Smith Peter G, George Matthew, Bradshaw Sarah
Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
Urology. 2009 Jun;73(6):1392-6. doi: 10.1016/j.urology.2008.11.052. Epub 2009 Apr 10.
To assess whether sympathetic reinnervation of the rat proximal urethra is affected by differences in estrogen levels. Sympathetic innervation mediates tonic contraction of proximal urethral smooth muscle, thus contributing to urinary continence. Urethral innervation is particularly susceptible to damage during vaginal delivery, a time characterized by decreasing estrogen levels.
Adult female rats were ovariectomized and implanted with pellets containing vehicle or estrogen to achieve serum levels similar to rodent pregnancy. The rats were injected intravenously with vehicle or the selective sympathetic neurotoxin 6-hydroxydopamine, which produces uniform and complete destruction of terminal sympathetic axons. At 1, 4, 12, and 25 days, tyrosine hydroxylase-immunoreactive sympathetic innervation of the proximal urethral smooth muscle was assessed quantitatively.
In rats with intact innervation, the proximal urethra is densely innervated, and nerve density is comparable, irrespective of estrogen status. 6-Hydroxydopamine induced marked sympathetic axon disruption by day 1 and complete denervation by 4 days after injection in the ovariectomized rats receiving vehicle or estrogen. In the vehicle-treated rats, few nerves were present at 12 days after sympathectomy, and innervation remained substantially less than normal levels at 25 days. In estrogen-treated rats, sympathetic reinnervation was twofold greater at 12 days and by 25 days was comparable to that of the controls.
Estrogen improves sympathetic reinnervation of the proximal urethra. Estrogen titers in individuals with urethral sympathetic nerve damage might, therefore, influence the rate and extent of urethral smooth muscle reinnervation.
评估大鼠近端尿道的交感神经再支配是否受雌激素水平差异的影响。交感神经支配介导近端尿道平滑肌的紧张性收缩,从而有助于尿失禁。尿道神经支配在阴道分娩期间特别容易受损,而阴道分娩期间雌激素水平会下降。
成年雌性大鼠行卵巢切除术,并植入含赋形剂或雌激素的药丸,以使血清水平与啮齿动物孕期相似。给大鼠静脉注射赋形剂或选择性交感神经毒素6-羟基多巴胺,该毒素可使终末交感神经轴突发生均匀且完全的破坏。在第1、4、12和25天,对近端尿道平滑肌中酪氨酸羟化酶免疫反应性交感神经支配进行定量评估。
在神经支配完整的大鼠中,无论雌激素状态如何,近端尿道均有密集的神经支配,且神经密度相当。在接受赋形剂或雌激素的去卵巢大鼠中,6-羟基多巴胺在注射后第1天引起明显的交感神经轴突破坏,4天后完全去神经支配。在接受赋形剂治疗的大鼠中,交感神经切除术后12天几乎没有神经,25天时神经支配仍显著低于正常水平。在接受雌激素治疗的大鼠中,交感神经再支配在12天时增加了两倍,到25天时与对照组相当。
雌激素可改善近端尿道的交感神经再支配。因此,尿道交感神经损伤个体的雌激素水平可能会影响尿道平滑肌再支配的速度和程度。