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Lithium as a disease-modifying agent for prion diseases

机译:锂作为病毒疾病的疾病改良剂

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Prion diseases still remain incurable despite multiple efforts to develop a treatment. Therefore, it is important to find strategies to at least reduce the symptoms. Lithium has been considered as a neuroprotective agent for years, and the objective of this preclinical study was to evaluate the efficacy of lithium delivered as a water-in-oil microemulsion (Aonys?). This delivery system allows using low doses of lithium and to avoid the toxicity observed in chronic treatments. C57BL/6J mice were intracranially inoculated with ME7 prion-infected brain homogenates and then were treated with lithium from day 90 post inoculation until their death. Lithium was administered at traditional doses (16?mg/kg/day) by the gavage route and at lower doses (40 or 160?μg/kg/day; Aonys?) by the rectal mucosa route. Low doses of lithium (Aonys?) improved the survival of prion-inoculated mice, and also decreased vacuolization, astrogliosis, and neuronal loss compared with controls (vehicle alone). The extent of the protective effects in mice treated with low-dose lithium was comparable or even higher than what was observed in mice that received lithium at the traditional dose. These results indicate that lithium administered using this innovative delivery system could represent a potential therapeutic approach not only for prion diseases but also for other neurodegenerative diseases.
机译:尽管开发治疗方法付出了许多努力,但on病毒仍然无法治愈。因此,重要的是找到至少减轻症状的策略。锂已被认为是一种神经保护剂,多年来,这项临床前研究的目的是评估锂作为油包水型微乳(Aonys ?)的功效。该输送系统允许使用低剂量的锂,并避免了在慢性治疗中观察到的毒性。 C57BL / 6J小鼠颅内接种ME7 ates病毒感染的脑匀浆,然后从接种后90天开始用锂治疗直至死亡。灌胃途径以传统剂量(16?mg / kg /天)施用锂,而直肠粘膜途径以较低剂量(40或160?μg/ kg /天; Aonys ?)施用锂。与对照(单独的车辆)相比,低剂量的锂(Aonys ?)提高了接种病毒的小鼠的存活率,并且还降低了空泡,星形胶质沉着和神经元丢失。用低剂量锂治疗的小鼠的保护作用程度与传统剂量接受锂的小鼠相当或什至更高。这些结果表明,使用这种创新的给药系统给药的锂不仅可以代表病毒疾病,还可以代表其他神经退行性疾病的潜在治疗方法。

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