Journals / Turkish Journal of Veterinary and Animal Sciences / 2019 / Cilt: 43 - Sayı: 4

Determination of antioxidants in bovine oviduct epithelial cell culture isolated at different periods of the estrous cycle

Pages
448–455
Publication Date
2022-11-04
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In conclusion,the antioxidant enzyme activity profile of BOEC did not differ by region or sexual cycle except for that of CAT, which was higherin the ampulla.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Oxidative stress interferes with oviduct functions including oocyte maturation, capacitation, fertilization, and embryo andgamete transport.
📊
Key Findings & Data:This study aimed to determine activity of the antioxidants glutathione peroxidase (GPX-I), superoxide dismutase(SOD), and catalase (CAT) in bovine oviduct epithelial cells (BOEC) isolated from the isthmus and ampulla of the oviduct at estral (n =7) and luteal phases (n = 7) of the estrous cycle.
💡
Conclusion & Impact:In conclusion,the antioxidant enzyme activity profile of BOEC did not differ by region or sexual cycle except for that of CAT, which was higherin the ampulla.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Oxidative stress interferes with oviduct functions including oocyte maturation, capacitation, fertilization, and embryo andgamete transport. This study aimed to determine activity of the antioxidants glutathione peroxidase (GPX-I), superoxide dismutase(SOD), and catalase (CAT) in bovine oviduct epithelial cells (BOEC) isolated from the isthmus and ampulla of the oviduct at estral (n =7) and luteal phases (n = 7) of the estrous cycle. The antioxidant activity was measured at the primary, first, and second passages of thecell culture, and was characterized by cytokeratin expression. The GPX activity increased over the passages in samples of the ampullaand the isthmus of each sexual phase without statistical significance. The SOD activity remained steady through the cell passages inboth sexual phases. CAT activity at the primary culture was higher in the ampulla compared to the isthmus in both sexual phases witha significant difference for the estral phase (P < 0.05), and it decreased over the passages with no significant differences. In conclusion,the antioxidant enzyme activity profile of BOEC did not differ by region or sexual cycle except for that of CAT, which was higherin the ampulla. Further studies should focus on SOD, GPX, and CAT activity for the mechanism of BOEC adaptation to an in vitroenvironment.

🔖

Cite This Article

KARAHAN, S., ÇINAR, M., KÜRÜM, A., KOCAMIŞ, H., ERGÜN, E. (2022). Determination of antioxidants in bovine oviduct epithelial cell culture isolated at different periods of the estrous cycle. Turkish Journal of Veterinary and Animal Sciences, Cilt: 43 - Sayı: 4, 448–455. https://ajindex.com/articles/614830

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Roy M, Gauvreau D, Bilodeau JF. Expression of superoxide dismutases in the bovine oviduct during the estrous cycle. Theriogenology 2008;70: 836-842
  2. Grippo AA, Way AL, Killian GJ. Effect of bovine ampullary and isthmic oviductal fluid on motility, acrosome reaction and fertility of bull spermatozoa. J Reprod Fertil 1995; 105: 57-64
  3. Abe H, Hoshi H. Bovine oviductal epithelial cells: Their cell culture and applications in studies for reproductive biology. Cytotechnology 1997; 23: 171-183
  4. Schoen J, Bondzio A, Topp K, Einspanier R. Establishment and characterization of an adherent pure epithelial cell line derived from the bovine oviduct. Theriogenology 2008; 69: 536-545
  5. Cerny KL, Garret E, Walton AJ, Anderson LH, Bridges PJ. A transcriptomal analysis of bovine oviductal epithelial cells collected during the follicular phase versus the luteal phase of the estrous cycle. Reprod Biol Endocrinol 2015; 13:84
  6. Mcnutt-Scott TL, Harris C. Modulation of intracellular glutathion and cysteine metabolism in bovine oviduct epithelial cells cultured in vitro. Biol Reprod 1998; 59: 314-320
  7. Agarwal A, Gupta S, Sharma RK. Role of oxidative stress in female reproduction. Reprod Biol Endocrinol 2005; 3: 28
  8. Agarwal A, Aponte-Mellado A, Premkumar BJ, Shaman A, Gupta S. The effects of oxidative stress on female reproduction: A review. Reprod Biol Endocrinol 2012; 10-49
  9. Ruder EH, Hartman TJ, Goldman MB. Impact of oxidative stress on female fertility. Curr Opin Obstet Gynecol. 2009; 21: 219-222
  10. Akkuş, İ. Serbest radikaller ve fizyopatolojik etkileri, Mimoza yayınları, (1995) Konya
  11. Davies KJA. Oxidative stress, antioxidant defenses, and damage removal, repair and replacement systems. IUBMB Life 2000; 50: 279-289
  12. Ho YS, Magnenat JL, Gargano M, Cao J. The nature of antioxidant defense mechanisms: a lesson from transgenic studies. Environ Health Perspect 1998; 5: 1219-1228
  13. Lapointe J, Bilodeau JF. Antioxidant defenses are modulated in the cow oviduct during the estrous cycle. Biol Reprod 2003; 68: 1157-1164
  14. Sanocka D, Kurpisz M. Reactive oxygen species and sperm cells. Reprod Biol Endocrinol 2004; 2-12
  15. Fujii J, Iuchi Y, Okada F. Fundamental roles of reactive oxygen species and protective mechanisms in the female reproductive system. Reprod Biol Endocrinol 2005; 3: 43
  16. Lapointe S, Sullivan R, Sirard MA. Binding of a bovine oviductal fluid catalase to mammalian spermatozoa. Biol Reprod 1998; 58: 747-753
  17. Lamirande E, J