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Blockade of mast cell histamine secretion in response to neurotensin by SR 48692, a nonpeptide antagonist of the neurotensin brain receptor.

机译:SR 48692(一种神经降压素脑受体的非肽拮抗剂)可响应神经降压素,阻止肥大细胞组胺的分泌。

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摘要

1. Pretreatment of rat isolated mast cells with SR 48692, a nonpeptide antagonist of the neurotensin (NT) receptor, prevented histamine secretion in response to NT. 2. This inhibition was rapid in onset (approximately 1 min) and dependent upon the concentration of SR 48692 (IC50 approximately 1-10 nM). 3. SR 48692 (1-1000 nM) did not inhibit histamine secretion elicited by substance P, bradykinin or compound 48/80, or by anti-IgE stimulation of sensitized mast cells. 4. When SR 48692 was injected intradermally (5 pmol in 50 microliters) into anaesthetized rats, 15 min before the intradermal injection of NT, it reduced the effect of NT on vascular permeability. 5. When injected intravenously, SR 48692 attenuated the effects of NT on haematocrit and blood stasis. 6. These results demonstrate that SR 48692 selectively antagonizes the actions of NT on rat isolated mast cells as well as mast cells in vivo. Given the demonstrated specific interaction of SR 48692 with receptors for NT in brain, our results suggest the presence of specific NT receptors on mast cells.
机译:1.用SR 48692(一种神经降压素(NT)受体的非肽拮抗剂)预处理大鼠分离的肥大细胞,可防止对NT的组胺分泌。 2.这种抑制作用起效较快(约1分钟),并取决于SR 48692的浓度(IC50约为1-10 nM)。 3. SR 48692(1-1000 nM)不会抑制P物质,缓激肽或化合物48/80或敏化肥大细胞的抗IgE刺激引起的组胺分泌。 4.在皮内注射NT之前15分钟,当将SR 48692皮内注射(5 pmol,50微升)注射到麻醉的大鼠中时,会降低NT对血管通透性的影响。 5.静脉注射时,SR 48692减弱了NT对血细胞比容和血瘀的影响。 6.这些结果表明,SR 48692选择性拮抗NT对大鼠分离的肥大细胞以及体内肥大细胞的作用。考虑到SR 48692与脑中NT受体的特异性相互作用,我们的结果表明肥大细胞上存在特定NT受体。

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