Table 1.
List of differentially expressed proteins after berberine8998 treatment in hamsters. The proteins were identified by TOF-AB 5600 (↑, upregulated; ↓, down-regulated).
| Protein name | Gene name | P-value | Fold of change | Protein function |
|---|---|---|---|---|
| Peroxisomal carnitine O-octanoyl transferase | Crot | 1.57×10−5 | 0.69↓ | Beta-oxidation of fatty acids. The highest activity concerns the C6 to C10 chain length substrate. |
| Alpha-N-acetyl galactosaminidase | Naga | 3.58×10−5 | 1.71↑ | Removes terminal alpha-N-acetylgalactosamine residues from glycolipids and glycopeptides. |
| Heterogeneous nuclear ribonucleoprotein K | Hnrnpk | 4.13×10−5 | 0.67↓ | One of the major pre-mRNA-binding proteins. |
| Peroxisomal acylcoenzyme A oxidase 1 | Acox1 | 1.24×10−3 | 0.52↓ | Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. |
| Acetyl-CoA acetyltransferase | Acta2 | 1.28×10−3 | 1.55↑ | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
| Apolipoprotein B-100 | Apob | 1.45×10−3 | 0.75↓ | Apolipoprotein B is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). |
| 1-phosphatidylinositol-4,5-bisphosphate phosphodiesterase delta-1 | Plcd1 | 1.58×10−3 | 1.37↑ | The production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) is mediated by activated phosphatidylinositol-specific phospholipase C enzymes. |
| Guanine nucleotide binding protein subunit beta-2-like 1 | Gnb2l1 | 2.16×10−3 | 0.69↓ | Involved in the recruitment, assembly and/or regulation of a variety of signaling molecules. |
| Uricase | Uox | 2.34×10−3 | 0.54↓ | Catalyzes the oxidation of uric acid to 5-hydroxyisourate, which is further processed to form (S)-allantoin. |
| 40S ribosomal protein S15 | Rps15 | 2.50×10−3 | 0.52↓ | Liver regeneration. Ribosomal small subunit assembly. |
| Long-chain-fatty-acid—CoA ligase 1 | ACSL1 | 2.10×10−3 | 0.50↓ | Activation of long-chain fatty acids for both synthesis of cellular lipids, and degradation via beta-oxidation. Preferentially uses oleate, arachidonate, eicosapentaenoate and docosahexaenoate as substrates. |