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Title:Molecular mechanisms of acute drug toxicity in polypharmacy : analgesic–psychotropic interactions
Authors:ID Rijavec, Nikolina (Author)
ID Rijavec, Boris (Author)
Files:.pdf PDF - Presentation file, download (1,24 MB)
MD5: 35B2809A44545F06CDBE2617DDEFE52C
 
URL URL - Source URL, visit https://www.mdpi.com/1422-0067/27/16/7168
 
Language:English
Typology:1.02 - Review Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Concurrent exposure to analgesic and psychotropic drugs is frequent in patients with pain, psychiatric comorbidity, frailty, or acute-care needs. The clinically important question is whether analgesics and psychotropic drugs act on the same metabolic, transporter, receptor, ion-channel, or cellular stress systems. This narrative mechanistic review discusses those points of contact. CYP-mediated inhibition or induction, phenoconversion, altered parent-to-metabolite ratios, and blood–brain barrier transporter effects can change both systemic and central exposure, particularly through CYP2D6, CYP3A4, CYP2C9, CYP2B6, and P-glycoprotein. Pharmacodynamic toxicity may involve serotonergic excess, opioid and GABAergic effects in respiratory-control networks, hERG/IKr-related loss of repolarization reserve, or dopamine D2 receptor blockade. Non-opioid analgesics and psychotropic background therapy add further pathways involving renal and gastrointestinal vulnerability, hematological toxicity, mitochondrial injury, and altered central nervous system function. At the cellular level, mitochondrial dysfunction, oxidative stress, calcium dysregulation, and endoplasmic reticulum stress are discussed primarily as mechanistic or preclinical contributors unless direct clinical evidence is available. Overall, analgesic–psychotropic co-exposure is presented as a clinically important example of pathway convergence, while pharmacogenomic and computational approaches are interpreted in relation to drug exposure, organ reserve, and patient-specific vulnerability.
Keywords:analgesics, psychotropic drugs, polypharmacy, acute toxicity, cytochrome P450
Publication status:Published
Publication version:Version of Record
Year of publishing:2026
Number of pages:str. 1-24
Numbering:Vol. 27, issue 16, [article no.] 7168
PID:20.500.12556/DiRROS-31895 New window
UDC:615
ISSN on article:1422-0067
DOI:10.3390/ijms27167168 New window
COBISS.SI-ID:287907587 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 17. 8. 2026;
Publication date in DiRROS:17.08.2026
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Downloads:22
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Record is a part of a journal

Title:International journal of molecular sciences
Shortened title:Int. j. mol. sci.
Publisher:MDPI
ISSN:1422-0067
COBISS.SI-ID:2779162 New window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:analgetiki, psihotropna zdravila, akutna toksičnost, citokorm p450


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