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ISSN 2063-5346
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SELF-ASSEMBLED ULTRA DEFORMABLE VESICULAR SYSTEM LOADED DRUG FOR TARGETED DRUG DELIVERY FOR THE TREATMENT OF DIABETES MELLITUS FOR MULTI-TARGETED DRUGS

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Mishra Namrata , M. Alagusundaram, Bhattacharya Vijeta ,VenkateswarluGoli
ยป doi: 10.31838/ecb/2023.12.si4.112

Abstract

Type 2 diabetes mellitus (T2DM) affects a large population worldwide. T2DM is a complex heterogeneous group of metabolic disorders including hyperglycemia and impaired insulin action and/or insulin secretion. T2DM causes dysfunctions in multiple organs or tissues. Current theories of T2DM include a defect in insulin-mediated glucose uptake in muscle, a dysfunction of the pancreatic b-cells, a disruption of the secretory function of adipocytes, and an impaired insulin action in the liver. The etiology of human T2DM is multifactorial, with genetic background and physical inactivity as two critical components. The pathogenesis of T2DM is not fully understood. Animal models of T2DM have been proven to be useful to study the pathogenesis of, and to find a new therapy for, the disease. Although different animal models share similar characteristics, each mimics a specific aspect of genetic, endocrine, metabolic, and morphologic changes that occur in human T2DM. The purpose of this review is to provide the recent progress and current theories in T2DM and to summarize animal models for studying the pathogenesis of the disease. Diabetes Mellitus (DM) is a multi-factorial chronic health condition that affects a large part of the population and according to the World Health Organization (WHO), the number of adults living with diabetes is expected to increase. Since type 2 diabetes mellitus (T2DM) is suffered by the majority of diabetic patients (around 90โ€“95%) and often the mono-target therapy fails in managing blood glucose levels and the other comorbidities, this review focuses on the potential drugs acting on multi-targets involved in the treatment of this type of diabetes. In particular, the review considers the main systems directly involved in T2DM or involved in diabetes comorbidities. Agonists acting on incretin, and glucagon systems, as well as on peroxisome proliferation-activated receptors are considered. Inhibitors that target either aldose reductase and tyrosine phosphatase 1B or sodium glucose transporters 1 and 2 are taken into account. Moreover, with a view at the multi-target approaches for T2DM some Phyto complexes are also discussed.

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