Quercetin enhances adiponectin secretion by a PPAR-gamma independent mechanism
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Quercetin enhances adiponectin secretion by a PPAR-gamma independent mechanism. / Wein, Silvia; Behm, Norma; Petersen, Rasmus Koefoed ; Kristiansen, Karsten; Wolffram, Siegfried.
In: European Journal of Pharmaceutical Sciences, Vol. 41, No. 1, 11.09.2010, p. 16-22.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Quercetin enhances adiponectin secretion by a PPAR-gamma independent mechanism
AU - Wein, Silvia
AU - Behm, Norma
AU - Petersen, Rasmus Koefoed
AU - Kristiansen, Karsten
AU - Wolffram, Siegfried
N1 - Copyright (c) 2010 Elsevier B.V. All rights reserved.
PY - 2010/9/11
Y1 - 2010/9/11
N2 - To study possible insulin sensitizing, anti-inflammatory and anti-oxidative effects of the flavonol quercetin, rats were fed a high-fat diet (19%, w/w) with (HFQ) or without (HF) 0.03% quercetin or a flavonoid-poor low-fat (5%, w/w) maintenance diet (LF) over 4 weeks. Body weight was measured weekly, and plasma concentrations of adiponectin, leptin, insulin, glucose, triacylglycerols, total cholesterol, as well as of markers of inflammation and oxidative stress were measured (12h fasted) at the end of the feeding period. Adiponectin and peroxisome-proliferator-activated-receptor (PPAR)-gamma mRNA were measured in adipose tissue (WAT) by real-time RT-PCR. PPAR-gamma transactivation was investigated by means of a reporter gene assay. HF feeding resulted in elevated fasted plasma glucose concentrations, while HFQ did not differ from LF feeding. In the HFQ group plasma concentrations and WAT mRNA levels of adiponectin were elevated compared with the HF group, however, PPAR-gamma mRNA concentration in WAT was decreased (HFQ vs. HF). Compared to both other groups quercetin feeding significantly reduced oxidative stress, measured by plasma 8-iso-PGF(2alpha), while body weight gain, body composition and plasma leptin levels were not affected. Neither quercetin nor its metabolites induced PPAR-gamma-mediated transactivation in vitro. Adiponectin stimulating effects of quercetin are PPAR-gamma-independent and prevent impairment of insulin sensitivity without affecting body weight and composition.
AB - To study possible insulin sensitizing, anti-inflammatory and anti-oxidative effects of the flavonol quercetin, rats were fed a high-fat diet (19%, w/w) with (HFQ) or without (HF) 0.03% quercetin or a flavonoid-poor low-fat (5%, w/w) maintenance diet (LF) over 4 weeks. Body weight was measured weekly, and plasma concentrations of adiponectin, leptin, insulin, glucose, triacylglycerols, total cholesterol, as well as of markers of inflammation and oxidative stress were measured (12h fasted) at the end of the feeding period. Adiponectin and peroxisome-proliferator-activated-receptor (PPAR)-gamma mRNA were measured in adipose tissue (WAT) by real-time RT-PCR. PPAR-gamma transactivation was investigated by means of a reporter gene assay. HF feeding resulted in elevated fasted plasma glucose concentrations, while HFQ did not differ from LF feeding. In the HFQ group plasma concentrations and WAT mRNA levels of adiponectin were elevated compared with the HF group, however, PPAR-gamma mRNA concentration in WAT was decreased (HFQ vs. HF). Compared to both other groups quercetin feeding significantly reduced oxidative stress, measured by plasma 8-iso-PGF(2alpha), while body weight gain, body composition and plasma leptin levels were not affected. Neither quercetin nor its metabolites induced PPAR-gamma-mediated transactivation in vitro. Adiponectin stimulating effects of quercetin are PPAR-gamma-independent and prevent impairment of insulin sensitivity without affecting body weight and composition.
KW - Adiponectin
KW - Animals
KW - Blood Glucose
KW - Cells, Cultured
KW - Cholesterol
KW - Chromatography, High Pressure Liquid
KW - Insulin
KW - Leptin
KW - Male
KW - Mice
KW - Oxidative Stress
KW - PPAR gamma
KW - Quercetin
KW - RNA, Messenger
KW - Rats
KW - Rats, Wistar
KW - Reverse Transcriptase Polymerase Chain Reaction
KW - Triglycerides
U2 - 10.1016/j.ejps.2010.05.004
DO - 10.1016/j.ejps.2010.05.004
M3 - Journal article
C2 - 20580672
VL - 41
SP - 16
EP - 22
JO - Norvegica Pharmaceutica Acta
JF - Norvegica Pharmaceutica Acta
SN - 0928-0987
IS - 1
ER -
ID: 35411607