Chance W T, Sheriff S, Foley-Nelson T, Fischer J E, Balasubramaniam A
Department of Surgery, University of Cincinnati Medical Center, OH 45267.
Peptides. 1989 Nov-Dec;10(6):1283-6. doi: 10.1016/0196-9781(89)90022-3.
Neuropeptide Y (NPY) is the most powerful peptide drug stimulating feeding in rats. Rats with paraventricular hypothalamic (PVH) cannulae were used to investigate the mechanisms involved in NPY-induced feeding. Consistent with previous reports, injection of 2 micrograms of NPY into the PVH significantly increased the cumulative food intake over 1-, 2- and 4-hr periods. Ad lib feeding decreased significantly two days after pertussis toxin (PT) administration, but recovered to nearly normal levels on the fourth day. PT had no immediate effect on NPY-induced feeding; however, four days after PT was injected NPY (2 micrograms) did not increase the food intake compared to control. In vitro investigations showed that isoproterenol-stimulated adenylate cyclase activity in the hypothalamus of control rats was inhibited by NPY. In PT-treated rats, however, no inhibition of cAMP production was observed. These results suggest that cAMP may mediate NPY-induced feeding and that a PT-sensitive G protein may be involved in this signal transduction.
神经肽Y(NPY)是刺激大鼠进食的最强效肽类药物。采用下丘脑室旁核(PVH)插管的大鼠来研究NPY诱导进食所涉及的机制。与先前的报道一致,向PVH注射2微克NPY可显著增加1小时、2小时和4小时内的累积食物摄入量。给予百日咳毒素(PT)两天后,自由进食量显著减少,但在第四天恢复到接近正常水平。PT对NPY诱导的进食没有即时影响;然而,注射PT四天后,与对照组相比,注射2微克NPY并未增加食物摄入量。体外研究表明,异丙肾上腺素刺激的对照大鼠下丘脑腺苷酸环化酶活性受到NPY的抑制。然而,在PT处理的大鼠中,未观察到cAMP生成的抑制。这些结果表明,cAMP可能介导NPY诱导的进食,并且一种对PT敏感的G蛋白可能参与了这一信号转导过程。