测定葡萄糖酸锌在小鼠体内的中位致死剂量并进行安全性评估

Yong-cai Wang, Xia Yang, Juan Xiao, Su-mei Wei, Ying Su, Xiu-qi Chen, Ting Huang, Qing-wen Shan
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摘要

葡萄糖酸锌 (ZG) 是一种安全有效的锌补充剂。然而,关于 ZG 静脉注射的最佳剂量和动物模型安全性评估的研究还很有限。本研究旨在确定 C57BL/6J 小鼠静脉注射 ZG 的安全剂量范围。通过剂量滴定实验确定了 ZG 在小鼠体内的半数致死剂量和 95% 置信区间 (95%CI)。根据半数致死剂量,评估了 ZG 的四个亚致死剂量 (SLD)。每种亚致死剂量小鼠注射三次并监测七天后,测定血清锌含量,并通过组织学染色确定小鼠肝脏、肾脏和脾脏组织的病理变化。剂量滴定实验确定 ZG 对小鼠的半数致死剂量为 39.6 毫克/千克,95%CI 为 31.8-49.3 毫克/千克。服用 SLD 后,小鼠血清锌的总体水平有显著差异(H = 36.912,P < 0.001)。配对比较显示,1/2 LD50组和3/4 LD50组的血清锌水平显著高于对照组(P < 0.001);3/4 LD50组的血清锌水平显著高于1/8 LD50组和1/4 LD50组(P < 0.05)。ZG 的不同 SLDs 与小鼠血清锌水平呈正相关(rs = 0.973,P < 0.001)。H&E 染色显示,所有实验组小鼠的肝、肾和脾组织均未出现明显的组织学异常或病变。该研究明确了C57BL/6J小鼠静脉注射ZG的适宜剂量范围,为今后的实验研究提供了参考。
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Determination of the median lethal dose of zinc gluconate in mice and safety evaluation
Zinc Gluconate (ZG) is a safe and effective supplement for zinc. However, there is limited research on the optimal dosage for intravenous injection and the safety evaluation of animal models for ZG. This study aims to determine the safe dose range of ZG for intravenous injection in C57BL/6J mice. A Dose titration experiment was conducted to determine the LD50 and 95% confidence interval (95%CI) of ZG in mice. Based on the LD50, four sub-lethal doses (SLD) of ZG were evaluated. Following three injections of each SLD and monitoring for seven days, serum zinc levels were measured, and pathological changes in the liver, kidney, and spleen tissues of mice were determined by histological staining. The dose titration experiment determined the LD50 of ZG in mice to be 39.6 mg/kg, with a 95%CI of 31.8-49.3 mg/kg. There was a statistically significant difference in the overall serum zinc levels (H = 36.912, P < 0.001) following SLD administration. Pairwise comparisons showed that the serum zinc levels of the 1/2 LD50 and 3/4 LD50 groups were significantly higher than those of the control group (P < 0.001); the serum zinc level of the 3/4 LD50 group was significantly higher than those of the 1/8 LD50 and 1/4 LD50 groups (P < 0.05). There was a positive correlation between the different SLDs of ZG and the serum zinc levels in mice (rs = 0.973, P < 0.001). H&E staining showed no significant histological abnormalities or lesions in the liver, kidney, and spleen tissues of mice in all experimental groups. The appropriate dose range of ZG for intravenous injection in C57BL/6J mice was clarified, providing a reference for future experimental research.
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