Influence of testosterone on phase II metabolism and availability of soy isoflavones in male Wistar rats
Influence of testosterone on phase II metabolism and availability of soy isoflavones in male Wistar rats
复制标题
睾酮对雄性 Wistar 大鼠 II 期代谢和大豆异黄酮有效性的影响
DOI:
10.1007/s00204-016-1853-1
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发表时间:
2016
影响因子:
6.1
通讯作者:
Kulling SE
中科院分区:
文献类型:
--
作者:
Soukup ST;Müller DR;Kurrat A;Diel P;Kulling SE
Genistein and daidzein are the main isoflavones in soy. Their potential beneficial or adverse effects in males like the prevention of prostate cancer or the impact on reproductive functions are controversially discussed. Major determinants of their bioactivity are the absorption and biotransformation of isoflavones. In this study, we focused on the influence of testosterone on plasma availability and phase II metabolism of isoflavones. Male Wistar rats, receiving an isoflavones rich diet, were randomized into three groups: Two groups were orchiectomized (ORX) at postnatal day (PND) 80 and treated for 11 days with testosterone propionate (TP) (ORX TP group) or a vehicle (ORX group) after a 7 days lasting hormonal decline. The third group served as control and remained intact. Rats were sacrificed at PND 98. ORX rats had reduced isoflavones plasma levels. Differently regulated mRNA expressions of transporters relevant for transport of phase II metabolites in liver and kidney may be responsible for this reduction, more precisely Slc10a1 and Slc21a1 in kidney as well as Slc22a8 in liver. While main phase II metabolites in intact rats were disulfates and sulfoglucuronides, the amount of sulfate conjugates was significantly diminished by ORX. In accordance with that, mRNA expression of different sulfotransferases was reduced in liver by ORX. The observed effects could be almost restored by TP treatment. In conclusion, testosterone, and likely further androgens, has a huge impact on phase II metabolism and availability of isoflavones by influencing the expression of different sulfotransferases and transporters.
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影响因子:
3.9
作者:
Shelby, MK;Cherrington, NJ;Klaassen, CD
通讯作者:
Klaassen, CD
DOI:
10.1124/jpet.301.1.145
发表时间:
2002-04-01
影响因子:
3.5
作者:
Buist, SCN;Cherrington, NJ;Klaassen, CD
通讯作者:
Klaassen, CD
影响因子:
4.2
作者:
Sfakianos, J;Coward, L;Barnes, S
通讯作者:
Barnes, S
DOI:
--
发表时间:
1998-06
期刊:
Drug metabolism and disposition: the biological fate of chemicals
影响因子:
--
作者:
Robert T. Dunn;Curtis D. Klaassen
通讯作者:
Robert T. Dunn;Curtis D. Klaassen
DOI:
--
发表时间:
1988
期刊:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
影响因子:
--
作者:
S. Andò;S. Aquila;E. Beraldi;M. Canonaco;M. L. Panno;A. Valenti;F. Dessì
通讯作者:
F. Dessì