Modulatory Effect of Lifestyle-Related, Environmental and Genetic Factors on Paraoxonase-1 Activity: A Review

Int J Environ Res Public Health. 2023 Feb 5;20(4):2813. doi: 10.3390/ijerph20042813.

Abstract

Paraoxonase-1 (PON1) is a calcium-dependent, HDL-bound serum hydrolase active toward a wide variety of substrates. PON1 displays three types of activities, among which lactonase, paraoxonase, arylesterase and phosphotriesterase can be distinguished. Not only is this enzyme a major organophosphate compound detoxifier, but it is also an important constituent of the cellular antioxidant system and has anti-inflammatory and antiatherogenic functions. The concentration and activity of PON1 is highly variable among individuals, and these differences can be both of genetic origin and be a subject of epigenetic regulation. Owing to the fact that, in recent decades, the exposure of humans to an increasing number of different xenobiotics has been continuously rising, the issues concerning the role and activity of PON1 shall be reconsidered with particular attention to growing pharmaceuticals intake, dietary habits and environmental awareness. In the following manuscript, the current state of knowledge concerning the influence of certain modifiable and unmodifiable factors, including smoking, alcohol intake, gender, age and genotype variation on PON1 activity, along with pathways through which these could interfere with the enzyme's protective functions, is presented and discussed. Since exposure to certain xenobiotics plays a key role in PON1 activity, the influence of organophosphates, heavy metals and several pharmaceutical agents is also specified.

Keywords: PON1 activity; PON1 polymorphisms; antioxidants; enzyme activity regulation; paraoxonase.

Publication types

  • Review

MeSH terms

  • Antioxidants / metabolism
  • Aryldialkylphosphatase* / genetics
  • Epigenesis, Genetic*
  • Humans
  • Life Style
  • Organophosphates / metabolism
  • Smoking

Substances

  • Aryldialkylphosphatase
  • Antioxidants
  • Organophosphates
  • PON1 protein, human

Grants and funding

This research received no external funding.