Heart Institute (InCor), University of São Paulo Medical School , São Paulo , Brazil.
Cancer Institute of the State of São Paulo, University of São Paulo Medical School , São Paulo , Brazil.
Am J Physiol Heart Circ Physiol. 2019 Jul 1;317(7):H1-H12. doi: 10.1152/ajpheart.00756.2018. Epub 2019 Apr 19.
The purpose of the present study was to test the hypothesis that doxorubicin (DX) and cyclophosphamide (CY) adjuvant chemotherapy (CHT) acutely impairs neurovascular and hemodynamic responses in women with breast cancer. Sixteen women (age: 47.0 ± 2.0 yr; body mass index: 24.2 ± 1.5 kg/m) with stage II-III breast cancer and indication for adjuvant CHT underwent two experimental sessions, saline (SL) and CHT. In the CHT session, DX (60 mg/m) and CY (600 mg/m) were administered over 45 min. In the SL session, a matching SL volume was infused in 45 min. Muscle sympathetic nerve activity (MSNA) from peroneal nerve (microneurography), calf blood flow (CBF; plethysmography) and calf vascular conductance (CVC), heart rate (HR; electrocardiography), and beat-to-beat blood pressure (BP; finger plethysmography) were measured at rest before, during, and after each session. Venous blood samples (5 ml) were collected before and after both sessions for assessment of circulating endothelial microparticles (EMPs; flow cytometry), a surrogate marker for endothelial damage. MSNA and BP responses were increased ( < 0.001), whereas CBF and CVC responses were decreased ( < 0.001), during and after CHT session when compared with SL session. Interestingly, the vascular alterations were also observed at the molecular level through an increased EMP response to CHT ( = 0.03, CHT vs. SL session). No difference in HR response was observed ( > 0.05). Adjuvant CHT with DX and CY in patients treated for breast cancer increases sympathetic nerve activity and circulating EMP levels and, in addition, reduces muscle vascular conductance and elevates systemic BP. These responses may be early signs of CHT-induced cardiovascular alterations and may represent potential targets for preventive interventions. It is known that chemotherapy regimens increase the risk of cardiovascular events in patients treated for cancer. Here, we identified that a single cycle of adjuvant chemotherapy with doxorubicin and cyclophosphamide in women treated for breast cancer dramatically increases sympathetic nerve activity and circulating endothelial microparticle levels, reduces the muscle vascular conductance, and elevates systemic blood pressure.
本研究旨在检验以下假设,即阿霉素(DX)和环磷酰胺(CY)辅助化疗(CHT)会急性损害患有乳腺癌女性的神经血管和血液动力学反应。16 名女性(年龄:47.0±2.0 岁;体重指数:24.2±1.5kg/m2)患有 II-III 期乳腺癌,需要辅助 CHT,她们进行了两次实验,盐水(SL)和 CHT。在 CHT 疗程中,DX(60mg/m)和 CY(600mg/m)在 45 分钟内输注。在 SL 疗程中,在 45 分钟内输注等量的 SL 溶液。腓肠神经(微神经生理学)的肌肉交感神经活动(MSNA)、小腿血流(容积描记法)和小腿血管传导性(CVC)、心率(心电图)和每搏血压(指容积描记法)在每个疗程前后的休息时间进行测量。在两次疗程前后采集 5ml 静脉血样,用于评估循环内皮微颗粒(EMPs;流式细胞术),这是内皮损伤的替代标志物。与 SL 疗程相比,CHT 疗程期间和之后,MSNA 和血压反应增加(<0.001),而 CBF 和 CVC 反应降低(<0.001)。有趣的是,通过 CHT 引起的 EMP 反应增加(=0.03,CHT 与 SL 疗程相比),也在分子水平上观察到血管变化。心率反应无差异(>0.05)。在接受乳腺癌治疗的患者中,用 DX 和 CY 进行辅助 CHT 会增加交感神经活动和循环 EMP 水平,并降低肌肉血管传导性和升高全身血压。这些反应可能是 CHT 引起的心血管改变的早期迹象,可能是预防干预的潜在目标。众所周知,化疗方案会增加癌症治疗患者发生心血管事件的风险。在这里,我们发现,在接受乳腺癌治疗的女性中,单次接受辅助化疗(阿霉素和环磷酰胺)会显著增加交感神经活动和循环内皮微颗粒水平,降低肌肉血管传导性,并升高全身血压。