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壬酸诱导胸腺基质淋巴细胞生成素产生并加剧小鼠过敏炎症。

Induction of thymic stromal lymphopoietin production by nonanoic acid and exacerbation of allergic inflammation in mice.

机构信息

Graduate School of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan.

出版信息

Allergol Int. 2013 Dec;62(4):463-71. doi: 10.2332/allergolint.13-OA-0552. Epub 2013 Sep 25.

Abstract

BACKGROUND

Thymic stromal lymphopoietin (TSLP) plays critical roles in the induction and exacerbation of allergic diseases. We tested various chemicals in the environment and found that xylene and 1,2,4-trimethylbenzene induced the production of TSLP in vivo. These findings prompted us to search for additional chemicals that induce TSLP production. In this study, we examined whether fatty acids could induce the production of TSLP in vivo and exacerbate allergic inflammation.

METHODS

Various fatty acids and related compounds were painted on the ear lobes of mice and the amount of TSLP in the homogenate of ear lobe tissue was determined. The effects of nonanoic acid on allergic inflammation were also examined.

RESULTS

Octanoic acid, nonanoic acid, and decanoic acid markedly induced TSLP production, while a medium-chain aldehyde and alcohol showed only weak activity. Nonanoic acid induced the production of TSLP with a maximum at 24 h. TSLP production was even observed in nonanoic acid-treated C3H/HeJ mice that lacked functional toll-like receptor 4. The aryl hydrocarbon receptor agonist β-naphthoflavone did not induce TSLP production. Nonanoic acid promoted sensitization to ovalbumin, resulting in an enhancement in the cutaneous anaphylactic response. In addition, painting of nonanoic acid after the sensitization augmented picryl chloride-induced thickening of the ear, which was reversed in TSLP receptor-deficient mice.

CONCLUSIONS

Nonanoic acid and certain fatty acids induced TSLP production, resulting in the exacerbation of allergic inflammation. We propose that TSLP-inducing chemical compounds such as nonanoic acid be recognized as chemical allergo-accelerators.

摘要

背景

胸腺基质淋巴细胞生成素(TSLP)在诱导和加剧过敏性疾病方面发挥着关键作用。我们测试了环境中的各种化学物质,发现二甲苯和 1,2,4-三甲苯在体内诱导 TSLP 的产生。这些发现促使我们寻找其他诱导 TSLP 产生的化学物质。在这项研究中,我们研究了脂肪酸是否能在体内诱导 TSLP 的产生并加剧过敏炎症。

方法

我们将各种脂肪酸和相关化合物涂在小鼠的耳垂上,然后测定耳垂组织匀浆中 TSLP 的含量。还研究了壬酸对过敏炎症的影响。

结果

辛酸、壬酸和癸酸能显著诱导 TSLP 的产生,而中链醛和醇则只有较弱的活性。壬酸诱导 TSLP 的产生在 24 小时达到最大值。在缺乏功能性 toll 样受体 4 的 C3H/HeJ 小鼠中,壬酸也能诱导 TSLP 的产生。芳基烃受体激动剂β-萘黄酮不能诱导 TSLP 的产生。壬酸促进对卵清蛋白的致敏,导致皮肤过敏反应增强。此外,致敏后涂抹壬酸会增强对二硝基氯苯引起的耳部增厚,而 TSLP 受体缺陷型小鼠则逆转了这种作用。

结论

壬酸和某些脂肪酸诱导 TSLP 的产生,导致过敏炎症的加剧。我们提出,壬酸等诱导 TSLP 产生的化学物质应被视为化学性变应原加速剂。

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