Effects of dopamine β-hydroxylase inhibition in pressure overload-induced right ventricular failure

被引:1
作者
Andersen, Stine [1 ,2 ]
Axelsen, Julie Sorensen [1 ,2 ]
Nielsen-Kudsk, Anders H. [1 ,2 ]
Schwab, Janne [1 ,2 ]
Jensen, Caroline D. [1 ,2 ]
Ringgaard, Steffen [3 ]
Andersen, Asger [1 ,2 ]
Smal, Rowan [4 ]
Llucia-Valldeperas, Aida [4 ]
de Man, Frances Handoko [4 ]
Igreja, Bruno [5 ]
Pires, Nuno [5 ]
机构
[1] Aarhus Univ Hosp, Dept Cardiol, Palle Juul Jensens Blvd 99, DK-8200 Aarhus, Denmark
[2] Aarhus Univ, Dept Clin Med, Aarhus, Denmark
[3] Aarhus Univ, MR Res Ctr, Dept Clin Med, Aarhus, Denmark
[4] Univ Amsterdam, Med Ctr, Dept Pulmonol, Amsterdam, Netherlands
[5] Portela & Ca SA, Dept Res, BIAL, Coronado, S Romao E S Mam, Portugal
关键词
animal study; dopamine beta-hydroxylase; noradrenaline; right heart failure; sympathetic nervous system; PULMONARY ARTERIAL-HYPERTENSION; NEUROHORMONAL ACTIVATION; HEART-FAILURE; ANIMAL-MODELS; RAT MODEL; DYSFUNCTION; BISOPROLOL; ETAMICASTAT; ZAMICASTAT;
D O I
10.1002/pul2.70008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Activation of the sympathetic nervous system is observed in pulmonary arterial hypertension patients. This study investigates whether inhibiting the conversion of dopamine into noradrenaline by dopamine beta-hydroxylase (D beta H) inhibition with BIA 21-5337 improved right ventricular (RV) function or remodeling in pressure overload-induced RV failure. RV failure was induced in male Wistar rats by pulmonary trunk banding (PTB). Two weeks after the procedure, PTB rats were randomized to vehicle (n = 8) or BIA 21-5337 (n = 11) treatment. An additional PTB group treated with ivabradine (n = 11) was included to control for the potential heart rate-reducing effects of BIA 21-5337. A sham group (n = 6) received vehicle treatment. After 5 weeks of treatment, RV function was assessed by echocardiography, magnetic resonance imaging, and invasive pressure-volume measurements before rats were euthanized. RV myocardium was analyzed to evaluate RV remodeling. PTB caused a fourfold increase in RV afterload which led to RV dysfunction, remodeling, and failure. Treatment with BIA 21-5337 reduced adrenal gland D beta H activity and 24-h urinary noradrenaline levels confirming relevant physiological response to the treatment. At end-of-study, there were no differences in RV function or RV remodeling between BIA 21-5337 and vehicle-treated rats. In conclusion, treatment with BIA 21-5337 did not have any beneficial-nor adverse-effects on the development of RV failure after PTB despite reduced adrenal gland D beta H activity.
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页数:13
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