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首页> 外文期刊>Digestive Diseases and Sciences >Moxibustion inhibits apoptosis and tumor necrosis factor-alpha/tumor necrosis factor receptor 1 in the colonic epithelium of crohn's disease model rats
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Moxibustion inhibits apoptosis and tumor necrosis factor-alpha/tumor necrosis factor receptor 1 in the colonic epithelium of crohn's disease model rats

机译:艾灸抑制克罗恩病模型大鼠结肠上皮细胞凋亡和肿瘤坏死因子-α/肿瘤坏死因子受体1

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摘要

Background: Previous studies have shown that moxibustion on Tianshu (ST25) and Qihai (CV6) is effective for treating Crohn's disease. However, the mechanism of moxibustion has not been clearly elucidated. Aim: The purpose of this study was to investigate the effect of moxibustion on the inhibition of colonic epithelial cell apoptosis and on tumor necrosis factor alpha (TNF-alpha) and tumor necrosis factor receptor TNF receptor-1 (TNFR1) and TNFR2 and to determine the mechanism of its protective effect using Crohn's disease (CD) model rats. Methods and Results: The experimental CD rat models were established by the administration of trinitrobenzene sulfonic acid. In the herbs-partitioned moxibustion (HPM) and mild-warm moxibustion (MWM) groups, moxibustion was administered to Tianshu (ST25) and Qihai (CV6) acupoints once daily for 14 days. In the salicylazosulfapyridine (SASP) group, SASP was administered twice daily for 14 days. A normal control (NC) group and a model control (MC) group were also studied. The levels of TNF-alpha and its mRNA, TNFR1 as well as the rate of colonic epithelial cell apoptosis were significantly decreased in the HPM, MWM and SASP groups compared with the MC group. The HPM and MWM groups had lower mRNA expression and lower protein levels of TNF-alpha compared to the SASP group. The HPM and MWM groups exhibited less apoptosis than the SASP group. Conclusions: Moxibustion may inhibit colonic epithelial cell apoptosis by reducing the high expression of TNF-alpha and TNFR1 to protect the defective colonic epithelial barrier in CD model rats.
机译:背景:以前的研究表明,艾灸天舒(ST25)和旗海(CV6)可有效治疗克罗恩氏病。但是,艾灸的机制尚未明确阐明。目的:本研究的目的是研究艾灸对结肠上皮细胞凋亡的抑制作用以及对肿瘤坏死因子α(TNF-alpha)和肿瘤坏死因子受体TNF受体-1(TNFR1)和TNFR2的影响,并确定克罗恩病(CD)模型大鼠的保护作用机制。方法与结果:通过给予三硝基苯磺酸建立了实验性CD大鼠模型。在以草药划分的艾灸(HPM)和轻度温灸(MWM)组中,每天对天枢(ST25)和and海(CV6)穴位进行一次艾灸,持续14天。在水杨基偶氮磺吡啶(SASP)组中,每天两次给药SASP,共14天。还研究了正常对照组(NC)和模型对照组(MC)。与MC组相比,HPM,MWM和SASP组的TNF-α及其mRNA,TNFR1的水平以及结肠上皮细胞凋亡的速率显着降低。与SASP组相比,HPM和MWM组具有更低的mRNA表达和更低的TNF-α蛋白水平。 HPM和MWM组显示出比SASP组少的凋亡。结论:艾灸可能通过降低TNF-α和TNFR1的高表达来抑制结肠上皮细胞凋亡,从而保护CD模型大鼠结肠上皮屏障的缺陷。

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