Yukmijihwang-tang protects against cyclophosphamide-induced reproductive toxicity

被引:36
|
作者
Oh, Myung Sook
Chang, Mun Seog
Park, Wansu
Kim, Do Rim
Bae, Hyunsu
Huh, Youngbuhm
Park, Seong Kyu
机构
[1] Kyung Hee Univ, Coll Oriental Med, Dept Prescriptionol, Seoul 130701, South Korea
[2] Kyung Hee Univ, Coll Oriental Med, Dept Physiol, Seoul 130701, South Korea
[3] Kyung Hee Univ, Coll Med, Dept Anat & Neurobiol, Seoul 130701, South Korea
关键词
Yukmijihwang-tang; cyclophosphamide; reproductive toxicity; sperm count; sperm motility; testosterone; lipid peroxidation; cAMP-responsive element modulator;
D O I
10.1016/j.reprotox.2007.05.007
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A side effect of cyclophosphamide (CP), an alkylating agent widely used to treat tumors and autoimmune disorders, is the alteration of male reproductive function. Yukmijihwang-tang (YJT) is a multi-herbal medicinal formula that has been used in traditional Asian medicine to treat male reproductive problems. In this study, we investigated the effects of YJT on CP-induced reproductive toxicities in rat testes. Eight-week-old male Wistar rats were divided into three groups: vehicle-treated (control), CP-treated and CP+YJT-treated groups. CP was administered for the first 7 days (20 mg/kg/day, p.o.), and YJT was administered for 56 days consecutively (1.0 g/kg/day, p.o.). The CP-treated group showed significant decreases in the weight of the testes, epididymal sperm count and sperm motility compared to the control group, while the CP+YJT-treated group had significant increases for these variables compared to the U-treated group. The enhancement of lipid peroxidation by CP in the rat testes was reduced by YJT treatment. CP diminished the expression of cAMP-responsive element modulator (CREM), a transcription factor that is highly expressed in male germ cells and is crucial to post-meiotic germ cell differentiation. YJT restored CREM at both the mRNA and protein levels. These results suggest that YJT has a protective effect against CP-induced reproductive toxicities by inhibiting the increases in lipid pet-oxidation and enhancing CREM expression. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:365 / 370
页数:6
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