Leukocytes Rolling Adhesion

Blood vessel endothelium at site of infection expresses selectin molecule P-selectin and E-selectin.Leukocytes such as neutrophils express the ligand for selectin in form of s-Lex .The binding of endothelial selectins to s-lex is weak and cannot hold the cell against the flow of blood .instead the cell rolls on the wall of the blood vessel making and breaking many interactions with the selectins

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Antigenic Drift

Pathogens such as influenza virus have receptors that enable them to bind host cell surfaces, Antibodies to these viral receptors prevent the virus to binding to and infecting the cells, these are neutralizing antibodies since they neutralize the ability to infect the cell. However some virus have mutation that alter the receptor in the ways to prevent binding of neutralizing antibodies, while leaving the virus able to bind to and infect host cells.

In this way the pattern of antigens expressed by the virus can change over time. This process of accumulation of small changes is called has antigenic drift and contributes our susceptibility to influenza infections.

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Germinal Centers

Germinal centers is place were B cells proliferates and undergoes both isotype switching and somatic hyper mutation,B cells are formed within Bcell follicle and lymphoid organs.
Formation of germinal center starts when dendritic cells display antigen on the surface ,which activates Antigen specific CD4 Tcells,which proliferate and mature into affector cells capable of activating Antigen specific B cells.


B cells enter into the follicle and begins to proliferate rapidly ,During this time it also undergoes somatic mutation to introduce new variation in the B cell receptor.
B cell undergoes process of selection after somatic mutation .When the receptors are tested for the ability to bind the antigen.
Those who fail to bind or fail to compete efficiently with other B cell receptors will die.

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Lymphocyte Trafficking

Naive T lymphocytes leave blood stream across the specialised endotherlial wall o blood vessel called High endothelial venule(HEV).
The specialized endothelium synthesis number of molecules which are involved in lymphocyte homing in the lymph node.In particlualr homing receptor GLYCAM1 and ICAM-1 and chemokine such as MIP3 beta.
Initial binding of Naive T cells to the vascular endothelium is mediated by L-selectin binding to GLYCAM1 ,subsequently chemokine binding occurs which triggers binding of intergin LFA-1 to its ligand ICAM1.

Lymphocytes are able to migrate across endothelium and into T cell area of lymph node.
Naive T cells can inspect Dendritic Cells in the lymph node for the presence of specific antigens.If T cells didn't recognise antigen,then T cells are not activated and passed out of lymph node to return to the circulation.
T cells that don meet the speciic antigen in the lymph node are activated and begins to proliferate and mature into effector cells.
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T Cell Granule Release

Cytotoxic T cells contains number of cytoplasmic organnels,cells like golgi apparatus and micro tubule prganising center are common to all the cells,others like cytotoxic garnaules are formed cD8 T cells and natural killers
During interaction of Cytotoxic T cells with the targets these organnels will become redistributed win cytoplasm of the T cells,So that it can allow T cells to deliver effective function directly on the target cells.

Th LFA1 mediates the initial contact with the potential target cells and binding to it in ICAM-1.If the T cell receptor finds no specific antigen on target cell,then T cell is not activated abd T cells Dis engages itself
If T cell receptor finds the specific antigen on the target cell,it becomes activated.Changes occur is\n cytosol of T cells in which cytoplasmic organelles in the T cells moves to face the target cells.
This Reorganization directs both granules and new protein synthesis into interphase between T cells and target cells.
Cytokines like interleukin 2 and interferon γ released from golgi and directed towards the target cells.

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Immunological Synapse

Immunological synapse is the interface between an antigen-presenting cell and a lymphocyte. It was first discovered by Abraham Kupfer at the National Jewish Center in Denver and the term was coined by Michael Dustin at NYU who studied it in further detail. Key molecules in the synapse are the T cell receptor and its counterpart the major histocompatibility complex (MHC). Also important are LFA-1, ICAM-1, CD28, and CD80/CD86. The structure is composed of concentric rings, the C-SMAC, the P-SMAC, and the D-SMAC each containing a peculiar mix of molecules.




Immunological synapse. (2009, June 3). In Wikipedia, The Free Encyclopedia. Retrieved 03:03, June 3, 2009, from http://en.wikipedia.org/w/index.php?title=Immunological_synapse&oldid=294087337

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Dendritic Cell Migration

Dendritic cells (DCs) are immune cells and form part of the mammalian immune system. Their main function is to process antigen material and present it on the surface to other cells of the immune system, thus functioning as antigen-presenting cells.

Dendritic cells are key presenting cells in the immune system,The are generated from Bone marrow nd migrate into proliferal tissue through the blood stream,Immature dendritic cell wait for pathogen entry(site of injury).
Dendritic cells express various pattern recognistion receptors that can recognse common features of many bacteria and fungal pathogens.Through this receptor dendritic cells bind and phagocyotsis pathogens,When this receptor bind to the pathogens the activate the dendritic cell which then starts to mature.
In this process dendritic cells migrate to the tissue and changes its behaviour to stop phagocytosis and start expressing immune stimulatory molecules
Activated dendritic cells migrate from tissue to lumphatic vessel,with lymphatic fluid drain to lymph node carrying dendritic cells with it.
T cells migrates through lymph node inspects teh dendritic cells for the presence of specific antigen.T cells which fail to recognize antigens on one dendritic cells carryon to inspect others.
T cells which recognise the specific antigen becomes activated and both proliferated and differntialte into a factor cells.

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TCR-APC Interaction

Antigen Presenting cells express both MHC molecules,in this case MHC II molecule co stimulator molecule such as CD80.Stimulation of T cells in this case CD4 tcell by the antigen presenting cell involves the interaction of T cell receptor and co receptor molecule with the MHC peptide complex.As well as the interaction between the  CD80 and CD28.The interaction of antigen presenting cell with T cell causes signals to pass in both direction.Signalling the antigen presenting cell to express additional co-stimulatary molecules such as CD86 and CD40.At the same time signals to T cell receptor and CD28 induce T cell to express CD40L(CD40 ligand).the interaction between CD40L and CD40 As well the additional stimulation through CD28 mediated by interaction with CD86 resolved in full activation of CD4 T cell.


Activation of CD8 T cell also requires multiple receptor ligand interaction ,the same activation siganals induce the antigen presenting cell to express other co-stimulatary molecules such as 4-1BBL ligand (4-1BBL),while initial activation of  CD8 T cells induces the expression of 4-1BB,Binding of 411B ligand to 41BB is thought to required for full activation of CD8 T cells. 

