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Kontrollü Ovaryen Hiperstimulasyon Uterusta Apelin ve Apelin Reseptör Ekspresyonunu Arttırır

Year 2023, Volume: 9 Issue: 2, 180 - 186, 01.05.2023
https://doi.org/10.53394/akd.1026446

Abstract

Amaç: Bu çalışmada, klinikle sıklıkla kullanılan süperovülasyon uygulamasının Apelin (APLN) ve Apelin Reseptör (APJ) ekspresyonunuterusta ne şekilde etkilediği araştırılmıştır.

Gereç ve Yöntemler: Bu çalışmada 6-8 haftalık on iki dişi Balb-C faresi kullanıldı. Gruplar şu şekilde oluşturuldu; herhangi bir uygulama yapılmayan çiftleşmemiş kontrol grubu (Knt), bir günlük gebe olan gebe kontrol grubu (GK) ve 5 IU/fare/intraperitoneal (ip) PMSG ve 5 IU/fare/ip hCG uygulanan ve gebe olan (P+H) grubu. P+H ve GK gruplarındaki farelerde, çiftleşmeye atıldıktan sonraki gün vajinal plak kontrolü yapılarak vajinal plak pozitif fareler gebeliğin 0.5. gününde kabul edildi. P+ H grubundaki fareler, hCG enjeksiyonundan 42 saat sonra sakrifiye edildi. Tüm gruplardan immünohistokimyasal analiz için uterus dokuları elde edilerek parafin kesitler elde edildi. Yağ dokusu pozitif kontrol olarak kullanıldı.

Bulgular: İmmunohistokimyasal boyanma yoğunluğu değerlendirildiğinde; APLN, Knt grubunda özellikle uterus bezlerinde ve bez etrafındaki stromal hücrelerde görüldü. APJ’nin uterustaki lokalizasyonu da APLN’ye benzerdi. GK grubunda APLN ve APJ ekspresyon seviyeleri kontrol grubu ile benzerdi. Ancak APJ’nin lokalizasyonu değerlendirildiğinde, Knt grubundan farklı olarak özellikle uterusun perimetriyal bezlerinde yoğun olarak ekspre edildiği izlendi. APLN ekspresyonu, Knt ve GK grupları ile karşılaştırıldığında P+H grubundaki endometrial bezlerde ve stromada belirgin olarak artmıştı (p<0.05).

Sonuçlar: PMSG ve hCG uygulaması sonrasında uterusta APLN ve APJ ekspresyon düzeyi artmıştır. Artışın, özellikle östradiol (E2) ve progesteron (P4) reseptörlerini içeren uterin bezleri, uterus epiteli ile stromal hücrelerde gözlenmesi, bu artışın hiperstimülasyon sonrasında kanda artan E2 ve/veya P4 düzeyleri ilişkili olabileceğini ve uterin metabolizmayı embriyo implantasyonu için düzenleyebileceğini düşündürmüştür. Bulgularımız, bu konuda yeni çalışmaların planlanmasına temel bilgi sağlamıştır.

