Lutein and Zeaxanthin Enhance, Whereas Oxidation, Fructosylation, and Low pH Damage High-Density Lipoprotein

Jingyuan Zheng1, Brian V Hong1, Joanne K Agus1

  • 1Department of Nutrition, University of California Davis, Davis, CA 95616, USA.

Insights

Chronic diseases impair high-density lipoproteins (HDL) function. Antioxidant carotenoids, lutein and zeaxanthin, protect HDL against functional loss, improving cholesterol efflux and antioxidant activity, while disease factors like oxidation and high fructose impair HDL function.

Area of Science:

  • Lipid Metabolism and Cardiovascular Health
  • Biochemistry of Oxidative Stress and Antioxidants

Background:

  • High-density lipoproteins (HDLs) are crucial for cholesterol homeostasis but lose function in chronic diseases.
  • Factors causing HDL functional decline and the protective roles of carotenoids remain unclear.

Purpose of the Study:

  • To investigate the impact of disease-associated factors (oxidants, pH, sugars, enzymes) on HDL functionality.
  • To determine the protective effects of carotenoid antioxidants lutein and zeaxanthin on HDL function.

Main Methods:

  • Isolated HDL from human plasma and exposed it to various chemical treatments.
  • Assessed HDL functionality by measuring cholesterol efflux capacity (CEC), LCAT activity, and PON1 activity.
  • Analyzed changes in HDL particle diameter.

Main Results:

  • Acidic pH, oxidation, and high fructose significantly reduced HDL's cholesterol efflux capacity.
  • Lutein and zeaxanthin improved HDL cholesterol efflux and antioxidant activity (PON1).
  • Oxidizing agents, high fructose, and low pH impaired HDL maturation and function; deglycosylation reduced antioxidant capacity.

Conclusions:

  • Oxidative stress, high fructose, and acidic pH are detrimental to HDL functionality, impacting cholesterol transport and particle integrity.
  • Lutein and zeaxanthin demonstrate significant potential in preserving and enhancing HDL's beneficial cholesterol efflux and antioxidant properties.
  • Understanding these interactions is key to developing strategies against HDL dysfunction in chronic diseases.

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