Department of Biochemistry and Molecular Biology, University of Texas-Houston Medical School, Houston, TX 77030, USA.
J Sex Med. 2011 Aug;8(8):2172-80. doi: 10.1111/j.1743-6109.2011.02316.x. Epub 2011 May 19.
Adenosine has been implicated in normal and abnormal penile erection. However, a direct role of endogenous adenosine in erectile physiology and pathology has not been established.
To determine the functional role of endogenous adenosine production in erectile function.
CD73-deficient mice (CD73(-/-)) and age-matched wild-type (WT) mice were used. Some WT mice were treated with alpha, beta-methylene adenosine diphosphate (ADP) (APCP), a CD73-specific inhibitor. High-performance liquid chromatography was used to measure adenosine levels in mouse penile tissues. In vivo assessment of intracorporal pressure (ICP) normalized to mean arterial pressure (MAP) in response to electrical stimulation (ES) of the cavernous nerve was used.
The main outcome measures of this study were the in vivo assessment of initiation and maintenance of penile erection in WT mice and mice with deficiency in CD73 (ecto-5'-nucleotidase), a key cell-surface enzyme to produce extracellular adenosine.
Endogenous adenosine levels were elevated in the erected state induced by ES of cavernous nerve compared to the flaccid state in WT mice but not in CD73(-/-) mice. At cellular levels, we identified that CD73 was highly expressed in the neuronal, endothelial cells, and vascular smooth muscle cells in mouse penis. Functionally, we found that the ratio of ES-induced ICP to MAP in CD73(-/-) mice was reduced from 0.48 ± 0.03 to 0.33 ± 0.05 and ES-induced slope was reduced from 0.30 ± 0.13 mm Hg/s to 0.15 ± 0.05 mm Hg/s (both P < 0.05). The ratio of ES-induced ICP to MAP in APCP-treated WT mice was reduced from 0.49 ± 0.03 to 0.38 ± 0.06 and ES-induced slope was reduced from 0.29 ± 0.11 mm Hg/s to 0.19 ± 0.04 mm Hg/s (both P < 0.05).
Overall, our findings demonstrate that CD73-dependent production of endogenous adenosine plays a direct role in initiation and maintenance of penile erection.
腺苷已被牵涉到正常和异常的阴茎勃起中。然而,内源性腺苷在勃起生理和病理中的直接作用尚未确定。
确定内源性腺苷产生在勃起功能中的作用。
使用 CD73 缺陷型(CD73(-/-))小鼠和年龄匹配的野生型(WT)小鼠。一些 WT 小鼠用 α,β-亚甲基腺苷二磷酸(ADP)(APCP)处理,一种 CD73 特异性抑制剂。使用高效液相色谱法测量小鼠阴茎组织中的腺苷水平。使用电刺激(ES)海绵状神经时的阴茎体内压力(ICP)与平均动脉压(MAP)的比值来评估体内反应。
本研究的主要观察指标是 WT 小鼠和 CD73 缺陷型(外切 5'-核苷酸酶)小鼠的阴茎勃起的起始和维持的体内评估,CD73 是产生细胞外腺苷的关键细胞表面酶。
与 WT 小鼠松弛状态相比,ES 诱导的海绵状神经勃起状态下内源性腺苷水平升高,但在 CD73(-/-)小鼠中则没有升高。在细胞水平上,我们发现 CD73 在小鼠阴茎的神经元、内皮细胞和血管平滑肌细胞中高表达。在功能上,我们发现 CD73(-/-) 小鼠的 ES 诱导的 ICP 与 MAP 的比值从 0.48±0.03 降低至 0.33±0.05,ES 诱导的斜率从 0.30±0.13mm Hg/s 降低至 0.15±0.05mm Hg/s(均 P<0.05)。APCP 处理的 WT 小鼠的 ES 诱导的 ICP 与 MAP 的比值从 0.49±0.03 降低至 0.38±0.06,ES 诱导的斜率从 0.29±0.11mm Hg/s 降低至 0.19±0.04mm Hg/s(均 P<0.05)。
总的来说,我们的研究结果表明,CD73 依赖性内源性腺苷的产生在阴茎勃起的起始和维持中起直接作用。