Literature DB >> 17905136

Exposure to the phytoestrogen daidzein attenuates apomorphine-induced penile erection concomitant with plasma testosterone level reduction in dose- and time-related manner in adult rats.

Lianjun Pan1, Xinyi Xia, Yao Feng, Chunxia Jiang, Yufeng Huang.   

Abstract

OBJECTIVES: To investigate the impact of exposure to the phytoestrogen daidzein on erectile function and sexual hormones. The negative effects of phytoestrogens on the male reproductive system, particularly on penile erection, have hardly been evaluated.
METHODS: Thirty adult male Sprague-Dawley rats were equally divided into a normal control group, three experimental groups, and one positive control group. The three experimental groups were given daidzein at doses of 2, 20, and 100 mg/kg body weight daily, and the positive control group received 0.1 mg diethylstilbestrol per animal daily for 90 days. The apomorphine-induced erection test was performed 0, 30, 60, and 90 days after daidzein administration to evaluate for erectile function or dysfunction. After each test, blood samples were collected for plasma testosterone and luteinizing hormone measurement.
RESULTS: High-dose daidzein (100 mg/kg) decreased erectile responses to apomorphine from the 30th day of daidzein treatment and lasted to the 90th day without significant differences compared with the diethylstilbestrol-treated rats. However, similar changes were observed in the medium-dose daidzein (20 mg/kg) group from the 60th day. Low-dose daidzein (2 mg/kg) had no significant effect on the erectile responses to apomorphine compared with the normal control group (P >0.05). The plasma testosterone and luteinizing hormone levels showed a declining trend similar to that of the apomorphine-induced erections.
CONCLUSIONS: The phytoestrogen daidzein has the potential to adversely affect erectile function in a dose and time-related manner that is at least partly attributable to androgen deficiency. These findings implicate that phytoestrogens, especially isoflavones, if overconsumed for a long period, might be a novel risk factor for erectile dysfunction.

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Year:  2007        PMID: 17905136     DOI: 10.1016/j.urology.2007.05.006

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  4 in total

1.  Lack of an effect of high dose isoflavones in men with prostate cancer undergoing androgen deprivation therapy.

Authors:  Preetika Sharma; Amy Wisniewski; Milena Braga-Basaria; Xiaoqiang Xu; Mary Yep; Samuel Denmeade; Adrian S Dobs; Theodore DeWeese; Michael Carducci; Shehzad Basaria
Journal:  J Urol       Date:  2009-09-16       Impact factor: 7.450

Review 2.  The role of soy in vegetarian diets.

Authors:  Mark Messina; Virginia Messina
Journal:  Nutrients       Date:  2010-08-06       Impact factor: 5.717

3.  Timing of supplementation of selenium and isoflavones determines prostate cancer risk factor reduction in rats.

Authors:  Jessica R Tolman; Edwin D Lephart; Kenneth Dr Setchell; Dennis L Eggett; Merrill J Christensen
Journal:  Nutr Metab (Lond)       Date:  2008-11-10       Impact factor: 4.169

4.  Hyperhomocysteinaemia in rats is associated with erectile dysfunction by impairing endothelial nitric oxide synthase activity.

Authors:  Weijun Jiang; Lei Xiong; Weiwei Li; Jing Zhang; Qing Zhou; Qiuyue Wu; Tianfu Li; Cui Zhang; Mingchao Zhang; Xinyi Xia
Journal:  Sci Rep       Date:  2016-05-25       Impact factor: 4.379

  4 in total

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