{"title":"Redox reactions in vitrified-warmed ovary","authors":"Atefe Rahimi D.V.M , Ali Shahriari Ph.D. , Farid Barati Ph.D.","doi":"10.1016/j.xfss.2023.11.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Backgrounds</h3><p>Ovary vitrification is a way for the preservation of fertility in women undergoing chemotherapy and for protecting the valuable or the endangered species. However, cryopreservation of complex tissues, which are composed of different cells and materials, encountered various challenges including oxidative stress damage.</p></div><div><h3>Objectives</h3><p>This study aimed to evaluate some oxidative stress indices in the vitrified bovine ovaries.</p></div><div><h3>Methods</h3><p>The pieces of the bovine ovarian cortex (1 × 1 × 1 mm<sup>3</sup><span>) were vitrified with final concentrations of ethylene glycol (25%) and glycerol (25%) and 0.5 M sucrose and then, after 48 h, were warmed with descending concentrations (0.5, 0.25, and 0.125 M) of sucrose. The ovaries were processed and some biochemical indicators of oxidative stresses were assayed.</span></p></div><div><h3>Results</h3><p><span>Total antioxidant capacity had a 45% decrease after vitrification (</span><em>P</em><span><.0001). This reduction was associated with a 4 times increase in malondialdehyde (</span><em>P</em>=.0002) and a 53% decrease in superoxide dismutase (<em>P</em>=.0081). The levels of protein carbonyl in vitrified-warmed ovaries were less than in fresh ovaries (<em>P</em>=.0325). Regression analysis showed that the components of oxidative stress indices in vitrified tissues are different from those of fresh tissues.</p></div><div><h3>Conclusion</h3><p>An extensive alteration was seen in oxidant/antioxidant balance during vitrification.</p></div>","PeriodicalId":73012,"journal":{"name":"F&S science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"F&S science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666335X23000678","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Backgrounds
Ovary vitrification is a way for the preservation of fertility in women undergoing chemotherapy and for protecting the valuable or the endangered species. However, cryopreservation of complex tissues, which are composed of different cells and materials, encountered various challenges including oxidative stress damage.
Objectives
This study aimed to evaluate some oxidative stress indices in the vitrified bovine ovaries.
Methods
The pieces of the bovine ovarian cortex (1 × 1 × 1 mm3) were vitrified with final concentrations of ethylene glycol (25%) and glycerol (25%) and 0.5 M sucrose and then, after 48 h, were warmed with descending concentrations (0.5, 0.25, and 0.125 M) of sucrose. The ovaries were processed and some biochemical indicators of oxidative stresses were assayed.
Results
Total antioxidant capacity had a 45% decrease after vitrification (P<.0001). This reduction was associated with a 4 times increase in malondialdehyde (P=.0002) and a 53% decrease in superoxide dismutase (P=.0081). The levels of protein carbonyl in vitrified-warmed ovaries were less than in fresh ovaries (P=.0325). Regression analysis showed that the components of oxidative stress indices in vitrified tissues are different from those of fresh tissues.
Conclusion
An extensive alteration was seen in oxidant/antioxidant balance during vitrification.
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