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1.
Mol Reprod Dev ; 36(2): 159-63, 1993 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8257565

RESUMO

The factors involved in the inhibition of ovarian follicular cellular growth after the luteinizing hormone (LH) surge are poorly established. The aim of this study was to investigate the production of an inhibitory growth factor by human ovarian cells. Luteinized granulosa cells were obtained from an assisted fertilization program and were cultured in the presence or absence of follicle-stimulating hormone (FSH) and estradiol. Data obtained by cell counting showed that the number of human luteinized granulosa cells cultured in the presence of fetal bovine serum (10%) increased 1.8-fold within a 2-day period. In serum-free medium, human luteinized granulosa cells were able to incorporate 3H-thymidine, measured during consecutive 48 h periods. During all the periods tested (up to 7 days), low basal levels of thymidine incorporation were measured and were further reduced in the presence of FSH (200 ng/ml) and estradiol (500 ng/ml). To elucidate the possible production of an inhibitory growth factor, 3H-thymidine incorporation by rat granulosa cell cultures was measured in the presence of conditioned media (CM; from human granulosa cell cultures). In this system, FSH and estradiol elicited a tenfold increase in thymidine incorporation. The addition of CM (10% v/v collected on day 2) to FSH- and estradiol-treated granulosa cell cultures produced an inhibition (61%) of thymidine incorporation. The active factor in CM withstood freeze-thawing, was stable for several weeks at -20 degrees C, became unstable at 4 degrees C, and was heat labile and sensitive to proteolysis. Ultrafiltration using membranes with different molecular weight cutoffs suggested that the factor had a molecular weight > 30,000 dalton.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Corpo Lúteo/metabolismo , Células da Granulosa/metabolismo , Inibidores do Crescimento/biossíntese , Hormônio Luteinizante/farmacologia , Animais , Fenômenos Fisiológicos Sanguíneos , Divisão Celular/efeitos dos fármacos , Células Cultivadas , Corpo Lúteo/efeitos dos fármacos , Meios de Cultivo Condicionados/farmacologia , Meios de Cultura Livres de Soro/farmacologia , Replicação do DNA/efeitos dos fármacos , Estradiol/farmacologia , Feminino , Hormônio Foliculoestimulante/farmacologia , Células da Granulosa/efeitos dos fármacos , Inibidores do Crescimento/isolamento & purificação , Inibidores do Crescimento/farmacologia , Humanos , Ratos , Ultrafiltração
2.
Fertil Steril ; 55(6): 1093-8, 1991 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-1903728

RESUMO

STUDY OBJECTIVE: To examine the progesterone (P) production by cultured granulosa cells and the hormonal content in the follicular fluid (FF) of ovarian-hyperstimulated women. DESIGN: Retrospective. SETTING: Private Fertility Clinic and National Research Institute. PATIENTS: Eighteen patients undergoing in vitro fertilization or gamete intrafallopian transfer programs. RESULTS: Progesterone levels Measured in the culture medium of granulosa cells decreased sixfold with culture time. Human luteinizing hormone (LH) increased P production only when basal P production was less than 1 microgram/mL. Granulosa cell P production in culture was negatively correlated with FF LH-human chorionic gonadotropin (hCG) levels. Follicular fluid follicle-stimulating hormone (FSH) levels were positively correlated with FF P and 17 beta-estradiol (E2) concentrations. Similar results were found between FF LH (hCG) and E2 levels, but there was no relationship between FF LH (hCG) and FF P values. CONCLUSION: The high dose of hCG administered during gonadotropin treatment could induce a decrease in the in vitro granulosa cell P production.


Assuntos
Células da Granulosa/fisiologia , Hormônio Luteinizante/farmacologia , Folículo Ovariano/fisiologia , Progesterona/biossíntese , Células Cultivadas , Feminino , Fertilização in vitro , Hormônio Foliculoestimulante/fisiologia , Transferência Intrafalopiana de Gameta , Células da Granulosa/efeitos dos fármacos , Humanos , Hormônio Luteinizante/fisiologia , Análise de Regressão
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