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丹皮总苷通过调节 TH1/TH2 细胞因子失衡缓解 2,4,6-三硝基苯磺酸/乙醇诱导的大鼠结肠炎。

Total glucosides of peony attenuates 2,4,6-trinitrobenzene sulfonic acid/ethanol-induced colitis in rats through adjustment of TH1/TH2 cytokines polarization.

机构信息

Department of Gastroenterology, Zhongnan Hospital of Wuhan University School of Medicine, Donghu Road 169, Wuhan, 430071, Hubei, People's Republic of China.

出版信息

Cell Biochem Biophys. 2014 Jan;68(1):83-95. doi: 10.1007/s12013-013-9696-3.


DOI:10.1007/s12013-013-9696-3
PMID:23771723
Abstract

The present study is to investigate effects of total glucosides of peony (TGP) on 2,4,6-trinitrobenzene sulfonic acid (TNBS)/ethanol-induced colitis in rats and to explore potential clinical use of TGP for treatment of inflammatory bowel disease. Sixty Sprague-Dawley rats were randomly grouped into normal controls, model controls, sulfasalazine (SASP) controls (100 mg/kg/day), and low, medium, and high-dose TGP groups (25, 50, and 100 mg/kg/day, respectively). 24 h following colonic instillation of TNBS, TGP, and SASP were given by gastric gavage three times a day for 7 days. Disease activity index (DAI), colon macroscopic damage index (CMDI), histopathological score (HPS), and myeloperoxidase (MPO) activity were evaluated. Levels of serum TNF-α, IL-1β, and IL-10 were measured by ELISA, and expression of TNF-α, IL-1β, and IL-10 mRNA and protein in colonic tissues was detected by RT-PCR and western blot, respectively. Compared with rats in the model controls, TGP (50 or 100 mg/kg/day)-treated rats with TNBS/ethanol-induced colitis showed significant improvements of DAI, CMDI, HPS, and MPO activity. Moreover, administration of TGP (50 or 100 mg/kg/day) decreased the up-regulated levels of serum TNF-α and IL-1β, and expression of TNF-α and IL-1β mRNA and protein in colonic tissues, and increased the serum IL-10 and colonic IL-10 mRNA and protein level. And there was no significant difference compared with administration of SASP (P > 0.05). TGP attenuates TNBS/ethanol-induced colitis in rats and its efficacy is similar to SASP, the potential mechanism might be related to the adjustment of Th1/Th2 cytokines polarization by decreasing pro-inflammatory cytokine TNF-α and IL-1β, and increasing anti-inflammatory cytokine IL-10.

摘要

本研究旨在探讨白芍总苷(TGP)对 2,4,6-三硝基苯磺酸(TNBS)/乙醇诱导的大鼠结肠炎的影响,并探讨 TGP 治疗炎症性肠病的潜在临床应用。将 60 只 Sprague-Dawley 大鼠随机分为正常对照组、模型对照组、柳氮磺胺吡啶(SASP)对照组(100mg/kg/天)和低、中、高剂量 TGP 组(25、50 和 100mg/kg/天)。TNBS 结肠灌胃后 24 小时,TGP 和 SASP 通过胃灌胃每天三次给药,共 7 天。评估疾病活动指数(DAI)、结肠大体损伤指数(CMDI)、组织病理学评分(HPS)和髓过氧化物酶(MPO)活性。通过 ELISA 测定血清 TNF-α、IL-1β 和 IL-10 水平,通过 RT-PCR 和 Western blot 分别检测结肠组织中 TNF-α、IL-1β 和 IL-10 mRNA 和蛋白的表达。与模型对照组大鼠相比,TNBS/乙醇诱导结肠炎的 TGP(50 或 100mg/kg/天)治疗大鼠的 DAI、CMDI、HPS 和 MPO 活性均显著改善。此外,TGP(50 或 100mg/kg/天)给药降低了血清 TNF-α 和 IL-1β 以及结肠组织中 TNF-α 和 IL-1β mRNA 和蛋白的上调水平,并增加了血清 IL-10 和结肠组织中 IL-10 mRNA 和蛋白水平。与 SASP 给药相比无显著差异(P>0.05)。TGP 减轻 TNBS/乙醇诱导的大鼠结肠炎,其疗效与 SASP 相似,其潜在机制可能与通过降低促炎细胞因子 TNF-α和 IL-1β、增加抗炎细胞因子 IL-10 来调节 Th1/Th2 细胞因子极化有关。

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