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  2. Histidine decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Histidine_decarboxylase

    The enzyme histidine decarboxylase (EC 4.1.1.22, HDC) is transcribed on chromosome 15, region q21.1-21.2, and catalyzes the decarboxylation of histidine to form histamine.In mammals, histamine is an important biogenic amine with regulatory roles in neurotransmission, gastric acid secretion and immune response.

  3. Histamine intolerance - Wikipedia

    en.wikipedia.org/wiki/Histamine_intolerance

    In the supposed histamine intolerance, these affected individuals supposedly have a lower threshold for histamine and can develop symptoms even after consuming foods with normal or moderate amounts of histamine, [1] [14] such as tomatoes, eggplants, spinach, strawberries—plants which naturally contain histamine [20] [15] —or wine. [15]

  4. Histamine liberators - Wikipedia

    en.wikipedia.org/wiki/Histamine_liberators

    During that time, many dietitians advised that a diet devoid of histamine-liberating foods was the ideal strategy to prevent symptoms of histamine intolerance from manifesting. Lists of foods deemed to be histamine-liberating were published in various scientific articles, which included fermented sausages , cured cheese , wine and beer.

  5. α-Fluoromethylhistidine - Wikipedia

    en.wikipedia.org/wiki/Α-fluoromethylhistidine

    It functions by forming a covalent linkage with a catalytic serine residue on the active site of HDC. Due to its efficacy in reducing histamine levels in tissue mast cells, it has many applications in the study of histaminergic systems. [2] It has potent sleep-inducing effects in mice.

  6. H3 receptor antagonist - Wikipedia

    en.wikipedia.org/wiki/H3_receptor_antagonist

    An H 3 receptor antagonist is a type of antihistaminic drug used to block the action of histamine at H 3 receptors.. Unlike the H 1 and H 2 receptors which have primarily peripheral actions, but cause sedation if they are blocked in the brain, H 3 receptors are primarily found in the brain and are inhibitory autoreceptors located on histaminergic nerve terminals, which modulate the release of ...

  7. H1 antagonist - Wikipedia

    en.wikipedia.org/wiki/H1_antagonist

    Time to peak Half-life b Metabolism Anticholinergic Diphenhydramine: 50 mg 2–3 hours 2–9 hours CYP2D6, others Yes Doxylamine: 25 mg 2–3 hours 10–12 hours CYP2D6, others Yes Hydroxyzine: 25–100 mg 2 hours 20 hours ADH, CYP3A4, others No Doxepin: 3–6 mg 2–3 hours 17 hours c: CYP2D6, others No (at low doses) Mirtazapine: 7.5–15 mg ...

  8. Diamine oxidase - Wikipedia

    en.wikipedia.org/wiki/Diamine_oxidase

    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.

  9. Antihistamine - Wikipedia

    en.wikipedia.org/wiki/Antihistamine

    [4] [5] Normally, histamine binds to the H 1 receptor and heightens the receptor's activity; the receptor antagonists work by binding to the receptor and blocking the activation of the receptor by histamine; by comparison, the inverse agonists bind to the receptor and both block the binding of histamine, and reduce its constitutive activity, an ...