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作 者:Dan Dan Wang Hai Yan Wang Ye Hong Zhou Chun Gui Zhao Chuan Dong Shao Min Shuang
机构地区:[1]School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China [2]Medical College of Shanxi Datong University, Datong 037000, China
出 处:《Chinese Chemical Letters》2007年第4期424-426,共3页中国化学快报(英文版)
基 金:the National Natural Science Foundation of China (No. 20575038).
摘 要:Characteristic of Fura-2-Ca^2+ interaction was studied based on the fluorescence technique. The apparent dissociation constants (Kd) of the Fura-2-Ca^2+ complex were determined at different temperature. The effect of cefotaxime (CEFA) on intracellular Ca^2+ concentration ([Ca^2+]i) was discussed by using a ratiometric fluorescence dye Fura-2 as a probe. The basal [Ca^2+]i in resting human peripheral lymphocytes was 100 4- 7 nmol/L but after treatment with cefotaxime, the changes of [Ca^2+]i were observed in different conditions. In the concentration range of 1-30 μmol/L of cefotaxime [Ca^2+]i increased, as a result of releasing intracellular Ca^2+ stores. Higher concentration of cefotaxime (50-500 μmol/L) stimulated to decrease of [Ca^2+]i.Characteristic of Fura-2-Ca^2+ interaction was studied based on the fluorescence technique. The apparent dissociation constants (Kd) of the Fura-2-Ca^2+ complex were determined at different temperature. The effect of cefotaxime (CEFA) on intracellular Ca^2+ concentration ([Ca^2+]i) was discussed by using a ratiometric fluorescence dye Fura-2 as a probe. The basal [Ca^2+]i in resting human peripheral lymphocytes was 100 4- 7 nmol/L but after treatment with cefotaxime, the changes of [Ca^2+]i were observed in different conditions. In the concentration range of 1-30 μmol/L of cefotaxime [Ca^2+]i increased, as a result of releasing intracellular Ca^2+ stores. Higher concentration of cefotaxime (50-500 μmol/L) stimulated to decrease of [Ca^2+]i.
关 键 词:FURA-2 LYMPHOCYTES CEFOTAXIME [Ca^2+]i
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