The aim of the present study was to investigate the origin and modulation of 5-hydroxytryptamine release in dorsal hippocampus of freely moving rats using brain microdialysis. 2. Basal release of 5-hydroxytryptamine and 5-hydroxyindole-acetic acid was 3.0 +/- 0.2 pg/15 min and 519 +/- 18 pg/15 min, respectively. Stimulation by 60 mM K+ increased 5-hydroxytryptamine release by 66%. Inclusion of 10 microM tetrodotoxin in the perfusion medium reduced 5-hydroxytryptamine release to approximately 5% of basal levels. 3. In addition, release could be modulated by the 5-hydroxytryptamine receptor agonist 8-hydroxy-2-(di-N-propylamino)-tetralin (50 % decrease) and this effect was completely blocked by the 5-hydroxytryptamine-1 receptor antagonist pindolol. 4. These data are in concordance with results from the ventral hippocampus and indicate that release of 5-hydroxytryptamine is predominantly of neuronal origin. In contrast with other studies, the authors found the non-selective 5-hydroxytryptamine-1 antagonist, pindolol, to increase 5-hydroxytryptamine release by 65% following systemic administration. This may hint at a different autoreceptor control in serotonergic fibers ascending from the median raphe as compared to the dorsal raphe nucleus.
摘要
本研究的目的是使用脑微透析技术研究自由活动大鼠背侧海马中5-羟色胺释放的起源和调节。2. 5-羟色胺和5-羟吲哚乙酸的基础释放量分别为3.0±0.2 pg/15分钟和519±18 pg/15分钟。60 mM K⁺刺激使5-羟色胺释放增加了66%。在灌注培养基中加入10 μM河豚毒素可使5-羟色胺释放降至基础水平的约5%。3. 此外,5-羟色胺受体激动剂8-羟基-2-(二-N-丙基氨基)-四氢萘可调节释放(降低50%),且该效应可被5-羟色胺-1受体拮抗剂吲哚洛尔完全阻断。4. 这些数据与腹侧海马的结果一致,表明5-羟色胺的释放主要源于神经元。与其他研究不同的是,作者发现全身给药后,非选择性5-羟色胺-1拮抗剂吲哚洛尔可使5-羟色胺释放增加65%。这可能暗示与背侧中缝核相比,从中缝正中上升的5-羟色胺能纤维存在不同的自身受体控制。