| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Megan Caldwell, Vanessa Ayo-Jibunoh, Josue Criollo Mendoza, Katherine R Brimblecombe, Lauren M Reynolds, Xin Yan Zhu Jiang, Colin Alarcon, Elizabeth Fiore, Jacquelyn N Tomaio, Greg R Phillips, Susana Mingote, Cecilia Flores, Patrizia Casaccia, Jia Liu, Stephanie J Cragg, Dan P McCloskey, Leora Yetnikof. Axo-glial interactions between midbrain dopamine neurons and oligodendrocyte lineage cells in the anterior corpus callosum. Brain structure & function. 2023-09-05. PMID:37668732. |
axo-glial interactions between midbrain dopamine neurons and oligodendrocyte lineage cells in the anterior corpus callosum. |
2023-09-05 |
2023-09-07 |
mouse |
| Megan Caldwell, Vanessa Ayo-Jibunoh, Josue Criollo Mendoza, Katherine R Brimblecombe, Lauren M Reynolds, Xin Yan Zhu Jiang, Colin Alarcon, Elizabeth Fiore, Jacquelyn N Tomaio, Greg R Phillips, Susana Mingote, Cecilia Flores, Patrizia Casaccia, Jia Liu, Stephanie J Cragg, Dan P McCloskey, Leora Yetnikof. Axo-glial interactions between midbrain dopamine neurons and oligodendrocyte lineage cells in the anterior corpus callosum. Brain structure & function. 2023-09-05. PMID:37668732. |
here, we provide evidence implicating midbrain dopamine neurons in the innervation of oligodendrocyte lineage cells in the anterior corpus callosum and nearby white matter tracts of male and female adult mice. |
2023-09-05 |
2023-09-07 |
mouse |
| Megan Caldwell, Vanessa Ayo-Jibunoh, Josue Criollo Mendoza, Katherine R Brimblecombe, Lauren M Reynolds, Xin Yan Zhu Jiang, Colin Alarcon, Elizabeth Fiore, Jacquelyn N Tomaio, Greg R Phillips, Susana Mingote, Cecilia Flores, Patrizia Casaccia, Jia Liu, Stephanie J Cragg, Dan P McCloskey, Leora Yetnikof. Axo-glial interactions between midbrain dopamine neurons and oligodendrocyte lineage cells in the anterior corpus callosum. Brain structure & function. 2023-09-05. PMID:37668732. |
these results suggest that oligodendrocyte lineage cells may respond to dopamine released from midbrain dopamine axons, which could affect myelination. |
2023-09-05 |
2023-09-07 |
mouse |
| Megan Caldwell, Vanessa Ayo-Jibunoh, Josue Criollo Mendoza, Katherine R Brimblecombe, Lauren M Reynolds, Xin Yan Zhu Jiang, Colin Alarcon, Elizabeth Fiore, Jacquelyn N Tomaio, Greg R Phillips, Susana Mingote, Cecilia Flores, Patrizia Casaccia, Jia Liu, Stephanie J Cragg, Dan P McCloskey, Leora Yetnikof. Axo-glial interactions between midbrain dopamine neurons and oligodendrocyte lineage cells in the anterior corpus callosum. Brain structure & function. 2023-09-05. PMID:37668732. |
together, this work broadens our understanding of neuron-glia interactions with important implications for myelin plasticity by identifying midbrain dopamine axons as a potential regulator of corpus callosal oligodendrocyte lineage cells. |
2023-09-05 |
2023-09-07 |
mouse |
| Kenta Abe, Yuki Kambe, Kei Majima, Zijing Hu, Makoto Ohtake, Ali Momennezhad, Hideki Izumi, Takuma Tanaka, Ashley Matunis, Emma Stacy, Takahide Itokazu, Takashi R Sato, Tatsuo K Sat. Enhanced Aversive Signals During Classical Conditioning in Dopamine Axons in Medial Prefrontal Cortex. bioRxiv : the preprint server for biology. 2023-09-04. PMID:37662305. |
midbrain dopamine neurons impact neural processing in the prefrontal cortex (pfc) through mesocortical projections. |
2023-09-04 |
2023-09-07 |
mouse |
| Min Jung Kim, Daniel J Gibson, Dan Hu, Ara Mahar, Cynthia J Schofield, Patlapa Sompolpong, Tomoko Yoshida, Kathy T Tran, Ann M Graybie. Dopamine Release Plateau and Outcome Signals in Dorsal Striatum Contrast with Classic Reinforcement Learning Formulations. bioRxiv : the preprint server for biology. 2023-08-30. PMID:37645888. |
in most sites, we found no evidence for a transition from outcome to cue signaling, a hallmark of temporal difference reinforcement learning as applied to midbrain dopamine activity. |
2023-08-30 |
2023-09-07 |
