Comparison of metabolites in the follicular fluid of bovine preovulatory and cystic ovarian follicles using nuclear magnetic resonance


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Authors

  • MANDEEP SINGH Veterinary Officer, VP & RRTC, Kaljharani, Bathinda
  • MRIGANK HONPARKHE Gynaecologist, Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab 141 001 India
  • AJEET KUMAR Assistant Professor, Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab 141 001 India
  • SUMIT SINGHAL Assistant Professor, Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab 141 001 India

https://doi.org/10.56093/ijans.v88i3.78261

Keywords:

Cattle, Cystic ovarian follicle, Follicular fluid, Metabolomics, Nuclear magnetic resonance, Transvaginal ablation

Abstract

Estimation of metabolites in cystic and normal preovulatory follicular fluid through proton Nuclear Magnetic Resonance (1H NMR) in cattle suffering from cystic ovarian follicle is highly desirable.The trans-vaginal ultrasound guided ablation was used to collect follicular fluid from cystic (15) and normally cycling (8) dairy cattle. NMR spectra of both fluids were recorded at a resonance frequency of 500.13 MHz on a Bruker Avance-500 spectrometer equipped with solid state probe (5 mm). Spectra were phased manually, baseline corrected, and calibrated against 3-(trimethylsilyl) propionic-2,2,3,3-d4 acid at 0.0 parts per million (ppm) using Prometab software running within MATLAB. The cystic ovarian follicle associated metabolites with variable importance in projection (VIP) scores >2 were lactate (1.98 ppm), UDP-G (5.62), pyruvate (2.34 and 2.38) and creatinine/creatine (3.14) in cystic and normal preovulatory follicular fluid.These metabolites showed identifiable peaks, and thus can be used as potential biomarkers for dairy cattle suffering from cystic ovarian follicle.

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References

AbdEllah M R, Hussein H A and Derar D R. 2010. Ovarian follicular fluid constituents in relation to stage of estrus cycle and size of the follicle in buffalo. Veterinary World 3: 263– 67.

Aich P, Jalal S, Czuba C, Schatte G, Herzog K, Olson D J, Ross A R, Potter A A, Babiuk L A and Griebel P. 2007. Comparative approaches to the investigation of responses to stress and viral infection in cattle. Journal of Integrative Biology OMICS 11: 413–34. DOI: https://doi.org/10.1089/omi.2007.0023

Bertoldo M J, Desbarats L N, Gerard N, Dubois A, Holyoake P K and Grupen C G. 2013. Differences in the metabolomic signatures of porcine follicular fluid collected from environments associated with good and poor oocyte quality. Reproduction 146: 221–31. DOI: https://doi.org/10.1530/REP-13-0142

Butler W R. 2003. Energy balance relationships with follicular development, ovulation and fertility in postpartum dairy cows. Livestock Production Science 83: 211–18. DOI: https://doi.org/10.1016/S0301-6226(03)00112-X

Douthwaite R and Dobson H. 2000. Comparison of different methods of diagnosis of cystic ovarian disease in cattle and an assessment of its treatment with a progesterone-releasing intravaginal device. Veterinary Record 147(13): 355–59. DOI: https://doi.org/10.1136/vr.147.13.355

Fernandez E C, Picton H M and Dumollard R. 2012. Metabolism throughout follicle and oocyte development in mammals. International Journal of Developmental Biology 56: 799–08. DOI: https://doi.org/10.1387/ijdb.120140ec

Fulmer G R, Miller A J M, Sherden N H, Gottlieb H E, Nudelman A, Stoltz B M, Bercaw J E and Goldberg K I. 2010. NMR chemical shifts of trace impurities: Common laboratory solvents, organics, and gases in deuterated solvents relevant to the organometallic chemist. Organometallics 29: 2176–79. DOI: https://doi.org/10.1021/om100106e

Gerard N, Fahiminiya S, Grupen C G and Desbarats L N. 2015. Reproductive physiology and ovarian folliculogenesis examined via 1H-NMR metabolomics signatures: a comparative study of large and small follicles in three mammalian species (Bos taurus, Sus scrofa domesticus and Equus ferus caballus). Journal of Integrative Biology 19: 31–40. DOI: https://doi.org/10.1089/omi.2014.0097

Gerard N, Loiseau S, Duchamp G and Seguin F. 2002. Analysis of the variations of follicular fluid composition during follicular growth and maturation in the mare using proton nuclear magnetic resonance (1H NMR). Reproduction 124: 241–48. DOI: https://doi.org/10.1530/rep.0.1240241

Gosden R G, Sadler I H, Reed D and Hunter R H F. 1990. Characterization of ovarian follicular fluids of sheep, pigs and cows using proton nuclear magnetic resonance spectroscopy. Experientia 46: 1012–15. DOI: https://doi.org/10.1007/BF01940658

GradoAhuir J A, Aad P Y and Spicer L J. 2011. New insights into the pathogenesis of cystic follicles in cattle: Microarray analysis of gene expression in granulosa cells. Journal of Animal Science 89: 1769–86. DOI: https://doi.org/10.2527/jas.2010-3463

Haliloglu S, Erdem H, Serpek B, Tekeli T and Bulut Z. 2008. The relationship among vitamin c, s-carotene, vitamin a, progesterone and oestradiol 17-s concentrations in plasma and cyst fluid of Holstein cows with ovarian cyst. Reproduction in Domestic Animals 43: 573–77. DOI: https://doi.org/10.1111/j.1439-0531.2007.00954.x

