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鸡脑体外电诱发单胺释放的药理学特性

Pharmacological characterisation of the electrically evoked release of monoamines from chicken brain in vitro.

作者信息

Jackson G, Hudson A L, Lalis M, Raj A B M

机构信息

Department of Clinical Veterinary Science, University of Bristol, Langford, England.

出版信息

Br Poult Sci. 2007 Feb;48(1):76-83. doi: 10.1080/00071660601157485.

Abstract
  1. A study was conducted to develop an in vitro model for examining the basal and electrical-stimulation-induced release of [3H]monoamines from chicken hyperstriatal neurones in order to demonstrate the presence of presynaptic autoreceptors for the three main monoamine transmitters: noradrenaline, dopamine and 5-HT. 2. Two sets of experiments were carried out: the first was to evaluate the effect of calcium and tetrodotoxin (TTX, sodium channel conductance inhibitor) in order to demonstrate that evoked release of monoamines was a consequence of exocytotic processes; the second to investigate the effect of selective agonists and antagonists on neurotransmitter release. 3. Ross and Cobb broiler chickens of either sex (approximately 7 to 8 weeks old) were used. Slices of hyperstriatal tissue were preincubated with [3H]noradrenaline, [3H]dopamine or [3H]5-hydroxytryptamine (5-HT), washed, perfused and electrically stimulated at three time points (S1, S2 and S3) which released [3H]noradrenaline, [3H]dopamine and [3H]5-HT, as determined by scintillation spectrometry. 4. When calcium was removed from, or TTX added to, the superfusion medium prior to and including the second period of electrical stimulation (S2) the evoked releases of [3H]noradrenaline, [3H]dopamine and [3H]5-HT at S2 were abolished. 5. In the presence of the selective alpha2-adrenoceptor agonist UK 14304 during the S2 period, the S2/S1 ratio was lower than the control ratio due to a reduction in the stimulated release of [3H]noradrenaline. The selective alpha2-adrenoceptor antagonist RX 821002 blocked the UK 14304-induced reduction of evoked release and the S2/S1 ratio was similar to the control ratio. 6. The D2-like receptor agonist quinpirole reduced the S2/S1 ratio for [3H]dopamine release, an effect blocked by the antagonist AJ 76. The 5-HT1B receptor agonist CP 94253 during S2 reduced the S2/S1 ratio due to a reduction in evoked [3H]5-HT. This effect was blocked by the 5-HT1B receptor antagonist GR 55562. 7. The results demonstrate, for the first time, the functional presence of presynaptic alpha2-adrenoceptors, presynaptic 5-HT1B autoreceptors and presynaptic D2-like autoreceptors in broiler chicken hyperstriatal neurones in vitro.
摘要
  1. 开展了一项研究,旨在建立一种体外模型,用于检测鸡超纹状体神经元基础状态下以及电刺激诱导的[3H]单胺释放,以证明三种主要单胺递质(去甲肾上腺素、多巴胺和5-羟色胺)的突触前自身受体的存在。2. 进行了两组实验:第一组是评估钙和河豚毒素(TTX,钠通道电导抑制剂)的作用,以证明单胺的诱发释放是胞吐过程的结果;第二组是研究选择性激动剂和拮抗剂对神经递质释放的影响。3. 使用了罗斯和科布肉鸡(性别不限,约7至8周龄)。将超纹状体组织切片先用[3H]去甲肾上腺素、[3H]多巴胺或[3H]5-羟色胺(5-HT)进行预孵育,洗涤后,在三个时间点(S1、S2和S3)进行灌注和电刺激,通过闪烁光谱法测定释放的[3H]去甲肾上腺素、[3H]多巴胺和[3H]5-HT。4. 在包括第二个电刺激期(S2)之前和期间,当从灌注培养基中去除钙或添加TTX时,S2期诱发的[3H]去甲肾上腺素、[3H]多巴胺和[3H]5-HT释放被消除。5. 在S2期存在选择性α2-肾上腺素能受体激动剂UK 14304的情况下,由于[3H]去甲肾上腺素刺激释放减少,S2/S1比值低于对照比值。选择性α2-肾上腺素能受体拮抗剂RX 821002阻断了UK 14304诱导的诱发释放减少,S2/S1比值与对照比值相似。6. D2样受体激动剂喹吡罗降低了[3H]多巴胺释放的S2/S1比值,拮抗剂AJ 76可阻断该作用。S2期5-HT1B受体激动剂CP 94253由于诱发的[3H]5-HT减少而降低了S2/S1比值。该作用被5-HT1B受体拮抗剂GR 55562阻断。7. 结果首次证明,体外培养的肉鸡超纹状体神经元中存在突触前α2-肾上腺素能受体、突触前5-HT1B自身受体和突触前D2样自身受体。

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