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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Presynaptic displacement of serotonin by alpha-methyl-5-hydroxytryptamine in the nucleus tractus solitarius of the rat.
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Presynaptic displacement of serotonin by alpha-methyl-5-hydroxytryptamine in the nucleus tractus solitarius of the rat.

机译:α-甲基-5-羟基色胺在大鼠孤束核中突触前5-羟色胺的置换。

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摘要

Rat brain slices containing the nucleus tractus solitarius loaded with [3H]5-hydroxytryptamine ([3H]5-HT) for superfusion were stimulated at (3 Hz, 25 mA, 1 min) resulting in fractional release ratios S2/S1 of 0.89 for [3H]5-HT in the presence of the serotonin uptake inhibitor 1.0 microM 6-nitroquipazine (6-NQ). alpha-Methylserotonin (alpha-Me-5-HT; 1.0 microM), a non-selective 5-HT1 and 5-HT2 receptor agonist, significantly reduced the S2/S1 ratio of [3H]5-HT without affecting the basal release ratios B2/B1 1.00 +/- 0.04. Without 6-NQ in the perfusion medium 1.0 microM alpha-Me-5-HT sharply increased the basal release B2/B1 to 2.21 (P < 0.01). In low Ca2+ medium the S2/S1 ratio was reduced to 0.06 and alpha-Me-5-HT promoted a B2/B1 release of 2.17 (P < 0.01). The 5-HT3 antagonist LY-278,584 did not block alpha-Me-5-HT induced basal release of [3H]5-HT. Both pindolol and LY-53,857 blocked the autoinhibitory effects of alpha-Me-5-HT, but only LY-53,857 and 6-NQ blocked the basal release induced by alpha-Me-5-HT. These results suggest that alpha-Me-5-HT reduces neurotransmitter release through the serotonin autoreceptor and displaces serotonin through a non-exocytotic release mechanism.
机译:在(3 Hz,25 mA,1分钟)刺激含有孤核细胞核并装有[3H] 5-羟基色胺([3H] 5-HT)的大鼠脑切片,以产生0.89的S2 / S1释放比例[3H] 5-HT在5-羟色胺摄取抑制剂1.0 microM 6-硝基喹嗪(6-NQ)的存在下。 α-甲基5-羟色胺(α-Me-5-HT; 1.0 microM),一种非选择性的5-HT1和5-HT2受体激动剂,可显着降低[3H] 5-HT的S2 / S1比,而不会影响基础释放比B2 / B1 1.00 +/- 0.04。在灌注培养基中没有6-NQ的情况下,1.0 microM alpha-Me-5-HT会使基础释放B2 / B1急剧增加至2.21(P <0.01)。在低Ca2 +培养基中,S2 / S1比降低至0.06,而α-Me-5-HT促进B2 / B1释放为2.17(P <0.01)。 5-HT3拮抗剂LY-278,584没有阻止α-Me-5-HT诱导的[3H] 5-HT的基础释放。品多洛尔和LY-53,857都阻断了α-Me-5-HT的自抑制作用,但是只有LY-53,857和6-NQ阻断了由α-Me-5-HT诱导的基础释放。这些结果表明,α-Me-5-HT通过5-羟色胺自身受体减少神经递质的释放,并通过非胞吐释放机制取代5-羟色胺。

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