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. 2017:2017:1583098.
doi: 10.1155/2017/1583098. Epub 2017 Mar 15.

Cinnamon Polyphenol Extract Inhibits Hyperlipidemia and Inflammation by Modulation of Transcription Factors in High-Fat Diet-Fed Rats

Affiliations

Cinnamon Polyphenol Extract Inhibits Hyperlipidemia and Inflammation by Modulation of Transcription Factors in High-Fat Diet-Fed Rats

Zeynep Tuzcu et al. Oxid Med Cell Longev. 2017.

Abstract

We evaluated the effects of cinnamon polyphenol extract on hepatic transcription factors expressions including SREBP-1c and LXR-α in rats fed high fat diet (HFD). Twenty-eight Wistar rats were allocated into four groups: (i) normal control: animals fed with normal chow; (ii) cinnamon: animals supplemented with cinnamon polyphenol; (iii) HFD: animals fed a high-fat diet; and (iv) HFD + cinnamon: animals fed a high-fat diet and treated with cinnamon polyphenol. Obesity was linked to hyperglycemia, hyperlipidemia, and oxidative stress as imitated by elevated serum glucose, lipid profile, and serum and liver malondialdehyde (MDA) concentrations. Cinnamon polyphenol decreased body weight, visceral fat, liver weight and serum glucose and insulin concentrations, liver antioxidant enzymes, and lipid profile (P < 0.05) and reduced serum and liver MDA concentration compared to HFD rats (P < 0.05). Cinnamon polyphenol also suppressed the hepatic SREBP-1c, LXR-α, ACLY, FAS, and NF-κB p65 expressions and enhanced the PPAR-α, IRS-1, Nrf2, and HO-1 expressions in the HFD rat livers (P < 0.05). In conclusion, cinnamon polyphenol reduces the hyperlipidemia, inflammation, and oxidative stress through activating transcription factors and antioxidative defense signaling pathway in HFD rat liver.

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Figures

Figure 1
Figure 1
Hepatic SREBP-1c, LXRs, ACLY, and FAS expression levels in cinnamon polyphenol supplemented high-fat diet- (HFD-) fed rats and control groups. (a)–(d) show the expression level of SREBP-1c, LXRs, ACLY, and FAS in various groups. The intensity of the bands shown in (e) was quantified by densitometric analysis. Data are expressed as a ratio of normal control value (set to 100%). Each bar represents the mean and standard error of mean. Blots were repeated at least 3 times (n = 3) and only a representative blot is shown in (e). β-Actin was included to ensure equal protein loading.
Figure 2
Figure 2
Hepatic PPARα and IRS expression levels in cinnamon polyphenol supplemented high-fat diet- (HFD-) fed rats and control groups. (a) and (b) show the expression level of PPARα and IRS in the groups. The intensity of the bands shown in (c) was quantified by densitometric analysis. Data are expressed as a ratio of normal control value (set to 100%). Each bar represents the mean and standard error of mean. Blots were repeated at least 3 times (n = 3) and only a representative blot is shown in (c). β-Actin was included to ensure equal protein loading.
Figure 3
Figure 3
Hepatic NF-κB p65, Nrf2, and HO-1 expression levels in cinnamon polyphenol supplemented high-fat diet- (HFD-) fed rats and control groups. (a)–(c) show the expression level of NF-κB p65, Nrf2, and HO-1 in the groups. The intensity of the bands shown in (d) was quantified by densitometric analysis. Data are expressed as a ratio of normal control value (set to 100%). Each bar represents the mean and standard error of mean. Blots were repeated at least 3 times (n = 3) and only a representative blot is shown in (d). β-Actin was included to ensure equal protein loading.

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