References

  • Referans 1. Zhou, H., et al., Fc-apelin fusion protein attenuates lipopolysaccharide-induced liver injury in mice. Sci Rep, 2018. 8(1): p. 11428.
  • Referans 2. Mercati, F., et al., Apelin system detection in the reproductive apparatus of ewes grazing on semi-natural pasture. Theriogenology, 2019. 139: p. 156-166.
  • Referans 3. Tatemoto, K., et al., Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor. Biochem Biophys Res Commun, 1998. 251(2): p. 471-6.
  • Referans 4. Antushevich, H. and M. Wojcik, Review: Apelin in disease. Clin Chim Acta, 2018. 483: p. 241-248.
  • Referans 5. O'Dowd, B.F., et al., A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11. Gene, 1993. 136(1-2): p. 355-60.
  • Referans 6. Kawamata, Y., et al., Molecular properties of apelin: tissue distribution and receptor binding. Biochim Biophys Acta, 2001. 1538(2-3): p. 162-71.
  • Referans 7. Xiong, Q., et al., Effect of the spinal apelinAPJ system on the pathogenesis of chronic constriction injury-induced neuropathic pain in rats. Mol Med Rep, 2017. 16(2): p. 1223-1231.
  • Referans 8. Liu, Q., et al., Apelin/Apelin receptor: A new therapeutic target in Polycystic Ovary Syndrome. Life Sci, 2020. 260: p. 118310.
  • Referans 9. Masoumi, J., et al., Role of Apelin/APJ axis in cancer development and progression. Adv Med Sci, 2020. 65(1): p. 202-213.
  • Referans 10. Kourtis, A., et al., Apelin levels in normal pregnancy. Clin Endocrinol (Oxf), 2011. 75(3): p. 367-71.
  • Referans 11. Yue, P., et al., Apelin is necessary for the maintenance of insulin sensitivity. Am J Physiol Endocrinol Metab, 2010. 298(1): p. E59-67.
  • Referans 12. Dray, C., et al., Apelin stimulates glucose utilization in normal and obese insulin-resistant mice. Cell Metab, 2008. 8(5): p. 437-45.
  • Referans 13. Paradisi, G., et al., Abnormal carbohydrate metabolism during pregnancy : association with endothelial dysfunction. Diabetes Care, 2002. 25(3): p. 560-4.
  • Referans 14. Ramos, M.P., et al., Fat accumulation in the rat during early pregnancy is modulated by enhanced insulin responsiveness. Am J Physiol Endocrinol Metab, 2003. 285(2): p. E318-28.
  • Referans 15. Dawid, M., et al., Apelin decreased placental hormone secretion by human trophoblast BeWo cells via apelin receptor, protein kinase A and extracellular signal-regulated kinases 1/2 activation. J Physiol Pharmacol, 2019. 70(6).
  • Referans 16. Ishimaru, Y., et al., Apelin protects against NMDA-induced retinal neuronal death via an APJ receptor by activating Akt and ERK1/2, and suppressing TNF-alpha expression in mice. J Pharmacol Sci, 2017. 133(1): p. 34-41.
  • Referans 17. Kon, H., R. Hokao, and M. Shinoda, Fertilizability of Superovulated Eggs by Estrous Stage-independent PMSG/hCG Treatment in Adult Wistar-Imamichi Rats. Exp Anim, 2014. 63(2): p. 175-82.
  • Referans 18. Ainsworth, L., et al., Interrelationships between follicular fluid steroid levels, gonadotropic stimuli, and oocyte maturation during preovulatory development of porcine follicles. Biol Reprod, 1980. 23(3): p. 621-7.
  • Referans 19. Homburg, R. and V. Insler, Ovulation induction in perspective. Hum Reprod Update, 2002. 8(5): p. 449-62.
  • Referans 20. Santos, M.A., E.W. Kuijk, and N.S. Macklon, The impact of ovarian stimulation for IVF on the developing embryo. Reproduction, 2010. 139(1): p. 23-34.
  • Referans 21. Yu, B., et al., Superovulation alters global DNA methylation in early mouse embryo development. Epigenetics, 2019. 14(8): p. 780-790.
  • Referans 22. Weinerman, R. and M. Mainigi, Why we should transfer frozen instead of fresh embryos: the translational rationale. Fertil Steril, 2014. 102(1): p. 10-8.
  • Referans 23. Sun, X., et al., Non-activated APJ suppresses the angiotensin II type 1 receptor, whereas apelin-activated APJ acts conversely. Hypertens Res, 2011. 34(6): p. 701-6.
  • Referans 24. Hehir, M.P. and J.J. Morrison, The adipokine apelin and human uterine contractility. Am J Obstet Gynecol, 2012. 206(4): p. 359 e1-5.
  • Referans 25. Kidoya, H., et al., The apelin/APJ system induces maturation of the tumor vasculature and improves the efficiency of immune therapy. Oncogene, 2012. 31(27): p. 3254-64.
  • Referans 26. Daviaud, D., et al., TNFalpha up-regulates apelin expression in human and mouse adipose tissue. FASEB J, 2006. 20(9): p. 1528-30.
  • Referans 27. Chi, Y., et al., Apelin inhibits the activation of the nucleotide-binding domain and the leucine-rich, repeat-containing family, pyrin-containing 3 (NLRP3) inflammasome and ameliorates insulin resistance in severely burned rats. Surgery, 2015. 157(6): p. 1142-52.
  • Referans 28. Ozkan, Z.S., et al., Investigation of apelin expression in endometriosis. J Reprod Infertil, 2013. 14(2): p. 50-5.
  • Referans 29. Handwerger, S. and M. Freemark, The roles of placental growth hormone and placental lactogen in the regulation of human fetal growth and development. J Pediatr Endocrinol Metab, 2000. 13(4): p. 343-56.
  • Referans 30. Bortoff, K.D., et al., Decreased maternal plasma apelin concentrations in preeclampsia. Hypertens Pregnancy, 2012. 31(4): p. 398-404.
  • Referans 31. Taheri, S., et al., The effects of centrally administered apelin-13 on food intake, water intake and pituitary hormone release in rats. Biochem Biophys Res Commun, 2002. 291(5): p. 1208-12.
  • Referans 32. Kelleher, A.M., et al., Uterine glands impact uterine receptivity, luminal fluid homeostasis and blastocyst implantation. Sci Rep, 2016. 6: p. 38078.
  • Referans 33. Couse, J.F. and K.S. Korach, Estrogen receptor null mice: what have we learned and where will they lead us? Endocr Rev, 1999. 20(3): p. 358-417.
  • Referans 34. Wang, H., H. Eriksson, and L. Sahlin, Estrogen receptors alpha and beta in the female reproductive tract of the rat during the estrous cycle. Biol Reprod, 2000. 63(5): p. 1331-40.
  • Referans 35. Winuthayanon, W., et al., Uterine epithelial estrogen receptor alpha is dispensable for proliferation but essential for complete biological and biochemical responses. Proc Natl Acad Sci U S A, 2010. 107(45): p. 19272-7.
  • Referans 36. Quarmby, V.E. and K.S. Korach, The influence of 17 beta-estradiol on patterns of cell division in the uterus. Endocrinology, 1984. 114(3): p. 694-702.
  • Referans 37. Stewart, C.A., et al., Uterine gland formation in mice is a continuous process, requiring the ovary after puberty, but not after parturition. Biol Reprod, 2011. 85(5): p. 954-64.
  • Referans 38. Joo, B.S., et al., Serum estradiol levels during controlled ovarian hyperstimulation influence the pregnancy outcome of in vitro fertilization in a concentration-dependent manner. Fertil Steril, 2010. 93(2): p. 442-6.