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T Cell Killing

Viruses are inter-cellular pathogen that infects the cells of the body. Degradation of virus protein inside the cell allows viral peptide to display on the surface of the cell bound to MHC class 1 protein.CD8 T cells, which recognize MHC peptide complexes, are activated and kill the infected cell. Having killed 1 cell the T cell can move to new target kill that cell and move on again




The killing process is initiated when the T cell receptors and CD8 together bind to MHC class 1 molecule bearing a viral peptide producing the signals that activate the T cell.

Cytotoxic T cell contain membrane vesicle called cytotoxic granules, which package the protein that kills target cells, The most important of these is protein called perforin and set of proteases called granzymes, these proteins are complexed with scaffolding protein called serglycin.

Activation of T cells causes the release content of the vesicles, delivering protein on the surface of the target cells,

Although the exact mechanism is not known the Perforin facilitates the delivery of the granzymes into the cytosol, at this point the target cell are destined for death and the T cell can migrate onward to find new target cells.

The process of cell death initiated by grandzymes uses the same basic cellular machinery that gives rise to apotosis. The granzymes target various cellular proteins that regulate apoptosis such as BID and pro-caspase-3, The granzymes cleaves the BID which in its truncated form causes cytocrome C to release from the mitochondria into the cytosol, simultaneously granzymes activates pro caspase -3 which in turn cleaves ICAD the inhibitor of CAD (caspase activated DNA)

The activated DNA migrates into the nucleus where it degrades the DNA ensuring the death of the cell.

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Lymph Node Development

Lymph node is an organ consisting of many types of cells, and is a part of the lymphatic system. Lymph nodes are found all through the body, and act as filters or traps for foreign particles. They contain white blood cells. Thus they are important in the proper functioning of the immune system.

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Chemokine Signaling

Chemokine receptors associate with G-proteins to transmit cell signals following ligand binding. Activation of G proteins, by chemokine receptors, causes the subsequent activation of an enzyme known as phospholipase C (PLC). PLC cleaves a molecule called phosphatidylinositol (4,5)-bisphosphate (PIP2) into two second messenger molecules known as Inositol triphosphate (IP3) and diacylglycerol (DAG) that trigger intracellular signaling events; DAG activates another enzyme called protein kinase C (PKC), and IP3 triggers the release of calcium from intracellular stores. These events promote many signaling cascades (such as the MAP kinase pathway) that generate responses like chemotaxis, degranulation, release of superoxide anions and changes in the avidity of cell adhesion molecules called integrins within the cell harbouring the chemokine receptor.

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DTH Response

Delayed type hypersensitivity (DTH) reactions are antigen-specific, cell-mediated immune responses which, depending on the antigen involved, mediate beneficial (resistance to viruses, bacteria, fungi, and tumors) or harmful (allergic dermatitis, autoimmunity) aspects of immune function. Cutaneous DTH reactions are initiated when CD4 memory T cells are activated by Langerhans cells and other antigen-presenting cells in the skin. Upon activation, CD4 T cells release inflammatory mediators which recruit effector cells to the site of antigen administration. While the monocyte/macrophage is thought to be the major effector cell in this model, CD8+ cytolytic T cells, and NK cells are also thought to serve as effector cells in DTH reactions. Activated effector cells mount an inflammatory response which results in the elimination of antigen and the extravasation of plasma accompanied by selling at the site of challenge. The magnitude of the response to the antigen is measured as an increase in swelling at the site of challenge.

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Killer T Cell

This video shows the actions of a killer T cell that attacks a fibroblast.

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Hemagglutinin

Hemogglutinin is a membrane fusion protein expressed on the surface of influenza virus. By mediating the fusion of viral and cellular membranes during infection it allows the viral genome to enter the cells.During the fusion reaction, hemoggluttinin inserts a hydrophobic fusion peptide into the host cell membrane and it becomes integral membrane protein in the two lipid bilayers



Tran membrane helix that anchors hemoggluttinin in the viral membrane is omitted from the structure.

Fusion reaction is triggered by low ph, which the virus encounters after the up taking endosomes of the host cell. This change in ph leads to massive structural change including the formation of long alpha helix in the core of protein.

Fusion peptide, which are previously tucked away from protein stock are displayed prominently in the tip of helix, ready to slip into host cell membrane.



Fusion peptide had to removed from the protein to be allowed for crystallization.
On the viral surface of hemogglutinin is a complex with 3 identical sub units.
It is likely the considered action of small number of hemogglutinin trimers is required to trigger a membrane fusion effect.

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Intracellular Listeria Infection

Listeriosis is an infection caused by the gram-positive motile bacterium Listeria monocytogenes.1,2 Listeriosis is relatively rare and occurs primarily in newborn infants, elderly patients, and patients who are immunocompromised.

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Leukocyte Rolling

Leukocytes are white blood cells that help in fighting infection (at site of injury, infection or inflammation). Cytokines are released which stimulate endothelial cells, which lines adjacent blood vessel. Endothelial cells express surface proteins called Selectins.


Selectins binds to carbohydrates in membrane of leukocytes causing it to stick to walls of blood vessel. Binding interaction is insufficient lower affinity that leukocytes can roll on along the vessel wall in search for points to exit.

Leukocytes adhere tightly and squeeze between endothelial cells without disturbing the vessel walls and crawl out of the blood vessel to adjacent connective tissue

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Listeria Parasites

Listeria parasites move throughout the cytosol of an infected cell by recruiting host cell actin.

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Plant Cell Division

Video on plant cell Division

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Mitotic Spindles Video

This video demonstrates the process of division in the mitotic spindles of a fly embryo

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Sea Urchin Fertilization

Video on Sea Urchin Fertilization

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Microtubule and ER Dynamics

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Organelle Movement on Microtubules

This video deomonsrates the movement of organlles on microtubules.

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Cell Compartments

Video on Cell compartment

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Exocytotic Transport

Video shows the path of proteins exiting the Golgi apparatus on the way to the cell surface.

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Endosome Fusion

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Intermediate Filaments

Animation on Intermediate Filaments,its structure andits function

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Microtubule Dynamics IN VIVO

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Neurite Outgrowth

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Neuronal Pathfinding

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Tomogram of a Mitochondrion

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Embryonic development of Tadpole

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Keratocytes

The fibroblastic stromal cell of the cornea. Keratocytes produce keratan-sulfate proteoglycans (KSPG), lumican and keratocan to form and sustain proper collagen interfibrillar spacing and fibril diameter of the cornea.

