Carter D A, Lightman S L
Exp Brain Res. 1987;65(3):699-702. doi: 10.1007/BF00235997.
The role of ascending noradrenergic pathways in the mediation of central opiate-induced cardiovascular effects has been investigated. The effects of selective kappa- and delta-opiate agonists microinjected into the nucleus tractus solitarius (NTS) of urethane anaesthetized rats were compared following 6-hydroxydopamine lesions of either the dorsal (DNAB) or ventral (VNAB) noradrenergic bundles. In sham lesioned animals both opiates elicited a significant pressor effect and a variable but consistent bradycardia. The delta-agonist responses were not modified in lesioned rats. In marked contrast the pressor effect of the kappa-agonist was abolished in both DNAB and VNAB lesioned rats. The bradycardic response was not significantly modified. These findings are consistent with previous observations that the cardiovascular effects of kappa- and delta-opiates in the NTS are mediated via different mechanisms, and provide evidence for selective functional actions of endogenous opioids within brain nuclei.
已对上行去甲肾上腺素能通路在介导中枢阿片类药物引起的心血管效应中的作用进行了研究。在对去甲肾上腺素能束的背侧(DNAB)或腹侧(VNAB)进行6-羟基多巴胺损伤后,比较了选择性κ-和δ-阿片类激动剂微量注射到乌拉坦麻醉大鼠孤束核(NTS)中的效应。在假损伤动物中,两种阿片类药物均引起显著的升压效应和可变但一致的心动过缓。损伤大鼠中δ-激动剂的反应未改变。与之形成鲜明对比的是,在DNAB和VNAB损伤的大鼠中,κ-激动剂的升压效应均被消除。心动过缓反应没有显著改变。这些发现与之前的观察结果一致,即NTS中κ-和δ-阿片类药物的心血管效应是通过不同机制介导的,并为脑内核团内内源性阿片类物质的选择性功能作用提供了证据。