Alan-Albayrak Elif, Simonsen Ulf
Department of Pharmacology, Faculty of Pharmacy, Ege University, Izmir, Turkey.
Department of Biomedicine, Pulmonary and Cardiovascular Pharmacology, Aarhus University, Aarhus, Denmark.
Basic Clin Pharmacol Toxicol. 2025 Nov;137(5):e70124. doi: 10.1111/bcpt.70124.
Cyanide is widely recognized for its potent toxicity, yet evidence shows that concentrations below 1 μM may enhance cytochrome c oxidase activity and have a regulatory function. Recent findings also demonstrate that mammalian cells, including endothelial cells, produce cyanide endogenously, where it can modulate mitochondrial bioenergetics. However, the vascular implications of this endogenous production remain unexplored. The review addresses this gap and evaluates the vascular effects of glycine, a proposed substrate for endogenous cyanide synthesis. This systematic review was conducted in accordance with PRISMA 2020 guidelines. Seventy-eight studies were included. Eligible studies with quantifiable vascular outcomes were screened and synthesized. Exogenous cyanide elicited vascular responses through mitochondrial inhibition, modulation of calcium signalling and interference with the soluble guanylyl cyclase/cyclic guanosine monophosphate pathway. Subchronic low-dose in vivo cyanide exposure reduced contractions and enhanced relaxation in endothelium-denuded aortic rings. Collectively, evidence indicates a biphasic pattern: high concentrations are cytotoxic, whereas low concentrations may exert protective/regulatory effects. Low-dose cyanide may have therapeutic potential in managing vascular disorders associated with endothelial dysfunction. Determining an effective and safe dosage range is crucial, and further studies are needed to clarify the role of endogenous cyanide in regulating vascular function.
氰化物因其强大的毒性而广为人知,但有证据表明,浓度低于1μM时可能会增强细胞色素c氧化酶的活性并具有调节功能。最近的研究结果还表明,包括内皮细胞在内的哺乳动物细胞会内源性产生氰化物,它可以调节线粒体生物能量学。然而,这种内源性产生对血管的影响仍未得到探索。这篇综述填补了这一空白,并评估了甘氨酸(一种内源性氰化物合成的潜在底物)对血管的影响。本系统综述是按照PRISMA 2020指南进行的。共纳入78项研究。对具有可量化血管结果的合格研究进行筛选和综合分析。外源性氰化物通过线粒体抑制、钙信号调节以及干扰可溶性鸟苷酸环化酶/环磷酸鸟苷途径引发血管反应。亚慢性低剂量体内氰化物暴露可减少去内皮主动脉环的收缩并增强其舒张。总体而言,证据表明存在一种双相模式:高浓度具有细胞毒性,而低浓度可能发挥保护/调节作用。低剂量氰化物在治疗与内皮功能障碍相关的血管疾病方面可能具有治疗潜力。确定有效且安全的剂量范围至关重要,需要进一步研究来阐明内源性氰化物在调节血管功能中的作用。