Curcumin mitigates lithium-induced thyroid dysfunction by modulating antioxidant status, apoptosis and inflammatory cytokines

IF 1.1 Q3 BIOLOGY
Sanaa M. Abd El-Twab, Manal Abdul-Hamid
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引用次数: 14

Abstract

Lithium is an integral drug used in the management of acute mania, unipolar and bipolar depression and prophylaxis of bipolar disorders. It has also been shown to reduce suicidal risk and short term mortality. Few experimental studies have demonstrated the thyroid toxicity caused by lithium as well as the possible protective effect of curcumin. Twenty four male albino rats were divided into three groups; group I (control group), group II received lithium carbonate daily for 6 weeks and group III received the same dose of lithium carbonate as group II concomitantly with curcumin for 6 weeks. The specimens were prepared for histopathological, immunohistochemical and biochemical examination. Lithium-induced thyroid dysfunction evidenced by the histopathological and immunohistochemical changes represented by detached cells and vacuolated cytoplasm of some follicular cells and highly significant increase in positive immunostained of thyroglobulin and caspase-3 respectively. Moreover, a significant decrease in serum free triiodothyonine (FT3), free thyroxine (FT4) concomitant with significantly increased thyroid stimulating hormone (TSH) and pro-inflammatory cytokines, and thyroid lipid peroxidation (MDA) and nitric oxide (NO) levels. Curcumin counteracted lithium-induced oxidative stress and inflammation as assessed by restoration of the antioxidant defenses and diminishing of pro-inflammatory cytokines and improvements in the degenerative changes of the thyroid gland. In conclusion, the present study provides evidence that curcumin exerts thyroprotective effects against lithium carbonate mediated by its antioxidant, anti-inflammatory and anti-apoptotic effect as indicated by caspase-3. This report also confers that the use of this drug should be justified for long treatment under direct medical supervision.

姜黄素通过调节抗氧化状态、细胞凋亡和炎症细胞因子减轻锂诱导的甲状腺功能障碍
锂是一种整体药物,用于管理急性躁狂,单极和双相抑郁症和双相情感障碍的预防。它也被证明可以降低自杀风险和短期死亡率。很少有实验研究证明锂引起的甲状腺毒性以及姜黄素可能的保护作用。24只雄性白化大鼠分为3组;ⅰ组(对照组)、ⅱ组每日给予碳酸锂治疗,连续6周,ⅲ组给予与ⅱ组相同剂量碳酸锂治疗,同时给予姜黄素治疗,连续6周。对标本进行组织病理学、免疫组织化学和生化检查。锂离子诱导的甲状腺功能障碍表现为组织病理学和免疫组织化学改变,部分滤泡细胞出现细胞分离和胞浆空泡,甲状腺球蛋白和caspase-3免疫染色阳性分别显著升高。此外,血清游离三碘甲状腺氨酸(FT3)、游离甲状腺素(FT4)显著降低,同时促甲状腺激素(TSH)、促炎细胞因子、甲状腺脂质过氧化(MDA)和一氧化氮(NO)水平显著升高。姜黄素通过恢复抗氧化防御、减少促炎细胞因子和改善甲状腺退行性变化来抵消锂诱导的氧化应激和炎症。综上所述,本研究证明姜黄素通过caspase-3的抗氧化、抗炎和抗凋亡作用,对碳酸锂具有甲状腺保护作用。该报告还认为,在直接医疗监督下长期使用这种药物是合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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48
审稿时长
47 weeks
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