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垂体腺苷酸环化酶激活肽对肠道蠕动下降松弛期的调节

Regulation of the descending relaxation phase of intestinal peristalsis by PACAP.

作者信息

Grider J R, Katsoulis S, Schmidt W E, Jin J G

机构信息

Department of Physiology, Medical College of Virginia, Richmond 23298.

出版信息

J Auton Nerv Syst. 1994 Dec 15;50(2):151-9. doi: 10.1016/0165-1838(94)90005-1.

DOI:10.1016/0165-1838(94)90005-1
PMID:7884155
Abstract

The presence of pituitary adenylate cyclase-activating peptide (PACAP), a homologue of vasoactive intestinal peptide (VIP), in enteric neurons suggests that it may involved in the regulation of the descending relaxation phase of the peristaltic reflex. The role of PACAP was evaluated by measurement of PACAP release and by immuno-neutralization with specific monoclonal antibodies to PACAP-27 and PACAP-38, and an antibody to VIP. Electrical field stimulation at 4 Hz caused a 12-fold increase in PACAP release that was inhibited by 53 +/- 6% (P < 0.01) by the nitric oxide synthase inhibitor, NG-nitro-L-arginine (L-NNA). Orad stretch of colonic segments elicited descending relaxation and PACAP release in proportion to the degree of stretch. PACAP release induced by 10-g stretch was inhibited by 67 +/- 10% (P < 0.01) by L-NNA. Previous studies (Am. J. Physiol., 264 (1993) G334-G340) showed that orad stretch elicits also VIP release and nitric oxide (NO) production and that VIP release is inhibited (59%) by L-NNA. Preincubation of the segments with PACAP-27 plus PACAP-38 antibodies (50 micrograms/ml each), or with VIP antibody (1:60) inhibited descending relaxation at all degrees of stretch (inhibition with PACAP antibodies: 90 +/- 8% with 2-g and 22 +/- 5% with 10-g stretch). Preincubation with both PACAP and VIP antibodies virtually abolished descending relaxation. A similar pattern was observed with the antagonists, PACAP6-38 and VIP10-28, alone and in combination.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

垂体腺苷酸环化酶激活肽(PACAP)是血管活性肠肽(VIP)的同源物,其在肠神经元中的存在表明它可能参与蠕动反射下行松弛阶段的调节。通过测量PACAP释放以及用针对PACAP - 27和PACAP - 38的特异性单克隆抗体和针对VIP的抗体进行免疫中和来评估PACAP的作用。4Hz的电场刺激使PACAP释放增加了12倍,一氧化氮合酶抑制剂NG - 硝基 - L - 精氨酸(L - NNA)可抑制53±6%(P<0.01)。结肠段的口侧拉伸引起下行松弛和与拉伸程度成比例的PACAP释放。10g拉伸诱导的PACAP释放被L - NNA抑制67±10%(P<0.01)。先前的研究(《美国生理学杂志》,264(1993)G334 - G340)表明,口侧拉伸也会引发VIP释放和一氧化氮(NO)生成,并且L - NNA可抑制VIP释放(59%)。用PACAP - 27加PACAP - 38抗体(各50μg/ml)或VIP抗体(1:60)预孵育各段,在所有拉伸程度下均抑制下行松弛(用PACAP抗体抑制:2g拉伸时为90±8%,10g拉伸时为22±5%)。用PACAP和VIP抗体预孵育实际上消除了下行松弛。单独或联合使用拮抗剂PACAP6 - 38和VIP10 - 28时观察到类似模式。(摘要截断于250字)

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