首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Life stress and diminished expression of genes encoding glucocorticoid receptor and beta(2)-adrenergic receptor in children with asthma
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Life stress and diminished expression of genes encoding glucocorticoid receptor and beta(2)-adrenergic receptor in children with asthma

机译:哮喘患儿的生活压力和糖皮质激素受体和β(2)-肾上腺素能受体编码基因的表达减少

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Despite evidence that stressful experience can exacerbate the symptoms of asthma, little is known about the biological mechanisms through which this occurs. This study examined whether life stress reduces expression of the genes coding for the glucocorticoid receptor and the beta(2)-adrenergic receptor. A total of 77 children were enrolled in the study (59% male; mean age, 13.5 years). Thirty-nine of them were physician-diagnosed with asthma, and 38 were healthy. After an in-depth interview regarding stressful experiences, leukocytes were collected through antecubital venipuncture, and real-time RT-PCR was used to quantify mRNA. Chronic stress was associated with reduced expression of mRNA for the beta(2)-adrenergic receptor among children with asthma. In the sample of healthy children, however, the direction of this effect was reversed. The occurrence of a major life event in the 6 months before the study was not sufficient to influence patterns of gene expression. When such events occurred in the context of a chronic stressor, however, their association with patterns of gene expression was accentuated. Children with asthma who simultaneously experienced acute and chronic stress exhibited a 5.5-fold reduction in glucocorticoid receptor mRNA and a 9.5-fold reduction in beta(2)-adrenergic receptor mRNA relative to children with asthma without comparable stressor exposure. These findings suggest that stressful experience diminishes expression of the glucocorticoid and beta(2)-adrenergic receptor genes in children with asthma. To the extent that it diminishes sensitivity to the antiinflammatory properties of glucocorticoids or the bronchodilatory properties of beta-agonists, this process could explain the increased asthma morbidity associated with stress.
机译:尽管有证据表明紧张的经历会加剧哮喘的症状,但对其发生的生物学机制知之甚少。这项研究检查了生活压力是否降低了糖皮质激素受体和β(2)-肾上腺素能受体编码基因的表达。研究共纳入77名儿童(男性59%;平均年龄13.5岁)。其中三十九名医生诊断为哮喘,其中三十八名健康。经过有关压力经历的深入访谈后,通过肘前静脉穿刺收集白细胞,并使用实时RT-PCR定量mRNA。慢性应激与哮喘儿童的β(2)-肾上腺素能受体mRNA表达降低有关。但是,在健康儿童的样本中,这种作用的方向相反。在研究前的6个月中发生的主要生命事件不足以影响基因表达方式。但是,当此类事件在慢性应激源的情况下发生时,它们与基因表达模式的关联就会加重。与没有可比的应激源暴露的哮喘儿童相比,同时经历急性和慢性压力的哮喘儿童表现出糖皮质激素受体mRNA降低5.5倍,β(2)-肾上腺素能受体mRNA降低9.5倍。这些发现表明,有压力的经历会减少哮喘儿童中糖皮质激素和β(2)-肾上腺素能受体基因的表达。在一定程度上降低了对糖皮质激素的抗炎特性或β受体激动剂的支气管扩张特性的敏感性,该过程可以解释与压力相关的哮喘发病率增加。

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