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促炎细胞因子对空肠营养物质转运的影响。

Effect of proinflammatory interleukins on jejunal nutrient transport.

作者信息

Hardin J, Kroeker K, Chung B, Gall D G

机构信息

Gastrointestinal Research Group, University of Calgary, Alberta, Canada.

出版信息

Gut. 2000 Aug;47(2):184-91. doi: 10.1136/gut.47.2.184.

DOI:10.1136/gut.47.2.184
PMID:10896908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1727997/
Abstract

AIM

We examined the effect of proinflammatory and anti-inflammatory interleukins on jejunal nutrient transport and expression of the sodium-glucose linked cotransporter (SGLT-1).

METHODS

3-O-methyl glucose and L-proline transport rates were examined in New Zealand White rabbit stripped, short circuited jejunal tissue. The effects of the proinflammatory cytokines interleukin (IL)-1alpha, IL-6, and IL-8, IL-1alpha plus the specific IL-1 antagonist, IL-1ra, and the anti-inflammatory cytokine IL-10 were investigated. In separate experiments, passive tissue permeability was assessed and brush border SGLT-1 expression was measured by western blot in tissues exposed to proinflammatory interleukins.

RESULTS

The proinflammatory interleukins IL-6, IL-1alpha, and IL-8 significantly increased glucose absorption compared with control levels. This increase in glucose absorption was due to an increase in mucosal to serosal flux. IL-1alpha and IL-8 also significantly increased L-proline absorption due to an increase in absorptive flux. The anti-inflammatory IL-10 had no effect on glucose transport. The receptor antagonist IL-1ra blocked the ability of IL-1alpha to stimulate glucose transport. IL-8 had no effect on passive tissue permeability. SGLT-1 content did not differ in brush border membrane vesicles (BBMV) from control or interleukin treated tissue.

CONCLUSIONS

These findings suggest that intestinal inflammation and release of inflammatory mediators such as interleukins increase nutrient absorption in the gut. The increase in glucose transport does not appear to be due to changes in BBMV SGLT-1 content.

摘要

目的

我们研究了促炎和抗炎白细胞介素对空肠营养物质转运及钠-葡萄糖协同转运蛋白(SGLT-1)表达的影响。

方法

在新西兰白兔剥离的、短路的空肠组织中检测3-O-甲基葡萄糖和L-脯氨酸的转运速率。研究了促炎细胞因子白细胞介素(IL)-1α、IL-6和IL-8、IL-1α加特异性IL-1拮抗剂IL-1ra以及抗炎细胞因子IL-10的作用。在单独的实验中,评估了被动组织通透性,并通过蛋白质印迹法测量了暴露于促炎白细胞介素的组织中刷状缘SGLT-1的表达。

结果

与对照水平相比,促炎白细胞介素IL-6、IL-1α和IL-8显著增加了葡萄糖吸收。葡萄糖吸收的增加是由于黏膜到浆膜通量的增加。IL-1α和IL-8还由于吸收通量的增加而显著增加了L-脯氨酸的吸收。抗炎性IL-10对葡萄糖转运没有影响。受体拮抗剂IL-1ra阻断了IL-1α刺激葡萄糖转运的能力。IL-8对被动组织通透性没有影响。对照组织或白细胞介素处理组织的刷状缘膜囊泡(BBMV)中SGLT-1含量没有差异。

结论

这些发现表明,肠道炎症以及白细胞介素等炎症介质 的释放会增加肠道对营养物质的吸收。葡萄糖转运的增加似乎不是由于BBMV中SGLT-1含量的变化。

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