首页> 外文期刊>Psychological science: a journal of the American Psychological Society >Targeted Rejection Predicts Decreased Anti-Inflammatory Gene Expression and Increased Symptom Severity in Youth With Asthma
【24h】

Targeted Rejection Predicts Decreased Anti-Inflammatory Gene Expression and Increased Symptom Severity in Youth With Asthma

机译:定向排斥预测哮喘青年的抗炎基因表达减少,症状严重程度增加

获取原文
获取原文并翻译 | 示例
       

摘要

Although responses to different stressors are sometimes assumed to be similar, recent research has demonstrated that certain types of stress, such as targeted rejection, are particularly potent. To test such associations in a chronic-disease model, we examined how noninterpersonal, interpersonal, and targeted-rejection major life events predicted changes in gene expression and symptom severity in 121 youths with asthma who were assessed every 6 months for 2 years. Youths who had recently experienced targeted rejection had lower messenger RNA expression for signaling molecules that control airway inflammation and obstruction (specifically, the glucocorticoid receptor and (2)-adrenergic receptor) than youths who had not experienced targeted rejection. These associations were specific to targeted rejection and stronger for youths higher in subjective social status. Higher-status youths exposed to targeted rejection (but not other types of stress) also reported more asthma symptoms. These data demonstrate stressor-specific associations with molecular-signaling pathways and the severity of asthma, and they suggest that threats to the social self may be particularly deleterious.
机译:尽管有时会假定对不同压力源的响应相似,但最近的研究表明,某些类型的压力(例如定向排斥)特别有效。为了在慢性病模型中测试这种关联,我们研究了非人际,人际和目标拒绝主要生活事件如何预测121名哮喘青年的基因表达和症状严重性的变化,这些青年每6个月评估2年。与未经历靶向排斥的年轻人相比,最近经历靶向排斥的年轻人的信号分子控制气道炎症和阻塞的信使RNA表达水平更低(特别是糖皮质激素受体和(2)-肾上腺素能受体)。这些协会专门针对有针对性的拒绝,对于主观社会地位较高的年轻人则更强。处于定向排斥状态(但没有其他类型的压力)的较高状态的年轻人也报告了更多的哮喘症状。这些数据表明应激源特异性与分子信号通路和哮喘的严重程度相关,并且表明对社会自我的威胁可能特别有害。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号