Effects of Lithium and Verapamil on Thyroid and Kidney Function in Mice: A Preclinical Study.

IF 3.1 4区 医学 Q3 TOXICOLOGY
Journal of Applied Toxicology Pub Date : 2026-11-01 Epub Date: 2026-03-20 DOI:10.1002/jat.70172
Mohammad Salem Hareedy, Mahmoud Hamdy Abdelrahem, Samar Sayed Hassan, Heba Hassan Elkaliny
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引用次数: 0

Abstract

Lithium (Li) salts are still one of the basic therapies for manic-depressive illness, which has a double-edged nature where the good efficacy is threatened by possible toxicity if Li levels are elevated. The effects of verapamil and N-acetylcysteine (NAC) on Li levels and Li-related toxicity in the thyroid gland and kidneys were studied. Five groups of mice (normal control, Li, verapamil, Li + verapamil, and Li + NAC) were evaluated for levels of urea, creatinine, thyroid hormones (T3 and T4), thyroid-stimulating hormone (TSH), sodium, and potassium after 6 weeks. Li levels were measured in all groups that received Li. Renal and thyroid tissues were assessed histologically. T4 and T3 were significantly elevated in the Li, Li + verapamil, and Li + NAC groups compared to the normal control (p < 0.0001), while TSH was significantly decreased (p < 0.001). Levels of Li, potassium, and urea were elevated by the co-administration of verapamil or NAC, while serum creatinine was significantly decreased compared to the Li-treated group. Verapamil and NAC elevated the serum levels of Li and augmented the effects of Li on the thyroid gland, urea, and potassium levels.

锂和维拉帕米对小鼠甲状腺和肾脏功能影响的临床前研究。
锂盐仍然是治疗躁狂抑郁症的基础药物之一,但锂盐具有双刃剑的性质,如果锂盐水平升高,其良好的疗效可能受到毒性的威胁。研究了维拉帕米和n -乙酰半胱氨酸(NAC)对大鼠甲状腺和肾脏中锂离子水平及锂相关毒性的影响。6周后测定5组小鼠(正常对照组、Li组、维拉帕米组、Li +维拉帕米组、Li + NAC组)的尿素、肌酐、甲状腺激素(T3、T4)、促甲状腺激素(TSH)、钠、钾水平。在所有接受Li治疗的组中测量Li水平。对肾脏和甲状腺组织进行组织学评估。与正常对照组相比,Li组、Li +维拉帕米组和Li + NAC组的T4和T3明显升高(p
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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