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雄激素对罗非鱼(尼罗罗非鱼)卵黄蛋白原基因表达的抑制作用。

Androgen inhibition of vitellogenin gene expression in tilapia (Oreochromis niloticus).

作者信息

Lazier C B, Langley S, Ramsey N B, Wright J M

机构信息

Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Gen Comp Endocrinol. 1996 Dec;104(3):321-9. doi: 10.1006/gcen.1996.0177.

Abstract

Treatment of mature female tilapia (Oreochromis niloticus) with high levels of androgen (17 alpha-methyltestosterone, 17 alpha MT) results in a pronounced decline in plasma vitellogenin levels as determined by gel electrophoresis. Total RNA extracted from livers of treated fish and vehicle-injected controls was analyzed by Northern and slot blot hybridization using an oligonucleotide complementary to a sequence in the 3' end of tilapia vitellogenin mRNA. The probe revealed an mRNA of 6.5 kb in liver from the control mature female fish which was decreased by 85% by androgen treatment. As expected, estradiol (E2) treatment induced the 6.5-kb mRNA in mature male tilapia. The antiestrogen, tamoxifen, strongly decreased vitellogenin mRNA levels in mature females. Radioimmunoassay of serum from control and 17 alpha MT-treated female tilapia showed a marked reduction in serum E2 levels, from 11.4 +/- 2.6 ng/ml in controls to 2.2 +/- 0.13 ng/ml in treated fish. Tamoxifen, however, resulted in increased serum E2 levels, probably by blocking E2 negative feedback. The serum E2-lowering effect of 17 alpha MT suggests an inhibitory site of action on gonadotropin production at the hypothalamic-pituitary axis, possibly through an androgen receptor or through an estrogen receptor after local aromatization of 17 alpha MT.

摘要

用高水平雄激素(17α-甲基睾酮,17αMT)处理成熟雌性罗非鱼(尼罗罗非鱼),通过凝胶电泳测定发现血浆卵黄蛋白原水平显著下降。使用与罗非鱼卵黄蛋白原mRNA 3'端序列互补的寡核苷酸,通过Northern和狭缝印迹杂交分析从处理过的鱼和注射溶剂的对照鱼肝脏中提取的总RNA。该探针在对照成熟雌鱼肝脏中检测到一个6.5 kb的mRNA,雄激素处理使其减少了85%。正如预期的那样,雌二醇(E2)处理诱导成熟雄性罗非鱼产生6.5 kb的mRNA。抗雌激素他莫昔芬可显著降低成熟雌鱼的卵黄蛋白原mRNA水平。对对照和17αMT处理的雌性罗非鱼血清进行放射免疫分析显示,血清E2水平显著降低,从对照鱼的11.4±2.6 ng/ml降至处理鱼的2.2±0.13 ng/ml。然而,他莫昔芬导致血清E2水平升高,可能是通过阻断E2的负反馈作用。17αMT降低血清E2的作用表明其作用位点可能在下丘脑-垂体轴上对促性腺激素产生有抑制作用,可能是通过雄激素受体,或者是在17αMT局部芳香化后通过雌激素受体起作用。

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