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Inflammation and metabolic dysfunction: links to cardiovascular diseases

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00907.2011

关键词

adipokines; adipose tissue

资金

  1. Ministerium fur Wissenschaft und Forschung des Landes Nordrhein-Westfalen (Ministry of Science and Research of the State of North Rhine-Westphalia)
  2. Bundesministerium fur Gesundheit (Federal Ministry of Health)
  3. Commission of the European Communities [HEALTH-F2-2008-201100]
  4. European Union COST [BM0602]
  5. Juhling Foundation

向作者/读者索取更多资源

Taube A, Schlich R, Sell H, Eckardt K, Eckel J. Inflammation and metabolic dysfunction: links to cardiovascular diseases. Am J Physiol Heart Circ Physiol 302: H2148-H2165, 2012. First published March 23, 2012; doi: 10.1152/ajpheart.00907.2011. -Abdominal obesity is a major risk factor for cardiovascular disease, and recent studies highlight a key role of adipose tissue dysfunction, inflammation, and aberrant adipokine release in this process. An increased demand for lipid storage results in both hyperplasia and hypertrophy, finally leading to chronic inflammation, hypoxia, and a phenotypic change of the cellular components of adipose tissue, collectively leading to a substantially altered secretory output of adipose tissue. In this review we have assessed the adipo-vascular axis, and an overview of adipokines associated with cardiovascular disease is provided. This resulted in a first list of more than 30 adipokines. A deeper analysis only considered adipokines that have been reported to impact on inflammation and NF-kappa B activation in the vasculature. Out of these, the most prominent link to cardiovascular disease was found for leptin, TNF-alpha, adipocyte fatty acid-binding protein, interleukins, and several novel adipokines such as lipocalin-2 and pigment epithelium-derived factor. Future work will need to address the potential role of these molecules as biomarkers and/or drug targets.

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