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点燃大鼠海马中[3H]氟硝西泮结合的长期及区域特异性变化。

Long-term and regional specific changes in [3H]flunitrazepam binding in kindled rat hippocampus.

作者信息

Titulaer M N, Kamphuis W, Lopes da Silva F H

机构信息

Graduate School for the Neurosciences, Institute of Neurobiology, Faculty of Biology, University of Amsterdam, The Netherlands.

出版信息

Neuroscience. 1995 Sep;68(2):399-406. doi: 10.1016/0306-4522(95)00158-f.

Abstract

The binding of the GABAA/benzodiazepine receptor agonist [3H]flunitrazepam was studied in the hippocampus of rats kindled by daily stimulation of the Schaffer collaterals, using semi-quantitative autoradiography. Two kindled stages were investigated: (i) 24 h after the last generalized tonic-clonic seizure (fully kindled) and (ii) 28 days after the last generalized seizure (long-term). The binding of [3H]flunitrazepam was determined at two concentrations, 3 and 16 nM. In the CA1 area, we found a small but significant decrease (ca. 10%), both in the 3 and 16 nM [3H]flunitrazepam binding at the fully kindled stage. In contrast, there was a significant increase in the 3 nM binding (c. 15%) at the long-term stage. The 16 nM binding was not significantly different from control binding at this stage. In the granular and molecular layers of the fascia dentata, we found at both kindled stages a significantly increased 3 nM (ca. 9 and 19%, respectively) and 16 nM (ca. 19 and 14%, respectively) binding. Furthermore, we found that muscimol was still able to enhance the [3H]flunitrazepam binding in kindled animals, indicating that the GABAA receptor agonist binding site and benzodiazepine agonist binding site are still functionally coupled. The changes in [3H]flunitrazepam binding at the fully kindled stage are in agreement with the recently observed kindling-induced changes in [3H]muscimol binding in the hippocampal formation of the same animals [Titulaer M. N. G. et al. (1994) Neuroscience 59, 817-826] and extend these observations to the benzodiazepine modulatory site of the GABAA receptor.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用半定量放射自显影技术,研究了GABAA/苯二氮䓬受体激动剂[3H]氟硝西泮在经每日刺激海马体的Schaffer侧支而点燃的大鼠海马体中的结合情况。研究了两个点燃阶段:(i) 最后一次全身性强直阵挛发作后24小时(完全点燃)和(ii) 最后一次全身性发作后28天(长期)。在3和16 nM这两种浓度下测定了[3H]氟硝西泮的结合情况。在CA1区,我们发现在完全点燃阶段,3和16 nM [3H]氟硝西泮结合均有小幅但显著的下降(约10%)。相比之下,在长期阶段,3 nM结合有显著增加(约15%)。此时16 nM结合与对照结合无显著差异。在齿状回颗粒层和分子层,我们发现在两个点燃阶段,3 nM(分别约为9%和19%)和16 nM(分别约为19%和14%)结合均显著增加。此外,我们发现蝇蕈醇仍能增强点燃动物中[3H]氟硝西泮的结合,表明GABAA受体激动剂结合位点和苯二氮䓬激动剂结合位点仍在功能上偶联。完全点燃阶段[3H]氟硝西泮结合的变化与最近在同一动物海马结构中观察到的点燃诱导的[3H]蝇蕈醇结合变化一致[Titulaer M. N. G.等人(1994年)《神经科学》59卷,817 - 826页],并将这些观察结果扩展到GABAA受体的苯二氮䓬调节位点。(摘要截短至250字)

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