4.7 Article

Therapeutic effects of chitosan-embedded vitamin C, E nanoparticles against cisplatin-induced gametogenic and androgenic toxicity in adult male rats

期刊

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
卷 28, 期 40, 页码 56319-56332

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-14516-y

关键词

Chitosan; Vitamin C; Vitamin E; Nanoparticle; Cisplatin toxicity; Reproduction; Rat

资金

  1. National Key Research and Development Programme of China [2016YFC1305301]
  2. National Natural Science Foundation of China [81570759, 81270938]
  3. Zhejiang Provincial Key Disciplines of Medicine (Innovation discipline) [11-CX24]
  4. Higher Education Commission (HEC) of Pakistan

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Vitamin C, E, and their nanoparticles have been found to effectively mitigate cisplatin-induced reproductive toxicity, restoring testicular function and improving tissue structure.
Cisplatin, an anticancer drug used in treating various types of cancers, can cause reproductive toxicities during chemotherapy. Keeping this in view, the present study was designed to investigate the possible protective effects of normal vitamin C and E and vitamin C and E nanoparticles (embedded in chitosan) against cisplatin-induced reproductive toxicities. Vitamins C, E, and their nanoparticles in this regard proved to be an effective therapy. The work aimed to treat cisplatin-induced reproductive toxicities through vitamin C and E and their nanoparticles. Cisplatin exposure caused significant reduction in the weight, testosterone level, and changed lipid profile. Similarly, cisplatin induced significant widespread testicular atrophy and testicular lesions as evidenced by the gaps in the epithelium and loss of differentiating germ cells. Vitamin C and E and their nanoparticles rescued the weight, testosterone level, and testicular disturbances, which is associated with improved histological view of testicular tissues. The current study highlights evidence that designing a medication of vitamin C and E nanoparticles is useful in mitigating cisplatin-induced reproductive toxicity in cancerous male patients underlying chemotherapy.

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