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多巴胺β-羟化酶抑制对压力超负荷诱导的右心室衰竭的影响。

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

作者信息

Andersen Stine, Axelsen Julie Sørensen, Nielsen-Kudsk Anders H, Schwab Janne, Jensen Caroline D, Ringgaard Steffen, Andersen Asger, Smal Rowan, Llucià-Valldeperas Aida, Handoko de Man Frances, Igreja Bruno, Pires Nuno

机构信息

Department of Cardiology Aarhus University Hospital Aarhus Denmark.

Department of Clinical Medicine Aarhus University Aarhus Denmark.

出版信息

Pulm Circ. 2024 Nov 13;14(4):e70008. doi: 10.1002/pul2.70008. eCollection 2024 Oct.

Abstract

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 -hydroxylase (DH) 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 ( = 8) or BIA 21-5337 ( = 11) treatment. An additional PTB group treated with ivabradine ( = 11) was included to control for the potential heart rate-reducing effects of BIA 21-5337. A sham group ( = 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 DH 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 DH activity.

摘要

在肺动脉高压患者中观察到交感神经系统的激活。本研究调查了用BIA 21-5337抑制多巴胺羟化酶(DH)将多巴胺转化为去甲肾上腺素是否能改善压力超负荷诱导的右心室(RV)衰竭中的右心室功能或重塑。通过肺动脉束带(PTB)在雄性Wistar大鼠中诱导RV衰竭。术后两周,将PTB大鼠随机分为接受溶剂对照(n = 8)或BIA 21-5337(n = 11)治疗。纳入另一组接受伊伐布雷定治疗的PTB组(n = 11)以控制BIA 21-5337潜在的心率降低作用。假手术组(n = 6)接受溶剂对照治疗。治疗5周后,在对大鼠实施安乐死之前,通过超声心动图、磁共振成像和有创压力-容积测量评估RV功能。分析RV心肌以评估RV重塑。PTB使RV后负荷增加了四倍,导致RV功能障碍、重塑和衰竭。用BIA 21-5337治疗可降低肾上腺DH活性和24小时尿去甲肾上腺素水平,证实了对该治疗的相关生理反应。在研究结束时,BIA 21-5337治疗组和溶剂对照治疗组的大鼠在RV功能或RV重塑方面没有差异。总之,尽管肾上腺DH活性降低,但BIA 21-5337治疗对PTB后RV衰竭的发展没有任何有益或不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db30/11558268/961878a01fba/PUL2-14-e70008-g004.jpg

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