Controlled ovarian hyperstimulation increases the expression of apelin and apelin receptor in uterus

Year 2023, Volume: 9 Issue: 2, 180 - 186, 01.05.2023
https://doi.org/10.53394/akd.1026446

Abstract

Objective; In this study, we investigated whether superovulation, which is frequently used in the clinic as controlled ovarian hyperstimulation, affect the expression of Apelin (APLN) and Apelin Receptor (APJ) in the uterus.

Methods: Twelve female Balb-C mice 6-8 weeks old were used in this study. The groups were established as follows; virgin control female group (Knt) which did not receive any treatment, the pregnant control group (GK) which was on their pregnancy day 1, and the PMSG+hCG group (P+H) that received 5 IU/mouse/intraperitoneal (ip) PMSG and 5 IU/mouse/ip hCG . Vaginal plaque control was performed on the day after mating in the P+H and GK groups, and vaginal plaque-positive mice were accepted at day 0.5 of pregnancy. Mice in the P+H group were sacrificed 42 hours after hCG injection. Uterine tissues were obtained from all groups for immunohistochemical analysis, and paraffin sections were obtained. Adipose tissue was used as a positive control.

Results: In the Knt group, APLN protein expression was present especially in the uterine glands and stromal cells that are located close to the glands. The localization of APJ protein expression was also similar to APLN. In the GK group, APLN and APJ expression levels were similar to the Knt group. However, when the localization of APJ was evaluated, it has been observed that APJ expression was intensely expressed especially in the perimetrial glands of the uterus, which was not present in the Knt group. In the P+H group, APLN expression significantly increased in the endometrial glands and stromal cells compared to the Knt and GK groups (p<0.05).

Conclusions: APLN and APJ proetin expression levels increased in uterus after PMSG and hCG administration. The increase was observed especially in uterine glands, uterine epithelium and stromal cells that are known to express estradiol (E2) and progesterone (P4) receptors. Altohgether these results suggest that the increase of APLN/APJ expression in these uterin compartments may be related to the increased E2 and/or P4 levels after hyperstimulation which may also regulate metabolism of the uterus for implantation. These results provided the first basic knowledge for the possible roles of APLN/APJ system in endometrium and established the need of planning new studies on this subject.

