Abstract
Research into the paraoxonase (PON) gene family has flourished over the past few years. In the 1970s and 1980s, only PON1 was known, and the investigations were conducted, essentially, by toxicologists focusing on protection against organophosphate poisoning. Since then, two new members of the family, PON2 and PON3, have been identified, both being shown to play antioxidant and anti-inflammatory roles. Evidence exists indicating that the PON family is central to a wide variety of human illnesses such as cardiovascular disease, diabetes mellitus, metabolic syndrome, obesity, non-alcoholic steatohepatitis, and several mental disorders. However, research is hampered considerably by the methods currently available to measure the activity of these enzymes. In this review, we summarize the state of knowledge on PON biochemistry and function, the influence of genetic variations, and the involvement of PON in several diseases. The problems associated with PON measurement, such as sample acquisition, lack of reference methods, and variety of substrates, will be presented. Also, we cover some of the present lines of research and propose some others for future progress in this field.
Acknowledgments
The authors of this manuscript belong to the Working Group on Markers of Oxidative Stress and Inflammation of the Spanish Society of Clinical Chemistry and Molecular Pathology. Some studies described in this article have been funded by grants from the Instituto de Salud Carlos III (FIS 02/0430, 04/1752, 05/1607, RCMN C03/08, and RD06), Ministerio de Sanidad, Madrid, Spain. J. M. is the recipient of a post-graduate fellowship from the Generalitat de Catalunya (FI 05/00068).
Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.