Resveratrol for patients with chronic obstructive pulmonary disease: hype or hope?

被引:47
作者
Beijers, Rosanne J. H. C. G. [1 ]
Gosker, Harry R. [1 ]
Schols, Annemie M. W. J. [1 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Resp Med, NUTRIM Sch Nutr & Translat Res Metab, POB 5800, NL-6202 AZ Maastricht, Netherlands
关键词
cardiovascular risk; chronic obstructive pulmonary disease; lung pathology; muscle mitochondrial function; resveratrol; MUSCLE OXIDATIVE PHENOTYPE; SKELETAL-MUSCLE; SYSTEMIC INFLAMMATION; MITOCHONDRIAL DYSFUNCTION; ALVEOLAR MACROPHAGES; INSULIN SENSITIVITY; RED WINE; STRESS; SUPPLEMENTATION; EXPRESSION;
D O I
10.1097/MCO.0000000000000444
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review Chronic obstructive pulmonary disease (COPD) is a progressive lung disease with a high prevalence of extrapulmonary manifestations and, frequently, cardiovascular comorbidity. Resveratrol is a food-derived compound with anti-inflammatory, antioxidant, metabolic and cardioprotective potential. Therefore, resveratrol might improve the pulmonary as well as extrapulmonary pathology in COPD. In this review, we will evaluate knowledge on the effects of resveratrol on lung injury, muscle metabolism and cardiovascular risk profile and discuss if resveratrol is a hype or hope for patients with COPD. Recent findings Experimental models of COPD consistently show decreased inflammation and oxidative stress in the lungs after resveratrol treatment. These beneficial anti-inflammatory and antioxidant properties of resveratrol can indirectly also improve both skeletal and respiratory muscle impairment in COPD. Recent clinical studies in non-COPD populations show improved mitochondrial oxidative metabolism after resveratrol treatment, which could be beneficial for both lung and muscle impairment in COPD. Moreover, preclinical studies suggest cardioprotective effects of resveratrol but results of clinical studies are inconclusive. Summary Resveratrol might be an interesting therapeutic candidate to counteract lung and muscle impairments characteristic to COPD. However, there is no convincing evidence that resveratrol will significantly decrease the cardiovascular risk in patients with COPD.
引用
收藏
页码:138 / 144
页数:7
相关论文
共 70 条
[1]
Resveratrol prevents dexamethasone-induced expression of the muscle atrophy-related ubiquitin ligases atrogin-1 and MuRF1 in cultured myotubes through a SIRT1-dependent mechanism [J].
Alamdari, Nima ;
Aversa, Zaira ;
Castillero, Estibaliz ;
Gurav, Aniket ;
Petkova, Victoria ;
Tizio, Steven ;
Hasselgren, Per-Olof .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 417 (01) :528-533
[2]
Barnes Peter J, 2004, Proc Am Thorac Soc, V1, P264, DOI 10.1513/pats.200402-014MS
[5]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[6]
Normal Weight but Low Muscle Mass and Abdominally Obese: Implications for the Cardiometabolic Risk Profile in Chronic Obstructive Pulmonary Disease [J].
Beijers, Rosanne J. H. C. G. ;
van de Bool, Coby ;
van den Borst, Bram ;
Franssen, Frits M. E. ;
Wouters, Emiel F. M. ;
Schols, Annemie M. W. J. .
JOURNAL OF THE AMERICAN MEDICAL DIRECTORS ASSOCIATION, 2017, 18 (06) :533-538
[7]
Resveratrol, an extract of red wine, inhibits lipopolysaccharide induced airway neutrophilia and inflammatory mediators through an NF-κB-independent mechanism [J].
Birrell, MA ;
McCluskie, K ;
Wong, SS ;
Donnelly, LE ;
Barnes, PJ ;
Belvisi, MG .
FASEB JOURNAL, 2005, 19 (02) :840-+
[8]
Metabolic effects of resveratrol: addressing the controversies [J].
Bitterman, Jacob L. ;
Chung, Jay H. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2015, 72 (08) :1473-1488
[9]
Resveratrol and Cardiovascular Diseases [J].
Bonnefont-Rousselot, Dominique .
NUTRIENTS, 2016, 8 (05)
[10]
Nutritional strategies to modulate inflammation and oxidative stress pathways via activation of the master antioxidant switch Nrf2 [J].
Cardozo, Ludmila F. M. F. ;
Pedruzzi, Liliana M. ;
Stenvinkel, Peter ;
Stockler-Pinto, Milena B. ;
Daleprane, Julio B. ;
Leite Jr, Maurilo ;
Mafra, Denise .
BIOCHIMIE, 2013, 95 (08) :1525-1533