Kreis M E, Haupt W, Kirkup A J, Grundy D
Department of General Surgery, University Hospital, 72076 Tübingen, Germany.
Am J Physiol. 1998 Oct;275(4):G675-80. doi: 10.1152/ajpgi.1998.275.4.G675.
The concept of functional interaction between mast cells and intestinal afferents is gaining support. We have therefore characterized the action of histamine on jejunal afferent discharge in the anesthetized rat. Whole nerve mesenteric afferent discharge was recorded in conjunction with intestinal pressure in response to a range of histamine agonists and antagonists. Histamine at 2, 4, and 8 micromol/kg (iv) evoked a dose-dependent biphasic increase in afferent discharge together with a biphasic rise in intestinal pressure. However, these two events were mediated independently, since nifedipine (1 mg/kg) substantially reduced the intestinal pressure increase but not the afferent discharge. These responses were completely inhibited by pyrilamine (5 mg/kg) but unaffected by ranitidine (5 mg/kg) or thioperamide (2 mg/kg). Neither the selective H2 receptor agonist dimaprit nor the selective H3 receptor agonist R-alpha-methylhistamine caused any modulation of afferent discharge. We conclude that histamine stimulates an H1 receptor-mediated increase in mesenteric afferent discharge that is independent of intestinal motor events. This suggests that histamine potentially acts as a mediator in mast cell-to-afferent nerve communication in the small intestine.
肥大细胞与肠传入神经之间功能相互作用的概念正获得越来越多的支持。因此,我们对组胺对麻醉大鼠空肠传入神经放电的作用进行了特征描述。记录了肠系膜全神经传入神经放电,并结合肠压力,以应对一系列组胺激动剂和拮抗剂。静脉注射2、4和8微摩尔/千克的组胺会引起传入神经放电呈剂量依赖性双相增加,同时肠压力也呈双相升高。然而,这两个事件是独立介导的,因为硝苯地平(1毫克/千克)可显著降低肠压力升高,但对传入神经放电没有影响。这些反应被吡拉明(5毫克/千克)完全抑制,但不受雷尼替丁(5毫克/千克)或硫代哌酰胺(2毫克/千克)影响。选择性H2受体激动剂二甲双胍和选择性H3受体激动剂R-α-甲基组胺均未对传入神经放电产生任何调节作用。我们得出结论,组胺刺激H1受体介导的肠系膜传入神经放电增加,这与肠道运动事件无关。这表明组胺可能在小肠肥大细胞与传入神经的通讯中起介质作用。