Goswami Sumanta Kumar, Vishwanath Manikanta, Gangadarappa Suma Kallahalli, Razdan Rema, Inamdar Mohammed Naseeruddin
Department of Pharmacology, Al-Ameen College of Pharmacy, Near Lalbagh main gate, Hosur Main Road, Bangalore, Karnataka, India.
Pharmacogn Mag. 2014 Aug;10(Suppl 3):S581-7. doi: 10.4103/0973-1296.139790.
Diabetes induced sexual dysfunction is a leading cause of male sexual disorder and an early indicator of cardiovascular complication. Reactive oxygen species generated in body during diabetes is a main causative factor for erectile dysfunction, a sexual dysfunction. Adjuvant antioxidant therapy along with phosphodiesterases type 5 enzyme inhibitor (PDE5i) is more effective than PDE5i alone.
The aim of the study was to investigate efficacy of ellagic acid a known antioxidant and sildenafil in diabetes induced erectile dysfunction.
Type 1 diabetes was induced in male rats and rats were treated with ellagic acid (50 mg/kg, p.o.) and a combination of ellagic acid (50 mg/kg, p.o.) and sildenafil (5 mg/kg, p.o.), a PDE5i for 28 days. Sexual function was observed in diabetic rat and compared with those of treatment group and normal rats. Effect of ellagic acid was studied on advanced glycation end products (AGE) and isolated rat corpus cavernosum in vitro.
Sexual function of diabetic rats was found to be reduced and ellegic acid treatment could preserve sexual function of diabetic rats to some extent. Ellagic acid + sildenafil treatment was more efficient in management of diabetes induced sexual dysfunction. Ellagic acid inhibited (AGE) in vitro implying its role in reducing oxidative stress in diabetes. The polyphenol could not increase sexual function in normal rats and relax isolated rat corpus cavernosum smooth muscle significantly.
The study proves usefulness of adjuvant antioxidant therapy in the management of erectile dysfunction in diabetes.
糖尿病诱发的性功能障碍是男性性功能障碍的主要原因,也是心血管并发症的早期指标。糖尿病期间体内产生的活性氧是勃起功能障碍(一种性功能障碍)的主要致病因素。辅助抗氧化治疗联合5型磷酸二酯酶抑制剂(PDE5i)比单独使用PDE5i更有效。
本研究旨在探讨已知抗氧化剂鞣花酸和西地那非对糖尿病诱发的勃起功能障碍的疗效。
诱导雄性大鼠患1型糖尿病,然后用鞣花酸(50毫克/千克,口服)以及鞣花酸(50毫克/千克,口服)与PDE5i西地那非(5毫克/千克,口服)的组合对大鼠进行为期28天的治疗。观察糖尿病大鼠的性功能,并与治疗组和正常大鼠进行比较。在体外研究鞣花酸对晚期糖基化终产物(AGE)和分离的大鼠海绵体的影响。
发现糖尿病大鼠的性功能降低,鞣花酸治疗可在一定程度上保留糖尿病大鼠的性功能。鞣花酸+西地那非治疗在糖尿病诱发的性功能障碍管理方面更有效。鞣花酸在体外抑制AGE,这表明其在减轻糖尿病氧化应激中的作用。该多酚不能增加正常大鼠的性功能,也不能使分离的大鼠海绵体平滑肌显著松弛。
该研究证明辅助抗氧化治疗在糖尿病勃起功能障碍管理中的有用性。