References

  • Referans 1. Zhou, H., et al., Fc-apelin fusion protein attenuates lipopolysaccharide-induced liver injury in mice. Sci Rep, 2018. 8(1): p. 11428.
  • Referans 2. Mercati, F., et al., Apelin system detection in the reproductive apparatus of ewes grazing on semi-natural pasture. Theriogenology, 2019. 139: p. 156-166.
  • Referans 3. Tatemoto, K., et al., Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor. Biochem Biophys Res Commun, 1998. 251(2): p. 471-6.
  • Referans 4. Antushevich, H. and M. Wojcik, Review: Apelin in disease. Clin Chim Acta, 2018. 483: p. 241-248.
  • Referans 5. O'Dowd, B.F., et al., A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11. Gene, 1993. 136(1-2): p. 355-60.
  • Referans 6. Kawamata, Y., et al., Molecular properties of apelin: tissue distribution and receptor binding. Biochim Biophys Acta, 2001. 1538(2-3): p. 162-71.
  • Referans 7. Xiong, Q., et al., Effect of the spinal apelinAPJ system on the pathogenesis of chronic constriction injury-induced neuropathic pain in rats. Mol Med Rep, 2017. 16(2): p. 1223-1231.
  • Referans 8. Liu, Q., et al., Apelin/Apelin receptor: A new therapeutic target in Polycystic Ovary Syndrome. Life Sci, 2020. 260: p. 118310.
  • Referans 9. Masoumi, J., et al., Role of Apelin/APJ axis in cancer development and progression. Adv Med Sci, 2020. 65(1): p. 202-213.
  • Referans 10. Kourtis, A., et al., Apelin levels in normal pregnancy. Clin Endocrinol (Oxf), 2011. 75(3): p. 367-71.
  • Referans 11. Yue, P., et al., Apelin is necessary for the maintenance of insulin sensitivity. Am J Physiol Endocrinol Metab, 2010. 298(1): p. E59-67.
  • Referans 12. Dray, C., et al., Apelin stimulates glucose utilization in normal and obese insulin-resistant mice. Cell Metab, 2008. 8(5): p. 437-45.
  • Referans 13. Paradisi, G., et al., Abnormal carbohydrate metabolism during pregnancy : association with endothelial dysfunction. Diabetes Care, 2002. 25(3): p. 560-4.
  • Referans 14. Ramos, M.P., et al., Fat accumulation in the rat during early pregnancy is modulated by enhanced insulin responsiveness. Am J Physiol Endocrinol Metab, 2003. 285(2): p. E318-28.
  • Referans 15. Dawid, M., et al., Apelin decreased placental hormone secretion by human trophoblast BeWo cells via apelin receptor, protein kinase A and extracellular signal-regulated kinases 1/2 activation. J Physiol Pharmacol, 2019. 70(6).
  • Referans 16. Ishimaru, Y., et al., Apelin protects against NMDA-induced retinal neuronal death via an APJ receptor by activating Akt and ERK1/2, and suppressing TNF-alpha expression in mice. J Pharmacol Sci, 2017. 133(1): p. 34-41.
  • Referans 17. Kon, H., R. Hokao, and M. Shinoda, Fertilizability of Superovulated Eggs by Estrous Stage-independent PMSG/hCG Treatment in Adult Wistar-Imamichi Rats. Exp Anim, 2014. 63(2): p. 175-82.
  • Referans 18. Ainsworth, L., et al., Interrelationships between follicular fluid steroid levels, gonadotropic stimuli, and oocyte maturation during preovulatory development of porcine follicles. Biol Reprod, 1980. 23(3): p. 621-7.
  • Referans 19. Homburg, R. and V. Insler, Ovulation induction in perspective. Hum Reprod Update, 2002. 8(5): p. 449-62.
  • Referans 20. Santos, M.A., E.W. Kuijk, and N.S. Macklon, The impact of ovarian stimulation for IVF on the developing embryo. Reproduction, 2010. 139(1): p. 23-34.
  • Referans 21. Yu, B., et al., Superovulation alters global DNA methylation in early mouse embryo development. Epigenetics, 2019. 14(8): p. 780-790.
  • Referans 22. Weinerman, R. and M. Mainigi, Why we should transfer frozen instead of fresh embryos: the translational rationale. Fertil Steril, 2014. 102(1): p. 10-8.
