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Ability of bronchodilators to prevent bovine - experimental

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Original

article

Ability

of bronchodilators to prevent bovine experimental respiratory distress

B GenicotP Lambert 2D Votion 1

R CloseJK

Lindsey

P Lekeux

1

Laboratoire

d'investigation fonctionnelle, faculté de médecine vétérinaire, université de

Liège,

bât B42, Sari Tilman, B-4000

Liège;

2

Département

de méthodologie quantitative, faculté d'économie, de gestion et de sciences sociales, université de

Liège,

bât B31, Sart

Tilman,

B-4000

Liège, Belgium

(Received

27 October

1994;
accepted

23 March

1995)

Summary ―

This cross-over trial

involving

6 Blue

Belgian

double-muscled calves aimed to investigate whether ipratropium bromide inhaled alone or in combination with clenbuterol hydrochloride could prevent the dramatic clinical and pulmonary disturbances that are observed during an experimentally induced bronchoconstriction. Inhaled bronchodilators significantly influenced the clinical and func- tional responses of bovines subjected to a

5-hydroxytryptamine perfusion.

However,

despite a mean (standard error) wash-out period of 11.2 (3.1) and 7.5 (0.9) d after the 1 st and the 2nd one-day chal- lenges, respectively, first-order carry-over effects (ie those remaining from the previous treatment), effects of the period during which the treatment was allocated and interaction effects did not allow a definitive interpretation of overall treatment differences. aerosol bronchodilator / clenbuterol / inhalation / ipratropium

Résumé ―

Aptitude

des bronchodilatateurs prévenir un syndrome de détresse respiratoire expé- rimentale chez le bovin. Six veaux hyperviandeux de race

Blanc Bleu

Belge ont été introduits dans cette

étude

dont le but fut de déterminer si le bromure d'ipratropium, inhalé seul ou en association avec de l'hydrochlorure de clenbutérol, permet de prévenir les perturbations cliniques et fonctionnelles observées lors d'une bronchoconstriction expérimentale.

Les bronchodilatateurs

influencèrent, de manière signi- ficative, la réponse clinique et fonctionnelle des bovins soumis à une perfusion lente de

5-hydroxy-

tryptamine.

Néanmoins,

malgré un intervalle d'attente moyen (erreur standard) de 11,2 (3, et 7,5 5 [0,9J j respectivement après le premier et le deuxième traitement, des interactions, des effets transfé- rés du traitement précédent et des effets de la période durant laquelle le traitement fut administré n'ont pas permis une interprétation définitive des différences thérapeutiques globales observées. aérosol / bronchodilatateur / cienbutéroi / inhalation / ipratropium

Correspondence

and reprints:

Pfizer Central

Research,

Clinical

Development,

rue

Laid-Burniat, 1,

B-1348

Louvain-la-Neuve,

Belgium.

INTRODUCTION

Due to the

morphological and functional peculiarities of their lungs, cattle are prone to develop rapid respiratory failure (Lekeux ef al, 1984). Deaths, reduced weight gains, additional labour and veterinary costs all contribute to the financial loss that is due to respiratory disease in calves. In the UK, such losses exceed £50 million annually (Gourlay etal, 1989). In

Belgium,

acute respiratory distress syn- drome is a common and dramatic syndrome in which the bovine respiratory syncytial virus (Wellemans and Leunen, 1975) plays an important role. Several studies concerning the pathogenesis and the physiological changes associated with the bovine respi- ratory syncytial virus have been undertaken (Lekeux ef al, 1985;

Kimman et al, 1989a,b;

Leblanc

etal,1991) and have shown that the syndrome can be associated with airway obstruction (Lekeux et al, 1985) and hyper- reactivity (Leblanc ef al, 1991 ). Conse- quently, an aerosol delivery equipment suit- able for calves has been designed.

Several

studies have been dedicated to the perfor- mances of this aerosol delivery equipment and to the physical properties of therapeutic droplets atomized by means of this equip- ment (Genicot et al, 1994a,b).

On the basis of this

background, the pre- sent study aimed to investigate whether ipratropium bromide inhaled alone or in com- bination with clenbuterol hydrochloride was able to prevent the dramatic clinical and pul- monary disturbances that are observed dur- ing an experimentally induced bronchocon- striction (BC).

MATERIALS AND METHODS

Animals

Six Blue

Belgian

double-muscled calves with a mean (se, standard error) bodyweight of 112.0 (2.9) kg were involved in this cross-over trial which lasted 32 d. The animals were randomly allocated to a treatment (A, B or

C) sequence (table I).

A mean (se) wash-out period of 11.2 (3.1) and 7.5 (0.9) d was introduced after the 1 st and the 2nd one-day challenge, respectively.

Examination under normal

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