TY - JOUR
T1 - Bilberry juice modulates plasma concentration of NF-κB related inflammatory markers in subjects at increased risk of CVD
AU - Karlsen, Anette
AU - Paur, Ingvild
AU - Bøhn, Siv K.
AU - Sakhi, Amrit K.
AU - Borge, Grethe I.
AU - Serafini, Mauro
AU - Erlund, Iris
AU - Laake, Petter
AU - Tonstad, Serena
AU - Blomhoff, Rune
N1 - Funding Information:
Acknowledgments This research received grants from the Norwegian Research Council and the Throne–Holst Foundation. The participation of study subjects recruited through an advertisement in a local newspaper and from the Department of Preventive Cardiology, Ullevål University Hospital, Oslo, Norway, is greatly appreciated. The enthusiastic support of Lisa Flakk at the Department of Preventive Cardiology at Ullevål University Hospital in coordinating the study is highly appreciated. Kari Holte has provided valuable help in the laboratory. We are also grateful to Dr Janne Reseland at Institute of Clinical Dentistry, University of Oslo, Norway, for providing their facilities for cytokine analysis. RB and ST formulated the present hypothesis. IP was responsible for the cell culture experiments, and the data handling and statistical analysis associated with these. ST was the overall principal investigator of the clinical study. RB and AK contributed to the clinical study design, intervention, sample handling and data collection. SKB was responsible for the analysis of inflammatory mediators in plasma samples. AKS was responsible for analysis of glutathione in plasma samples. GIB was responsible for the analysis of ORAC in plasma. MS was responsible for the analysis of TRAP in plasma. IE was responsible for the analysis of polyphenols in plasma. AK was responsible for analysis of additional parameters in plasma samples. AK and PL were responsible for the statistical analysis for the clinical study. AK and IP were responsible for writing the manuscript. All authors approved the final version of the manuscript before submission.
PY - 2010/9
Y1 - 2010/9
N2 - Purpose: Bilberries are abundant in polyphenols. Dietary polyphenols have been associated with strategies for prevention and treatment of chronic inflammatory diseases. We investigated the effect of bilberry juice on serum and plasma biomarkers of inflammation and antioxidant status in subjects with elevated levels of at least one risk factor for cardiovascular disease (CVD). Methods: In a randomized controlled trial, participants consumed either bilberry juice (n = 31) or water (n = 31) for 4 weeks. Results: Supplementation with bilberry juice resulted in significant decreases in plasma concentrations of C-reactive protein (CRP), interleukin (IL)-6, IL-15, and monokine induced by INF-γ (MIG). Unexpectedly, an increase in the plasma concentration of tumor nuclear factor-α (TNF-α) was observed in the bilberry group. CRP, IL-6, IL15, MIG, and TNF-α are all target genes of nuclear factor- kappa B (NF-κB), -a transcription factor that is crucial in orchestrating inflammatory responses. Plasma quercetin and p-coumaric acid increased in the bilberry group, otherwise no differences were observed for clinical parameters, oxidative stress or antioxidant status. Furthermore, we studied the effect of polyphenols from bilberries on lipopolysaccharide (LPS)-induced NF-κB activation in a monocytic cell line. We observed that quercetin, epicatechin, and resveratrol inhibited NF-κB activation. Conclusions: These findings suggest that supplementation with bilberry polyphenols may modulate the inflammation processes. Further testing of bilberry supplementation as a potential strategy in prevention and treatment of chronic inflammatory diseases is warranted. © 2010 Springer-Verlag.
AB - Purpose: Bilberries are abundant in polyphenols. Dietary polyphenols have been associated with strategies for prevention and treatment of chronic inflammatory diseases. We investigated the effect of bilberry juice on serum and plasma biomarkers of inflammation and antioxidant status in subjects with elevated levels of at least one risk factor for cardiovascular disease (CVD). Methods: In a randomized controlled trial, participants consumed either bilberry juice (n = 31) or water (n = 31) for 4 weeks. Results: Supplementation with bilberry juice resulted in significant decreases in plasma concentrations of C-reactive protein (CRP), interleukin (IL)-6, IL-15, and monokine induced by INF-γ (MIG). Unexpectedly, an increase in the plasma concentration of tumor nuclear factor-α (TNF-α) was observed in the bilberry group. CRP, IL-6, IL15, MIG, and TNF-α are all target genes of nuclear factor- kappa B (NF-κB), -a transcription factor that is crucial in orchestrating inflammatory responses. Plasma quercetin and p-coumaric acid increased in the bilberry group, otherwise no differences were observed for clinical parameters, oxidative stress or antioxidant status. Furthermore, we studied the effect of polyphenols from bilberries on lipopolysaccharide (LPS)-induced NF-κB activation in a monocytic cell line. We observed that quercetin, epicatechin, and resveratrol inhibited NF-κB activation. Conclusions: These findings suggest that supplementation with bilberry polyphenols may modulate the inflammation processes. Further testing of bilberry supplementation as a potential strategy in prevention and treatment of chronic inflammatory diseases is warranted. © 2010 Springer-Verlag.
KW - Bilberry
KW - Cell culture
KW - Cytokines
KW - Human intervention
KW - NF-κB
KW - Polyphenols
KW - Vaccinium myrtillus/chemistry
KW - Humans
KW - Middle Aged
KW - Anti-Inflammatory Agents, Non-Steroidal/pharmacology
KW - Phenols/pharmacology
KW - Flavonoids/pharmacology
KW - Male
KW - Cardiovascular Diseases/blood
KW - U937 Cells
KW - Adult
KW - Biomarkers/blood
KW - Female
KW - Beverages/analysis
KW - Risk Factors
KW - Monocytes/drug effects
KW - C-Reactive Protein/analysis
KW - Cytokines/blood
KW - Fruit/chemistry
KW - Inflammation Mediators/blood
KW - Aged
KW - NF-kappa B/antagonists & inhibitors
KW - Dietary Supplements
KW - Lipopolysaccharides/toxicity
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UR - https://www.mendeley.com/catalogue/1757995c-cbfe-3221-aa5a-083c8d175656/
U2 - 10.1007/s00394-010-0092-0
DO - 10.1007/s00394-010-0092-0
M3 - Article
C2 - 20119859
SN - 1436-6207
VL - 49
SP - 345
EP - 355
JO - European Journal of Nutrition
JF - European Journal of Nutrition
IS - 6
ER -