Fentanyl overdose: Temporal effects and prognostic factors in SKH1 mice

Basic Clin Pharmacol Toxicol. 2024 Apr;134(4):460-471. doi: 10.1111/bcpt.13984. Epub 2024 Jan 29.

Abstract

Fentanyl exposure and overdose are growing concerns in public health and occupational safety. This study aimed to establish parameters of fentanyl lethality in SKH1 mice for future overdose research. Lethality was determined using the up-down procedure, with subjects monitored post-administration using pulse oximetry (5 min) and then whole-body plethysmography (40 min). Following the determination of subcutaneous dose-response, [18F]Fluorodeoxyglucose positron emission tomography (18 F-FDG PET) was performed after LD10 fentanyl at 40 min, 6 h, 24 h or 7 days post-dose. LD10 and LD50 were observed to be 110 and 135 mg/kg, respectively, and consistent with four-parameter logistic fit values of 111.2 and 134.6 mg/kg (r2 = 0.9996). Overdose (LD10 or greater) yielded three distinct cardiovascular groups: survival, non-survival with blood oxygen saturation (SpO2) minimum ≥37% and non-survival with SpO2 <37%. Breaths per minute, minute volume and inspiratory quotient were significantly different between surviving and non-surviving animals for up to 40 min post-injection. 18 F-FDG PET revealed decreased glucose uptake in the heart, lungs and brain for up to 24 h. These findings provide critical insights into fentanyl lethality in SKH1 mice, including non-invasive respiratory effects and organ-specific impacts that are invaluable for future translational studies investigating the temporal effects of fentanyl overdose.

Keywords: SKH1 mouse; fentanyl; opioid; overdose; wooden chest syndrome.

MeSH terms

  • Analgesics, Opioid / therapeutic use
  • Animals
  • Drug Overdose* / drug therapy
  • Fentanyl / toxicity
  • Fluorodeoxyglucose F18* / therapeutic use
  • Humans
  • Mice
  • Positron-Emission Tomography
  • Prognosis

Substances

  • Fluorodeoxyglucose F18
  • Fentanyl
  • Analgesics, Opioid