Li W, Zheng T, Wang J, Altura B T, Altura B M
Department of Physiology, State University of New York, Health Science Center at Brooklyn, 11203, USA.
Alcohol. 1999 Jun-Jul;18(2-3):221-4. doi: 10.1016/s0741-8329(99)00007-5.
Acute exposure of cultured canine cerebral vascular smooth muscle cells to methanol (10-400 mM) results in concentration-dependent elevation of the concentration of intracellular free calcium ion ([Ca2+]i) as measured with the fluorescent indicator, fura-2, and digital imaging microscopy. The resting level of [Ca2+]i in the cerebral vascular smooth muscle cells was 89.3+/-5.3 nM. Exposure of these cells to 10 mM methanol for only 5 min resulted in significant elevation in [Ca2+]i (i.e., to 105.7+/-4.6) (p < 0.05). Methanol (10 mM) is a concentration found in the blood of victims demonstrating early CNS toxicity. Other, higher concentrations of methanol rapidly raised [Ca2+]i upwards of 60% over basal resting levels. These result suggest that methanol-induced cerebral vasospasm is a consequence of large rises in intracellular Ca2+. These events could play a crucial role in methanol-induced cerebral edema, brain hemorrhage, and cerebral and retinal infarcts, eventuating in severe deficits in brain blood flow and the known, subsequent CNS disturbances.
用荧光指示剂fura - 2和数字成像显微镜测量发现,培养的犬脑血管平滑肌细胞急性暴露于甲醇(10 - 400 mM)会导致细胞内游离钙离子浓度([Ca2+]i)呈浓度依赖性升高。脑血管平滑肌细胞中[Ca2+]i的静息水平为89.3±5.3 nM。将这些细胞仅暴露于10 mM甲醇5分钟就导致[Ca2+]i显著升高(即升至105.7±4.6)(p < 0.05)。甲醇(10 mM)是在表现出早期中枢神经系统毒性的受害者血液中发现的浓度。其他更高浓度的甲醇会使[Ca2+]i迅速升高至比基础静息水平高出60%以上。这些结果表明,甲醇诱导的脑血管痉挛是细胞内Ca2+大幅升高的结果。这些事件可能在甲醇诱导的脑水肿、脑出血以及脑和视网膜梗死中起关键作用,最终导致脑血流量严重不足以及随后已知的中枢神经系统紊乱。