Protein fingerprinting of the extracellular matrix remodelling in a rat model of liver fibrosis—a serological evaluation. (26th December 2012)
- Record Type:
- Journal Article
- Title:
- Protein fingerprinting of the extracellular matrix remodelling in a rat model of liver fibrosis—a serological evaluation. (26th December 2012)
- Main Title:
- Protein fingerprinting of the extracellular matrix remodelling in a rat model of liver fibrosis—a serological evaluation
- Authors:
- Leeming, Diana J.
Byrjalsen, Inger
Jiménez, Wladimiro
Christiansen, Claus
Karsdal, Morten A. - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="liv12044-abs-0001"> <title>Abstract</title> <sec id="liv12044-sec-0001" sec-type="section"> <title>Background/Aim</title> <p>We investigated nine novel biomarkers of extracellular matrix (ECM) remodelling in a rat model of liver fibrosis.</p> </sec> <sec id="liv12044-sec-0002" sec-type="section"> <title>Methods</title> <p>Liver fibrosis was induced in 52 male Wistar rats by inhalation of carbon tetrachloride and the level of hepatic fibrosis was assessed by Sirius red staining compared with controls. The novel serum biochemical markers assessed in the model were type I‐(C1M), type III‐(C3M), type IV‐(C4M) and type VI‐(C6M) collagen, citrullinated vimentin (VICM) and biglycan (BGM) all protein fragments generated by matrix metalloproteinases; and formation markers of type III‐(P3NP), type VI (P4NP 7S) and type V (P5CP) collagen; hepatic mRNA type I collagen alpha‐1 chain levels, serum potassium, sodium, osmolarity, alanine aminotransferase, lactate dehydrogenase, albumin and creatinine.</p> </sec> <sec id="liv12044-sec-0003" sec-type="section"> <title>Results</title> <p>Stratification of the CCl<sub>4</sub>‐treated rats according to total hepatic collagen showed that the degradation markers were significantly elevated in mild to severe fibrosis except for C6M which was also elevated in early fibrosis (<italic>P </italic>&lt; 0.05). The highest Z‐scores in early and moderate fibrosis were provided by P4NP 7S and alanine<abstract abstract-type="main" xml:lang="en" id="liv12044-abs-0001"> <title>Abstract</title> <sec id="liv12044-sec-0001" sec-type="section"> <title>Background/Aim</title> <p>We investigated nine novel biomarkers of extracellular matrix (ECM) remodelling in a rat model of liver fibrosis.</p> </sec> <sec id="liv12044-sec-0002" sec-type="section"> <title>Methods</title> <p>Liver fibrosis was induced in 52 male Wistar rats by inhalation of carbon tetrachloride and the level of hepatic fibrosis was assessed by Sirius red staining compared with controls. The novel serum biochemical markers assessed in the model were type I‐(C1M), type III‐(C3M), type IV‐(C4M) and type VI‐(C6M) collagen, citrullinated vimentin (VICM) and biglycan (BGM) all protein fragments generated by matrix metalloproteinases; and formation markers of type III‐(P3NP), type VI (P4NP 7S) and type V (P5CP) collagen; hepatic mRNA type I collagen alpha‐1 chain levels, serum potassium, sodium, osmolarity, alanine aminotransferase, lactate dehydrogenase, albumin and creatinine.</p> </sec> <sec id="liv12044-sec-0003" sec-type="section"> <title>Results</title> <p>Stratification of the CCl<sub>4</sub>‐treated rats according to total hepatic collagen showed that the degradation markers were significantly elevated in mild to severe fibrosis except for C6M which was also elevated in early fibrosis (<italic>P </italic>&lt; 0.05). The highest Z‐scores in early and moderate fibrosis were provided by P4NP 7S and alanine aminotransferase. All nine markers of ECM remodelling were highly related to the extent of liver fibrosis induced by CCl<sub>4</sub>. The novel collagen formation marker, P4NP 7S, was reliable for the detection of early fibrosis, while the combination of the two markers, C6M and P5CP provided the best correlation with hepatic fibrosis in all fibrosis levels.</p> </sec> <sec id="liv12044-sec-0004" sec-type="section"> <title>Conclusion</title> <p>As the markers can be used for translational science, these markers may provide valuable information for the evaluation of liver fibrosis in clinical settings.</p> </sec> </abstract> … (more)
- Is Part Of:
- Liver international. Volume 33:Number 3(2013:Mar.)
- Journal:
- Liver international
- Issue:
- Volume 33:Number 3(2013:Mar.)
- Issue Display:
- Volume 33, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 33
- Issue:
- 3
- Issue Sort Value:
- 2013-0033-0003-0000
- Page Start:
- 439
- Page End:
- 447
- Publication Date:
- 2012-12-26
- Subjects:
- Liver -- Periodicals
Liver -- Diseases -- Periodicals
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1478-3231 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/liv.12044 ↗
- Languages:
- English
- ISSNs:
- 1478-3223
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5280.514000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3676.xml