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Studies on Androgen Receptor mRNA expression in Pancreas,Hypothalamus and Ovary of Androgen Sterilized Rats

Studies on Androgen Receptor mRNA expression in Pancreas,Hypothalamus and Ovary of Androgen Sterilized Rats
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摘要 Objective To investigate the androgen receptor (AR) mRNA expression in pancreas, hypothalamus and ovary of androgen sterilized rats (ASR).Methods ASR model was established by subcutaneous injection of testosterone propionate to SD female rats at the age of 9 days. Around the age of 106 days (proestrus), all rats were killed, serum Δ4-andronestedione (Δ 4-A), total testosterone (TT), free testosterone (FT), insulin (Ins) and C-peptide (C-P) were measured by radioimmunoassay (RIA). Total RNA in pancreas, hypothalamus and ovary were extracted and the amount of AR mRNA was quantitatedly analyzed by RT-PCR with single base mutant template as inner standard. Results Serum concentrations of Δ4-A, TT, FT, Ins and C-P in ASR model rats were significantly higher than those in control group (P〈0.05, P〈0.01). The expression of AR mRNA in pancreas, hypothalamus and ovary increased significantly (P〈0. 05, P〈0.01) of model rats as compared with control group. Conclusion The elevated serum androgen levels in ASR model could enhance the expression of AR mRNA levels in pancreas, hypothalamus and ovary, which further induce hyperinsulinemia and anovulation. Objective To investigate the androgen receptor (AR) mRNA expression in pancreas, hypothalamus and ovary of androgen sterilized rats (ASR).Methods ASR model was established by subcutaneous injection of testosterone propionate to SD female rats at the age of 9 days. Around the age of 106 days (proestrus), all rats were killed, serum Δ4-andronestedione (Δ 4-A), total testosterone (TT), free testosterone (FT), insulin (Ins) and C-peptide (C-P) were measured by radioimmunoassay (RIA). Total RNA in pancreas, hypothalamus and ovary were extracted and the amount of AR mRNA was quantitatedly analyzed by RT-PCR with single base mutant template as inner standard. Results Serum concentrations of Δ4-A, TT, FT, Ins and C-P in ASR model rats were significantly higher than those in control group (P〈0.05, P〈0.01). The expression of AR mRNA in pancreas, hypothalamus and ovary increased significantly (P〈0. 05, P〈0.01) of model rats as compared with control group. Conclusion The elevated serum androgen levels in ASR model could enhance the expression of AR mRNA levels in pancreas, hypothalamus and ovary, which further induce hyperinsulinemia and anovulation.
出处 《Journal of Reproduction and Contraception》 CAS 2004年第4期233-238,共6页 生殖与避孕(英文版)
关键词 androgen sterilized rat androgen receptor ANDROGEN INSULIN androgen sterilized rat androgen receptor androgen insulin
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