Neumann Detlef, Seifert Roland
Institute of Pharmacology, Hannover Medical School, Germany.
Institute of Pharmacology, Hannover Medical School, Germany.
Biochem Pharmacol. 2014 Sep 1;91(1):12-7. doi: 10.1016/j.bcp.2014.06.004. Epub 2014 Jun 11.
In the intestine of patients suffering from inflammatory bowel disease concentrations of histamine are increased compared to healthy controls. Genetic ablation of histamine production in mice ameliorates the course of experimentally induced colitis. These observations and first pharmacological studies indicate a function of histamine in the pathogenesis of inflammatory bowel disease. However, a closer examination reveals that available data are highly heterogeneous, limiting the rational design of strategies addressing specific histamine receptor subtypes as possible target for pharmacological interaction. However, very recently first clinical data indicate that antagonism at the histamine receptor subtype H4 provides a beneficial effect in at least the skin. Here, we discuss the available data on histamine effects and histamine receptor subtype functions in inflammatory bowel disease with a special emphasis on the histamine H4-receptor.
与健康对照相比,炎症性肠病患者肠道中的组胺浓度会升高。小鼠体内组胺生成的基因消融改善了实验性诱导结肠炎的病程。这些观察结果和最初的药理学研究表明组胺在炎症性肠病的发病机制中发挥作用。然而,仔细研究发现现有数据高度异质性,限制了针对特定组胺受体亚型作为药物相互作用可能靶点的策略的合理设计。不过,最近的首批临床数据表明,组胺受体亚型H4的拮抗作用至少在皮肤方面具有有益效果。在此,我们讨论关于组胺作用以及组胺受体亚型在炎症性肠病中的功能的现有数据,特别强调组胺H4受体。