University Heart Center Hamburg, Hamburg, Germany.
Institute of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sci Rep. 2019 Apr 5;9(1):5708. doi: 10.1038/s41598-019-42239-1.
The purpose of the present study was to assess whether 6-week ranolazine application on top of guideline-based treatment impacts on the arginine/NO pathway and urinary isoprostane 8-iso-PGF as marker of oxidative stress in patients directly after a myocardial infarction. 20 patients with unstable angina pectoris and proof of acute cardiac ischemia entered the study. 10 subjects received the study drug ranolazine in addition to standard treatment, the others received only standard treatment. Urine and venous blood were collected before and after treatment. At the end of the study and compared to baseline, homoarginine levels had increased in the control group. This was not the case in ranolazine-patients. Interestingly, in ranolazine-treated-patients arginine plasma levels were significantly higher at the end of the study than at baseline (difference +26 µmol/L, 95% CI 8.6 to 44 µmol/L). ADMA and SDMA levels were not different. Urine levels of the oxidative stress marker 8-iso-PGF tended to be lower in ranolazine-treated patients (-144 pmol/mg creatinine). Findings of this hypothesis-driven study give evidence that ranolazine treatment enhances arginine plasma levels and lowers oxidative stress.
本研究旨在评估在基于指南的治疗基础上加用 6 周雷诺嗪治疗是否会影响急性心肌梗死后即刻患者的精氨酸/NO 途径和尿 8-异前列腺素 F2α(氧化应激的标志物)。20 例不稳定型心绞痛患者和急性心肌缺血的证据进入了这项研究。10 名患者接受研究药物雷诺嗪加标准治疗,其余患者仅接受标准治疗。在治疗前后采集尿液和静脉血。与基线相比,对照组的同型精氨酸水平在研究结束时升高。雷诺嗪患者则不然。有趣的是,在接受雷诺嗪治疗的患者中,研究结束时的血浆精氨酸水平明显高于基线(差异+26µmol/L,95%CI8.6 至 44µmol/L)。ADMA 和 SDMA 水平无差异。尿中氧化应激标志物 8-异前列腺素 F2α的水平在接受雷诺嗪治疗的患者中呈下降趋势(-144pmol/mg 肌酐)。这项基于假设的研究结果表明,雷诺嗪治疗可提高血浆精氨酸水平并降低氧化应激。