Changes in the gene expression of adiponectin and adiponectin receptors (AdipoR1 and AdipoR2) in ovarian follicular cells of dairy cow at different stages of development

Theriogenology

Volumn 73, Issue 5, 2010, Pages 659-669

  Tabandeh, M R ^a   Hosseini, A ^b   Saeb, M ^c   Kafi, M ^c   Saeb, S ^c  

^a SHAHID CHAMRAN UNIVERSITY OF AHVAZ   (Iran)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c SHIRAZ UNIVERSITY   (Iran)

Author keywords

Adiponectin; Adiponectin receptors; Cow; Follicular development; Gene expression; Ovary

Indexed keywords

ADIPONECTIN; ADIPONECTIN RECEPTOR; ESTRADIOL; PROGESTERONE;

ANIMAL; ARTICLE; BLOOD; CATTLE; CORPUS LUTEUM; DAIRYING; FEMALE; FOLLICULAR PHASE; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; LUTEAL CELL; METABOLISM; OVARY FOLLICLE; PHYSIOLOGY; VALIDATION STUDY;

ADIPONECTIN; ANIMALS; CATTLE; CORPUS LUTEUM; DAIRYING; ESTRADIOL; FEMALE; FOLLICULAR PHASE; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; LUTEAL CELLS; OVARIAN FOLLICLE; PROGESTERONE; RECEPTORS, ADIPONECTIN; VALIDATION STUDIES AS TOPIC;

BOS; BOVINAE;

EID: 75949107388     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2009.11.006     Document Type: Article

References (49)

