Journal article
Dipeptidyl peptidase IV inhibitors as novel regulators of vascular disease
- Abstract:
- Dipeptidyl peptidase IV (DPP-IV) has been revealed as an adipokine with potential relevance in cardiovascular disease (CVD), while clinically used DPP-IV inhibitors have demonstrated beneficial cardiovascular effects in several experimental studies. Perivascular adipose tissue (PVAT) is a unique adipose tissue depot in close anatomical proximity and bidirectional functional interaction with the vascular wall, which is a source of DPP-IV and its biology may be influenced by DPP-IV inhibition. Recently, DPP-IV inhibition has been associated with decreased local inflammation and oxidative stress both in the vascular wall and the PVAT, potentially regulating atherogenesis progression in vivo. DPP-IV inhibition may thus be a promising target in cardiovascular disease. However, the exact pleiotropic mechanisms that underlie the cardiovascular effects of DPP-IV inhibition need to be clarified, while the in vivo benefit of DPP-IV inhibition in humans remains unclear.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 540.6KB, Terms of use)
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- Publisher copy:
- 10.1016/j.vph.2017.07.001
Authors
+ NovoNordisk Foundation
More from this funder
- Funding agency for:
- Antoniades, C
- Grant:
- NNF15CC0018486
+ British Heart Foundation
More from this funder
- Funding agency for:
- Antoniades, C
- Grant:
- NNF15CC0018486
+ National Institute for Health Research
More from this funder
- Funding agency for:
- Antoniades, C
- Grant:
- NNF15CC0018486
- Publisher:
- Elsevier
- Journal:
- Vascular Pharmacology More from this journal
- Volume:
- 96-98
- Pages:
- 1-4
- Publication date:
- 2017-07-08
- Acceptance date:
- 2017-07-01
- DOI:
- EISSN:
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1879-3649
- ISSN:
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1537-1891
- Language:
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English
- Keywords:
- Pubs id:
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pubs:708117
- UUID:
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uuid:a6b83ba7-b817-4476-a5d7-6c4652cd8c2e
- Local pid:
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pubs:708117
- Source identifiers:
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708117
- Deposit date:
-
2017-07-21
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier Inc
- Copyright date:
- 2017
- Notes:
- Copyright © 2017 Elsevier Inc. This is the accepted manuscript version of the article. The final version is available online from Elsevier at: https://doi.org/10.1016/j.vph.2017.07.001
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