Effects of oxymatrine on the serum levels of T helper cell 1 and 2 cytokines and the expression of the S gene in hepatitis B virus S gene transgenic mice: A study on the anti-hepatitis B virus mechanism of oxymatrine

التفاصيل البيبلوغرافية
العنوان: Effects of oxymatrine on the serum levels of T helper cell 1 and 2 cytokines and the expression of the S gene in hepatitis B virus S gene transgenic mice: A study on the anti-hepatitis B virus mechanism of oxymatrine
المؤلفون: Yu-hong Dong, Kan Jiang, Liuzhe Li, Qin-huan Wang, Hongli Xi, Yan-yan Yu
المصدر: Journal of Gastroenterology and Hepatology. 17:1299-1306
بيانات النشر: Wiley, 2002.
سنة النشر: 2002
مصطلحات موضوعية: Hepatitis B virus, Transgene, medicine.medical_treatment, Mice, Transgenic, Biology, medicine.disease_cause, Antiviral Agents, Interferon-gamma, Mice, chemistry.chemical_compound, Alkaloids, Interferon, medicine, Animals, Hepatology, Gastroenterology, Interleukin, T helper cell, Molecular biology, Interleukin-10, Oxymatrine, Cytokine, medicine.anatomical_structure, chemistry, HBeAg, Immunology, Interleukin-2, Interleukin-4, Quinolizines, medicine.drug
الوصف: BACKGROUND Oxymatrine has been shown to have a remarkable inhibitory activity to hepatitis B virus (HBV) infection with a hepatitis B virus e antigen (HBeAg) serum conversion rate of approximately 45%. In order to explore the anti-HBV mechanism of oxymatrine, the effects of oxymatrine on serum levels of T helper (h)1 cytokines (interferon (IFN)-gamma and interleukin (IL)-2) and Th2 cytokines (IL-4 and IL-10), and the expression of S gene in HBV S gene transgenic mice were studied. METHODS Each transgenic mouse was either injected with oxymatrine or saline intraperitoneally once a day for 30 days. Serum levels of IFN-gamma, IL-2, IL-4 and IL-10 were quantitated and compared to the data before the treatment. The expression of HBV S gene in transgenic mice was analyzed at the DNA, mRNA and protein levels. RESULTS The serum levels of IFN-gamma in transgenic mice before or after oxymatrine treatment were 3.108 +/- 3.172 and 11.059 +/- 6.971 pg/mL, respectively. In contrast, serum levels before and after oxymatrine treatment for IL-4 were 29.045 +/- 13.235 and 13.024 +/- 9.002 pg/mL, respectively (P < 0.001). The serum levels of IL-2 in the control (saline injection) and oxymatrine-treated mice were 1.070 +/- 0.447 and 5.537 +/- 2.887 pg/mL, respectively (P < 0.0001); and that of IL-10 were 97.226 +/- 73.306 and 33.607 +/- 23.154 pg/mL, respectively (P < 0.01). No significant differences were observed in the expression of HBV S gene in the transgenic mice at the DNA, mRNA and protein levels before or after oxymatrine treatment. CONCLUSIONS The fact that Th1 cytokines are increased while Th2 cytokines are decreased suggests that oxymatrine treatment triggers the change of immune response to hepatitis B infection in transgenic mice, which leads to improved HBV inhibitory activities. The study can help us better understand the mechanisms of the anti-HBV drug, oxymatrine, and how it has potential as an application in clinical chronic hepatitis B treatment.
تدمد: 1440-1746
0815-9319
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d761f657c093f54c196c64982596081Test
https://doi.org/10.1046/j.1440-1746.2002.02885.xTest
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....0d761f657c093f54c196c64982596081
قاعدة البيانات: OpenAIRE