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Infobox disclaimer and references
Histamine is a biogenic amine involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter. As part of an immune response to foreign pathogens, histamine is produced by basophils and by mast cells found in nearby connective tissues. Histamine increases the permeability of the capillaries to white blood cells and other proteins, in order to allow them to engage foreign invaders in the affected tissues. It is found in virtually all animal body cells.[How to reference and link to summary or text]
Properties[edit | edit source]
Histamine forms colorless hygroscopic crystals that melt at 84°C, and are easily dissolved in water or ethanol, but not in ether. In aqueous solution histamine exists in two tautomeric forms, Nπ-H-histamine and Nτ-H-histamine.
Histamine has two basic centres, namely the aliphatic amino group and whichever nitrogen atom of the imidazole ring does not already have a proton. Under physiological conditions, the aliphatic amino group (having a pKa around 9.4) will be protonated, whereas the second nitrogen of the imidazole ring (pKa ≈ 5.8) will not be protonated. Thus, histamine is normally protonated to a singly-charged cation.
Synthesis and metabolism[edit | edit source]
Once formed, histamine is either stored or rapidly inactivated. Histamine released into the synapses is broken down by acetaldehyde dehydrogenase. It is the deficiency of this enzyme that triggers an allergic reaction as histamines pool in the synapses. Histamine is broken down by histamine-N-methyltransferase and diamine oxidase. Some forms of foodborne disease, so-called "food poisonings," are due to conversion of histidine into histamine in spoiled food, such as fish.
Storage and release[edit | edit source]
Most histamine in the body is generated in granules in mast cells or in white blood cells called basophils. Mast cells are especially numerous at sites of potential injury - the nose, mouth, and feet, internal body surfaces, and blood vessels. Non-mast cell histamine is found in several tissues, including the brain, where it functions as a neurotransmitter. Another important site of histamine storage and release is the enterochromaffin-like (ECL) cell of the stomach.
The most important pathophysiologic mechanism of mast cell and basophil histamine release is immunologic. These cells, if sensitized by IgE antibodies attached to their membranes, degranulate when exposed to the appropriate antigen. Certain amines and alkaloids, including such drugs as morphine, and curare alkaloids, can displace histamine in granules and cause its release. Antibiotics like polymyxin are also found to be stimulating histamine release.
Mechanism of action[edit | edit source]
Histamine exerts its actions by combining with specific cellular histamine receptors. The four histamine receptors that have been discovered are designated H1 through H4.
|H1 histamine receptor||Found on smooth muscle, endothelium, and central nervous system tissue||Causes vasodilation, bronchoconstriction, bronchial smooth muscle contraction, separation of endothelial cells (responsible for hives), and pain and itching due to insect stings; the primary receptors involved in allergic rhinitis symptoms and motion sickness.|
|H2 histamine receptor||Located on parietal cells||Primarily stimulate gastric acid secretion|
|H3 histamine receptor||Found on central nervous system and to a lesser extent peripheral nervous system tissue||Decreased neurotransmitter release: histamine, acetylcholine, norepinephrine, serotonin|
|H4 histamine receptor||Found primarily in the basophils and in the bone marrow. It is also found on thymus, small intestine, spleen, and colon.||Plays a role in chemotaxis.|
Roles in the body[edit | edit source]
Sleep regulation[edit | edit source]
Histamine is released as a neurotransmitter. The cell bodies of neurons which release histamine are found in the posterior hypothalamus, in various tuberomammillary nuclei. From here, these histaminergic neurons project throughout the brain, to the cortex through the medial forebrain bundle. Histaminergic action is known to modulate sleep. Classically, antihistamines (H1 histamine receptor antagonists) produce sleep. Likewise, destruction of histamine releasing neurons, or inhibition of histamine synthesis leads to an inability to maintain vigilance. Finally, H3 receptor antagonists (which stimulate histamine release) increase wakefulness.
It has been shown that histaminergic cells have the most wakefulness-related firing pattern of any neuronal type thus far recorded. They fire rapidly during waking, fire more slowly during periods of relaxation/tiredness and completely stop firing during REM and NREM (non-REM) sleep. Histaminergic cells can be recorded firing just before an animal shows signs of waking.
Sexual response[edit | edit source]
Research has shown that histamine is released as part of the human orgasm from mast cells in the genitals. If this response is lacking this may be a sign of histapenia (histamine deficiency). In such cases, a doctor may prescribe diet supplements with folic acid and niacin (which used in conjunction can increase blood histamine levels and histamine release), or L-histidine.
Schizophrenia[edit | edit source]
It has been found that about half the patients classified as suffering from schizophrenia have low histamine levels in the blood. This may be because of antipsychotics that have unwanted effect on histamine, such as quetiapine. Although, in these cases, as histamine levels were increased, their health improved.
Disorders[edit | edit source]
Nomenclature[edit | edit source]
"H substance" or "substance H" are occasionally used in medical literature for histamine or a hypothetical histamine-like diffusible substance released in allergic reactions of skin and in the responses of tissue to inflammation.
See also[edit | edit source]
See also[edit | edit source]
References[edit | edit source]
Histamine and Histamine intolerance
- Marieb, E. (2001). Human anatomy & physiology, 414, San Francisco: Benjamin Cummings.
- Di Guiseppe, Maurice; et al. (2003). Nelson Biology 12, Toronto: Thomson Canada Ltd..
- Paiva T.B., Tominaga M. & Paiva A.C. (1970). Ionization of histamine, N-acetylhistamine, and their iodinated derivatives. J. Med. Chem., 13, 689–692.
- What is Schizophrenia?
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