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脑片中去甲肾上腺素释放的自抑制反馈控制的数学建模与量化

Mathematical modelling and quantification of the autoinhibitory feedback control of noradrenaline release in brain slices.

作者信息

Feuerstein T J, Sauermann W, Allgaier C, Singer E A

机构信息

Neuropharmakologisches Labor, Neurologischen Universitätsklinik, Freiburg, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1993 Feb;347(2):171-9. doi: 10.1007/BF00169263.

Abstract

Concentration-response curves, reflecting alpha 2-autoreceptor-mediated inhibition of [3H]-noradrenaline release by exogenous noradrenaline in rat cerebral cortex and rabbit hippocampus slices, were analysed in order to test the usefulness of a mathematical model describing the relation between the independent variable, exogenous noradrenaline, and the dependent variable, inhibition of release. This model was based on the assumption of direct proportionality between receptor occupation and response, implying that there is correspondence between the shape of a concentration-binding curve and a concentration-response curve. The experimental concentration-response curves were obtained by different approaches: noradrenaline release from brain slices prelabelled with [3H]-noradrenaline was elicited electrically either by pseudo-one-pulse (POP) stimulation or by stimulation with 36 pulses applied with a frequency of 3 Hz. POP stimulation avoids autoinhibition by released noradrenaline and, therefore, was a suitable touchstone for the applied mathematical model which evaluates by nonlinear regression analysis two primary parameters: the dissociation constant between noradrenaline and the alpha 2-adrenoceptor and the biophase concentration of noradrenaline which reflects the extent of autoinhibition and should be zero under POP conditions. In rat cerebral cortex tissue, the corresponding biophase concentration of endogenous noradrenaline was indeed estimated to be zero and the dissociation constant was Kd = 10(-7.62 +/- 0.14) mol/l. With 3 Hz stimulation, the biophase concentration was 10(-7.80 +/- 0.05) mol/l, which has to be interpreted with respect to a simultaneously estimated Kd of 10(-7.63 +/- 0.12) mol/l.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了检验一个描述自变量(外源性去甲肾上腺素)与因变量(释放抑制)之间关系的数学模型的实用性,分析了反映大鼠大脑皮层和兔海马切片中外源性去甲肾上腺素通过α2 - 自身受体介导抑制[3H] - 去甲肾上腺素释放的浓度 - 反应曲线。该模型基于受体占据与反应之间直接比例关系的假设,这意味着浓度 - 结合曲线和浓度 - 反应曲线的形状存在对应关系。实验性浓度 - 反应曲线通过不同方法获得:用[3H] - 去甲肾上腺素预标记的脑切片中的去甲肾上腺素释放,可通过伪单脉冲(POP)刺激或3Hz频率施加36个脉冲的刺激来电诱发。POP刺激避免了释放的去甲肾上腺素的自身抑制,因此,它是所应用数学模型的合适试金石,该模型通过非线性回归分析评估两个主要参数:去甲肾上腺素与α2 - 肾上腺素能受体之间的解离常数以及反映自身抑制程度且在POP条件下应为零的去甲肾上腺素的生物相浓度。在大鼠大脑皮层组织中,内源性去甲肾上腺素的相应生物相浓度确实估计为零,解离常数为Kd = 10(-7.62±0.14)mol/l。在3Hz刺激下,生物相浓度为10(-7.80±0.05)mol/l,这必须结合同时估计的Kd为10(-7.63±0.12)mol/l来解释。(摘要截断于250字)

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