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1.
Journal of Clinical Hepatology ; (12): 955-958, 2021.
Article in Chinese | WPRIM | ID: wpr-875911

ABSTRACT

Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease with unknown etiology, and patients with poor response to ursodeoxycholic acid and obeticholic acid may eventually progress to liver cirrhosis and even liver failure. Liver transplantation is the only effective treatment method for PBC at present. This article elaborates on liver transplantation, survival time after liver transplantation, complications, recurrence of PBC after liver transplantation, and prospects and challenges of liver transplantation in patients with PBC, so as to provide a reference for clinical outcome and treatment after liver transplantation for PBC.

2.
Chinese Journal of Pathophysiology ; (12): 1425-1429, 2016.
Article in Chinese | WPRIM | ID: wpr-495876

ABSTRACT

AIM:To investigate the role of heat shock protein 70(HSP70)in hepatitis B virus (HBV) replica-tion.METHODS:The effect of HBV replication on the expression of HSP 70 was analyzed by RT-qPCR.The overexpres-sion efficiency of HSP70 was confirmed by Western blot .The effect of HSP70 overexpression on HBV DNA replicative in-termediates was analyzed by RT-qPCR and Southern blot .The effects of HSP70 overexpression on the expression level of HBV 3.5 kb mRNA and HBV core protein were measured by RT-qPCR and Western blot, respectively.The Effect of HSP70 overexpression on HBV promoter activity was detected by dual luciferase reporter system .RESULTS: The mRNA levels of HSP70 were inhibited by HBV replication .Overexpression of HSP70 repressed the expression of HBV DNA repli-cative intermediates, 3.5 kb mRNA and core protein, as well as HBV core promoter activity .CONCLUSION:HBV rep-lication inhibits the expression of HSP70.Overexpression of HSP70 represses HBV replication.These data suggest that HSP70 repressed HBV replication by inhibiting HBV core promoter activity .

3.
Yonsei Medical Journal ; : 625-633, 2015.
Article in English | WPRIM | ID: wpr-93957

ABSTRACT

PURPOSE: The role of IL28B gene variants and expression in hepatitis B virus (HBV) infections are not well understood. Here, we evaluated whether IL28B gene expression and rs12979860 variations are associated with HBV outcomes. MATERIALS AND METHODS: IL28B genetic variations (rs12979860) were genotyped by pyrosequencing of DNA samples from 137 individuals with chronic HBV infection [50 inactive carriers (IC), 34 chronic hepatitis B (CHB), 27 cirrhosis, 26 hepatocellular carcinoma (HCC)], and 19 healthy controls. IL28A/B mRNA expression in peripheral blood mononuclear cells was determined by qRT-PCR, and serum IL28B protein was measured by ELISA. RESULTS: Patients with IL28B C/C genotype had greater IL28A/B mRNA expression and higher IL28B protein levels than C/T patients. Within the various disease stages, compared to IC and healthy controls, IL28B expression was reduced in the CHB, cirrhosis, and HCC cohorts (CHB vs. IC, p=0.02; cirrhosis vs. IC, p=0.01; HCC vs. IC, p=0.001; CHB vs. controls, p<0.01; cirrhosis vs. controls, p<0.01; HCC vs. controls, p<0.01). When stratified with respect to serum HBV markers in the IC and CHB cohorts, IL28B mRNA and protein levels were higher in HBeAg-positive than negative individuals (p=0.01). Logistic regression analysis revealed that factors associated with high IL28B protein levels were C/C versus C/T genotype [p=0.016, odds ratio (OR)=0.25, 95% confidence interval (CI)=0.08-0.78], high alanine aminotransferase values (p<0.001, OR=8.02, 95% CI=2.64-24.4), and the IC stage of HBV infection (p<0.001). CONCLUSION: Our data suggest that IL28B genetic variations may play an important role in long-term development of disease in chronic HBV infections.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Alanine Transaminase/blood , Asian People/genetics , Biomarkers/blood , Carcinoma, Hepatocellular/genetics , Case-Control Studies , China , DNA, Viral/blood , Enzyme-Linked Immunosorbent Assay , Genotype , Hepatitis B virus/genetics , Hepatitis B, Chronic/ethnology , Interleukins/blood , Leukocytes, Mononuclear , Liver Cirrhosis/blood , Liver Neoplasms/genetics , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction
4.
China Journal of Chinese Materia Medica ; (24): 1717-1719, 2009.
Article in Chinese | WPRIM | ID: wpr-344548

