首页> 外文期刊>European Journal of Pharmacology: An International Journal >Protective effect of the antipsychotic drug zotepine on dizocilpine-induced neuropathological changes in rat retrosplenial cortex.
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Protective effect of the antipsychotic drug zotepine on dizocilpine-induced neuropathological changes in rat retrosplenial cortex.

机译:抗精神病药佐替平对地佐西平诱导的大鼠脾后皮质神经病理变化的保护作用。

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An atypical antipsychotic drug, zotepine, which is pharmacologically and clinically related to clozapine, has unique therapeutic effects on patients with schizophrenia. It has been demonstrated that clozapine blocks neurotoxicity in the rat retrosplenial cortex induced by administration of the noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist dizocilpine ((+)-MK-801). We examined whether or not zotepine has the ability to block neurotoxicity in the rat retrosplenial cortex induced by administration of dizocilpine. Female Sprague-Dawley rats were injected intraperitoneally (i.p.) with vehicle (1 mg/kg), zotepine (5, 10 or 20 mg/kg) or clozapine (20 mg/kg). Fifteen minutes later, animals were injected intraperitoneally (i.p.) with vehicle (1 ml/kg) or dizocilpine (0.5 mg/kg). Neuropathological changes (neuronal vacuolization) were assessed 4 h after administration of dizocilpine. Immunohistochemical analysis of heat shock protein HSP-70, a marker of reversible neuronal injury, was performed 24 h after administration of dizocilpine. The pretreatment with zotepine (5, 10 or 20 mg/kg) significantly decreased the number of vacuolized neurons in the rat retrosplenial cortex 4 h after the administration of dizocilpine (0.5 mg/kg), in a dose-dependent manner. The potency of zotepine (20 mg/kg) for dizocilpine-induced neurotoxicity was similar to that of clozapine (20 mg/kg). Furthermore, similar to the case with clozapine (20 mg/kg, i.p.), zotepine (20 mg/kg, i.p.) significantly attenuated the expression of HSP-70 in the rat retrosplenial cortex induced by dizocilpine (0.5 mg/kg, i.p.). The present study suggests that the neuroprotective effects of zotepine- on dizocilpine-induced neurotoxicity are equipotent to those of clozapine. Based on the NMDA receptor hypofunction hypothesis of schizophrenia, the efficacy of zotepine in this study may partly contribute to the unique therapeutic effects of zotepine in patients with schizophrenia.
机译:非典型的抗精神病药物佐替平在药理和临床上与氯氮平有关,对精神分裂症患者具有独特的治疗作用。业已证明,氯氮平可阻断非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂地佐西平((+)-MK-801)的给药所诱导的大鼠脊髓后皮质的神经毒性。我们检查了佐替平是否具有阻断由二唑西平引起的大鼠脾后皮质中神经毒性的能力。给雌性Sprague-Dawley大鼠腹膜内(i.p.)注射媒介物(1 mg / kg),唑替平(5、10或20 mg / kg)或氯氮平(20 mg / kg)。 15分钟后,向动物腹膜内(i.p.)注射赋形剂(1ml / kg)或地佐西平(0.5mg / kg)。在给予地佐西平4小时后评估神经病理学改变(神经空泡)。给予地佐西平24小时后,进行了热休克蛋白HSP-70(一种可逆性神经元损伤的标志物)的免疫组织化学分析。佐佐平(5、10或20 mg / kg)预处理以剂量依赖性方式显着降低地佐西平(0.5 mg / kg)给药后4 h大鼠脾后皮质皮层中空泡神经元的数量。佐替平(20 mg / kg)对地佐西平诱导的神经毒性的效力与氯氮平(20 mg / kg)相似。此外,类似于氯氮平(20 mg / kg,ip)的情况,佐替平(20 mg / kg,ip)显着减弱了地佐西平(0.5 mg / kg,ip)在大鼠脾后皮质中HSP-70的表达。 。本研究表明,佐替平对双唑西平诱导的神经毒性的神经保护作用与氯氮平等效。基于精神分裂症的NMDA受体功能减退假说,唑替平的功效在本研究中可能部分有助于佐替平对精神分裂症患者的独特治疗作用。

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