采用新型Ca2+荧光指示剂Fura-2建立双波长荧光法测定分离的大鼠神经细胞内游离钙浓度([Ca2+]i).结果显示,在静息状态下,其[Ca2+]i为109±12nmol/L.30mmol/L KCl可显著增加[Ca2+]i,并且KCl的这种效应呈一定的剂量依赖关系,提示该法灵敏、可靠.
The intracellular free Ca2+ concentration ([Ca2+]i) was measured in isolated neurocytes prepared from Sprague-Dawley rats with Fura-2 double-wavelength fluoremetry. The results showed that the [Ca2+]i, of the resting neurocytes in Ca2+-containing solution was 109±12nmol/L(x±s, n=9).KCl (30mmol/L) markedly evoked [Ca2+] of the neurocytes (P<0.01, n=9),and the rises of [Ca2+]i by KCl is a concentration-dependent response.These results suggest that the adoption of Fura-2 double-wavelength fluoremetry in dissociated rat neurocytes in a useful and relatively easily applicable technique for monitoring intracellular Ca2+ changes.
卢步峰,黄诒森,鲁友明.用Fura-2双波长荧光法测定神经细胞内游离钙[J].生物化学与生物物理进展,1994,21(3):275-277
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