Volkoff H, Peter R E
Department of Biological Sciences, University of Alberta, Alberta, T6G 2E9, Edmonton, Canada.
Regul Pept. 2001 Sep 15;101(1-3):59-72. doi: 10.1016/s0167-0115(01)00261-0.
The neuropeptides orexin A (OXA), neuropeptide Y (NPY) and galanin (GAL) have been shown to play a role in the regulation of food intake in mammals. They also significantly stimulate feeding in goldfish. In order to assess the interactions between these peptides in the control of feeding in goldfish, we investigated the effects of central injection of specific receptor antagonists for NPY (BIBP 3226) and GAL (M40) on OXA-induced feeding and the effects of desensitization of orexin receptors on NPY- and GAL-induced feeding. We investigated the effects of BIBP 3226 on GAL-induced feeding and the effects of M40 on NPY-induced feeding. We also examined the effects of coinjection of each pair of neuropeptides on feeding behavior. Injections of 10 ng/g OXA, 5 ng/g NPY and 10 ng/g GAL each induced an increase in feeding. Fish treated with 5 ng/g BIBP or 20 ng/g M40 had food consumption similar to saline controls. BIBP at 5 ng/g significantly reduced NPY- and OXA-induced feeding. Injections of 20 ng/g M40 significantly decreased GAL-induced feeding, but had no effect on OXA-induced feeding. Blocking of orexin receptors by treatment with high doses of OXA (100 ng/g) resulted in a decrease in both NPY- and GAL-induced feeding. Coinjection with 0.5 ng/g OXA and either 0.5 ng/g NPY or 0.5 ng/g GAL resulted in a food intake higher than that observed in saline control fish and in fish treated with NPY or GAL alone at 0.5 ng/g. NPY mRNA expression was increased in the telencephalon and in the hypothalamus compared to saline-treated fish, following injection of OXA. These results indicate that both NPY and GAL are at least, in part, dependent on coaction with OXA for the stimulation of food intake and feeding behavior in goldfish. In addition, the effects of OXA are mediated, in part, by the NPY pathway. This suggests a functional interdependence between these three peptidergic systems in the control of energy balance in goldfish.
神经肽食欲素A(OXA)、神经肽Y(NPY)和甘丙肽(GAL)已被证明在哺乳动物的食物摄入调节中发挥作用。它们也能显著刺激金鱼进食。为了评估这些肽在金鱼进食控制中的相互作用,我们研究了向金鱼脑内注射NPY特异性受体拮抗剂(BIBP 3226)和GAL特异性受体拮抗剂(M40)对OXA诱导进食的影响,以及食欲素受体脱敏对NPY和GAL诱导进食的影响。我们研究了BIBP 3226对GAL诱导进食的影响以及M40对NPY诱导进食的影响。我们还检查了每对神经肽共同注射对进食行为的影响。注射10 ng/g OXA、5 ng/g NPY和10 ng/g GAL均可使进食量增加。用5 ng/g BIBP或20 ng/g M40处理的金鱼的食物消耗量与生理盐水对照组相似。5 ng/g的BIBP显著降低了NPY和OXA诱导的进食量。注射20 ng/g M40显著降低了GAL诱导的进食量,但对OXA诱导的进食量没有影响。用高剂量OXA(100 ng/g)处理以阻断食欲素受体,导致NPY和GAL诱导的进食量均减少。0.5 ng/g OXA与0.5 ng/g NPY或0.5 ng/g GAL共同注射导致的食物摄入量高于生理盐水对照鱼以及单独用0.5 ng/g NPY或GAL处理的鱼。与生理盐水处理的鱼相比,注射OXA后,端脑和下丘脑的NPY mRNA表达增加。这些结果表明,在金鱼中,NPY和GAL至少部分依赖于与OXA共同作用来刺激食物摄入和进食行为。此外,OXA的作用部分是由NPY途径介导的。这表明这三种肽能系统在金鱼能量平衡控制中存在功能上的相互依赖关系。