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Eutreptiella

Eutreptiella use both flagella and pronounced cell shape changes to swim.

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Fluidity of the Lipid Bilayer

Video on Fuluidity of Lipid Bilayer

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Red blood cell treated with Detergent

When detergent is added to red blood cell the membrane ruptures and cytosol spills out

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Red Blood Cell Membrane

Animation is about Red blood cells membrane,it talks about different functions of red blood cell membrane .

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Hair cells

  • The sound sensitive cells in our ear is called hair cells, Each has a tough spiky extensions called Stereocilia on its upper surface and each sends signal to auditory nerve fibers through its basal surface.
  • Hair cells are embedded in a layer supporting cells and are sandwiched between two sheaths extra cellular matrix, the tectorial membrane and basilar membrane.


  • Sound vibrations cause the basilar membrane to vibrate, and this motion pushes the Stereocilia against the tectoral membrane.
  • Stereocilia tilt, triggering an electrical response in the hair cells, the activated hair cell in turn activates the auditory nerve cells.
  • Hair cell membrane contains stretch activated ion channels; these channels are closed when Stereocilia is not tilted.
  • However, when the steroecilia tilt a linking the filament from one Stereocilium to the channel neighboring stereocilium pulls at the channel opening it. Positive charged ions flow into the cell and depolarizing the membrane

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Synaptic Signaling

Neurons transmits chemical signal across synapses. The synapse converts the electrical signal of the action potential in the pre synaptic cell into a chemical signal.

When the action potential reaches then nerve terminal it opens voltage-gated calcium channels in the plasma membrane allowing calcium ions to flow into the terminal.


Increased calcium in the nerve terminal stimulates synaptic vesicle to fuse with the plasma membrane releasing the neural transmitter cargo into the synaptic cleft.

Released neuro transmitters diffuse across the synaptic cleft where the bind to and open transmitter gated ion channels in plasma membrane of postsynaptic cell.

Resulting ion flows depolarize the plasma membrane of the postsynaptic cell, thereby converting neurotransmitters chemical signal back into an electrical one that can be propagated as a new action potential.

Enzymes that destroy it or reuptake into nerve terminals or neighboring cells remove neural transmitter quickly from synaptic cleft.

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Animal Cell Division

Animation on Animal Cell Division

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Wound Healing animation

This Animation shows how cell react to wound and how healing takes place

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MHC Class I Processing

  • Folding assembly of MHC class 1 molecule takes place in the lumen of ER.Initially folding of Class1 alpha chain is aided by calnexin chaperone.
  • Partially folded chain is transferred to second chaperone calrecticulam,which further  aids   folding  the chain and association with beta 2-Microglobulin.
  • Other proteins Frp57 and tapasin associate with it.
  • Class I molecule binds with the TAP Transporter to form peptide Loading complex.
  • The peptides that bind to MHC class 1 proteins are geneated by Proteosomes.
  • In cytoplasm Proteasome generates peptide fragments which will bind to MHC class 1 Protein.
  • The proteasome degrades protein into shorter fragments within cytosol and transports it to ER by TAP transporter.
  • By the process of Peptide ending ,non-binding and unstable peptides are released from ER.
  • Peptides with stable affinity binds with MHC molecule form stable complex.
  • Final phase of folding MHC class 1 molecule takes place.
  • Disassociation of Peptide Holding Complex takes place.
  • Peptide loaded with MHC class 1 molecule exits from ER and Moves to Cell surface with help of Golgi apparatus.where its recognized by by Antigen Receptors of CD8 Tcells.

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MHC Class 1 Protein

MHC class I proteins display short peptides, or antigens, derived from normal cell proteins. Peptide-loaded MHC proteins are located on the cell surface where they can be examined by passing T cells of the immune system. The MHC complex has two subunits. The smaller subunit, b2 microglobulin, resembles an immunoglobulin domain.

The larger a subunit also has an immunoglobulin-like domain which is linked to a head domain containing the antigen-binding groove. The antigen-binding groove in the MHC head domain is built from two walls composed of long alpha helices that rest on a floor composed of an eight stranded beta sheet. The peptide on display fits snugly between the helices in the groove.The peptide backbone is bound at both ends by highly conserved regions of the MHC protein. Some peptide side chains extend downwards into specific binding pockets in the groove, while other peptide side chains project upwards where they can be recognized by T cells. MHC class I proteins display their bound peptides on the cell surface for immune surveillance. Immune cells, called cytotoxic or killer T cells, for example, express T-cell receptors that bind to the MHC head domain and the bound peptide. If the cell expressing the MHC protein displays a peptide foreign to the immune system, the T cell is activated by this receptor-MHC interaction. The activated T cell then proceeds to destroy the abnormal cell. Cut-away views of this peptide-bound MHC protein complexed with a T-cell receptor reveal the exquisite precision with which the interacting surfaces fit together.

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HCV infection and Immune Response Video

This Animation shows how HCV infection and Replication


This animation shows The cells Response To HCV



These two Animation shows TCell response to HCV
T cell response to MHC II



Proliferation of T cell by IL-10

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Anatomy and Diseases of the Basal Ganglia

Basal ganglia (or basal nuclei) are a group of nuclei in the brain interconnected with the cerebral cortex, thalamus and brainstem. Mammalian basal ganglia are associated with a variety of functions: motor control, cognition, emotions, and learning. In modern use the term 'ganglia' is in this instance considered a misnomer; 'ganglion' refers to concentrations of neural nuclei in the periphery only (for example those of the autonomic nervous system), and the term 'basal nuclei' is preferred.


The five individual nuclei that make up the primate basal ganglia, along with their major subdivisions, are:
rostral
the striatum, which consists of
putamen
caudate nucleus
external segment of the globus pallidus (GPe)
internal segment of the globus pallidus (GPi)
caudal
subthalamic nucleus (STN)
substantia nigra (SN)
substantia nigra pars compacta (SNc)
substantia nigra pars reticulata (SNr)
substantia nigra pars lateralis (SNl)
There are 2 sets of basal ganglia in the mammalian brain, mirrored in the left and right hemispheres.
Two coronal sections are used to show the basal ganglia; the STN and substantia nigra lie deeper back in the brain (more caudal). Images show two schematic coronal cross-sections of the human brain with nuclei of the basal ganglia labeled on the right side.
Functionally, the basal ganglia consist of a series of circuits, such as skeletomotor, limbic and occulomotor circuits. Each circuit projects to specific nuclei within the basal ganglia and its projections e.g. the skeletomotor circuit projects to the ventral lateral, lateral ventral anterior and centromedian thalamic nuclei.


