Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, Baltimore, MD 21224, USA.
Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, Baltimore, MD 21224, USA.
Brain Res. 2023 Apr 1;1804:148251. doi: 10.1016/j.brainres.2023.148251. Epub 2023 Jan 20.
Among the numerous general anesthetics utilized in rodent surgical procedures, the co-administration of ketamine and xylazine is the current standard for induction and maintenance of surgical planes of anesthesia and pain control. In contrast to classical GABAergic anesthetics, which act to inhibit CNS activity, inducing muscle relaxation, sedation, hypothermia, and brain hypoxia, ketamine and xylazine act through different mechanisms to induce similar effects while also providing potent analgesia. By using three-point thermorecording in freely moving rats, we show that the ketamine-xylazine mixture induces modest brain hyperthermia, resulting from increased intra-cerebral heat production due to metabolic brain activation and increased heat loss due to skin vasodilation. The first effect derives from ketamine, which alone increases brain and body temperatures due to brain metabolic activation and skin vasoconstriction. The second effect derives from xylazine, which increases heat loss due to potent skin vasodilation. By using oxygen sensors coupled with amperometry, we show that the ketamine-xylazine mixture modestly decreases brain oxygen levels that results from relatively weak respiratory depression. This tonic pharmacological effect was preceded by a strong but transient oxygen increase that may result from a stressful injection or unknown, possibly peripheral action of this drug combination. This pattern of physiological effects elicited by the ketamine-xylazine mixture differs from the effects of other general anesthetic drugs, particularly barbiturates.
在用于啮齿动物手术的众多全身麻醉剂中,氯胺酮和甲苯噻嗪的联合使用是目前诱导和维持麻醉和疼痛控制手术平面的标准。与经典的 GABA 能麻醉剂不同,后者通过抑制中枢神经系统(CNS)活动来发挥作用,导致肌肉松弛、镇静、体温过低和脑缺氧,而氯胺酮和甲苯噻嗪通过不同的机制发挥作用,产生类似的效果,同时提供强大的镇痛作用。通过在自由活动的大鼠中使用三点温度记录,我们表明氯胺酮-甲苯噻嗪混合物会引起适度的大脑发热,这是由于代谢性脑激活导致的颅内产热增加和皮肤血管扩张导致的热量损失增加所致。第一种作用源自氯胺酮,它单独通过大脑代谢激活和皮肤血管收缩导致大脑和体温升高。第二种作用源自甲苯噻嗪,它通过强烈的皮肤血管扩张导致热量损失增加。通过使用氧传感器结合安培法,我们表明氯胺酮-甲苯噻嗪混合物会适度降低大脑氧水平,这是由于相对较弱的呼吸抑制所致。这种紧张的药理学作用之前是一个强烈但短暂的氧增加,可能是由于这种药物组合的注射压力或未知的、可能是外周作用。这种由氯胺酮-甲苯噻嗪混合物引起的生理效应模式与其他全身麻醉药物(特别是巴比妥类药物)的效应不同。