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膳食血红素尽管诱导热休克蛋白表达,仍可导致大鼠实验性结肠炎恶化。

Dietary heme adversely affects experimental colitis in rats, despite heat-shock protein induction.

机构信息

Top Institute Food and Nutrition, Wageningen, The Netherlands.

出版信息

Nutrition. 2011 May;27(5):590-7. doi: 10.1016/j.nut.2010.05.002. Epub 2010 Aug 12.

Abstract

OBJECTIVE

Research on dietary modulation of inflammatory bowel disease is in its infancy. Dietary heme, mimicking red meat, is cytotoxic to colonic epithelium and thus may aggravate colitis. Alternatively, heme-induced colonic stress might also result in potential protective heat-shock proteins (HSPs). Therefore, we investigated the effect of dietary heme on trinitrobenzene sulfonic acid (TNBS)-induced colitis in rats.

METHODS

Rats were fed a high-fat control diet or a similar diet supplemented with heme. After dietary adaptation, rats were rectally infused with TNBS for colitis induction or saline for sham treatment. Colitis severity was evaluated and several markers were quantified in colonic mucosa isolated 1 wk after colitis induction. Furthermore, cytotoxicity of fecal water and serum α-1-acid glycoprotein were measured.

RESULTS

Dietary heme increased cytotoxicity of the fecal water. Heme-fed sham-treated rats had higher colonic HSP-25 and heme-oxygenase-1 mRNA levels, which was confirmed by immunohistochemistry. HSP induction by heme was associated with decreased protein levels of myeloperoxidase and interleukin-1β after subsequent TNBS infusion. However, no dietary effects were observed on histologic colitis score. Furthermore, body weight gain, colon length, and food intake were lower and α-1-acid glycoprotein concentrations were higher in heme-fed colitic rats. In addition, somatostatin, involved in mucosal repair, was not changed with TNBS infusion in heme-fed rats.

CONCLUSION

Dietary heme adversely affects colitis, despite HSP induction. We speculate that the irritating influence of dietary heme, being continuously present in the colon, impairs recovery after colitis induction. A diet high in red meat might be a risk factor for inflammatory bowel disease development.

摘要

目的

关于饮食调控炎症性肠病的研究尚处于起步阶段。膳食血红素模仿红肉,对结肠上皮具有细胞毒性,因此可能加重结肠炎。或者,血红素诱导的结肠应激也可能导致潜在的保护性热休克蛋白(HSP)。因此,我们研究了膳食血红素对三硝基苯磺酸(TNBS)诱导的大鼠结肠炎的影响。

方法

大鼠喂食高脂肪对照饮食或类似饮食补充血红素。在饮食适应后,大鼠通过直肠输注 TNBS 诱导结肠炎或盐水诱导假处理。在结肠炎诱导后 1 周分离结肠黏膜,评估结肠炎严重程度并定量测定几种标志物。此外,还测量粪便水和血清α-1-酸性糖蛋白的细胞毒性。

结果

膳食血红素增加粪便水的细胞毒性。血红素喂养的假处理大鼠结肠 HSP-25 和血红素加氧酶-1 mRNA 水平较高,免疫组化证实了这一点。血红素诱导的 HSP 与随后 TNBS 输注后髓过氧化物酶和白细胞介素-1β的蛋白水平降低有关。然而,饮食对组织学结肠炎评分没有影响。此外,血红素喂养的结肠炎大鼠体重增加、结肠长度和食物摄入量减少,α-1-酸性糖蛋白浓度升高。此外,在血红素喂养的大鼠中,参与黏膜修复的生长抑素在 TNBS 输注后没有变化。

结论

尽管诱导 HSP,但膳食血红素对结肠炎有不利影响。我们推测,膳食血红素的刺激性影响持续存在于结肠中,会损害结肠炎诱导后的恢复。高红肉饮食可能是炎症性肠病发展的危险因素。

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