Test source

Basal ganglia. (2009, May 19). In Wikipedia, The Free Encyclopedia. Retrieved 22:08, May 19, 2009, from http://en.wikipedia.org/w/index.php?title=Basal_ganglia&oldid=291041764

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Intestinal Fatty Acid Binding Protein

The intestinal fatty acid binding protein (I-FABP) belongs to a family of 15 kDa clamshell-like proteins that are found in many different tissues. So far, nine types have been identified. Their primary structures are highly conserved between species but somewhat less so among the different types. The function of these proteins, many of which are highly expressed, is not well understood. Their ability to bind lipid ligands suggests a role in lipid metabolism, but direct evidence for this idea is still lacking.

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What causes neuronal death in Alzheimer's disease.

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Pathophysiology of Schizophrenia

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Lipoproteins that Circulate in the Blood Collecting Fat

High-density lipoproteins (HDL), often referred to as the "Good Cholesterol", circulates in the blood stream collecting fat and cholesterol from arteries and transporting them to the liver for removal. The movie shows how these lipoproteins (in blue and green) can gather the fat molecules (in white and brown) into small particles allowing them to flow through blood vessels.

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EGFR Pathway

EGFR is a transmembrane tyrosine kinase receptor that plays a central role in regulating cell division and death. EGFR belongs to the HER family of receptors which comprise four related proteins (EGFR(HER1/ErbB1), ERBB2(HER2), ERBB3(HER3) and ERBB4(HER4)). The HER receptors are known to be activated by binding to different ligands, including EGF, TGFA, heparin-binding EGF-like growth factor, amphiregulin, betacellulin, and epiregulin. After a ligand binds to the extracellular domain of the receptor, the receptor forms functionally active dimers (EGFR-EGFR (homodimer) or EGFR-HER2, EGFR-HER3, EGFR-HER4 (heterodimer)). Dimerization induces the activation of the tyrosine kinase domain, which leads to autophosphorylation of the receptor on multiple tyrosine residues. This leads to recruitment of a range of adaptor proteins (such as SHC, GRB2) and activates a series of intracellular signaling cascades to affect gene transcription, which in turn results in cancer cell proliferation, reduced apoptosis, invasion and metastasis and also stimulates tumor-induced angiogenesis.



The pathways mediating downstream effects of EGFR have been well studied and three major signalling pathways have been identified. The first pathway involves RAS-RAF-MAPK pathway, where phosphorylated EGFR recruits the guanine-nucleotide exchange factor via the GRB2 and Shcadapter proteins, activating RAS and subsequently stimulating RAF and the MAP kinase pathway to affect cell proliferation, tumor invasion, and metastasis. The second pathway involves PI3K/AKT pathway, which activates the major cellular survival and anti-apoptosis signals via activating nuclear transcription factors such as NFKB. The third pathway involves JAK/STAT pathway which is also implicated in activating transcription of genes associated with cell survival. EGFR activation may also lead to phosphorylation of PLCG and subsequent hydrolysis of phosphatidylinositol 4,5 biphosphate (PIP2) into inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG), resulting in activation of protein kinase C (PRKC) and CAMK.

Given the prominent importance of EGFR signaling in cancer development, both anti-EGFR monoclonal antibodies and small-molecule EGFR tyrosine kinase inhibitors have been developed. Anti-EGFR antibodies, eg. cetuximab and panitumumab, bind to the extracellular domain of EGFR monomer and compete for receptor binding by the endogenous ligands; in this way they block ligand-induced receptor activation. The small molecule EGFR inhibitors, such as erlotinib, gefitinib and lapatinib, compete with ATP to bind the catalytic domain of the kinase which in turn inhibits EGFR autophosphorylation and downstream signaling. However, these inhibitors are known to be effective in only a small subset of patients. Mutations in the EGFR gene and possible down-stream effectors have been shown to be associated with various clinical outcomes associated with EGFR inhibitor treatments

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EGFR

The epidermal growth factor receptor (EGFR; ErbB-1; HER1 in humans) is the cell-surface receptor for members of the epidermal growth factor family (EGF-family) of extracellular protein ligands. The epidermal growth factor receptor is a member of the ErbB family of receptors, a subfamily of four closely related receptor tyrosine kinases: EGFR (ErbB-1), HER2/c-neu (ErbB-2), Her 3 (ErbB-3) and Her 4 (ErbB-4). Mutations affecting EGFR expression or activity could result in cancer.


Function


EGFR (epidermal growth factor receptor) exists on the cell surface and is activated by binding of its specific ligands, including epidermal growth factor and transforming growth factor α (TGFα) (note, a full list of the ligands able to activate EGFR and other members of the ErbB family is given in the ErbB article). ErbB2 has no known direct activating ligand, and may be in an activated state constitutively or become active upon heterodimerization with other family members such as EGFR.

Upon activation by its growth factor ligands, EGFR undergoes a transition from an inactive monomeric form to an active homodimer - although there is some evidence that preformed inactive dimers may also exist before ligand binding. In addition to forming homodimers after ligand binding, EGFR may pair with another member of the ErbB receptor family, such as ErbB2/Her2/neu, to create an activated heterodimer. There is also evidence to suggest that clusters of activated EGFRs form, although it remains unclear whether this clustering is important for activation itself or occurs subsequent to activation of individual dimers.

EGFR dimerization stimulates its intrinsic intracellular protein-tyrosine kinase activity. As a result, autophosphorylation of several tyrosine (Y) residues in the C-terminal domain of EGFR occurs. These include Y992, Y1045, Y1068, Y1148 and Y1173 as shown in the diagram to the left.This autophosphorylation elicits downstream activation and signaling by several other proteins that associate with the phosphorylated tyrosines through their own phosphotyrosine-binding SH2 domains. These downstream signaling proteins initiate several signal transduction cascades, principally the MAPK, Akt and JNK pathways, leading to DNA synthesis and cell proliferation. Such proteins modulate phenotypes such as cell migration, adhesion, and proliferation. Activation of the receptor is important for the innate immune response in human skin . The kinase domain of EGFR can also cross-phosphorylate tyrosine residues of other receptors it is aggregated with, and can itself be activated in that manner.

