首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Radioligand binding analysis of knockout mice reveals 5-hydroxytryptamine(7) receptor distribution and uncovers 8-hydroxy-2-(di-n-propylamino)tetralin interaction with alpha(2) adrenergic receptors.
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Radioligand binding analysis of knockout mice reveals 5-hydroxytryptamine(7) receptor distribution and uncovers 8-hydroxy-2-(di-n-propylamino)tetralin interaction with alpha(2) adrenergic receptors.

机译:敲除小鼠的放射性配体结合分析揭示了5-羟基色胺(7)受体分布,并揭示了与α(2)肾上腺素受体的8-羟基-2-(二-正丙基氨基)四氢萘相互作用。

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摘要

In the present autoradiographic study, we took advantage of 5-hydroxytryptamine(7) (5-HT(7)) receptor knockout mice to analyze the brain distribution of 5-HT(7) receptor binding sites using [(3)H]5-carboxamidotryptamine (5-CT; a 5-HT(1A/1B/1D/5/7) receptor ligand) and [(3)H]8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; a 5-HT(1A/7) receptor ligand). Low to moderate densities of [(3)H]5-CT (2 nM) binding sites insensitive to pindolol (10 microM, for 5-HT(1A/1B) receptor blockade) and GR-127935 (1 microM; for 5-HT(1D) receptor blockade) were observed in wild-type mice (mainly in thalamus and hypothalamus) but not in 5-HT(7) receptor knockout mice. Surprisingly, moderate to high densities of [(3)H]8-OH-DPAT (10 nM) binding sites insensitive to pindolol (10 microM) remained in 5-HT(7) receptor knockout mouse brain. These non-5-HT(1A), non-5-HT(7) binding sites were found to be adrenergic alpha(2A) receptor binding sites. In alpha(2A) receptor knockout mice low to moderate densities of [(3)H]8-OH-DPAT binding sites insensitive to pindolol but sensitive to the selective 5-HT(7) receptor antagonist SB-269970 (300 nM) were observed mainly in thalamus and hypothalamus. Therefore, in addition to 5-HT(1A) and 5-HT(7) binding sites, [(3)H]8-OH-DPAT also binds to alpha(2A) receptor binding sites in wild-type mouse brain. [(3)H]8-OH-DPAT (in the presence of pindolol and 1 microM RX-821002 for alpha(2) receptor blockade) and [(3)H]5-CT (in the presence of pindolol and GR-127935) bind to a similar receptor binding population corresponding to 5-HT(7) binding sites. Detailed anatomical mapping of 5-HT(7) receptor binding sites in wild-type mouse brain was then performed using both radioligands in the presence of suitable pharmacological agents for non-5-HT(7) receptor binding sites blockade. The mapping revealed binding sites consistent with the mRNA distribution with the highest densities found in anterior thalamic nuclei.
机译:在本放射自显影研究中,我们利用5-羟色胺(7)(5-HT(7))敲除小鼠来利用[(3)H] 5分析5-HT(7)受体结合位点的大脑分布-羧酰胺基色胺(5-CT; 5-HT(1A / 1B / 1D / 5/7)受体配体)和[(3)H] 8-羟基-2-(二-正丙基氨基)四氢化萘(8-OH -DPAT; 5-HT(1A / 7)受体配体)。低至中等密度的[(3)H] 5-CT(2 nM)结合位点,对哌多洛尔(10 microM,对5-HT(1A / 1B)受体阻滞不敏感)和GR-127935(1 microM;对5-在野生型小鼠(主要在丘脑和下丘脑)中观察到HT(1D)受体阻滞,但在5-HT(7)受体敲除小鼠中未观察到。令人惊讶的是,对哌多洛尔(10 microM)不敏感的[(3)H] 8-OH-DPAT(10 nM)结合位点的中高密度仍保留在5-HT(7)受体敲除小鼠脑中。这些非-5-HT(1A),非-5-HT(7)结合位点被发现是肾上腺素α(2A)受体结合位点。在alpha(2A)受体敲除小鼠中,对匹多洛尔不敏感但对选择性5-HT(7)受体拮抗剂SB-269970(300 nM)敏感的[(3)H] 8-OH-DPAT结合位点的密度低至中等主要观察到丘脑和下丘脑。因此,除了5-HT(1A)和5-HT(7)结合位点,[(3H)] 8-OH-DPAT还与野生型小鼠脑中的alpha(2A)受体结合位点结合。 [(3)H] 8-OH-DPAT(在存在潘多洛尔和1 microM RX-821002的情况下,以进行alpha(2)受体阻断)和[(3)H] 5-CT(在存在潘多洛尔和GR- 127935)与对应于5-HT(7)结合位点的相似受体结合群体结合。然后,在适合非5-HT(7)受体结合位点的合适药理剂存在下,使用两种放射性配体对野生型小鼠大脑中5-HT(7)受体结合位点进行详细的解剖定位。该作图揭示了与在丘脑前核中发现的具有最高密度的mRNA分布一致的结合位点。

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