The enzyme is expressed inbilateria, a biological group ofanimals. The enzyme is encoded by theAOC1 gene. This gene is highly conserved across thebilateria group which includesmammals,birds,reptiles,fish andinsects, to name a few.
Histamine, a biogenic amine, undergoes metabolism through three distinct enzymatic pathways:[2]
The first pathway (see the reaction illustrated below) involves the deamination of histamine by the enzyme diamine oxidase to form imidazole acetaldehyde.[2]
In the second pathway, histamine is metabolized into Nτ-methylhistamine (also known as1-Methylhistamine), which also has some biological activity, albeit much weaker than that of histamine.[3] Still, NMT, being a product in a reaction catalyzed by HNMT, may inhibit expression of HNMT in a negative feedback loop.[4] This reaction is Nτ-methylation of histamine by thehistamine N-methyltransferase (HNMT) enzyme. The Nτ-methylhistamine, unless excreted by the kindney, is subsequently oxidized into Nτ-methylimidazoleacetic acid (NτMIAA) by the enzymemonoamine oxidase (MAO). This two-step process effectively reduces the activity of histamine in the body and is particularly important for quick deactivation of histamine in the brain.[2]
The third pathway involves the acetylation of histamine by an acetylase to form 4-(-acetylaminoethyl)imidazole. However, it’s important to note that this pathway is found exclusively in enterobacteria and has not been identified in mammals. This suggests a unique metabolic pathway for histamine in these bacteria.[2]
These pathways highlight the complex and varied mechanisms through which histamine is metabolized in different organisms. Understanding these pathways is crucial for biomedical professionals as it can provide insights into the regulation of histamine levels and its role in various physiological and pathological processes.[2]DAO catalyzes theoxidative deamination ofpolyamines, such as histamine andputrescine, to produceaminoaldehydes,[2]hydrogen peroxide,[2] andammonia.[2]
DAO is involved in the physiology of digestion and other physiological processes, such as inflammation, immune response, and wound healing. Dysfunction of DAO has been associated with various diseases, including allergies, autoimmune disorders, and cancer. DAO also plays a role in healthy pregnancy in placental mammals.
Inplacental mammals, including humans, the highest levels of DAO expression are observed in the digestive tract (intestinal mucosa) and theplacenta. DAO expression is also observed in kidney of various species.
In humans, a certain subtype of cells of the placenta, namely the extravilloustrophoblasts, express the enzyme and secrete it into the blood stream of a pregnant woman.[11]
During pregnancy, DAO helps maintaining fetal growth and development by regulating histamine levels.[11] DAO levels in the blood circulation increase vastly in pregnant women suggesting a protective mechanism against adverse histamine.[12] Histamine is a potent vasodilator and can cause uterine contractions, which can lead to premature labor. DAO in the placenta breaks down histamine to prevent its accumulation and maintain a healthy pregnancy. Low levels of DAO in the placenta may contribute to preeclampsia, a pregnancy-related disorder characterized by mother's high blood pressure and damage to mother's organs such as the liver and kidneys; the baby may also be affected if the condition is severe or left untreated, but it is not the primary target of the disorder.
Lowered diamine oxidase values in maternal blood in early pregnancy might be an indication for trophoblast-related pregnancy disorders like early-onsetpreeclampsia.[12]
Exogenous DAO (supplements) are being studied as complementary treatment[13] for the relief of symptoms associated withhistamine intolerance, and for the relief of other conditions, such as migraine[14] or fibromyalgia.[15] However, the results are inconclusive because studies to date have involved small study populations and short intervention periods.[16][17][18]
In the United States, DAO supplements are availableover the counter but are notFDA-approved.[19]
In Europe, two investigations, financially backed by the manufacturer of the oral DAO supplementation, have posited that DAO supplementation could alleviate patient symptoms.[20] The first study sought to "objectify and quantify histamine-associated symptoms and to analyze whether oral administration of the histamine-degrading enzyme DAO caused a reduction of symptoms".[20] In this study, neither major nor minor symptoms could be replicated in 39 patients who initially responded to an open challenge with 75 mg histamine in peppermint tea, using a double-blind, placebo-controlled challenge.[20] Consequently, the primary endpoint of the study was not achieved, and the basis for the authors' conclusion that DAO supplementation intake resulted in a "statistically significant reduction in symptoms" remains unclear. The second study was purely observational, lacking a control group: it compared symptomatology with and without DAO use in 28 patients.[20] The chosen design was not suitable to demonstrate causal effects and carried a high risk of attributing placebo effects.[20] The effectiveness of DAO supplementation has not been scientifically validated and is not recommended by the medical associations in Germany, Austria and Switzerland.[20]
DAO is related on possible links to migraine conditions. During migraine episodes, there is a noted elevation in the plasma concentrations of both calcitonin gene-related peptide (CGRP) and histamine. These substances are known for their potent vasodilatory effects and have been observed to mutually stimulate each other's release within the trigeminovascular system, potentially contributing to the onset of migraines, so that individuals with genetic variants in the DAO gene often experience migraines when consuming a diet high in histamine. As such, exploring the functional interplay between exogenous histamine and CGRP could provide valuable insights into the mechanisms underlying diet-induced migraines. This area of research continues to be actively investigated.[21]
^Wolvekamp MC, de Bruin RW (1994). "Diamine oxidase: an overview of historical, biochemical and functional aspects".Digestive Diseases.12 (1):2–14.doi:10.1159/000171432.PMID8200121.
^Mohammed T (2010). "Biological and Pharmacological Aspects of Histamine Receptors and Their Ligands".Biomedical Aspects of Histamine. Springer. pp. 61–100.doi:10.1007/978-90-481-9349-3_4.ISBN978-90-481-9348-6.
^Peters LJ, Kovacic JP (2009). "Histamine: Metabolism, physiology, and pathophysiology with applications in veterinary medicine".Journal of Veterinary Emergency and Critical Care.19 (4):311–328.doi:10.1111/j.1476-4431.2009.00434.x.PMID25164630.
^Izquierdo-Casas J, Comas-Basté O, Latorre-Moratalla ML, Lorente-Gascón M, Duelo A, Soler-Singla L, et al. (February 2019). "Diamine oxidase (DAO) supplement reduces headache in episodic migraine patients with DAO deficiency: A randomized double-blind trial".Clin Nutr.38 (1):152–158.doi:10.1016/j.clnu.2018.01.013.hdl:2445/162978.PMID29475774.S2CID3511305.
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