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P物质对猫小肠血流、液体转运及血管活性肠肽释放的影响。

Substance P effects on blood flow, fluid transport and vasoactive intestinal polypeptide release in the feline small intestine.

作者信息

Brunsson I, Fahrenkrug J, Jodal M, Sjöqvist A, Lundgren O

机构信息

Department of Physiology, Göteborg University, Sweden.

出版信息

J Physiol. 1995 Mar 15;483 ( Pt 3)(Pt 3):727-34. doi: 10.1113/jphysiol.1995.sp020617.

Abstract
  1. Substance P (SP) infusions were given close I.A. to the feline small intestine in vivo in a dose that produced plasma concentrations of 1-5 microM. This infusion regularly evoked a net fluid secretion measured with a gravimetric technique. Concomitantly, the release into blood of vasoactive intestinal polypeptide (VIP), a putative neurotransmitter of the enteric nervous system, increased. 2. The SP-induced fluid secretion was blocked by tetrodotoxin (7 micrograms close I.A.), a blocker of fast sodium channels in excitable tissues, and hexamethonium (10 mg (kg body wt)-1, I.V.), a nicotinic receptor antagonist, suggesting that the SP effect was mediated by the enteric nervous system. In line with this it was shown that the SP-evoked release of VIP was also significantly diminished by hexamethonium. 3. Close I.A. infusions of methionine enkephalin (Met-enkephalin; 7-23 nmol min-1) or electrical stimulation of the sympathetic nerve fibres (6 Hz) to the intestine markedly diminished net fluid secretion and the release of VIP caused by SP given close I.A. 4. The cyclo-oxygenase inhibitor diclofenac (5 mg (kg body wt)-1, I.V.) or the histamine-1 receptor antagonist pyrilamine (10 mg (kg body wt)-1, I.V.) did not influence the fluid secretion caused by SP, indicating that the effects of SP were not due to the actions of prostaglandins or histamine. 5. It is proposed that SP activates a nervous reflex arch that we have shown to be activated by various luminal stimuli, including cholera toxin.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在猫体内,将P物质(SP)以能使血浆浓度达到1 - 5微摩尔的剂量经肠内(I.A.)靠近猫小肠处注入。这种注入方式通过重量测定技术可定期诱发净液体分泌。与此同时,作为肠神经系统一种假定神经递质的血管活性肠肽(VIP)向血液中的释放增加。2. SP诱导的液体分泌被河豚毒素(7微克,经肠内靠近处)阻断,河豚毒素是可兴奋组织中快速钠通道的阻滞剂,以及六甲铵(10毫克/(千克体重),静脉注射),一种烟碱受体拮抗剂,这表明SP的作用是由肠神经系统介导的。与此一致的是,已表明六甲铵也能显著减少SP诱发的VIP释放。3. 经肠内靠近处注入甲硫氨酸脑啡肽(Met - 脑啡肽;7 - 23纳摩尔/分钟)或对肠的交感神经纤维进行电刺激(6赫兹),可显著减少经肠内靠近处给予SP所引起的净液体分泌和VIP释放。4. 环氧化酶抑制剂双氯芬酸(5毫克/(千克体重),静脉注射)或组胺 - 1受体拮抗剂吡咯胺(10毫克/(千克体重),静脉注射)不影响SP引起的液体分泌,这表明SP的作用不是由于前列腺素或组胺的作用。5. 有人提出,SP激活了一种神经反射弧,我们已证明该反射弧可被包括霍乱毒素在内的各种腔内刺激所激活。(摘要截短至250字)

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