| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Mohammad-Reza Zarrindast, Shamseddin Ahmadi, Ali Haeri-Rohani, Ameneh Rezayof, Mohammad-Reza Jafari, Majid Jafari-Sabe. GABA(A) receptors in the basolateral amygdala are involved in mediating morphine reward. Brain research. vol 1006. issue 1. 2004-06-07. PMID:15047023. |
gaba(a) receptors in the basolateral amygdala are involved in mediating morphine reward. |
2004-06-07 |
2023-08-12 |
rat |
| Mohammad-Reza Zarrindast, Shamseddin Ahmadi, Ali Haeri-Rohani, Ameneh Rezayof, Mohammad-Reza Jafari, Majid Jafari-Sabe. GABA(A) receptors in the basolateral amygdala are involved in mediating morphine reward. Brain research. vol 1006. issue 1. 2004-06-07. PMID:15047023. |
it can be concluded that gaba(a) receptors in the amygdala are involved in morphine reward. |
2004-06-07 |
2023-08-12 |
rat |
| Alicia Izquierdo, Elisabeth A Murra. Combined unilateral lesions of the amygdala and orbital prefrontal cortex impair affective processing in rhesus monkeys. Journal of neurophysiology. vol 91. issue 5. 2004-05-25. PMID:14711973. |
to assess whether there is a hemispheric functional specialization for the processing of emotion or reward or both in nonhuman primates, rhesus monkeys (macaca mulatta) with combined lesions of the amygdala and pfo in one hemisphere, either left or right, were compared with unoperated controls on a battery of tasks that tax affective processing, including two tasks that tax reward processing and two that assess emotional reactions. |
2004-05-25 |
2023-08-12 |
human |
| Jean A King, Jeffrey Tenney, Victoria Rossi, Lauralea Colamussi, Stacy Burdic. Neural substrates underlying impulsivity. Annals of the New York Academy of Sciences. vol 1008. 2004-03-26. PMID:14998882. |
furthermore, new emerging data on neural substrates underlying impulsivity have incorporated brain regions involved in reinforcement, reward, and decision making such as the nucleus accumbens, cerebellum, and amygdala. |
2004-03-26 |
2023-08-12 |
Not clear |
| George F Koo. Neuroadaptive mechanisms of addiction: studies on the extended amygdala. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. vol 13. issue 6. 2004-03-01. PMID:14636960. |
the brain reward system implicated in the development of addiction is comprised of key elements of a basal forebrain macrostructure termed the extended amygdala and its connections. |
2004-03-01 |
2023-08-12 |
Not clear |
| George F Koo. Neuroadaptive mechanisms of addiction: studies on the extended amygdala. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. vol 13. issue 6. 2004-03-01. PMID:14636960. |
neuropharmacologic studies in animal models of addiction have provided evidence for the dysregulation of specific neurochemical mechanisms not only in specific brain reward circuits (opioid peptides, gamma-aminobutyric acid, glutamate and dopamine) but also recruitment of brain stress systems (corticotropin-releasing factor) that provide the negative motivational state that drives addiction, and also are localized in the extended amygdala. |
2004-03-01 |
2023-08-12 |
Not clear |
| Lisa Stefanacci, Robert E Clark, Stuart M Zol. Selective neurotoxic amygdala lesions in monkeys disrupt reactivity to food and object stimuli and have limited effects on memory. Behavioral neuroscience. vol 117. issue 5. 2004-01-05. PMID:14570552. |
monkeys with bilateral neurotoxic amygdala lesions and normal monkeys were administered tests of emotional reactivity, recognition memory, and reward association memory. |
2004-01-05 |
2023-08-12 |
monkey |
| Lisa Stefanacci, Robert E Clark, Stuart M Zol. Selective neurotoxic amygdala lesions in monkeys disrupt reactivity to food and object stimuli and have limited effects on memory. Behavioral neuroscience. vol 117. issue 5. 2004-01-05. PMID:14570552. |
these findings underscore the role of the amygdala in aspects of emotional reactivity and reward association memory, but not in recognition memory. |
2004-01-05 |
2023-08-12 |
monkey |
| George F Koo. Alcoholism: allostasis and beyond. Alcoholism, clinical and experimental research. vol 27. issue 2. 2003-12-02. PMID:12605072. |
the brain reward system implicated in the development of alcoholism comprises key elements of a basal forebrain macrostructure termed the extended amygdala that includes the central nucleus of the amygdala, the bed nucleus of the stria terminalis, and a transition zone in the medial (shell) part of the nucleus accumbens. |
2003-12-02 |
2023-08-12 |
human |
| William D S Killgore, Ashley D Young, Lisa A Femia, Piotr Bogorodzki, Jadwiga Rogowska, Deborah A Yurgelun-Tod. Cortical and limbic activation during viewing of high- versus low-calorie foods. NeuroImage. vol 19. issue 4. 2003-10-23. PMID:12948696. |
findings suggest that the amygdala may be responsive to a general category of biologically relevant stimuli such as food, whereas separate ventromedial prefrontal systems may be activated depending on the perceived reward value or motivational salience of food stimuli. |
