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. 2019 Sep 6;9:12848. doi: 10.1038/s41598-019-49262-2

Table 7.

Messenger expression of genes involved in the pathogenic mechanisms of fatty liver showing 2-fold or greater regulation in liver between controls and MCDD rats treated with vehicle or CeO2NPs.

Genes MCDD rats
Vehicle (n = 5) CeO2NPs (n = 4)
Insulin Signaling Pathway:
Igf1 −2.14* −4.27*,†
Igfbp1 43.05 16.71
Pklr −3.51** −4.23**
Ppargc1a 8.13 4.97**
Slc2a4 −4.88 −7.75*
Socs3 2.59 1.26
Srebf1 −1.75 −3.27*
Adipokine Signaling Pathway:
Adipor1 2.09 1.05
Cd36 7.25** 3.23***,†
Lepr 2.76 −1.02
Slc2a1 2.69 1.19
Metabolic Pathways:
Acly −2.18 −2.82
Abcg1 5.66* 2.83*
Acaca −2.17 −4.17**
Acadl 2.25 1.59
Acsm3 −1.61 −2.76
Apoa1 2.61* 1.86*
Apoc3 −1.92* −2.83**
Atp5c1 2.14 1.21
Cyp2e1 2.98 1.70
Cyp7a1 2.50 2.18
Cpt1a 3.07* 1.42
Fabp3 3.35 2.05
Fasn −2.87 −3.46
G6pc −1.24 −2.02
G6pd 3.32 1.90**
Gck 2.09 3.30
Gk 2.33* 1.44
Hmgcr 3.07 1.98
Lpl 16.11* 9.24**
Mlxipl −1.64 −2.34
Nr1h4 −2.18 −2.46*
Pck2 6.25 4.35*
Pdk4 3.01 1.24
Ppard 2.96 1.69
Scd1 −45.15*** −27.08**
Slc27a5 −5.52** −7.02*
Srebf2 2.42 1.23
Inflammatory Response:
Il1B 3.48* 1.10
Tnf 6.33 2.65
Apoptosis:
Casp3 2.34 1.14
Fas 4.41* 2.29*
Serpine1 13.76* 7.26*

Abcg1, ATP-binding cassette, subfamily G (WHITE), member 1; Acaca, Acetyl-coenzyme A carboxylase alpha; Acadl, Acyl-CoA Dehydrogenase, Long Chain; Acly, ATP citrate lyase; Acsm3, Acyl-CoA synthetase medium-chain family member 3; Adipor1, Adiponectin receptor 1; ApoA1, apolipoprotein A-1; Apoc3, Apolipoprotein C-III; Atp5c1, ATP synthase subunit gamma, mitochondrial; Casp3, Caspase 3; Cd36, Cd36 molecule (thrombospondin receptor); Cpt1a, Carnitine palmitoyltransferase 1a, liver; Cyp2e1, Cytochrome P450, family 2, subfamily e, polypeptide 1; Cyp7a1, Cytochrome P450, family 7, subfamily a, polypeptide 1; Fabp3, Fatty acid binding protein 3, muscle and heart; Fas, Fas (TNF receptor superfamily, member 6); Fasn, Fatty acid synthase; G6pc, Glucose-6-phosphatase, catalytic subunit; G6pd, Glucose-6-phosphate dehydrogenase; Gck, Glucokinase; Gk, Glycerol kinase; Hmgcr, 3-hydroxy-3-methylglutaryl-Coenzyme A reductase; Igf1, Insulin-like growth factor 1; Igfbp1, Insulin-like growth factor binding protein 1; Il1B, Interleukin 1 beta; Lepr, leptin receptor; Lpl, Lipoprotein lipase; Mlxipl, MLX interacting protein-like; Nr1h4, Nuclear receptor subfamily 1, group H, member 4; Pck2, Phosphoenolpyruvate carboxykinase 2 (mitochondrial); Pdk4, Pyruvate dehydrogenase kinase, isozyme 4; Pklr, Pyruvate kinase, liver and RBC; Ppard, Peroxisome proliferator-activated receptor delta; Ppargc1a, Peroxisome proliferator-activated receptor gamma, coactivator 1 alpha; Scd1, Stearoyl-Coenzyme A desaturase 1; Serpine1, Serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1; Slc27a5, Solute carrier family 27 (fatty acid transporter), member 5; Slc2a1, Solute carrier family 2 (facilitated glucose transporter), member 1; Slc2a4, Solute carrier family 2 (facilitated glucose transporter), member 4; Socs3, Suppressor of cytokine signaling 3; Srebf1, Sterol regulatory element binding transcription factor 1; Srebf2, Sterol regulatory element binding transcription factor 2; Tnf, Tumor necrosis factor (TNF superfamily, member 2). *p < 0.05, **p < 0.01, ***p < 0.001 vs. control rats. p < 0.05 vs. MCDD rats receiving vehicle. Unpaired Student’s t-test.