Počet záznamů: 1  

Cow body condition affects the hormonal release of ovarian cells and their responses to gonadotropic and metabolic hormones

  1. 1.
    0489567 - ÚŽFG 2019 RIV US eng J - Článek v odborném periodiku
    Sirotkin, A. V. - Makarevich, A. V. - Laurinčík, Jozef - Alawasel, S. - Harrath, A. H.
    Cow body condition affects the hormonal release of ovarian cells and their responses to gonadotropic and metabolic hormones.
    Theriogenelogy. Roč. 110, č. 3 (2018), s. 142-147. ISSN 0093-691X. E-ISSN 1879-3231
    Grant CEP: GA MŠMT EF15_003/0000460
    Institucionální podpora: RVO:67985904
    Klíčová slova: ovary * body condition * progesterone
    Obor OECD: Developmental biology
    Impakt faktor: 2.299, rok: 2018

    The body condition score (BCS) of cows affects their reproductive efficiency, but the underlying mechanism is unclear. We examined the effect of BCS on the basic ovarian cell functions and their responses to gonadotropic and metabolic hormones. We isolated ovarian cells from cows with a tendency toward emaciation (BCS2) and those with an average body condition (BCS3), and we compared their hormonal release and responses to FSH, leptin, ghrelin, and neuropeptide Y (NPY) added at doses of 0, 1, 10, or 100 ng/mL Progesterone, testosterone, estradiol, and insulin-like growth factor I (IGF-I) release were evaluated by RIA. No differences were found in progesterone or testosterone release between BCS2 and BCS3 cells, however, ovarian cells from BCS2 cows released more estradiol and IGF-I than cells from BCS3 cows. FSH, ghrelin, and NPY promoted progesterone release in BCS2 cells but had no stimulatory or inhibitory effect on BCS3 cells. In contrast, leptin promoted progesterone release in BCS3 cells and inhibited progesterone release in BCS2 cells. FSH also promoted testosterone release in both BCS2 and BCS3 cells but inhibited progesterone at a low dose in BCS3 cells. Leptin inhibited testosterone release in BCS3 cells but not in BCS2 cells. Estradiol release was promoted by leptin and ghrelin in BCS3 cells, however, it was unaffected by leptin and inhibited by ghrelin in BCS2 cells. IGF-I production was promoted by FSH and inhibited by leptin in both groups. Ghrelin suppressed IGF-I release in BCS2 cells and increased IGF-I release in BCS3 cells. NPY promoted IGF-I release in BCS2 cells but not in BCS3 cells. Our results demonstrate the effects of BCS on ovarian cell estradiol and IGF-I (but not progesterone or testosterone) release, as well as on the responses of ovarian cells to FSH, leptin, ghrelin, and NPY.
    Trvalý link: http://hdl.handle.net/11104/0283966

     
     
Počet záznamů: 1  

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