Ciccocioppo R, Onori L, Messori E, Candura S M, Coccini T, Tonini M
Department of Internal Medicine and Therapeutics, University of Pavia, Italy.
J Pharmacol Exp Ther. 1994 Sep;270(3):929-37.
Previous findings, which have been confirmed in this study, indicate that nitric oxide (NO)-dependent and -independent (apamin-sensitive) mechanisms underlie the electrically induced non-adrenergic, noncholinergic (NANC) relaxation in the circular muscle of rabbit distal colon. Based on this evidence, we further investigated whether, and to what extent, these separate NANC components participate in the maintenance of circular muscle tone, reflex relaxations evoked by localized balloon distension or during peristalsis (descending inhibition) and in the accommodation of colonic wall in response to graded intraluminal fluid delivery. NG-nitro-L-arginine (L-NNA) (10-300 microM), apamin (100 nM) and tetrodotoxin (60 nM), enhanced the spontaneous low tone and phasic activity in circular muscle strips. In experiments on peristalsis, L-NNA (30 and 300 microM) shortened the latency of peristaltic wave initiation and increased the velocity of propulsion of an intraluminally distended balloon (range, 0.1-1 ml). The latter effect was mimicked by the NO scavenger oxyhemoglobin (30 microM). Velocity of propulsion was enhanced by apamin (100 nM) at low balloon distension (0.1 and 0.2 ml), whereas it was reduced at high distension volumes (1 ml), due to disruption of descending inhibition. A combination of L-NNA (300 microM) and apamin (100 nM) blocked peristalsis, due to persisting spasms of the circular muscle. L-NNA (300 microM) did not affect the amplitude of distension-evoked ascending reflex contraction and slightly inhibited the descending reflex relaxation. By contrast, the latter reflex was virtually abolished by apamin (100 nM).(ABSTRACT TRUNCATED AT 250 WORDS)
先前的研究结果在本研究中得到了证实,这些结果表明,一氧化氮(NO)依赖和非依赖(蜂毒明肽敏感)机制是兔远端结肠环形肌电诱导的非肾上腺素能、非胆碱能(NANC)舒张的基础。基于这一证据,我们进一步研究了这些独立的NANC成分是否以及在多大程度上参与环形肌张力的维持、局部气囊扩张或蠕动(下行抑制)诱发的反射性舒张以及结肠壁对腔内液体输送分级反应的适应性调节。NG-硝基-L-精氨酸(L-NNA)(10-300微摩尔)、蜂毒明肽(100纳摩尔)和河豚毒素(60纳摩尔)增强了环形肌条的自发性低张力和阶段性活动。在蠕动实验中,L-NNA(30和300微摩尔)缩短了蠕动波起始的潜伏期,并增加了腔内扩张气囊(范围为0.1-1毫升)的推进速度。后者的效应被NO清除剂氧合血红蛋白(30微摩尔)模拟。在低气囊扩张(0.1和0.2毫升)时,蜂毒明肽(100纳摩尔)可提高推进速度,而在高扩张体积(1毫升)时,由于下行抑制的破坏,推进速度降低。L-NNA(300微摩尔)和蜂毒明肽(100纳摩尔)联合使用可阻断蠕动,原因是环形肌持续痉挛。L-NNA(300微摩尔)不影响扩张诱发的上行反射收缩的幅度,并轻微抑制下行反射舒张。相比之下,后者的反射几乎被蜂毒明肽(100纳摩尔)消除。(摘要截断于250字)