共 165 条
Molecular Mechanisms of SGLT2 Inhibitor on Cardiorenal Protection
被引:69
作者:

Hou, Yi-Chou
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机构:
Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan
Taipei Med Univ, Coll Med, Sch Med, Grad Inst Clin Med, Taipei 110, Taiwan Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan

Zheng, Cai-Mei
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机构:
Taipei Med Univ, Dept Internal Med, Div Nephrol, Shuang Ho Hosp, New Taipei 235, Taiwan
Taipei Med Univ, Coll Med, Sch Med, Div Nephrol,Dept Internal Med, Taipei 110, Taiwan
Taipei Med Univ, Res Ctr Urol & Kidney, Taipei 110, Taiwan Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan

Yen, Tzung-Hai
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机构:
Chang Gung Mem Hosp, Dept Internal Med, Div Nephrol, Taipei 105, Taiwan
Chang Gung Univ, Coll Med, Dept Med, Taoyuan 333, Taiwan Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan

Lu, Kuo-Cheng
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机构:
Taipei Tzu Chi Hosp, Buddhist Tzu Chi Med Fdn, Dept Med, Div Nephrol, New Taipei 231, Taiwan Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan
机构:
[1] Fu Jen Catholic Univ, Cardinal Tien Hosp, Sch Med, Dept Med,Div Nephrol, New Taipei 234, Taiwan
[2] Taipei Med Univ, Coll Med, Sch Med, Grad Inst Clin Med, Taipei 110, Taiwan
[3] Taipei Med Univ, Dept Internal Med, Div Nephrol, Shuang Ho Hosp, New Taipei 235, Taiwan
[4] Taipei Med Univ, Coll Med, Sch Med, Div Nephrol,Dept Internal Med, Taipei 110, Taiwan
[5] Taipei Med Univ, Res Ctr Urol & Kidney, Taipei 110, Taiwan
[6] Chang Gung Mem Hosp, Dept Internal Med, Div Nephrol, Taipei 105, Taiwan
[7] Chang Gung Univ, Coll Med, Dept Med, Taoyuan 333, Taiwan
[8] Taipei Tzu Chi Hosp, Buddhist Tzu Chi Med Fdn, Dept Med, Div Nephrol, New Taipei 231, Taiwan
关键词:
cardiovascular disease;
chronic kidney disease;
SGLT2;
diabetes mellitus;
COTRANSPORTER;
2;
INHIBITOR;
SYMPATHETIC-NERVOUS-SYSTEM;
GLOMERULAR-FILTRATION RATE;
GLUCOSE-TRANSPORTER SGLT2;
NA+/H+ EXCHANGER NHE3;
BLOOD-PRESSURE;
DIABETIC-NEPHROPATHY;
URIC-ACID;
KIDNEY-DISEASE;
URINARY-EXCRETION;
D O I:
10.3390/ijms21217833
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页码:1 / 25
页数:25
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