|Jmol-3D images||Image 1|
|Molar mass||111.15 g mol−1|
|Melting point||83.5 °C (182.3 °F)|
|Boiling point||209.5 °C (409.1 °F)|
|Solubility in water||Easily soluble in cold water, hot water1|
|Solubility||Easily soluble in methanol. Very slightly soluble in diethyl ether.1 Easily soluble in ethanol.|
|Acidity (pKa)||imidazole: 6.04
| (what is: / ?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Histamine is an organic nitrogenous compound involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter.2 Histamine is involved in the inflammatory response. 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 some proteins, to allow them to engage pathogens in the infected tissues.3
- 1 Properties
- 2 Synthesis and metabolism
- 3 Storage and release
- 4 Mechanism of action
- 5 Roles in the body
- 6 Disorders
- 7 History
- 8 See also
- 9 References
- 10 External links
Histamine forms coloured 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. The imidazole ring has two nitrogens. The nitrogen farthest away from the side chain is the 'tele' nitrogen and is denoted by a lowercase tau sign. The nitrogen closest to the side chain is the 'pros' nitrogen and is denoted by the pi sign. The position of the nitrogen with the hydrogen on it determines how the tautomer is named. If the nitrogen with the hydrogen is in the tele position, then histamine is in the tele-tautomer form. The tele-tautomer is preferred in solution.
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.4 Thus, histamine is normally protonated to a singly charged cation.
Once formed, histamine is either stored or rapidly inactivated by its primary degradative enzymes, histamine-N-methyltransferase or diamine oxidase. In the central nervous system, histamine released into the synapses is primarily broken down by histamine-N-methyltransferase, while in other tissues both enzymes may play a role. Several other enzymes, including MAO-B and ALDH2, further process the immediate metabolites of histamine for excretion or recycling.
Bacteria also are capable of producing histamine using histidine decarboxylase enzymes unrelated to those found in animals. A non-infectious form of foodborne disease, scombroid poisoning, is due to histamine production by bacteria in spoiled food, particularly fish. Fermented foods and beverages naturally contain small quantities of histamine due to a similar conversion performed by fermenting bacteria or yeasts. Sake contains histamine in the 20–40 mg/L range; wines contain it in the 2–10 mg/L range.5
Most histamine in the body is generated in granules in mast cells and in white blood cells called basophils and eosinophils. 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 stimulate histamine release.
Histamine release occurs when allergens bind to mast-cell-bound IgE antibodies. Reduction of IgE overproduction may lower the likelihood of allergens finding sufficient free IgE to trigger a mast-cell-release of histamine.
In binding to the H2 receptor, histamine is protonated at the end-chain amine group. This amine group interacts with aspartic acid in the transmembrane domains of the receptor. The other nitrogens interact with threonine and aspartic acid in different transmembrane domains; collectively, this is referred to as a three-pronged interaction. Bringing the transmembrane domains close to each other, it initiates a signal transduction cascade.6
It should be noted that all of the known physiological reactions of histamine are a series of weak interactions; the histamine backbone remains unchanged.6
Histamine receptors in insects, like Drosophila melanogaster, are ligand-gated chloride channels that act to reduce neuronal activity.7 Histamine-gated chloride channels are implicated in the transmission of peripheral sensory information in insects, especially in photoreception/vision. Two receptor subtypes have been identified in Drosophila: HClA and HClB.8 There are no known GPCRs for histamine in insects.
Increased vascular permeability causes fluid to escape from capillaries into the tissues, which leads to the classic symptoms of an allergic reaction: a runny nose and watery eyes. Allergens can bind to IgE-loaded mast cells in the nasal cavity's mucous membranes. This can lead to three clinical responses:12
- sneezing due to histamine-associated sensory neural stimulation
- hyper-secretion from glandular tissue
- nasal congestion due to vascular engorgement associated with vasodilation and increased capillary permeability
Although histamine is small compared to other biological molecules (containing only 17 atoms), it plays an important role in the body. It is known to be involved in 23 different physiological functions. Histamine is known to be involved in so many physiological functions because of its chemical properties that allow it to be so versatile in binding. It is Coulombic (able to carry a charge), conformational, and flexible. This allows it to interact and bind more easily.6
Histamine is released as a neurotransmitter. The cell bodies of histaminergics, the neurons which release histamine, are found in the posterior hypothalamus, in various tuberomammillary nuclei. From here, these 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 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.
Enterochromaffin-like cells, located within the gastric glands of the stomach, release histamine that stimulates nearby parietal cells by binding to the apical H2 receptor. Stimulation of the parietal cell induces the uptake of carbon dioxide and water from the blood, which is then converted to carbonic acid by the enzyme carbonic anhydrase. Inside the cytoplasm of the parietal cell, the carbonic acid readily dissociates into hydrogen and bicarbonate ions. The bicarbonate ions diffuse back through the basilar membrane and into the bloodstream, while the hydrogen ions are pumped into the lumen of the stomach via a K⁺/H⁺ ATPase pump. Histamine release is halted when the pH of the stomach starts to decrease. Antagonist molecules, like antacids, block the H2 receptor and prevent histamine from binding, causing decreased hydrogen ion secretion.
