Bisabololoxide A (BSBO), main constituents in German chamomile extract, is responsible for antipruritic effect. In previous study, the incubation with 30-100 μM BSBO for 24 h exerted cytotoxic and proapoptotic effects on rat thymocytes. To further characterize BSBO cytotoxicity, the effect on the cells suffering from calcium overload by calcium ionophore A23187 was examined. A23187 induced Ca(2+) -dependent cell death. Contrary to our expectation, 1-10 μM BSBO inhibited A23187-induced increase in cell lethality of rat thymocytes. BSBO attenuated A23187-induced increases in populations of shrunken living cells, phosphatidylserine-exposed living cells, and dead cells, without affecting the increase in intracellular Ca(2+) concentration and the Ca(2+) -dependent hyperpolarization. The effect of BSBO on A23187-treated cells may be unique because the activation of Ca(2+) -dependent K(+) channels is required for cell shrinkage, externalization of phosphatidylserine, and cell death in some cells. The cell death induced by A23187 was not inhibited by Z-VAD-FMK, a pan-inhibitor of caspases. Thus, the cell death may be a necrosis with some features observed during an early stage of apoptosis. These results suggest that BSBO at low micromolar concentrations is cytoprotective against calcium overload.

译文

双药物氧A (BSBO),德国洋甘菊提取物的主要成分,负责止痒作用。在先前的研究中,与30-100  μ mbsbo孵育24  h对大鼠胸腺细胞具有细胞毒性和促凋亡作用。为了进一步表征BSBO的细胞毒性,研究了钙离子载体A23187对遭受钙超载的细胞的影响。A23187诱导Ca(2 +) 依赖性细胞死亡。与我们的预期相反,1-10  μ mbsbo A23187-induced抑制大鼠胸腺细胞致死率的增加。BSBO减弱了收缩的活细胞,磷脂酰丝氨酸暴露的活细胞和死细胞的A23187-induced增加,而不影响细胞内Ca(2) 浓度和Ca(2) 依赖性超极化的增加。BSBO对A23187-treated细胞的作用可能是独特的,因为某些细胞的细胞收缩,磷脂酰丝氨酸的外部化和细胞死亡需要激活Ca(2) 依赖性K () 通道。A23187诱导的细胞死亡不受胱天蛋白酶泛抑制剂Z-VAD-FMK的抑制。因此,细胞死亡可能是坏死,在凋亡的早期阶段观察到某些特征。这些结果表明,低微摩尔浓度的BSBO对钙超载具有细胞保护作用。

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