Archives of Medical Science · 2016 · 41 citations · 16 references
Veterinary MedicineBiochemistryPathobiologyApoptosisInflammationNutritional BiochemistryAntifibrotic TherapyFibrosisHepatic FibrosisHepatic PathophysiologyLiver DiseaseLiver PhysiologyC-jun N-terminal Kinase SignalingC/ebp Homologous ProteinEndoplasmic Reticulum StressEndoplasmic Reticulum Stress ResponsesJnk Signaling PathwayJnk-mediated ApoptosisJnk-mediated Apoptotic SignalingJun N-terminal Kinase Signaling
INTRODUCTION: (SPJ) against fatty liver fibrosis in mice. In this study, fatty liver fibrosis was induced by a high-fat (HF) diet combined with intraperitoneal injection of porcine serum. MATERIAL AND METHODS: The fatty liver fibrosis model was induced by HF diet combined with intraperitoneal injection of porcine serum. The endoplasmic reticulum stress (ERS) response and C/EBP homologous protein (CHOP) and p-Jun N-terminal kinase (JNK)-mediated apoptosis and inflammation were assessed by serum biochemistry, hematoxylin-eosin (H + E), Masson and electronic microscopy staining, Hyp content detection, Western blotting and real time polymerase chain reaction (RT-PCR). RESULTS: could significantly improve liver function and decrease the lipid level in the serum. The liver steatosis, collagen fibers and inflammatory cell infiltration were significantly improved in the SPJ group according to microscope observation. The RT-PCR analysis revealed that the collagen I (Coll), α smooth muscle actin (α-SMA), tissue inhibitors of MMPs (TIMP), CHOP and GRP78 mRNA expression levels were distinctly weakened by SPJ treatment; and western blotting analysis indicated that the phosphorylated JNK (p-JNK), Coll and 78 kD glucose-regulated protein (GRP78) protein expression levels were significantly alleviated, which might be associated with the inhibition of the ERS response and the CHOP and JNK-mediated apoptosis and inflammation pathway. CONCLUSIONS: Based on this research, SPJ as a preventive medicine has great potential in prevention of liver fibrosis.
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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
PubMed · 1997 · 66.6K citations
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Medicine, Endocrinology, Hepatology +14
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