Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43610
Title: Pyridoxamine Alleviates Cardiac Fibrosis and Oxidative Stress in Western Diet-Induced Prediabetic Rats
Authors: D'HAESE, Sarah 
Claes, Lisa
Jaeken, Eva
DELUYKER, Dorien 
EVENS, Lize 
HEEREN, Ellen 
HAESEN, Sibren 
VASTMANS, Lotte 
LAMBRICHTS, Ivo 
WOUTERS, Kristiaan 
Schalkwijk, Casper
HANSEN, Dominique 
OP 'T EIJNDE, Bert 
BITO, Virginie 
Issue Date: 2024
Source: International journal of molecular sciences (Print), 25 (15)
Abstract: 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 B6 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.
Keywords: pyridoxamine;type 2 diabetes;Western diet;adverse cardiac remodeling;prevention;cardioprotection
Document URI: http://hdl.handle.net/1942/43610
ISSN: 1661-6596
e-ISSN: 1422-0067
DOI: 10.3390/ijms25158508
ISI #: WOS:001287874900001
Rights: 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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