Abstract | BACKGROUND: METHODS: The HCVR was tested in 20 patients using a rebreathing method and the HVR was examined using a progressive isocapnic hypoxic method. The HCVR and HVR were assessed by calculating the slopes of plots of occlusion pressure (P0.1) and ventilation (VE) against end tidal carbon dioxide pressure (PETCO2) and arterial oxygen saturation (SaO2), respectively. Spirometric values, lung volumes, and respiratory muscle strength were also measured. The HCVR and HVR were examined after the oral administration of fenoterol (15 mg/day) or placebo for seven days. RESULTS:
Fenoterol treatment increased the forced expiratory volume in one second (FEV1) and inspiratory muscle strength. In the HCVR the slope of P0.1 versus PETCO2 was increased by fenoterol from 0.35 (0.23) to 0.43 (0.24) (p < 0.01). Moreover, the P0.1 at PETCO2 of 8 kPa was higher on fenoterol than on placebo (p < 0.05) and the VE was also greater (p < 0.01). In the HVR fenoterol treatment increased the P0.1 at 80% SaO2 from 0.90 (0.72) to 0.97 (0.55) kPa (p < 0.05) while the slopes of the response of P0.1 and VE were not changed. CONCLUSIONS:
Fenoterol increases the ventilatory response to hypercapnia in patients with COPD, presumably by stimulation of the central chemoreceptor. The hypoxic ventilatory response is only slightly affected by fenoterol.
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Authors | S Suzuki, Y Watanuki, Y Yoshiike, T Okubo |
Journal | Thorax
(Thorax)
Vol. 52
Issue 2
Pg. 125-9
(Feb 1997)
ISSN: 0040-6376 [Print] England |
PMID | 9059471
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Adrenergic beta-Agonists
- Fenoterol
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Topics |
- Adrenergic beta-Agonists
(therapeutic use)
- Aged
- Aged, 80 and over
- Chemoreceptor Cells
(drug effects)
- Cross-Over Studies
- Double-Blind Method
- Female
- Fenoterol
(therapeutic use)
- Humans
- Hypercapnia
(physiopathology)
- Hypoxia
(physiopathology)
- Lung Diseases, Obstructive
(drug therapy, physiopathology)
- Male
- Middle Aged
- Respiratory Muscles
(drug effects, physiopathology)
- Stimulation, Chemical
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