首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Autoradiographic distribution of tachykinin NK(2) binding sites in the rat brain: comparison with NK(1) and NK(3) binding sites.
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Autoradiographic distribution of tachykinin NK(2) binding sites in the rat brain: comparison with NK(1) and NK(3) binding sites.

机译:速激肽NK(2)结合位点在大鼠脑中的放射自显影分布:与NK(1)和NK(3)结合位点的比较。

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摘要

The autoradiographic distribution of tachykinin NK(2) binding sites was determined in the adult rat brain using [(125)I]neurokinin A in the presence of either senktide (NK(3) agonist) and [Pro(9)]substance P (NK(1) agonist) or senktide and SR 140333 (NK(1) antagonist). Indeed, this radioligand labels two subtypes of NK(1) binding sites (which present a high affinity not only for SP but also for neurokinin A, neuropeptide K and neuropeptide gamma) as well as NK(3) binding sites. The distribution of NK(2) binding sites was also compared with those of NK(1) and NK(3) binding sites, these sites being labeled with [(125)I]Bolton and Hunter substance P and [(125)I]Bolton and Hunter eledoisin, respectively. In agreement with our results obtained with membranes from various brain structures, NK(2)-sensitive [(125)I]neurokinin A labeling was mainly observed in few structures including the dorsal and ventral hippocampus, the septum, the thalamus and the prefrontal cortex. The density of NK(2) binding sites was weak when compared with those of NK(1) and NK(3) binding sites. Marked differences were observed in the distributions of NK(1), NK(2) and NK(3) binding sites. These results are discussed taking into consideration differences or similarities between the distributions of NK(2)-sensitive [(125)I]neurokinin A binding sites and of their endogenous ligands (neurokinin A, neuropeptide K and neuropeptide gamma) but also local NK(2) agonist responses blocked by NK(2) antagonists. Insights on the roles of endogenous tachykinins in several brain functions are also discussed on the basis of the respective distributions of different neurokinin binding sites.
机译:速激肽NK(2)结合位点的放射自显影分布在senktide(NK(3)激动剂)和[Pro(9)]物质P( NK(1)激动剂)或senktide和SR 140333(NK(1)拮抗剂)。确实,这种放射性配体标记了NK(1)结合位点的两个亚型(不仅对SP而且对神经激肽A,神经肽K和神经肽γ都具有很高的亲和力)以及NK(3)结合位点。还比较了NK(2)结合位点的分布与NK(1)和NK(3)结合位点的分布,这些位点用[(125)I] Bolton和Hunter物质P和[(125)I]标记Bolton和Hunter eledoisin分别。与我们从各种大脑结构的膜获得的结果一致,NK(2)-敏感的[(125)I]神经激肽A标记主要在少数结构中观察到,包括背侧和腹侧海马,中隔,丘脑和前额叶皮层。与NK(1)和NK(3)结合位点相比,NK(2)结合位点的密度较弱。在NK(1),NK(2)和NK(3)结合位点的分布中观察到明显差异。讨论这些结果时要考虑到NK(2)敏感[[125)I]神经激肽A结合位点及其内源性配体(神经激肽A,神经肽K和神经肽γ)之间的分布差异或相似性,还包括局部NK( 2)被NK(2)拮抗剂阻断的激动剂反应。还根据不同神经激肽结合位点的各自分布,探讨了内源性速激肽在几种脑功能中的作用。

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