Bouali S M, Fournier A, Jolicoeur F B
Department of Psychiatry, Faculty of Medicine, University of Sherbrooke, Québec, Canada.
Regul Pept. 1994 Dec 15;54(2-3):367-72. doi: 10.1016/0167-0115(94)90534-7.
Many effects of NPY have been attributed to a decrease in the activity of adenylate cyclase. Pre-treatment with pertussis toxin (PTx) has been shown to inhibit many pharmacological effects of NPY including increased feeding following administration in the paraventricular nucleus (PVN). In the present study, we examined the influence of PTx pretreatment on the effects of NPY on body temperature following administration in the preoptic area (POA), a region which seems to be the most sensitive to the effects of the peptide on body temperature. The effects of the same pre-treatment on the action of NPY2-36 was also studied since we have found previously that this fragment produced opposite effects on body temperature to that of NPY when injected in the POA. PTx was administered 3 days prior to the injection of NPY or NPY2-36. Results indicate that the hypothermic effect of NPY produced in the POA was blocked by PTx whereas the hyperthermic effect of NPY2-36 was not affected. These results are important as they provide evidence that, in the POA at least, the receptors mediating the hypothermic effect of NPY might be biochemically different from those mediating the hyperthermic effect of NPY2-36.
神经肽Y(NPY)的许多作用都归因于腺苷酸环化酶活性的降低。研究表明,用百日咳毒素(PTx)预处理可抑制NPY的许多药理作用,包括在室旁核(PVN)给药后摄食量增加。在本研究中,我们研究了PTx预处理对NPY在视前区(POA)给药后对体温影响的作用,视前区似乎是对该肽对体温影响最敏感的区域。由于我们之前发现,当在视前区注射时,该片段对体温产生的作用与NPY相反,因此我们也研究了相同预处理对NPY2-36作用的影响。在注射NPY或NPY2-36前3天给予PTx。结果表明,PTx可阻断视前区产生的NPY的降温作用,而NPY2-36的升温作用不受影响。这些结果很重要,因为它们提供了证据,至少在视前区,介导NPY降温作用的受体在生化性质上可能与介导NPY2-36升温作用的受体不同。