Pyridoxamine Alleviates Cardiac Fibrosis and Oxidative Stress in Western Diet-Induced Prediabetic Rats.
Sarah D'HaeseLisa ClaesEva JaekenDorien DeluykerLize EvensEllen HeerenSibren HaesenLotte VastmansIvo LambrichtsKristiaan A M WoutersCasper G SchalkwijkDominique HansenB O EijndeVirginie BitoPublished in: International journal of molecular sciences (2024)
Individuals with type 2 diabetes mellitus (T2DM) are at an increased risk for heart failure, yet preventive cardiac care is suboptimal in this population. Pyridoxamine (PM), a vitamin B 6 analog, has been shown to exert protective effects in metabolic and cardiovascular diseases. In this study, we aimed to investigate whether PM limits adverse cardiac remodeling and dysfunction in rats who develop T2DM. Male rats received a standard chow diet or Western diet (WD) for 18 weeks to induce prediabetes. One WD group received additional PM (1 g/L) via drinking water. Glucose tolerance was assessed with a 1 h oral glucose tolerance test. Cardiac function was evaluated using echocardiography and hemodynamic measurements. Histology on left ventricular (LV) tissue was performed. Treatment with PM prevented the increase in fasting plasma glucose levels compared to WD-fed rats ( p < 0.05). LV cardiac dilation tended to be prevented using PM supplementation. In LV tissue, PM limited an increase in interstitial collagen deposition ( p < 0.05) seen in WD-fed rats. PM tended to decrease 3-nitrotyrosine and significantly lowered 4-hydroxynonenal content compared to WD-fed rats. We conclude that PM alleviates interstitial fibrosis and oxidative stress in the hearts of WD-induced prediabetic rats.
Keyphrases
- particulate matter
- left ventricular
- air pollution
- polycyclic aromatic hydrocarbons
- oxidative stress
- heavy metals
- heart failure
- drinking water
- water soluble
- south africa
- dna damage
- diabetic rats
- emergency department
- risk assessment
- blood glucose
- blood pressure
- acute myocardial infarction
- health risk assessment
- mitral valve
- pain management
- mouse model
- drug induced
- ejection fraction
- ischemia reperfusion injury
- liver fibrosis
- preterm birth
- adipose tissue
- endothelial cells
- quality improvement
- induced apoptosis
- wound healing
- combination therapy