Exercise reverses OVA-induced inhibition of glucocorticoid receptor and increases anti-inflammatory cytokines in asthma

被引:36
作者
Silva, R. A. [1 ,2 ]
Almeida, F. M. [2 ]
Olivo, C. R. [2 ]
Saraiva-Romanholo, B. M. [2 ,3 ]
Martins, M. A. [2 ]
Carvalho, C. R. F. [1 ,2 ]
机构
[1] Univ Sao Paulo, Sch Med, Dept Phys Therapy, BR-01246903 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Sch Med, Dept Clin Med LIM 20, BR-01246903 Sao Paulo, SP, Brazil
[3] Univ City Sao Paulo UNICID, Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Exercise; allergy; cytokine regulator; structural changes; hormone; AIRWAY SMOOTH-MUSCLE; AEROBIC EXERCISE; GLYCEMIC CONTROL; REDUCED RISK; MOUSE MODEL; EXPRESSION; INFLAMMATION; ACTIVATION; REACTIVITY; RESPONSES;
D O I
10.1111/sms.12411
中图分类号
G8 [体育];
学科分类号
040301 [体育人文社会学];
摘要
The purpose of this study was to determine the effect of aerobic exercise training (AT) on the expression of glucocorticoid receptors (GR) and anti-inflammatory cytokines in an asthma model. BALB/c mice were divided into groups control (CT; nonsensitized/nontrained), aerobic training (AT; nonsensitized/trained), ovalbumin (OVA; sensitized/not trained), and OVA+AT (sensitized/trained). OVA groups received OVA by inhalation, and the AT groups completed 1, 3, or 7 days of exercise (60min/session). Expression of GR, IL-4, IL-5, IL-10, IL-1ra, NF-B, TGF-, VEGF, ICAM-1, VCAM-1; eosinophils counting; and airway remodeling (AR) features [airway smooth muscle (ASM) and epithelial thickness and collagen fiber deposition] were quantified. OVA sensitization induced a decrease in the expression of GR and increases in the eosinophil, IL-4, IL-5, NF-B, TGF-, VEGF, ICAM-1, VCAM-1, and AR features (P<0.05). After 3 days, AT reversed the OVA-induced reduction in the expression of GR, and subsequently induced increases in the expression of IL-10 and IL-1ra (seventh day). In contrast, the eosinophil migration, the expression of NF-B, IL-4, IL-5, TGF-, RANTES, VEGF, ICAM-1, VCAM-1, and the AR features (P<0.05) were reduced. AT increases the expression of GR and anti-inflammatory cytokines (IL-10 and IL-1ra) and reduces the expression of inflammatory mediators and airway inflammation in an animal model of asthma.
引用
收藏
页码:82 / 92
页数:11
相关论文
共 53 条
[1]
EFFECTS OF GLUCOCORTICOIDS ON TRANSCRIPTION FACTOR ACTIVATION IN HUMAN PERIPHERAL-BLOOD MONONUCLEAR-CELLS [J].
ADCOCK, IM ;
BROWN, CR ;
GELDER, CM ;
SHIRASAKI, H ;
PETERS, MJ ;
BARNES, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (02) :C331-C338
[2]
Extracellular matrix components and regulators in the airway smooth muscle in asthma [J].
Araujo, B. B. ;
Dolhnikoff, M. ;
Silva, L. F. F. ;
Elliot, J. ;
Lindeman, J. H. N. ;
Ferreira, D. S. ;
Mulder, A. ;
Gomes, H. A. P. ;
Fernezlian, S. M. ;
James, A. ;
Mauad, T. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (01) :61-69
[3]
The balance between IL-1 and IL-1Ra in disease [J].
Arend, WR .
CYTOKINE & GROWTH FACTOR REVIEWS, 2002, 13 (4-5) :323-340
[4]
The Inflammatory Preatherosclerotic Remodeling Induced by Intermittent Hypoxia Is Attenuated by RANTES/CCL5 Inhibition [J].
Arnaud, Claire ;
Beguin, Pauline C. ;
Lantuejoul, Sylvie ;
Pepin, Jean-Louis ;
Guillermet, Christiane ;
Pelli, Graziano ;
Burger, Fabienne ;
Buatois, Vanessa ;
Ribuot, Christophe ;
Baguet, Jean-Philippe ;
Mach, Francois ;
Levy, Patrick ;
Dematteis, Maurice .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 184 (06) :724-731
[5]
Differential gene expression and cytokine production from neutrophils in asthma phenotypes [J].
Baines, K. J. ;
Simpson, J. L. ;
Bowden, N. A. ;
Scott, R. J. ;
Gibson, P. G. .
EUROPEAN RESPIRATORY JOURNAL, 2010, 35 (03) :522-531
[6]
[7]
Brown JR, 1998, CLIN EXP IMMUNOL, V114, P137
[8]
Castellani ML, 2009, J BIOL REGUL HOMEOST, V24, P1
[9]
Corticosteroid insensitivity of chemokine expression in airway smooth muscle of patients with severe asthma [J].
Chang, Po-Jui ;
Bhavsar, Pankaj K. ;
Michaeloudes, Charalambos ;
Khorasani, Nadia ;
Chung, Kian Fan .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 130 (04) :877-+
[10]
Inhibition of airway remodeling in IL-5-deficient mice [J].
Cho, JY ;
Miller, M ;
Baek, KJ ;
Han, JW ;
Nayar, J ;
Lee, SY ;
McElwain, K ;
McElwain, S ;
Friedman, S ;
Broide, DH .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (04) :551-560