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Airway Exposure to 1,3-Beta-d-Glucan Induces Airway Hyperresponsiveness in Guinea Pigs
You Shuei Lin1,2, Yueh-Yin Chen2, Nai-Ju Chan2
1Department of Physiology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Abstract:
1,3-Beta-d-glucan (β-glucan) is a component of mold cell walls and is frequently found in fungi and house dust mites. The studies of β-glucan are inconsistent, although it has been implicated in airway adverse responses. This study was carried out to determine whether airway hyperresponsiveness was seen 24 h after airway exposure to β-glucan in guinea pigs. Two matching guinea pigs were exposed intratracheally to either β-glucan or its vehicle. Twenty-four hours after intratracheal instillation, there was no difference between these two groups in the baseline of the total pulmonary resistance (R L), dynamic lung compliance (C dyn), arterial blood pressure, and heart rate. In contrast, the responses of R L to capsaicin injection were significantly increased in β-glucan animals; capsaicin at the same dose of 3.2 μg/kg increased R L by 184% in vehicle animals and by 400% in β-glucan animals. The effective dose 200% to capsaicin injection was lower in the β-glucan animals. Furthermore, the increases in R L were partially reduced after transient lung hyperinflation to recruit the occluding airways; however, the R L induced by capsaicin injection after lung hyperinflation was significantly larger than the baseline in β-glucan animals; also, the lung wet-to-dry ratio in capsaicin-injected animals was augmented in the β-glucan group. Moreover, the airway hyperresponsiveness was accompanied by increases in neutrophils in the bronchoalveolar lavage fluid in the β-glucan animals. Furthermore, the levels of substance P and the calcitonin gene-related peptide in the bronchoalveolar lavage fluid collected after capsaicin injection were increased in β-glucan animals. We provide definitive evidence that β-glucan can induce airway hyperresponsiveness in guinea pigs, and the neuropeptide releases play an important role in this airway hyperresponsiveness.
Insights
1,3-Beta-d-glucan (β-glucan) exposure in guinea pigs induced airway hyperresponsiveness. This study demonstrates β-glucan
Area of Science:
- Pulmonary immunology
- Respiratory physiology
- Environmental health
Background:
- 1,3-Beta-d-glucan (β-glucan), a mold cell wall component, is linked to adverse airway responses.
- Previous studies on β-glucan's respiratory effects are inconsistent.
- The role of β-glucan in airway hyperresponsiveness requires further investigation.
Purpose of the Study:
- To determine if airway exposure to β-glucan induces airway hyperresponsiveness in guinea pigs 24 hours post-exposure.
- To investigate the underlying mechanisms, including neuropeptide release and inflammatory cell infiltration.
Main Methods:
- Guinea pigs were intratracheally instilled with either β-glucan or a vehicle.
- Airway responsiveness to capsaicin was assessed by measuring pulmonary resistance (RL).
- Bronchoalveolar lavage fluid (BALF) was analyzed for inflammatory cells and neuropeptides (substance P, CGRP).
Main Results:
- β-glucan exposure significantly increased airway hyperresponsiveness to capsaicin compared to controls.
- Increased neutrophils and neuropeptides (substance P, CGRP) were observed in BALF of β-glucan-treated animals.
- Lung wet-to-dry ratio was augmented in β-glucan animals post-capsaicin challenge.
Conclusions:
- 1,3-Beta-d-glucan induces airway hyperresponsiveness in guinea pigs.
- Neuropeptide release and neutrophil infiltration play a significant role in β-glucan-mediated airway hyperresponsiveness.
- Findings provide definitive evidence for β-glucan's role in respiratory adverse responses.
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