Miyazato Minoru, Kaiho Yasuhiro, Kamo Izumi, Chancellor Michael B, Sugaya Kimio, de Groat William C, Yoshimura Naoki
Department. of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Am J Physiol Renal Physiol. 2008 Jul;295(1):F264-71. doi: 10.1152/ajprenal.90241.2008. Epub 2008 May 14.
We investigated the effect of duloxetine, a norepinephrine (NE) and serotonin (5-HT) reuptake inhibitor, on the neurally evoked urethral continence reflex induced by sneezing in rats. To clarify the role of noradrenergic and serotonergic mechanisms in preventing stress urinary incontinence (SUI) during sneezing, we examined the effect of duloxetine followed by intrathecal (it) methiothepin maleate (5-HT receptor and alpha1-adrenoceptor antagonist) or terazosin or idazoxan (selective alpha1- and alpha2-adrenoceptor antagonists, respectively). Amplitude of urethral pressure responses during sneezing (A-URS), urethral baseline pressure (UBP) at the midurethra, and sneeze-induced leak point pressure (S-LPP) were measured in normal adult female rats and rats with SUI induced by vaginal distension (VD). In normal and VD rats, intravenous application of duloxetine (1 mg/kg) increased A-URS by 35% and 34% and UBP by 21% and 34%, respectively. Sneezing-induced fluid leakage from the urethral orifice was observed in VD rats but not in normal rats. S-LPP was increased from 39.1 to 92.2 cmH2O by intravenous duloxetine in incontinent VD rats. Duloxetine-mediated enhancement of A-URS was inhibited by terazosin but not methiothepin maleate (it). In addition, simultaneous intrathecal application of methiothepin and terazosin induced a reduction in A-URS during sneezing, which was not increased by intravenous duloxetine. However, the reduced A-URS after intrathecal application of methiothepin and terazosin returned to the control level when duloxetine (iv) was applied after intrathecal idazoxan administration. These results indicate that duloxetine can prevent SUI by facilitating noradrenergic and serotonergic systems in the spinal cord to enhance the sneeze-induced active urethral closure mechanism.
我们研究了去甲肾上腺素(NE)和5-羟色胺(5-HT)再摄取抑制剂度洛西汀对大鼠打喷嚏诱发的神经源性尿道控尿反射的影响。为阐明去甲肾上腺素能和5-羟色胺能机制在预防打喷嚏期间压力性尿失禁(SUI)中的作用,我们先给予度洛西汀,随后鞘内注射马来酸甲硫哒嗪(5-HT受体和α1-肾上腺素能受体拮抗剂)或特拉唑嗪或咪唑克生(分别为选择性α1-和α2-肾上腺素能受体拮抗剂),观察其效果。在正常成年雌性大鼠和经阴道扩张(VD)诱导SUI的大鼠中,测量打喷嚏期间尿道压力反应的幅度(A-URS)、尿道中尿道基线压力(UBP)以及打喷嚏诱发的漏点压力(S-LPP)。在正常和VD大鼠中,静脉注射度洛西汀(1 mg/kg)分别使A-URS增加35%和34%,使UBP增加21%和34%。在VD大鼠中观察到打喷嚏诱发的尿道口漏液,而正常大鼠未观察到。静脉注射度洛西汀使失禁的VD大鼠的S-LPP从39.1 cmH2O增加到92.2 cmH2O。特拉唑嗪可抑制度洛西汀介导的A-URS增强,但马来酸甲硫哒嗪(鞘内注射)则无此作用。此外,鞘内同时注射甲硫哒嗪和特拉唑嗪可使打喷嚏期间的A-URS降低,静脉注射度洛西汀后该值未增加。然而,鞘内注射甲硫哒嗪和特拉唑嗪后降低的A-URS在鞘内注射咪唑克生后再静脉注射度洛西汀时恢复到对照水平。这些结果表明,度洛西汀可通过促进脊髓中的去甲肾上腺素能和5-羟色胺能系统来增强打喷嚏诱发的主动尿道闭合机制,从而预防SUI。