Hayashi Narihiko, Bella Anthony J, Wang Guifang, Lin Guiting, Deng Donna Y, Nunes Lora, Lue Tom F
Knuppe Molecular Urology Lab, Department of Urology, University of California, San Francisco, Calif.
Can Urol Assoc J. 2007 Sep;1(3):256-63. doi: 10.5489/cuaj.79.
We tested the hypothesis that extended-term (5-week) estrogen therapy would negatively impact voiding function in a postpartum, ovariectomized rat model.
Immediately after delivery, 30 primiparous Sprague-Dawley rats underwent intravaginal balloon dilation, followed by ovariectomy 1 week later. Cystometry at postpartum week 2 determined normal or abnormal voiding patterns. After randomization, one-half the normal and abnormal voiding rats received 5 weeks of estrogen therapy, while the remainder received placebo. Estrogen effect was determined by repeat cystometry and immunohistochemical analysis of the urethra and vagina.
Abnormal voiding increased from 60.0% to 73.3% in the estrogen- treated group and declined from 60% to 33% for the placebo group. Rats were then divided into 4 groups for comparison: normal voiding versus placebo (group 1), abnormal voiding versus placebo (group 2), normal voiding versus estrogen (group 3) and abnormal voiding versus estrogen (group 4). Bladder capacity, leak point pressure and maximum voiding pressure were most depressed in group 4. Estrogen treatment was associated with a significant downregulation of alpha(1A) and alpha(1D)-adrenoceptors in the urethral submucosa but an upregulation of nNOS in the urethral smooth muscle.
Extended-term estrogen therapy in a rat model of simulated birth trauma and ovariectomy resulted in a higher rate of incontinence. Immunohistochemical examination demonstrated significant downregulation of urethral alpha(1A)- and alpha(1D)-adrenoceptors and upregulation of neuronal nitric oxide synthase (nNOS) in the urethra of estrogen-treated groups. These studies question the use of hormone replacement therapy in the treatment of postmenopausal incontinence.
我们检验了这样一个假设,即在产后去卵巢大鼠模型中,长期(5周)雌激素治疗会对排尿功能产生负面影响。
30只初产的Sprague-Dawley大鼠在分娩后立即接受阴道内气囊扩张,1周后进行卵巢切除术。产后第2周进行膀胱测压以确定排尿模式正常或异常。随机分组后,正常排尿和异常排尿的大鼠各有一半接受5周的雌激素治疗,其余接受安慰剂治疗。通过重复膀胱测压以及对尿道和阴道进行免疫组织化学分析来确定雌激素的作用。
雌激素治疗组异常排尿率从60.0%增至73.3%,而安慰剂组则从60%降至33%。然后将大鼠分为4组进行比较:正常排尿与安慰剂组(第1组)、异常排尿与安慰剂组(第2组)、正常排尿与雌激素组(第3组)以及异常排尿与雌激素组(第4组)。第4组的膀胱容量、漏点压力和最大排尿压力下降最为明显。雌激素治疗与尿道黏膜下层α(1A)和α(1D) -肾上腺素能受体的显著下调有关,但与尿道平滑肌中神经元型一氧化氮合酶(nNOS)的上调有关。
在模拟分娩创伤和卵巢切除的大鼠模型中,长期雌激素治疗导致更高的尿失禁发生率。免疫组织化学检查显示,雌激素治疗组尿道中α(1A) -和α(1D) -肾上腺素能受体显著下调,而神经元型一氧化氮合酶(nNOS)上调。这些研究对激素替代疗法用于治疗绝经后尿失禁提出了质疑。