Effects of Prolactin on Prostate Androgen Receptors in Male Rats

Five groups of immature (30‐day‐old) intact male rats were injected daily for ten days with different doses of ovine prolactin (5, 10, 25, 50, or 500 μg per rat per day). At the end of the treatment period, the animals were killed, serum was collected for LH and androgens measurements and weights of...

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Autores principales: Barañao, José Lino S., Tesone, Marta, Calvo, Juan Carlos, Charreau, Eduardo Hernán
Publicado: 1982
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v3_n5_p281_BARANAO
http://hdl.handle.net/20.500.12110/paper_01963635_v3_n5_p281_BARANAO
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spelling paper:paper_01963635_v3_n5_p281_BARANAO2023-06-08T15:20:29Z Effects of Prolactin on Prostate Androgen Receptors in Male Rats Barañao, José Lino S. Tesone, Marta Calvo, Juan Carlos Charreau, Eduardo Hernán androgen receptors immature male rats prolactin prostate Five groups of immature (30‐day‐old) intact male rats were injected daily for ten days with different doses of ovine prolactin (5, 10, 25, 50, or 500 μg per rat per day). At the end of the treatment period, the animals were killed, serum was collected for LH and androgens measurements and weights of testes, prostates, and epididymides were recorded. Available and exchangeable cytoplasmic and total nuclear KC1‐extractable androgen binding sites in the prostate gland were determined using the synthetic androgen R1881 as radioligand. A significant increase in the weights of testes and accessory reproductive glands was observed with the highest dose injected (500 μg per rat per day) as follows: testes, 583 ± 21 (SEM) versus 448 ± 38 mg (P <0.05); prostate, 80.0 ± 4.0 versus 64.7 ± 3.1 mg (P <0.05); epididymis, 72.1 ± 5.0 versus 58.2 ± 4.0 mg (P <0.05). Serum levels of LH were significantly higher in prolactin‐treated animals. Maximal values of serum LH were attained with the dose of 50 μg (99.0 ± 11.2 versus 32.0 ± 4.6 ng/ml; P < 0.05). Increasing doses of prolactin produced a concomitant rise in serum 3α‐androstanediol (2.21 ± 0.45 versus 6.63 ± 0.42 ng/ml in the group treated with 50 μg), whereas testosterone plus dihydrotestosterone levels remained unchanged. A decrease in the concentration of exchangeable cytosolic androgen binding sites in the prostate (fmoleslmg protein) was observed in prolactin injected animals (88.2 ± 0.8 in the control group versus 80.6 ± 0.3 and 74.9 ± 0.3 for doses of 5 and 50 μg, respectively; P <0.05). No changes in androgen binding sites were detected in the group treated with 500 μg per rat per day. On the other hand, prolactin treatment did not alter the number of available androgen binding sites in the prostate gland. Increasing doses of prolactin induced a dose‐related increase in the total number of nuclear KC1‐extractable receptors, expressed per mg DNA or per organ. In addition, the total content of androgen receptors (cytosolic plus nuclear binding sites) was significantly higher in animals treated with 500 μg of prolactin (385 ± 34 versus 228 ± 37 fmoles per organ; P < 0.05). These results suggest that, in addition to the previously described effects of prolactin on Leydig cell responsiveness to LH and on androgen metabolism, this hormone could also modify peripheral LH and androgen levels as well as the androgen receptor content in the rat prostate gland. 1982 American Society of Andrology Fil:BARAÑAO, J.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:TESONE, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:CALVO, J.C. 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. 1982 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v3_n5_p281_BARANAO http://hdl.handle.net/20.500.12110/paper_01963635_v3_n5_p281_BARANAO
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic androgen receptors
immature male rats
prolactin
prostate
spellingShingle androgen receptors
immature male rats
prolactin
prostate
Barañao, José Lino S.
Tesone, Marta
Calvo, Juan Carlos
Charreau, Eduardo Hernán
Effects of Prolactin on Prostate Androgen Receptors in Male Rats
topic_facet androgen receptors
immature male rats
prolactin
prostate
description Five groups of immature (30‐day‐old) intact male rats were injected daily for ten days with different doses of ovine prolactin (5, 10, 25, 50, or 500 μg per rat per day). At the end of the treatment period, the animals were killed, serum was collected for LH and androgens measurements and weights of testes, prostates, and epididymides were recorded. Available and exchangeable cytoplasmic and total nuclear KC1‐extractable androgen binding sites in the prostate gland were determined using the synthetic androgen R1881 as radioligand. A significant increase in the weights of testes and accessory reproductive glands was observed with the highest dose injected (500 μg per rat per day) as follows: testes, 583 ± 21 (SEM) versus 448 ± 38 mg (P <0.05); prostate, 80.0 ± 4.0 versus 64.7 ± 3.1 mg (P <0.05); epididymis, 72.1 ± 5.0 versus 58.2 ± 4.0 mg (P <0.05). Serum levels of LH were significantly higher in prolactin‐treated animals. Maximal values of serum LH were attained with the dose of 50 μg (99.0 ± 11.2 versus 32.0 ± 4.6 ng/ml; P < 0.05). Increasing doses of prolactin produced a concomitant rise in serum 3α‐androstanediol (2.21 ± 0.45 versus 6.63 ± 0.42 ng/ml in the group treated with 50 μg), whereas testosterone plus dihydrotestosterone levels remained unchanged. A decrease in the concentration of exchangeable cytosolic androgen binding sites in the prostate (fmoleslmg protein) was observed in prolactin injected animals (88.2 ± 0.8 in the control group versus 80.6 ± 0.3 and 74.9 ± 0.3 for doses of 5 and 50 μg, respectively; P <0.05). No changes in androgen binding sites were detected in the group treated with 500 μg per rat per day. On the other hand, prolactin treatment did not alter the number of available androgen binding sites in the prostate gland. Increasing doses of prolactin induced a dose‐related increase in the total number of nuclear KC1‐extractable receptors, expressed per mg DNA or per organ. In addition, the total content of androgen receptors (cytosolic plus nuclear binding sites) was significantly higher in animals treated with 500 μg of prolactin (385 ± 34 versus 228 ± 37 fmoles per organ; P < 0.05). These results suggest that, in addition to the previously described effects of prolactin on Leydig cell responsiveness to LH and on androgen metabolism, this hormone could also modify peripheral LH and androgen levels as well as the androgen receptor content in the rat prostate gland. 1982 American Society of Andrology
author Barañao, José Lino S.
Tesone, Marta
Calvo, Juan Carlos
Charreau, Eduardo Hernán
author_facet Barañao, José Lino S.
Tesone, Marta
Calvo, Juan Carlos
Charreau, Eduardo Hernán
author_sort Barañao, José Lino S.
title Effects of Prolactin on Prostate Androgen Receptors in Male Rats
title_short Effects of Prolactin on Prostate Androgen Receptors in Male Rats
title_full Effects of Prolactin on Prostate Androgen Receptors in Male Rats
title_fullStr Effects of Prolactin on Prostate Androgen Receptors in Male Rats
title_full_unstemmed Effects of Prolactin on Prostate Androgen Receptors in Male Rats
title_sort effects of prolactin on prostate androgen receptors in male rats
publishDate 1982
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v3_n5_p281_BARANAO
http://hdl.handle.net/20.500.12110/paper_01963635_v3_n5_p281_BARANAO
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