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Modulation of the perforant path-evoked potential in dentate gyrus as a function of intrahippocampal β-adrenoceptor agonist concentration in urethane-anesthetized rat

机译:调节海马齿状回中的穿孔路径诱发电位作为氨基甲酸酯麻醉大鼠海马内β-肾上腺素能受体激动剂浓度的函数

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摘要

udBackgroundudβ-adrenoceptor activation in the hippocampus is sufficient to induce heterosynaptic long-term potentiation of perforant path input to the dentate gyrus. However, in vitro and in vivo studies suggest the plasticity effects of β-adrenoceptor activation may vary depending on the level of receptor activation.ududMethodsudThe present experiments use an in vivo model concurrently infusing differing concentrations of the β-adrenoceptor agonist, isoproterenol (ISO; 0, 0.1, 1, 10, and 100 μmol/L in aCSF; 1 μL over 12.5 min) in the dentate gyrus, while monitoring changes in the perforant path-evoked potential at the same site.ududResultsudLong-term depression (LTD) of fEPSP slope was elicited by 0.1 μmol/L ISO. Higher doses did not alter fEPSP slope. Maximal long-term potentiation of the perforant path-evoked population spike (183% >3 h) occurred at 10 μmol/L ISO. Transient depression of spike amplitude occurred at 0.1 μmol/L ISO.udududConclusionsudududThese data demonstrate concentration-dependent effects of β-adrenoceptor activation on the perforant path-evoked potential. Long-term depression and long-term potentiation of perforant path-evoked responses are variably elicited as a function of the degree of receptor activation.
机译:海马中的 udBackground udβ-肾上腺素受体激活足以诱导向齿状回输入的穿孔路径的异突触长期增强。但是,体外和体内研究表明,β-肾上腺素受体活化的可塑性效应可能会根据受体活化水平而变化。 ud ud方法 ud本实验使用体内模型,同时注入不同浓度的β-肾上腺素受体激动剂,齿状回中的异丙肾上腺素(ISO;在aCSF中为0、0.1、1、10和100μmol/ L;在12.5分钟内为1μL),同时监测同一部位的穿孔诱发电位的变化。 udResults ud通过0.1μmol/ L ISO引起fEPSP斜率的长期降低(LTD)。较高剂量不会改变fEPSP斜率。在10μmol/ L ISO下,发生通径诱发的群体峰值的最大长期增强作用(183%> 3 h)。尖峰幅度的瞬时降低发生在0.1μmol/ L ISO处。 ud ud ud结论 ud ud ud这些数据表明,β-肾上腺素受体激活对穿孔路径诱发电位的浓度依赖性影响。根据受体激活程度的变化,可引起长期的抑郁和穿孔诱导的反应的长期增强。

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