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Erschienen in: Cough 1/2005

Open Access 01.12.2005 | Research

Phosphodiesterase 3 inhibition and cough in elderly asthmatics

verfasst von: Yoshihisa Ishiura, Masaki Fujimura, Kouichi Nobata, Miki Abo, Takayoshi Oribe, Shigeharu Myou, Hiroyuki Nakamura

Erschienen in: Cough | Ausgabe 1/2005

Abstract

Aims

Cough is a common symptom of bronchial asthma, a chronic inflammatory airway disease. Recently, the therapeutic effects of selective phosphodiesterase (PDE) inhibitors have been focused on bronchial asthma. This study was designed to investigate the clinical effect of PDE 3 inhibition on cough reflex sensitivity in elderly patients with bronchial asthma.

Methods

Effects of cilostazol, a PDE 3 inhibitor, on cough response to inhaled capsaicin were examined in 11 patients over 70 years with stable asthma in a randomized, placebo-controlled cross over study. Capsaicin cough threshold, defined as the lowest concentration of capsaicin eliciting five or more coughs, was measured as an index of airway cough reflex sensitivity.

Results

The cough threshold was significantly (p < 0.05) increased after two-week treatment with cilostazol (100 mg twice a day orally) compared with placebo [48.8 (GSEM 1.4) vs. 29.2 (GSEM 1.3) μM].

Conclusion

These findings indicate that PDE 3 inhibition may be a novel therapeutic option for elderly patients with asthma, especially for their cough symptoms.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1745-9974-1-11) contains supplementary material, which is available to authorized users.
Abkürzungen
cyclic-AMP
adenosine 3' 5'-cyclic monophosphate
CVA
cough variant asthma
FEV1
forced expiratory volume in one second
FVC
forced vital capacity
GSEM
geometric standard error of the mean
PDE
phosphodiesterase
PGD2
prostaglandin D2
PGE2
prostaglandin E2
PGF2α
prostaglandin F2α
TNF-α
tumor necrosis factor-α
TxA2
thromboxane A2
TxB2
thromboxane B2.

Introduction

Chronic cough is a frequent problem in general practice and one of the commonest reasons for referral to respiratory clinic. A patient's quality of life becomes severely affected through loss of sleep, interruption of work and social embarrassment. Every effort should be made to clarify the cause of cough because specific therapy has a higher likelihood of success than empirical therapy. A previous study revealed that patients with persistent cough had three times the risk of developing chronic wheezing as compared to normal subjects [2]. Thus, it is important to disclose the mechanism of persistent cough and to develop more efficacious treatment. Though cough has been considered to result from stimulation of airway sensory nerve endings within the respiratory tract [1], the potential mechanism by which the cough reflex may be altered in humans remains obscure.
Recently, considerable attention has been focused on the potential use of selective inhibitors of cyclic nucleotide phosphodiesterases (PDEs) in the treatment of respiratory diseases as PDE isoenzymes may play an important role in the regulation of airway caliber and bronchial smooth muscle function [3]. It has been shown that PDE 3 and PDE 4 are the major adenosine 3' 5'-cyclic monophosphate (cyclic-AMP) – hydrolyzing enzymes and that human airway smooth muscle contains isozymes of the PDE families [4, 5]. Furthermore, human lung tissue contains multiple PDE isozymes [6]. Therefore, it is important to determine the possible role of inhibition of these PDE isozymes in vivo. Though previous research failed to prove a bronchodilator effect of a PDE 3 and PDE 4 dual inhibitor, zardaverine, in patients with partially reversible chronic airway obstruction [7], others indicated the protective effect of selective PDE 3 and PDE 4 inhibitors [8, 9]. We have demonstrated that a phosphodiesterase 3 inhibitor, cilostazol, reduces bronchial hyperresponsiveness to inhaled methacholine in elderly patients with stable asthma [10].
Based on these findings, this study was designed to elucidate the potential importance of orally administered cilostazol on cough reflex sensitivity to inhaled capsaicin in asthmatic elderly patients.

