Metformin Affects Cardiac Arachidonic Acid Metabolism and Cardiac Lipid Metabolite Storage in a Prediabetic Rat Model
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
IN 00023001
Ministerstvo Zdravotnictví Ceské Republiky
IGA_LF_2021_013
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
34299301
PubMed Central
PMC8305829
DOI
10.3390/ijms22147680
PII: ijms22147680
Knihovny.cz E-zdroje
- Klíčová slova
- arachidonic acid, cytochrome P450, fatty acid profile, lipotoxic intermediates, metformin, myocardial function, myocardial phospholipids, stearoyl-CoA desaturase,
- MeSH
- bazální metabolismus účinky léků MeSH
- biologické markery krev MeSH
- desaturasy mastných kyselin metabolismus MeSH
- hyperlipoproteinemie typ IV farmakoterapie metabolismus MeSH
- hypoglykemika farmakologie MeSH
- kardiotonika farmakologie MeSH
- krysa rodu Rattus MeSH
- kyselina arachidonová metabolismus MeSH
- mediátory zánětu krev MeSH
- metabolismus lipidů účinky léků MeSH
- metformin farmakologie MeSH
- modely nemocí na zvířatech MeSH
- myokard metabolismus MeSH
- potkani Wistar MeSH
- prediabetes farmakoterapie metabolismus MeSH
- rizikové faktory MeSH
- srdce účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery MeSH
- desaturasy mastných kyselin MeSH
- hypoglykemika MeSH
- kardiotonika MeSH
- kyselina arachidonová MeSH
- mediátory zánětu MeSH
- metformin MeSH
Metformin can reduce cardiovascular risk independent of glycemic control. The mechanisms behind its non-glycemic benefits, which include decreased energy intake, lower blood pressure and improved lipid and fatty acid metabolism, are not fully understood. In our study, metformin treatment reduced myocardial accumulation of neutral lipids-triglycerides, cholesteryl esters and the lipotoxic intermediates-diacylglycerols and lysophosphatidylcholines in a prediabetic rat model (p < 0.001). We observed an association between decreased gene expression and SCD-1 activity (p < 0.05). In addition, metformin markedly improved phospholipid fatty acid composition in the myocardium, represented by decreased SFA profiles and increased n3-PUFA profiles. Known for its cardioprotective and anti-inflammatory properties, metformin also had positive effects on arachidonic acid metabolism and CYP-derived arachidonic acid metabolites. We also found an association between increased gene expression of the cardiac isoform CYP2c with increased 14,15-EET (p < 0.05) and markedly reduced 20-HETE (p < 0.001) in the myocardium. Based on these results, we conclude that metformin treatment reduces the lipogenic enzyme SCD-1 and the accumulation of the lipotoxic intermediates diacylglycerols and lysophosphatidylcholine. Increased CYP2c gene expression and beneficial effects on CYP-derived arachidonic acid metabolites in the myocardium can also be involved in cardioprotective effect of metformin.
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