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锂中毒会导致脑损伤吗?——一项大鼠组织病理学研究。

Does lithium poisoning induce brain injuries?-A histopathological rat study.

作者信息

Klein Mathieu, Naffaa Vanessa, Chevillard Lucie, Risède Patricia, Saubaméa Bruno, Adle-Biassette Homa, Mégarbane Bruno

机构信息

Université Paris Cité, Inserm UMRS-1144, Paris, France.

Université Paris Cité, Inserm NeuroDiderot, Laboratoire d'Anatomie Pathologique, Hôpital Lariboisière, AP-HP, Paris, France.

出版信息

Basic Clin Pharmacol Toxicol. 2023 May;132(5):449-453. doi: 10.1111/bcpt.13847. Epub 2023 Feb 26.

Abstract

Due to a narrow therapeutic index, prolonged lithium treatment and overdose may result in neurotoxicity. Neurotoxicity is deemed reversible with lithium clearance. However, echoing the report of syndrome of irreversible lithium-effectuated neurotoxicity (SILENT) in rare severe poisonings, lithium-induced histopathological brain injuries including extensive neuronal vacuolization, spongiosis and ageing-like neurodegenerative changes were described in the rat following acute toxic and pharmacological exposure. We aimed to investigate the histopathological consequences of lithium exposure in rat models mimicking prolonged treatment and all three patterns of acute, acute-on-chronic and chronic poisonings observed in humans. We performed histopathology and immunostaining-based analyses using optic microscopy of brains obtained from male Sprague-Dawley rats randomly assigned to lithium or saline (controls) and treated according to the therapeutic or to the three poisoning models. No lesion was observed in any brain structure in any of the models. Neuron and astrocyte counts did not differ significantly between lithium-treated rats and controls. Our findings support that lithium-induced neurotoxicity is reversible and brain injury not a common feature of toxicity.

摘要

由于治疗指数较窄,长期锂治疗及过量使用可能导致神经毒性。随着锂的清除,神经毒性被认为是可逆的。然而,与罕见严重中毒中不可逆锂所致神经毒性综合征(SILENT)的报告一致,在急性毒性和药理学暴露后的大鼠中,描述了锂诱导的组织病理学脑损伤,包括广泛的神经元空泡化、海绵样变和类似衰老的神经退行性变化。我们旨在研究锂暴露在模拟长期治疗以及人类中观察到的急性、慢性中毒基础上的急性中毒和慢性中毒这三种模式的大鼠模型中的组织病理学后果。我们对随机分配到锂组或生理盐水组(对照组)并根据治疗方案或三种中毒模型进行处理的雄性Sprague-Dawley大鼠的大脑进行了组织病理学和基于免疫染色的光学显微镜分析。在任何模型的任何脑结构中均未观察到病变。锂治疗组大鼠与对照组之间的神经元和星形胶质细胞计数无显著差异。我们的研究结果支持锂诱导的神经毒性是可逆的,脑损伤并非毒性的常见特征。

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