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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Pennig, J; Scherrer, P; Gissler, MC; Anto-Michel, N; Hoppe, N; Füner, L; Härdtner, C; Stachon, P; Wolf, D; Hilgendorf, I; Mullick, A; Bode, C; Zirlik, A; Goldberg, IJ; Willecke, F.
Glucose lowering by SGLT2-inhibitor empagliflozin accelerates atherosclerosis regression in hyperglycemic STZ-diabetic mice.
Sci Rep. 2019; 9(1):17937-17937 Doi: 10.1038/s41598-019-54224-9 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Anto Michel Nathaly
Zirlik Andreas
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Abstract:
Diabetes worsens atherosclerosis progression and leads to a defect in repair of arteries after cholesterol reduction, a process termed regression. Empagliflozin reduces blood glucose levels via inhibition of the sodium glucose cotransporter 2 (SGLT-2) in the kidney and has been shown to lead to a marked reduction in cardiovascular events in humans. To determine whether glucose lowering by empagliflozin accelerates atherosclerosis regression in a mouse model, male C57BL/6J mice were treated intraperitoneally with LDLR- and SRB1- antisense oligonucleotides and fed a high cholesterol diet for 16 weeks to induce severe hypercholesterolemia and atherosclerosis progression. At week 14 all mice were rendered diabetic by streptozotocin (STZ) injections. At week 16 a baseline group was sacrificed and displayed substantial atherosclerosis of the aortic root. In the remaining mice, plasma cholesterol was lowered by switching to chow diet and treatment with LDLR sense oligonucleotides to induce atherosclerosis regression. These mice then received either empagliflozin or vehicle for three weeks. Atherosclerotic plaques in the empagliflozin treated mice were significantly smaller, showed decreased lipid and CD68+ macrophage content, as well as greater collagen content. Proliferation of plaque resident macrophages and leukocyte adhesion to the vascular wall were significantly decreased in empagliflozin-treated mice. In summary, plasma glucose lowering by empagliflozin improves plaque regression in diabetic mice.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Atherosclerosis - blood
Atherosclerosis - drug therapy
Atherosclerosis - etiology
Benzhydryl Compounds - therapeutic use
Blood Glucose - analysis
Diabetes Mellitus, Experimental - blood
Diabetes Mellitus, Experimental - complications
Diabetes Mellitus, Experimental - drug therapy
Glucosides - therapeutic use
Male -
Mice -
Mice, Inbred C57BL -
Plaque, Atherosclerotic - blood
Plaque, Atherosclerotic - drug therapy
Plaque, Atherosclerotic - etiology
Sodium-Glucose Transporter 2 Inhibitors - therapeutic use

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