Department of Toxicology, School of Pharmacy, Hoshi University, 2–4–41 Ebara, Shinagawa-ku, Tokyo 142–8501, Japan.
Biol Pharm Bull. 2012;35(12):2243-6. doi: 10.1248/bpb.b12-00542.
The present study was designed to clarify whether the arachidonic acid cascade contributes to the decreased threshold for pentylenetetrazole-induced seizure under benzodiazepine withdrawal in mice. The seizure threshold for pentylenetetrazole was significantly decreased by the discontinuation of chronic treatment with diazepam. The decrease in the seizure threshold for pentylenetetrazole during diazepam withdrawal was significantly suppressed by intracerebroventricular (i.c.v.) pretreatment with the phospholipase A(2) inhibitor quinacrine (30, 100 nmol) and the lipoxygenase inhibitor nordihydroguaiaretic acid (10, 30 nmol). In contrast, the decreased seizure threshold in the diazepam-withdrawal group was intensified by pretreatment with the cyclooxygenase inhibitor diclofenac (56 nmol). These compounds did not alter the threshold for seizure in a control group. These findings suggest that enhancement of the arachidonic acid cascade may contribute to the hypersusceptibility to pentylenetetrazole-induced seizure during diazepam withdrawal.
本研究旨在阐明花生四烯酸级联是否有助于在苯二氮䓬类药物戒断下降低戊四氮诱发癫痫的阈值。长期应用地西泮治疗的停药可显著降低戊四氮诱发癫痫的阈值。鞘内预先给予磷脂酶 A2 抑制剂奎尼丁(30、100nmol)和脂氧合酶抑制剂 nordihydroguaiaretic 酸(10、30nmol)可显著抑制地西泮戒断时戊四氮诱发癫痫的阈值降低。相比之下,预先给予环氧化酶抑制剂双氯芬酸(56nmol)可增强地西泮戒断组的癫痫发作阈值降低。这些化合物在对照组中不改变癫痫发作的阈值。这些发现表明,花生四烯酸级联的增强可能有助于苯二氮䓬类药物戒断期间对戊四氮诱发癫痫的高敏感性。