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Under physiological conditions, the aliphatic amino group (having a pK a around 9.4) ... The role of histamine in health and disease is an area of ongoing research ...
The histamine receptors are a class of G protein–coupled receptors which bind histamine as their primary endogenous ligand. [1] [2] Histamine receptors are proteins that bind with histamine, a neurotransmitter involved in various physiological processes. There are four main types: H1, H2, H3, and H4.
Like all histamine receptors, the H 3 receptor is a G-protein coupled receptor. The H 3 receptor is coupled to the G i G-protein , so it leads to inhibition of the formation of cAMP . Also, the β and γ subunits interact with N-type voltage gated calcium channels , to reduce action potential mediated influx of calcium and hence reduce ...
Histamine is a ubiquitous messenger molecule released from mast cells, enterochromaffin-like cells, and neurons. [5] Its various actions are mediated by histamine receptors H 1, H 2, H 3 and H 4. The histamine receptor H 2 belongs to the rhodopsin-like family of G protein-coupled receptors.
Histamine N-methyltransferase (HNMT) is a protein encoded by the HNMT gene in humans. It belongs to the methyltransferases superfamily of enzymes and plays a role in the inactivation of histamine, a biomolecule that is involved in various physiological processes.
Histamine is an organic compound that primarily functions in service of the human body's immune responses as well as for the regulation of many physiological functions. [1] Since their discovery in 1910, [ 2 ] histamines have been known to trigger inflammatory responses such as itching as part of an immune response to foreign pathogens; for ...
Virgin Australia crew members were allegedly sexually assaulted and robbed in one of Fiji's nightclub areas on New Year's Day, the island country's Deputy Prime Minister Viliame Gavoka announced.
Cimetidine was the prototypical histamine H 2 receptor antagonist from which later drugs were developed. Cimetidine was the culmination of a project at Smith, Kline & French (SK&F; now GlaxoSmithKline) by James W. Black, C. Robin Ganellin, and others to develop a histamine receptor antagonist that would suppress stomach acid secretion.