Interleukin-6 regulates the expression of hepatic canalicular efflux drug transporters after cecal ligation and puncture-induced sepsis: A comparison with lipopolysaccharide treatment. (1st February 2023)
- Record Type:
- Journal Article
- Title:
- Interleukin-6 regulates the expression of hepatic canalicular efflux drug transporters after cecal ligation and puncture-induced sepsis: A comparison with lipopolysaccharide treatment. (1st February 2023)
- Main Title:
- Interleukin-6 regulates the expression of hepatic canalicular efflux drug transporters after cecal ligation and puncture-induced sepsis: A comparison with lipopolysaccharide treatment
- Authors:
- Ashino, Takashi
Nakamura, Yuki
Ohtaki, Hirokazu
Iwakura, Yoichiro
Numazawa, Satoshi - Abstract:
- Abstract: Hepatic multidrug transporters expressed on the canalicular membrane play a role in the hepatobiliary excretion of xenobiotics and endogenous substrates. The aim of this study was to elucidate the role of pro-inflammatory cytokines in the regulation of hepatic drug transporter expression after cecal ligation and puncture (CLP), a valuable tool for studying polymicrobial sepsis, and to compare CLP with lipopolysaccharide (LPS) treatment. CLP reduced the expression of Mdr2/Abcb4, Mrp2/Abcc2, Bsep/Abcb11, Bcrp/Abcg2, and Mate1/Slc47a1 mRNAs in wild-type (WT) mouse livers in a time-dependent manner up to 48 h postoperation. LPS also reduced the expression of all transporters in WT mouse livers 24 h posttreatment; thereafter, expression levels tended to return to normal by 48 h posttreatment. IL-6 −/− mice exhibited inhibited downregulation of drug transporters following CLP, although IL-1 −/− and TNFα −/− mice exhibited the reduced expression of all transporters in a manner similar to that found in WT mice. Compared with CLP, LPS treatment reduced the expression of all transporters in all cytokine-deficient mouse livers, except for the expression of Mrp2/Abcc2 in IL-6 −/− mice. Overall, these findings suggest that IL-6 is major factor in the downregulation of hepatic multidrug transporters following the onset of polymicrobial sepsis but not after LPS treatment. Graphical Abstract: ga1 Highlights: Cecal ligation and puncture-induced sepsis downregulate hepatic drugAbstract: Hepatic multidrug transporters expressed on the canalicular membrane play a role in the hepatobiliary excretion of xenobiotics and endogenous substrates. The aim of this study was to elucidate the role of pro-inflammatory cytokines in the regulation of hepatic drug transporter expression after cecal ligation and puncture (CLP), a valuable tool for studying polymicrobial sepsis, and to compare CLP with lipopolysaccharide (LPS) treatment. CLP reduced the expression of Mdr2/Abcb4, Mrp2/Abcc2, Bsep/Abcb11, Bcrp/Abcg2, and Mate1/Slc47a1 mRNAs in wild-type (WT) mouse livers in a time-dependent manner up to 48 h postoperation. LPS also reduced the expression of all transporters in WT mouse livers 24 h posttreatment; thereafter, expression levels tended to return to normal by 48 h posttreatment. IL-6 −/− mice exhibited inhibited downregulation of drug transporters following CLP, although IL-1 −/− and TNFα −/− mice exhibited the reduced expression of all transporters in a manner similar to that found in WT mice. Compared with CLP, LPS treatment reduced the expression of all transporters in all cytokine-deficient mouse livers, except for the expression of Mrp2/Abcc2 in IL-6 −/− mice. Overall, these findings suggest that IL-6 is major factor in the downregulation of hepatic multidrug transporters following the onset of polymicrobial sepsis but not after LPS treatment. Graphical Abstract: ga1 Highlights: Cecal ligation and puncture-induced sepsis downregulate hepatic drug transporters. IL-6 is important for the downregulation of drug transporters following sepsis. Lipopolysaccharide downregulates hepatic drug transporters in IL-6-deficient mice. … (more)
- Is Part Of:
- Toxicology letters. Volume 374(2023)
- Journal:
- Toxicology letters
- Issue:
- Volume 374(2023)
- Issue Display:
- Volume 374, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 374
- Issue:
- 2023
- Issue Sort Value:
- 2023-0374-2023-0000
- Page Start:
- 40
- Page End:
- 47
- Publication Date:
- 2023-02-01
- Subjects:
- ABC ATP-binding cassette -- SLC solute carrier -- LPS lipopolysaccharide -- IL interleukin -- TNF tumor necrosis factor -- mdr multidrug resistance protein -- mrp multidrug resistance-associated protein -- bcrp breast cancer resistance protein -- bsep bile-salt export pump -- mate multidrug and toxin extrusion -- WT wild type -- i.p. intraperitoneally -- CLP cecal ligation and puncture -- PCR real-time polymerase chain reaction
Drug transporter -- Cecal ligation and puncture -- Sepsis -- Lipopolysaccharide -- Interleukin -- Tumor necrosis factor
Toxicology -- Periodicals
363.179 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03784274 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.toxlet.2022.12.003 ↗
- Languages:
- English
- ISSNs:
- 0378-4274
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.042000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26990.xml