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- Publisher Website: 10.1186/s12944-018-0905-3
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- PMID: 30428911
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Article: Dysregulation of cardiac lipid parameters in high-fat high-cholesterol diet-induced rat model
Title | Dysregulation of cardiac lipid parameters in high-fat high-cholesterol diet-induced rat model |
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Authors | |
Keywords | adipocyte animal experiment animal modelanimal tissue cardiovascular disease cell damage |
Issue Date | 2018 |
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.lipidworld.com |
Citation | Lipids in Health and Disease, 2018, v. 17 n. 1, p. article no. 255 How to Cite? |
Abstract | Background:
Lipid dysregulation is a classical risk factor for cardiovascular disease (CVD), yet scanty evidence existed regarding cardiac lipid metabolism that is directly related to heart damage. Recently, the relationship between dyslipidemia and pro-inflammatory insults has led to further understanding on the CVD-predisposing effects of dyslipidemia. The aims of the present study were to investigate whether high-fat high-cholesterol (HFHC) diet-induced hyperlipidemia would cause heart damage and to study the potential role of local cardiac lipid dysregulation in the occurrence of cellular injury.
Methods:
Male Sprague–Dawley rats were divided into normal chow or HFHC diet groups, and sacrificed after 2 or 4 weeks, respectively. Lipid peroxidation marker level was measured. Lipid parameters in the rat hearts were detected. Cardiac damage was evaluated.
Results:
HFHC diet increased serum levels of cholesterol and free fatty acids (FFAs) and led to systemic oxidative stress and pro-inflammatory status. Cardiac lipid dysregulation, which was characterized by elevated levels of cholesterol and adipocyte (A)- and heart (H)-fatty acid binding proteins (FABPs), occurred after HFHC diet for 4 weeks. Cardiac damage was further evident with elevated circulating H-FABP levels, increased cardiac interstitial fibrosis and the loss of troponin I.
Conclusion:
Our data demonstrated that HFHC diet led to systemic and cardiac lipid dysregulation, accompanied by systemic oxidative and pro-inflammatory stresses, and these may finally cooperate to cause a series of pathological changes of the heart tissue. Our findings suggest that maintenance of lipid regulation may be essential in the prevention of heart damage. |
Persistent Identifier | http://hdl.handle.net/10722/273401 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.112 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Han, Q | - |
dc.contributor.author | Yeung, SC | - |
dc.contributor.author | Ip, MSM | - |
dc.contributor.author | Mak, JCW | - |
dc.date.accessioned | 2019-08-06T09:28:16Z | - |
dc.date.available | 2019-08-06T09:28:16Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Lipids in Health and Disease, 2018, v. 17 n. 1, p. article no. 255 | - |
dc.identifier.issn | 1476-511X | - |
dc.identifier.uri | http://hdl.handle.net/10722/273401 | - |
dc.description.abstract | Background: Lipid dysregulation is a classical risk factor for cardiovascular disease (CVD), yet scanty evidence existed regarding cardiac lipid metabolism that is directly related to heart damage. Recently, the relationship between dyslipidemia and pro-inflammatory insults has led to further understanding on the CVD-predisposing effects of dyslipidemia. The aims of the present study were to investigate whether high-fat high-cholesterol (HFHC) diet-induced hyperlipidemia would cause heart damage and to study the potential role of local cardiac lipid dysregulation in the occurrence of cellular injury. Methods: Male Sprague–Dawley rats were divided into normal chow or HFHC diet groups, and sacrificed after 2 or 4 weeks, respectively. Lipid peroxidation marker level was measured. Lipid parameters in the rat hearts were detected. Cardiac damage was evaluated. Results: HFHC diet increased serum levels of cholesterol and free fatty acids (FFAs) and led to systemic oxidative stress and pro-inflammatory status. Cardiac lipid dysregulation, which was characterized by elevated levels of cholesterol and adipocyte (A)- and heart (H)-fatty acid binding proteins (FABPs), occurred after HFHC diet for 4 weeks. Cardiac damage was further evident with elevated circulating H-FABP levels, increased cardiac interstitial fibrosis and the loss of troponin I. Conclusion: Our data demonstrated that HFHC diet led to systemic and cardiac lipid dysregulation, accompanied by systemic oxidative and pro-inflammatory stresses, and these may finally cooperate to cause a series of pathological changes of the heart tissue. Our findings suggest that maintenance of lipid regulation may be essential in the prevention of heart damage. | - |
dc.language | eng | - |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.lipidworld.com | - |
dc.relation.ispartof | Lipids in Health and Disease | - |
dc.rights | Lipids in Health and Disease. Copyright © BioMed Central Ltd. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | adipocyte | - |
dc.subject | animal experiment | - |
dc.subject | animal modelanimal tissue | - |
dc.subject | cardiovascular disease | - |
dc.subject | cell damage | - |
dc.title | Dysregulation of cardiac lipid parameters in high-fat high-cholesterol diet-induced rat model | - |
dc.type | Article | - |
dc.identifier.email | Yeung, SC: flag@hkucc.hku.hk | - |
dc.identifier.email | Ip, MSM: msmip@hku.hk | - |
dc.identifier.email | Mak, JCW: judithmak@hku.hk | - |
dc.identifier.authority | Ip, MSM=rp00347 | - |
dc.identifier.authority | Mak, JCW=rp00352 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/s12944-018-0905-3 | - |
dc.identifier.pmid | 30428911 | - |
dc.identifier.pmcid | PMC6237003 | - |
dc.identifier.scopus | eid_2-s2.0-85056584431 | - |
dc.identifier.hkuros | 300327 | - |
dc.identifier.volume | 17 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | article no. 255 | - |
dc.identifier.epage | article no. 255 | - |
dc.identifier.isi | WOS:000450505600001 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1476-511X | - |