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慢性阻塞性肺疾病中的氧化途径与病情加重:N-乙酰半胱氨酸的作用

Oxidation pathway and exacerbations in COPD: the role of NAC.

作者信息

Matera Maria Gabriella, Calzetta Luigino, Cazzola Mario

机构信息

a Department of Systems Medicine, Unit of Respiratory Clinical Pharmacology , University of Rome Tor Vergata , Rome , Italy.

出版信息

Expert Rev Respir Med. 2016;10(1):89-97. doi: 10.1586/17476348.2016.1121105. Epub 2015 Dec 15.

Abstract

Oxidative stress is an important trait in the pathogenesis of chronic obstructive pulmonary disease (COPD). Consequently, targeting oxidative stress is likely to be beneficial as a treatment in COPD. Glutathione (GSH) is an intracellular antioxidant that protects against a variety of different antioxidant species. The increase of lung GSH in COPD is an attempt to counter excess oxidant production but it is inadequate during exacerbations due to the excessive production of ROS. N-acetyl-l-cysteine (NAC) acts as a precursor for the substrate cysteine in synthesis of GSH and also as a mucolytic and anti-inflammatory agent. NAC prevents COPD exacerbations at high dosage (≥1200 mg daily), while a regular treatment with 600 mg daily is enough in chronic bronchitis. Nonetheless, we must still establish whether the level of bronchial obstruction may influence its effects, the effect of high-dose NAC in Caucasian patients with COPD, and the role of NAC in the escalation and de-escalation of therapy in COPD.

摘要

氧化应激是慢性阻塞性肺疾病(COPD)发病机制中的一个重要特征。因此,针对氧化应激进行治疗可能对COPD有益。谷胱甘肽(GSH)是一种细胞内抗氧化剂,可抵御多种不同的抗氧化物质。COPD患者肺内GSH增加是为了对抗过量的氧化剂产生,但在急性加重期由于活性氧(ROS)产生过多,这种增加并不足够。N-乙酰半胱氨酸(NAC)作为合成GSH的底物半胱氨酸的前体,同时还具有黏液溶解和抗炎作用。高剂量(≥1200毫克/天)的NAC可预防COPD急性加重,而对于慢性支气管炎患者,每天600毫克的常规治疗就足够了。尽管如此,我们仍需确定支气管阻塞程度是否会影响其疗效、高剂量NAC对高加索COPD患者的疗效,以及NAC在COPD治疗升级和降级中的作用。

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