Li Wen Ji, Xu Mingxi, Gu Meng, Zheng Da-Chao, Guo Jianhua, Cai Zhikang, Wang Zhong
Cell Physiol Biochem. 2017;42(1):333-345. doi: 10.1159/000477388. Epub 2017 May 25.
BACKGROUND/AIMS: Transforming growth factor-β1 (TGF-β1) plays important roles in penile corporal fibrosis and veno-occlusive dysfunction (CVOD). Angiotensin II (Ang II) is critically involved in erectile dysfunction, and blocking of Ang II is more important than inhibition of TGF-β in non-penile tissue fibrosis. However, the role of Ang II in corporal fbrosis and CVOD in a diabetic condition has not been investigated.
Diabetic rats were treated with sildenafil or losartan (an Ang II antagonist) alone or in combination. Intracavernosal pressure, dynamic infusion cavernosometry, and histological and molecular alterations of the corpus cavernosum were examined.
Diabetic rats exhibited decreases in erectile response, severe CVOD, apoptosis, fibrosis, and activation of the TGF-β1 pathway. Treatment with sildenafil had a modest effect on erectile response and an insignificant suppressive effect on CVOD, apoptosis, fibrosis, and the TGF-β1 pathway. Although losartan greatly improved the histological and molecular changes and CVOD as compared with sildenafil, its effect on erectile response was low. The combination of sildenafil and losartan had superior effects on these parameters than did either compound alone.
Ang II activation may be involved in apoptosis and fibrosis of the corpus cavernosum through Smad and non-Smad pathways, resulting in CVOD and ED. The low efficacy of sildenafil in a diabetic ED rat model was at least partly due to its inadequate effects on apoptosis, fibrosis, and CVOD.
背景/目的:转化生长因子-β1(TGF-β1)在阴茎海绵体纤维化和静脉闭塞功能障碍(CVOD)中起重要作用。血管紧张素II(Ang II)与勃起功能障碍密切相关,在非阴茎组织纤维化中,阻断Ang II比抑制TGF-β更重要。然而,Ang II在糖尿病状态下海绵体纤维化和CVOD中的作用尚未得到研究。
对糖尿病大鼠单独或联合使用西地那非或氯沙坦(一种Ang II拮抗剂)进行治疗。检测阴茎海绵体内压、动态灌注海绵体测压以及阴茎海绵体的组织学和分子改变。
糖尿病大鼠勃起反应降低,出现严重的CVOD、细胞凋亡、纤维化以及TGF-β1途径激活。西地那非治疗对勃起反应有一定作用,但对CVOD、细胞凋亡、纤维化和TGF-β1途径的抑制作用不显著。与西地那非相比,氯沙坦虽然能显著改善组织学和分子变化以及CVOD,但其对勃起反应的作用较弱。西地那非和氯沙坦联合使用对这些参数的效果优于单独使用任何一种药物。
Ang II激活可能通过Smad和非Smad途径参与阴茎海绵体的细胞凋亡和纤维化,导致CVOD和勃起功能障碍(ED)。西地那非在糖尿病性ED大鼠模型中的疗效较低,至少部分原因是其对细胞凋亡、纤维化和CVOD的作用不足。