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DMT biosynthesis

Dimethyltryptamine (DMT), also known as N,N-dimethyltryptamine, is a naturally-occurring tryptamine and potent psychedelic drug,found not only in many plants, but also in trace amounts in the human body where its natural function is undetermined. Structurally, it is analogous to the neurotransmitter serotonin and other psychedelic tryptamines such as 5-MeO-DMT and 4-HO-DMT. DMT is created in small amounts by the human body during normal metabolism by the enzyme tryptamine-N-methyltransferase. Many cultures, indigenous and modern, ingest DMT as a psychedelic in extracted or synthesized forms. Pure DMT at room temperature is a clear or white to yellowish-red crystalline solid. A laboratory synthesis of DMT was first reported in 1931, and it was later found in many plants


Dimethyltryptamine. (2009, June 16). In Wikipedia, The Free Encyclopedia. Retrieved 03:23, June 16, 2009, from http://en.wikipedia.org/w/index.php?title=Dimethyltryptamine&oldid=296681896

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Stroke Basics

Stroke is the third leading killer and the most common cause of adult disability in the United States. When a stroke happens, minutes matter. Knowing the signs of a stroke and acting quickly are essential. Join David Granet, MD, and his guest, Patrick Delaney, MD, noted stroke expert and author of The Legend Healer, as they discuss stroke basics.

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Darvocet

Dextropropoxyphene, manufactured by Eli Lilly and Company, is an analgesic in the opioid category. It is used to treat mild pain and is additionally an anti-tussive and local anesthetic.

Dextropropoxyphene is sometimes combined with acetaminophen or acetylsalicylic acid. Trade-names include Darvocet-N and DigesicDarvon with APAP for dextropropoxyphene and paracetamol and Darvon with ASA for dextropropoxyphene and aspirin. The paracetamol combination(s) are known as co-proxamol or in the United Kingdom, Capadex or Di-Gesic in Australia, and Lentogesic in South Africa.

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SDS-PAGE

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Genomic Revolution

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Genomic Advances on a Grand Scale

For more than two decades J. Craig Venter and his research teams have been pioneers in genomic research. Regarded as one of the leading scientist of the 21st century, Venter discusses how he is applying tools and techniques developed to sequence the human genomes to discover new genes of microbes from around the world.
J. Craig Venter is an American biologist and businessman. Venter founded The Institute for Genomic Research and has been credited with being instrumental in mapping the human genome.His for-profit efforts used public domain data generated by the Human Genome Project, but could be used to generate high quality data on their own. He was listed on Time Magazine's 2007 and 2008 Time 100 list of the most influential people in the world.

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Muscle contractile protiens

Myofibrils (obsolete term: sarcostyles) are cylindrical organelles. They are found within muscle cells. They are bundles of actomyosin filaments that run from one end of the cell to the other and are attached to the cell surface membrane at each end.

Actomyosin motors are important in muscle contraction (relying in this case on "classical myosins") as well as other processes like retraction of membrane blebs, filiopod retraction, and uropodium advancement (relying in this case on "nonclassical myosins").

Structure

The filaments of myofibrils, myofilaments, consist of two types, thick and thin.

* Thin filaments consist primarily of the protein actin, coiled with nebulin filaments.
* Thick filaments consist primarily of the protein myosin, held in place by titin filaments.

The protein complex composed of actin and myosin is sometimes referred to as "actomyosin."

In striated muscle, such as skeletal and cardiac muscle, the actin and myosin filaments each have a specific and constant length on the order of a few micrometers, far less than the length of the elongated muscle cell (a few millimeters in the case of human skeletal muscle cells). The filaments are organized into repeated subunits along the length of the myofibril. These subunits are called sarcomeres. The muscle cell is nearly filled with myofibrils running parallel to each other on the long axis of the cell. The sarcomeric subunits of one myofibril are in nearly perfect alignment with those of the myofibrils next to it. This alignment gives rise to certain optical properties which cause the cell to appear striped or striated. In smooth muscle cells, this alignment is absent, hence there are no apparent striations and the cells are called smooth.
Myofibril. (2009, June 13). In Wikipedia, The Free Encyclopedia. Retrieved 00:09, June 13, 2009, from http://en.wikipedia.org/w/index.php?title=Myofibril&oldid=296076817

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Ion Channel Coupled Receptors

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Low Back Pain

Dr. John Chardos Department of Medicine (VA) on the cause, treatment and prevention of low back pain. Most people have experienced low back pain at one time or another, so it is no surprise that it is one of the most common problems in primary care. Although it is so common, it is not clear how to best treat back pain. John Chardos, MD presents information to better understand back pain and what can be done to manage it

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Male Physiology

Spermatogenesis is the process by which male spermatogonia develop into mature spermatozoa. Spermatozoa are the mature male gametes in many sexually reproducing organisms. Thus, spermatogenesis is the male version of gametogenesis. In mammals it occurs in the male testes and epididymis in a stepwise fashion, and for humans takes approximately 64 days.permatogenesis is highly dependent upon optimal conditions for the process to occur correctly, and is essential for sexual reproduction. It starts at puberty and usually continues uninterrupted until death, although a slight decrease can be discerned in the quantity of produced sperm with increase in age. The entire process can be broken up into several distinct stages, each corresponding to a particular type of cell:

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Nano Hazards nanosilver enviroment

This is a video about nanosilver, which you can find in many of your daily products. It is explained here, what happens to it, when you have used the product, & what it could do to the enviroment.

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Woolly Mammoth DNA discovered

Scientists in the U.S. have discovered the genetic code of the woolly mammoth, an animal that's been extinct since the Ice Age. It's led to fevered speculation that there might one day be hope of reviving it.Researchers who bought mammoth hair on the internet have decoded 70% of the creature's genome, marking the first time the nearly complete genome of an extinct animal has been sequenced


The woolly mammoth (Mammuthus primigenius), also called the tundra mammoth, is an extinct species of mammoth. This animal is known from bones and frozen carcasses from northern North America and northern Eurasia with the best preserved carcasses in Siberia.

This mammoth species was first recorded in (possibly 150,000 years old) deposits of the second last glaciation in Eurasia. They were derived from steppe mammoths (Mammuthus trogontherii).

It disappeared from most of its range at the end of the Pleistocene (10,000 years ago), with a dwarfed race still living on Wrangel Island until roughly 1700 BC.

