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右美托咪定、ST-91和可乐定的慢性脊髓输注:脊髓α2肾上腺素能受体亚型及内在活性。

Chronic spinal infusion of dexmedetomidine, ST-91 and clonidine: spinal alpha 2 adrenoceptor subtypes and intrinsic activity.

作者信息

Takano Y, Yaksh T L

机构信息

Department of Anesthesiology, University of California, San Diego, La Jolla.

出版信息

J Pharmacol Exp Ther. 1993 Jan;264(1):327-35.

PMID:8093729
Abstract

The antinociceptive effect (hot plate test) and behavioral changes produced by the continuous 7-day i.t. infusion of alpha 2 adrenoceptor agonists dexmedetomidine (10 and 3 nmol/hr), clonidine (100 and 30 nmol/hr) and 2-(2,6-diethylphenylamino)-2-imidazoline (ST-91) (30 and 10 nmol/hr) were examined in rats. The highest doses of each agonist produced an equivalent increase in hot plate latency on day 1 of infusion. These effects diminished to near base line by 5 to 7 days. In separate groups, i.t. dose-response curves were obtained with dexmedetomidine, clonidine and ST-91 in groups of rats which had received a 7-day infusion of saline or the equianalgesic concentrations of dexmedetomidine (10 nmol/hr) or ST-91 (30 nmol/hr). Dose-response curves in drug-infused animals showed a right shift as compared to the vehicle-infused rats. Calculation of the ratio of the ED50 values (tolerance ratio: drug vs. control) in animals receiving the continuous infusion of dexmedetomidine vs. saline indicated: 8- (6-12), 36- (19-54) and 1.0- (0.6-1.5) (ratio with 95% Cl) fold rightward shifts of dexmedetomidine, clonidine and ST-91 dose-response curves, respectively. Chronic infusion of ST-91 resulted in 62- (36-127), 22- (13-46) and 0.9- (0.7-1.1) fold rightward shift of the ST-91, clonidine and dexmedetomidine dose-response curves, respectively. Previously, we have shown that dexmedetomidine and clonidine act upon spinal alpha 2 adrenoceptor, which appeared distinguishable from that acted upon by ST-91.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在大鼠中检测了连续7天鞘内输注α2肾上腺素能受体激动剂右美托咪定(10和3 nmol/小时)、可乐定(100和30 nmol/小时)和2-(2,6-二乙基苯基氨基)-2-咪唑啉(ST-91)(30和10 nmol/小时)产生的抗伤害感受作用(热板试验)和行为变化。每种激动剂的最高剂量在输注第1天使热板潜伏期产生同等程度的增加。这些作用在5至7天时减弱至接近基线水平。在单独的几组中,在接受7天生理盐水输注或等效镇痛浓度右美托咪定(10 nmol/小时)或ST-91(30 nmol/小时)输注的大鼠组中获得了右美托咪定、可乐定和ST-91的鞘内剂量-反应曲线。与输注赋形剂的大鼠相比,药物输注动物的剂量-反应曲线右移。计算接受连续输注右美托咪定与生理盐水的动物的ED50值之比(耐受比:药物与对照)表明:右美托咪定、可乐定和ST-91剂量-反应曲线分别向右移位8-(6-至12)、36-(19-至54)和1.0-(0.6-至1.5)倍(含95%可信区间的比值)。长期输注ST-91导致ST-91、可乐定和右美托咪定剂量-反应曲线分别向右移位62-(36-至127)、22-(13-至46)和0.9-(0.7-至1.1)倍。此前,我们已表明右美托咪定和可乐定作用于脊髓α2肾上腺素能受体,这似乎与ST-91作用的受体不同。(摘要截短于250字)

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