Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice
Context: We identified an active prenylated derivative of genistein, 8-prenylgenistein (8PG) from Erythrina variegata L. (Leguminosae) and found that 8PG increased osteoprotective effects of genistein in oestrogen-deficient mice. Objective: This study investigated and compared the oestrogenic effect...
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oai:doaj.org-article:fbe9b6dae6094669b7cb7fa66cc16f152021-11-17T14:21:56ZDifferential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice1388-02091744-511610.1080/13880209.2019.1590422https://doaj.org/article/fbe9b6dae6094669b7cb7fa66cc16f152019-01-01T00:00:00Zhttp://dx.doi.org/10.1080/13880209.2019.1590422https://doaj.org/toc/1388-0209https://doaj.org/toc/1744-5116Context: We identified an active prenylated derivative of genistein, 8-prenylgenistein (8PG) from Erythrina variegata L. (Leguminosae) and found that 8PG increased osteoprotective effects of genistein in oestrogen-deficient mice. Objective: This study investigated and compared the oestrogenic effects of genistein and 8PG on uterus and vagina of immature mice. Materials and methods: Immature female CD-1 mice were orally treated with vehicle (Control, n = 10) or genistein (75 mg/kg, n = 10) or 8PG with low (8PG-L, 75 mg/kg, n = 10) and high dose (8PG-H, 150 mg/kg, n = 10) for 7 consecutive days by intragastric gavage. The uterus and vagina were harvested for histological and molecular measurements. Results: Treatment with genistein and 8PG-H significantly increased uterus index (1.98 ± 0.21 & 1.49 ± 0.16 mg/g) and vagina index (3.83 ± 0.11 & 3.13 ± 0.25 mg/g) as compared to untreated control (uterus, 1.12 ± 0.13 mg/g; vagina, 2.32 ± 0.18 mg/g). Accordingly, both genistein and 8PG-H made vaginal cells keratinized and induced uterine and vaginal hypertrophy associated with the endometrial proliferation. 8PG-L did not affect oestrus cycle and histology of uterus and vagina. Treatment of immature mice with genistein or 8PG-H upregulated protein expression of oestrogen receptor-α (ER-α) and proliferating cell nuclear antigen (PCNA), but 8PG-L did not alter ER-α and PCNA expression in uterus and vagina. Conclusion: This study indicated that 8-prenylgenistein exerted oestrogenic effects in immature female mice. The efficacy and safety of 8-prenylgenistein when applied in improving oestrogen deficiency-induced syndrome requires further elucidation.Xiao-Li LiLi SuiFu-Hui LinYin LianLian-Zhong AiYan ZhangTaylor & Francis Grouparticleoestrogen receptorphytoestrogenuterusvaginaTherapeutics. PharmacologyRM1-950ENPharmaceutical Biology, Vol 57, Iss 1, Pp 226-230 (2019) |
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oestrogen receptor phytoestrogen uterus vagina Therapeutics. Pharmacology RM1-950 |
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oestrogen receptor phytoestrogen uterus vagina Therapeutics. Pharmacology RM1-950 Xiao-Li Li Li Sui Fu-Hui Lin Yin Lian Lian-Zhong Ai Yan Zhang Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
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Context: We identified an active prenylated derivative of genistein, 8-prenylgenistein (8PG) from Erythrina variegata L. (Leguminosae) and found that 8PG increased osteoprotective effects of genistein in oestrogen-deficient mice. Objective: This study investigated and compared the oestrogenic effects of genistein and 8PG on uterus and vagina of immature mice. Materials and methods: Immature female CD-1 mice were orally treated with vehicle (Control, n = 10) or genistein (75 mg/kg, n = 10) or 8PG with low (8PG-L, 75 mg/kg, n = 10) and high dose (8PG-H, 150 mg/kg, n = 10) for 7 consecutive days by intragastric gavage. The uterus and vagina were harvested for histological and molecular measurements. Results: Treatment with genistein and 8PG-H significantly increased uterus index (1.98 ± 0.21 & 1.49 ± 0.16 mg/g) and vagina index (3.83 ± 0.11 & 3.13 ± 0.25 mg/g) as compared to untreated control (uterus, 1.12 ± 0.13 mg/g; vagina, 2.32 ± 0.18 mg/g). Accordingly, both genistein and 8PG-H made vaginal cells keratinized and induced uterine and vaginal hypertrophy associated with the endometrial proliferation. 8PG-L did not affect oestrus cycle and histology of uterus and vagina. Treatment of immature mice with genistein or 8PG-H upregulated protein expression of oestrogen receptor-α (ER-α) and proliferating cell nuclear antigen (PCNA), but 8PG-L did not alter ER-α and PCNA expression in uterus and vagina. Conclusion: This study indicated that 8-prenylgenistein exerted oestrogenic effects in immature female mice. The efficacy and safety of 8-prenylgenistein when applied in improving oestrogen deficiency-induced syndrome requires further elucidation. |
format |
article |
author |
Xiao-Li Li Li Sui Fu-Hui Lin Yin Lian Lian-Zhong Ai Yan Zhang |
author_facet |
Xiao-Li Li Li Sui Fu-Hui Lin Yin Lian Lian-Zhong Ai Yan Zhang |
author_sort |
Xiao-Li Li |
title |
Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
title_short |
Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
title_full |
Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
title_fullStr |
Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
title_full_unstemmed |
Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
title_sort |
differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice |
publisher |
Taylor & Francis Group |
publishDate |
2019 |
url |
https://doaj.org/article/fbe9b6dae6094669b7cb7fa66cc16f15 |
work_keys_str_mv |
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