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[雄激素与大鼠海绵体平滑肌中兰尼碱受体1和电压门控钙通道1.3的表达相关]

[Androgen correlates with expressions of ryanodine receptor 1 and voltage-gated calcium channel 1.3 in rat corpus cavernosum smooth muscle].

作者信息

Luo Hua, Yang Hai-fan, Jiang Rui

机构信息

Department of Urology, The Affiliated Hospital of Luzhou Medical College, Luzhou, Sichuan 646000, China.

出版信息

Zhonghua Nan Ke Xue. 2009 Oct;15(10):895-900.

Abstract

OBJECTIVE

To study the expressions of ryanodine receptor 1 (RyR1) and voltage-gated calcium channel 1.3 (CaV1.3) in the corpus cavernosum smooth muscle of castrated rats and to investigate their role in androgen deficiency-related erectile dysfunction.

METHODS

Forty 8-week-old SD rats were equally randomized into Groups A (2-week sham-operation), B (4-week sham-operation), C (2-week castration), and D (4-week castration). After surgery, the levels of serum testosterone in different groups of rats were determined, and the expressions of RyR1 and CaV1.3 in the corpus cavernosum were detected by immunohistochemical staining and RT-PCR.

RESULTS

The levels of serum testosterone were significantly decreased in Groups C ([15.97 +/- 5.67] nmol/L) and D ([2.03 +/- 1.57] nmol/L) as compared with A ([90.54 +/- 20.13] nmol/L) and B ([120.35 +/- 30.32] nmol/L) (P < 0.05). RyR1 and CaV1.3 expressed in all the groups. RyR1 mRNA, CaV1.3 mRNA and their proteins were remarkably reduced in Groups C (0.51 +/- 0.24, 0.50 +/- 0.12, 120.36 +/- 25.78, 103.37 +/- 39.52, respectively) and D (0.33 +/- 0.15, 0.32 +/- 0.07, 67.39 +/- 30.54, 67.56 +/- 20.12, respectively) in comparison with A (1.53 +/- 0.25, 1.33 +/- 0.05, 300.96 +/- 135.12, 298.68 +/- 126.35, respectively) and B (1.37 +/- 0.23, 1.25 +/- 0.03, 330.38 +/- 128.59, 327.35 +/- 117.37, respectively) (P < 0.05). The androgen level was positively correlated with the expressions of RyR1 and CaV1.3.

CONCLUSION

Androgen can regulate erectile function via RyR1 and CaV1.3.

摘要

目的

研究兰尼碱受体1(RyR1)和电压门控钙通道1.3(CaV1.3)在去势大鼠阴茎海绵体平滑肌中的表达,并探讨其在雄激素缺乏相关性勃起功能障碍中的作用。

方法

将40只8周龄SD大鼠随机均分为A组(假手术2周)、B组(假手术4周)、C组(去势2周)和D组(去势4周)。术后测定不同组大鼠血清睾酮水平,采用免疫组织化学染色和RT-PCR检测阴茎海绵体中RyR1和CaV1.3的表达。

结果

与A组([90.54±20.13]nmol/L)和B组([120.35±30.32]nmol/L)相比,C组([15.97±5.67]nmol/L)和D组([2.03±1.57]nmol/L)血清睾酮水平显著降低(P<0.05)。所有组均有RyR1和CaV1.3表达。与A组(分别为1.53±0.25、1.33±0.05、300.96±135.12、298.68±126.35)和B组(分别为1.37±0.23、1.25±0.03、330.38±128.59、327.35±117.37)相比,C组(分别为0.51±0.24、0.50±0.12、120.36±25.78、103.37±39.52)和D组(分别为0.33±0.15、0.32±0.07、67.39±3·54、67.56±20.12)的RyR1 mRNA、CaV1.3 mRNA及其蛋白显著降低(P<0.05)。雄激素水平与RyR1和CaV1.3的表达呈正相关。

结论

雄激素可通过RyR1和CaV1.3调节勃起功能。

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