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FR167653是白细胞介素-1和肿瘤坏死因子-α产生的强效抑制剂,可改善实验性诱导的急性结肠炎中的结肠病变。

FR167653, a potent suppressant of interleukin-1 and tumor necrosis factor-alpha production, ameliorates colonic lesions in experimentally induced acute colitis.

作者信息

Blandino I I, Otaka M, Jin M, Komatsu K, Odashima M, Konishi N, Sato T, Kato S, Watanabe S

机构信息

First Department of Internal Medicine, Akita University School of Medicine, Akita City, Akita, Japan.

出版信息

J Gastroenterol Hepatol. 2001 Oct;16(10):1105-11. doi: 10.1046/j.1440-1746.2001.02584.x.

Abstract

BACKGROUND

Interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha) are believed to play a significant role in the pathogenesis of inflammatory bowel disease (IBD). Interleukin-1 and TNF-alpha possess overlapping and synergetic activities inducing the production in cascade of other cytokines, adhesion molecules, arachidonic acid metabolites, as well as activating immune and non-immune cells. FR167653 (C24H18FN5O2-H2SO4-H2O) is a newly synthesized organic compound with a potent inhibitory effect on IL-1beta and TNF-alpha production. We hypothesized that the suppression of IL-1 and TNF-alpha induced by FR167653 could effectively attenuate experimentally induced colonic damage.

METHODS

Colonic lesions were induced in male Sprague-Dawley rats (250-300 g) by intrarectal instillation of 4% acetic acid. The effect of FR167653 administration at 1.0, 1.5, 2.5 mg/kg per 6 h subcutaneously on acetic acid-induced colonic damage was assessed. The lesion area, microscopic findings, colonic and serum levels of TNF-alpha and IL-1beta were also evaluated.

RESULTS

Treatment with FR167653 at 1.5 and 2.5 mg/kg per 6 h was able to ameliorate the gross macroscopic appearance of colonic lesions significantly, as well as ameliorate the lesion area induced by acetic acid. Colonic mucosal TNF-alpha and IL-1beta levels of rats treated with FR167653 showed significant decrease in a dose-dependent fashion compared with the control group. In the same manner, serum TNF-alpha of rats treated with FR167653 was significantly lower than that of respective controls.

CONCLUSIONS

Subcutaneous administration of FR167653 was able to ameliorate the acute changes induced by acetic acid instillation in a dose-dependent manner. This is the first report to evaluate the dual inhibition of the production of IL-1 and TNF-alpha, offered by FR167653, in acute experimental colitis. Further studies are necessary to evaluate FR167653's efficacy and safety on long-term conditions.

摘要

背景

白细胞介素-1(IL-1)和肿瘤坏死因子-α(TNF-α)被认为在炎症性肠病(IBD)的发病机制中起重要作用。白细胞介素-1和肿瘤坏死因子-α具有重叠和协同活性,可诱导其他细胞因子、黏附分子、花生四烯酸代谢产物的级联产生,并激活免疫细胞和非免疫细胞。FR167653(C24H18FN5O2-H2SO4-H2O)是一种新合成的有机化合物,对IL-1β和TNF-α的产生具有强效抑制作用。我们假设FR167653诱导的IL-1和TNF-α的抑制可有效减轻实验性诱导的结肠损伤。

方法

通过直肠内注入4%乙酸在雄性Sprague-Dawley大鼠(250-300克)中诱导结肠损伤。评估每6小时皮下注射1.0、1.5、2.5毫克/千克FR167653对乙酸诱导的结肠损伤的影响。还评估了病变面积、微观发现、结肠和血清中TNF-α和IL-1β的水平。

结果

每6小时用1.5和2.5毫克/千克的FR167653治疗能够显著改善结肠病变的大体外观,并改善乙酸诱导的病变面积。与对照组相比,用FR167653治疗的大鼠结肠黏膜TNF-α和IL-1β水平呈剂量依赖性显著降低。同样,用FR167653治疗的大鼠血清TNF-α明显低于各自的对照组。

结论

皮下注射FR167653能够以剂量依赖性方式改善乙酸注入诱导的急性变化。这是第一份评估FR167653在急性实验性结肠炎中对IL-1和TNF-α产生的双重抑制作用的报告。有必要进行进一步研究以评估FR167653在长期情况下的疗效和安全性。

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