干预褪黑激素以预防纳米材料暴露引起的损害:体外和体内研究的系统回顾和荟萃分析。

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-08-01 DOI:10.1002/jat.4676
Xuejiao Wang, Yang Zhou, Dongli Xie, Fei Yin, Yunxia Liang, Xiaogang Luo
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引用次数: 0

摘要

褪黑激素(MEL)具有抗氧化、抗炎和抗细胞凋亡的特性,是一种改善睡眠障碍的保健食品,因此被认为可以防止纳米材料暴露引起的毒性。然而,不同研究得出的结论似乎并不一致。我们对所有可用的临床前研究进行了荟萃分析,以研究 MEL 对纳米材料诱发的损害的影响。通过搜索截至 2023 年 12 月的五个电子数据库,共检索到 18 项相关研究。荟萃分析表明,相对于对照组,MEL 处理可显著提高细胞活力(标准化平均差 [SMD = 1.27]),减轻动物肝功能(降低 AST [SMD = -3.89] 和 ALT [SMD = -5.89])、骨形成(增强 BV/TV [SMD = 4.13],减轻侵蚀骨表面 [SMD = -5.40])和脑神经(抑制 AChE 活性 [SMD = -3.60])损伤。MEL 对纳米材料暴露所造成的损害的保护机制与其抗凋亡机制(降低 Bax/Bcl-2 比率 [SMD = -4.50] 和 caspase-3 水平 [剂量] = 4.13])有关。
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Melatonin intervention to prevent nanomaterial exposure-induced damages: A systematic review and meta-analysis of in vitro and in vivo studies.

Given its antioxidant, anti-inflammatory, and antiapoptotic properties, melatonin (MEL), a health-caring food to improve sleep disorders, is hypothesized to protect against nanomaterial exposure-induced toxicity. However, the conclusion derived from different studies seemed inconsistent. A meta-analysis of all available preclinical studies was performed to examine the effects of MEL on nanomaterial-induced damages. Eighteen relevant studies were retrieved through searching five electronic databases up to December 2023. The meta-analysis showed that relative to control, MEL treatment significantly increased cell viability (standardized mean difference [SMD = 1.27]) and alleviated liver function (lowered AST [SMD = -3.89] and ALT [SMD = -5.89]), bone formation (enhanced BV/TV [SMD = 4.13] and lessened eroded bone surface [SMD = -5.40]), and brain nerve (inhibition of AChE activity [SMD = -3.60]) damages in animals. The protective mechanisms of MEL against damages caused by nanomaterial exposure were associated with its antiapoptotic (decreased Bax/Bcl-2 ratio [SMD = -4.50] and caspase-3 levels [dose <100 μM: SMD = -3.66]), antioxidant (decreased MDA [in vitro: SMD = -2.84; in vivo: SMD = -4.27]), and anti-inflammatory (downregulated TNF-α [in vitro: SMD = -5.41; in vivo: SMD = -3.21] and IL-6 [in vitro: SMD = -5.90; in vivo: SMD = -2.81]) capabilities. In conclusion, our study suggests that MEL should be supplemented to prevent damages in populations exposed to nanomaterials.

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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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