| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Ting Mei, Linchuan Ma, Fanzhen Kon. Sodium aescinate improve behavioral performance by inhibiting dorsal raphe nucleus NLRP3 inflammasome in Post-traumatic stress disorder Rat Model. Biochemical and biophysical research communications. vol 671. 2023-06-11. PMID:37302291. |
growing evidence suggest that nlrp3 inflammasome activation in hippocampus and amygdala is involved in the pathophysiology of ptsd. |
2023-06-11 |
2023-08-14 |
rat |
| Sara Florén Lind, Frida Stam, Sofia Zelleroth, Evelina Meurling, Andreas Frick, Alfhild Grönblad. Acute caffeine differently affects risk-taking and the expression of BDNF and of adenosine and opioid receptors in rats with high or low anxiety-like behavior. Pharmacology, biochemistry, and behavior. 2023-06-11. PMID:37302662. |
thus, the aim of this study was to investigate general behavior, risk-taking, and anxiety-like behavior, as well as mrna expression (adenosine a2a and a1, dopamine d2, and, μ, κ, δ opioid, receptors, bdnf, c-fos, igf-1) in amygdala, caudate putamen, frontal cortex, hippocampus, hypothalamus, after an acute dose of caffeine. |
2023-06-11 |
2023-08-14 |
rat |
| Dipan C Patel, Nathaniel Swift, Bhanu P Tewari, Jack L Browning, Courtney Prim, Lata Chaunsali, Ian Kimbrough, Michelle L Olsen, Harald Sontheime. Infection-induced epilepsy is caused by increased expression of chondroitin sulfate proteoglycans in hippocampus and amygdala. bioRxiv : the preprint server for biology. 2023-06-09. PMID:37292901. |
infection-induced epilepsy is caused by increased expression of chondroitin sulfate proteoglycans in hippocampus and amygdala. |
2023-06-09 |
2023-08-14 |
Not clear |
| Mate Abraham, Kirsten Schmerder, Malin Hedtstück, Kimberly Bösing, Annakarina Mundorf, Nadja Freun. Maternal separation and its developmental consequences on anxiety and parvalbumin interneurons in the amygdala. Journal of neural transmission (Vienna, Austria : 1996). 2023-06-09. PMID:37294327. |
altered gabaergic activity in the hippocampus and the amygdala have been identified in humans diagnosed with depression or anxiety disorders, as well as in respective animal models. |
2023-06-09 |
2023-08-14 |
rat |
| Zhaosong Chu, Lijin Yuan, Mengxin He, Yuqi Cheng, Yi Lu, Xiufeng Xu, Zonglin She. Atrophy of bilateral nucleus accumbens in melancholic depression. Neuroreport. vol 34. issue 10. 2023-06-04. PMID:37270840. |
evidence from previous literature suggests that the nucleus accumbens (nac), hippocampus, and amygdala play critical roles in the reward circuit. |
2023-06-04 |
2023-08-14 |
human |
| Zhaosong Chu, Lijin Yuan, Mengxin He, Yuqi Cheng, Yi Lu, Xiufeng Xu, Zonglin She. Atrophy of bilateral nucleus accumbens in melancholic depression. Neuroreport. vol 34. issue 10. 2023-06-04. PMID:37270840. |
however, few studies have investigated the structural alterations of the nac, hippocampus, and amygdala in depression with anhedonia as the main clinical manifestation. |
2023-06-04 |
2023-08-14 |
human |
| Zhaosong Chu, Lijin Yuan, Mengxin He, Yuqi Cheng, Yi Lu, Xiufeng Xu, Zonglin She. Atrophy of bilateral nucleus accumbens in melancholic depression. Neuroreport. vol 34. issue 10. 2023-06-04. PMID:37270840. |
thus, the current study aimed to explore the structural changes of the subcortical regions among melancholic depression (md) patients, especially in the nac, hippocampus, and amygdala, to provide a theoretical basis for understanding the pathological mechanisms of md. |
2023-06-04 |
2023-08-14 |
human |
| Robin Nguyen, Konstantinos Koukoutselos, Thomas Forro, Stéphane Ciocch. Fear extinction relies on ventral hippocampal safety codes shaped by the amygdala. Science advances. vol 9. issue 22. 2023-05-31. PMID:37256958. |
fear extinction relies on ventral hippocampal safety codes shaped by the amygdala. |
2023-05-31 |
2023-08-14 |
Not clear |
| Robin Nguyen, Konstantinos Koukoutselos, Thomas Forro, Stéphane Ciocch. Fear extinction relies on ventral hippocampal safety codes shaped by the amygdala. Science advances. vol 9. issue 22. 2023-05-31. PMID:37256958. |
here, we performed activity-dependent engram tagging and in vivo single-unit electrophysiological recordings from the ventral hippocampus (vh) while optogenetically manipulating basolateral amygdala (bla) inputs during the formation of cued fear extinction memory. |
2023-05-31 |
2023-08-14 |
Not clear |
| Laura Göschel, Lea Kurz, Andrea Dell'Orco, Theresa Köbe, Peter Körtvélyessy, Ariane Fillmer, Semiha Aydin, Layla Tabea Riemann, Hui Wang, Bernd Ittermann, Ulrike Grittner, Agnes Flöe. 7T amygdala and hippocampus subfields in volumetry-based associations with memory: A 3-year follow-up study of early Alzheimer's disease. NeuroImage. Clinical. vol 38. 2023-05-30. PMID:37253284. |
7t amygdala and hippocampus subfields in volumetry-based associations with memory: a 3-year follow-up study of early alzheimer's disease. |
2023-05-30 |
2023-08-14 |
Not clear |
| Cristina Dettori, Francesca Ronca, Marco Scalese, Federica Saponar. Parathyroid Hormone (PTH)-Related Peptides Family: An Intriguing Role in the Central Nervous System. Journal of personalized medicine. vol 13. issue 5. 2023-05-27. PMID:37240884. |
