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肝苏颗粒对实验性黄疸大鼠肝功能的保护及其机制 被引量:1

A study on the protective actions and mechanisms of gansu capsule in experimental icteritious rats
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摘要 目的观察肝苏颗粒对实验性黄疸大鼠的保护作用及其机制的初步探讨。方法采用α-萘异硫氰酸酯(ANIT)灌胃制备大鼠黄疸模型,共60只大鼠,设正常组、模型组、熊去氧胆酸(UDCA)组、肝苏颗粒小剂量组和肝苏颗粒大剂量组,检测不同组血清ALT、TBil和一氧化氮(NO)、IL-6的变化,流式细胞仪检测肝细胞凋亡,免疫组化检测肝细胞Bcl-2、Bax蛋白的表达。结果肝苏颗粒大、小剂量治疗组和UDCA组与模型组比较,ALT及TBil降低明显,ALT分别为(547.20±79.41)U/L、(573.34±68.79)U/L、(535.60±69.39)U/L、(642.30±92.70)U/L,TBil分别为(47.10±11.54)μmol/L、(50.87±13.46)μmol/L、(45.22±14.46)μmol/L、(66.19±10.67)μmol/L,差异有统计学意义(P<0.05或P<0.01)。肝苏颗粒治疗组和UDCA组NO、IL-6水平与模型组比较下降显著,差异有统计学意义(P<0.01或P<0.05)。肝苏颗粒治疗组、UDCA组与模型组比较,肝细胞凋亡率下降,差异有统计学意义(P<0.01或P<0.05);肝苏颗粒大剂量治疗组、UDCA组Bcl-2和Bax阳性表达及Bax/Bcl-2相对比率明显低于模型组,差异有统计学意义(P<0.01或P<0.05)。结论肝苏颗粒对实验性黄疸大鼠的肝功能具保护作用,影响血清NO、IL-6及抑制肝细胞凋亡可能是其退黄、恢复肝脏功能的作用机制之一。 Objective To study the effect and mechanisms of gansu capsule in experimental icteritious rats. Methods The experimental icteritious model was made by per/using alpha-naphthyli- sothiocyanate (ANIT) by mouth in Wistar rats. Normal control group, experimental icteritious model group, ursodeoxycholic acid (UDCA) group, gansu capsule low dose group and gansu capsule high dose group were set up. The levels of alanine aminotransferase (ALT), total bilirubin (TBil), nitric oxide (NO), interleukin-6 (IL-6) in blood plasma of the five groups were examined. The rates of apoptosis of hepatocytes were analysed by flow cytometry. The expression of Bax and Bcl-2 was detected qualitatively and quantitatively by immunohistochemistry assay using an image analysis system. Results The levels of ALT and TBil in the gansu capsule treatment group (large dose group and small dose group) and UDCA group were lower than those of the experimental icteritious model group. ALT was (547.20 ± 79.41) U/L, (573.34 ±68.79) U/L, (535.60 ± 69.39) U/L, (642.30 ±92.70) U/L respectively and TBil was (47.10± 11.54) μ/mol/L, (50.87 ± 13.46) μmol/L, (45.22 ±14.46)μmol/L, (66.19 ±10.67) μmol/L respectively. The differences between the gansu capsule groups or UDCA group and the model group were significant (P 〈0.01 or P 〈 0.05). The levels of NO and IL-6 in the gansu capsule groups and the UDCA group were lower than those of the model group, and the differences were significant (P 〈 0.01 or P 〈 0.05) . The rates of hepatocytes apoptosis of the gansu capsule treatment groups or the UDCA group were lower than that of the model group, and the differences were significant (P 〈 0.01 or P 〈0.05). The comparing ratios of Bax and Bcl-2 proteins (Bax/Bcl-2) expressed in hepatocytes in gansu capsule high dose group and UDCA group were lower than that of the model group, the differences were significant (P 〈 0.01 or P 〈 0. 05). Conclusion Gansu capsule influence secretion of NO and IL-6 level in plasma and inhibit hepatocytes apoptosis to protect liver.
出处 《中华传染病杂志》 CAS CSCD 北大核心 2007年第3期143-146,共4页 Chinese Journal of Infectious Diseases
关键词 肝苏颗粒 黄疸 一氧化氮 白细胞介素6 细胞凋亡 Gansu capsule Jaundice Nitric oxide Interleukin-6 Apoptosis
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  • 1Povero D, Busletta C, Novo E, et al. Liver fibrosis: a dynamic and potentially reversible process. Histol Histopathol, 2010, 25 (8): 1075-1091.
  • 2Pinzani M, Rombouts K. Liver fibrosis: from the bench to clinical targets. Dig Liver Dis, 2004, 36 (4): 231-242.
  • 3Desmyter L, Fan YD, Praet M, et al. Rating of CCl(4)- induced rat liver fibrosis by blood serum glycomics. J Gastroenterol Hepatol, 2007, 22 (7): 1148-1154.
  • 4Huang Q, Xie Q, Shi CC, et al. Expression of angiotensin-converting enzyme 2 in CCIA-induced rat liver fibrosis. Int J Mol Med. 2009. 23 (6): 717-723.
  • 5Muriel P, Moreno MG, Hernandez Mdel C, et al. Resolution of liver fibrosis in chronic CC14 administration in the rat after discontinuation of treatment: effect of silymarin, silibinin, eolehicine and trimethylcolehieinic acid. Basic Clin Pharmacol Toxicol, 2005, 96 (5): 375- 380.
  • 6Molina MF, Sanchez-Reus I, Iglesias I, et al. Quercetin, a flavonoid antioxidant, prevents and protects against ethanoMnduced oxidative stress in mouse liver. Biol Pharm Bull, 2003, 26 (10): 1398-1402.
  • 7Renugadevi J, Prabu SM. Quercetin protects against oxidative stress-related renal dysfunction by cadmium in rats. Exp Toxicol Pathol, 2010, 62 (5): 471-481.
  • 8Liu CM, Ma JQ, Sun YZ. Quercetin protects the rat kidney against oxidative stress-mediated DNA damage and apoptosis induced by lead. Environ Toxicol Pharmacol, 30 (3): 264-271.
  • 9Shinno E, Shimoji M, Imaizumi N, et al. Activation of rat liver microsomal glutathione S-transferase by gallic acid. Life Sci, 2005, 78 (1): 99-106.
  • 10Rasool MK, Sabina EP, Ramya SR, et al. Hepatoprotective and antioxidant effects of gallic acid in paracetamol-induced liver damage in mice. J Pharm Pharmacol, 2010, 62 (5): 638-643.

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