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Potential Role of Dipeptidyl Peptidase IV in the Pathophysiology of Heart Failure
被引:17
|作者:
Salles, Thiago A.
[1
]
dos Santos, Leonardo
[2
]
Barauna, Valerio G.
[2
]
Girardi, Adriana C. C.
[1
]
机构:
[1] Univ Sao Paulo, Heart Inst InCor, Lab Genet & Mol Cardiol, Sch Med, BR-05403000 Sao Paulo, SP, Brazil
[2] Univ Fed Espirito Santo, Dept Physiol Sci, BR-29043900 Vitoria, ES, Brazil
基金:
巴西圣保罗研究基金会;
关键词:
GLUCAGON-LIKE PEPTIDE-1;
BRAIN NATRIURETIC PEPTIDE;
VASOACTIVE-INTESTINAL-PEPTIDE;
LEFT-VENTRICULAR DYSFUNCTION;
IMPROVES CARDIAC-FUNCTION;
EXCHANGER ISOFORM NHE3;
PLASMA NEUROPEPTIDE-Y;
MYOCARDIAL-INFARCTION;
CD26;
EXPRESSION;
DIASTOLIC DYSFUNCTION;
D O I:
10.3390/ijms16024226
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:
Dipeptidyl peptidase IV (DPPIV) is a widely expressed multifunctional serine peptidase that exists as a membrane-anchored cell surface protein or in a soluble form in the plasma and other body fluids. Numerous substrates are cleaved at the penultimate amino acid by DPPIV, including glucagon-like peptide-1 (GLP-1), brain natriuretic peptide (BNP) and stromal cell-derived factor-1 (SDF-alpha), all of which play important roles in the cardiovascular system. In this regard, recent reports have documented that circulating DPPIV activity correlates with poorer cardiovascular outcomes in human and experimental heart failure (HF). Moreover, emerging evidence indicates that DPPIV inhibitors exert cardioprotective and renoprotective actions in a variety of experimental models of cardiac dysfunction. On the other hand, conflicting results have been found when translating these promising findings from preclinical animal models to clinical therapy. In this review, we discuss how DPPIV might be involved in the cardio-renal axis in HF. In addition, the potential role for DPPIV inhibitors in ameliorating heart disease is revised, focusing on the effects of the main DPPIV substrates on cardiac remodeling and renal handling of salt and water.
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页码:4226 / 4249
页数:24
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