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Molecular basis of mood and cognitive adverse events elucidated via a combination of pharmacovigilance data mining and functional enrichment analysis

Andronis, Christos (author)
Biovista, 34 Rodopoleos St, Athens 16777, Greece
Silva, João Pedro (author)
Univ Porto, Fac Pharm, Dept Biol Sci, Lab Toxicol,UCIBIO,REQUIMTE, P-4050313 Porto, Portugal
Lekka, Eftychia (author)
Biovista, 34 Rodopoleos St, Athens 16777, Greece
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Virvilis, Vassilis (author)
Biovista, 34 Rodopoleos St, Athens 16777, Greece
Carmo, Helena (author)
Univ Porto, Fac Pharm, Dept Biol Sci, Lab Toxicol,UCIBIO,REQUIMTE, P-4050313 Porto, Portugal
Bampali, Konstantina (author)
‎Med Univ Vienna, Dept Mol Neurosci, Spitalgasse 4, A-1090 Vienna, Austria
Ernst, Margot (author)
‎Med Univ Vienna, Dept Mol Neurosci, Spitalgasse 4, A-1090 Vienna, Austria
Hu, Yang, 1989- (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab
Loryan, Irena, 1977- (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab
Richard, Jacques (author)
Sanofi R&D, 371 Ave Prof Blayac, F-34000 Montpellier, France
Carvalho, Félix (author)
Univ Porto, Fac Pharm, Dept Biol Sci, Lab Toxicol,UCIBIO,REQUIMTE, P-4050313 Porto, Portugal
Savić, Miroslav M (author)
Univ Belgrade, Fac Pharm, Dept Pharmacol, Vojvode Stepe 450, Belgrade 11000, Serbia
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 (creator_code:org_t)
2020-06-05
2020
English.
In: Archives of Toxicology. - : Springer Nature. - 0340-5761 .- 1432-0738. ; 94:8, s. 2829-2845
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Drug-induced Mood- and Cognition-related adverse events (MCAEs) are often only detected during the clinical trial phases of drug development, or even after marketing, thus posing a major safety concern and a challenge for both pharmaceutical companies and clinicians. To fill some gaps in the understanding and elucidate potential biological mechanisms of action frequently associated with MCAEs, we present a unique workflow linking observational population data with the available knowledge at molecular, cellular, and psychopharmacology levels. It is based on statistical analysis of pharmacovigilance reports and subsequent signaling pathway analyses, followed by evidence-based expert manual curation of the outcomes. Our analysis: (a) ranked pharmaceuticals with high occurrence of such adverse events (AEs), based on disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database, and (b) identified 120 associated genes and common pathway nodes possibly underlying MCAEs. Nearly two-thirds of the identified genes were related to immune modulation, which supports the critical involvement of immune cells and their responses in the regulation of the central nervous system function. This finding also means that pharmaceuticals with a negligible central nervous system exposure may induce MCAEs through dysregulation of the peripheral immune system. Knowledge gained through this workflow unravels putative hallmark biological targets and mediators of drug-induced mood and cognitive disorders that need to be further assessed and validated in experimental models. Thereafter, they can be used to substantially improve in silico/in vitro/in vivo tools for predicting these adversities at a preclinical stage.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

Adverse outcome pathways
Cross-talk analysis
Neurotoxicity
Pharmaceuticals’ safety
Psychiatric/psychological adverse events

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ref (subject category)
art (subject category)

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