Wake Forest Institute for Regenerative Medicine, Wake Forest University Primate Center, Department of Comparative Medicine, Wake Forest University Health Sciences, Winston Salem, NC 27157, USA.
Eur Urol. 2009 Dec;56(6):1055-66. doi: 10.1016/j.eururo.2008.12.016. Epub 2008 Dec 25.
Despite the advent of effective oral therapies for erectile dysfunction (ED), many patients are not successfully treated, and side effects have been documented.
To further evaluate the potential utility of naked DNA-based gene transfer as an attractive treatment option for ED.
DESIGN, SETTING AND PARTICIPANTS: The effects of gene transfer on erectile function and sexual behavior were evaluated in eight male cynomolgus monkeys with ED secondary to moderately severe, diet-induced atherosclerosis.
Following establishment of baseline characteristics, animals were subjected to intracavernous injection of a smooth-muscle-specific gene transfer vector (pSMAA-hSlo) encoding the pore-forming subunit of the human large-conductance, calcium-sensitive potassium channel (Maxi-K).
For the sexual behavior studies, 2 wk of baseline data were obtained, and then animals were placed in the presence of estrogen-implanted females (n=2) three times per week for 30 min, and sexual behavior was recorded. The intracavernous pressure response to papaverine injection was also monitored.
Dramatic changes in erectile function and sexual behavior were observed after intracorporal gene transfer. The frequency of partial (6±2 to 10±2) and full (2±1.5 to 5±1.4) erections were significantly increased, with a parallel 2-3-fold increase in the duration of the observed erections. The frequency and latency of ejaculation were increased and decreased, respectively. Frequency and duration of grooming by the female were increased, and the latency decreased. Increased latency and decreased frequency of body contact was also observed, and this is characteristic of the typical drop in consort intimacy that occurs after mating in most macaque species. In addition, an increased responsiveness to intracavernous papaverine injection was observed.
The data indicate that intracorporal Maxi-K-channel gene transfer enhances erectile capacity and sexual behavior; the data imply that increased erectile function per se may lead to increased sexual function.
尽管有有效的口服治疗勃起功能障碍(ED)的方法,但许多患者并未得到成功治疗,并且已经记录到了副作用。
进一步评估将裸露 DNA 基因转移作为 ED 有吸引力的治疗选择的潜力。
设计、设置和参与者:将基因转移对勃起功能和性行为的影响评估应用于 8 只因饮食诱导的动脉粥样硬化而导致 ED 的雄性食蟹猴。
在建立基线特征后,动物接受了平滑肌特异性基因转移载体(pSMAA-hSlo)的海绵体内注射,该载体编码人类大电导、钙敏钾通道(Maxi-K)的孔形成亚基。
在性行为研究中,获得了 2 周的基线数据,然后每周 3 次将动物置于雌激素植入的雌性(n=2)的存在下 30 分钟,并记录性行为。还监测了罂粟碱注射引起的海绵体内压反应。
在体内基因转移后,观察到勃起功能和性行为的显著变化。部分(6±2 至 10±2)和完全(2±1.5 至 5±1.4)勃起的频率显著增加,观察到的勃起持续时间增加了 2-3 倍。射精的频率和潜伏期分别增加和减少。雌性的梳理频率和持续时间增加,潜伏期减少。还观察到接触身体的频率增加和潜伏期增加,这是大多数猕猴物种交配后伴侣亲密关系典型下降的特征。此外,还观察到对海绵体内罂粟碱注射的反应性增加。
数据表明,海绵体内 Maxi-K 通道基因转移增强了勃起能力和性行为;数据表明,勃起功能的增加本身可能导致性功能的增加。