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10.3390/ijms21217833

http://scihub22266oqcxt.onion/10.3390/ijms21217833
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33105763!7660105!33105763
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suck abstract from ncbi


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pmid33105763      Int+J+Mol+Sci 2020 ; 21 (21): ä
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  • Molecular Mechanisms of SGLT2 Inhibitor on Cardiorenal Protection #MMPMID33105763
  • Hou YC; Zheng CM; Yen TH; Lu KC
  • Int J Mol Sci 2020[Oct]; 21 (21): ä PMID33105763show ga
  • The development of sodium-glucose transporter 2 inhibitor (SGLT2i) broadens the therapeutic strategies in treating diabetes mellitus. By inhibiting sodium and glucose reabsorption from the proximal tubules, the improvement in insulin resistance and natriuresis improved the cardiovascular mortality in diabetes mellitus (DM) patients. It has been known that SGLT2i also provided renoprotection by lowering the intraglomerular hypertension by modulating the pre- and post- glomerular vascular tone. The application of SGLT2i also provided metabolic and hemodynamic benefits in molecular aspects. The recent DAPA-CKD trial and EMPEROR-Reduced trial provided clinical evidence of renal and cardiac protection, even in non-DM patients. Therefore, the aim of the review is to clarify the hemodynamic and metabolic modulation of SGLT2i from the molecular mechanism.
  • |Animals[MESH]
  • |Anti-Inflammatory Agents, Non-Steroidal/pharmacology[MESH]
  • |Autonomic Nervous System Diseases/*drug therapy/physiopathology[MESH]
  • |Cardio-Renal Syndrome/*drug therapy/physiopathology[MESH]
  • |Clinical Trials as Topic[MESH]
  • |Diabetes Mellitus/*drug therapy/physiopathology[MESH]
  • |Glomerular Filtration Rate[MESH]
  • |Hemodynamics/drug effects[MESH]
  • |Humans[MESH]
  • |Ketosis/chemically induced[MESH]
  • |Kidney Glomerulus/physiopathology[MESH]
  • |Sodium-Glucose Transporter 2 Inhibitors/*pharmacology[MESH]


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