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Riociguat for treatment of pulmonary hypertension in COPD: a translational study
被引:29
|作者:
Pichl, Alexandra
[1
,2
,3
,4
]
Sommer, Natascha
[1
,2
,3
,4
]
Bednorz, Mariola
[1
,2
,3
,4
]
Seimetz, Michael
[1
,2
,3
,4
]
Hadzic, Stefan
[1
,2
,3
,4
]
Kuhnert, Stefan
[1
,2
,3
,4
]
Kraut, Simone
[1
,2
,3
,4
]
Roxlau, Elsa T.
[1
,2
,3
,4
]
Kojonazarov, Baktybek
[1
,2
,3
,4
]
Wilhelm, Jochen
[1
,2
,3
,4
]
Gredic, Marija
[1
,2
,3
,4
]
Gall, Henning
[1
,2
,3
,4
]
Tello, Khodr
[1
,2
,3
,4
]
Richter, Manuel J.
[1
,2
,3
,4
]
Pak, Oleg
[1
,2
,3
,4
]
Petrovic, Aleksandar
[1
,2
,3
,4
]
Hecker, Matthias
[1
,2
,3
,4
]
Schermuly, Ralph T.
[1
,2
,3
,4
]
Grimminger, Friedrich
[1
,2
,3
,4
]
Seeger, Werner
[1
,2
,3
,4
,5
]
Ghofrani, Hossein A.
[1
,2
,3
,4
]
Weissmann, Norbert
[1
,2
,3
,4
]
机构:
[1] Univ Giessen, Excellence Cluster Cardiopulm Syst, Aulweg 130, D-35392 Giessen, Germany
[2] Marburg Lung Ctr UGMLC, Aulweg 130, D-35392 Giessen, Germany
[3] German Ctr Lung Res DZL, Giessen, Germany
[4] Justus Liebig Univ, Giessen, Germany
[5] Max Planck Inst Heart & Lung Res, Bad Nauheim, Germany
关键词:
SOLUBLE GUANYLATE-CYCLASE;
MATRIX METALLOPROTEINASES;
DISEASE;
SILDENAFIL;
EMPHYSEMA;
D O I:
10.1183/13993003.02445-2018
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Chronic obstructive pulmonary disease (COPD), which comprises the phenotypes of chronic bronchitis and emphysema, is often associated with pulmonary hypertension (PH). However, currently, no approved therapy exists for PH-COPD. Signalling of the nitric oxide (NO)-cyclic guanosine monophosphate (cGMP) axis plays an important role in PH and COPD. We investigated the treatment effect of riociguat, which promotes the NO-cGMP pathway, in the mouse model of smoke-induced PH and emphysema in a curative approach, and retrospectively analysed the effect of riociguat treatment on PH in single patients with PH-COPD. In mice with established PH and emphysema (after 8 months of cigarette smoke exposure), riociguat treatment for another 3 months fully reversed PH. Moreover, histological hallmarks of emphysema were decreased. Microarray analysis revealed involvement of different signalling pathways, e.g. related to matrix metalloproteinases (MMPs). MMP activity was decreased in vivo by riociguat. In PH-COPD patients treated with riociguat (n=7), the pulmonary vascular resistance, airway resistance and circulating MMP levels decreased, while oxygenation at rest was not significantly changed. Riociguat may be beneficial for treatment of PH-COPD. Further long-term prospective studies are necessary to investigate the tolerability, efficacy on functional parameters and effect specifically on pulmonary emphysema in COPD patients.
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