首页> 外文期刊>European Journal of Pharmacology: An International Journal >Activators of potassium M currents have anticonvulsant actions in two rat models of encephalitis.
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Activators of potassium M currents have anticonvulsant actions in two rat models of encephalitis.

机译:钾M电流激活剂在两种大鼠脑炎模型中均具有惊厥作用。

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Opioid systems in hippocampus regulate excitability and kappa opioids have a role in anticonvulsant protection, but their mechanisms of action are incompletely understood. We examined the ability of opioid and nonopioid agents with overlapping ionic mechanisms and actions similar to kappa opioid agonists, to block seizures in rat models of encephalitis due to Borna Disease virus and Herpes Simplex Virus Type-1. Naltrindole, a delta antagonist and thus a kappa opioid sparing agent, (10 mg/kg s.c.) blocked spontaneous and naloxone (opioid antagonist)-induced seizures in the models, but produced somatic signs similar to opioid withdrawal. Given that delta antagonists as well as kappa opioid agonists in hippocampus enhance potassium M currents (I(M)), we tested the effect of the I(M) augmenter flupirtine. Flupirtine (20 mg/kg i.p.) prevented seizures in Borna and herpes infected rats, without signs of withdrawal, hypotonia or sedation. The results support the efficacy of opioid and nonopioid drugs in modulating naloxone-induced seizures in critical illness due to viral encephalitis and by analogy, opioid withdrawal seizures.
机译:海马中的阿片类药物系统调节兴奋性,κ阿片类药物在抗惊厥保护中起作用,但其作用机理尚不完全清楚。我们检查了与阿片类阿片激动剂类似的具有重叠离子机制和作用的阿片类药物和非阿片类药物的能力,以阻止由博尔纳病病毒和单纯疱疹病毒1型引起的脑炎大鼠模型的癫痫发作。 Naltrindole是一种δ拮抗剂,因此是一种阿片类阿片保护剂(10 mg / kg s.c.)在模型中阻断了自发的和纳洛酮(阿片类拮抗剂)诱导的癫痫发作,但产生类似于阿片类药物戒断的体征。考虑到海马中的δ拮抗剂和κ阿片样物质激动剂会增强钾离子电流(I(M)),因此我们测试了I(M)增强氟吡汀的作用。氟吡汀(20 mg / kg i.p.)预防了感染Borna和疱疹的大鼠的癫痫发作,没有停药,肌张力低下或镇静的迹象。该结果支持阿片类药物和非阿片类药物在调节由病毒性脑炎和类阿片类戒断发作所致的危重疾病中纳洛酮诱发的癫痫发作中的功效。

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