Differential effects of minocycline on microvascular complications in murine models of type 1 and type 2 diabetes
Year: 2021
Type: article
Abstract: Diabetes is a global healthcare problem associated with enormous healthcare and personal costs. Despite glucose lowering agents that control glycaemia, both type 1 (T1D) and type (T2D) diabetes patients often develop microvascular complications that increase morbidity and mortality. Current interventions rely on careful glycemic control and healthy lifestyle choices, but these are ineffective at reversing or completely preventing the major microvascular complications, diabetic peripheral neuropathy (DPN), diabetic retinopathy (DR), and diabetic kidney disease (DKD). Minocycline, a tetracycline antibiotic with anti-inflammatory and anti-apoptotic properties, has been proposed as a protective agent in diabetes. However, there are no reported studies evaluating the therapeutic efficacy of minocycline in T1D and T2D models for all microvascular complications (DPN, DR, and DKD). Therefore, we performed metabolic profiling in streptozotocin-induced T1D and db/db T2D models and compared the efficacy of minocycline in preventing complications to that of insulin and pioglitazone in both models. Minocycline partially ameliorated DR and DKD in T1D and T2D animals, but was less effective than insulin or pioglitazone, and failed to improve DPN in either model. These results suggest that minocycline is unlikely to improve outcomes beyond that achieved with current available therapies in patients with T1D or T2D associated microvascular complications.
Source: Journal of Translational Science
DOI: 10.15761/jts.1000431
Institutions: University of Michigan, Michigan Medicine
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
Awards: Integrated Systems Biology Approach to Diabetic Microvascular Complications, Michigan Mouse Metabolic Phenotyping Center, Inflammatory Resolution and Vascular Restoration in Diabetic Retinopathy, Molecular Regulation of Photoreceptor Cell Death, University of Michigan O'Brien Kidney Translational Core Center, Cincinnati Mouse Metabolic Phenotyping Center, Linking Nerve Bioenergetics with Metabolomics: New Insights into Diabetic Neuroapthy, Cincinnati Mouse Metabolic Phenotyping Center, Regulation of Retinal Cell Death in Diabetes, University of Michigan Vision Research Center, Michigan Nutrition Obesity Research Center
OpenAlex ID: W3127874994
