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肌间神经丛中间神经元对肠纵肌兴奋性神经输入的调节。

Regulation of excitatory neural input to longitudinal intestinal muscle by myenteric interneurons.

作者信息

Grider J R

机构信息

Departments of Physiology and Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia 23298-0551, USA.

出版信息

Am J Physiol. 1998 Nov;275(5):G973-8. doi: 10.1152/ajpgi.1998.275.5.G973.

Abstract

The circuit of myenteric interneurons that regulate excitatory input to longitudinal colonic muscle was identified using dispersed ganglia and longitudinal muscle strips with adherent myenteric plexus from rat distal colon. The preparations enabled measurement of neurotransmitter release from interneurons and/or excitatory motoneurons innervating longitudinal muscle. 1, 1-Dimethyl-4-phenylpiperizinium (DMPP) and somatostatin were used to activate myenteric neurons in dispersed ganglia and muscle strips, respectively. DMPP-stimulated vasoactive intestinal peptide (VIP) release in dispersed ganglia was inhibited by [Met]enkephalin and bicuculline and augmented by naloxone and GABA, implying that inhibitory opioid and stimulatory GABA neurons regulate the activity of VIP interneurons. In muscle strips, VIP stimulated basal and augmented somatostatin-induced substance P (SP) release; the somatostatin-induced increase in SP release was inhibited by VIP-(10-28) and NG-nitro-L-arginine, implying that excitatory VIP neurons regulate tachykinin motoneurons innervating longitudinal muscle. Somatostatin inhibited [Met]enkephalin and stimulated VIP release; basal and somatostatin-stimulated VIP release were inhibited by [Met]enkephalin and bicuculline and augmented by naloxone and GABA, implying that inhibitory pathways linking somatostatin, opioid, and GABA neurons regulate VIP interneurons, which in turn regulate tachykinin and probably cholinergic motoneurons.

摘要

利用大鼠远端结肠的分散神经节和带有附着肌间神经丛的纵行肌条,确定了调节结肠纵行肌兴奋性输入的肠肌间神经元回路。这些标本能够测量来自支配纵行肌的中间神经元和/或兴奋性运动神经元的神经递质释放。分别使用1,1 - 二甲基 - 4 - 苯基哌嗪鎓(DMPP)和生长抑素激活分散神经节和肌条中的肠肌间神经元。在分散神经节中,DMPP刺激的血管活性肠肽(VIP)释放受到[甲硫氨酸]脑啡肽和荷包牡丹碱的抑制,并被纳洛酮和GABA增强,这意味着抑制性阿片样物质和刺激性GABA神经元调节VIP中间神经元的活性。在肌条中,VIP刺激基础状态下的P物质(SP)释放并增强生长抑素诱导的SP释放;生长抑素诱导的SP释放增加受到VIP - (10 - 28)和NG - 硝基 - L - 精氨酸的抑制,这意味着兴奋性VIP神经元调节支配纵行肌的速激肽运动神经元。生长抑素抑制[甲硫氨酸]脑啡肽并刺激VIP释放;基础状态下和生长抑素刺激的VIP释放受到[甲硫氨酸]脑啡肽和荷包牡丹碱的抑制,并被纳洛酮和GABA增强,这意味着连接生长抑素、阿片样物质和GABA神经元的抑制性通路调节VIP中间神经元,而VIP中间神经元又反过来调节速激肽以及可能的胆碱能运动神经元。

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