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S1P1 基因转染可改善自发性高血压大鼠的勃起功能。

S1P1 Gene Transfection Improves Erectile Function in Spontaneously Hypertensive Rats.

机构信息

Department of Urology, Affiliated Hospital, Southwest medical University, Luzhou, China.

Department of thyroid Surgery, Affiliated Hospital, Southwest medical University, Luzhou, China.

出版信息

Urology. 2019 Nov;133:249.e1-249.e7. doi: 10.1016/j.urology.2019.08.025. Epub 2019 Aug 30.

Abstract

OBJECTIVE

To investigate the relationship between the upregulated expression of sphingosine-1-phosphate receptor 1 (S1P1) in the corpus cavernosum and erectile function in spontaneously hypertensive rats (SHRs).

METHODS

Twelve-week-old healthy male Wistar-Kyoto rats (WKY) and SHR rats were randomly divided into 4 groups: WKY, SHR, WKY transfection, and SHR transfection (n = 5). A lentiviral vector carrying the S1P1 gene was injected into the corpus cavernosum penis of rats in the transfection groups (1 × 10 TU/mL, 20 μL). After 1 week, the maximum penile intracavernous pressure/mean arterial pressure (ICP/MAP), nitric oxide (NO) content, and the expression of eNOS, P-eNOS, ROCK1, ROCK2, and S1P1 in the corpus cavernosum penis of rats in each group were measured.

RESULTS

The ICP/MAP value was significantly higher in the SHR transfection group than in the SHR group under 3-V and 5-V electrical stimulations (P <.01). The expression of S1P1 and P-eNOS proteins significantly increased (P <.01), while that of ROCK1 and ROCK2 proteins significantly decreased (P <.01) in the SHR transfected group compared with the SHR group. The NO content was significantly higher in the SHR transfection group than in the SHR group (P <.01).

CONCLUSION

The upregulated expression of S1P1 in SHR corpus cavernosum penis may improve the SHR erectile function by upregulating the P-eNOS/eNOS ratio and inhibiting the RhoA/Rho kinase signaling pathway.

摘要

目的

探讨阴茎海绵体中鞘氨醇-1-磷酸受体 1(S1P1)表达上调与自发性高血压大鼠(SHR)勃起功能的关系。

方法

将 12 周龄健康雄性 Wistar-Kyoto 大鼠(WKY)和 SHR 大鼠随机分为 4 组:WKY 组、SHR 组、WKY 转染组和 SHR 转染组(n=5)。转染组大鼠阴茎海绵体注射携带 S1P1 基因的慢病毒载体(1×10 TU/mL,20 μL)。1 周后,测量各组大鼠阴茎海绵体最大腔内压/平均动脉压(ICP/MAP)、一氧化氮(NO)含量及阴茎海绵体组织中 eNOS、磷酸化 eNOS(P-eNOS)、Rho 激酶 1(ROCK1)、Rho 激酶 2(ROCK2)和 S1P1 的表达。

结果

3-V 和 5-V 电刺激时,SHR 转染组大鼠的 ICP/MAP 值明显高于 SHR 组(P<.01)。与 SHR 组相比,SHR 转染组大鼠 S1P1 和 P-eNOS 蛋白表达显著增加(P<.01),ROCK1 和 ROCK2 蛋白表达显著降低(P<.01)。与 SHR 组相比,SHR 转染组大鼠 NO 含量显著升高(P<.01)。

结论

SHR 阴茎海绵体中 S1P1 的表达上调可能通过上调 P-eNOS/eNOS 比值并抑制 RhoA/Rho 激酶信号通路来改善 SHR 的勃起功能。

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