Kiyatkin Eugene A
Behavioral Neuroscience Branch, National Institute on Drug Abuse, Intramural Research Program, National Institutes of Health, DHHS, Baltimore, Maryland, United States.
Am J Physiol Lung Cell Mol Physiol. 2024 Dec 1;327(6):L930-L948. doi: 10.1152/ajplung.00251.2024. Epub 2024 Oct 15.
Respiratory depression that diminishes oxygen delivery to the brain is the most dangerous effect of opioid drugs. Although plethysmography is a valuable tool to examine drug-induced changes in respiration, the primary cause of brain abnormalities induced by opioids is the global decrease in brain oxygen levels. The primary goal of this review is to provide an overview and discussion on fluctuations in brain oxygen levels induced by opioids, with a focus on heroin and fentanyl. To evaluate fluctuations in brain oxygen levels, we used oxygen sensors coupled with high-speed amperometry in awake, freely moving rats. First, we provide an overview of brain oxygen responses induced by natural physiological stimuli and discuss the mechanisms regulating oxygen entry into brain tissue. Then, we present data on brain oxygen responses induced by heroin and fentanyl and review their underlying mechanisms. These data allowed us to compare the effects of these drugs on brain oxygen regarding their latency, potency, time-dependency, and potential lethality at high doses as well as their relationships with peripheral oxygen responses. We also discuss data on the effects of naloxone on brain oxygen responses induced by heroin and fentanyl in the paradigms of both the pretreatment and treatment, when naloxone is administered at different times after the primary opioid drug. Although most data discussed were obtained in rats, they may have clinical relevance for understanding the mechanisms underlying the physiological effects of opioids and developing rational treatment strategies to decrease acute lethality and long-term health complications of opioid misuse.
呼吸抑制会减少大脑的氧气供应,这是阿片类药物最危险的作用。尽管体积描记法是检测药物引起的呼吸变化的一种有价值的工具,但阿片类药物引起的大脑异常的主要原因是大脑氧气水平的整体下降。本综述的主要目的是概述和讨论阿片类药物引起的大脑氧气水平波动,重点是海洛因和芬太尼。为了评估大脑氧气水平的波动,我们在清醒、自由活动的大鼠中使用了与高速安培法相结合的氧气传感器。首先,我们概述了自然生理刺激引起的大脑氧气反应,并讨论了调节氧气进入脑组织的机制。然后,我们展示了海洛因和芬太尼引起的大脑氧气反应的数据,并回顾了其潜在机制。这些数据使我们能够比较这些药物对大脑氧气的影响,包括它们的潜伏期、效力、时间依赖性以及高剂量时的潜在致死性,以及它们与外周氧气反应的关系。我们还讨论了在预处理和治疗范式中,纳洛酮在主要阿片类药物给药后的不同时间给药时,对海洛因和芬太尼引起的大脑氧气反应的影响的数据。尽管所讨论的大多数数据是在大鼠中获得的,但它们可能与理解阿片类药物生理作用的潜在机制以及制定合理的治疗策略以降低阿片类药物滥用的急性致死率和长期健康并发症具有临床相关性。