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首页> 外文期刊>Current opinion in pulmonary medicine >Anticholinergic agents in asthma: chronic bronchodilator therapy, relief of acute severe asthma, reduction of chronic viral inflammation and prevention of airway remodeling.
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Anticholinergic agents in asthma: chronic bronchodilator therapy, relief of acute severe asthma, reduction of chronic viral inflammation and prevention of airway remodeling.

机译:哮喘中的抗胆碱能药物:慢性支气管扩张剂治疗,急性重症哮喘的缓解,慢性病毒性炎症的减轻和气道重塑的预防。

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PURPOSE OF REVIEW: It is difficult to identify specific groups of asthmatic patients who may benefit from acute or chronic use of anticholinergic agents. Therefore, an important consideration is how anticholinergic agents can be used to achieve clinically effective treatment of asthma. RECENT FINDINGS: A genotype-stratified study revealed that greater bronchoprotective effect of anticholinergic agents was observed in asthmatic patients with the Arg/Arg genotype of the beta2-adrenergic receptor. Anticholinergic agents could add to the bronchodilation obtained with beta2-agonists on acute severe asthma. CD8+ T lymphocytes induced by chronic hepatitis C viral infection causes chronic obstructive pulmonary disease-like inflammation in asthma. Virus-specific CD8+ T lymphocytes may induce cholinergic activation in asthma through M2 receptor dysfunction. Therefore, anticholinergic agents are highly effective for asthma associated with chronic viral infection. In contrast, asthma with chronic obstructive pulmonary disease-like inflammation appears to be poorly responsive to beta2-agonists and can lead to partially irreversible airflow limitation. Moreover, a recent report suggested that treatment with inhaled tiotropium bromide markedly inhibited the increase in airway smooth muscle mass, myosin expression, and contractility in asthma. SUMMARY: Anticholinergic agents may benefit stable asthmatics, particularly those who have the Arg/Arg genotype. These agents have a demonstrated role in combination with beta2-agonists in the treatment of acute severe asthma, and may benefit asthmatics with chronic obstructive pulmonary disease-like inflammation. Moreover, these agents could be also beneficial in preventing airway remodeling in asthmatic airways.
机译:审查目的:很难确定可能从急性或长期使用抗胆碱能药物中受益的特定哮喘患者群体。因此,重要的考虑因素是如何使用抗胆碱能药物实现临床上有效的哮喘治疗。最近的发现:一项基因型分层研究显示,在具有β2-肾上腺素能受体Arg / Arg基因型的哮喘患者中,抗胆碱能药的支气管保护作用更高。抗胆碱能药物可能会加重用β2受体激动剂治疗急性重症哮喘的支气管扩张作用。慢性丙型肝炎病毒感染诱导的CD8 + T淋巴细胞在哮喘中引起慢性阻塞性肺疾病样炎症。病毒特异性CD8 + T淋巴细胞可能通过M2受体功能障碍诱导哮喘中的胆碱能激活。因此,抗胆碱能药对与慢性病毒感染有关的哮喘非常有效。相反,患有慢性阻塞性肺疾病样炎症的哮喘患者对β2受体激动剂的反应较差,并可能导致部分不可逆的气流受限。此外,最近的报告表明,吸入噻托溴铵治疗可明显抑制哮喘患者气道平滑肌质量,肌球蛋白表达和收缩力的增加。摘要:抗胆碱能药可能有益于稳定的哮喘患者,尤其是那些具有Arg / Arg基因型的哮喘患者。这些药物与β2-激动剂联用具有治疗急性严重哮喘的作用,并可能使患有慢性阻塞性肺疾病样炎症的哮喘患者受益。而且,这些试剂在预防哮喘气道中的气道重塑方面也可能是有益的。

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