mouse |
| Licia Vellucci, Mariateresa Ciccarelli, Elisabetta Filomena Buonaguro, Michele Fornaro, Giordano D'Urso, Giuseppe De Simone, Felice Iasevoli, Annarita Barone, Andrea de Bartolomei. The Neurobiological Underpinnings of Obsessive-Compulsive Symptoms in Psychosis, Translational Issues for Treatment-Resistant Schizophrenia. Biomolecules. vol 13. issue 8. 2023-08-26. PMID:37627285. |
an integrative view exploring this topic should take into account the following aspects: (i) the implication for glutamate, dopamine, and serotonin neurotransmission as demonstrated by genetic findings; (ii) the growing neuroimaging evidence of the common brain regions and dysfunctional circuits involved in both diseases; (iii) the pharmacological modulation of dopaminergic, serotoninergic, and glutamatergic systems as current therapeutic strategies in schizophrenia ocs; (iv) the recent discovery of midbrain dopamine neurons and dopamine d1- and d2-like receptors as orchestrating hubs in repetitive and psychotic behaviors; (v) the contribution of n-methyl-d-aspartate receptor subunits to both psychosis and ocd neurobiology. |
2023-08-26 |
2023-09-07 |
Not clear |
| Shweta Jain, Andrew G Yee, James Maas, Sarah Gierok, Hongfei Xu, Jasmine Stansil, Jacob Eriksen, Alexandra Nelson, Katlin Silm, Christopher P Ford, Robert H Edward. Adaptor Protein-3 Produces Synaptic Vesicles that Release Phasic Dopamine. bioRxiv : the preprint server for biology. 2023-08-23. PMID:37609166. |
the burst firing of midbrain dopamine neurons releases a phasic dopamine signal that mediates reinforcement learning. |
2023-08-23 |
2023-09-07 |
Not clear |
| Adrien T Stanley, Michael R Post, Clay Lacefield, David Sulzer, Maria Concetta Miniac. Norepinephrine release in the cerebellum contributes to aversive learning. Nature communications. vol 14. issue 1. 2023-08-10. PMID:37563141. |
the modulation of dopamine release from midbrain projections to the striatum has long been demonstrated in reward-based learning, but the synaptic basis of aversive learning is far less characterized. |
2023-08-10 |
2023-08-16 |
mouse |
| Jens Devoght, Joris Comhair, Giovanni Morelli, Jean-Michel Rigo, Rudi D'Hooge, Chadi Touma, Rupert Palme, Ilse Dewachter, Martin vandeVen, Robert J Harvey, Serge N Schiffmann, Elisabeth Piccart, Bert Br\\xc3\\xb4n. Dopamine-mediated striatal activity and function is enhanced in GlyR\\xce\\xb12 knockout animals. iScience. vol 26. issue 8. 2023-08-09. PMID:37554441. |
we show that depletion of glyr\xce\xb12 enhances dopamine-induced increases in the activity of putative dopamine d1 receptor-expressing striatal projection neurons, but does not alter midbrain dopamine neuron activity. |
2023-08-09 |
2023-08-16 |
mouse |
| Emmi Pakarinen, P\\xc3\\xa4ivi Lindhol. CDNF and MANF in the brain dopamine system and their potential as treatment for Parkinson's disease. Frontiers in psychiatry. vol 14. 2023-08-09. PMID:37555005. |
parkinson's disease (pd) is a progressive neurodegenerative disease characterized by gradual loss of midbrain dopamine neurons, leading to impaired motor function. |
2023-08-09 |
2023-08-16 |
human |
| Mengxi Yun, Masafumi Nejime, Takashi Kawai, Jun Kunimatsu, Hiroshi Yamada, HyungGoo R Kim, Masayuki Matsumot. Distinct roles of the orbitofrontal cortex, ventral striatum, and dopamine neurons in counterfactual thinking of decision outcomes. Science advances. vol 9. issue 32. 2023-08-09. PMID:37556536. |
here we report a clear distinction among the roles of the orbitofrontal cortex, ventral striatum and midbrain dopamine neurons in processing counterfactual outcomes in monkeys. |
2023-08-09 |
2023-08-16 |
monkey |
| Hiroyasu Murasawa, Hitomi Soumiya, Hiroyuki Kobayashi, Jun Imai, Takahiko Nagase, Hidefumi Fukumits. Neonatal bilateral whisker trimming in male mice age-dependently alters brain neurotransmitter levels and causes adolescent onsets of social behavior abnormalities. Biomedical research (Tokyo, Japan). vol 44. issue 4. 2023-08-06. PMID:37544736. |
