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Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina
BACKGROUND: The isoflavone genistein (GEN) is found in soy (Glycine max) and red clover (Trifolium pratense). The estrogenic activity of GEN is known, and it is widely advertised as a phytoestrogen useful in alleviating climacteric complaints and other postmenopausal disorders. Knowledge of effects...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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National Institute of Environmental Health Sciences
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174401/ https://www.ncbi.nlm.nih.gov/pubmed/18174952 http://dx.doi.org/10.1289/ehp.9367 |
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author | Rimoldi, Guillermo Christoffel, Julie Seidlova-Wuttke, Dana Jarry, Hubertus Wuttke, Wolfgang |
author_facet | Rimoldi, Guillermo Christoffel, Julie Seidlova-Wuttke, Dana Jarry, Hubertus Wuttke, Wolfgang |
author_sort | Rimoldi, Guillermo |
collection | PubMed |
description | BACKGROUND: The isoflavone genistein (GEN) is found in soy (Glycine max) and red clover (Trifolium pratense). The estrogenic activity of GEN is known, and it is widely advertised as a phytoestrogen useful in alleviating climacteric complaints and other postmenopausal disorders. Knowledge of effects of long-term administration of GEN in laboratory animals is scarce, and effects in the uterus and mammary gland after long-term administration have not been studied. The uterus and mammary gland are known to be negatively influenced by estrogens used in hormone therapy. OBJECTIVES: We administered two doses of GEN [mean daily uptake 5.4 (low) or 54 mg/kg (high) body weight (bw)] orally over a period of 3 months to ovariectomized (ovx) rats and compared the effects with a treatment with two doses of 17β-estradiol [E(2); 0.17 (low) or 0.7 mg/kg bw (high)]. Mammary glands, vaginae, and uteri were investigated morphologically and immunohistochemically. We quantified the expression of proliferating cell nuclear antigen (PCNA) and progesterone receptor (PR) in the mammary gland. RESULTS: In rats treated with either of the E(2) doses or the high GEN dose, we found increased uterine weight, and histologic analysis showed estrogen-induced features in the uteri. In vaginae, either E(2) dose or GEN high induced hyperplastic epithelium compared with the atrophic controls. In the mammary gland, E(2) (either dose) or GEN increased proliferation and PR expression. Serum levels of luteinizing hormone were decreased by E(2) (both doses) but not by GEN. CONCLUSIONS: In summary, E(2) and GEN share many effects in the studied organs, particularly in the vagina, uterus, and mammary gland but not in the hypothalamo/pituitary unit. |
format | Text |
id | pubmed-2174401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-21744012008-01-03 Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina Rimoldi, Guillermo Christoffel, Julie Seidlova-Wuttke, Dana Jarry, Hubertus Wuttke, Wolfgang Environ Health Perspect Monograph BACKGROUND: The isoflavone genistein (GEN) is found in soy (Glycine max) and red clover (Trifolium pratense). The estrogenic activity of GEN is known, and it is widely advertised as a phytoestrogen useful in alleviating climacteric complaints and other postmenopausal disorders. Knowledge of effects of long-term administration of GEN in laboratory animals is scarce, and effects in the uterus and mammary gland after long-term administration have not been studied. The uterus and mammary gland are known to be negatively influenced by estrogens used in hormone therapy. OBJECTIVES: We administered two doses of GEN [mean daily uptake 5.4 (low) or 54 mg/kg (high) body weight (bw)] orally over a period of 3 months to ovariectomized (ovx) rats and compared the effects with a treatment with two doses of 17β-estradiol [E(2); 0.17 (low) or 0.7 mg/kg bw (high)]. Mammary glands, vaginae, and uteri were investigated morphologically and immunohistochemically. We quantified the expression of proliferating cell nuclear antigen (PCNA) and progesterone receptor (PR) in the mammary gland. RESULTS: In rats treated with either of the E(2) doses or the high GEN dose, we found increased uterine weight, and histologic analysis showed estrogen-induced features in the uteri. In vaginae, either E(2) dose or GEN high induced hyperplastic epithelium compared with the atrophic controls. In the mammary gland, E(2) (either dose) or GEN increased proliferation and PR expression. Serum levels of luteinizing hormone were decreased by E(2) (both doses) but not by GEN. CONCLUSIONS: In summary, E(2) and GEN share many effects in the studied organs, particularly in the vagina, uterus, and mammary gland but not in the hypothalamo/pituitary unit. National Institute of Environmental Health Sciences 2007-12 2007-06-08 /pmc/articles/PMC2174401/ /pubmed/18174952 http://dx.doi.org/10.1289/ehp.9367 Text en This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original DOI. |
spellingShingle | Monograph Rimoldi, Guillermo Christoffel, Julie Seidlova-Wuttke, Dana Jarry, Hubertus Wuttke, Wolfgang Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title | Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title_full | Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title_fullStr | Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title_full_unstemmed | Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title_short | Effects of Chronic Genistein Treatment in Mammary Gland, Uterus, and Vagina |
title_sort | effects of chronic genistein treatment in mammary gland, uterus, and vagina |
topic | Monograph |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174401/ https://www.ncbi.nlm.nih.gov/pubmed/18174952 http://dx.doi.org/10.1289/ehp.9367 |
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