2020
DOI: 10.3164/jcbn.20-88
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Trans-portal hepatic infusion of cultured bone marrow-derived mesenchymal stem cells in a steatohepatitis murine model

Abstract: The incidence of nonalcoholic steatohepatitis related liver cirrhosis is increasing. We used a steatohepatitis murine model fed a choline deficient, L amino acid defined (CDAA) diet with a single injection of carbon tetrachloride (CCl 4) to evaluate the efficacy of trans portal hepatic infusion of bone marrow derived mesenchymal stem cells (BMSCs) for liver fibrosis, liver steatosis, and oxidative stress. Mice were fed a CDAA diet and injected with a single intra peritoneal dose of CCl 4 (0.5 ml/kg) after 4 we… Show more

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Cited by 3 publications
(4 citation statements)
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“…Notably, under feeding with Western diet (WD) supplemented with 5% fructose (WDF), CCl 4 reduced the induction time and aggravated liver fibrosis in FATZO mice [93]. In comparison to CDAA-treated mice, additional treatment with a single dose of CCl 4 resulted in not merely hepatic lipid deposition but also peri-hepatocellular fibrosis [94]. HFFC diet combined with a low-dose of CCl 4 injection intraperitoneally to establish a murine NASH model with extensive fibrosis and rapid HCC progression [95].…”
Section: High-fat Diet Plus Carbon Tetrachloride (Ccl 4 ) Inductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Notably, under feeding with Western diet (WD) supplemented with 5% fructose (WDF), CCl 4 reduced the induction time and aggravated liver fibrosis in FATZO mice [93]. In comparison to CDAA-treated mice, additional treatment with a single dose of CCl 4 resulted in not merely hepatic lipid deposition but also peri-hepatocellular fibrosis [94]. HFFC diet combined with a low-dose of CCl 4 injection intraperitoneally to establish a murine NASH model with extensive fibrosis and rapid HCC progression [95].…”
Section: High-fat Diet Plus Carbon Tetrachloride (Ccl 4 ) Inductionmentioning
confidence: 99%
“…Because the pathogenesis of fatty liver is diverse and heterogenous, the mouse models available have similar pathological features but not necessarily the same processes as we see in the clinic. The ARRIVE guideline which was established by the editors of major biomedical journals provides some principles for selecting the right type of animal models in scientific research 94 .…”
Section: Mouse Models Of Nafldmentioning
confidence: 99%
“…BMMSCs showed antioxidative activity in endstage liver diseases. BMMSCs migrated into injured sites in liver fibrosis animal models [74,75], significantly reduced ROS production [76], downregulated lipid peroxidation (LPO) [75], improved SOD activity [76,77], and increased GSH [74,75] and antioxidant enzyme levels via Nrf2/HO-1 signaling pathway [75,78]. In addition to BMMSCs, human amniotic membrane-derived MSCs significantly reduced oxidative stress in decompensated liver cirrhosis [79].…”
Section: Antioxidative Capacitymentioning
confidence: 99%
“…162 Similar results were confirmed by Sasaki et al, demonstrating improved liver fibrosis, liver steatosis, and oxidative stress following intraportal injection of bone marrow-derived MSCs in a steatohepatitis murine model. 163 None of these models determined preinjection portal-lung shunt values to account for cell loss.…”
Section: Delivery Routes Of Stem Cellsmentioning
confidence: 99%