Matla J, Langwiński R
Pol J Pharmacol Pharm. 1982;34(1-3):135-44.
The effects of benzodiazepine (mainly diazepam) on the following central action of narcotic analgesics were tested: antinociceptive action (Randall-Selitto and hot plate tests), hypermotility, inhibition of methylphenidate stereotypy, catalepsy. Diazepam, in doses not affecting the pain threshold markedly potentiated morphine, codeine, etorphine, pentazocine and fentanyl antinociception. Hypermotility produced by morphine and fentanyl was inhibited by pretreatment with chlordiazepoxide, diazepam and clonazepam. Diazepam potentiated the inhibitory effect of opiates on methylphenidate-induced stereotyped gnawing in mice and increased the catalepsy induced by morphine and fentanyl in rats. In all experiments the effects of diazepam were suppressed by the substances which impair GABA-ergic neurotransmission: bicuculline and picrotoxin. Obtained results indicate that benzodiazepine potentiate the antinociceptive and cataleptogenic effects of opiates and their inhibitory influence on methylphenidate stereotypy. However, these drugs antagonize locomotor hyperactivity in mice. All these actions seem to be related to facilitation of GABA-ergic neurotransmission by benzodiazepines.
测试了苯二氮䓬类药物(主要是地西泮)对麻醉性镇痛药以下中枢作用的影响:抗伤害感受作用(兰德尔-塞利托试验和热板试验)、运动亢进、对哌醋甲酯刻板行为的抑制作用、僵住症。地西泮在不明显影响痛阈的剂量下,显著增强了吗啡、可待因、埃托啡、喷他佐辛和芬太尼的抗伤害感受作用。氯氮䓬、地西泮和氯硝西泮预处理可抑制吗啡和芬太尼引起的运动亢进。地西泮增强了阿片类药物对小鼠哌醋甲酯诱导的刻板啃咬的抑制作用,并增加了吗啡和芬太尼在大鼠中诱导的僵住症。在所有实验中,地西泮的作用均被损害γ-氨基丁酸能神经传递的物质:荷包牡丹碱和印防己毒素所抑制。获得的结果表明,苯二氮䓬类药物增强了阿片类药物的抗伤害感受和致僵住症作用及其对哌醋甲酯刻板行为的抑制影响。然而,这些药物拮抗小鼠的运动性多动。所有这些作用似乎都与苯二氮䓬类药物对γ-氨基丁酸能神经传递的促进作用有关。