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1.
Respir Med ; 102(3): 377-81, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18061423

ABSTRACT

Exhaled breath condensate (EBC) is being used increasingly to sample airway fluid. EBC pH may be a biomarker of airway inflammation in asthma. In this study, we assessed the long-term reproducibility of EBC pH in asthma. We examined 31 asthmatic patients and eight healthy subjects three times over a 1-year period (winter, autumn and summer). EBC pH was measured after argon deaeration. Repeatability of pH measurements was assessed using intraclass correlation coefficients (ICC) and the limits of agreement (LOA) between seasons were calculated according to Bland-Altman method. No significant differences in EBC pH between seasons were detected in healthy subjects and asthmatic patients. EBC pH showed high repeatability either in healthy subjects (ICC=0.94) or in asthmatics (ICC=0.97). Variability between seasons was greater in asthmatics than in healthy subjects: winter-autumn LOA -0.68/+0.52 and -0.31/+0.31, autumn-summer LOA -0.75/+0.67 and -0.24/+0.15, winter-summer LOA -0.92/+0.67 and -0.34/+0.23 in asthmatic and healthy subjects, respectively. In a subgroup of 11 asthmatics who remained in stable conditions during the study, no substantially different LOA were observed in EBC pH compared with the whole group of asthmatics. Asthmatic smokers (n=10) tended to have lower EBC pH (7.57+/-0.46) than asthmatic non-smokers (n=21) (7.74+/-0.21; p=0.063) and wider LOA. In conclusion, we demonstrated that EBC pH exhibits good repeatability in long-term assessment. EBC pH in asthmatics tended to fluctuate more than in healthy subjects. However, EBC pH variability in asthma was not influenced by changes in clinical status. Rather, we suggest that cigarette smoke may be implicated in EBC pH variability.


Subject(s)
Asthma/diagnosis , Breath Tests/methods , Adult , Asthma/physiopathology , Biomarkers/analysis , Case-Control Studies , Female , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Reproducibility of Results , Respiratory Function Tests/standards , Seasons
2.
J Neurosci ; 25(47): 10822-30, 2005 Nov 23.
Article in English | MEDLINE | ID: mdl-16306395

ABSTRACT

The Na+/Ca2+ exchangers NCX1, NCX2, and NCX3 are vital for the control of cellular Ca2+ homeostasis. Here, we show that a doublet of downstream regulatory element sites in the promoter of the NCX3 gene mediates transcriptional repression of NCX3 by the Ca2+-modulated transcriptional repressor downstream regulatory element antagonist modulator (DREAM). Overexpression of a DREAM EF-hand mutant insensitive to Ca2+ (EFmDREAM) in hippocampus and cerebellum of transgenic mice significantly reduced NCX3 mRNA and protein levels without modifying NCX1 and NCX2 expression. Cerebellar granules from EFmDREAM transgenic mice showed increased levels of cytosolic Ca2+ and were more vulnerable to increased Ca2+ influx after partial opening of voltage-gated plasma membrane Ca2+ channels induced by increasing K+ in the culture medium but survived better in the conditions of reduced Ca2+ influx prevailing in low extracellular K+. Overexpression of NCX3 in EFmDREAM transgenic granules using a lentiviral vector restored the normal survival response to high K+ observed in wild-type granules. Thus, the downregulation of the regulator of Ca2+ homeostasis NCX3 by Ca2+-regulated DREAM is a striking example of the autoregulatory property of the Ca2+ signal in neurons.


Subject(s)
Calcium/metabolism , Cerebellum/physiology , Homeostasis/physiology , Kv Channel-Interacting Proteins/physiology , Membrane Transport Proteins/metabolism , Neurons/physiology , Sodium-Calcium Exchanger/metabolism , Amino Acid Motifs/genetics , Animals , Brain/metabolism , Calcium Signaling/physiology , Cell Line, Tumor , Cell Survival/physiology , Cerebellum/metabolism , Cytoplasmic Granules/metabolism , Down-Regulation , Humans , Intracellular Membranes/metabolism , Kv Channel-Interacting Proteins/genetics , Membrane Transport Proteins/genetics , Mice , Mice, Transgenic , Mutation , Neurons/metabolism , Osmolar Concentration , Promoter Regions, Genetic , Sodium-Calcium Exchanger/genetics
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