首页> 外文期刊>British Journal of Pharmacology >Evidence that 5-hydroxytryptamine release in rat dorsal raphe nucleus is controlled by 5-HT_(1A), 5-HT_(1B) and 5-HT_(1D) autoreceptors
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Evidence that 5-hydroxytryptamine release in rat dorsal raphe nucleus is controlled by 5-HT_(1A), 5-HT_(1B) and 5-HT_(1D) autoreceptors

机译:在大鼠背缝核中5-羟色胺释放受5-HT_(1A),5-HT_(1B)和5-HT_(1D)自体受体控制的证据

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Electrically stimulated 5-hydroxytryptamine (5-HT) release was monitored in slices of rat dorsal raphe nucleus (DRN) by fast cylic voltammetry. Pseudo-single pulse stimulations (5 pulses at 100 Hz) were used to enable the effect of various receptor agonists to be seen without competition from endogenously released transmitter. The selective 5-HT_(1A) receptor agonist, (+)-8-OH-DPAT (1.0 μM) decreased stimulated 5-HT release to 31 ± 3% of controls. This decrease was inhibited by the 5-HT_(1A) receptor antagonists, ( + )-WAY-100135 (1.0 μM) and WAY-100635 (0.1 μM) but not by the 5-HT_(1D/B) antagonist, GR127935 (0.05 μM). The selective 5-HT_(1B) receptor agonist, CP-93129 (0.3 μM) decreased stimulated 5-HT release to 61 ± 4% of control. This effect was antagonized by the 5-HT_(1B) receptor antagonist, isamoltane (0.5 μM) but not by ( + )-WAY-100135. The 5-HT_(1D) agonist, sumatriptan (0.5 μM) decreased stimulated 5-HT release to 52 ± 2 % of controls. This decrease was blocked by GR-127935 but not by WAY-100635. These results suggest that 5-HT release in the rat DRN is under the control of 5-HT_(1A), 5-HT_(1B) and 5-HT_(1D) autoreceptors.
机译:通过快速循环伏安法监测大鼠背缝核(DRN)切片中电刺激的5-羟基色胺(5-HT)释放。使用伪单脉冲刺激(在100 Hz时有5个脉冲)可以观察到各种受体激动剂的作用,而不会与内源释放的递质竞争。选择性5-HT_(1A)受体激动剂(+)-8-OH-DPAT(1.0μM)将刺激的5-HT释放降低至对照组的31±3%。 5-HT_(1A)受体拮抗剂(+)-WAY-100135(1.0μM)和WAY-100635(0.1μM)抑制了这一下降,但5-HT_(1D / B)拮抗剂GR127935( 0.05μM)。选择性5-HT_(1B)受体激动剂CP-93129(0.3μM)将刺激的5-HT释放降低至对照组的61±4%。这种作用被5-HT_(1B)受体拮抗剂异烟酰胺(0.5μM)拮抗,但(+)-WAY-100135却没有。 5-HT_(1D)激动剂舒马曲坦(0.5μM)将刺激的5-HT释放降低至对照组的52±2%。 GR-127935阻止了此减少,但WAY-100635并未阻止。这些结果表明,大鼠DRN中5-HT的释放受5-HT_(1A),5-HT_(1B)和5-HT_(1D)自体受体的控制。

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