Tramadol and Codeine Stacking/Boosting Dose Exposure Induced Neurotoxic Behaviors, Oxidative Stress, Mitochondrial Dysfunction, and Neurotoxic Genes in Adolescent Mice
- PMID: 35829998
- DOI: 10.1007/s12640-022-00539-x
Tramadol and Codeine Stacking/Boosting Dose Exposure Induced Neurotoxic Behaviors, Oxidative Stress, Mitochondrial Dysfunction, and Neurotoxic Genes in Adolescent Mice
Abstract
In spite of the increasing epidemic of pharmaceutical opioids (codeine and tramadol) misuse and abuse among the adolescents, little is known about the neurotoxic consequences of the widespread practice of tramadol and codeine abuse involving increasing multiple doses across days, referred to as stacking and boosting. Hence, in this study, we replicated stacking and boosting doses of tramadol, codeine alone, or in combination on spontaneous motor activity and cognitive function in adolescent mice and adduced a plausible mechanism of possible neurotoxicity. Ninety-six adolescent mice were randomly distributed into 4 groups (n = 24 per group) and treated thrice daily for 9 days with vehicle, tramadol (20, 40, or 80 mg/kg), codeine (40, 80, or 160 mg/kg), or their combinations. Exposure of mice to tramadol induced hyperactivity and stereotypic behavior while codeine exposure caused hypoactivity and nootropic effect but tramadol-codeine cocktail led to marked reduction in spontaneous motor activity and cognitive function. In addition, tramadol, codeine, and their cocktail caused marked induction of nitroso-oxidative stress and inhibition of mitochondrial complex I activity in the prefrontal cortex (PFC) and midbrain (MB). Real-time PCR expression profiling of genes encoding neurotoxicity (RT) showed that tramadol exposure upregulate 57 and downregulate 16 neurotoxic genes, codeine upregulate 45 and downregulate 25 neurotoxic genes while tramadol-codeine cocktail upregulate 52 and downregulate 20 neurotoxic genes in the PFC. Findings from this study demonstrate that the exposure of adolescents mice to multiple and increasing doses of tramadol, codeine, or their cocktail lead to spontaneous motor coordination deficits indicative of neurotoxicity through induction of oxidative stress, inhibition of mitochondrial complex I activity and upregulation of neurotoxicity encoding genes in mice.
Keywords: Codeine-tramadol cocktail; Mitochondrial dysfunction; Neurodegeneration; Neurotoxic genes; Oxidative stress; Stereotypic behavior.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Similar articles
-
Combined molecular, structural and memory data unravel the destructive effect of tramadol on hippocampus.Neurosci Lett. 2022 Feb 6;771:136418. doi: 10.1016/j.neulet.2021.136418. Epub 2021 Dec 23. Neurosci Lett. 2022. PMID: 34954113
-
Tramadol/acetaminophen combination tablets and codeine/acetaminophen combination capsules for the management of chronic pain: a comparative trial.Clin Ther. 2001 Sep;23(9):1429-45. doi: 10.1016/s0149-2918(01)80118-1. Clin Ther. 2001. PMID: 11589258 Clinical Trial.
-
Pharmaceutical opioid poisonings in Victoria, Australia: Rates and characteristics of a decade of emergency department presentations among nine pharmaceutical opioids.Addiction. 2022 Mar;117(3):623-636. doi: 10.1111/add.15653. Epub 2021 Sep 18. Addiction. 2022. PMID: 34338377 Free PMC article.
-
"Weak" opioid analgesics. Codeine, dihydrocodeine and tramadol: no less risky than morphine.Prescrire Int. 2016 Feb;25(168):45-50. Prescrire Int. 2016. PMID: 27042732 Review.
-
Pain management in dental practice: tramadol vs. codeine combinations.J Am Dent Assoc. 1999 Jul;130(7):1075-9. doi: 10.14219/jada.archive.1999.0338. J Am Dent Assoc. 1999. PMID: 10422401 Review.
Cited by
-
Does Tramadol Exposure Have Unfavorable Effects on Hippocampus? A Review Study.Addict Health. 2024 Jul;16(3):213-223. doi: 10.34172/ahj.1481. Epub 2024 Jul 29. Addict Health. 2024. PMID: 39439859 Free PMC article. Review.
-
Minocycline Acts as a Neuroprotective Agent Against Tramadol-Induced Neurodegeneration: Behavioral and Molecular Evidence.Int J Prev Med. 2024 Sep 28;15:47. doi: 10.4103/ijpvm.ijpvm_10_24. eCollection 2024. Int J Prev Med. 2024. PMID: 39539580 Free PMC article.
-
Street adolescents in low income setting exposed to hepatitis B and C, and disadvantaged by lifestyle: a Togolese cross-sectional study.BMC Public Health. 2024 Jul 16;24(1):1901. doi: 10.1186/s12889-024-19415-8. BMC Public Health. 2024. PMID: 39014371 Free PMC article.
-
Potent Ameliorative Effects of Rosmarinic Acid on Tramadol-Induced Neurotoxicity in the Brain and Hippocampus; by Suppressing Oxidative stress, Apoptosis, ER stress, and Regulating Cognitive Functions.Mol Neurobiol. 2025 Aug;62(8):10245-10263. doi: 10.1007/s12035-025-04892-8. Epub 2025 Apr 7. Mol Neurobiol. 2025. PMID: 40193018 Free PMC article.
References
-
- Achukwu PU, Omorodion NT, Tosan E, Aloh HE, Eze C, Okoyeocha OME (2019) Codeine and its histopathological effect on brain of albino rats: an experimental study. Acta Scientific Nutr Health 3(2):125–133
-
- Arora S, Herbert ME (2001) Myth: codeine is a powerful and effective analgesic. West J Med 174(6):428. https://doi.org/10.1136/ewjm.174.6.428 - DOI - PubMed - PMC
-
- Awadalla EA, Salah-Eldin A (2015) Histopathological and molecular studies on tramadol mediated hepato-renal toxicity in rats. IOSR J Pharm Biol Sci 10(6):90–102
-
- Azmy SM, Abd El Fattah MA, Abd El-Rahman SS et al (2018) Does nicotine impact tramadol abuse? Insights from neurochemical and neurobehavioral changes in mice. Neurotoxicology 67:245–258
-
- Baldacchino A, Tolomeo S, Balfour DJ, Matthews K (2019) Profiles of visuospatial memory dysfunction in opioid-exposed and dependent populations. Psychol Med 49(7):1174–1184. https://doi.org/10.1017/S0033291718003318 - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous