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雌性兔膀胱颈及尿道近端、中段和远端的肾上腺素能、胆碱能和非肾上腺素能非胆碱能神经介导的收缩。

The adrenergic, cholinergic and NANC nerve-mediated contractions of the female rabbit bladder neck and proximal, medial and distal urethra.

作者信息

Deplanne V, Palea S, Angel I

机构信息

Synthélabo Recherche, Department of Internal Medicine, Rueil-Malmaison, France.

出版信息

Br J Pharmacol. 1998 Apr;123(8):1517-24. doi: 10.1038/sj.bjp.0701757.

Abstract
  1. The nerve-mediated contraction of the female rabbit bladder neck and different portions of the urethra (proximal, medial and distal) was studied in vitro by electrical stimulation (50 V, 30 Hz, 0.05 ms width, trains of 5 s every 5 min) by use of a superfusion system. 2. The amplitude (Emax) and the duration (Dmax) of the stimulated contraction were studied in the four tissues. The Emax value was significantly higher in distal urethra (2.07+/-0.15 g) compared to the bladder neck (1.08+/-0.10 g), proximal urethra (0.73+/-0.07 g) and medial urethra (0.87+/-0.07 g). In contrast, the Dmax value appeared slightly but significantly lower (P<0.05) in distal urethra (68.5+/-2.3 s) than in bladder neck (76.7+/-6.0 s), proximal urethra (84.5+/-5.0 s) and medial urethra (81.3+/-3.5 s). 3. Cocaine (1 microM) significantly increased the basal Emax values in medial and distal urethra and the basal Dmax values in the four tissues. 4. Prazosin (1 microM) significantly reduced E max value in proximal, medial and distal urethra and Dmax value in bladder neck and proximal urethra. Atropine (1 microM) also significantly reduced Emax values in bladder neck and proximal urethra and reduced Dmax value in bladder neck, but not in other tissues. Yohimbine (0.1 microM) was devoid of effect in the four tissues. 5. The association of prazosin (1 microM) and atropine (1 microM) did not modify the Emax and the Dmax values of the electrically-induced contractions, except in proximal urethra and in bladder neck where an additive inhibitory effect (on Emax only) was observed compared to prazosin and atropine alone. 6. The residual contractile response after combined treatment with prazosin and atropine was significantly diminished by tetrodotoxin (TTX; 1 microM) but not completely abolished. These NANC contractions were insensitive to P2X-purinoceptor desensitization by continuous tissue perfusion with alpha,beta-methylene ATP (30 microM). 7. These results demonstrate that bladder neck and proximal urethra are mainly innervated by the parasympathetic nervous system, whereas medial and distal urethras are to a greater extent under the control of the sympathetic innervation. The residual responses, insensitive to prazosin and atropine, may indicate a NANC innervation in the four tissues. However, the nature of the NANC neurotransmitter remains to be identified.
摘要
  1. 采用体外实验,利用灌流系统,通过电刺激(50V,30Hz,0.05ms脉宽,每5分钟刺激5秒的串刺激)研究雌性兔膀胱颈及尿道不同部位(近端、中段和远端)的神经介导收缩。2. 研究了这四个组织中刺激收缩的幅度(Emax)和持续时间(Dmax)。与膀胱颈(1.08±0.10g)、近端尿道(0.73±0.07g)和中段尿道(0.87±0.07g)相比,远端尿道的Emax值显著更高(2.07±0.15g)。相反,远端尿道的Dmax值(68.5±2.3秒)比膀胱颈(76.7±6.0秒)、近端尿道(84.5±5.0秒)和中段尿道(81.3±3.5秒)略低但有显著差异(P<0.05)。3. 可卡因(1μM)显著增加了中段和远端尿道的基础Emax值以及四个组织的基础Dmax值。4. 哌唑嗪(1μM)显著降低了近端、中段和远端尿道的Emax值以及膀胱颈和近端尿道的Dmax值。阿托品(1μM)也显著降低了膀胱颈和近端尿道的Emax值,并降低了膀胱颈的Dmax值,但对其他组织无此作用。育亨宾(0.1μM)对这四个组织无影响。5. 哌唑嗪(1μM)和阿托品(1μM)联合使用未改变电诱导收缩的Emax和Dmax值,但在近端尿道和膀胱颈,与单独使用哌唑嗪和阿托品相比,观察到了相加的抑制作用(仅对Emax)。6. 与哌唑嗪和阿托品联合治疗后的残余收缩反应被河豚毒素(TTX;1μM)显著减弱,但未完全消除。通过用α,β-亚甲基ATP(30μM)持续组织灌注使P2X嘌呤受体脱敏后,这些非肾上腺素能非胆碱能(NANC)收缩不受影响。7. 这些结果表明,膀胱颈和近端尿道主要由副交感神经系统支配,而中段和远端尿道在更大程度上受交感神经支配。对哌唑嗪和阿托品不敏感的残余反应可能表明这四个组织中存在NANC神经支配。然而,NANC神经递质的性质仍有待确定。

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