| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Teruko Danjo, Kenji Yoshimi, Kazuo Funabiki, Satoshi Yawata, Shigetada Nakanish. Aversive behavior induced by optogenetic inactivation of ventral tegmental area dopamine neurons is mediated by dopamine D2 receptors in the nucleus accumbens. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 17. 2014-06-24. PMID:24737889. |
dopamine (da) transmission from the ventral tegmental area (vta) is critical for controlling both rewarding and aversive behaviors. |
2014-06-24 |
2023-08-13 |
Not clear |
| Teruko Danjo, Kenji Yoshimi, Kazuo Funabiki, Satoshi Yawata, Shigetada Nakanish. Aversive behavior induced by optogenetic inactivation of ventral tegmental area dopamine neurons is mediated by dopamine D2 receptors in the nucleus accumbens. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 17. 2014-06-24. PMID:24737889. |
silencing of da neurons in the vta was thus indispensable for inducing aversive responses and learning through dopamine d2 receptors in the nac. |
2014-06-24 |
2023-08-13 |
Not clear |
| Dennis R Sparta, Frederic Woodward Hopf, Stuart L Gibb, Saemi L Cho, Garret D Stuber, Robert O Messing, Dorit Ron, Antonello Bonc. Binge ethanol-drinking potentiates corticotropin releasing factor R1 receptor activity in the ventral tegmental area. Alcoholism, clinical and experimental research. vol 37. issue 10. 2014-05-15. PMID:23763790. |
here, we examined whether brief binge etoh consumption leads to crf receptor adaptations within the ventral tegmental area (vta), a structure involved in signaling rewarding and aversive events and important in the development and expression of drug and alcohol addiction. |
2014-05-15 |
2023-08-12 |
Not clear |
| Meaghan C Creed, Niels R Ntamati, Kelly R Ta. VTA GABA neurons modulate specific learning behaviors through the control of dopamine and cholinergic systems. Frontiers in behavioral neuroscience. vol 8. 2014-03-10. PMID:24478655. |
the task of signaling both rewarding and aversive events from the vta to the nac has mostly been ascribed to da neurons and the role of gaba neurons has been largely neglected until recently. |
2014-03-10 |
2023-08-12 |
Not clear |
| Meaghan C Creed, Niels R Ntamati, Kelly R Ta. VTA GABA neurons modulate specific learning behaviors through the control of dopamine and cholinergic systems. Frontiers in behavioral neuroscience. vol 8. 2014-03-10. PMID:24478655. |
the results gathered with each of these approaches suggest that vta gaba neurons bi-directionally modulate activity of local da neurons, underlying reward or aversion at the behavioral level. |
2014-03-10 |
2023-08-12 |
Not clear |
| Alice M Stamatakis, Joshua H Jennings, Randall L Ung, Grace A Blair, Richard J Weinberg, Rachael L Neve, Frederick Boyce, Joanna Mattis, Charu Ramakrishnan, Karl Deisseroth, Garret D Stube. A unique population of ventral tegmental area neurons inhibits the lateral habenula to promote reward. Neuron. vol 80. issue 4. 2014-01-15. PMID:24267654. |
lateral habenula (lhb) neurons convey aversive and negative reward conditions through potent indirect inhibition of ventral tegmental area (vta) dopaminergic neurons. |
2014-01-15 |
2023-08-12 |
Not clear |
| Miriam Melis, Marta De Felice, Salvatore Lecca, Liana Fattore, Marco Pisti. Sex-specific tonic 2-arachidonoylglycerol signaling at inhibitory inputs onto dopamine neurons of Lister Hooded rats. Frontiers in integrative neuroscience. vol 7. 2014-01-13. PMID:24416004. |
the ventral tegmental area (vta) where dopamine (da) cells are located is a key component of brain reward circuitry, whereas the rostromedial tegmental nucleus (rmtg) critically regulates aversive behaviors. |
2014-01-13 |
2023-08-12 |
rat |
| Elham Ghanbarian, Fereshteh Motamed. Ventral tegmental area inactivation suppresses the expression of CA1 long term potentiation in anesthetized rat. PloS one. vol 8. issue 3. 2013-12-27. PMID:23536829. |
in this study we examined the effect of vta reversible inactivation on the induction and maintenance of early ltp in the ca1 area of anesthetized rats, and also on different phases of learning of a passive avoidance (pa) task. |
2013-12-27 |
2023-08-12 |
rat |
| Elham Ghanbarian, Fereshteh Motamed. Ventral tegmental area inactivation suppresses the expression of CA1 long term potentiation in anesthetized rat. PloS one. vol 8. issue 3. 2013-12-27. PMID:23536829. |
moreover, vta inactivation immediately after training impaired memory in the passive avoidance task, while its blockade before or 20 min after training produced no memory deficit. |
2013-12-27 |
2023-08-12 |
rat |
| Tasha Ahmad, Nicole M Lauzon, Xavier de Jaeger, Steven R Laviolett. Cannabinoid transmission in the prelimbic cortex bidirectionally controls opiate reward and aversion signaling through dissociable kappa versus μ-opiate receptor dependent mechanisms. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 33. issue 39. 2013-11-25. PMID:24068830. |
we further report that cb1-mediated intra-plc opiate motivational signaling is mediated through a μ-opiate receptor-dependent reward pathway, or a κ-opiate receptor-dependent aversion pathway, directly within the ventral tegmental area. |
2013-11-25 |
2023-08-12 |
rat |
| Chang-Liang Liu, Ming Gao, Guo-Zhang Jin, Xuechu Zhe. GABA neurons in the ventral tegmental area responding to peripheral sensory input. PloS one. vol 7. issue 12. 2013-06-03. PMID:23251560. |
