Blinder K J, Dickerson L W, Gray A L, Lauenstein J M, Newsome J T, Bingaman M T, Gatti P J, Gillis R A, Massari V J
Department of Pharmacology, Howard University College of Medicine, 50 W Street, NW, Washington, DC 20059, USA.
Brain Res. 1998 Nov 9;810(1-2):251-6. doi: 10.1016/s0006-8993(98)00877-4.
Previous research from this laboratory has shown that substance P-immunoreactive (SP) terminals synapse upon negative chronotropic vagal preganglionic neurons (VPNs), but not upon negative dromotropic VPNs, of the ventrolateral nucleus ambiguus (NA-VL). Moreover, SP agonists injected into NA-VL cause bradycardia without decreasing AV conduction. In the current study, we have: (1) defined the electron microscopic characteristics of the SP neurons of NA-VL in dog; and (2) tested the hypothesis that SP nerve terminals synapse upon negative inotropic VPNs of NA-VL, retrogradely labeled from the cranial medial ventricular (CMV) ganglion. Numerous SP terminals and a few SP neurons were observed in the vicinity of retrogradely labeled neurons. SP terminals were observed forming synapses with unlabeled dendrites and with SP dendrites, but never with the retrogradely labeled neurons. Together, these results and earlier findings suggest that SP agonists may be able to induce bradycardia without decreasing AV conduction or ventricular contractility.
该实验室先前的研究表明,P物质免疫反应性(SP)终末与腹外侧疑核(NA-VL)中负性变时性迷走神经节前神经元(VPNs)形成突触,但不与负性变传导性VPNs形成突触。此外,注入NA-VL的SP激动剂可引起心动过缓,而不降低房室传导。在本研究中,我们:(1)确定了犬NA-VL中SP神经元的电子显微镜特征;(2)检验了以下假设,即SP神经终末与从颅内侧心室(CMV)神经节逆行标记的NA-VL中负性变力性VPNs形成突触。在逆行标记神经元附近观察到大量SP终末和少数SP神经元。观察到SP终末与未标记的树突以及SP树突形成突触,但从未与逆行标记的神经元形成突触。这些结果和早期发现共同表明,SP激动剂可能能够在不降低房室传导或心室收缩力的情况下诱发心动过缓。