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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.
Wang, Xuejiao; Zhou, Yang; Xie, Dongli; Yin, Fei; Liang, Yunxia; Luo, Xiaogang.
Afiliación
  • Wang X; College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
  • Zhou Y; School of Textile Science and Engineering/National Engineering Laboratory for Advanced Yarn and Clean Production, Wuhan Textile University, Wuhan, China.
  • Xie D; College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
  • Yin F; College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
  • Liang Y; College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
  • Luo X; College of Textile and Clothing Engineering, Soochow University, Suzhou, China.
J Appl Toxicol ; 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39090837
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Appl Toxicol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Appl Toxicol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido