Amirjanians Matthieu, Egemnazarov Bakytbek, Sydykov Akylbek, Kojonazarov Baktybek, Brandes Ralf, Luitel Himal, Pradhan Kabita, Stasch Johannes-Peter, Redlich Gorden, Weissmann Norbert, Grimminger Friedrich, Seeger Werner, Ghofrani Hossein, Schermuly Ralph
University of Giessen Lung Center, Giessen, Germany.
Institute for Cardiovascular Physiology, J.W. Goethe University, Frankfurt, Germany.
Oncotarget. 2017 May 2;8(18):29613-29624. doi: 10.18632/oncotarget.16769.
Dysfunction of the NO/sGC/cGMP signaling pathway has been implicated in the pathogenesis of pulmonary hypertension (PH). Therefore, agents stimulating cGMP synthesis via sGC are important therapeutic options for treatment of PH patients. An unwanted effect of this novel class of drugs is their systemic hypotensive effect. We tested the hypothesis that aerosolized intra-tracheal delivery of the sGC stimulator BAY41-8543 could diminish its systemic vasodilating effect.Pharmacodynamics and -kinetics of BAY41-8543 after single intra-tracheal delivery was tested in healthy rats. Four weeks after a single injection of monocrotaline (MCT, 60 mg/kg s.c.), rats were randomized to a two-week treatment with either placebo, BAY 41-8543 (10 mg/kg per os (PO)) or intra-tracheal (IT) instillation (3 mg/kg or 1 mg/kg).Circulating concentrations of the drug 10 mg/kg PO and 3 mg/kg IT were comparable. BAY 41-8543 was detected in the lung tissue and broncho-alveolar fluid after IT delivery at higher concentrations than after PO administration. Systemic arterial pressure transiently decreased after oral BAY 41-8543 and was unaffected by intratracheal instillation of the drug. PO 10 mg/kg and IT 3 mg/kg regimens partially reversed pulmonary hypertension and improved heart function in MCT-injected rats. Minor efficacy was noted in rats treated IT with 1 mg/kg. The degree of pulmonary vascular remodeling was largely reversed in all treatment groups.Intratracheal administration of BAY 41-8543 reverses PAH and vascular structural remodeling in MCT-treated rats. Local lung delivery is not associated with systemic blood pressure lowering and represents thus a further development of PH treatment with sGC stimulators.
一氧化氮/可溶性鸟苷酸环化酶/环磷酸鸟苷(NO/sGC/cGMP)信号通路功能障碍与肺动脉高压(PH)的发病机制有关。因此,通过刺激sGC来促进cGMP合成的药物是治疗PH患者的重要治疗选择。这类新型药物的一个不良作用是其全身降压作用。我们检验了以下假设:经气管内雾化递送sGC刺激剂BAY41-8543可减弱其全身血管舒张作用。在健康大鼠中测试了单次气管内递送BAY41-8543后的药效学和药代动力学。单次注射野百合碱(MCT,60mg/kg皮下注射)四周后,将大鼠随机分为两组,分别接受为期两周的安慰剂、BAY41-8543(10mg/kg口服(PO))或气管内(IT)滴注(3mg/kg或1mg/kg)治疗。口服10mg/kg和气管内滴注3mg/kg的药物循环浓度相当。IT给药后,肺组织和支气管肺泡液中检测到的BAY41-8543浓度高于口服给药后。口服BAY41-8543后,体动脉压短暂下降,而气管内滴注该药物对其无影响。口服10mg/kg和气管内滴注3mg/kg方案可部分逆转MCT注射大鼠的肺动脉高压并改善心脏功能。气管内注射1mg/kg治疗的大鼠疗效较差。所有治疗组的肺血管重塑程度在很大程度上都得到了逆转。气管内给予BAY41-8543可逆转MCT治疗大鼠的肺动脉高压和血管结构重塑。肺部局部给药与全身血压降低无关,因此代表了sGC刺激剂治疗PH的进一步发展。