While histamine has stimulatory effects upon neurons, it also has suppressive ones that protect against the susceptibility to convulsion, drug sensitization, denervation supersensitivity, ischemic lesions and stress.13 It has also been suggested that histamine controls the mechanisms by which memories and learning are forgotten.14
Libido loss and erectile failure can occur during treatment while using of histamine (H2) receptor antagonists such as cimetidine, ranitidine, and risperidone.15 The injection of histamine into the corpus cavernosum in men with psychogenic impotence produces full or partial erections in 74% of them.16 It has been suggested that H2 antagonists may cause sexual difficulties by reducing the uptakeclarification needed of testosterone.15
Metabolites of histamine are increased in the cerebrospinal fluid of people with schizophrenia, while the efficiency of H(1) receptor binding sites is decreased. Many atypical antipsychotic medications have the effect of decreasing histamine production (antagonist), because its use seems to be imbalanced in people with that disorder.17
Histamine therapy for treatment of multiple sclerosis is currently being studied. The different H receptors have been known to have different effects on the treatment of this disease. The H1 and H4 receptors, in one study, have been shown to be counterproductive in the treatment of MS. The H1 and H4 receptors are thought to increase permeability in the Blood Brain Barrier, thus increasing infiltration of unwanted cells in the Central Nervous System. This can cause inflammation, and MS symptom worsening. The H2 and H3 receptors are thought to be helpful when treating MS patients. Histamine has been shown to help with T-cell differentiation. This is important because in MS, the body's immune system attacks its own myelin sheaths on nerve cells (which causes loss of signaling function and eventual nerve degeneration). By helping T cells to differentiate, the T cells will be less likely to attack the body's own cells, and instead attack invaders.18
As an integral part of the immune system, histamine may be involved in immune system disorders and allergies. Mastocytosis is a rare disease in which there is a proliferation of mast cells that produce excess histamine.19
"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.citation needed
- Marieb, E. (2001). Human anatomy & physiology. San Francisco: Benjamin Cummings. p. 414. ISBN 0-8053-4989-8.
- Di Giuseppe, M., et al. (2003). Nelson Biology 12. Toronto: Thomson Canada. p. 473. ISBN 0-17-625987-2.
- Paiva, T. B.; Tominaga, M.; Paiva, A. C. M. (1970). "Ionization of histamine, N-acetylhistamine, and their iodinated derivatives". Journal of Medicinal Chemistry 13 (4): 689–692. doi:10.1021/jm00298a025. PMID 5452432.
- Noszal, B.; Kraszni, M.; Racz, A. (2004). "Histamine: fundamentals of biological chemistry". In Falus, A.; Grosman, N.; Darvas, Z. Histamine: Biology and Medical Aspects. Budapest: SpringMed. pp. 15–28. ISBN 380557715X.
- Hardie RC (June 1989). "A histamine-activated chloride channel involved in neurotransmission at a photoreceptor synapse". Nature 339 (6227): 704–6. doi:10.1038/339704a0. PMID 2472552.
- Pantazis A, Segaran A, Liu CH, et al. (July 2008). "Distinct roles for two histamine receptors (hclA and hclB) at the Drosophila photoreceptor synapse". J. Neurosci. 28 (29): 7250–9. doi:10.1523/JNEUROSCI.1654-08.2008. PMID 18632929.
- Lee, HS; Lee, BY; Waterhouse, BD (2005 May 10). "Retrograde study of projections from the tuberomammillary nucleus to the dorsal raphe and the locus coeruleus in the rat.". Brain research 1043 (1-2): 65–75. PMID 15862519.
- Köhler, C; Swanson, LW; Haglund, L; Wu, JY (1985 Sep). "The cytoarchitecture, histochemistry and projections of the tuberomammillary nucleus in the rat.". Neuroscience 16 (1): 85–110. PMID 2423918.
- Blandina, Patrizio; Munari, Leonardo; Provensi, Gustavo; Passani, Maria B. (2012). "Histamine neurons in the tuberomamillary nucleus: a whole center or distinct subpopulations?". Frontiers in Systems Neuroscience 6. doi:10.3389/fnsys.2012.00033.
- Monroe EW, Daly AF, Shalhoub RF (February 1997). "Appraisal of the validity of histamine-induced wheal and flare to predict the clinical efficacy of antihistamines". J. Allergy Clin. Immunol. 99 (2): S798–806. PMID 9042073.
- Yanai, K; Tashiro, M (2007). "The physiological and pathophysiological roles of neuronal histamine: an insight from human positron emission tomography studies.". Pharmacology & therapeutics 113 (1): 1–15. doi:10.1016/j.pharmthera.2006.06.008. PMID 16890992.
- Alvarez, EO (2009). "The role of histamine on cognition.". Behavioural Brain Research 199 (2): 183–9. doi:10.1016/j.bbr.2008.12.010. PMID 19126417.
- White, JM; Rumbold, GR (1988). "Behavioural effects of histamine and its antagonists: a review.". Psychopharmacology 95 (1): 1–14. PMID 3133686.
- Cará, AM; Lopes-Martins, RA; Antunes, E; Nahoum, CR; De Nucci, G (1995). "The role of histamine in human penile erection.". British Journal of Urology 75 (2): 220–4. doi:10.1111/j.1464-410X.1995.tb07315.x. PMID 7850330.
- Ito, C (2004). "The role of the central histaminergic system on schizophrenia". Drug News & Perspectives 17 (6): 383–7. doi:10.1358/dnp.2004.17.6.829029. PMID 15334189.
- Jadidi-Niaragh F, Mirshafiey A (September 2010). "Histamine and histamine receptors in pathogenesis and treatment of multiple sclerosis". Neuropharmacology 59 (3): 180–9. doi:10.1016/j.neuropharm.2010.05.005. PMID 20493888.
- Valent P, Horny HP, Escribano L, et al. (July 2001). "Diagnostic criteria and classification of mastocytosis: a consensus proposal". Leuk. Res. 25 (7): 603–25. PMID 11377686.
- Dale HH, Laidlaw PP (December 1910). "The physiological action of β-iminazolylethylamine" (PDF). J. Physiol. (Lond.) 41 (5): 318–44. PMC 1512903. PMID 16993030.