dopamine (da) neurons in the ventral tegmental area (vta) not only participate in reward processing, but also respond to aversive stimuli. |
2013-06-03 |
2023-08-12 |
rat |
| Joshua H Jennings, Dennis R Sparta, Alice M Stamatakis, Randall L Ung, Kristen E Pleil, Thomas L Kash, Garret D Stube. Distinct extended amygdala circuits for divergent motivational states. Nature. vol 496. issue 7444. 2013-04-29. PMID:23515155. |
the extended amygdala, including the bed nucleus of the stria terminalis (bnst), modulates fear and anxiety, but also projects to the ventral tegmental area (vta), a region implicated in reward and aversion, thus providing a candidate neural substrate for integrating diverse emotional states. |
2013-04-29 |
2023-08-12 |
mouse |
| Joshua H Jennings, Dennis R Sparta, Alice M Stamatakis, Randall L Ung, Kristen E Pleil, Thomas L Kash, Garret D Stube. Distinct extended amygdala circuits for divergent motivational states. Nature. vol 496. issue 7444. 2013-04-29. PMID:23515155. |
these data demonstrate that functionally opposing bnst to vta circuits regulate rewarding and aversive motivational states, and may serve as a crucial circuit node for bidirectionally normalizing maladaptive behaviours. |
2013-04-29 |
2023-08-12 |
mouse |
| Farzaneh Nazari-Serenjeh, Ameneh Rezayo. Cooperative interaction between the basolateral amygdala and ventral tegmental area modulates the consolidation of inhibitory avoidance memory. Progress in neuro-psychopharmacology & biological psychiatry. vol 40. 2013-03-26. PMID:23063440. |
cooperative interaction between the basolateral amygdala and ventral tegmental area modulates the consolidation of inhibitory avoidance memory. |
2013-03-26 |
2023-08-12 |
rat |
| Farzaneh Nazari-Serenjeh, Ameneh Rezayo. Cooperative interaction between the basolateral amygdala and ventral tegmental area modulates the consolidation of inhibitory avoidance memory. Progress in neuro-psychopharmacology & biological psychiatry. vol 40. 2013-03-26. PMID:23063440. |
the aim of the current study was to examine the existence of a cooperative interaction between the basolateral nucleus of amygdala (bla) and the ventral tegmental area (vta) in inhibitory avoidance task. |
2013-03-26 |
2023-08-12 |
rat |
| Farzaneh Nazari-Serenjeh, Ameneh Rezayo. Cooperative interaction between the basolateral amygdala and ventral tegmental area modulates the consolidation of inhibitory avoidance memory. Progress in neuro-psychopharmacology & biological psychiatry. vol 40. 2013-03-26. PMID:23063440. |
the bla and the vta regions of adult male wistar rats were simultaneously cannulated and memory consolidation was measured in a step-through type inhibitory avoidance apparatus. |
2013-03-26 |
2023-08-12 |
rat |
| Dipesh Chaudhury, Jessica J Walsh, Allyson K Friedman, Barbara Juarez, Stacy M Ku, Ja Wook Koo, Deveroux Ferguson, Hsing-Chen Tsai, Lisa Pomeranz, Daniel J Christoffel, Alexander R Nectow, Mats Ekstrand, Ana Domingos, Michelle S Mazei-Robison, Ezekiell Mouzon, Mary Kay Lobo, Rachael L Neve, Jeffrey M Friedman, Scott J Russo, Karl Deisseroth, Eric J Nestler, Ming-Hu Ha. Rapid regulation of depression-related behaviours by control of midbrain dopamine neurons. Nature. vol 493. issue 7433. 2013-03-04. PMID:23235832. |
we show that optogenetic induction of phasic, but not tonic, firing in vta dopamine neurons of mice undergoing a subthreshold social-defeat paradigm rapidly induced a susceptible phenotype as measured by social avoidance and decreased sucrose preference. |
2013-03-04 |
2023-08-12 |
mouse |
| Anna K Radke, Jonathan C Gewirt. Increased dopamine receptor activity in the nucleus accumbens shell ameliorates anxiety during drug withdrawal. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. vol 37. issue 11. 2013-02-26. PMID:22692565. |
these results suggest that transient activation of the ventral tegmental area mesolimbic dopamine system triggers the expression of anxiety and aversion during withdrawal from multiple classes of abused drugs. |
2013-02-26 |
2023-08-12 |
Not clear |
| Matthew T C Brown, Kelly R Tan, Eoin C O'Connor, Irina Nikonenko, Dominique Muller, Christian Lüsche. Ventral tegmental area GABA projections pause accumbal cholinergic interneurons to enhance associative learning. Nature. vol 492. issue 7429. 2013-02-12. PMID:23178810. |
the task of signalling such events, both rewarding and aversive, from the vta to the nac has largely been ascribed to dopamine neurons. |
2013-02-12 |
2023-08-12 |
mouse |
| Iván Gómez-Milanés, Pilar Almela, Juan-Antonio García-Carmona, M Salud García-Gutiérrez, Auxiliadora Aracil-Fernández, Jorge Manzanares, María Victoria Milanés Maquilón, M Luisa Laorde. Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice. Neurochemistry international. vol 61. issue 3. 2013-01-22. PMID:22713675. |
the purpose of the present study was to evaluate: (i) the turnover of da, na and 5-ht in the nucleus accumbens (nac), one of the most important substrates for aversive states, (ii) the changes in tyrosine hydroxylase (th) gene expression in the ventral tegmental area, and (iii) total th protein levels and th phosphorylation in the nac after naloxone-induced morphine withdrawal. |
2013-01-22 |
2023-08-12 |
mouse |