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定量受体放射自显影术在孤束核受体 - 受体相互作用研究中的应用

Quantitative receptor radioautography in the study of receptor-receptor interactions in the nucleus tractus solitarii.

作者信息

Fior-Chadi D R, Fuxe K

机构信息

Departamento de Fisiologia, Universidade de São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1998 Feb;31(2):225-30. doi: 10.1590/s0100-879x1998000200006.

Abstract

The nucleus tractus solitarii (NTS) in the dorsomedial medulla comprises a wide range of neuropeptides and biogenic amines. Several of them are related to mechanisms of central blood pressure control. Angiotensin II (Ang II), neuropeptide Y (NPY) and noradrenaline (NA) are found in the NTS cells, as well as their receptors. Based on this observation we have evaluated the modulatory effect of these peptide receptors on alpha 2-adrenoceptors in the NTS. Using quantitative receptor radioautography, we observed that NPY and Ang II receptors decreased the affinity of alpha 2-adrenoceptors for their agonists in the NTS of the rat. Cardiovascular experiments agreed with the in vitro data. Coinjection of a threshold dose of Ang II or of the NPY agonists together with an ED50 dose of adrenergic agonists such as NA, adrenaline and clonidine counteracted the depressor effect produced by the alpha 2-agonist in the NTS. The results provide evidence for the existence of an antagonistic interaction between Ang II AT1 receptors and NPY receptor subtypes with the alpha 2-adrenoceptors in the NTS. This receptor interaction may reduce the transduction over the alpha 2-adrenoceptors which can be important in central cardiovascular regulation and in the development of hypertension.

摘要

延髓背内侧的孤束核(NTS)包含多种神经肽和生物胺。其中一些与中枢血压控制机制有关。在NTS细胞及其受体中发现了血管紧张素II(Ang II)、神经肽Y(NPY)和去甲肾上腺素(NA)。基于这一观察结果,我们评估了这些肽受体对NTS中α2-肾上腺素能受体的调节作用。使用定量受体放射自显影技术,我们观察到NPY和Ang II受体降低了大鼠NTS中α2-肾上腺素能受体对其激动剂的亲和力。心血管实验与体外数据一致。将阈剂量的Ang II或NPY激动剂与ED50剂量的肾上腺素能激动剂(如NA、肾上腺素和可乐定)共同注射,可抵消α2-激动剂在NTS中产生的降压作用。这些结果为NTS中Ang II AT1受体和NPY受体亚型与α2-肾上腺素能受体之间存在拮抗相互作用提供了证据。这种受体相互作用可能会减少α2-肾上腺素能受体的信号转导,这在中枢心血管调节和高血压的发生发展中可能很重要。

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