Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, 333 Cassell Drive, Baltimore, MD 21224, USA.
Behavioral Neuroscience Branch, National Institute on Drug Abuse - Intramural Research Program, National Institutes of Health, DHHS, 333 Cassell Drive, Baltimore, MD 21224, USA.
Neuropharmacology. 2017 Nov;126:271-280. doi: 10.1016/j.neuropharm.2017.07.025. Epub 2017 Jul 27.
Here we examined how intravenous heroin at a dose that maintains self-administration (0.1 mg/kg) affects brain temperature homeostasis in freely moving rats under conditions that seek to mimic some aspects of human drug use. When administered under standard laboratory conditions (quiet rest at 22 °C ambient temperature), heroin induced moderate temperature increases (1.0-1.5 °C) in the nucleus accumbens (NAc), a critical structure of the brain motivation-reinforcement circuit. By simultaneously recording temperatures in the temporal muscle and skin, we demonstrate that the hyperthermic effects of heroin results primarily from inhibition of heat loss due to strong and prolonged skin vasoconstriction. Heroin-induced brain temperature increases were enhanced during behavioral activation (i.e., social interaction) and in a moderately warm environment (29 °C). By calculating the "net" effects of the drug in these two conditions, we found that this enhancement results from the summation of the hyperthermic effects of heroin with similar effects induced by either social interaction or a warmer environment. When the dose of heroin was increased (to 0.2, 0.4, 0.8, 1.6, 3.2, and 6.4 mg/kg), brain temperature showed a biphasic down-up response. The initial temperature decrease was dose-dependent and resulted from a transient inhibition of intra-brain heat production coupled with increased heat loss via skin surfaces-the effects typically induced by general anesthetics. These initial inhibitory effects induced by large-dose heroin injections could be related to profound CNS depression-the most serious health complications typical of heroin overdose in humans.
在这里,我们研究了在模拟人类用药某些方面的条件下,静脉给予维持自我给药剂量的海洛因(0.1mg/kg)如何影响自由活动大鼠的大脑体温稳态。在标准实验室条件下(在 22°C 的环境温度下安静休息)给予海洛因时,会导致伏隔核(NAc)中的体温适度升高(1.0-1.5°C),NAc 是大脑动机-强化回路的关键结构。通过同时记录颞肌和皮肤的温度,我们证明海洛因的致热作用主要是由于强烈和持久的皮肤血管收缩导致散热抑制所致。在行为激活(即社交互动)和较温暖的环境(29°C)中,海洛因引起的大脑温度升高会增强。通过计算这两种情况下药物的“净”效应,我们发现这种增强是由于海洛因的致热作用与社交互动或更温暖的环境引起的类似作用的叠加所致。当海洛因剂量增加(至 0.2、0.4、0.8、1.6、3.2 和 6.4mg/kg)时,大脑温度表现出双相下降-上升反应。初始温度下降与剂量相关,是由于大脑内热产生的短暂抑制以及通过皮肤表面增加散热所致——这些作用通常是由全身麻醉剂引起的。大剂量海洛因注射引起的这些初始抑制作用可能与中枢神经系统深度抑制有关——这是人类海洛因过量最严重的健康并发症。