1. Butler W.R. Nutritional interactions with reproductive performance in dairy cattle. Anim Reprod Sci 60-61 (2000) 449-457
2. Fernandez-Fernandez R., Martini A.C., Navarro V.M., Castellano J.M., Dieguez C., Aguilar E., et al. Novel signals for the integration of energy balance and reproduction. Mol Cell Endocrinol 254-255 (2006) 127-132
3. Wathes D.C., Fenwick M., Cheng Z., Bourne N., Liewellyn S., Morris D.G., et al. Influence of negative energy balance on cyclicity and fertility in high producing dairy cow. Theriogenology 68 (2007) 232-241
4. Campos D.B., Palin M.F., Bordignon V., and Murphy B.D. The 'beneficial' adipokines in reproduction and fertility. Int J Obes 32 (2008) 223-231
5. Scherer P.E., Williams S., Fogliano M., Baldini G., and Lodish H.F. A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem 270 (1995) 26746-26749
6. Maeda K., Okubo K., Shimomura I., Funahashi T., Matsuzawa Y., and Matsubara K. cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (adipose most abundant gene transcript 1). Biochem Biophys Res Commun 221 (1996) 286-289
7. Das K., Lin Y., Widen E., Zhang Y., and Scherer P.E. Chromosomal localization, expression pattern, and promoter analysis of the mouse gene encoding adipocyte-specific secretory protein Acrp30. Biochem Biophys Res Commun 280 (2001) 1120-1129
8. Donohoue P.A. Adiponectin: a multifunctional adipokine. Contemporary Endocrinology: Energy Metabolism and Obesity: Research and Clinical Applications. 1st edition (2008), Humana Press pp. 87-105
9. Kadowaki T., and Yamouchi T. Adiponectin and adiponectin receptors. The Endocrine Society. Endocr Rev 26 (2005) 439-451
10. Yamauchi T., Kamon J., Ito Y., Tsuchida A., Yokomizo T., Kita S., et al. Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature 423 (2003) 762-769
11. Lord E., Ledoux S., Murphy B.D., Beaudry D., and Palin M.F. Expression of adiponectin and its receptors in swine. J Anim Sci 83 (2005) 565-578
12. Dai M.H., Xia T., Zhang G.D., Chen X.D., Gan L., Feng S.Q., et al. Cloning, expression and chromosome localization of porcine adiponectin and adiponectin receptors genes. Domest Anim Endocrinol 30 (2006) 117-125
13. Ramachandran R., Ocon-Grove O.M., and Metzger S.L. Molecular cloning and tissue expression of chicken AdipoR1 and AdipoR2 complementary deoxyribonucleic acids. Domest Anim Endocrinol 33 (2007) 19-31
14. Chabrolle C., Tosca L., Crochet S., Tesseraud S., and Dupont J. Expression of AdipoR1 and AdipoR2 in chicken ovary: potential role in ovarian steroidogenesis. Domest Anim Endocrinol 33 (2007) 480-487 this issue
15. Motoshima H., Wu X., Mahadev K., and Goldstein B.J. Adiponectin suppresses proliferation and superoxide generation and enhances eNOS activity in endothelial cells treated with oxidized LDL. Biochem Biophys Res Commun 315 (2004) 264-271
16. Combs T.P., Berg A.H., Rajala M.W., Klebanov S., Iyengar P., Jimenez-Chillaron J.C., et al. Sexual differentiation, pregnancy, calorie restriction, and aging affect the adipocyte-specific secretory protein adiponectin. Diabetes 52 (2003) 268-276
17. Kubota N., Yano W., Kubota T., Yamauchi T., Itoh S., Kumagai H., et al. Adiponectin stimulates AMP-activated protein kinase in the hypothalamus and increases food intake. Cell Metabolism 6 (2007) 55-68
18. Wena J.P., Lv W.S., Yang J., Nie A.F., Cheng X.B., Yang Y., et al. Globular adiponectin inhibits GnRH secretion from GT1-7 hypothalamic GnRH neurons by induction of hyperpolarization of membrane potential. Biochem Biophys Res Commun 371 (2008) 756-761
19. Rodriguez-Pacheco F., Martinez-Fuentes A.J., Tovar S., Pinilla L., Tena-Sempere M., Dieguez C., et al. Regulation of pituitary cell function by adiponectin. Endocrinology 148 (2008) 401-410
20. Mitchell M., Armstrong D.T., Robker R.L., and Norman R.J. Adipokines: implications for female fertility and obesity. Reproduction 130 (2005) 583-597
21. Ledoux S., Campos D.B., Lopes F.L., Dobias-Goff M., Palin M.F., and Murphy B.D. Adiponectin induces periovulatory changes in ovarian follicular cells. Endocrinology 147 (2006) 5178-5186 this issue
22. Lagaly D.V., Aad P.Y., Grado-Ahuir G.A., Hulsey L.B., and Spicer L.J. Role of adiponectin in regulating ovarian theca and granulosa cell function. Mol Cell Endocrinol 284 (2005) 38-45 this issue
23. Dafopoulos K., Sourlas D., Kallitsaris A., Pournaras S., and Messinis I.E. Blood ghrelin, resistin, and adiponectin concentrations during the normal menstrual cycle. Fertil Steril 92 (2009) 1389-1394
24. Chabrolle C., Tosca1 T., and Dupont J. Regulation of adiponectin and its receptors in rat ovary by human chorionic gonadotrophin treatment and potential involvement of adiponectin in granulosa cell steroidogenesis. Reproduction 133 (2007) 719-731 this issue
25. Dupont J., Chabrolle C., Rame C., Tosca L., and Coyral-Castel S. Role of the peroxisome proliferator-activated receptors, adenosine monophosphate-activated kinase, and adiponectin in the ovary. PPAR Res 2008 (2008) 1-9