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Ghrelin Hormone

Ghrelin is a hormone produced mainly by P/D1 cells lining the fundus of the human stomach and epsilon cells of the pancreas that stimulates hunger. Ghrelin levels increase before meals and decrease after meals. It is considered the counterpart of the hormone leptin, produced by adipose tissue, which induces satiation when present at higher levels. In some bariatric procedures, the level of ghrelin is reduced in patients, thus causing satiation before it would normally occur.
Recently Scientist found that Ghrelin chages how your brain perceives food.



Mechanism of action

Ghrelin has emerged as the first circulating hunger hormone. Ghrelin and synthetic ghrelin mimetics (the growth hormone secretagogues) increase food intake and increase fat mass by an action exerted at the level of the hypothalamus. They activate cells in the arcuate nucleus that include the orexigenic neuropeptide Y (NPY) neurons. Ghrelin-responsiveness of these neurones is both leptin- and insulin-sensitive. Ghrelin also activates the mesolimbic cholinergic-dopaminergic reward link, a circuit that communicates the hedonic and reinforcing aspects of natural rewards, such as food, as well as of addictive drugs, such as ethanol.



Text reference:"Ghrelin." Wikipedia, The Free Encyclopedia. 23 Jun 2009, 02:34 UTC. 23 Jun 2009 <http://en.wikipedia.org/w/index.php?title=Ghrelin&oldid=298044461>.

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From cell to Embryo

An embryo is a multicellular diploid eukaryote in its earliest stage of development, from the time of first cell division until birth, In humans, it is called an embryo until about eight weeks after fertilization


Stages of Development

Week 1-3 5-7 days after fertilization, the blastula attaches to the wall of the uterus (endometrium). When it comes into contact with the endometrium it performs implantation. Implantation connections between the mother and the embryo will begin to form, including the umbilical cord. The embryo's growth centers around an axis, which will become the spine and spinal cord. The brain, spinal cord, heart, and gastrointestinal tract begin to form.

Week 4-5 Chemicals produced by the embryo stop the woman's menstrual cycle. Neurogenesis is underway, showing brain activity at about the 6th week. "The heart will begin to beat around the same time. Limb buds appear where the arms and legs will grow later. Organogenesis begins. The head represents about one half of the embryo's axial length, and more than half of the embryo's mass. The brain develops into five areas. Tissue formation occurs that develops into the vertebra and some other bones. The heart starts to beat and blood starts to flow.

Week 6-8 Myogenesis and neurogenesis have progressed to where the embryo is capable of motion, and the eyes begin to form. Organogenesis and growth continue. Hair has started to form along with all essential organs. Facial features are beginning to develop. At the end of the 8th week, the embryonic stage is over, and the fetal stage begins.

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Mulitplex Microarray Hybridization

ArrayIt® has developed an innovative solution to multi-well microarrays that includes glass substrate slides containing a hydrophobic mask for well creation and a submersible hybridization cassette that allows temperature-controlled reactions without sample evaporation. Twenty four microarrays in a 3 x 8 pattern can be printed, reacted, scanned and quantified on a single glass substrate slide, offering highly affordable sample multiplexing for research and diagnostics.



Designed for up to 24 high or low biochemical reactions on a single microarray substrate or slide. The unit is air tight to prevent evaporation and water proof, therefore short and extended reactions can be run in a high or low temperature controlled water bath or oven. This 24 well submersible hybridization cassette fits one 24 well masked substrate for 24 separate microarray reactions using a single cassette. No cover slips required.

This submersible cassette is made from a durable, flat, precision-machined corrosion resistant alloy and high quality black rubber gasket to ensure proper alignment and no leaking from “well to well”.


For more Information Visit:http://www.arrayit.com/Products/Microarray_Tools/Multiplex_Microarrays/multiplex_microarrays.html

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Swine Flu Immunity video

Swine influenza (also called swine flu, hog flu, and pig flu) refers to influenza caused by those strains of influenza virus, called swine influenza virus (SIV), that usually infect pigs. Swine influenza is common in pigs in the midwestern United States (and occasionally in other states), Mexico, Canada, South America, Europe (including the United Kingdom, Sweden, and Italy), Kenya, Mainland China, Taiwan, Japan and other parts of eastern Asia.

Transmission of swine influenza virus from pigs to humans is not common and properly cooked pork poses no risk of infection. When transmitted, the virus does not always cause human influenza and often the only sign of infection is the presence of antibodies in the blood, detectable only by laboratory tests. When transmission results in influenza in a human, it is called zoonotic swine flu. People who work with pigs, especially people with intense exposures, are at risk of catching swine flu. However, only about fifty such transmissions have been recorded since the mid-20th Century, when identification of influenza subtypes became possible. Rarely, these strains of swine flu can pass from human to human. In humans, the symptoms of swine flu are similar to those of influenza and of influenza-like illness in general, namely chills, fever, sore throat, muscle pains, severe headache, coughing, weakness and general discomfort.

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Using Dendritic Cells to Create Cancer Vaccines

Edgar Engleman, MD, medical director of the Stanford Blood Center, discusses his research involving the use of a special type of white blood cell as a treatment for cancer. Engleman, who is also a professor of pathology at the Stanford School of Medicine, and his team of researchers have been interested in dendritic cells, or DCs, which can provoke an immune response in the body.


The goal of this laboratory is to better understand dendritic cell biology with the objective of using this information to discover and develop more effective immunotherapeutic approaches to disease. We pursue this goal by performing experiments in both mice and humans. In our initial clinical studies antigen pulsed dendritic cells were administered to patients with cancer or life-threatening viral infections in order to induce specific immunity. The results of these trials have been extremely encouraging. More recently we have focused our studies on the development and life cycle of dendritic cells, including Langerhans cells, and the results have not only shed new light on dendritic cell biology but also have led to our ability to target dendritic cells in vivo without having to manipulate these cells in vitro. We believe that this new approach will eventually make it possible to downregulate as well as upregulate the immune system in an antigen specific manner.

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Bird flu

Avian influenza, sometimes Avian flu, and commonly Bird flu, refers to "influenza caused by viruses adapted to birds." Of greatest concern is highly pathogenic avian influenza (HPAI).

"Bird flu" is a phrase similar to "Swine flu," "Dog flu," "Horse flu," or "Human flu" in that it refers to an illness caused by any of many different strains of influenza viruses that have adapted to a specific host. All known viruses that cause influenza in birds belong to the species: Influenza A virus. All subtypes (but not all strains of all subtypes) of Influenza A virus are adapted to birds, which is why for many purposes avian flu virus is the Influenza A virus (note that the "A" does not stand for "avian").

