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作 者:李杨[1] 赵丹[1] 王洪军[1] 王蔚东[1] 田庚[1] 赵雪俭[1]
机构地区:[1]白求恩医科大学生殖病理生理研究室
出 处:《生殖与避孕》1996年第1期65-69,T004,共5页Reproduction and Contraception
摘 要:30只日本大耳白雄兔,分为输精管结扎25月组(VG25)和假手术25月组(SOG25),输精管结扎6月组(VG6)和假手术6月组(SOG6)。应用放射免疫技术测定血浆睾酮含量;应用大鼠雄激素受体(AR)cDNA探针,Northern杂交方法检测睾丸组织的ARmRNA表达,分析输精管结扎对睾丸ARmRNA表达强度的影响。结果表明(1)血浆睾酮含量以VG6为最低(8.06±2.78nmol/L),但与SOG6(10.68±0.99nmol/L)比较,P>0.05.VG25(12.10±2.44nmol/L)略高于SOG25(10.93±1.28nmol/L),并显著地高于VG6(t=3.09,P<0.01)。(2)睾丸组织ARmRNA的Northern杂交分析证明,家兔睾丸组织的ARmRNA与大鼠有同源性,杂交信号位于28s之后。在VG6、SOG6、VG25和SOG25均有ARmRNA的表达,VG6强于SOG6,VG25与SOG25无明显差异。该结果显示了睾酮对ARmRNA表达的下调节作用,而输精管结扎对家兔ARmRNA的长度无影响。Thirty male Japan white rabbits were divided into four groups:Vasectomy Groups in 6 and 25 months (VG6 .VG25) and the corresponding Sham Operation Groups (SOG6.SOG25).Plasma testosterone content (T) was detected by RIA ; Androgen receptor (AR) mRNA concentrations were determined by Northern blotting with rat AR cDNA probe. The results showed that: (1) Tin VG6 (8. 06 ±2. 78nmol/L) was the lowest in four groups,but compared with in SOG6 (10. 68 ±0. 99nmol/L) P > 0. 05; T in VG25 (12. 10 ±2. 44nmol/L) was slightly higher than that in SOG25 (10. 93± 1. 28nmol/L) and significantly higher than that in VG6 as well (t= 3. 09,P<0. 01). (2) AR mRNA of rabbit testis showed a homology with rat. The major AR mRNA species was behind 28s, and although ARmRNA expression was detected in VG6. SOG6. VG25 and SOG25, concentration of AR mRNA was the highest in VG6 and the lowest in VG25. Taken together, these data demonstrated that androgen down regulated the concentration of AR mRNA in testis;no changes were found in the length of AR mRNA.
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