Osinski M A, Bass P, Gaumnitz E A
Section for Gastroenterology, Department of Medicine, Wisconsin 53705, USA.
Am J Physiol. 1999 Jan;276(1):G125-31. doi: 10.1152/ajpgi.1999.276.1.G125.
Orphanin FQ (OFQ), also known as nociceptin, is a recently isolated endogenous peptide with a structure similar to the endogenous opioid peptides. The present study examines the actions of centrally administered OFQ on in vivo murine gastrointestinal and colonic transit as well as the actions of OFQ on the isolated colon. Intracerebroventricular injections of OFQ dose dependently inhibited colonic propulsive activity. OFQ inhibition of colonic propulsion was unaffected by coadministration of the competitive opioid receptor antagonist naltrexone. A subadditive response was observed when approximately equipotent doses of either morphine sulfate or the delta-agonist DPDPE were coadministered with OFQ. No subadditivity was observed with coadministration of the micro-agonist DAMGO, suggesting a functional interaction between OFQ and delta-opioid central pathways regulating colonic transit. High, but not low, doses of OFQ also inhibited the transit of a nonabsorbable charcoal marker through the stomach and/or small intestine. OFQ potently contracted isolated colon preparations; contractile activity was abolished by TTX or chlorpromazine. Our results suggest that OFQ may be an important peptide ligand acting on a novel inhibitory neural pathway that modulates gastrointestinal transit.
孤啡肽(OFQ),也被称为痛敏肽,是一种最近分离出的内源性肽,其结构与内源性阿片肽相似。本研究考察了脑室内注射OFQ对小鼠体内胃肠道和结肠转运的作用,以及OFQ对离体结肠的作用。脑室内注射OFQ剂量依赖性地抑制结肠推进活动。OFQ对结肠推进的抑制作用不受竞争性阿片受体拮抗剂纳曲酮共同给药的影响。当硫酸吗啡或δ激动剂DPDPE与OFQ共同给予大约等效剂量时,观察到亚相加反应。与微激动剂DAMGO共同给药时未观察到亚相加性,这表明OFQ与调节结肠转运的δ阿片中枢途径之间存在功能相互作用。高剂量而非低剂量的OFQ也抑制了不可吸收的炭标记物通过胃和/或小肠的转运。OFQ使离体结肠标本强烈收缩;收缩活性被TTX或氯丙嗪消除。我们的结果表明,OFQ可能是一种重要的肽配体,作用于一条调节胃肠转运的新型抑制性神经通路。