ABSTRACT

<p><b>OBJECTIVE</b>To establish an HPLC method for determination of catalpol in CSF (cerebrospinal fluid) of rats.</p><p><b>METHOD</b>Rats were intravenously injected 1.0 g x L(-1) catalpol physiological saline, and the sample of CSF from subarachnoid space of the cerebrum 40 minutes of injection. The sample of CSF from normal rats was used for blank control, the all samples were preserved in a refrigerator of - 20 degrees C, and use HPLC was employed to determine the catalpol content. The separation of catalpol was performed on Hypersil C18 reversion phase chromatographic column. The mobile phase consisted of water-acetonitrile (99.5: 0.5) with a flow rate of 1.0 mL x min(-1) and detection wavelength of 210 nm.</p><p><b>RESULT</b>The linear range of catalpol in CSF was 0.5-40 mg x L(-1) (r = 0.999 7). The absolute recoveries were (90.2 +/- 1.71)%, (89.1 +/- 1.17)% and (86.9 +/- 0.98)%; and the methodological recoveries were (99.8 +/- 1.98)%, (101.1 +/- 3.04)%, (100.1 +/- 2.30)% respectively. The within-day and between-day derivation RSD were less than 4%. Catalpol was stable in a refrigerator of -20 degrees C for 15 days.</p><p><b>CONCLUSION</b>The method is simple and accurate for the determination of the content of catalpol in CSF.</p>


Subject(s)
Animals , Male , Rats , Chromatography, High Pressure Liquid , Glucosides , Cerebrospinal Fluid , Iridoid Glucosides , Iridoids , Cerebrospinal Fluid , Random Allocation , Rats, Sprague-Dawley
5.
Journal of Jilin University(Medicine Edition) ; (6)2006.
Article in Chinese | WPRIM | ID: wpr-591256

ABSTRACT

Objective To investigate the proportion of CD4+CD25highTreg and CD4+CD25+CD127low/-Treg in peripheral blood in patients with chronic hepatitis B(CHB) and determine the relationship between the proportion of CD4+CD25+Treg and clinical parameters.Methods Fresh isolated peripheral blood mononuclear cells(PBMCs) of 28 patients with CHB and 24 healthy donors were analyzed for the proportion of CD4+CD25+Treg using flow cytometry by surface staining for CD4-PC5,CD25-FITC,CD127-PE.HBsAg,HBsAb,HBeAg,HBeAb and HBcAb were evaluated.HBV DNA levels were measured using real-time RT-PCR.Results The proportions of CD4+CD25highTreg to CD4+ T cells(3.36%?2.59%) and CD4+CD25+CD127low/-Treg(4.05%?1.63%) to CD4+ T cells in patients with CHB were higher than those in health controls(1.60%?0.66%,1.75%?0.83%,P100U?L-1) had a higher fraction(4.26%?3.10%) of CD4+CD25highTreg in peripheral blood than those patients with low level ALT(ALT

6.
Chinese Journal of Medical Education Research ; (12)2005.
Article in Chinese | WPRIM | ID: wpr-623897

ABSTRACT

This article manages to find some methods to improve students' innovative spirit and ability with some pharmaceutical teaching practice

7.
Journal of Chongqing Medical University ; (12)2003.
Article in Chinese | WPRIM | ID: wpr-571691

ABSTRACT

Objective:To acquaint with situation of drug quantity of dissolving out of pharmacy tablet,we investigated the speed of dissolving out situation of domestic carbamazepine tablets(0.1?100) produced by six pharmaceutical factories.Methods:Refer to testing second methods of degree of dissolving out of pharmacy tablet in 《Pharmacopeia of China》2000 year edition,second portion.Results:Speed of dissolving out of the carbamazepine tablets(0.1g?100)produced by six pharmaceutical factories are greatly different among them,even in same one.Some accord with stipulation of degree of dissolving out of the drug within 30 minutes;while some accord with stipulation of degree of dissolving out of the drug within 60 minutes.Conclusion:speed of dissolving out of the domestic carbamazepine tablets(0.1g?100) produced by six pharmaceutical factories is quite different.

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