NOD Mice Recapitulate the Cardiac Disturbances Observed in Type 1 Diabetes

被引:0
作者
Ygor Schleier
Oscar Moreno-Loaiza
Maria Micaela López Alarcón
Eduarda Gabrielle Lopes Martins
Bruno Cabral Braga
Isalira Peroba Ramos
Antonio Galina
Emiliano Horacio Medei
机构
[1] Federal University of Rio de Janeiro,Laboratory of Cardioimmunology, Institute of Biophysics Carlos Chagas Filho
[2] Federal University of Rio de Janeiro,Laboratory of Bioenergetics and Mitochondrial Physiology, Institute of Medical Biochemistry Leopoldo de Meis, Center for Health Sciences
[3] Federal University of Rio de Janeiro,National Center for Structural Biology and Bioimaging
[4] Carlos Chagas Filho Biophysics Institute – UFRJ,undefined
来源
Journal of Cardiovascular Translational Research | 2021年 / 14卷
关键词
Type 1 diabetes; Arrhythmias; Mitochondria; NOD mice; Electrophysiology;
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中图分类号
学科分类号
摘要
This work aimed at testing the hypothesis that NOD/ShiLtJ mice (NOD) recapitulate the cardiac disturbances observed on type 1 diabetes (T1D). NOD mice were studied 4 weeks after the onset of hyperglycemia, and NOR/Lt mice matched as control. Cardiac function was evaluated by echocardiography and electrocardiography (ECG). Action potentials (AP) and Ca2+ transients were evaluated at whole heart level. Heart mitochondrial function was evaluated by high-resolution respirometry and H2O2 release. NOD mice presented a reduction in hearth weight. Mitochondrial oxygen fluxes and H2O2 release were similar between NOD and NOR mice. ECG revealed a QJ interval prolongation in NOD mice. Furthermore, AP duration at 30% of repolarization was increased, and it depicted slower Ca2+ transient kinetics. NOD mice presented greater number/severity of ventricular arrhythmias both in vivo and in vitro. In conclusion, NOD mice evoked cardiac electrical and calcium handling disturbances similar to the observed in T1D.
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页码:271 / 282
页数:11
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[31]   REDUCTION OF DIABETES INCIDENCE IN NOD MICE BY NEONATAL GLUCOSE TREATMENT [J].
BOCK, T ;
KJAER, TW ;
JORGENSEN, M ;
JOSEFSEN, K ;
RYGAARD, J ;
BUSCHARD, K .
APMIS, 1991, 99 (11) :989-992
[32]   Synthetic glycolipid OCH prevents insulitis and diabetes in NOD mice [J].
Mizuno, M ;
Masumura, M ;
Tomi, C ;
Chiba, A ;
Oki, S ;
Yamamura, T ;
Miyake, S .
JOURNAL OF AUTOIMMUNITY, 2004, 23 (04) :293-300
[33]   Immunization with streptozotocin-treated NOD mouse islets inhibits the onset of autoimmune diabetes in NOD mice [J].
Rayat, GR ;
Rajotte, RV ;
Lyon, JG ;
Dufour, JM ;
Hacquoil, BV ;
Korbutt, GS .
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[34]   Mouse models for the study of autoimmune type 1 diabetes: a NOD to similarities and differences to human disease [J].
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