Liraglutide Decreases Hepatic Inflammation and Injury in Advanced Lean Non‐Alcoholic Steatohepatitis. Issue 6 (30th July 2018)
- Record Type:
- Journal Article
- Title:
- Liraglutide Decreases Hepatic Inflammation and Injury in Advanced Lean Non‐Alcoholic Steatohepatitis. Issue 6 (30th July 2018)
- Main Title:
- Liraglutide Decreases Hepatic Inflammation and Injury in Advanced Lean Non‐Alcoholic Steatohepatitis
- Authors:
- Ipsen, David H.
Rolin, Bidda
Rakipovski, Günaj
Skovsted, Gry F.
Madsen, Anette
Kolstrup, Stefanie
Schou‐Pedersen, Anne Marie
Skat‐Rørdam, Josephine
Lykkesfeldt, Jens
Tveden‐Nyborg, Pernille - Abstract:
- Abstract: Although commonly associated with obesity, non‐alcoholic fatty liver disease (NAFLD) is also present in the lean population representing a unique disease phenotype. Affecting 25% of the world's population, NAFLD is associated with increased mortality especially when progressed to non‐alcoholic steatohepatitis (NASH). However, no approved pharmacological treatments exist. Current research focuses mainly on NASH associated with obesity, leaving the effectiveness of promising treatments in lean NASH virtually unknown. This study therefore aimed to evaluate the effect of liraglutide (glucagon‐like peptide 1 analogue) and dietary intervention, alone and in combination, in guinea pigs with non‐obese NASH. After 20 weeks of high‐fat feeding (20% fat, 15% sucrose, 0.35% cholesterol), 40 female guinea pigs were block‐randomized based on weight into four groups receiving one of four treatments for 4 weeks: continued high‐fat diet (HF, control), high‐fat diet and liraglutide treatment (HFL), chow diet (4% fat, 0% sucrose, 0% cholesterol; HFC) or chow diet and liraglutide treatment (HFCL). High‐fat feeding induced NASH with severe fibrosis. Liraglutide decreased inflammation ( p < 0.05) and hepatocyte ballooning ( p < 0.05), while increasing hepatic α‐tocopherol ( p = 0.0154). Dietary intervention did not improve liver histopathology significantly, but decreased liver weight ( p = 0.004), plasma total cholesterol ( p = 0.0175), LDL‐cholesterol ( p = 0.0063), VLDL‐cholesterol (Abstract: Although commonly associated with obesity, non‐alcoholic fatty liver disease (NAFLD) is also present in the lean population representing a unique disease phenotype. Affecting 25% of the world's population, NAFLD is associated with increased mortality especially when progressed to non‐alcoholic steatohepatitis (NASH). However, no approved pharmacological treatments exist. Current research focuses mainly on NASH associated with obesity, leaving the effectiveness of promising treatments in lean NASH virtually unknown. This study therefore aimed to evaluate the effect of liraglutide (glucagon‐like peptide 1 analogue) and dietary intervention, alone and in combination, in guinea pigs with non‐obese NASH. After 20 weeks of high‐fat feeding (20% fat, 15% sucrose, 0.35% cholesterol), 40 female guinea pigs were block‐randomized based on weight into four groups receiving one of four treatments for 4 weeks: continued high‐fat diet (HF, control), high‐fat diet and liraglutide treatment (HFL), chow diet (4% fat, 0% sucrose, 0% cholesterol; HFC) or chow diet and liraglutide treatment (HFCL). High‐fat feeding induced NASH with severe fibrosis. Liraglutide decreased inflammation ( p < 0.05) and hepatocyte ballooning ( p < 0.05), while increasing hepatic α‐tocopherol ( p = 0.0154). Dietary intervention did not improve liver histopathology significantly, but decreased liver weight ( p = 0.004), plasma total cholesterol ( p = 0.0175), LDL‐cholesterol ( p = 0.0063), VLDL‐cholesterol ( p = 0.0034), hepatic cholesterol ( p < 0.0001) and increased hepatic vitamin C ( p = 0.0099). Combined liraglutide and dietary intervention induced a rapid weight loss, necessitating periodical liraglutide dose adjustment/discontinuation, limiting the strength of the findings from this group. Collectively, this pre‐clinical study supports the beneficial effect of liraglutide on NASH and extends this notion to lean NASH. … (more)
- Is Part Of:
- Basic & clinical pharmacology & toxicology. Volume 123:Issue 6(2018)
- Journal:
- Basic & clinical pharmacology & toxicology
- Issue:
- Volume 123:Issue 6(2018)
- Issue Display:
- Volume 123, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 123
- Issue:
- 6
- Issue Sort Value:
- 2018-0123-0006-0000
- Page Start:
- 704
- Page End:
- 713
- Publication Date:
- 2018-07-30
- Subjects:
- Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology, Clinical -- Periodicals
Computer network resources
Electronic journals
615.1 - Journal URLs:
- http://firstsearch.oclc.org/journal=1742-7835;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1742-7843 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=pto ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcpt.13082 ↗
- Languages:
- English
- ISSNs:
- 1742-7835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1863.914250
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8507.xml