Suppr超能文献

垂体腺苷酸环化酶激活肽对豚鼠肠道正常及药物损害蠕动的刺激作用。

Stimulant action of pituitary adenylate cyclase-activating peptide on normal and drug-compromised peristalsis in the guinea-pig intestine.

作者信息

Heinemann A, Holzer P

机构信息

Department of Experimental and Clinical Pharmacology, University of Graz, Austria.

出版信息

Br J Pharmacol. 1999 Jun;127(3):763-71. doi: 10.1038/sj.bjp.0702602.

Abstract
  1. Pituitary adenylate cyclase-activating peptide (PACAP) is known to influence the activity of intestinal smooth muscle. This study set out to examine the action of PACAP on normal and drug-inhibited peristalsis and to shed light on its site and mode of action. 2. Peristalsis in isolated segments of the guinea-pig small intestine was elicited by distension through a rise of the intraluminal pressure. Drug-induced motility changes were quantified by alterations of the peristaltic pressure threshold at which aborally moving peristaltic contractions were triggered. 3. PACAP (1-30 nM) stimulated normal peristalsis as deduced from a concentration-related decrease in the peristaltic pressure threshold (maximum decrease by 55%). The peptide's stimulant effect remained intact in segments pre-exposed to apamin (0.5 microM), N-nitro-L-arginine methyl ester (300 microM), naloxone (0.5 microM), atropine (1 microM) plus naloxone (0.5 microM) or hexamethonium (100 microM) plus naloxone (0.5 microM). 4. PACAP (10 nM) restored peristalsis blocked by morphine (10 microM), noradrenaline (1 microM) or N6-cyclopentyladenosine (0.3 microM) and partially reinstated peristalsis blocked by Rp-adenosine-3',5'-cyclic monophosphothioate triethylamine (100 microM) but failed to revive peristalsis blocked by hexamethonium (100 microM) or atropine (1 microM). The peptide's spectrum of properistaltic activity differed from that of naloxone (0.5 microM) and forskolin (0.3 microM). 5. The distension-induced ascending reflex contraction of the circular muscle was facilitated by PACAP (1-30 nM) which itself evoked transient nerve-mediated contractions of intestinal segment preparations. 6. These data show that PACAP stimulates normal peristalsis and counteracts drug-induced peristaltic arrest by a stimulant action on excitatory enteric motor pathways, presumably at the intrinsic sensory neurone level. The action of PACAP seems to involve multiple signalling mechanisms including stimulation of adenylate cyclase.
摘要
  1. 已知垂体腺苷酸环化酶激活肽(PACAP)会影响肠道平滑肌的活性。本研究旨在研究PACAP对正常蠕动和药物抑制蠕动的作用,并阐明其作用部位和作用方式。2. 通过升高管腔内压力引起豚鼠小肠离体节段的蠕动。药物诱导的运动变化通过引发向口侧移动的蠕动收缩的蠕动压力阈值的改变来量化。3. PACAP(1 - 30 nM)刺激正常蠕动,这可从蠕动压力阈值与浓度相关的降低中推断出来(最大降低55%)。在预先暴露于蜂毒明肽(0.5 microM)、N - 硝基 - L - 精氨酸甲酯(300 microM)、纳洛酮(0.5 microM)、阿托品(1 microM)加纳洛酮(0.5 microM)或六甲铵(100 microM)加纳洛酮(0.5 microM)的节段中,该肽的刺激作用仍然完整。4. PACAP(10 nM)恢复了被吗啡(10 microM)、去甲肾上腺素(1 microM)或N6 - 环戊基腺苷(0.3 microM)阻断的蠕动,并部分恢复了被Rp - 腺苷 - 3',5' - 环化单磷酸硫代乙酯三乙胺(100 microM)阻断的蠕动,但未能恢复被六甲铵(100 microM)或阿托品(1 microM)阻断的蠕动。该肽的促蠕动活性谱与纳洛酮(0.5 microM)和福斯可林(0.3 microM)不同。5. PACAP(1 - 30 nM)促进了扩张诱导的环行肌向心性反射收缩,其本身可诱发肠段制剂的短暂神经介导收缩。6. 这些数据表明,PACAP通过对兴奋性肠运动通路(可能是在内在感觉神经元水平)的刺激作用来刺激正常蠕动并抵消药物诱导的蠕动停止。PACAP的作用似乎涉及多种信号传导机制,包括刺激腺苷酸环化酶。

相似文献

本文引用的文献

3
Intrinsic primary afferent neurons of the intestine.肠道的内在初级传入神经元。
Prog Neurobiol. 1998 Jan;54(1):1-18. doi: 10.1016/s0301-0082(97)00051-8.
7
PACAP and VIP inhibit pyloric muscle through VIP/PACAP-preferring receptors.
Regul Pept. 1997 Aug 29;71(3):185-90. doi: 10.1016/s0167-0115(97)01031-8.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验