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Naslov:Molecular mechanisms of acute drug toxicity in polypharmacy : analgesic–psychotropic interactions
Avtorji:ID Rijavec, Nikolina (Avtor)
ID Rijavec, Boris (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,24 MB)
MD5: 35B2809A44545F06CDBE2617DDEFE52C
 
URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/1422-0067/27/16/7168
 
Jezik:Angleški jezik
Tipologija:1.02 - Pregledni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek: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.
Ključne besede:analgesics, psychotropic drugs, polypharmacy, acute toxicity, cytochrome P450
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2026
Št. strani:str. 1-24
Številčenje:Vol. 27, issue 16, [article no.] 7168
PID:20.500.12556/DiRROS-31895 Novo okno
UDK:615
ISSN pri članku:1422-0067
DOI:10.3390/ijms27167168 Novo okno
COBISS.SI-ID:287907587 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 17. 8. 2026;
Datum objave v DiRROS:17.08.2026
Število ogledov:37
Število prenosov:21
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:International journal of molecular sciences
Skrajšan naslov:Int. j. mol. sci.
Založnik:MDPI
ISSN:1422-0067
COBISS.SI-ID:2779162 Novo okno

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:analgetiki, psihotropna zdravila, akutna toksičnost, citokorm p450


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