Department of Urology, Affiliated Hospital, Southwest medical University, Luzhou, China.
Department of thyroid Surgery, Affiliated Hospital, Southwest medical University, Luzhou, China.
Urology. 2019 Nov;133:249.e1-249.e7. doi: 10.1016/j.urology.2019.08.025. Epub 2019 Aug 30.
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).
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.
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).
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.
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。
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。
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)。
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。