26. Chappaz E., Albornoz M.S., Camposb D., Chea L., Palin M.F., Bruce D., et al. Adiponectin enhances in vitro development of swine embryos. Domest Anim Endocrinol 35 (2008) 198-207
27. Ireland J.J., Murphee R.L., and Coulson P.B. Accuracy of predicting stages of bovine estrous cycle by gross appearance of the corpus luteum. J Dairy Sci 63 (1980) 155
28. Fortune J.E., Rivera G.M., Evans A.C., and Turzillo A.M. Differentiation of dominant versus subordinate follicles in cattle. Biol Reprod 65 (2001) 648-654
29. Silvan R., Illera J.C., Illera M.J., and Lorenzo P. Percentage of atretic and non atretic follicles in different follicular sizes of heifers and cows. Theriogenology 39 (2001) 311
30. Kruip T.A., and Dieleman S.J. Steroid hormone concentrations in the fluid of bovine follicles relative to size, quality and stage of estrous cycle. Theriogenology 24 (1985) 395-401
31. Ohno K., Araki N., Yanase T., Nawata H., and Iida M. A novel nonradioactive method for measuring aromatase activity using a human ovarian granulosa-like tumor cell line and an estrone ELISA. Toxicol Sci 82 (2004) 443-450
32. Hayashi K., Acosta T.J., Berisha B., Kobayashi S., Ohtani M., Schamsc D., and Miyamotoa A. Changes in prostaglandin secretion by the regressing bovine corpus luteum. Prostaglandins Other Lipid Mediat 70 (2003) 339-349
33. Bettegowda A., Patel O.V., Ireland J.J., and Smith G.W. Quantitative analysis of messenger RNA abundance for ribosomal protein L-15, cyclophilin-A, phosphoglycerokinase, beta-glucuronidase, glyceraldehyde 3-phosphate dehydrogenase, beta-actin, and histone H2A during bovine oocyte maturation and early embryogenesis in vitro. Mol Reprod Dev 73 (2006) 267-278
34. Ryan N.K., Van der Hoek K.H., Robertson S.A., and Norman R.J. Leptin and leptin receptor expression in the rat ovary. Endocrinology 144 (2003) 5006-5013
35. Wang A.M., Doyle M.V., and Mark D.F. Quantification of mRNA by the polymerase chain reaction. Proc Natl Acad Sci U S A 86 (1989) 9717-9721
36. Dorak M.T. Real-time PCR. 1st edition (2006), Taylor & Francis Group p. 63-73
37. Hazeleger N.L., Hill D.J., Stubbings R.B., and Walton J.S. Relationship of morphology and follicular fluid environment of bovine oocytes to their developmental potential in vitro. Theriogenology 43 (1995) 509-522
38. Hirshfield A.N. Development of follicles in the mammalian ovary. Int Rev Cytol 124 (1991) 43-101
39. Tan B.K., Chen J., Digby J.E., Keay S.D., Kennedy C.R., and Randeva H.S. Upregulation of adiponectin receptor 1 and 2 mRNA and protein in adipose tissue and adipocytes in insulin-resistant women with polycystic ovary syndrome. Diabetologia 49 (2006) 2723-2728
40. Chabrolle C., Pierre E.J., Tosca L., Rame C., and Dupont J. Effects of high level of glucose on the steroidogenesis and the expression of adiponectin receptors in rat ovarian cells. Reprod Biol Endocrinol 6 (2008) 11-25
41. Ouchi N., Kobayashi H., Kihara S., Kumada M., Sato K., Inoue T., et al. Adiponectin stimulates angiogenesis by promoting cross-talk between AMP-activated protein kinase and Akt signaling in endothelial cells. J Biol Chem 279 (2004) 1304-1309
42. Downs S.M., Hudson E.R., and Hardie D.G. A potential role of AMP activated protein kinase in meiotic induction in mouse oocytes. Dev Biol 245 (2002) 200-212
43. Rieger D., and Loskutoff N.M. Changes in the metabolism of glucose, pyruvate, glutamine and glycine during the maturation of cattle oocytes in vitro. J Reprod Fertil 100 (1994) 257-262
44. Sutton-McDowall M.L., Gilchrist R.B., and Thompson J.G. Cumulus expansion and glucose utilisation by bovine cumulus-oocyte complexes during in vitro maturation: the influence of glucosamine and follicle-stimulating hormone. Reproduction 128 (2004) 313-319
45. Mayes M.A., Laforest M.F., Guillemette C., Gilchrist R.B., and Richard F.J. Adenosine 5-monophosphate kinase-activated protein kinase (PRKA) activators delay meiotic resumption in porcine oocytes. Biol Reprod 76 (2007) 589-597
46. Tsai S.J., and Wiltbank M.C. Prostaglandin F2 regulates distinct physiological changes in early and midcycle bovine corpora lutea. Biol Reprod 58 (1998) 346-352
47. Del Vecchio R.P., Sutherland W.D., and Sasser R.G. Bovine luteal cell production in vitro of prostaglandin E2, oxytocin and progesterone in response to pregnancy-specific protein B and prostaglandin F2α. J Reprod Fertil 107 (1996) 131-136
48. Fields M.J., Barros C.M., Watkins W.B., and Fields P.R. Characterization of large luteal cells and their secretory granules throughout the estrous cycle of the cow. Biol Reprod 46 (1992) 535-545
49. Sakurai T., Tamura K., and Kogo H. Vascular endothelial growth factor increases messenger RNAs encoding cyclooxygenase II and membrane-associated prostaglandin E synthase in rat luteal cells. J Endocrinol 183 (2004) 527-533