Local and systemic alterations of the L-arginine/nitric oxide pathway in aputum, blood, and urine of pediatric cystic fibrosis patients and effects of antibiotic treatment

• Verfasst von: Hanusch, Beatrice [VerfasserIn]
• Verfasst von: Brinkmann, Folke [VerfasserIn]
• Verfasst von: Mayorandan, Sebene [VerfasserIn]
• Verfasst von: Chobanyan-Jürgens, Kristine [VerfasserIn]
• Verfasst von: Wiemers, Anna [VerfasserIn]
• Verfasst von: Jansen, Kathrin [VerfasserIn]
• Verfasst von: Ballmann, Manfred [VerfasserIn]
• Verfasst von: Schmidt-Choudhury, Anjona [VerfasserIn]
• Verfasst von: Bollenbach, Alexander [VerfasserIn]
• Verfasst von: Derichs, Nico [VerfasserIn]
• Verfasst von: Tsikas, Dimitrios [VerfasserIn]
• Verfasst von: Lücke, Thomas [VerfasserIn]
• Titel: Local and systemic alterations of the L-arginine/nitric oxide pathway in aputum, blood, and urine of pediatric cystic fibrosis patients and effects of antibiotic treatment
• Verf.angabe: Beatrice Hanusch, Folke Brinkmann, Sebene Mayorandan, Kristine Chobanyan-Jürgens, Anna Wiemers, Kathrin Jansen, Manfred Ballmann, Anjona Schmidt-Choudhury, Alexander Bollenbach, Nico Derichs, Dimitrios Tsikas and Thomas Lücke
• E-Jahr: 2020
• Jahr: 24 November 2020
• Umfang: 19 S.
• Fussnoten: Gesehen am 09.02.2022
• Titel Quelle: Enthalten in: Journal of Clinical Medicine
• Ort Quelle: Basel : MDPI, 2012
• Jahr Quelle: 2020
• Band/Heft Quelle: 9(2020), 12, Artikel-ID 3802, Seite 1-19
• ISSN Quelle: 2077-0383
• DOI: doi:10.3390/jcm9123802
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: <i>Pseudomonas aeruginosa</i>
• Sach-SW: antibiotics
• Sach-SW: cystic fibrosis
• Sach-SW: inflammation
• Sach-SW: nitric oxide
• K10plus-PPN: 1788666631

Abstract

Alterations in the L-arginine (Arg)/nitric oxide (NO) pathway have been reported in cystic fibrosis (CF; OMIM 219700) as the result of various factors including systemic and local inflammatory activity in the airways. The aim of the present study was to evaluate the Arg/NO metabolism in pediatric CF patients with special emphasis on lung impairment and antibiotic treatment. Seventy CF patients and 78 healthy controls were included in the study. CF patients (43% male, median age 11.8 years) showed moderately impaired lung functions (FEV1 90.5 ± 19.1% (mean ± SD); 21 (30%) had a chronic Pseudomonas aeruginosa (PSA) infection, and 24 (33%) had an acute exacerbation). Plasma, urinary, and sputum concentrations of the main Arg/NO metabolites, nitrate, nitrite, Arg, homoarginine (hArg), and asymmetric dimethylarginine (ADMA) were determined in pediatric CF patients and in healthy age-matched controls. Clinical parameters in CF patients included lung function and infection with PSA. Additionally, the Arg/NO pathway in sputum samples of five CF patients was analyzed before and after routine antibiotic therapy. CF patients with low fractionally exhaled NO (FENO) showed lower plasma Arg and nitrate concentrations. During acute exacerbation, sputum Arg and hArg levels were high and dropped after antibiotic treatment: Arg: pre-antibiotics: 4.14 nmol/25 mg sputum vs. post-antibiotics: 2.33 nmol/25 mg sputum, p = 0.008; hArg: pre-antibiotics: 0.042 nmol/25 mg sputum vs. post-antibiotics: 0.029 nmol/25 mg sputum, p = 0.035. The activated Arg/NO metabolism in stable CF patients may be a result of chronic inflammation. PSA infection did not play a major role regarding these differences. Exacerbation increased and antibiotic therapy decreased sputum Arg concentrations.