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首页> 外文期刊>American Journal of Physiology >Involvement of pituitary adenylate cyclase-activating peptide in opossum internal anal sphincter relaxation.
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Involvement of pituitary adenylate cyclase-activating peptide in opossum internal anal sphincter relaxation.

机译:垂体腺苷酸环化酶激活肽参与负鼠内部肛门括约肌松弛。

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摘要

Despite its widespread distribution and significance in the gut, the role of pituitary adenylate cyclase-activating peptide (PACAP) in internal anal sphincter (IAS) relaxation has not been examined. This study examined the role of PACAP in nonadrenergic noncholinergic (NANC) nerve-mediated relaxation of IAS smooth muscle. Circular smooth muscle strips from the opossum IAS were prepared for measurement of isometric tension. The influence of PACAP and vasoactive intestinal peptide (VIP) antagonists and tachyphylaxis on the neurally mediated IAS relaxation was examined either separately or in combination. The release of these neuropeptides in response to NANC nerve stimulation before and after the nitric oxide (NO) synthase inhibitor Nomega-nitro-L-arginine and NO was also investigated. Both PACAP and VIP antagonists caused significant attenuation of IAS relaxation by NANC nerve stimulation. The combination of the antagonists, however, did not have an additive effect on IAS relaxation. VIP tachyphylaxis caused significant suppression of IAS relaxation by NANC nerve stimulation. PACAP and VIP were found to be released by NANC nerve stimulation and exogenous NO. The data suggest the involvement of PACAP in IAS relaxation primarily by the activation of PACAP1/VIP receptor and lack of its independent role in the relaxation. Furthermore, NO may regulate the presynaptic release of PACAP and VIP.
机译:尽管其在肠道中广泛分布并具有重要意义,但尚未检查垂体腺苷酸环化酶激活肽(PACAP)在肛门内括约肌(IAS)松弛中的作用。这项研究检查了PACAP在非肾上腺能非胆碱能(NANC)神经介导的IAS平滑肌松弛中的作用。制备了负鼠IAS的圆形平滑肌条,用于测量等轴测张力。分别或联合检查了PACAP和血管活性肠肽(VIP)拮抗剂和速激肽对神经介导IAS松弛的影响。还研究了一氧化氮(NO)合酶抑制剂Nomega-nitro-L-精氨酸和NO之前和之后响应于NANC神经刺激而释放的这些神经肽。 PACAP和VIP拮抗剂均通过NANC神经刺激引起IAS松弛明显减弱。但是,拮抗剂的组合对IAS松弛没有累加作用。 VIP速激肽通过NANC神经刺激显着抑制IAS松弛。发现PACAP和VIP由NANC神经刺激和外源性NO释放。数据表明,PACAP参与IAS放松主要是通过激活PACAP1 / VIP受体而缺乏的,它在放松中没有独立的作用。此外,NO可能会调节PACAP和VIP的突触前释放。

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