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spelling todo:paper_00379727_v174_n1_p123_Tesone2023-10-03T14:48:12Z Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats Tesone, M. Ladenheim, R.G. Oliveira-Filho, R.M. Chiauzzi, V.A. Foglia, V.G. Charreau, E.H. chorionic gonadotropin i 125 chorionic gonadotropin receptor cyclic amp h 3 gonadotropin receptor insulin isophane insulin progesterone progesterone h 3 radioisotope streptozocin unclassified drug animal experiment article corpus luteum diestrus endocrine system estrus etiology female genital system intravenous drug administration nonhuman ovary insufficiency rat reproduction streptozocin diabetes Animals Binding Sites Blood Glucose Chorionic Gonadotropin Corpus Luteum Cyclic AMP Diabetes Mellitus, Experimental Female Insulin Organ Size Ovary Progesterone Rats Animalia The effect of streptozotocin diabetes on some ovarian functions in adult rats was examined. Diabetic diestrus animals showed reduced ovary weight and lower circulating levels of progesterone. Scatchard plots of binding data derived from ovarian paniculate fractions of normal and streptozotocin diabetic rats revealed the presence of one class of binding sites with high affinity for 125I-hCG. The apparent association constant of the hCG receptors of diabetic ovaries was comparable to that of normal gonads. However, a marked decrease (42%) in the number of hCG binding sites was found in diabetic animals. With isolated luteal cells similar results were obtained, and the administration of insulin to streptozotocin diabetic rats restored to normality the number of hCG binding sites. The maximal response of progesterone production by luteal cells from control ovaries was obtained with 10-10 M hCG. A 100-fold higher concentration of hCG was required for the maximum stimulation of cAMP synthesis. The cAMP response of cells from diabetic rats was significantly higher than that of control cells. However, luteal cells from diabetic rats showed some loss of sensitivity in the synthesis of progesterone during incubation with hCG. Most of the alterations seen in diabetic female rats could be restored with insulin therapy, indicating that insulin plays an important role in the regulation and maintenance of normal reproductive functions. It is suggested that the diminution of the LH receptor population causes the disruption of normal luteal cell function. This fact could be responsible for some of the reproductive alterations in the diabetic female rat. © 1983, SAGE Publications. All rights reserved. Fil:Tesone, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ladenheim, R.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Charreau, E.H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00379727_v174_n1_p123_Tesone
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic chorionic gonadotropin i 125
chorionic gonadotropin receptor
cyclic amp h 3
gonadotropin receptor
insulin
isophane insulin
progesterone
progesterone h 3
radioisotope
streptozocin
unclassified drug
animal experiment
article
corpus luteum
diestrus
endocrine system
estrus
etiology
female genital system
intravenous drug administration
nonhuman
ovary insufficiency
rat
reproduction
streptozocin diabetes
Animals
Binding Sites
Blood Glucose
Chorionic Gonadotropin
Corpus Luteum
Cyclic AMP
Diabetes Mellitus, Experimental
Female
Insulin
Organ Size
Ovary
Progesterone
Rats
Animalia
spellingShingle chorionic gonadotropin i 125
chorionic gonadotropin receptor
cyclic amp h 3
gonadotropin receptor
insulin
isophane insulin
progesterone
progesterone h 3
radioisotope
streptozocin
unclassified drug
animal experiment
article
corpus luteum
diestrus
endocrine system
estrus
etiology
female genital system
intravenous drug administration
nonhuman
ovary insufficiency
rat
reproduction
streptozocin diabetes
Animals
Binding Sites
Blood Glucose
Chorionic Gonadotropin
Corpus Luteum
Cyclic AMP
Diabetes Mellitus, Experimental
Female
Insulin
Organ Size
Ovary
Progesterone
Rats
Animalia
Tesone, M.
Ladenheim, R.G.
Oliveira-Filho, R.M.
Chiauzzi, V.A.
Foglia, V.G.
Charreau, E.H.
Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
topic_facet chorionic gonadotropin i 125
chorionic gonadotropin receptor
cyclic amp h 3
gonadotropin receptor
insulin
isophane insulin
progesterone
progesterone h 3
radioisotope
streptozocin
unclassified drug
animal experiment
article
corpus luteum
diestrus
endocrine system
estrus
etiology
female genital system
intravenous drug administration
nonhuman
ovary insufficiency
rat
reproduction
streptozocin diabetes
Animals
Binding Sites
Blood Glucose
Chorionic Gonadotropin
Corpus Luteum
Cyclic AMP
Diabetes Mellitus, Experimental
Female
Insulin
Organ Size
Ovary
Progesterone
Rats
Animalia
description The effect of streptozotocin diabetes on some ovarian functions in adult rats was examined. Diabetic diestrus animals showed reduced ovary weight and lower circulating levels of progesterone. Scatchard plots of binding data derived from ovarian paniculate fractions of normal and streptozotocin diabetic rats revealed the presence of one class of binding sites with high affinity for 125I-hCG. The apparent association constant of the hCG receptors of diabetic ovaries was comparable to that of normal gonads. However, a marked decrease (42%) in the number of hCG binding sites was found in diabetic animals. With isolated luteal cells similar results were obtained, and the administration of insulin to streptozotocin diabetic rats restored to normality the number of hCG binding sites. The maximal response of progesterone production by luteal cells from control ovaries was obtained with 10-10 M hCG. A 100-fold higher concentration of hCG was required for the maximum stimulation of cAMP synthesis. The cAMP response of cells from diabetic rats was significantly higher than that of control cells. However, luteal cells from diabetic rats showed some loss of sensitivity in the synthesis of progesterone during incubation with hCG. Most of the alterations seen in diabetic female rats could be restored with insulin therapy, indicating that insulin plays an important role in the regulation and maintenance of normal reproductive functions. It is suggested that the diminution of the LH receptor population causes the disruption of normal luteal cell function. This fact could be responsible for some of the reproductive alterations in the diabetic female rat. © 1983, SAGE Publications. All rights reserved.
format JOUR
author Tesone, M.
Ladenheim, R.G.
Oliveira-Filho, R.M.
Chiauzzi, V.A.
Foglia, V.G.
Charreau, E.H.
author_facet Tesone, M.
Ladenheim, R.G.
Oliveira-Filho, R.M.
Chiauzzi, V.A.
Foglia, V.G.
Charreau, E.H.
author_sort Tesone, M.
title Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
title_short Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
title_full Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
title_fullStr Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
title_full_unstemmed Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats
title_sort ovarian dysfunction in streptozotocin-lnduced diabetic rats
url http://hdl.handle.net/20.500.12110/paper_00379727_v174_n1_p123_Tesone
work_keys_str_mv AT tesonem ovariandysfunctioninstreptozotocinlnduceddiabeticrats
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AT oliveirafilhorm ovariandysfunctioninstreptozotocinlnduceddiabeticrats
AT chiauzziva ovariandysfunctioninstreptozotocinlnduceddiabeticrats
AT fogliavg ovariandysfunctioninstreptozotocinlnduceddiabeticrats
AT charreaueh ovariandysfunctioninstreptozotocinlnduceddiabeticrats
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