[3H]唑尼沙胺在大鼠脑中的结合。

Medical journal of Osaka University Pub Date : 1990-03-01
T Mimaki, Y Suzuki, T Tagawa, T Karasawa, H Yabuuchi
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引用次数: 0

摘要

我们之前报道过唑尼沙胺抑制[3H]氟硝西泮和[3H]muscimol在大鼠脑中的结合。在本研究中,发现[3H]zonisamide以饱和方式与大鼠全脑粗突触体部分结合。Scatchard图中结合数据的线性回归分析表明,Kd为90 nM,最大结合能力为1.40 × 10(3) fmol/mg蛋白。置换研究显示氯硝西泮的抑制作用和GABA对特异性[3H]唑尼沙胺结合的增强作用。这些结果表明,大鼠脑内特定的[3H]唑尼沙胺结合位点可能与苯二氮卓受体密切相关。
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[3H]zonisamide binding in rat brain.

We previously reported that zonisamide inhibits both [3H]flunitrazepam and [3H]muscimol binding in rat brain. In the present study, [3H]zonisamide was found to bind in a saturable fashion to the crude synaptosomal fraction of whole rat brain. Linear regression analysis of the binding data in the Scatchard plot indicated a Kd of 90 nM, and a maximal binding capacity of 1.40 x 10(3) fmol/mg protein. Displacement studies revealed an inhibitory effect of clonazepam and an enhancement effect of GABA on specific [3H]zonisamide binding. These results suggest that specific [3H]zonisamide binding sites may have a tight correlationship with benzodiazepine receptors in rat brain.

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