12- and 15-lipoxygenases in adipose tissue inflammation
► 12- and 15-lipoxygenases are expressed in many tissues, including adipose tissue. ► 12- and 15-lipoxygenases can generate pro- and anti-inflammatory metabolites. ► 12-Lipoxygenase activity in adipocytes is required for adipocyte differentiation. ► 12- and 15-lipoxygenases in obesity promote the on...
Saved in:
Published in | Prostaglandins & other lipid mediators Vol. 104-105; pp. 84 - 92 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.07.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | ► 12- and 15-lipoxygenases are expressed in many tissues, including adipose tissue. ► 12- and 15-lipoxygenases can generate pro- and anti-inflammatory metabolites. ► 12-Lipoxygenase activity in adipocytes is required for adipocyte differentiation. ► 12- and 15-lipoxygenases in obesity promote the onset of metabolic dysfunction. ► Therapeutics against 12- and 15-lipoxygenases may treat metabolic dysfunction.
The lipoxygenases (LOs) are principal enzymes involved in the oxidative metabolism of polyunsaturated fatty acids, including arachidonic acid. 12- and 15-LO and their lipid metabolites have been implicated in the development of insulin resistance and diabetes. Adipose tissue, and in particular visceral adipose tissue, plays a primary role in the development of the inflammation seen in these conditions. 12- and 15-LO and their lipid metabolites act as upstream regulators of many of the cytokines involved in the inflammatory response in adipose tissue. While the role that 12- and 15-LO play in chronically inflamed adipose tissue is becoming clearer, there are still many questions that remain unanswered regarding their activation, signaling pathways, and roles in healthy fat. 12- and 15-LO also generate products with anti-inflammatory properties that are under investigation. Therefore, 12- and 15-LO have the potential to be very important targets for therapeutics aimed at reducing insulin resistance and the comorbid conditions associated with obesity. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 |
ISSN: | 1098-8823 |
DOI: | 10.1016/j.prostaglandins.2012.07.004 |