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有意识的膀胱出口梗阻及未梗阻大鼠的排尿:脊髓α1肾上腺素能受体的作用

Micturition in conscious rats with and without bladder outlet obstruction: role of spinal alpha 1-adrenoceptors.

作者信息

Ishizuka O, Persson K, Mattiasson A, Naylor A, Wyllie M, Andersson K

机构信息

Department of Urology, Lund University Hospital, Sweden.

出版信息

Br J Pharmacol. 1996 Mar;117(5):962-6. doi: 10.1111/j.1476-5381.1996.tb15288.x.

Abstract
  1. In normal rats and rats with bladder hypertrophy secondary to outflow obstruction, undergoing continuous cytometry, we examined the responses to the selective alpha 1-adrenoceptor antagonist doxazosin given intrathecally (i.t.) and intra-arterially (i.a.). In addition, we investigated the effects of the drug on L-dopa-induced bladder hyperactivity in normal, unobstructed rats. 2. Doxazosin 50 nmol (approximately 60 micrograms kg-1), given i.t., decreased micturition pressure in normal rats and in animals with post-obstruction bladder hypertrophy. The effect was much more pronounced in the animals with hypertrophied/overactive bladders. Doxazosin did not markedly affect the frequency or amplitude of the unstable contractions observed in obstructed rats. In contrast, however, doxazosin reduced L-dopa-induced bladder overactivity. When tested, the enantiomers of doxazosin produced qualitatively similar effects to doxazosin, but there was no evidence of stereoselectivity. 3. The results suggest that in addition to the well documented action on prostatic and lower urinary tract smooth muscle, and an effect on the sympathetic outflow to the bladder, bladder neck, prostate, and external urethral sphincter, doxazosin may have an action at the level of the spinal cord and ganglia, thereby reducing activity in the parasympathetic nerves to the bladder. This effect is more pronounced in rats with bladder hypertrophy than in normal rats.
摘要
  1. 在正常大鼠以及继发于流出道梗阻的膀胱肥大大鼠中,我们通过连续细胞计数法,研究了鞘内注射(i.t.)和动脉内注射(i.a.)选择性α1 - 肾上腺素能受体拮抗剂多沙唑嗪后的反应。此外,我们还研究了该药物对正常、未梗阻大鼠中左旋多巴诱导的膀胱活动亢进的影响。2. 鞘内注射50 nmol(约60微克/千克)多沙唑嗪可降低正常大鼠以及梗阻后膀胱肥大动物的排尿压力。在膀胱肥大/活动亢进的动物中,这种作用更为明显。多沙唑嗪对梗阻大鼠中观察到的不稳定收缩的频率或幅度没有明显影响。然而,相比之下,多沙唑嗪可减轻左旋多巴诱导的膀胱活动亢进。对多沙唑嗪的对映体进行测试时,其产生的效果在性质上与多沙唑嗪相似,但没有立体选择性的证据。3. 结果表明,除了对前列腺和下尿路平滑肌有充分记录的作用,以及对膀胱、膀胱颈、前列腺和尿道外括约肌的交感神经流出有影响外,多沙唑嗪可能在脊髓和神经节水平发挥作用,从而降低膀胱副交感神经的活性。这种作用在膀胱肥大的大鼠中比在正常大鼠中更为明显。

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