Sivam S P, Ho I K
Life Sci. 1985 Jul 22;37(3):199-208. doi: 10.1016/0024-3205(85)90645-9.
Drugs affecting various steps of GABA transmission exhibit analgesia in a variety of experimental models in animals; this analgesic response generally requires high doses of the drugs and does not appear to be opiate-like since the GABAergic analgesia is naloxone-insensitive and lacks dependence liability. The outcome of the analgesia response is variable when opiate and GABAergic drugs are administered together; however, directly acting GABA receptor stimulants and GABA-transaminase inhibitors generally enhance the analgesic effect of opiates. The development of newer GABAergic drugs with greater potency and specificity may offer an alternative to opiate analgesics. The results obtained over the years, on the possible involvement of the GABA system in morphine tolerance and dependence are equivocal. Studies on region-specific changes in opiate-GABA interaction as well as opiate-GABA-benzodiazepine interaction are needed to further elucidate the role of GABA on opiate system.
影响γ-氨基丁酸(GABA)传递各个步骤的药物在多种动物实验模型中均表现出镇痛作用;这种镇痛反应通常需要高剂量的药物,并且似乎不像阿片类药物,因为GABA能镇痛对纳洛酮不敏感且不存在依赖性。当同时给予阿片类药物和GABA能药物时,镇痛反应的结果是可变的;然而,直接作用的GABA受体激动剂和GABA转氨酶抑制剂通常会增强阿片类药物的镇痛效果。开发更高效、更具特异性的新型GABA能药物可能为阿片类镇痛药提供一种替代选择。多年来获得的关于GABA系统可能参与吗啡耐受性和依赖性的结果并不明确。需要对阿片类药物与GABA相互作用以及阿片类药物与GABA-苯二氮䓬相互作用的区域特异性变化进行研究,以进一步阐明GABA在阿片类药物系统中的作用。