Roberto M, Brunelli M
Department of Physiology and Biochemistry, Institute Giuseppe Moruzzi, University of Pisa, Pisa, Italy.
Learn Mem. 2000 Sep-Oct;7(5):303-11. doi: 10.1101/lm.34200.
Specific receptors for pituitary adenylate cyclase-activating polypeptide (PACAP), a novel peptide with neuroregulatory and neurotrophic functions, have been identified recently in different brain regions, including the hippocampus. In this study, we examined the effects of PACAP-38 on the excitatory postsynaptic field potentials (fEPSPs) evoked at the Schaffer collateral-CA1 synapses. Brief bath application of PACAP-38 (0.05 nM) induced a long-lasting facilitation of the basal transmission. Enhancement of this response was occluded in part by previous high-frequency-induced long-term potentiation (LTP). PACAP-38 did not significantly alter the paired-pulse facilitation (PPF). PACAP-38 has been shown to have a presynaptic effect on the septohippocampal cholinergic terminals, which results in an increase in basal acetylcholine (ACh) release. To assess whether the PACAP-38 enhancement of CA1 synapses was related to the activation of the cholinergic system we examined the effect of this peptide in the presence of atropine, a muscarinic receptor antagonist. The enhancement of the fEPSPs by PACAP-38 was blocked by bath application of atropine. These results show that PACAP-38 induces facilitation of hippocampal synaptic transmission through activation of the cholinergic system via the muscarinic receptors.
垂体腺苷酸环化酶激活多肽(PACAP)是一种具有神经调节和神经营养功能的新型肽,最近已在包括海马体在内的不同脑区中鉴定出其特异性受体。在本研究中,我们检测了PACAP-38对在Schaffer侧支-CA1突触处诱发的兴奋性突触后场电位(fEPSP)的影响。短暂浴用PACAP-38(0.05 nM)可诱导基础传递的持久易化。先前高频诱导的长期增强(LTP)部分阻断了这种反应的增强。PACAP-38并未显著改变双脉冲易化(PPF)。已证明PACAP-38对隔海马胆碱能终末有突触前作用,这导致基础乙酰胆碱(ACh)释放增加。为了评估PACAP-38对CA1突触的增强作用是否与胆碱能系统的激活有关,我们在毒蕈碱受体拮抗剂阿托品存在的情况下检测了该肽的作用。浴用阿托品可阻断PACAP-38对fEPSP的增强作用。这些结果表明,PACAP-38通过毒蕈碱受体激活胆碱能系统诱导海马突触传递的易化。