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机构地区:[1]第三军医大学附属大坪医院野战外科研究所第三研究室
出 处:《第三军医大学学报》1997年第6期513-515,共3页Journal of Third Military Medical University
摘 要:目的:探索甲啡肽(ME)、纳络酮(NLX)对红藻氨酸(KA)诱发大鼠癫痫发作的行为和组织学效应。方法:大鼠经戊巴比妥钠腹腔麻醉后固定于SN-1型立体定位仪上,按大鼠海马定位图谱把直径为0.5mm的金属导管植于海马双侧CA1区:用微量注射器将ME、NLX于10min内注入,随即腹腔内注射KA10mg/kg或12mg/kg。海马组织石蜡切片、HE染色,显微镜观测。结果:海马内微量注入ME可易化癫痫的发生,加重海马组织损伤。NLX可拮抗ME的作用,减轻海马组织损伤。结论:内源性阿片肽在KA诱发大鼠癫痫发作中,对海马的兴奋性的调节起重要作用。Objective: To investigate the behavioral and histological effects of metenkephalin (ME) and naloxone (NLX) on kainic acidinduced epilepsy in rats. Methods: After the rats were anesthetized with intraperitoneal injection of sodium pentobarbital (30 mg/kg), their heads were mounted onto a SN1 stereotaxic apparatus (Narishige). Guiding cannula with a tip diameter of 0.5 mm was slowly implanted in CA1 area of the hippocampus (APO:3.0; RL:3.0; HO:3.0) on both sides. ME and NAL were microinjected through the implanted cannula into the bilateral CA1 areas of awake rats within 10 min. Intraperitoneal injection of 10 mg/kg or 12 mg/kg was immediately conducted. The extracted hippocampal tissue was embedded with paraffin and sectioned. The sections were then stained with HE and observed with microscopy. Results: Intrahippocampal microinjection of ME augmented epileptogenic action and neurotoxic effects of kainic acid (KA) while NLX retarded them. Conclusion: The endogenous opioid peptides may play an important role in regulating hippocampal excitability in KAinduced epilepsy in rats.
分 类 号:R742.1[医药卫生—神经病学与精神病学]
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