  • Referans 23. Sun, X., et al., Non-activated APJ suppresses the angiotensin II type 1 receptor, whereas apelin-activated APJ acts conversely. Hypertens Res, 2011. 34(6): p. 701-6.
  • Referans 24. Hehir, M.P. and J.J. Morrison, The adipokine apelin and human uterine contractility. Am J Obstet Gynecol, 2012. 206(4): p. 359 e1-5.
  • Referans 25. Kidoya, H., et al., The apelin/APJ system induces maturation of the tumor vasculature and improves the efficiency of immune therapy. Oncogene, 2012. 31(27): p. 3254-64.
  • Referans 26. Daviaud, D., et al., TNFalpha up-regulates apelin expression in human and mouse adipose tissue. FASEB J, 2006. 20(9): p. 1528-30.
  • Referans 27. Chi, Y., et al., Apelin inhibits the activation of the nucleotide-binding domain and the leucine-rich, repeat-containing family, pyrin-containing 3 (NLRP3) inflammasome and ameliorates insulin resistance in severely burned rats. Surgery, 2015. 157(6): p. 1142-52.
  • Referans 28. Ozkan, Z.S., et al., Investigation of apelin expression in endometriosis. J Reprod Infertil, 2013. 14(2): p. 50-5.
  • Referans 29. Handwerger, S. and M. Freemark, The roles of placental growth hormone and placental lactogen in the regulation of human fetal growth and development. J Pediatr Endocrinol Metab, 2000. 13(4): p. 343-56.
  • Referans 30. Bortoff, K.D., et al., Decreased maternal plasma apelin concentrations in preeclampsia. Hypertens Pregnancy, 2012. 31(4): p. 398-404.
  • Referans 31. Taheri, S., et al., The effects of centrally administered apelin-13 on food intake, water intake and pituitary hormone release in rats. Biochem Biophys Res Commun, 2002. 291(5): p. 1208-12.
  • Referans 32. Kelleher, A.M., et al., Uterine glands impact uterine receptivity, luminal fluid homeostasis and blastocyst implantation. Sci Rep, 2016. 6: p. 38078.
  • Referans 33. Couse, J.F. and K.S. Korach, Estrogen receptor null mice: what have we learned and where will they lead us? Endocr Rev, 1999. 20(3): p. 358-417.
  • Referans 34. Wang, H., H. Eriksson, and L. Sahlin, Estrogen receptors alpha and beta in the female reproductive tract of the rat during the estrous cycle. Biol Reprod, 2000. 63(5): p. 1331-40.
  • Referans 35. Winuthayanon, W., et al., Uterine epithelial estrogen receptor alpha is dispensable for proliferation but essential for complete biological and biochemical responses. Proc Natl Acad Sci U S A, 2010. 107(45): p. 19272-7.
  • Referans 36. Quarmby, V.E. and K.S. Korach, The influence of 17 beta-estradiol on patterns of cell division in the uterus. Endocrinology, 1984. 114(3): p. 694-702.
  • Referans 37. Stewart, C.A., et al., Uterine gland formation in mice is a continuous process, requiring the ovary after puberty, but not after parturition. Biol Reprod, 2011. 85(5): p. 954-64.
  • Referans 38. Joo, B.S., et al., Serum estradiol levels during controlled ovarian hyperstimulation influence the pregnancy outcome of in vitro fertilization in a concentration-dependent manner. Fertil Steril, 2010. 93(2): p. 442-6.
There are 38 citations in total.

Details

Primary Language Turkish
Subjects Clinical Sciences
Journal Section Research Article
Authors

Sema Avcı 0000-0002-2860-5592

Çiler Çelik-özenci 0000-0003-0370-8680

Early Pub Date April 28, 2023
Publication Date May 1, 2023
Submission Date November 20, 2021
Published in Issue Year 2023 Volume: 9 Issue: 2

Cite

APA Avcı, S., & Çelik-özenci, Ç. (2023). Kontrollü Ovaryen Hiperstimulasyon Uterusta Apelin ve Apelin Reseptör Ekspresyonunu Arttırır. Akdeniz Tıp Dergisi, 9(2), 180-186. https://doi.org/10.53394/akd.1026446