Vincristine (VCR) is a microtubule-destabilizing chemotherapeutic agent commonly administered for the treatment of cancers in patients, which can induce severe side effects including neurotoxicity. In context of the effects on female fertility, ovarian toxicity has been found in patients and mice model after VCR exposure. However, the influence of VCR exposure on oocyte quality has not been elucidated. We established VCR exposure in vitro and in vivo model. The results indicated in vitro VCR exposure contributed to failure of oocyte maturation through inducing defects in spindle assembly, activation of SAC, oxidative stress, mitochondrial dysfunction, and early apoptosis, which were confirmed by using in vivo exposure model. Moreover, in vivo VCR exposure caused aneuploidy, reduced oocyte-sperm binding ability, and the number of cortical granules in mouse oocyte cortex. Taken together, this study demonstrated that VCR could cause meiotic arrest and poor quality of mouse oocyte.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/iub.2797 | DOI Listing |
Heliyon
December 2024
Department of Geological Engineering, Universitas Muhammadiyah Kalimantan Timur, 75243, Kalimantan Timur, Kota Samarinda, Indonesia.
Phytomedicine
December 2024
College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China. Electronic address:
Clin Pharmacol Ther
October 2024
Infection, Immunity, Inflammation Section, UCL Institute of Child Health, London, UK.
Sci Rep
July 2024
Division of Urology, Department of Surgery, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Vincristine (VCR) is one of the most widely used chemotherapy agents in treating pediatric cancer. Nonetheless, it is known to cause dose-dependent neurotoxicity which can impact virtually every organ system. Despite its widespread use, the precise impact of VCR on the lower urinary tract (LUT) remains inadequately elucidated.
View Article and Find Full Text PDFNeurotoxicology
March 2024
Pacific Biosciences Research Center, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Selenium (Se) is required for synthesis of selenocysteine (Sec), an amino acid expressed in the active sites of Se-dependent enzymes (selenoenzymes), including forms with essential functions in fetal development, brain activities, thyroid hormone metabolism, calcium regulation, and to prevent or reverse oxidative damage. Homeostatic mechanisms normally ensure the brain is preferentially supplied with Se to maintain selenoenzymes, but high methylmercury (CHHg) exposures irreversibly inhibit their activities and impair Sec synthesis. Due to Hg's high affinity for sulfur, CHHg initially binds with the cysteine (Cys) moieties of thiomolecules which are selenoenzyme substrates.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!