4.3 Article

Ghrelin treatment suppresses neutrophil-dominant inflammation in airways of patients with chronic respiratory infection

期刊

PULMONARY PHARMACOLOGY & THERAPEUTICS
卷 21, 期 5, 页码 774-779

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pupt.2008.05.001

关键词

Ghrelin; Respiratory tract infection; Neutrophil; Cachectic state; IGF-1; Translational research

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation (NIBIO) of Japan
  3. Takeda Scientific Foundation

向作者/读者索取更多资源

Background: Persistent neutrophil influx into the airways is a characteristic of chronic respiratory infection and contributes to the deterioration of pulmonary function. Ghrelin is a novel growth hormone (GH)-releasing peptide with potential anti-inflammatory activities. The present study investigated whether or not ghrelin can reduce neutrophil-dominant inflammation in airways of patients with chronic respiratory infection. Populations and methods: Synthesized ghrelin was administered intravenously for 3 weeks to 7 cachectic patients with chronic respiratory infection to confirm ghrelin's effects on airway inflammation and nutrition state. Neutrophils, neutrophil products and inflammatory cytokines in sputum were used as markers of airway inflammation. Changes in serum protein levels were also evaluated along with plasma catecholamine levels. Exercise tolerance was assessed by measuring 6-min walking distance before and after 3 weeks of ghrelin treatment. Results: Three-week ghrelin administration decreased neutrophil density and inflammatory cytokine levels in sputum, reduced plasma norepinephrine level, and increased body weight, serum protein level, and 6-min walking distance. Conclusions: Ghrelin administration suppressed airway inflammation by decreasing neutrophil accumulation in lungs and increased body weight. These findings may contribute to the development of supportive therapies for patients with refractory chronic respiratory infection. (c) 2008 Elsevier Ltd. All rights reserved.

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