Prediabetes Induced by Fructose-Enriched Diet Influences Cardiac Lipidome and Proteome
and Leads to Deterioration of Cardiac Function prior to the Development of Excessive
Oxidative Stress and Cell Damage
Modern orvostudományi diagnosztikus eljárások és terápiák fejlesztése transzlációs
megközelítésbe...(EFOP-3.6.2-16-2017-00006) Támogató: EFOP
Szakterületek:
Általános orvostudomány
Biokémia és molekuláris biológia
Diabetológia
Szervfiziológia és kórélettan
Szív és keringési rendszer
Prediabetes is a condition affecting more than 35% of the population. In some forms,
excessive carbohydrate intake (primarily refined sugar) plays a prominent role. Prediabetes
is a symptomless, mostly unrecognized disease which increases cardiovascular risk.
In our work, we examined the effect of a fructose-enriched diet on cardiac function
and lipidome as well as proteome of cardiac muscle. Male Wistar rats were divided
into two groups. The control group received a normal diet while the fructose-fed group
received 60% fructose-supplemented chow for 24 weeks. Fasting blood glucose measurement
and oral glucose tolerance test (OGTT) showed slightly but significantly elevated
values due to fructose feeding indicating development of a prediabetic condition.
Both echocardiography and isolated working heart perfusion performed at the end of
the feeding protocol demonstrated diastolic cardiac dysfunction in the fructose-fed
group. Mass spectrometry-based, high-performance lipidomic and proteomic analyses
were executed from cardiac tissue. The lipidomic analysis revealed complex rearrangement
of the whole lipidome with special emphasis on defects in cardiolipin remodeling.
The proteomic analysis showed significant changes in 75 cardiac proteins due to fructose
feeding including mitochondria-, apoptosis-, and oxidative stress-related proteins.
Nevertheless, just very weak or no signs of apoptosis induction and oxidative stress
were detected in the hearts of fructose-fed rats. Our results suggest that fructose
feeding induces marked alterations in the cardiac lipidome, especially in cardiolipin
remodeling, which leads to mitochondrial dysfunction and impaired cardiac function.
However, at the same time, several adaptive responses are induced at the proteome
level in order to maintain a homeostatic balance. These findings demonstrate that
even very early stages of prediabetes can impair cardiac function and can result in
significant changes in the lipidome and proteome of the heart prior to the development
of excessive oxidative stress and cell damage.