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Histamine is an active substance found in a large range of living organisms that plays a major role in allergic reaction, dilating blood vessels and increasing the permeability of vessel walls. It also acts as a neurotransmitter or chemical messenger that carries signals from one nerve to another, as well as performing several other important functions in various bodily tissues.
Histamine is classified as an amine because it is based on the structure of ammonia and is formed through decarboxylation of the amino acid histidine. Histamine is an autacoid, which means it acts similarly to a local hormone, near its site of synthesis. It is produced as part of the local immune response to invading bodies and triggers inflammation.
Histamine exerts its effects by binding to histamine receptors on cells’ surfaces. There are four types of histamine receptor: H1, H2, H3 and H4. The binding of histamine to these receptors stimulates them to produce functional responses and these are described in more detail below:
Anithistamines are drugs used to block the activity of histamines, by preventing the ability of histamine to bind to histamine receptors. These agents are therefore referred to as histamine antagonists. The traditional antihistamines that are used to treat allergy block H1 receptors, while H2 antagonists inhibit gastric acid secretion to help treat peptic ulcers. The H4 receptor is a potential target for treating allergic and inflammatory conditions such as asthma and allergic rhinitis. The ability of the H3 receptor to modulate various neurotransmitters makes this receptor a novel therapeutic target in the relief of symptoms caused by several conditions including movement disorders, obesity, schizophrenia, abnormal sleep/wake patterns and ADHD.