Mizoguchi H, Yoshiike M, Suzuki T, Misawa M
Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.
Life Sci. 1993;53(22):PL365-70. doi: 10.1016/0024-3205(93)90211-k.
The effects of Ca2+ channel blockers on the development of physical dependence on diazepam were examined in mice. Co-administration of flunarizine (T-type Ca2+ channel sensitive blocker), but not of either nifedipine or diltiazem (L-type Ca2+ channel sensitive blockers), with diazepam significantly suppressed the hypersensitivity to FG 7142 following chronic treatment with diazepam. The hypersensitivity to FG 7142 may reflect benzodiazepine withdrawal convulsions. These results suggest that flunarizine, but not nifedipine or diltiazem, may suppress the development of physical dependence on diazepam, and that T-type Ca2+ channels in the brain, rather than L-type Ca2+ channels, may be involved in the development of physical dependence on diazepam.
在小鼠中研究了钙通道阻滞剂对安定身体依赖性发展的影响。与安定联合给予氟桂利嗪(T型钙通道敏感阻滞剂),而非硝苯地平或地尔硫䓬(L型钙通道敏感阻滞剂),可显著抑制安定长期治疗后对FG 7142的超敏反应。对FG 7142的超敏反应可能反映了苯二氮䓬类药物戒断惊厥。这些结果表明,氟桂利嗪而非硝苯地平或地尔硫䓬可能抑制安定身体依赖性的发展,并且大脑中的T型钙通道而非L型钙通道可能参与安定身体依赖性的发展。