Stuart J, Mojiminiyi F B, Stone P C, Culliford S J, Ellory J C
Department of Haematology, Medical School, University of Birmingham.
Br J Haematol. 1994 Apr;86(4):820-3. doi: 10.1111/j.1365-2141.1994.tb04836.x.
To study the effect of anti-sickling drugs on cellular dehydration induced by entry of Ca, sickle cells were subjected to cyclical oxygenation-deoxygenation for 15 h in Ca-containing buffer. The consequential loss of cation (K) via the Ca-dependent K efflux (Gardos) channel caused cell dehydration and loss of deformability. Inhibition of a specific fraction of Ca entry by verapamil had no rheologically protective effect, whereas inhibition of the Gardos channel by clotrimazole or nitrendipine had a marked protective effect. When Gardos channel inhibition (by either clotrimazole or nitrendipine) was combined with stabilization of the oxy-conformation of sickle haemoglobin (by the substituted benzaldehyde 12C79), an additive protective rheological effect was achieved with 60-78% reduction in clogging rate of 5 microns diameter pores when compared with no drug. Therapeutic use of anti-sickling compounds in combination may achieve increased efficacy with lower toxicity.
为研究抗镰状化药物对钙离子内流诱导的细胞脱水的影响,将镰状细胞置于含氯化钙的缓冲液中进行15小时的周期性氧合-脱氧处理。随后通过钙依赖性钾离子外流(加尔多斯)通道导致阳离子(钾)的流失,引起细胞脱水和变形性丧失。维拉帕米抑制特定部分的钙离子内流没有流变学保护作用,而克霉唑或尼群地平抑制加尔多斯通道则具有显著的保护作用。当加尔多斯通道抑制(通过克霉唑或尼群地平)与镰状血红蛋白氧构象稳定(通过取代苯甲醛12C79)相结合时,与未用药相比,直径5微米的孔堵塞率降低60%-78%,从而实现了附加的流变学保护作用。联合使用抗镰状化化合物进行治疗可能会在降低毒性的同时提高疗效。