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首页> 外文期刊>American Journal of Physiology >Histamine sensitivity of mesenteric afferent nerves in the rat jejunum.
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Histamine sensitivity of mesenteric afferent nerves in the rat jejunum.

机译:大鼠空肠肠系膜传入神经的组胺敏感性。

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摘要

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.
机译:肥大细胞和肠传入细胞之间的功能相互作用的概念正在获得支持。因此,我们表征了组胺对麻醉大鼠空肠传入放电的作用。记录了对一系列组胺激动剂和拮抗剂反应的全神经肠系膜传入放电与肠道压力。组胺浓度分别为2、4和8 micromol / kg(iv)引起传入放电剂量依赖性双相增加以及肠道压力双相增加。然而,由于硝苯地平(1 mg / kg)显着降低了肠内压力的升高,但未降低传入的排出量,因此这两个事件是独立介导的。这些反应完全被吡拉明(5 mg / kg)抑制,但不受雷尼替丁(5 mg / kg)或硫代过酰胺(2 mg / kg)的影响。选择性H2受体激动剂dimaprit或选择性H3受体激动剂R-α-甲基组胺都不会引起传入放电的任何调节。我们得出的结论是,组胺刺激H1受体介导的肠系膜传入性放电的增加,而独立于肠运动事件。这表明,组胺可能在小肠中肥大细胞与喜怒无常的神经沟通中充当介质。

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