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从大鼠脑分离的神经末梢对放射性钙的摄取:药理学研究。

Uptake of radiocalcium by nerve endings isolated from rat brain: pharmacological studies.

作者信息

Gripenberg J, Heinonen E, Jansson S E

出版信息

Br J Pharmacol. 1980;71(1):273-8. doi: 10.1111/j.1476-5381.1980.tb10936.x.

Abstract

1 The uptake of radiocalcium by nerve-ending particles isolated from the striatum of rat brain was studied using lanthanum as a quenching agent. 2 High potassium-induced calcium uptake occurred in two phases: an initial rapid phase and a late slow phase. Following preincubation with CaCl2 2.2 mmol/l for 1 h, dopamine at 1 to 2 x 10(-4) mol/l reduced the high potassium-induced calcium uptake which occurred during the initial rapid phase by 66 and 25% at 2 and 4 s of incubation, respectively, but had no effect on the late slow uptake phase. 3 Haloperidol at 1 x 10(-6) mol/l abolished the inhibitory effect of dopamine on the initial rapid phase of the high potassium-induced calcium uptake. Haloperidol per se had no effect on the calcium uptake. 4 Dibutyryl cyclic adenosine monophosphate at 2.5 x 10(-3) mol/l or prostaglandin E1 (PGE1) at 1 x 10(-5) mol/l had no effect on the initial rapid phase of the high potassium-induced calcium uptake by striatal synaptosomes. Neither of these agents affect calcium uptake by whole brain synaptosomes. 5 It appears that in the striatum, dopamine regulates the depolarization-induced influx of calcium in presynaptic nerve endings. This mechanism could constitute a feed-back inhibition for transmitter release in the striatum.

摘要
  1. 以镧作为猝灭剂,研究了从大鼠脑纹状体分离出的神经末梢颗粒对放射性钙的摄取。2. 高钾诱导的钙摄取分两个阶段进行:初始快速阶段和后期缓慢阶段。在2.2 mmol/l氯化钙中预孵育1小时后,1至2×10(-4) mol/l的多巴胺分别在孵育2秒和4秒时,使初始快速阶段高钾诱导的钙摄取减少了66%和25%,但对后期缓慢摄取阶段没有影响。3. 1×10(-6) mol/l的氟哌啶醇消除了多巴胺对高钾诱导的钙摄取初始快速阶段的抑制作用。氟哌啶醇本身对钙摄取没有影响。4. 2.5×10(-3) mol/l的二丁酰环磷酸腺苷或1×10(-5) mol/l的前列腺素E1(PGE1)对纹状体突触体高钾诱导的钙摄取初始快速阶段没有影响。这两种药物都不影响全脑突触体的钙摄取。5. 看来在纹状体中,多巴胺调节突触前神经末梢去极化诱导的钙内流。这种机制可能构成纹状体中递质释放的反馈抑制。

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