The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex

碩士 === 國立陽明大學 === 藥理學研究所 === 87 === Noradrenergic and dopaminergic projections converge in the medial prefrontal cortex (mPFC) and there is growing evidence of an interaction between dopamine (DA) and norepinephrine (NE). In our study, local infusion of NE (90 nM、150 nM and 300...

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Main Authors: Sze-Yuan Yang, 楊思源
Other Authors: Wynn H. T. Pan
Format: Others
Language:zh-TW
Published: 1999
Online Access:http://ndltd.ncl.edu.tw/handle/35236850289138697906
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spelling ndltd-TW-087YM0005500142015-10-13T11:50:26Z http://ndltd.ncl.edu.tw/handle/35236850289138697906 The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex 探討多巴胺神經與正腎上腺素神經在內前額皮質區的交互作用 Sze-Yuan Yang 楊思源 碩士 國立陽明大學 藥理學研究所 87 Noradrenergic and dopaminergic projections converge in the medial prefrontal cortex (mPFC) and there is growing evidence of an interaction between dopamine (DA) and norepinephrine (NE). In our study, local infusion of NE (90 nM、150 nM and 300 nM) into the mPFC concentration-dependently increased extracellular DA (110±2%、160±4% and 183±6%) in chloral hydrate anaesthetized rats. The a1 receptor antagonist prazosin (10 mM) could block the 300 nM NE-induced increase of DA in the mPFC; but not the 2 receptor antagonist, piperoxan (100 mM). Local application of NE uptake inhibitor, desipramine (DMI; 1 mM), into the mPFC increased extracellular DA (158±5%) as well as NE (194±9%) in this area. Co-infusion of DMI and the a1 receptor antagonist prazosin (10 M) could decrease the DMI-induced increase of DA (125±5%) and NE (130±6%). On the other hand, local application of DA (12 nM、20 nM and 40 nM) into the mPFC concentration-dependently increased extracellular NE (119±3%、135±6% and 160±6%) in the mPFC. The D1 receptor antagonist SCH 23390 (10nM), but not D2 receptor antagonist eticlopride (1nM), could block the increase of extracellular NE, which was induced by local infusion of 40 nM DA. These results suggest that in the mPFC (1) when the extracellular NE concentration increased, the DA concentration would also increase, which may be due to the action of NE on a1 receptors (heteroreceptor regulation) and the competitive effect of DA with NE for reuptake sites on the NE terminals (heterotransporter regulation); (2) DA terminals can regulate extracellular NE and this is due to the action of DA on D1 receptors to enhance NE release (heteroreceptor regulation). Wynn H. T. Pan 潘懷宗 1999 學位論文 ; thesis 85 zh-TW
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description 碩士 === 國立陽明大學 === 藥理學研究所 === 87 === Noradrenergic and dopaminergic projections converge in the medial prefrontal cortex (mPFC) and there is growing evidence of an interaction between dopamine (DA) and norepinephrine (NE). In our study, local infusion of NE (90 nM、150 nM and 300 nM) into the mPFC concentration-dependently increased extracellular DA (110±2%、160±4% and 183±6%) in chloral hydrate anaesthetized rats. The a1 receptor antagonist prazosin (10 mM) could block the 300 nM NE-induced increase of DA in the mPFC; but not the 2 receptor antagonist, piperoxan (100 mM). Local application of NE uptake inhibitor, desipramine (DMI; 1 mM), into the mPFC increased extracellular DA (158±5%) as well as NE (194±9%) in this area. Co-infusion of DMI and the a1 receptor antagonist prazosin (10 M) could decrease the DMI-induced increase of DA (125±5%) and NE (130±6%). On the other hand, local application of DA (12 nM、20 nM and 40 nM) into the mPFC concentration-dependently increased extracellular NE (119±3%、135±6% and 160±6%) in the mPFC. The D1 receptor antagonist SCH 23390 (10nM), but not D2 receptor antagonist eticlopride (1nM), could block the increase of extracellular NE, which was induced by local infusion of 40 nM DA. These results suggest that in the mPFC (1) when the extracellular NE concentration increased, the DA concentration would also increase, which may be due to the action of NE on a1 receptors (heteroreceptor regulation) and the competitive effect of DA with NE for reuptake sites on the NE terminals (heterotransporter regulation); (2) DA terminals can regulate extracellular NE and this is due to the action of DA on D1 receptors to enhance NE release (heteroreceptor regulation).
author2 Wynn H. T. Pan
author_facet Wynn H. T. Pan
Sze-Yuan Yang
楊思源
author Sze-Yuan Yang
楊思源
spellingShingle Sze-Yuan Yang
楊思源
The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
author_sort Sze-Yuan Yang
title The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
title_short The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
title_full The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
title_fullStr The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
title_full_unstemmed The Interaction between Dopaminergic and Noradrenergic Neurons in the Medial Prefrontal Cortex
title_sort interaction between dopaminergic and noradrenergic neurons in the medial prefrontal cortex
publishDate 1999
url http://ndltd.ncl.edu.tw/handle/35236850289138697906
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