Subjects and Methods

Subjects

Eleven patients over 70 years with stable bronchial asthma (4 males and 7 females) with a mean age of 74.9 ± 1.3 (± SEM) (range 70–81) yrs participated in this study. All patients were lifetime nonsmokers or ex-smokers with no history of viral infection for at least 4 weeks prior to the study. Informed consent was obtained from all subjects. Characteristics of individual patients are shown in table 1. This study was approved by the Ethics Committee of our hospital.
Each asthmatic patient satisfied the American Thoracic Society definition of asthma, with symptoms of episodic wheezing, cough, shortness of breath responding to bronchodilators and reversible airflow obstruction documented on at least one previous pulmonary function study [11]. Reversibility was defined as greater than 12% increase in the forced expiratory volume in one second (FEV1) following inhalation of 200 μg salbutamol sulfate. All patients had bronchial hyperresponsiveness as shown in table 1 and were taking oral (short-acting clenbuterol) and/or aerosol β2-agonists (short-acting procaterol), inhaled steroids (beclomethasone dipropionate) and/or mucolytic agents (carbocysteine). They had not received oral theophylline or oral steroid therapy for at least eight weeks. This study was carried out when their symptoms were mild and stable.
Table 1
Clinical characteristics of asthmatic patients
           
Treatment
Patient number
Age (yr)
Sex
Height (cm)
Type
Severity
Total IgE in serum (IU/ml)
Specific IgE in serum
Complication of allergic disease
RT20-FEV1 (mg/ml)*
Bronchodilator response (%)**
BDP (μg/day)
Theophylline (mg/day)
Clenbuterol (μg/day)
Carbocysteine (mg/day)
1
81
M
154
Int
Moderate
75
-
-
2.50
34.0
800
0
40
1500
2
72
F
151
Ext
Moderate
464
HD
AR
2.50
25.4
800
0
0
0
3
80
F
143
Ext
Moderate
3
Mite, HD
-
1.25
27.0
800
0
40
0
4
72
F
148
Int
Mild
28
-
-
0.08
19.4
0
0
0
1000
5
79
F
142
Int
Moderate
37
-
-
5.00
27.6
800
0
20
1500
6
72
F
150
Int
Moderate
57
-
-
0.31
22.3
400
0
40
0
7
72
F
147
Ext
Moderate
647
HD, Ceder
-
0.31
31.8
800
0
20
1500
8
70
F
140
Int
Moderate
17
-
-
1.25
17.6
800
0
40
1500
9
75
M
162
Ext
Moderate
148
HD, Ceder
AR
2.50
14.1
800
0
40
1500
10
71
M
165
Ext
Moderate
133
Mite, Ceder
AR
1.25
14.6
0
0
40
1500
11
80
M
165
Int
Moderate
2
-
-
2.50
12.6
400
0
0
0
Ext, extrinsic; Int, intrinsic; HD, house dust; AR, allergic rhinitis; BDP, beclomethasone diproprionate inhalation.
*PC20-FEV1 shows concentration of inhaled methacholine causing a 20% fall in FEV1.
**Bronchodilator response means percent increase in forced expiratory volume in 1s (FEV1) from the baseline value after inhalation of 300 μg of salbutamol sulfate.
All patients used inhaled β2-agonists (salbutamol or procaterol) on demand.

Assessment of cough reflex sensitivity to inhaled capsaicin

Cough reflex sensitivity was assessed by a capsaicin provocation test [12]. Capsaicin (30.5 mg) was dissolved in Tween 80 (1 mL) and ethanol (1 mL) and then dissolved in physiological saline (8 mL) to make a stock solution of 1 × 10-2 M, which was stored at -20°C. This solution was diluted with physiological saline to make solutions starting at a concentration of 0.49 μM and increased by doubling concentrations up to 1000 μM. Each subject inhaled a control solution of physiological saline followed by progressively increasing concentrations of the capsaicin solution. Solutions were inhaled by the subjects for 15 s every 60 s, by tidal mouth-breathing whilst wearing a noseclip from a Bennett Twin nebulizer (3012-60 cc, Puritan-Bennett Co., Carlsbad, California, USA). Increasing concentrations were inhaled until five or more coughs were elicited. The nebulizer output was 0.21 mL/min. The number of capsaicin-induced coughs were counted by a blindfolded medical technician in our pulmonary function laboratory. The cough threshold was defined as the lowest concentration of capsaicin that elicited five or more coughs.

