4.7 Article

Lycopene intervention reduces inflammation and improves HDL functionality in moderately overweight middle-aged individuals

Journal

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
Volume 24, Issue 1, Pages 163-168

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2012.03.015

Keywords

Lycopene; HDL2&3 functionality; Inflammation; Serum amyloid A; HDL-associated enzymes

Funding

  1. Foods Standards Agency/Department of Health [NO2038]
  2. MRC [MR/K023241/1] Funding Source: UKRI
  3. Medical Research Council [MR/K023241/1] Funding Source: researchfish

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The management of overweight subjects by interventions aimed at reducing inflammation is highly desirable. To date, observational studies have identified a link between increased dietary antioxidant intake and reduced cardiovascular morbidity. However, direct trial evidence regarding the ability of antioxidants to influence inflammation is lacking. Therefore, this study examined lycopene's ability to lower systemic and high-density lipoprotein (HDL)-associated inflammation in moderately overweight middle-aged subjects. Serum was collected before and after a 12-week intervention from 54 moderately overweight, middle-aged individuals. Subjects were randomised to one of three groups: control diet (<10 mg lycopene/week), lycopene-rich diet (224-350 mg lycopene/week) and lycopene supplement (70 mg lycopene/week). HDL was subfractionated into HDL2&3 by rapid ultracentrifugation. Compliance was monitored by assessing lycopene concentration in serum and HDL2&3. Systemic and HDL-associated inflammation was assessed by measuring serum amyloid A (SAA) levels. HDL functionality was determined by monitoring the activities of paraoxonase-1 (PON-1), cholesteryl ester transfer protein (CETP) and lecithin cholesterol acyltransferase (LCAT). Lycopene increased in serum and HDL2&3 following both lycopene interventions (P<.001, for all), while SAA decreased in serum following the lycopene supplement and in HDL3 following both lycopene interventions (P<.05 for all). PON-1 activity increased in serum and HDL2&3 in both lycopene groups (P<.05, for all). Furthermore, the activity of CETP decreased in serum following the lycopene supplement, while the activity of LCAT increased in serum and HDL3 following both lycopene interventions (P<.05 for all). These results demonstrate that in moderately overweight, middle-aged subjects, increasing lycopene intake leads to changes to HDL2&3, which we suggest enhanced their antiatherogenic properties. Overall, these results show the heart-protective properties of increased lycopene intake. (C) 2013 Elsevier Inc. All rights reserved.

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