Matsumoto R R, Brinsfield K H, Patrick R L, Walker J M
Department of Psychology, Brown University, Providence, Rhode Island.
J Pharmacol Exp Ther. 1988 Jul;246(1):196-203.
The regulation of motor behavior by mu, delta and kappa opiate receptors in the substantia nigra was examined. Unilateral microinjections of specific mu (DAGO), delta (DPDPE) and kappa (U-50,488H) ligands into the substantia nigra pars reticulata of rats produced dose-dependent contralateral turning. The opiate antagonist naloxone blocked these effects, suggesting that the circling was mediated through opiate receptors. The involvement of midbrain dopaminergic systems in this behavior was tested in two ways. Unilateral 6-hydroxydopamine lesions of the medial forebrain bundle decreased the circling produced by DPDPE and DAGO but increased the circling produced by U-50,488H. In contrast, activating dopaminergic systems with systemic injections of amphetamine increased the circling produced by DAGO and DPDPE but had no effect on the circling produced by U-50,488H. These findings suggest that kappa opioids exert opposite effects on locomotion: motor activation through the SNR and motor inhibition through actions in the SNC. Furthermore, the data suggest that the actions of kappa opioids in the SNC are opposite to those produced by mu and delta opioids.
研究了黑质中μ、δ和κ阿片受体对运动行为的调节作用。向大鼠黑质网状部单侧微量注射特异性μ(DAGO)、δ(DPDPE)和κ(U-50,488H)配体可产生剂量依赖性的对侧旋转。阿片拮抗剂纳洛酮可阻断这些效应,表明这种旋转是通过阿片受体介导的。通过两种方式测试了中脑多巴胺能系统在这种行为中的作用。内侧前脑束的单侧6-羟基多巴胺损伤减少了DPDPE和DAGO产生的旋转,但增加了U-50,488H产生的旋转。相反,全身注射苯丙胺激活多巴胺能系统增加了DAGO和DPDPE产生的旋转,但对U-50,488H产生的旋转没有影响。这些发现表明,κ阿片类物质对运动产生相反的作用:通过黑质网状部激活运动,通过黑质致密部的作用抑制运动。此外,数据表明κ阿片类物质在黑质致密部的作用与μ和δ阿片类物质产生的作用相反。