Lim Jeongwook, Cho Young Dae, Byoun Hyoung Soo
Department of Neurosurgery, Chungnam National University Sejong Hospital, Chungnam National University School of Medicine, Daejeon, Korea (Republic of).
Department of Radiology, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, 03080, Seoul, Korea (Republic of).
Clin Neuroradiol. 2022 Dec;32(4):1011-1017. doi: 10.1007/s00062-022-01151-4. Epub 2022 Mar 16.
Intra-arterial (IA) infusion of calcium channel blockers (CCBs) has been widely applied in treating medically refractory vasospasm; however, surprisingly little is known regarding their vasodilatory duration. This study was undertaken to compare attributes of nicardipine and dantrolene, focusing on efficacy and capacity for sustained vasodilation.
In New Zealand white rabbits (N = 22), vasospasm was individually provoked through experimentally induced subarachnoid hemorrhage and confirmed via conventional angiography, grouping animals by IA-infused drug (nicardipine vs. dantrolene). Controls received normal saline. After chemoangioplasty, follow-up angiography was performed at intervals of 1-3 h for 6 h to compare vasospastic and dilated (i.e., treated) arterial diameters. Drug efficacy, duration of action, and changes in mean arterial pressure (relative to baseline) were analyzed by group.
Compared with controls, effective vasodilation was evident in both nicardipine and dantrolene test groups after IA infusion. Vasodilatory effects of nicardipine peaked at 1 h, returning to former vasospastic states at 3 h. In dantrolene recipients, vasodilation endured longer, lasting >6 h. Only the nicardipine group showed a significant 3‑h period of lowered blood pressure.
Unlike the vasodilatory action of a CCB, sustained for < 3 h after IA infusion, the effect of dantrolene endured for > 6 h. This outcome suggests that IA dantrolene infused alone or together with a conventional CCB infusion may be a new means of prolonging vasodilatory effect. Further research is needed to assess durations of IA-infused vasodilatory drug based on perfusion status.
动脉内(IA)输注钙通道阻滞剂(CCB)已广泛应用于治疗药物难治性血管痉挛;然而,令人惊讶的是,关于其血管舒张持续时间的了解却很少。本研究旨在比较尼卡地平和丹曲林的特性,重点关注疗效和持续血管舒张能力。
在新西兰白兔(N = 22)中,通过实验性诱导蛛网膜下腔出血单独诱发血管痉挛,并通过传统血管造影术确认,根据IA注入的药物(尼卡地平与丹曲林)对动物进行分组。对照组接受生理盐水。化学血管成形术后,每隔1 - 3小时进行一次随访血管造影,持续6小时,以比较血管痉挛和扩张(即治疗后)动脉直径。按组分析药物疗效、作用持续时间和平均动脉压(相对于基线)的变化。
与对照组相比,IA输注后尼卡地平和丹曲林试验组均出现明显的有效血管舒张。尼卡地平的血管舒张作用在1小时达到峰值,3小时恢复到先前的血管痉挛状态。在接受丹曲林的动物中,血管舒张持续时间更长,持续> 6小时。只有尼卡地平组在3小时内出现显著的血压降低。
与IA输注后持续< 3小时的CCB血管舒张作用不同,丹曲林的作用持续> 6小时。这一结果表明,单独输注IA丹曲林或与传统CCB输注联合使用可能是延长血管舒张作用的新方法。需要进一步研究以根据灌注状态评估IA输注血管舒张药物的持续时间。