Study protocol

The subjects' concomitant medication was stopped at 9.00 p.m. on the previous day to allow a washout time of 12 h or more before the measurement of cough threshold to inhaled capsaicin at 10.00 a.m. on each test day to reduce the diurnal variability of cough response.
Each patient attended 4 times, once every 2 weeks, at the same time each day. A control measurement of capsaicin cough threshold was carried out before the first treatment. After a two week wash out period, treatment with cilostazol and a placebo was performed in a randomized, cross-over fashion, with a washout period of 2 weeks between treatments. Two cilostazol tablets (100 mg) or their placebo were taken orally two times a day for 14 days at 8.00 a.m. on the test day. FEV1 was measured on a dry wedge spirometer (Transfer Test, P.K. Morgan Ltd., UK) before the capsaicin challenge to assess the bronchoactive effect of the treatment regimens.

Data analysis

Capsaicin cough threshold values were expressed as a geometric mean with a geometric standard error of the mean (GSEM). Forced vital capacity (FVC) and FEV1 were shown as arithmetic mean values ± SEM. The cough threshold, the FVC and the FEV1 values were compared between each pair of the four test periods (run-in, placebo treatment, wash out and cilostazol treatment) by the Wilcoxon signed-ranks test. Data was transformed to logarithmic values for cough threshold at this test. A p-value of 0.05 or less was taken as significant.

Results

Cough threshold to inhaled capsaicin before each treatment (run-in and washout period) and after treatment with cilostazol and placebo are shown in figure 1. Geometric mean values for the cough threshold were 25.9 (GSEM 1.4) μM in run-in period, 27.5 (GSEM 1.4) μM in washout period, 48.8 (GSEM 1.4) μM after cilostazol treatment and 29.2 (GSEM 1.3) μM after placebo treatment. The cough threshold after the cilostazol treatment was significantly (p < 0.05) greater than the value after the placebo treatment. FVC or FEV1 value was not significantly different between run-in period, washout period, cilostazol treatment and placebo treatment as shown in table 2.
There were no changes in serum IgE and peripheral blood eosinophils, therefore, treatment with cilostazol did not affect the IgE production or peripheral blood eosinophil count. After the administration of cilostazol, none of the patients complained of headache. Other adverse effects such as palpitations, flushing and dizziness were not observed with the cilostazol treatment in patients participating in this study, since the side effects of cilostazol are less frequent in elderly patients as shown in our previous study [10].
Table 2
Pulmonary function on cilostazol and placebo treatments in patients with bronchial asthma
 
Run-in
Placebo
Wash out
Cilostazol
FVC as % pred. (%)
102.3 ± 5.7
104.7 ± 5.8
102.1 ± 5.1
108.4 ± 4.7
FEV1 as% pred. (%)
98.5 ± 8.2
100.4 ± 7.7
98.5 ± 6.6
106.3 ± 7.3
Data are shown as mean value ± standard error of the mean.