Adaptation is non-exclusive. Being adapted towards a particular species does not preclude adaptations, or partial adaptations, towards infecting different species. In this way strains of influenza viruses are adapted to multiple species, though may be preferential towards a particular host. For example, viruses responsible for influenza pandemics are adapted to both humans and birds. Recent influenza research into the genes of the Spanish Flu virus shows it to have genes adapted to both birds and humans; with more of its genes from birds than less deadly later pandemic strains.

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Electrophysiology of the Heart

Some tissues such as heart and nerves are able to generate electrical signals without external electrical stimulation.Heart's electrical impulses are conducted by two types of cardiac tissues ,a specialized cardiac conduction system .including sinoatrial Node or SA node,inter nodal track,Atrioventricular Node(AV node),Bundle of HIS, right and left Bundle branches,purkinje network and myocardium.

SA node the primary pacemaker of the heart exhibits rapid automaticity firing at regular rate and causes heart to be at rhythmically.Electrical impulses generated other than the SA nodes are abnormal and disrupts the normal heart rhythm

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G-Protein Coupled Receptors



Animation describing the role of G-protein coupled receptors in neurotransmission.

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Digestive Enzymes Therapy, Pancreatic Enzyme Therapy, Sytemic and Proteolytic Enzyme Therapy -

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Amniocentesis

Amniocentesis is a medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections , in which a small amount of amniotic fluid, which contains fetal tissues, is extracted from the amnion or amniotic sac surrounding a developing fetus, and the fetal DNA is examined for genetic abnormalities.





Procedure


Before the actual procedure, a local anesthetic is sometimes given to relieve the pain when inserting the needle used to withdraw the fluid. A needle is usually inserted through the mother's abdominal wall through the wall of the uterus into the amniotic sac. With the aid of ultrasound-guidance, a physician aims towards an area of the sac that is away from the fetus and extracts approximately 20ml of amniotic fluid for testing. The puncture heals, and the amniotic sac replenishes the liquid over a day or so. After the amniotic fluid is extracted, the fetal cells are separated from it. The cells are grown in a culture medium, then fixed and stained. Under a microscope the chromosomes are examined for abnormalities. The most common abnormalities detected are Down syndrome, Edward syndrome [Trisomy 18] and Turner syndrome [Monosomy X]. Amniocentesis is most safely performed after the 14th-16th week of pregnancy, does not need to be done before then due to risk it can do to the babys limbs. Usually genetic counseling is offered prior to amniocentesis.

Text source Refered From:http://en.wikipedia.org/wiki/Amniocentesis

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Female Physiology

part 2 Part 3

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Aldosterone Action on the Kidney

Aldosterone is a hormone that increases the reabsorption of sodium and water and the release (secretion) of potassium in the kidneys. This increases blood volume and therefore, increases blood pressure. Many drugs, such as spironolactone, lower blood pressure by blocking the aldosterone receptor. Aldosterone is part of the renin-angiotensin system.


Function
Aldosterone is the primary of several endogenous members of the class of mineralocorticoids in human. Deoxycorticosterone is another important member of this class. At the late distal tubule & collecting duct, aldosterone has three main actions:

  • Acting on the nuclear mineralocorticoid receptors (MR) within the principal cells of the distal tubule and the collecting duct of the kidney nephron, it increases the permeability of the apical (luminal) membrane to potassium and sodium and activates the basolateral Na+/K+ pumps, stimulating ATP hydrolysis leading to phosphorylation of the pump and a conformational change in the pump exposes the Na+ ions to the outside. The phosphorylated form of the pump has a low affinity for Na+ ions, hence reabsorbing sodium (Na+) ions and water into the blood, and secreting potassium (K+) ions into the urine. (Chlorine anions are also reabsorbed in conjunction with sodium cations to maintain the system's electrochemical balance.)
  • Aldosterone stimulates H+ secretion by intercalated cells in the collecting duct, regulating plasma bicarbonate (HCO3−) levels and its acid/base balance.
  • Aldosterone may act on the central nervous system via the posterior pituitary gland to release vasopressin (ADH) which serves to conserve water by direct actions on renal tubular reabsorption.

Aldosterone is responsible for the reabsorption of about 2% of filtered sodium in the kidneys, which is nearly equal to the entire sodium content in human blood under normal GFR (glomerular filtration rate).

Aldosterone, most probably acting through mineralocorticoid receptors, may positively influence neurogenesis in the dentate gyrus.


References


"Aldosterone." Wikipedia, The Free Encyclopedia. 22 Jun 2009, 02:13 UTC. 22 Jun 2009 <http://en.wikipedia.org/w/index.php?title=Aldosterone&oldid=297835998>.

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Anatomy of the Lens

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Ultram

Tramadol is a centrally acting analgesic, used for treating moderate to severe pain. It is a synthetic opioid and it appears to have actions at the μ-opioid receptor as well as the noradrenergic and serotonergic systems. Tramadol was developed by the German pharmaceutical company Grünenthal GmbH in the late 1970s and marketed under the trade name Tramal.


The mode of action of tramadol has yet to be fully understood, but it is believed to work through modulation of the noradrenergic and serotonergic systems in addition to its mild agonism of the μ-opioid receptor. The contribution of non-opioid activity is demonstrated by the fact that the analgesic effects of tramadol is not fully antagonised by the μ-opioid receptor antagonist naloxone.

Tramadol is marketed as a racemic mixture with a weak affinity for the μ-opioid receptor (approximately 1/6000th that of morphine; Gutstein & Akil, 2006). The (+)-enantiomer is approximately four times more potent than the (-)-enantiomer in terms of μ-opioid receptor affinity and 5-HT reuptake, whereas the (-)-enantiomer is responsible for noradrenaline reuptake effects (Shipton, 2000). These actions appear to produce a synergistic analgesic effect, with (+)-tramadol exhibiting 10-fold higher analgesic activity than (-)-tramadol (Goeringer et al., 1997).

The serotonergic-modulating properties of tramadol give tramadol the potential to interact with other serotonergic agents. There is an increased risk of serotonin syndrome when tramadol is taken in combination with serotonin reuptake inhibitors (e.g., SSRIs) or with use of a light box, since these agents not only potentiate the effect of 5-HT but also inhibit tramadol metabolism. Tramadol is also thought to have some NMDA-type antagonist effects, which has given it a potential application in neuropathic pain states.

