Mereu G, Fanni B, Serra M, Concas A, Biggio G
Eur J Pharmacol. 1983 Dec 9;96(1-2):129-32. doi: 10.1016/0014-2999(83)90539-3.
Diazepam (0.5 mg/kg i.v.) was found to inhibit the firing rate of substantia nigra pars reticulata (SN-PR) cells by 50%. In contrast, beta-CCM, at the doses of 125 and 250 micrograms/kg i.v. increased the firing rate by 90 and 150%, respectively, while DMCM produced similar increases at doses of 250 and 500 micrograms/kg i.v. Both beta-carboline-induced excitation and diazepam-induced inhibition were reversed to baseline values by the specific antagonist of benzodiazepine recognition sites, Ro15-1788 (2.0 mg/kg i.v.). Moreover, the stimulant effect of beta-carbolines was also reversed by diazepam (1.0 mg/kg) to about 50% of baseline. The results indicate that beta-carbolines specifically influence the activity of SN-PR cells through a mechanism opposite to that of benzodiazepines themselves, acting on benzodiazepine recognition sites.
地西泮(静脉注射0.5毫克/千克)可使黑质网状部(SN-PR)细胞的放电频率降低50%。相比之下,β-CCM静脉注射剂量为125和250微克/千克时,放电频率分别增加了90%和150%,而DMCM静脉注射剂量为250和500微克/千克时也产生了类似的增加。苯二氮䓬识别位点的特异性拮抗剂Ro15-1788(静脉注射2.0毫克/千克)可使β-咔啉诱导的兴奋和地西泮诱导的抑制作用恢复到基线值。此外,地西泮(1.0毫克/千克)也可使β-咔啉的兴奋作用恢复到基线值的约50%。结果表明,β-咔啉通过与苯二氮䓬本身相反的机制,作用于苯二氮䓬识别位点,特异性地影响SN-PR细胞的活性。