Malatynska E, Knapp R J, Ikeda M, Yamamura H I
University of Arizona, Department of Pharmacology, Tucson 85724.
Life Sci. 1988;43(4):303-7. doi: 10.1016/0024-3205(88)90107-5.
Convulsive seizures are a potential side effect of antidepressant drug treatment and can be produced by all classes of antidepressants. It is also known that some convulsant and anticonvulsant drug actions are mediated by the GABA-receptor chloride-ionophore complex. Drugs acting at this complex appear to induce convulsions by inhibiting chloride conductance through the associated chloride channel. Using the method of GABA-stimulated 36Cl-uptake by rat cerebral cortical vesicles, we show that some antidepressant drugs (imipramine, amitryptyline, and mianserine) can inhibit the GABA-receptor chloride uptake, and that the degree of chloride channel inhibition by these drugs correlates with the frequency of convulsive seizures induced by them.
惊厥性癫痫发作是抗抑郁药物治疗的一种潜在副作用,所有类型的抗抑郁药都可能引发。此外,已知一些惊厥药物和抗惊厥药物的作用是由γ-氨基丁酸(GABA)受体-氯离子载体复合物介导的。作用于该复合物的药物似乎通过抑制相关氯离子通道的氯电导来诱发惊厥。通过大鼠大脑皮质囊泡摄取GABA刺激的36Cl-的方法,我们发现一些抗抑郁药物(丙咪嗪、阿米替林和米安色林)能够抑制GABA受体对氯的摄取,并且这些药物对氯离子通道的抑制程度与它们所诱发的惊厥性癫痫发作频率相关。