AI Article Synopsis

  • Cisplatin is a medicine that can harm the ovaries and uterus by causing stress to the cells, while Pycnogenol is an antioxidant that helps protect against this damage.
  • In a study with female rats, there were three groups: one group got only cisplatin, one group got both Pycnogenol and cisplatin, and the last group was healthy.
  • The results showed that the rats treated with Pycnogenol had better health in their ovaries and uterus compared to those only given cisplatin, meaning Pycnogenol helped to reduce the damage caused by cisplatin.

Article Abstract

Introduction: Cisplatin is an antineoplastic agent, which is thought to act on tissues with increased levels of reactive oxygen species and decreased levels of antioxidants. Pycnogenol is a potent antioxidant that is used in medical conditions caused by oxidative stress. The aim of our study is to demonstrate the effects of pycnogenol on cisplatin-induced uterine and ovarian damage in rats.

Material And Methods: Wistar albino female rats were randomly divided into 3 groups before the experiment as follows: a 2.5 mg/kg cisplatin group (CG; = 10), a 40 mg/kg pycnogenol + 2.5 mg/kg cisplatin group (PCG; = 10), and a healthy control group (HG; = 10). Then, the ovaries and uteri of the rats were examined to determine malondialdehyde (MDA), total glutathione (tGSH) and superoxide dismutase (SOD) biochemical levels and the histopathological findings.

Results: Our study demonstrated that, in uterine and ovarian tissues of rats administered with cisplatin, there was a decrease in the levels of tGSH and SOD, while MDA was increased; however, it was observed that these ratios were reversed in the PCG group ( < 0.05). The number of follicles in the ovarian tissues was examined in all 3 groups. When the CG group was compared with the other two groups, the number of primordial, developing and atretic follicles was low, but there was no difference in the corpus luteum count.

Conclusions: Pycnogenol pretreatment alleviates cisplatin-induced uterine and ovarian injury in rats because of its antioxidative effect.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479720PMC
http://dx.doi.org/10.5114/aoms.2019.90414DOI Listing

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