however, reduced levels of dopamine (da) and their metabolites were more significantly identified at p8w in the nuclear origins of monoamine (midbrain and medulla oblongata) and the limbic system (frontal cortex, amygdala, and hippocampus) than at p4w. |
2023-08-06 |
2023-08-14 |
mouse |
| Emil W\\xc3\\xa4rnberg, Arvind Kuma. Feasibility of dopamine as a vector-valued feedback signal in the basal ganglia. Proceedings of the National Academy of Sciences of the United States of America. vol 120. issue 32. 2023-08-01. PMID:37527344. |
inspired by the recent observations that besides rpe, the firing rates of midbrain dopaminergic neurons correlate with motor and cognitive variables, we propose a model in which dopamine signal in the striatum carries a vector-valued error feedback signal (a loss gradient) instead of a homogeneous scalar error (a loss). |
2023-08-01 |
2023-08-14 |
Not clear |
| Olivia K Swanson, Priscilla E Yevoo, David Richard, Arianna Maffe. Altered Thalamocortical Signaling in a Mouse Model of Parkinson's Disease. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2023-08-01. PMID:37527923. |
a well-accepted idea in pd research, albeit not tested experimentally, is that the loss of midbrain dopamine leads to decreased activation of m1 by the motor thalamus (mthal). |
2023-08-01 |
2023-08-14 |
mouse |
| Olivia K Swanson, Priscilla E Yevoo, David Richard, Arianna Maffe. Altered Thalamocortical Signaling in a Mouse Model of Parkinson's Disease. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2023-08-01. PMID:37527923. |
here, we report that midbrain dopamine loss altered mthal input in a laminar- and cell type-specific fashion and induced laminar-specific changes in intracortical synaptic transmission. |
2023-08-01 |
2023-08-14 |
mouse |
| Michael B Prit. Nuclei and tracts in the epithalamus of crocodiles. The Journal of comparative neurology. 2023-07-29. PMID:37507852. |
the medial component is related to the limbic system and serotonergic raphe, while the lateral nucleus is more interconnected with the basal ganglia and midbrain dopamine systems. |
2023-07-29 |
2023-08-14 |
Not clear |
| Zizhen Si, Xidi Wang, Zhaoying Yu, Yuer Ruan, Liyin Qian, Shujun Lin, Xinshuang Gong, Longhui Li, Jing Huang, Yu Li. EGCG attenuates METH self-administration and reinstatement of METH seeking in mice. Addiction biology. vol 28. issue 8. 2023-07-27. PMID:37500489. |
in addition, we found that meth sa led to a decrease in inhibitory postsynaptic currents (ipscs) and increase in the ampar/nmdar ratio and excitation/inhibition (e/i) ratio in ex vivo midbrain slices from ventral tegmental area (vta) dopamine neurons. |
2023-07-27 |
2023-08-14 |
mouse |
| Briana Hempel, Madeline Crissman, Sruti Pari, Benjamin Klein, Guo-Hua Bi, Hannah Alton, Zheng-Xiong X. PPAR\\xce\\xb1 and PPAR\\xce\\xb3 are expressed in midbrain dopamine neurons and modulate dopamine- and cannabinoid-mediated behavior in mice. Molecular psychiatry. 2023-07-21. PMID:37479780. |
ppar\xce\xb1 and ppar\xce\xb3 are expressed in midbrain dopamine neurons and modulate dopamine- and cannabinoid-mediated behavior in mice. |
2023-07-21 |
2023-08-14 |
mouse |
| Woori Kim, Mohit Tripathi, Chunhyung Kim, Satyapavan Vardhineni, Young Cha, Shamseer Kulangara Kandi, Melissa Feitosa, Rohit Kholiya, Eric Sah, Anuj Thakur, Yehan Kim, Sanghyeok Ko, Kaiya Bhatia, Sunny Manohar, Young-Bin Kong, Gagandeep Sindhu, Yoon-Seong Kim, Bruce Cohen, Diwan S Rawat, Kwang-Soo Ki. An optimized Nurr1 agonist provides disease-modifying effects in Parkinson's disease models. Nature communications. vol 14. issue 1. 2023-07-18. PMID:37463889. |
the nuclear receptor, nurr1, is critical for both the development and maintenance of midbrain dopamine neurons, representing a promising molecular target for parkinson's disease (pd). |
2023-07-18 |
2023-08-14 |
mouse |