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  • Key words: Bronchial epithelial cells — Cl− currents — Cl− channels — Patch-clamp — Intracellular Ca2+— ATP — UTP  (1)
  • Key words: Eosinophils—Asthma—Atopy—Bronchial hyperresponsiveness—Methacholine—Bronchoalveolar lavage—Bronchial lavage—Inflammation.  (1)
  • Procalpain activation  (1)
Material
Years
Keywords
  • Key words: Bronchial epithelial cells — Cl− currents — Cl− channels — Patch-clamp — Intracellular Ca2+— ATP — UTP  (1)
  • Key words: Eosinophils—Asthma—Atopy—Bronchial hyperresponsiveness—Methacholine—Bronchoalveolar lavage—Bronchial lavage—Inflammation.  (1)
  • Procalpain activation  (1)
  • (Human)  (1)
  • Ca^2^+  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular 831 (1985), S. 335-339 
    ISSN: 0167-4838
    Keywords: (Human) ; Ca^2^+ ; Calpain ; Erythrocyte membrane ; Procalpain activation ; Proteinase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 156 (1997), S. 297 -305 
    ISSN: 1432-1424
    Keywords: Key words: Bronchial epithelial cells — Cl− currents — Cl− channels — Patch-clamp — Intracellular Ca2+— ATP — UTP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract. The perforated-patch technique was used to study the response of human bronchial cells to extracellular nucleotides. ATP or UTP (100 μm) elicited a complex response consisting of a large transient membrane current increase followed by a relatively small sustained level. These two phases were characterized by different current kinetics. Throughout the transient phase (2–3 min) the membrane current (I p ) displayed slow activation and deactivation kinetics at depolarizing and hyperpolarizing potentials respectively. At steady-state (I s ) the relaxation at hyperpolarizing potential disappeared whereas at positive membrane potentials the current became slightly deactivating. The I s amplitude was dependent on the extracellular Ca2+ concentration, being completely inhibited in Ca2+-free medium. Cell pre-incubation with the membrane-permeable chelating agent BAPTA/AM prevented completely the response to nucleotides, thus suggesting that both I p and I s were dependent on intracellular Ca2+. The presence of a hypertonic medium during nucleotide stimulation abolished I s leaving I p unchanged. On the contrary, niflumic acid, a blocker of Ca2+-activated Cl− channels, prevented completely I p without reducing significantly I s . 1,9-dideoxyforskolin fully inhibited I s but also reduced I p . Replacement of extracellular Cl− with aspartate demonstrated that the currents activated by nucleotides were Cl− selective. I p resulted five times more Cl− selective than I s with respect to aspartate. Taken together, our results indicate that ATP and UTP activate two types of Cl− currents through a Ca2+-dependent mechanism.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1750
    Keywords: Key words: Eosinophils—Asthma—Atopy—Bronchial hyperresponsiveness—Methacholine—Bronchoalveolar lavage—Bronchial lavage—Inflammation.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. To characterize the cellular inflammation at the bronchial and bronchoalveolar levels, we evaluated 43 patients with asthma who were sensitized to house dust mites. On 2 consecutive days patients underwent methacholine challenge and allergen bronchial challenge. In addition, 6, 24, or 72 h after allergen challenge, fiberoptic bronchoscopy with bronchial lavage (BL) and bronchoalveolar lavage (BAL) was performed. Patients belonging to the 6-h, 24-h, or 72-h group were divided further into two subgroups: those with isolated early response to allergen (LAR−), and those with dual response to allergen (LAR+). The percentage of eosinophils and of epithelial cells in BAL fluid was significantly higher in LAR+ than in LAR− patients in the 6-h group (p 〈 0.05, each comparison), but not 24 or 72 h after (p 〉 0.05, each comparison). Similarly, the proportion of BL eosinophils was also higher in LAR+ than in LAR− patients, both in the 6-h and in the 24-h group (p 〈 0.05, each comparison). In addition, increased proportions of BL neutrophils were present in the LAR+ patients belonging to the 24-h group (p 〈 0.05). Comparing ``proximal'' = BL vs ``distal'' = BAL data, we found a significantly higher proportion of epithelial cells in BL compared with BAL, in both LAR− and LAR+ subjects, either 6, or 24, or 72 h after challenge (p 〈 0.01, each comparison) and increased percentages of BL neutrophils and eosinophils in LAR+ patients (p 〈 0.05, each comparison), but not in LAR− patients, in the 24-h group. The percentages of BL or BAL macrophages and lymphocytes did not differ significantly among the different patient groups. These data indicate that the development of LAR after allergen inhalation challenge is associated with an early recruitment of eosinophils and with epithelial desquamation in the airways. In addition, after allergen challenge epithelial desquamation is more pronounced in the proximal than in the distal airways, independently of the type of bronchial response.
    Type of Medium: Electronic Resource
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