{"title":"Regulation of opioid peptides on the release of arginine vasotocin in the hen.","authors":"T Sasaki, K Shimada, N Saito","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Arginine vasotocin (AVT), an avian neurohypophysial hormone, is released during osmotic stimulation and oviposition. In the present study, the role of opioid peptides on AVT release was studied by examining the effects of an opioid agonist and antagonist on osmotic- and oviposition-induced secretion of AVT. The administration of hypertonic saline (1.5 M NaCl) induced an increase in the plasma levels of AVT. The simultaneous administration of morphine, an opioid receptor agonist, inhibited the osmotically induced increase in plasma levels of AVT in a dose-dependent manner. On the other hand, the co-administration of morphine with naloxone, an opioid receptor antagonist, attenuated the inhibitory effect of morphine. Moreover, injection of naloxone alone enhanced the osmotically induced increase in plasma levels of AVT. However, the administration of morphine did not inhibit the oviposition-induced increase in plasma levels of AVT. These results suggest that osmotic-induced release of AVT may be under opioid regulation, while oviposition-induced release of AVT may be controlled by a different mechanism. J. Exp. Zool. 286:481-486, 2000.</p>","PeriodicalId":15686,"journal":{"name":"Journal of Experimental Zoology","volume":"286 5","pages":"481-6"},"PeriodicalIF":0.0000,"publicationDate":"2000-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Zoology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Arginine vasotocin (AVT), an avian neurohypophysial hormone, is released during osmotic stimulation and oviposition. In the present study, the role of opioid peptides on AVT release was studied by examining the effects of an opioid agonist and antagonist on osmotic- and oviposition-induced secretion of AVT. The administration of hypertonic saline (1.5 M NaCl) induced an increase in the plasma levels of AVT. The simultaneous administration of morphine, an opioid receptor agonist, inhibited the osmotically induced increase in plasma levels of AVT in a dose-dependent manner. On the other hand, the co-administration of morphine with naloxone, an opioid receptor antagonist, attenuated the inhibitory effect of morphine. Moreover, injection of naloxone alone enhanced the osmotically induced increase in plasma levels of AVT. However, the administration of morphine did not inhibit the oviposition-induced increase in plasma levels of AVT. These results suggest that osmotic-induced release of AVT may be under opioid regulation, while oviposition-induced release of AVT may be controlled by a different mechanism. J. Exp. Zool. 286:481-486, 2000.
精氨酸催产素(AVT)是一种鸟类的神经垂体激素,在渗透刺激和产卵过程中释放。在本研究中,通过检测阿片受体激动剂和拮抗剂对渗透和排卵诱导的AVT分泌的影响,研究了阿片肽对AVT释放的作用。高渗盐水(1.5 M NaCl)可引起血浆AVT水平升高。同时给予吗啡,一种阿片受体激动剂,以剂量依赖的方式抑制渗透诱导的血浆AVT水平的增加。另一方面,吗啡与纳洛酮(一种阿片受体拮抗剂)联合使用,减弱了吗啡的抑制作用。此外,单独注射纳洛酮可增强渗透诱导的血浆AVT水平升高。然而,吗啡的施用并没有抑制排卵引起的血浆AVT水平的升高。这些结果表明,渗透诱导的AVT释放可能受阿片调节,而排卵诱导的AVT释放可能受不同机制的控制。[j] .中国生物医学工程学报,2006,31(2):481-486。