Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats

<p>Abstract</p> <p>Background</p> <p>The dopaminergic (DA) neurons in the ventral tegmental area (VTA) are widely implicated in the addiction and natural reward circuitry of the brain. These neurons project to several areas of the brain, including prefrontal cortex (PFC...

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Main Authors: Akay Yasemin M, Dragomir Andrei, Zhang Die, Chen Ting Y, Akay Metin
Format: Article
Language:English
Published: BMC 2011-02-01
Series:Journal of NeuroEngineering and Rehabilitation
Online Access:http://www.jneuroengrehab.com/content/8/1/13
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spelling doaj-2dd090c8058a400fa5b482e8a9de0ddf2020-11-24T21:18:38ZengBMCJournal of NeuroEngineering and Rehabilitation1743-00032011-02-01811310.1186/1743-0003-8-13Complexity of VTA DA neural activities in response to PFC transection in nicotine treated ratsAkay Yasemin MDragomir AndreiZhang DieChen Ting YAkay Metin<p>Abstract</p> <p>Background</p> <p>The dopaminergic (DA) neurons in the ventral tegmental area (VTA) are widely implicated in the addiction and natural reward circuitry of the brain. These neurons project to several areas of the brain, including prefrontal cortex (PFC), nucleus accubens (NAc) and amygdala. The functional coupling between PFC and VTA has been demonstrated, but little is known about how PFC mediates nicotinic modulation in VTA DA neurons. The objectives of this study were to investigate the effect of acute nicotine exposure on the VTA DA neuronal firing and to understand how the disruption of communication from PFC affects the firing patterns of VTA DA neurons.</p> <p>Methods</p> <p>Extracellular single-unit recordings were performed on Sprague-Dawley rats and nicotine was administered after stable recording was established as baseline. In order to test how input from PFC affects the VTA DA neuronal firing, bilateral transections were made immediate caudal to PFC to mechanically delete the interaction between VTA and PFC.</p> <p>Results</p> <p>The complexity of the recorded neural firing was subsequently assessed using a method based on the Lempel-Ziv estimator. The results were compared with those obtained when computing the entropy of neural firing. Exposure to nicotine triggered a significant increase in VTA DA neurons firing complexity when communication between PFC and VTA was present, while transection obliterated the effect of nicotine. Similar results were obtained when entropy values were estimated.</p> <p>Conclusions</p> <p>Our findings suggest that PFC plays a vital role in mediating VTA activity. We speculate that increased firing complexity with acute nicotine administration in PFC intact subjects is due to the close functional coupling between PFC and VTA. This hypothesis is supported by the fact that deletion of PFC results in minor alterations of VTA DA neural firing when nicotine is acutely administered.</p> http://www.jneuroengrehab.com/content/8/1/13
collection DOAJ
language English
format Article
sources DOAJ
author Akay Yasemin M
Dragomir Andrei
Zhang Die
Chen Ting Y
Akay Metin
spellingShingle Akay Yasemin M
Dragomir Andrei
Zhang Die
Chen Ting Y
Akay Metin
Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
Journal of NeuroEngineering and Rehabilitation
author_facet Akay Yasemin M
Dragomir Andrei
Zhang Die
Chen Ting Y
Akay Metin
author_sort Akay Yasemin M
title Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
title_short Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
title_full Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
title_fullStr Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
title_full_unstemmed Complexity of VTA DA neural activities in response to PFC transection in nicotine treated rats
title_sort complexity of vta da neural activities in response to pfc transection in nicotine treated rats
publisher BMC
series Journal of NeuroEngineering and Rehabilitation
issn 1743-0003
publishDate 2011-02-01
description <p>Abstract</p> <p>Background</p> <p>The dopaminergic (DA) neurons in the ventral tegmental area (VTA) are widely implicated in the addiction and natural reward circuitry of the brain. These neurons project to several areas of the brain, including prefrontal cortex (PFC), nucleus accubens (NAc) and amygdala. The functional coupling between PFC and VTA has been demonstrated, but little is known about how PFC mediates nicotinic modulation in VTA DA neurons. The objectives of this study were to investigate the effect of acute nicotine exposure on the VTA DA neuronal firing and to understand how the disruption of communication from PFC affects the firing patterns of VTA DA neurons.</p> <p>Methods</p> <p>Extracellular single-unit recordings were performed on Sprague-Dawley rats and nicotine was administered after stable recording was established as baseline. In order to test how input from PFC affects the VTA DA neuronal firing, bilateral transections were made immediate caudal to PFC to mechanically delete the interaction between VTA and PFC.</p> <p>Results</p> <p>The complexity of the recorded neural firing was subsequently assessed using a method based on the Lempel-Ziv estimator. The results were compared with those obtained when computing the entropy of neural firing. Exposure to nicotine triggered a significant increase in VTA DA neurons firing complexity when communication between PFC and VTA was present, while transection obliterated the effect of nicotine. Similar results were obtained when entropy values were estimated.</p> <p>Conclusions</p> <p>Our findings suggest that PFC plays a vital role in mediating VTA activity. We speculate that increased firing complexity with acute nicotine administration in PFC intact subjects is due to the close functional coupling between PFC and VTA. This hypothesis is supported by the fact that deletion of PFC results in minor alterations of VTA DA neural firing when nicotine is acutely administered.</p>
url http://www.jneuroengrehab.com/content/8/1/13
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