Macrovascular and microvascular type 2 diabetes complications are interrelated in a mouse model


Por: Cifuentes-Mendiola S.E., Solís-Suarez D.L., Martínez-Davalos A., García-Hernández A.L.

Publicada: 1 ene 2023 Ahead of Print: 1 mar 2023
Resumen:
Aim: Evaluate the development of multiple complications, their interactions, and common mechanisms in the same individual with T2D. Material and methods: 4-week-old male C57BL/6J mice were divided into: control (n = 6) and T2D (n = 6). T2D was induced through a high-carbohydrate-diet and low doses of streptozotocin. T2D was validated by metabolic parameters. Diabetic neuropathy was evaluated by mechanical and thermal sensitivity tests. We performed a histopathological analysis of the heart, kidney, liver, and parotid salivary glands and changes in bone microarchitecture by µCT. We calculated the relative risk (RR), odd ratios (OR) and Pearson correlation coefficients between the different complications and metabolic features. Results: T2D mice have cardiomyopathy, neuropathy, nephropathy, liver steatosis and fibrosis, structural damage in parotid salivary glands, and bone porosity. RR analysis shows that all complications are interrelated by hyperglycaemia, insulin resistance, obesity, and systemic inflammation. Conclusions: T2D mice develop multiple complications simultaneously, which are related to each other, and this is associated with metabolic alterations. Our findings open up new approaches for the study and new therapeutic approaches of the pathophysiology of T2D and its complications. © 2023

Filiaciones:
Laboratory of Dental Research, Section of Osteoimmunology and Oral Immunology, FES Iztacala, National Autonomous University of Mexico, A. Jiménez Gallardo SN, San Sebastián Xhala, Estado de México, Cuautitlán Izcalli, CP 54714, Mexico
Physics Institute, National Autonomous University of Mexico, Circuito de la Investigación Científica, Ciudad Universitaria, México City, 04510, Mexico
ISSN: 10568727
Editorial
ELSEVIER SCIENCE INC, 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 37 Número: 5
Páginas:
WOS Id: 000971499800001
ID de PubMed: 36963291

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