Journal article
Unravelling the adiponectin paradox: novel roles of adiponectin in the regulation of cardiovascular disease
- Abstract:
- Adipose tissue (AT) has recently been identified as a dynamic endocrine organ secreting a wide range of adipokines. Adiponectin is one such hormone, exerting endocrine and paracrine effects on the cardiovascular system. At a cellular and molecular level, adiponectin has anti‐inflammatory, antioxidant and anti‐apoptotic roles, thereby mitigating key mechanisms underlying cardiovascular disease (CVD) pathogenesis. However, adiponectin expression in human AT as well as its circulating levels are increased in advanced CVD states, and it is actually considered by many as a ‘rescue hormone’. Due to the complex mechanisms regulating adiponectin's biosynthesis in the human AT, measurement of its levels as a biomarker in CVD is highly controversial, given that adiponectin exerts protective effects on the cardiovascular system but at the same time its increased levels flag advanced CVD. In this review article, we present the involvement of adiponectin in CVD pathogenesis and we discuss its role as a clinical biomarker.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 385.4KB, Terms of use)
-
- Publisher copy:
- 10.1111/bph.13619
Authors
+ British Heart Foundation
More from this funder
- Funding agency for:
- Antoniades, C
- Grant:
- PG/13/56/30383
- Publisher:
- Wiley
- Journal:
- British Journal of Pharmacology More from this journal
- Volume:
- 174
- Issue:
- 22
- Pages:
- 4007-4020
- Publication date:
- 2016-09-15
- Acceptance date:
- 2016-08-31
- DOI:
- EISSN:
-
1476-5381
- ISSN:
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0007-1188
- Pmid:
-
27629236
- Language:
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English
- Keywords:
- Pubs id:
-
pubs:645889
- UUID:
-
uuid:9e4f8041-a66d-44c1-ae6c-09d0c26f7671
- Local pid:
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pubs:645889
- Source identifiers:
-
645889
- Deposit date:
-
2016-10-05
Terms of use
- Copyright holder:
- The British Pharmacological Society
- Copyright date:
- 2016
- Notes:
- © 2016 The British Pharmacological Society. This is the accepted manuscript version of the article. The final version is available online from Wiley at: https://doi.org/10.1111/bph.13619
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