Units of Drug Sciences (P.M., E.S., G.M.), Cardiovascular Sciences (V.C.), Oncology (G.A.), Hematology (O.A.), and Radiation Oncology (C.G.), Department of Medicine and Center for Integrated Research, University Campus Bio-Medico, Rome, Italy; Hematology and Stem Cell Transplant Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy, (F.M.); and Mediservice S.r.l., Agrate Brianza, Monza, Italy (G.R.).
Units of Drug Sciences (P.M., E.S., G.M.), Cardiovascular Sciences (V.C.), Oncology (G.A.), Hematology (O.A.), and Radiation Oncology (C.G.), Department of Medicine and Center for Integrated Research, University Campus Bio-Medico, Rome, Italy; Hematology and Stem Cell Transplant Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy, (F.M.); and Mediservice S.r.l., Agrate Brianza, Monza, Italy (G.R.)
J Pharmacol Exp Ther. 2018 Jul;366(1):158-168. doi: 10.1124/jpet.118.249235. Epub 2018 May 2.
B-type natriuretic peptide (BNP) is widely used as a diagnostic marker of systolic dysfunction. We previously conducted a clinical study in which anthracycline or nonanthracycline chemotherapy did not cause systolic dysfunction in cancer patients; however, some patients showed asymptomatic alterations in diastolic relaxation, whereas others showed persistent elevations of BNP, measured as prohormone BNP amino-terminal fragment. Here we describe post hoc pharmacologic analyses showing that: 1) impaired relaxation and persistent elevations of BNP were mutually exclusive manifestations of diastolic dysfunction; 2) in some patients, BNP elevations were induced by an early compromise of myocardial relaxation; 3) BNP elevations then halted further deterioration of relaxation in a concentration-dependent manner; and 4) high BNP increased heart rate (HR). BNP elevations therefore caused positive lusitropy and chronotropism, which might be explained by activation of natriuretic receptor-associated guanylyl cyclase and production of cGMP in ventricular myocytes and sinoatrial node, respectively. BNP levels also influenced responses to a lusitropic drug, ranolazine, that was given to treat diastolic dysfunction. For patients with impaired relaxation and normal or only transiently high levels of BNP, ranolazine improved myocardial relaxation without inducing chronotropic effects. For patients in whom relaxation abnormalities were corrected by persistently high BNP levels, ranolazine substituted for BNP and decreased HR by diminishing BNP levels. These findings describe a pharmacologic scenario in which cancer drugs cause an early diastolic dysfunction that in some patients is both heralded and modulated by BNP elevations. Patients showing BNP elevations should therefore receive the adequate pharmacologic treatment of correcting diastolic dysfunction and tachycardia.
B 型利钠肽(BNP)被广泛用作收缩功能障碍的诊断标志物。我们之前进行了一项临床研究,其中蒽环类或非蒽环类化疗并未在癌症患者中引起收缩功能障碍;然而,一些患者表现出舒张松弛的无症状改变,而其他患者则表现出 BNP 的持续升高,以 BNP 前体氨基末端片段来衡量。在这里,我们描述了事后药理学分析结果,表明:1)松弛受损和 BNP 的持续升高是舒张功能障碍的相互排斥的表现;2)在一些患者中,BNP 的升高是由心肌松弛的早期受损引起的;3)BNP 的升高以浓度依赖性方式阻止了松弛的进一步恶化;4)高 BNP 增加了心率(HR)。因此,BNP 的升高导致正性变力和变时作用,这可以通过心肌细胞和窦房结中利钠肽受体相关鸟苷酸环化酶的激活和 cGMP 的产生来解释。BNP 水平也影响了对舒张功能障碍治疗药物雷诺嗪的反应。对于松弛受损且 BNP 水平正常或仅短暂升高的患者,雷诺嗪改善了心肌松弛而没有引起变时作用。对于松弛异常通过持续升高的 BNP 水平得到纠正的患者,雷诺嗪替代 BNP,并通过降低 BNP 水平来降低 HR。这些发现描述了一种药理学情况,其中癌症药物引起早期舒张功能障碍,在某些患者中,BNP 升高既预示又调节舒张功能障碍。因此,出现 BNP 升高的患者应接受纠正舒张功能障碍和心动过速的适当药物治疗。