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α2 激动剂和拮抗剂对大鼠下尿路的影响。

The effect of alpha 2 agonists and antagonists on the lower urinary tract of the rat.

作者信息

Harada T, Constantinou C E

机构信息

Spinal Cord Injury Service, Department of Veterans Affairs, Stanford, California.

出版信息

J Urol. 1993 Jan;149(1):159-64. doi: 10.1016/s0022-5347(17)36030-5.

Abstract

The pharmacologic potential of selective alpha 2 adrenergic agents in modulating vesicourethral function was evaluated in urethane-anesthetized and conscious rats. The bladder was exposed through a midline incision and intubated via a cystostomy to measure pressure. The bladder was filled with saline at 0.05 ml./min. In six animals intravenous dexmedetomidine 0.6 micrograms./kg. followed by 2 micrograms./kg. was given. In another six rats the infusion was made with atipamezole at the same concentration. The parameters obtained were pressure/volume during cystometry, detrusor voiding pressures, and evidence of urine leakage. Conscious rats were placed in a restrainer outfitted with a voided volume sensor and a data recorder. The animals were divided in three groups. In controls, group I (n = 8), the animals were injected with a subcutaneous (SC) load of 5 ml. saline in which furosemide 10.0 mg./kg. was added. In group II (n = 6), dexmedetomidine was added in group III (n = 6), atipamezole was added. Parameters obtained were volume per micturition, latency, frequency of micturition, and patterns of micturition (such as dribbling), and total volume produced after a three hour recording. Values are expressed as mean +/- standard deviation. The results show that in an anesthetized preparation, the alpha 2 agonist dexmedetomidine produced inhibitory effects on the volume evoked micturition reflex (VEMR) at a dose level of 2.0 micrograms./kg. There was a significant decrease in peak pressure from 26.4 +/- 3.6 to 6.8 +/- 2.1 cm. H2O (p < 0.01). Urine leakage was observed at the external meatus. Atipamezole, the alpha 2 agonist, gradually increased bladder baseline pressure and inhibited VEMR. At a critical pressure there was continuous leakage from the external meatus. There was a significant elevation of baseline bladder pressure by atipamezole from 6.3 +/- 1.7 to 29.8 +/- 4.6 cm. H2O (p < 0.005). In conscious rats, the alpha 2 agonist produced urinary dribbling at approximately 20 minutes after SC injection, while the antagonists produced delayed dribbling 70 minutes after SC injection. Leakage occurred in 3 of 6 rats at a dose of 10 micrograms./kg. of atipamezole and in 5 of 6 rats at a dose of 30 micrograms./kg. The alpha 2 agonist caused a diuretic effect and a dose-dependent increase in the frequency of voiding (p < 0.05), while the antagonist decreased the frequency of voiding. Bladder capacity was decreased with the alpha 2 agonist while the antagonist increased capacity.

摘要

在氨基甲酸乙酯麻醉和清醒的大鼠中评估了选择性α2肾上腺素能药物调节膀胱尿道功能的药理学潜力。通过中线切口暴露膀胱,并通过膀胱造口术插管以测量压力。以0.05毫升/分钟的速度向膀胱内注入生理盐水。给6只动物静脉注射右美托咪定0.6微克/千克,随后注射2微克/千克。在另外6只大鼠中,以相同浓度输注阿替美唑。获得的参数包括膀胱测压期间的压力/容量、逼尿肌排尿压力以及尿液泄漏的证据。将清醒的大鼠置于配备有排尿量传感器和数据记录器的约束装置中。动物分为三组。在对照组I(n = 8)中,给动物皮下注射5毫升生理盐水,其中加入10.0毫克/千克速尿。在II组(n = 6)中加入右美托咪定,在III组(n = 6)中加入阿替美唑。获得的参数包括每次排尿量、潜伏期、排尿频率和排尿模式(如滴沥),以及3小时记录后产生的总尿量。数值以平均值±标准差表示。结果表明,在麻醉制剂中,α2激动剂右美托咪定在剂量为2.0微克/千克时对容量诱发排尿反射(VEMR)产生抑制作用。峰值压力从26.4±3.6显著降至6.8±2.1厘米水柱(p < 0.01)。在外尿道口观察到尿液泄漏。α2拮抗剂阿替美唑逐渐增加膀胱基线压力并抑制VEMR。在临界压力下,外尿道口持续漏尿。阿替美唑使膀胱基线压力从6.3±1.7显著升高至29.8±4.6厘米水柱(p < 0.005)。在清醒大鼠中,α2激动剂在皮下注射后约20分钟产生尿滴沥,而拮抗剂在皮下注射后70分钟产生延迟滴沥。在剂量为10微克/千克的阿替美唑时6只大鼠中有3只发生泄漏,在剂量为30微克/千克时6只大鼠中有5只发生泄漏。α2激动剂产生利尿作用并使排尿频率呈剂量依赖性增加(p < 0.05),而拮抗剂降低排尿频率。α2激动剂使膀胱容量减小,而拮抗剂增加容量。

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