Harlow C R, Winston R M L, Margara R A and Hillier S G. 1987. Gonadotropic control of human granulosa-cell glycolysis. Human Reproduction 2: 649–53. DOI: https://doi.org/10.1093/oxfordjournals.humrep.a136609

Harris S E, Adriaens I, Leese H J, Gosden R G and Picton H M. 2007. Carbohydrate metabolism by murine ovarian follicles and oocytes grown in vitro. Reproduction 134: 415–24. DOI: https://doi.org/10.1530/REP-07-0061

Khan F A, Das G K, Pande M, Pathak M K and Sarkar M. 2011. Biochemical and hormonal composition of follicular cysts in water buffalo (Bubalus bubalis). Animal Reproduction Science 124: 61–64. DOI: https://doi.org/10.1016/j.anireprosci.2011.02.020

Kumar A, Kroetsch T, Blondin P and Anzar M. 2015. Fertilityassociated metabolites in bull seminal plasma and blood serum: 1H nuclear magnetic resonance analysis. Molecular Reproduction Development 82: 123–31. DOI: https://doi.org/10.1002/mrd.22450

Maniwa J, Izumi S, Isobe N and Terada T. 2005. Studies on substantially increased proteins in follicular fluid of bovine ovarian follicular cysts using 2–D PAGE and MALDI-TOF MS. Reproduction Biology Endocrinology 3: 23. DOI: https://doi.org/10.1186/1477-7827-3-23

Ortega H H, Salvetti N R and Padmanabhan V. 2009. Developmental programming: prenatal androgen excess disrupts ovarian steroid receptor balance. Reproduction 137: 865–77. DOI: https://doi.org/10.1530/REP-08-0491

Peter A T. 2004. An update on cystic ovarian degeneration in cattle. Reproduction in Domestic Animals 39(1): 1–7. DOI: https://doi.org/10.1046/j.0936-6768.2003.00466.x

Revelli A, Piane L D, Casano S, Molinari E, Massobrio M and Rinaudo P. 2009. Follicular fluid content and oocyte quality: from single biochemical markers to metabolomics. Reproduction Biology Endocrinology 7: 40. DOI: https://doi.org/10.1186/1477-7827-7-40

Rubingh C M, Bijlsma S, Derks E P, Bobeldijk I, Verheij E R, Kochhar S and Smilde A K. 2006. Assessing the performance of statistical validation tools for megavariate metabolomics data. Metabolomics 2: 53–61. DOI: https://doi.org/10.1007/s11306-006-0022-6

Singh J, Dadarwal D, Honparkhe M and Kumar A. 2009. Incidences of etiological factors responsible for repeat breeding syndrome in cattle and buffaloes. International Journal of Veterinary Medicine 6(1): 1–8. DOI: https://doi.org/10.5580/2b9

Salvetti N R, Alfaro N S, Velazquez M M L, Amweg A N, Matiller V, Dyaz P U and Ortega H H. 2012. Alteration in localization of steroid hormone receptors and coregulatory proteins in follicles from cows with induced ovarian follicular cysts. Reproduction 144: 723–35. DOI: https://doi.org/10.1530/REP-12-0188

Sarty G E, Kendall E J, Adams G P and Pierson R A. 2006. Nuclear magnetic resonance spectroscopy of bovine ovarian follicular fluid at four selected times of the oestrous cycle. Reproduction Fertility and Development 18: 559–71. DOI: https://doi.org/10.1071/RD06010

Thomas F H, Leask R, Srsen V, Riley S C, Spears N and Telfer E E. 2001. Effect of ascorbic acid on health and morphology of bovine preantral follicles during long-term culture. Reproduction 122: 487–95. DOI: https://doi.org/10.1530/rep.0.1220487

Vanholder T, Opsomer G and de Kruif A. 2006. Aetiology and pathogenesis of cystic ovarian follicles in dairy cattle: a review. Reproduction Nutrition and Development 46(2): 105–19. DOI: https://doi.org/10.1051/rnd:2006003

Wathes D C, Fenwick M, Cheng Z, Bourne Z, Llewellyn S, Morris D G, Kenny D, Murphy J and Fitzpatrick R. 2007. Influence of negative energy balance on cyclicity and fertility in the high producing dairy cow. Theriogenology 22: 2232–41. DOI: https://doi.org/10.1016/j.theriogenology.2007.04.006

Zhao Y, Fu L, Li R, Wang L N, Yang Y, Liu N N, Zhang C M, Wang Y, Liu P, Tu B, Zhang X and Qiao J. 2012. Metabolic profiles characterizing different phenotypes of polycystic ovary syndrome: plasma metabolomics analysis. BMC Medicine 10: 153. DOI: https://doi.org/10.1186/1741-7015-10-153

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Submitted

2018-03-22

Published

2018-03-26

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How to Cite

SINGH, M., HONPARKHE, M., KUMAR, A., & SINGHAL, S. (2018). Comparison of metabolites in the follicular fluid of bovine preovulatory and cystic ovarian follicles using nuclear magnetic resonance. The Indian Journal of Animal Sciences, 88(3), 290-294. https://doi.org/10.56093/ijans.v88i3.78261
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