Rodrigues Stephen F, de Oliveira Maria Aparecida, Martins Joilson O, Sannomiya Paulina, de Cássia Tostes Rita, Nigro Dorothy, Carvalho Maria Helena C, Fortes Zuleica Bruno
Laboratory of Hypertension, Department of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, 05508-900, Av. Prof. Lineu Prestes, 1524 São Paulo, SP, Brazil.
Life Sci. 2006 Sep 20;79(17):1630-7. doi: 10.1016/j.lfs.2006.05.019. Epub 2006 May 26.
The proper use of anesthetics in animal experimentation has been intensively studied. In this study we compared the use of chloral hydrate (500 mg kg(-1)) and ketamine (167 mg kg(-1)) combined with xylazine (33 mg kg(-1)) by the s.c. route in male Wistar rats. Chloral hydrate and ketamine/xylazine produced a depth of anesthesia and analgesia sufficient for surgical procedures. The decrease of systolic and diastolic blood pressure was of a higher magnitude in rats anesthetized with chloral hydrate than with ketamine/xylazine. The initial microvascular diameter and blood flow velocity did not differ between both agents. On the other hand, ketamine/xylazine reduced the heart rate more intensively than chloral hydrate. Both anesthetics promoted an increase in arterial pCO(2) and a decrease in pH levels compared to unanesthetized animals. The blood glucose levels were of a higher magnitude in rats after ketamine/xylazine anesthesia than after chloral hydrate. In mesenteric arterioles studied in vivo, ketamine/xylazine anesthesia reduced the constrictive effect of noradrenaline and the dilator effect of bradykinin. However, both anesthetics did not modify the vasodilator effect promoted by acetylcholine. Based on our data, we concluded that both anesthetics alter metabolic and hemodynamic parameters, however the use of chloral hydrate in studies of microvascular reactivity in vivo is more appropriate since ketamine/xylazine reduces the responses to vasoactive agents and increases blood glucose levels.
在动物实验中麻醉剂的合理使用已得到深入研究。在本研究中,我们比较了水合氯醛(500 mg kg⁻¹)以及氯胺酮(167 mg kg⁻¹)与赛拉嗪(33 mg kg⁻¹)联合经皮下途径用于雄性Wistar大鼠的情况。水合氯醛和氯胺酮/赛拉嗪产生的麻醉深度和镇痛效果足以进行外科手术。与氯胺酮/赛拉嗪麻醉的大鼠相比,水合氯醛麻醉的大鼠收缩压和舒张压下降幅度更大。两种药物初始时的微血管直径和血流速度并无差异。另一方面,氯胺酮/赛拉嗪比水合氯醛更显著地降低心率。与未麻醉的动物相比,两种麻醉剂均使动脉血二氧化碳分压升高,pH值降低。氯胺酮/赛拉嗪麻醉后大鼠的血糖水平高于水合氯醛麻醉后。在体内研究的肠系膜小动脉中,氯胺酮/赛拉嗪麻醉减弱了去甲肾上腺素的收缩作用和缓激肽的舒张作用。然而,两种麻醉剂均未改变乙酰胆碱促进的血管舒张作用。基于我们的数据,我们得出结论,两种麻醉剂都会改变代谢和血流动力学参数,然而在体内微血管反应性研究中使用水合氯醛更为合适,因为氯胺酮/赛拉嗪会降低对血管活性药物的反应并升高血糖水平。