Dipeptidyl peptidase-4 inhibition and renoprotection: the role of antifibrotic effects

被引:18
作者
Takagaki, Yuta [1 ]
Koya, Daisuke [1 ,2 ]
Kanasaki, Keizo [1 ,2 ]
机构
[1] Kanazawa Med Univ, Dept Diabetol & Endocrinol, Uchinada, Ishikawa, Japan
[2] Kanazawa Med Univ, Div Anticipatory Mol Food Sci & Technol, Uchinada, Ishikawa, Japan
基金
日本学术振兴会;
关键词
EndMT; fibrosis; integrin; microRNA; TGF-; TO-MESENCHYMAL TRANSITION; INDUCED DIABETIC-RATS; DPP-4; INHIBITION; CARDIOVASCULAR OUTCOMES; ADENOSINE-DEAMINASE; ATTENUATES KIDNEY; OXIDATIVE STRESS; CELL-ACTIVATION; RENAL FIBROSIS; MOUSE MODEL;
D O I
10.1097/MNH.0000000000000291
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewThis article analyzes the potential beneficial effects of dipeptidyl peptidase (DPP)-4 inhibitors on renal diseases.Recent findingsThe pathological significance of DPP-4, either dependent or independent on catalytic activities, on renal diseases has been reported in preclinical studies. With regard to this, we have shown that damaged endothelial cells are converted to a mesenchymal cell phenotype, which is associated with the induction of DPP-4 in endothelial cells. The endothelial mesenchymal transition may contribute to kidney fibrosis; indeed, the antifibrotic effects of DPP-4 inhibitors have been reported elsewhere. However, even though such potential benefits of DPP-4 inhibitors on renal diseases were shown in preclinical studies, clinical trials have not yet revealed significant benefits in renal hard outcomes of DPP-4 inhibitors.SummaryTo completely understand the beneficial effects of DPP-4 inhibitors, both the following studies are required: first, preclinical studies that analyze deeper molecular mechanisms of DPP-4 inhibition, and, second, clinical studies that investigate whether such potential beneficial effects of DPP-4 inhibitors are relevant to the patients in the clinic.
引用
收藏
页码:56 / 66
页数:11
相关论文
共 89 条
[1]   DPP-4 inhibitor sitagliptin prevents inflammation and oxidative stress of heart and kidney in two kidney and one clip (2K1C) rats [J].
Alam, Md. Ashraful ;
Chowdhury, Mohammed Riaz Hasan ;
Jain, Preeti ;
Sagor, Md. Abu Taher ;
Reza, Hasan Mahmud .
DIABETOLOGY & METABOLIC SYNDROME, 2015, 7
[2]   DPP-4 Inhibition on Top of Angiotensin Receptor Blockade Offers a New Therapeutic Approach for Diabetic Nephropathy [J].
Alter, Markus L. ;
Ott, Ina M. ;
von Websky, Karoline ;
Tsuprykov, Oleg ;
Sharkovska, Yuliya ;
Krause-Relle, Katharina ;
Raila, Jens ;
Henze, Andrea ;
Klein, Thomas ;
Hocher, Berthold .
KIDNEY & BLOOD PRESSURE RESEARCH, 2012, 36 (01) :119-130
[3]   Des-serine-proline brain natriuretic peptide 3-32 in cardiorenal regulation [J].
Boerrigter, Guido ;
Costello-Boerrigter, Lisa C. ;
Harty, Gail J. ;
Lapp, Harald ;
Burnett, John C., Jr. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2007, 292 (02) :R897-R901
[4]   Renal fibrosis: novel insights into mechanisms and therapeutic targets [J].
Boor, Peter ;
Ostendorf, Tammo ;
Floege, Juergen .
NATURE REVIEWS NEPHROLOGY, 2010, 6 (11) :643-656
[5]   Dipeptidyl peptidase inhibition prevents diastolic dysfunction and reduces myocardial fibrosis in a Mouse model of Western diet induced obesity [J].
Bostick, Brian ;
Habibi, Javad ;
Ma, Lixin ;
Aroor, Annayya ;
Rehmer, Nathan ;
Hayden, Melvin R. ;
Sowers, James R. .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2014, 63 (08) :1000-1011
[6]   Dilpeptidyl-peptidase IV converts intact B-type natriuretic peptide into its des-SerPro form [J].
Brandt, I ;
Lambeir, AM ;
Ketelslegers, JM ;
Vanderheyden, M ;
Scharpé, S ;
De Meester, I .
CLINICAL CHEMISTRY, 2006, 52 (01) :82-87
[7]   Dipeptidylpeptidase 4 negatively regulates colony-stimulating factor activity and stress hematopoiesis [J].
Broxmeyer, Hal E. ;
Hoggatt, Jonathan ;
O'Leary, Heather A. ;
Mantel, Charlie ;
Chitteti, Brahmananda R. ;
Cooper, Scott ;
Messina-Graham, Steven ;
Hangoc, Giao ;
Farag, Sherif ;
Rohrabaugh, Sara L. ;
Ou, Xuan ;
Speth, Jennifer ;
Pelus, Louis M. ;
Srour, Edward F. ;
Campbell, Timothy B. .
NATURE MEDICINE, 2012, 18 (12) :1786-+
[8]   FGF Regulates TGF-β Signaling and Endothelial-to-Mesenchymal Transition via Control of let-7 miRNA Expression [J].
Chen, Pei-Yu ;
Qin, Lingfeng ;
Barnes, Carmen ;
Charisse, Klaus ;
Yi, Tai ;
Zhang, Xinbo ;
Ali, Rahmat ;
Medina, Pedro P. ;
Yu, Jun ;
Slack, Frank J. ;
Anderson, Daniel G. ;
Kotelianski, Victor ;
Wang, Fen ;
Tellides, George ;
Simons, Michael .
CELL REPORTS, 2012, 2 (06) :1684-1696
[9]   One site mutation disrupts dimer formation in human DPP-IV proteins [J].
Chien, CH ;
Huang, LH ;
Chou, CY ;
Chen, YS ;
Han, YS ;
Chang, GG ;
Liang, PH ;
Chen, X .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (50) :52338-52345
[10]   On the origin of serum CD26 and its altered concentration in cancer patients [J].
Cordero, Oscar J. ;
Salgado, Francisco J. ;
Nogueira, Montserrat .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2009, 58 (11) :1725-1749