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Breast cancer surgery: Modified Mastectomy

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Stem Cell in Facelifts Video

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Digital Tomosynthesis

Digital tomosynthesis creates a 3-dimensional picture of the breast using x-rays. Currently, digital tomosynthesis is available only for research purposes.
Digital tomosynthesis of the breast is different from a standard mammogram in the same way a CT scan of the chest is different from a standard chest x-ray. Or think of the difference between a ball and a circle. One is 3-dimensional, the other is flat.




Mammography usually takes two x-rays of each breast from different angles: top to bottom and side to side. The breast is pulled away from the body, compressed, and held between two glass plates to ensure that the whole breast is viewed. Regular mammography records the pictures on film, and digital mammography records the pictures on the computer. The images are then read by a radiologist. Breast cancer, which is denser than most healthy nearby breast tissue, appears as irregular white areas — sometimes called shadows.

Mammograms are very good, but they have some significant limitations:

  •  The compression of the breast that's required during a mammogram can be uncomfortable. Some women hate it, and it could deter them from getting the test.
  •  The compression also causes overlapping of the breast tissue. A breast cancer can be hidden in the overlapping tissue and not show up on the mammogram.
  •  Mammograms take only one picture, across the entire breast, in two directions: top to bottom and side to side. It's like standing on the edge of a forest, looking for a bird somewhere inside. To find the bird, it would be better to take 10 steps at a time through the forest and look all around you with each move.

Digital tomosynthesis is a new kind of test that's trying to overcome these three big issues. It takes multiple x-ray pictures of each breast from many angles. The breast is positioned the same way it is in a conventional mammogram, but only a little pressure is applied — just enough to keep the breast in a stable position during the procedure. The x-ray tube moves in an arc around the breast while 11 images are taken during a 7-second examination. Then the information is sent to a computer, where it is assembled to produce clear, highly focused 3-dimensional images throughout the breast.

Early results with digital tomosynthesis are promising. Researchers believe that this new breast imaging technique will make breast cancers easier to see in dense breast tissue and will make breast screening more comfortable.

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Herpes zoster

Herpes zoster (or simply zoster), commonly known as shingles, is a viral disease characterized by a painful skin rash with blisters in a limited area on one side of the body, often in a stripe. The initial infection with varicella zoster virus (VZV) causes the acute (short-lived) illness chickenpox, and generally occurs in children and young people. Once an episode of chickenpox has resolved, the virus is not eliminated from the body but can go on to cause shingles—an illness with very different symptoms—often many years after the initial infection.




The causative agent for herpes zoster is varicella zoster virus (VZV), a double-stranded DNA virus related to the Herpes simplex virus group. Most people are infected with this virus as children, and suffer from an episode of chickenpox. The immune system eventually eliminates the virus from most locations, but it remains dormant (or latent) in the ganglia adjacent to the spinal cord (called the dorsal root ganglion) or the ganglion semilunare (ganglion Gasseri) in the base of the skull. However, repeated attacks of herpes zoster are rare, and it is extremely rare for patients to suffer more than three recurrences.

Herpes zoster occurs only in people who have had chickenpox, and although it can occur at any age, the majority of sufferers are more than 50 years old. The disease results from the virus reactivating in a single sensory ganglion. In contrast to Herpes simplex virus, the latency of VZV is poorly understood. The virus has not been recovered from human nerve cells by cell culture and the location and structure of the viral DNA is not known. Virus-specific proteins continue to be made by the infected cells during the latent period, so true latency, as opposed to a chronic low-level infection, has not been proven. Although VZV has been detected in autopsies of nervous tissue, there are no methods to find dormant virus in the ganglia in living people.

Unless the immune system is compromised, it suppresses reactivation of the virus and prevents herpes zoster. Why this suppression sometimes fails is poorly understood, but herpes zoster is more likely to occur in people whose immune system is impaired due to aging, immunosuppressive therapy, psychological stress, or other factors. Upon reactivation, the virus replicates in the nerve cells, and virions are shed from the cells and carried down the axons to the area of skin served by that ganglion. In the skin, the virus causes local inflammation and blisters. The short and long-term pain caused by herpes zoster comes from the widespread growth of the virus in the infected nerves, which causes inflammation.

The symptoms of herpes zoster cannot be transmitted to another person. However, during the blister phase, direct contact with the rash can spread VZV to a person who has no immunity to the virus. This newly-infected individual may then develop chickenpox, but will not immediately develop shingles. Until the rash has developed crusts, a person is extremely contagious. A person is also not infectious before blisters appear, or during postherpetic neuralgia (pain after the rash is gone). The person is no longer contagious after the virus has disappeared.

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Vasectomy

Vasectomy is a minor surgical procedure wherein the vasa deferentia of a man are severed, and then tied or sealed in a manner such to prevent sperm from entering the seminal stream
Types

Typically done in an outpatient setting, a traditional vasectomy involves numbing (local anesthetic) of the scrotum after which 1 (or 2) small incisions are made, allowing a surgeon to gain access to the vas deferens. The "tubes" are cut and sealed by tying, stitching, cauterization (burning), or otherwise clamped to prevent sperm from entering the seminal stream. Variations of the procedure have been explored/used in hopes of reducing recovery time and pain (in recovery and post-surgery). The "Vas-Clip" method does not require cutting the Vas Deferens, but rather uses a clip to squeeze shut the flow of sperm. This method claims reduced pain in recovery, but statistics suggest a lower overall success rate compared to traditional methods. The No-Scalpel method (coined Key-Hole),[2] in which a sharp hemostat, rather than a scalpel, is used to puncture the scrotum may reduce healing times as well as mitigate the chance of infection. An "open-ended" vasectomy obstructs (seals) only one end of the vas deferens, which allows continued streaming of sperm (by virtue of the un-sealed vas-deferens) into the scrotum. This method may avoid build-up of pressure in the epididymis. Testicular pain (from "backup pressure") may also be reduced using this method.

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Physiology of the Cornea

Light enters to the eye through cornea, subsequently traveling to the Aqueous humour, pupil, lens and Vitreous humour before reaching the retina,Cornea is transparent layer of fibrous connective tissues that has no blood supply, Cornea is first intera-ocular structure that refract or bends the light rays.

After passing through cornea light passes to the aqueous humour. Aqueous humour is a clear fluid continually produced by capillaries in the ciliary body, Function of Aqueous humour is to maintain the shape of the front of the eye and to supply oxygen and nutrients to both cornea and lens.


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