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出 处:《重庆医科大学学报》1996年第3期199-202,共4页Journal of Chongqing Medical University
摘 要:本文系统地研究了影响小鼠大脑皮层细胞突触体^(45)Ca摄取的实验条件。发现:在前4min内。^(45)Ca摄取量与温育时间呈直线关系;突触体膜蛋白投入量以0.063~0.250mg为宜超过0.250mg则^(45)Ca摄取呈下降趋势;与无钙和正常钙(1.20mmol/L)培养液相比.低钙培养液(0.6mmo-l/L)更有利于突触体的钙摄取,且钙拮抗剂硝砒乙甲酯在低钙(0.6mmol/L)培养液中对^(45)Ca进入突触体有促进作用;高钾刺激促进^(45)Ca摄取,但浓度以30~50mmol/L为宜;溶剂二甲亚砜(DMSO)低浓度(0.05%)有促进^(45)Ca摄取的作用;但乙醇和丙酮浓度在0.05~6.25%范围内则无明显影。上述实验结果为准确进行突触体钙摄取实验和测定药物对钙进入的影响提供了基础资料。he experunental conditions of 45Ca uptake into synaptosome from the mice cerebral corticeswere studied.It was found that during the firot 4 minutes there was a straight relationshipbetween amount of 45Ca uptake and incubation tune. The range of suitable membrane protein ofsynaptosame used was between 0.063~0.250 mg and 45Ca uptake would decline when membraneprotein was more than 0.250mg Low calcium medium(0.6mmol/L)was more beneficial to the 45Cauptake than zero or normal calcium(12mmol/L)medium,and nitrendipine had a promoting effecton 45Ca uptake in the former medium. The rang of kalium concentrations for the best stunulationof 45Ca uptake was grom 30 to 50 mmol/L. DMSO had a potential effect on 45Ca uptake at theconcentration of 0.05%,but ethanol and acetone failed to show an influence on it at theconcentrations of 0.05~6.25%。All results above provide essential data for correctly carrying outexperunents of 45Ca uptake into synaptcoolne and determining the effects of drugs on 45Ca uptake.
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