Wang Xuejiao, Zhou Yang, Xie Dongli, Yin Fei, Liang Yunxia, Luo Xiaogang
College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
School of Textile Science and Engineering/National Engineering Laboratory for Advanced Yarn and Clean Production, Wuhan Textile University, Wuhan, China.
J Appl Toxicol. 2025 Feb;45(2):179-199. doi: 10.1002/jat.4676. Epub 2024 Aug 1.
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.
鉴于褪黑素(MEL)具有抗氧化、抗炎和抗凋亡特性,是一种有助于改善睡眠障碍的健康食品,因此推测它可预防纳米材料暴露所致的毒性。然而,不同研究得出的结论似乎并不一致。我们进行了一项对所有可用临床前研究的荟萃分析,以检验MEL对纳米材料诱导损伤的影响。截至2023年12月,通过检索五个电子数据库,共检索到18项相关研究。荟萃分析表明,与对照组相比,MEL治疗显著提高了细胞活力(标准化均值差[SMD = 1.27]),并减轻了肝功能损伤(降低了AST[SMD = -3.89]和ALT[SMD = -5.89])、骨形成损伤(增强了骨体积分数[SMD = 4.13]并减少了骨侵蚀表面[SMD = -5.40])以及脑神经损伤(抑制乙酰胆碱酯酶活性[SMD = -3.60])。MEL对纳米材料暴露所致损伤的保护机制与其抗凋亡能力(降低Bax/Bcl-2比值[SMD = -4.50]和caspase-3水平[剂量<100μM:SMD = -3.66])、抗氧化能力(降低丙二醛[体外:SMD = -2.84;体内:SMD = -4.27])和抗炎能力(下调TNF-α[体外:SMD = -5.41;体内:SMD = -3.21]和IL-6[体外:SMD = -5.90;体内:SMD = -2.81])有关。总之,我们的研究表明,应补充MEL以预防纳米材料暴露人群的损伤。