Hypoxic effects of heroin and fentanyl and their basic physiological mechanisms.

Am J Physiol Lung Cell Mol Physiol

Behavioral Neuroscience Branch, National Institute on Drug Abuse, Intramural Research Program, National Institutes of Health, DHHS, Baltimore, Maryland, United States.

Published: December 2024

AI Article Synopsis

  • Opioids, particularly heroin and fentanyl, can cause respiratory depression, significantly reducing oxygen flow to the brain and leading to harmful effects.
  • This review uses oxygen sensors in rats to study how these drugs affect brain oxygen levels, comparing their impacts on latency, potency, and potential lethality.
  • The research also explores how naloxone, an opioid antagonist, influences brain oxygen responses both before and after opioid administration, providing insights that could inform treatment strategies for opioid overdose and long-term health issues.

Article Abstract

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.

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Source
http://dx.doi.org/10.1152/ajplung.00251.2024DOI Listing

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