Kakizaki H, de Groat W C
Department of Urology, Hokkaido University School of Medicine, Sapporo, Japan.
J Urol. 1997 Oct;158(4):1562-7.
It is known that reflex activity of the urinary bladder can be inhibited or facilitated by perineal cutaneous stimulation. This study was undertaken to examine the urethral striated (EUS) and smooth muscle responses evoked by perineal cutaneous stimulation in the rat.
Urethral perfusion pressure and EUS-EMG were monitored in urethane-anesthetized normal and chronic spinal rats (4-5 weeks after T(8-9) spinalization) of either sex. Somatic perineal stimulation was performed by tactile or pinch stimulation to the perineum.
In both normal and chronic spinal rats, perineal stimulation elicited a transient increase in EUS-EMG activity which was abolished following neuromuscular blockade with alpha-bungarotoxin i.v. In normal rats treated with alpha-bungarotoxin perineal stimulation did not elicit a detectable urethral smooth muscle response. However, in chronic spinal rats perineal stimulation increased urethral pressure by smooth muscle contraction in males and decreased urethral pressure by smooth muscle relaxation in females. The evoked urethral smooth muscle contraction in males was significantly reduced or abolished by atropine i.v., but not by sympathetic nerve transection or prazosin i.v., whereas the relaxation in females was significantly reduced or abolished by N-nitro-L-arginine methyl ester (a nitric oxide synthase inhibitor, i.v.).
These data indicate that spinal cord injury unmasks somato-urethral smooth muscle reflexes mediated by lumbosacral parasympathetic efferent pathways. The reflexes consist of a nitric oxide-mediated urethral relaxation in females and an atropine-sensitive urethral contraction in male rats.
已知膀胱的反射活动可被会阴皮肤刺激所抑制或促进。本研究旨在检测大鼠会阴皮肤刺激所诱发的尿道横纹肌(EUS)和平滑肌反应。
在氨基甲酸乙酯麻醉的正常和慢性脊髓大鼠(T(8-9)脊髓横断4-5周后)中监测尿道灌注压和EUS-EMG,雌雄不限。通过对会阴进行触觉或捏压刺激来进行躯体会阴刺激。
在正常和慢性脊髓大鼠中,会阴刺激均引起EUS-EMG活动短暂增加,静脉注射α-银环蛇毒素进行神经肌肉阻滞后该增加消失。在用α-银环蛇毒素处理的正常大鼠中,会阴刺激未引发可检测到的尿道平滑肌反应。然而,在慢性脊髓大鼠中,会阴刺激在雄性中通过平滑肌收缩使尿道压力升高,在雌性中通过平滑肌舒张使尿道压力降低。静脉注射阿托品可显著降低或消除雄性中诱发的尿道平滑肌收缩,但交感神经横断或静脉注射哌唑嗪则无此作用,而雌性中的舒张反应可被N-硝基-L-精氨酸甲酯(一种一氧化氮合酶抑制剂,静脉注射)显著降低或消除。
这些数据表明脊髓损伤揭示了由腰骶部副交感传出通路介导的躯体-尿道平滑肌反射。这些反射包括雌性中一氧化氮介导的尿道舒张和雄性大鼠中对阿托品敏感的尿道收缩。