Director of “Bronchial Remodelling” team, Inserm Unit U1045
Cardio-Thoracic Research Centre of Bordeaux
+ 33 (0)5 57 57 16 94
A team of Inserm researchers from the Cardio-Thoracic Research Centre of Bordeaux (Inserm/University of Bordeaux and Bordeaux University Hospital) has demonstrated the clinical efficacy of gallopamil in 31 patients with severe asthma. This chronic disease is characterised by remodelling of the bronchi, which exacerbates the obstruction of the airways already seen in “classic” asthma. In contrast to the reference treatment, gallopamil has proved capable of reducing the bronchial smooth muscle mass. This work is published in the 29 January 2015 issue of the American Journal of Respiratory and Critical Care Medicine.
Severe asthma is a chronic condition of the airways that affects between 1 and 3% of the world population to a highly variable extent, depending on the country. It is characterised by persistent breathing difficulty, restricted physical activity, frequent nocturnal attacks, and prolonged asthma attacks that require systemic treatment. These symptoms lead to a considerable number of emergency hospital admissions, have a serious impact on the quality of life for patients, and can even result in death.
In severe asthma, bronchial obstruction causes a strong reduction in respiratory capacity. This bronchial obstruction is due to remodelling of the airways, particularly the thickening of the bronchial smooth muscle (BSM) that surrounds them. This phenomenon is associated with a poor prognosis and resistance to even intensive treatment. Until now, no pharmaceutical drug has succeeded in preventing the excessive proliferation of these muscle cells, including corticosteroids, the reference treatment for severe asthma.
In previous work, Patrick Berger and his colleagues had already demonstrated in vitro and ex vivo that this disproportionate growth was triggered by an abnormal entry of calcium into these bronchial smooth muscle cells. In this same article, the scientists had demonstrated in vitro the anti-proliferative effect of gallopamil, which is normally prescribed for certain heart conditions because of its blocking action on calcium channels.
© Inserm, Pelletier L. The left pictures show the characteristic look of lung inflammation in asthma with thickening of the bronchial wall, a lot of inflammatory cells and an abnormal production of mucus. Mice treated with the calcium channel inhibitor (on the right) are completely protected.
To assess its in vivo efficacy, the researchers then initiated a clinical trial sponsored by Bordeaux University Hospital and supported by the French Ministry and Health and Inserm. For 12 months, they thus measured the effect of the drug on the thickness of the BSM and bronchial wall, and the frequency of asthma attacks in 31 patients.
On analysis, the data showed a significant reduction in BSM in asthmatic patients treated with gallopamil compared with the placebo group. The drug therefore enabled a significant reduction in the thickness of the bronchial wall in patients.
After this phase, both patient groups were monitored for 3 months after stopping treatment. It then became apparent that individuals treated with gallopamil had significantly fewer prolonged attacks than the placebo group.
 Berger P. et al., Bronchial smooth muscle remodeling involves calcium-dependent enhanced mitochondrial biogenesis in asthma. J Exp Med 2007; 204:3173-3181
La chirurgie bariatrique est un traitement efficace de l’obésité sévère mais améliore également les co-morbidités associées dont le diabète de type 2 (DT2) par une restauration de la sécrétion d’insuline déficitaire. ...
Atopic dermatitis, or eczema, primarily affects infants and children, and manifests itself in hypersensitivity to allergens in the environment. A skin disease characterized by flare-ups, it is often treated with topical anti-inflammatories. A new study shows that immune cells and sensory neurons ...
Calcium channel blocker reduces airway remodeling in severe asthma: a Proof-of-concept study Pierre-Olivier Girodet1,2,3, Gael Dournes1,2,3, Matthieu Thumerel1,2,3, Hugues Begueret3, Pierre Dos Santos1,2,3, Annaig Ozier1,2,3, Isabelle Dupin1,2, Thomas Trian1,2, Michel Montaudon1,2,3, François Laurent1,2,3, Roger Marthan1,2,3, Patrick Berger1,2,3
1. University of Bordeaux, Cardio-Thoracic Research Centre of Bordeaux, U1045, Department of Pharmacology, CIC1401, F-33000, Bordeaux, France
2. INSERM, Cardio-Thoracic Research Centre of Bordeaux, U1045, CIC1401, F-33000, Bordeaux, France
3. Bordeaux University Hospital CIC1401, Functional Respiratory Exploration Service, Diagnostic and Therapeutic Imaging Service, Thoracic Surgery Service, Cardiology Service, F33604 Pessac, France American Journal of Respiratory and Critical Care Medicine, 29th january 2015