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曲马多对猫的呼吸抑制作用:阿片受体的参与

Respiratory depression by tramadol in the cat: involvement of opioid receptors.

作者信息

Teppema Luc J, Nieuwenhuijs Diederik, Olievier Cees N, Dahan Albert

机构信息

Department of Physiology, Leiden University Medical Center, The Netherlands.

出版信息

Anesthesiology. 2003 Feb;98(2):420-7. doi: 10.1097/00000542-200302000-00023.

Abstract

BACKGROUND

Tramadol hydrochloride (tramadol) is a synthetic opioid analgesic with a relatively weak affinity at opioid receptors. At analgesic doses, tramadol seems to cause little or no respiratory depression in humans, although there are some conflicting data. The aim of this study was to examine whether tramadol causes dose-dependent inhibitory effects on the ventilatory carbon dioxide response curve and whether these are reversible or can be prevented by naloxone.

METHODS

Experiments were performed in cats under alpha-chloralose-urethane anesthesia. The effects of tramadol and naloxone were studied by applying square-wave changes in end-tidal pressure of carbon dioxide (Petco2; 7.5-11 mmHg) and by analyzing the dynamic ventilatory responses using a two-compartment model with a fast peripheral and a slow central component, characterized by a time constant, carbon dioxide sensitivity, time delay, and a single offset (apneic threshold).

RESULTS

In five animals 1, 2, and 4 mg/kg tramadol (intravenous) increased the apneic threshold (control: 28.3 +/- 4.8 mmHg [mean +/- SD]; after 4 mg/kg: 36.7 +/- 7.1 mmHg; P < 0.05) and decreased the total carbon dioxide sensitivity (control: 109.3 +/- 41.3 ml x min(-1) x mmHg(-1) ) by 31, 59, and 68%, respectively, caused by proportional equal reductions in sensitivities of the peripheral and central chemoreflex loops. Naloxone (0.1 mg/kg, intravenous) completely reversed these effects. In five other cats, 4 mg/kg tramadol caused an approximately 70% ventilatory depression at a fixed Pet co2 of 45 mmHg that was already achieved after 15 min. A third group of five animals received the same dose of tramadol after pretreatment with naloxone. At a fixed Petco of 45 mmHg, naloxone prevented more than 50% of the expected ventilatory depression in these animals.

CONCLUSIONS

Because naloxone completely reversed the inhibiting effects of tramadol on ventilatory control and it prevented more than 50% of the respiratory depression after a single dose of tramadol, the authors conclude that this analgesic causes respiratory depression that is mainly mediated by opioid receptors.

摘要

背景

盐酸曲马多是一种合成阿片类镇痛药,对阿片受体的亲和力相对较弱。在镇痛剂量下,尽管存在一些相互矛盾的数据,但曲马多似乎在人体中很少或不会引起呼吸抑制。本研究的目的是检查曲马多是否对通气二氧化碳反应曲线产生剂量依赖性抑制作用,以及这些作用是否可逆或可被纳洛酮预防。

方法

实验在α-氯醛糖-乌拉坦麻醉的猫身上进行。通过在呼气末二氧化碳压力(Petco2;7.5-11 mmHg)上施加方波变化,并使用具有快速外周和缓慢中枢成分的双室模型分析动态通气反应,研究曲马多和纳洛酮的作用,该模型的特征包括时间常数、二氧化碳敏感性、时间延迟和单个偏移(呼吸暂停阈值)。

结果

在5只动物中,静脉注射1、2和4 mg/kg曲马多增加了呼吸暂停阈值(对照组:[平均±标准差]28.3±4.8 mmHg;4 mg/kg后:36.7±7.1 mmHg;P<0.05),并使总二氧化碳敏感性(对照组:109.3±41.3 ml·min⁻¹·mmHg⁻¹)分别降低了31%、59%和68%,这是由外周和中枢化学反射环敏感性成比例同等降低所致。静脉注射0.1 mg/kg纳洛酮完全逆转了这些作用。在另外5只猫中,4 mg/kg曲马多在固定的45 mmHg Petco2下导致约70%的通气抑制,15分钟后即已出现。第三组5只动物在预先用纳洛酮处理后接受相同剂量的曲马多。在固定的45 mmHg Petco下,纳洛酮在这些动物中预防了超过50%的预期通气抑制。

结论

由于纳洛酮完全逆转了曲马多对通气控制的抑制作用,并且在单次给予曲马多后预防了超过50%的呼吸抑制,作者得出结论,这种镇痛药引起的呼吸抑制主要由阿片受体介导。

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