Pharmaceutical Science Program (CiPharma), School of Pharmacy, Federal University of Ouro Preto, Campus Morro do Cruzeiro, s/n, Ouro Preto, Minas Gerais, 35400-000, Brazil.
Department of Pharmaceutical Products, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Cardiovasc Toxicol. 2021 Feb;21(2):93-105. doi: 10.1007/s12012-020-09599-x. Epub 2020 Aug 26.
Caspofungin is an echinocandin, exhibiting efficacy against most Candida species invasive infection. Its cardiotoxicity was reported in isolated rat heart and ventricular myocytes, but in vivo and clinical studies are insufficient. Our objective was to evaluate caspofungin in vivo cardiac effects using an efficacious dose against Candida albicans. Female Swiss mice were infected with C. albicans, and treated with caspofungin, 5 or 10 mg/kg, intraperitoneal along 5 days. Survival rate and colony-forming units (CFU) into vital organs were determined. For cardiac effects study, mice were treated with caspofungin 10 mg/kg, and electrocardiogram (ECG) signal was obtained on C. albicans-infected mice, single dose-treated, and uninfected mice treated along 5 days, both groups to measure ECG intervals. Besides, ECG was also obtained by telemetry on uninfected mice to evaluate heart rate variability (HRV) parameters. The MIC for caspofungin on the wild-type C. albicans SC5314 strain was 0.3 μg/ml, indicating the susceptible. Survival rate increased significantly in infected mice treated with caspofungin compared to mice treated with vehicle. None of the survived infected mice presented positive CFU after treatment with 10 mg/kg. C. albicans infection induced prolongation of QRS, QT, and QTc intervals; caspofungin did not alter this effect. Caspofungin induced increase of PR and an additional increase of QRS after 24 h of a single dose in infected mice. No significant alterations occurred in ECG intervals and HRV parameters of uninfected mice, after caspofungin treatment. Caspofungin showed in vivo cardiac relative safety maintaining its antifungal efficacy against C. albicans.
卡泊芬净是一种棘白菌素,对大多数侵袭性感染的念珠菌具有疗效。其在离体大鼠心脏和心室肌细胞中已有心脏毒性的报道,但体内和临床研究尚不充分。我们的目的是使用对白色念珠菌有效的剂量评估卡泊芬净的体内心脏效应。雌性瑞士小鼠感染白色念珠菌,并用卡泊芬净(5 或 10mg/kg)腹膜内注射,共 5 天。测定存活率和对重要器官的菌落形成单位(CFU)。为了进行心脏效应研究,用卡泊芬净(10mg/kg)处理小鼠,对白色念珠菌感染的小鼠、单次剂量处理的小鼠和连续 5 天处理的未感染小鼠进行心电图(ECG)信号检测,以测量 ECG 间期。此外,还对未感染的小鼠进行遥测心电图以评估心率变异性(HRV)参数。卡泊芬净对野生型白色念珠菌 SC5314 株的 MIC 为 0.3μg/ml,表明敏感。与用载体处理的小鼠相比,用卡泊芬净处理的感染小鼠的存活率显著增加。用 10mg/kg 治疗后,存活的感染小鼠均未出现阳性 CFU。白色念珠菌感染导致 QRS、QT 和 QTc 间期延长;卡泊芬净未改变这种作用。卡泊芬净在感染小鼠单次剂量后 24 小时内引起 PR 延长和 QRS 进一步延长。未感染小鼠在卡泊芬净治疗后,心电图间期和 HRV 参数无明显变化。卡泊芬净显示出体内心脏相对安全性,同时保持对白色念珠菌的抗真菌疗效。