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锯叶棕提取物对大鼠排尿反射及其自主受体结合活性的影响。

Effects of saw palmetto extract on micturition reflex of rats and its autonomic receptor binding activity.

作者信息

Oki Tomomi, Suzuki Mayumi, Nishioka Yasuhiko, Yasuda Akio, Umegaki Keizo, Yamada Shizuo

机构信息

Department of Biopharmacy and Center of Excellence Program in the 21st Century, School of Pharmaceutical Sciences, University of Shizuoka, Japan.

出版信息

J Urol. 2005 Apr;173(4):1395-9. doi: 10.1097/01.ju.0000146273.26591.f5.

Abstract

PURPOSE

We examined the effects of saw palmetto extract (SPE) on the rat micturition reflex and on autonomic receptors in the lower urinary tract.

MATERIALS AND METHODS

The effect of SPE was examined on cystometrograms of anesthetized rats induced by intravesical infusion of saline or 0.1% acetic acid. SHR/NDmc-cp (cp/cp) rats received repeat oral administration of SPE and nighttime urodynamic function was determined. The autonomic receptor binding activity of SPE in the rat bladder and prostate was examined by radioligand binding assay.

RESULTS

Intraduodenal administration of SPE (60 mg/kg) in anesthetized rat cystometry caused a significant increase in the micturition interval, micturition volume and bladder capacity during intravesical saline infusion. Also, similar administration of SPE at doses of 12 and 20 mg/kg significantly reversed the shortened micturition interval as well as the decreased micturition volume and bladder capacity due to 0.1% acetic acid infusion in a dose dependent manner. In conscious SHR/NDmc-cp (cp/cp) rats repeat oral administration of SPE (6 mg/kg daily) constantly increased the micturition interval and concomitantly decreased voiding frequency. SPE inhibited specific binding of [H]NMS ([N-methyl-H]scopolamine methyl chloride) (bladder) and [H]prazosin (prostate) with IC50 values of 46.1 and 183 microg/ml, respectively.

CONCLUSIONS

SPE significantly alleviates urodynamic symptoms in hyperactive rat bladders by increasing bladder capacity and subsequently prolonging the micturition interval. Our data may support the clinical efficacy of SPE for the treatment of lower urinary tract symptoms.

摘要

目的

我们研究了锯棕榈提取物(SPE)对大鼠排尿反射及下尿路自主受体的影响。

材料与方法

通过膀胱内注入生理盐水或0.1%乙酸诱导麻醉大鼠的膀胱测压图,研究SPE的作用。给SHR/NDmc-cp(cp/cp)大鼠重复口服SPE,并测定夜间尿动力学功能。通过放射性配体结合试验检测SPE在大鼠膀胱和前列腺中的自主受体结合活性。

结果

在麻醉大鼠膀胱测压中十二指肠内给予SPE(60mg/kg),在膀胱内注入生理盐水期间,排尿间隔、排尿量和膀胱容量显著增加。此外,以12mg/kg和20mg/kg剂量给予类似的SPE给药,以剂量依赖方式显著逆转了由于注入0.1%乙酸导致的排尿间隔缩短以及排尿量和膀胱容量减少。在清醒的SHR/NDmc-cp(cp/cp)大鼠中,重复口服SPE(每日6mg/kg)持续增加排尿间隔并同时降低排尿频率。SPE抑制[H]NMS([N-甲基-H]东莨菪碱甲基氯)(膀胱)和[H]哌唑嗪(前列腺)的特异性结合,IC50值分别为46.1和183μg/ml。

结论

SPE通过增加膀胱容量并随后延长排尿间隔,显著减轻大鼠膀胱活动亢进的尿动力学症状。我们的数据可能支持SPE治疗下尿路症状的临床疗效。

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