Discussion

The present study showed that two-week treatment with a PDE 3 inhibitor, cilostazol, increased the cough threshold to inhaled capsaicin in elderly patients with stable asthma. No difference could be found in the baseline pulmonary function, peripheral blood eosinophil counts and IgE production between cilostazol and placebo treatments. From these findings, PDE 3 inhibition may be useful in elderly patients suffering from bronchial asthma, especially cough predominant asthma.
Although cough is a protective reflex that facilitates the expulsion of mucus from the airways, chronic cough causes major functional limitation in a great number of people who seek medical service. It is well known that cough can be the sole manifestation in some asthmatic patients [13], however, the precise mechanism correlating to the cough reflex in this disorder remains obscure. A recent study revealed that inflammatory mediators play major roles in the pathogenesis of bronchial asthma, however, the relationship between inflammatory mediators and airway cough reflex sensitivity also remains unclear. Previous studies showed that some inflammatory mediators can modulate the sensitivity of the cough reflex [14, 15]. We indicated that intrinsic thromboxane A2 (TxA2) is a possible modulator, augmenting both airway cough reflex sensitivity and bronchial responsiveness whilst not having a bronchoconstricting effect in stable asthmatics [14, 16, 17]. Other studies reported that prostaglandin F2α (PGF2α) enhances airway cough reflex sensitivity with bronchoconstricting effect [18, 19]. It has also been shown that inhaled prostaglandin E2 (PGE2), which acts as a bronchodilator, enhances cough reflex sensitivity [19, 20]. These findings indicate the variable role of inflammatory mediators in the local control of cough reflex with no relation to bronchoconstriction.
Previous studies have shown the effects of selective inhibition of PDE isozymes in inhibition of inflammatory cell function and relaxation of airway smooth muscle in asthmatic airways [39, 21]. Bachelet et al have shown that alveolar macrophages from asthmatic patients have increased PDE activity [22]. Other researchers have indicated that PDE 3 is closely coupled to the regulation of prostaglandin D2 (PGD2) generation [23]. Recently we demonstrated the bronchoprotective effect of PDE 3 inhibition in asthmatic patients [10, 24, 25], on the basis that PDE 3 is indeed present in human airway smooth muscle [26]. We, therefore, carried out this study on the assumption that PDE 3 activity in an asthmatic airway might also lead to increased sensitivity of airway cough response and concluded that a selective PDE 3 inhibitor, cilostazol, can modulate to reduce the airway cough sensitivity to inhaled capsaicin. We also showed that there was no improvement in lung function despite our previous study [10]. Though the precise mechanism for this discordant remains obscure, we stipulate that the difference in the cilostazol administration period may be a possible cause of the discordant, because in our previous study, bronchodilation was observed with a single administration of cilostazol. Precise mechanisms for the improvement of cough reflex sensitivity indicated in this study also remains unclear because we did not measure PC20. One of the possible mechanisms is that elevation of cyclic-AMP induced by PDE 3 inhibition may play some role in the regulation of cell activity and airway cough reflex sensitivity [26].
Furthermore, the bronchoprotective effect of PDE 3 inhibition for non-asthmatic subjects was not examined. There is therefore a need for further studies in patients with other bronchial disorders and normal subjects.
In conclusion, the present study clearly indicates that PDE 3 inhibition can attenuate cough reflex sensitivity in the airways of elderly asthmatic patients. Oral administration of cilostazol may be a novel therapeutic option for patients with bronchial asthma, for whom cough is an especially troublesome symptom. This is the first report demonstrating the efficacy of PDE 3 inhibition in view of cough reflex sensitivity in elderly asthmatics. Further studies are required to investigate the role of other PDE isozymes in airway cough reflex sensitivity in bronchial asthma.
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://​creativecommons.​org/​licenses/​by/​2.​0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Metadaten
Titel
Phosphodiesterase 3 inhibition and cough in elderly asthmatics
verfasst von
Yoshihisa Ishiura
Masaki Fujimura
Kouichi Nobata
Miki Abo
Takayoshi Oribe
Shigeharu Myou
Hiroyuki Nakamura
Publikationsdatum
01.12.2005
Verlag
BioMed Central
Erschienen in
Cough / Ausgabe 1/2005
Elektronische ISSN: 1745-9974
DOI
https://doi.org/10.1186/1745-9974-1-11

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Echinokokkose medikamentös behandeln oder operieren?

06.05.2024 DCK 2024 Kongressbericht

Die Therapie von Echinokokkosen sollte immer in spezialisierten Zentren erfolgen. Eine symptomlose Echinokokkose kann – egal ob von Hunde- oder Fuchsbandwurm ausgelöst – konservativ erfolgen. Wenn eine Op. nötig ist, kann es sinnvoll sein, vorher Zysten zu leeren und zu desinfizieren. 

Umsetzung der POMGAT-Leitlinie läuft

03.05.2024 DCK 2024 Kongressbericht

Seit November 2023 gibt es evidenzbasierte Empfehlungen zum perioperativen Management bei gastrointestinalen Tumoren (POMGAT) auf S3-Niveau. Vieles wird schon entsprechend der Empfehlungen durchgeführt. Wo es im Alltag noch hapert, zeigt eine Umfrage in einem Klinikverbund.

Proximale Humerusfraktur: Auch 100-Jährige operieren?

01.05.2024 DCK 2024 Kongressbericht

Mit dem demographischen Wandel versorgt auch die Chirurgie immer mehr betagte Menschen. Von Entwicklungen wie Fast-Track können auch ältere Menschen profitieren und bei proximaler Humerusfraktur können selbst manche 100-Jährige noch sicher operiert werden.

Die „Zehn Gebote“ des Endokarditis-Managements

30.04.2024 Endokarditis Leitlinie kompakt

Worauf kommt es beim Management von Personen mit infektiöser Endokarditis an? Eine Kardiologin und ein Kardiologe fassen die zehn wichtigsten Punkte der neuen ESC-Leitlinie zusammen.

Update Innere Medizin

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