Zubrzycka M, Janecka A
Department of Experimental Physiology, Medical University, Lodz, Poland.
J Physiol Pharmacol. 2007 Sep;58(3):479-86.
Substance P (SP), vasoactive intestinal polypeptide (VIP) and galanin (GAL), present in primary sensory neurons, are involved in transmission of nociceptive signaling from the peripheral to central nervous system. In this study we investigated the effect of GAL on SP-induced or VIP-induced evoked tongue jerks (ETJ) in response to noxious tooth pulp stimulation during perfusion of the cerebral ventricles with SP or VIP solutions. The experiments were carried out on rats under chloralose anesthesia. It was shown that both, SP and VIP, perfused through the cerebral ventricles enhanced the ETJ amplitude as compared with control, but the effect produced by SP was stronger. The intracerebroventricular perfusion of GAL 5 minutes before SP caused a dose-dependent inhibition of SP-induced ETJ, whereas GAL perfused through the cerebral ventricles 5 minutes before VIP did not reduce the excitatory effect of VIP on ETJ. These results indicate that the antinociceptive effect of GAL perfused through the cerebral ventricles, tested on the trigemino-hypoglossal reflex in rats, is specifically mediated by the SP-ergic system.
P物质(SP)、血管活性肠肽(VIP)和甘丙肽(GAL)存在于初级感觉神经元中,参与伤害性信号从外周神经系统向中枢神经系统的传递。在本研究中,我们在向脑室灌注SP或VIP溶液期间,研究了GAL对有害牙髓刺激引起的SP诱导或VIP诱导的诱发舌抽搐(ETJ)的影响。实验在氯醛糖麻醉的大鼠身上进行。结果表明,与对照组相比,通过脑室灌注的SP和VIP均增强了ETJ幅度,但SP产生的效应更强。在SP灌注前5分钟脑室内灌注GAL可导致SP诱导的ETJ出现剂量依赖性抑制,而在VIP灌注前5分钟通过脑室灌注GAL并未降低VIP对ETJ的兴奋作用。这些结果表明,通过脑室灌注的GAL的抗伤害感受作用,在大鼠三叉神经-舌下神经反射中进行测试,是由SP能系统特异性介导的。