Su Yudong, Shui Jinman, Qi Danshi, Bai Jie, Xu Xiaoxia, Huang Yongchun, Li Ruilian, Wu Qiong, Wang Haiyan, Cao Chengzhu, Su Zhanhai, Zhang Shoude
School of Pharmacy, Qinghai University, Xining, Qinghai, People's Republic of China.
Department of Basic Medical Sciences, Qinghai University Medical College, Xining, Qinghai, People's Republic of China.
Drug Des Devel Ther. 2025 Apr 30;19:3351-3361. doi: 10.2147/DDDT.S514209. eCollection 2025.
Erectile dysfunction (ED), a prevalent form of male sexual dysfunction, is predominantly treated with Phosphodiesterase type 5 inhibitors (PDE5Is). Our previous research highlighted procyanidin, a natural compound, as a notably effective PDE5I. In the current study, we intend to further validate the inhibitory activity of procyanidin on PDE5A through in vitro and in vivo assessments. This study aims to validate the efficacy of procyanidin as a treatment for ED.
The binding affinity of procyanidin for PDE5A was assessed by molecular docking, molecular dynamics (MD) simulations, and microscale thermophoresis (MST) assay. The toxicity of procyanidin on penile corpus cavernosum smooth muscle (CCSM) cells (n=5) was evaluated. Additionally, its effects on intracellular cyclic guanosine monophosphate (cGMP) levels in CCSM cells (n=5) were evaluated. The absorption of procyanidin was evaluated by measuring plasma levels at various times after oral gavage to Sprague-Dawley (SD) rats (n=6). Subsequently, the effects of procyanidin on intracavernous pressure (ICP) and cGMP levels in penile cavernous tissue were evaluated in SD rats (n=6).
Procyanidin forms three hydrogen bonds with PDE5A and stabilizes the complex structure, exhibiting equilibrium dissociation constants (K) value of 7.77 ± 2.39 µmol/L. Additionally, procyanidin exhibits minimal cytotoxicity toward CCSM cells and significantly elevates intracellular cGMP levels compared to the control group. In vivo studies demonstrate that procyanidin is rapidly absorbed, achieving peak blood concentrations within one hour. Simultaneously, procyanidin significantly increases ICP and cGMP levels in rats compared to the control group.
These findings indicate that procyanidin sustains elevated cGMP levels within cells by targeting PDE5A, thereby exhibiting therapeutic efficacy in improving ICP. Procyanidin emerges as a promising PDE5I for treating ED and potentially other related conditions.
勃起功能障碍(ED)是男性性功能障碍的一种常见形式,主要采用5型磷酸二酯酶抑制剂(PDE5Is)进行治疗。我们之前的研究强调了原花青素这种天然化合物是一种特别有效的PDE5I。在当前研究中,我们打算通过体外和体内评估进一步验证原花青素对PDE5A的抑制活性。本研究旨在验证原花青素作为ED治疗方法的疗效。
通过分子对接、分子动力学(MD)模拟和微尺度热泳(MST)分析评估原花青素对PDE5A的结合亲和力。评估原花青素对阴茎海绵体平滑肌(CCSM)细胞(n = 5)的毒性。此外,评估其对CCSM细胞(n = 5)内细胞内环磷酸鸟苷(cGMP)水平的影响。通过测量对Sprague-Dawley(SD)大鼠(n = 6)灌胃后不同时间的血浆水平来评估原花青素的吸收情况。随后,在SD大鼠(n = 6)中评估原花青素对阴茎海绵体内压(ICP)和阴茎海绵体组织中cGMP水平的影响。
原花青素与PDE5A形成三个氢键并稳定复合物结构,表现出平衡解离常数(K)值为7.77±2.39µmol/L。此外,与对照组相比,原花青素对CCSM细胞表现出最小的细胞毒性,并显著提高细胞内cGMP水平。体内研究表明,原花青素吸收迅速,在一小时内达到血药浓度峰值。同时,与对照组相比,原花青素显著提高大鼠的ICP和cGMP水平。
这些发现表明,原花青素通过靶向PDE5A维持细胞内cGMP水平升高,从而在改善ICP方面表现出治疗效果。原花青素成为一种有前景的用于治疗ED及潜在其他相关病症的PDE5I。