Zingiber officinale extract administration diminishes steroyl-CoA desaturase gene expression and activity in hyperlipidemic hamster liver by reducing the oxidative and endoplasmic reticulum stress

Phytomedicine. 2018 Sep 15:48:62-69. doi: 10.1016/j.phymed.2018.04.059. Epub 2018 May 7.

Abstract

Background: Stearoyl CoA desaturases (SCD) are enzymes that convert saturated to monounsaturated fatty acids and have increased activity in hepatic steatosis.

Purpose: We aimed to investigate the potential of ginger extract (GIN) to modulate the liver SCD1 expression and activity in hyperlipidemic (HL) conditions, in order to lower lipid accumulation in the steatotic liver.

Study design/methods: Male Golden Syrian hamsters were divided in three groups: (i) fed with standard chow (N), (ii) fed with standard chow plus 3% cholesterol and 15% butter for 21 weeks (HL), (iii) HL treated with GIN (800 µg/kg body weight/day) in the last 5 weeks of fat diet (HL-GIN). Cholesterol (C), triglycerides (TG), non-esterified fatty acids (NEFA), SCD1 estimated activity (C16:1n7/C16:0; C18:1n9/C18:0) and gene expression, acetyl-CoA carboxylase (ACC), thiobarbituric acid reactive substances (TBARS), paraoxonase1 (PON1) and myeloperoxidase (MPO) were determined in the plasma and liver of all hamsters. We measured protein expression of endoplasmic reticulum stress (ERS) markers, gene and protein expression of liver X receptor α/β (LXRα/β), peroxisome proliferator-activated receptor γ (PPARγ), ATP-binding cassette sub-family G member 5/8 (ABCG5/G8) and 7α-hydroxylase1 (CYP7A1) in all hamsters' livers.

Results: In plasma, in HL-GIN versus HL hamsters, SCD1 estimated activity was lower (27%; 15%, p < 0.05), NEFA levels decreased by 91%, p < 0.001, while C and TG levels did not vary; the oxidative stress expressed as MPO and TBARS levels decreased (15%; 11%, p < 0.01), while PON1 protein increased (75%, p < 0.05). In the liver of HL-GIN versus HL, C, TG, NEFA, MPO and TBARS levels decreased (8-40%, p < 0.05) and PON1 protein levels increased (30%, p < 0.05), SCD1 estimated activity decreased (8%; 9%, p < 0.05), in parallel with the reduced gene expression of SCD1 and ACC (70-80%, p < 0.05). The protein expression of the ERS sensors decreased (30-65%, p < 0.05), while that of ABCG5/G8, CYP7A1, LXRα/β and PPARγ increased in HL-GIN (20-30%, p < 0.05) versus HL liver.

Conclusion: GIN reduces SCD1 estimated activity and expression, as well as the lipids accumulated in the livers of HL hamsters. This is achieved through a mechanism involving the decrease of the oxidative and ERS, and the enhancement of cholesterol efflux.

Keywords: ATP binding cassette transporter G5/G8; Endoplasmic reticulum stress; Ginger extract; Paraoxonase 1; Stearoyl CoA desaturases; Steatotic liver.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 5 / metabolism
  • ATP Binding Cassette Transporter, Subfamily G, Member 8 / metabolism
  • Acetyl-CoA Carboxylase / metabolism
  • Animals
  • Aryldialkylphosphatase / metabolism
  • Cholesterol / blood
  • Cholesterol 7-alpha-Hydroxylase / metabolism
  • Cricetinae
  • Endoplasmic Reticulum Stress*
  • Fatty Acids, Nonesterified / blood
  • Fatty Liver / enzymology*
  • Gene Expression
  • Liver / drug effects
  • Liver / enzymology
  • Liver X Receptors / metabolism
  • Male
  • Oxidation-Reduction
  • Oxidative Stress*
  • PPAR gamma / metabolism
  • Peroxidase / metabolism
  • Plant Extracts / pharmacology*
  • Stearoyl-CoA Desaturase / genetics
  • Stearoyl-CoA Desaturase / metabolism*
  • Thiobarbituric Acid Reactive Substances / analysis
  • Triglycerides / blood
  • Zingiber officinale / chemistry*

Substances

  • ATP Binding Cassette Transporter, Subfamily G, Member 5
  • ATP Binding Cassette Transporter, Subfamily G, Member 8
  • Fatty Acids, Nonesterified
  • Liver X Receptors
  • PPAR gamma
  • Plant Extracts
  • Thiobarbituric Acid Reactive Substances
  • Triglycerides
  • Cholesterol
  • Peroxidase
  • Cholesterol 7-alpha-Hydroxylase
  • Stearoyl-CoA Desaturase
  • Aryldialkylphosphatase
  • Acetyl-CoA Carboxylase