Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Clinical & experimental allergy 33 (2003), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Objective Cough variant asthma and atopic cough are different clinical manifestations of eosinophilic airway inflammation presenting with isolated chronic non-productive cough. The aim of this study was to examine the longitudinal change in pulmonary function in cough variant asthma and atopic cough.Methods Longitudinal change in FEV1 was prospectively examined in 20 patients with cough variant asthma, 14 patients with atopic cough and 271 asymptomatic healthy subjects. All were lifetime non-smokers. Of the 20 cough variant asthma patients, 13 were taking long-term inhaled corticosteroid therapy (ICS) (beclomethasone dipropionate 615 ± 58 µg/day) and the other seven were not. Spirometry was taken at first visit, after cough was almost completely relieved on therapy, and at least once every year for 5 or more years afterwards.Results The slope of longitudinal change in FEV1 was not significantly different among cough variant asthma patients (− 0.029 ± 0.007/year), atopic cough patients (− 0.021 ± 0.022/year) and asymptomatic subjects (− 0.028 ± 0.002 L/year). In patients with cough variant asthma, the slope in patients not taking inhaled corticosteroids (ICS) was 0.032 ± 0.007 L/year, which was not significantly different from that in patients taking ICS (− 0.027 ± 0.010 L/year).Conclusion Pulmonary function decline is not greater in cough variant asthma than atopic cough and the normal population, and long-term ICS has no effect on the decline in cough variant asthma.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background Cough receptor hypersensitivity is a fundamental feature of some conditions presenting with chronic non-productive cough. Suplatast tosilate, an anti-allergic agent, is a T helper (Th)2 cytokine inhibitor that inhibits the synthesis of interleukin (IL)-4, IL-5, immunoglobulin (Ig)E production, and local eosinophil accumulation.Objective The purpose of this study was to investigate the effect of suplatast on antigen-induced airway cough hypersensitivity and eosinophil infiltration into the airway.Methods Number of coughs elicited by inhalation of increasing concentrations of capsaicin (10−8, 10−6 and 10−4 M) was counted 24 h after an antigen challenge in conscious guinea-pigs and then bronchoalveolar lavage was performed. We investigated the effect of single (before antigen challenge or capsaicin provocation) or repetitive treatment with intraperitoneal suplatast at a dose of 10 or 30 mg/kg on antigen-induced cough hypersensitivity.Results Twenty-four hours after antigen challenge, guinea-pigs developed an increase in cough receptor sensitivity to inhaled capsaicin and eosinophil infiltration in the airways. After a 2-week treatment with suplatast, but not after only a single treatment before antigen challenge or capsaicin provocation, the antigen-induced early phase bronchoconstriction, cough hypersensitivity, and airway eosinophilia were inhibited in a dose-dependent manner.Conclusion These results indicate that suplatast inhibits airway cough hypersensitivity underlying allergic eosinophilic inflammation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background Indoor formaldehyde (FA) might worsen allergies and be an underlying factor for the increasing incidence and severity of asthma; the exact mechanism, however, remains unclear.Objective The present study examined the effects of repeated exposure to FA on methacholine- and antigen-induced bronchoconstriction in guinea-pigs in vivo.Methods First, non-sensitized guinea-pigs were transnasally treated with 0.1 or 1.0% FA or saline three times a week for 6 weeks, and increasing concentrations of methacholine (50, 100, and 200 μg/mL) were inhaled at 5-min intervals. Second, guinea-pigs pre-treated with transnasal administration of FA or saline using the same protocol were passively sensitized with anti-ovalbumin (OA) serum 7 days before antigen challenge. Third, guinea-pigs were actively sensitized with OA and pre-treated with transnasal administration of FA or saline using the same protocol. The lateral pressure of the tracheal tube (Pao) was measured under anesthesia and artificial ventilation.Results The antigen-induced increase in Pao in actively sensitized guinea-pigs was significantly potentiated by FA exposure in a dose-dependent manner. The dose–response curve of the methacholine-induced increase in Pao in non-sensitized guinea-pigs or of the antigen-induced increase in Pao in passively sensitized guinea-pigs was not altered by FA exposure. Transnasal administration of FA significantly increased the serum anti-OA homocytotropic antibody titre (IgG) as measured by the passive cutaneous anaphylaxis reaction in actively sensitized guinea-pigs.Conclusion The results suggest that repeated exposure to FA worsens allergic bronchoconstriction through enhancing antigen sensitization.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0022-2836
    Keywords: [abr] 2,4-dinitrophenyl ; [abr] 2-nitro-4-azidophenylglycine ; [abr] 3-(3-amino-3-carboxypropyl)uridine at tRNA^P^h^e position 47 ; [abr] 4-thiouridine at tRNA^P^h^e position 8 ; [abr] 6-(2-nitro-4-azidophenylamino)caproate ; [abr] AA-tRNA ; [abr] APA ; [abr] APA bromide ; [abr] APA thioether of s^4U ; [abr] APA-Br ; [abr] APA-s^4U"8 ; [abr] DNAB ; [abr] DNP ; [abr] DTT ; [abr] EF ; [abr] GDPCP ; [abr] GTP ; [abr] Ig ; [abr] Me"2SO ; [abr] N-(2,4-dinitrophenyl)-γ-aminobutyric acid ; [abr] N-hydroxysuccinimide ; [abr] NAG ; [abr] NAG-NOS ; [abr] NAK ; [abr] NAK-NOS ; [abr] NAK-acp^3U"4"7 ; [abr] NOS ; [abr] NOS ester of NAG ; [abr] NOS ester of NAK ; [abr] Phe-tRNA ; [abr] XLTC ; [abr] [^3H]A"7"6-tRNA^P^h^e ; [abr] acp^3 amide of NAK (see Fig. 1); NAG-acp^3U"4"7 ; [abr] acp^3U amide of NAG (see Fig. 1) ; [abr] acp^3U"4"7 ; [abr] aminoacyl-tRNA ; [abr] crosslinked ternary complex of EFTu. ; [abr] dimethylsulfoxide ; [abr] dithiothreitol ; [abr] elongation factor ; [abr] guanylyl-(β,γ-methylene)-diphosphonate ; [abr] immunoglobulin ; [abr] p-azidophenacyl ; [abr] s^4U"8 ; [abr] tRNA"A"P"A ; [abr] tRNA"N"A"G ; [abr] tRNA"N"A"K ; [abr] tRNA^P^h^e modified at acp^3U"4"7 with NAK or NAG ; [abr] tRNA^P^h^e modified at s^4U"8 with APA ; [abr] tRNA^P^h^e whose 3'-terminal adenosine has been replaced with
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...