the pth/pthrp/pth1r system has been found to be expressed in many areas of the brain (hippocampus, amygdala, hypothalamus, caudate nucleus, corpus callosum, subthalamic nucleus, thalamus, substantia nigra, cerebellum), and literature data suggest the system exercises a protective action against neuroinflammation and neurodegeneration, with positive effects on memory and hyperalgesia. |
2023-05-27 |
2023-08-14 |
Not clear |
| Michelle Ulrich, Evangelia Pollali, Gürsel Çalışkan, Oliver Stork, Anne Albrech. Sex differences in anxiety and threat avoidance in GAD65 knock-out mice. Neurobiology of disease. 2023-05-25. PMID:37230180. |
anxiety disorders have been linked to a disbalance of excitation and inhibition in a network of brain structures comprising frontal cortical regions, the amygdala and the hippocampus, among others. |
2023-05-25 |
2023-08-14 |
mouse |
| Jin Li, Dan Cao, Shan Yu, Xinyu Xiao, Lukas Imbach, Lennart Stieglitz, Johannes Sarnthein, Tianzi Jian. Functional specialization and interaction in the amygdala-hippocampus circuit during working memory processing. Nature communications. vol 14. issue 1. 2023-05-22. PMID:37217494. |
both the hippocampus and amygdala are involved in working memory (wm) processing. |
2023-05-22 |
2023-08-14 |
Not clear |
| Jin Li, Dan Cao, Shan Yu, Xinyu Xiao, Lukas Imbach, Lennart Stieglitz, Johannes Sarnthein, Tianzi Jian. Functional specialization and interaction in the amygdala-hippocampus circuit during working memory processing. Nature communications. vol 14. issue 1. 2023-05-22. PMID:37217494. |
here, we simultaneously recorded intracranial eeg from the amygdala and hippocampus of epilepsy patients while performing a wm task, and compared their representation patterns during the encoding and maintenance periods. |
2023-05-22 |
2023-08-14 |
Not clear |
| Jin Li, Dan Cao, Shan Yu, Xinyu Xiao, Lukas Imbach, Lennart Stieglitz, Johannes Sarnthein, Tianzi Jian. Functional specialization and interaction in the amygdala-hippocampus circuit during working memory processing. Nature communications. vol 14. issue 1. 2023-05-22. PMID:37217494. |
wm encoding and maintenance were associated with bidirectional information flow between the amygdala and the hippocampus in low-frequency bands (1-40 hz). |
2023-05-22 |
2023-08-14 |
Not clear |
| Jin Li, Dan Cao, Shan Yu, Xinyu Xiao, Lukas Imbach, Lennart Stieglitz, Johannes Sarnthein, Tianzi Jian. Functional specialization and interaction in the amygdala-hippocampus circuit during working memory processing. Nature communications. vol 14. issue 1. 2023-05-22. PMID:37217494. |
furthermore, the decoding accuracy on wm load was higher by using representational features in the amygdala during encoding and in the hippocampus during maintenance, and by using information flow from the amygdala during encoding and that from the hippocampus during maintenance, respectively. |
2023-05-22 |
2023-08-14 |
Not clear |
| Volodymir I Pidoplichko, Taiza H Figueiredo, Maria Fm Braga, Hongna Pan, Ann M Marin. Alpha-linolenic acid enhances the facilitation of GABAergic neurotransmission in the BLA and CA1. Experimental biology and medicine (Maywood, N.J.). 2023-05-20. PMID:37208920. |
however, the effect of ala on gabaergic neurotransmission in hyperexcitable brain regions involved in neuropsychiatric disorders, such as the basolateral amygdala (bla) and ca1 subfield of the hippocampus, is unknown. |
2023-05-20 |
2023-08-14 |
Not clear |
| Huanhua Lu, Xueting Li, Yinan Wang, Yiying Song, Jia Li. Hippocampus links perceived social support with self-esteem. Social neuroscience. 2023-05-18. PMID:37200111. |
therefore, we used voxel-based morphometry to explore whether the hippocampus and amygdala function as the neuroanatomical basis linking perceived social support with self-esteem in a cohort of 243 young healthy adults (128 women; mean age 22.64 years, standard deviation 1.01 years). |
2023-05-18 |
2023-08-14 |
Not clear |
| Pantelis Antonoudiou, Bradly Stone, Phillip L W Colmers, Aidan Evans-Strong, Najah Walton, Jamie Maguir. Influence of chronic stress on network states governing valence processing: Potential relevance to the risk for psychiatric illnesses. Journal of neuroendocrinology. 2023-05-15. PMID:37186481. |
valence assignment involves neural computations performed in emotional processing hubs, including the amygdala, prefrontal cortex, and ventral hippocampus, which can be influenced by neuroendocrine mediators. |
2023-05-15 |
2023-08-14 |
Not clear |
| Robert J McDonald, Nancy S Hong, Jan S Trow, Chelsea Kaupp, R J Balog, London Gokarn, Erin A Falkenberg, Keiko J McCreary, Nasrin Soltanpour, Carter Witbeck, Aimee McKenna, Gerlinde A S Met. Effects of maternal social isolation on adult rodent offspring cognition. Scientific reports. vol 13. issue 1. 2023-05-14. PMID:37173349. |
accordingly, for this study we were interested in the effects of maternal stress induced via social isolation on adult offspring cognitive functions including spatial, stimulus-response, and emotional learning and memory that are mediated by different networks centered on the hippocampus, dorsal striatum, and amygdala, respectively. |
2023-05-14 |
2023-08-14 |
rat |