2003-10-23 |
2023-08-12 |
human |
| Pierre Veinante, Marie-Elisabeth Stoeckel, François Lasbennes, Marie-José Freund-Mercie. c-Fos and peptide immunoreactivities in the central extended amygdala of morphine-dependent rats after naloxone-precipitated withdrawal. The European journal of neuroscience. vol 18. issue 5. 2003-10-23. PMID:12956728. |
the central extended amygdala, a forebrain macrostructure, may represent a common substrate for acute drug reward and the dysphoric effects of drug withdrawal. |
2003-10-23 |
2023-08-12 |
rat |
| Christopher A Gadd, Patricia Murtra, Carmen De Felipe, Stephen P Hun. Neurokinin-1 receptor-expressing neurons in the amygdala modulate morphine reward and anxiety behaviors in the mouse. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 23. issue 23. 2003-10-08. PMID:12967989. |
neurokinin-1 receptor-expressing neurons in the amygdala modulate morphine reward and anxiety behaviors in the mouse. |
2003-10-08 |
2023-08-12 |
mouse |
| Christopher A Gadd, Patricia Murtra, Carmen De Felipe, Stephen P Hun. Neurokinin-1 receptor-expressing neurons in the amygdala modulate morphine reward and anxiety behaviors in the mouse. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 23. issue 23. 2003-10-08. PMID:12967989. |
in a preliminary investigation, bilateral ablation of these neurons from the amygdala, but not the nucleus accumbens and dorsomedial caudate putamen, brought about reductions in morphine reward behavior. |
2003-10-08 |
2023-08-12 |
mouse |
| Christopher A Gadd, Patricia Murtra, Carmen De Felipe, Stephen P Hun. Neurokinin-1 receptor-expressing neurons in the amygdala modulate morphine reward and anxiety behaviors in the mouse. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 23. issue 23. 2003-10-08. PMID:12967989. |
nk1 receptor-expressing neurons in the mouse amygdala therefore modulate morphine reward behaviors. |
2003-10-08 |
2023-08-12 |
mouse |
| Jay A Gottfried, John O'Doherty, Raymond J Dola. Encoding predictive reward value in human amygdala and orbitofrontal cortex. Science (New York, N.Y.). vol 301. issue 5636. 2003-09-04. PMID:12934011. |
encoding predictive reward value in human amygdala and orbitofrontal cortex. |
2003-09-04 |
2023-08-12 |
human |
| Jay A Gottfried, John O'Doherty, Raymond J Dola. Encoding predictive reward value in human amygdala and orbitofrontal cortex. Science (New York, N.Y.). vol 301. issue 5636. 2003-09-04. PMID:12934011. |
thus, differential activity in amygdala and orbitofrontal cortex encodes the current value of reward representations accessible to predictive cues. |
2003-09-04 |
2023-08-12 |
human |
| Naoya Aoki, Ei-Ichi Izawa, Shin Yanagihara, Toshiya Matsushim. Neural correlates of memorized associations and cued movements in archistriatum of the domestic chick. The European journal of neuroscience. vol 17. issue 9. 2003-07-16. PMID:12752793. |
the ventral part of intermediate archistriatum proved to contain a group of neurons that selectively responded to the reward-associated colours before the reward was actually presented, possibly coding the memorized associations. |
2003-07-16 |
2023-08-12 |
chicken |
| S Ahn, A G Phillip. Independent modulation of basal and feeding-evoked dopamine efflux in the nucleus accumbens and medial prefrontal cortex by the central and basolateral amygdalar nuclei in the rat. Neuroscience. vol 116. issue 1. 2003-06-24. PMID:12535961. |
interactions of the central and basolateral nuclei of the amygdala with the mesocorticolimbic dopamine system are implicated in the acquisition and performance of conditioned responses for food reward. |
2003-06-24 |
2023-08-12 |
rat |
| Huiyuan Zheng, Michele Corkern, Irina Stoyanova, Laurel M Patterson, Rui Tian, Hans-Rudolf Berthou. Peptides that regulate food intake: appetite-inducing accumbens manipulation activates hypothalamic orexin neurons and inhibits POMC neurons. American journal of physiology. Regulatory, integrative and comparative physiology. vol 284. issue 6. 2003-06-17. PMID:12736179. |
corticolimbic circuits involving the prefrontal cortex, amygdala, and ventral striatum determine the reward value of food and might play a role in environmentally induced obesity. |
2003-06-17 |
2023-08-12 |
rat |
| Meg Waraczynsk. Lidocaine inactivation demonstrates a stronger role for central versus medial extended amygdala in medial forebrain bundle self-stimulation. Brain research. vol 962. issue 1-2. 2003-04-01. PMID:12543469. |
given recent attention to the role of the extended amygdala (ea) in brain reward processes, this study examines the relative contributions of the medial versus central aspects of that forebrain macrostructure to the rewarding effects of medial forebrain bundle (mfb) stimulation. |
2003-04-01 |
2023-08-12 |
rat |