Deng W, Bivalacqua T J, Champion H C, Hellstrom W J, Murthy Subramanyam N, Kadowitz Philip J
Department of Pharmacology, Tulane University Health Sciences Center, New Orleans, LA, USA.
Methods Mol Biol. 2010;610:213-27. doi: 10.1007/978-1-60327-029-8_13.
Erectile dysfunction (ED) is defined as the inability to attain and/or maintain penile erection sufficient for satisfactory sexual performance. Oxidative stress has been demonstrated to be involved in the pathophysiology of age- or diabetes-related ED. Superoxide dismutase (SOD), an antioxidant enzyme catalyzing the conversion of superoxide anion (O(2) (-)) to hydrogen peroxide (H(2)O(2)) and molecular oxygen (O(2)), is a promising therapeutic target for ED. In vivo gene therapy and adult stem cell-based ex vivo gene therapy are two attractive current gene therapies for the treatment of ED. In this chapter we describe the use of two potent gene transfer techniques to deliver the therapeutic gene extracellular superoxide dismutase (ecSOD) into the penis of aged or diabetic rats for therapy of ED: adenoviral-mediated intracavernosal ecSOD gene transfer for gene therapy of ED and ecSOD gene-modified marrow stromal cells, also known as mesenchymal stem cells, based stem cell and gene therapy.
勃起功能障碍(ED)被定义为无法获得和/或维持足以实现满意性功能的阴茎勃起。氧化应激已被证明与年龄相关或糖尿病相关的ED的病理生理学有关。超氧化物歧化酶(SOD)是一种抗氧化酶,可催化超氧阴离子(O(2) (-))转化为过氧化氢(H(2)O(2))和分子氧(O(2)),是治疗ED的一个有前景的治疗靶点。体内基因治疗和基于成体干细胞的体外基因治疗是目前治疗ED的两种有吸引力的基因治疗方法。在本章中,我们描述了使用两种有效的基因转移技术将治疗性基因细胞外超氧化物歧化酶(ecSOD)导入老年或糖尿病大鼠的阴茎以治疗ED:腺病毒介导的海绵体内ecSOD基因转移用于ED的基因治疗,以及基于ecSOD基因修饰的骨髓基质细胞(也称为间充质干细胞)的干细胞和基因治疗。