| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Taro Okunomiya, Hiroyuki Hioki, Chika Nishimura, Satoshi Yawata, Itaru Imayoshi, Ryoichiro Kageyama, Ryosuke Takahashi, Dai Watanab. Generation of a MOR-CreER knock-in mouse line to study cells and neural circuits involved in mu opioid receptor signaling. Genesis (New York, N.Y. : 2000). vol 58. issue 1. 2020-09-08. PMID:31651080. |
we show that the mor-creer allele undergoes tm-dependent recombination in a discrete subtype of neurons that express mor in the adult nervous system, including the olfactory bulb, cerebral cortex, striosome compartments in the striatum, hippocampus, amygdala, thalamus, hypothalamus, interpeduncular nucleus, superior and inferior colliculi, periaqueductal gray, parabrachial nuclei, cochlear nucleus, raphe nuclei, pontine and medullary reticular formation, ambiguus nucleus, solitary nucleus, spinal cord, and dorsal root ganglia. |
2020-09-08 |
2023-08-13 |
mouse |
| M Ghonghadze, K Pachkoria, M Okujava, N Antelava, N Gongadz. ENDOCANNABINOIDS RECEPTORS MEDIATED CENTRAL AND PERIPHERAL EFFECTS (REVIEW). Georgian medical news. issue 298. 2020-06-19. PMID:32141867. |
cb1 receptors are distributed in the central and peripheral nervous system being identified in the greater amounts in the brain cortex, basal ganglia, spinal cord, cerebellum, hippocampus and olfactory areas, owing for the modulatory action of ecs on cognitive function, memory, behaviour, emotion and locomotor activity. |
2020-06-19 |
2023-08-13 |
Not clear |
| Wei-Kang Xue, Wei-Jiang Zhao, Xiang-He Meng, Hui-Fan Shen, Pei-Zhi Huan. Spinal cord injury induced Neuregulin 1 signaling changes in mouse prefrontal cortex and hippocampus. Brain research bulletin. vol 144. 2020-01-16. PMID:30529367. |
spinal cord injury induced neuregulin 1 signaling changes in mouse prefrontal cortex and hippocampus. |
2020-01-16 |
2023-08-13 |
mouse |
| Niannian Huang, Chun Yang, Dongyu Hua, Shan Li, Gaofeng Zhan, Ning Yang, Ailin Luo, Hui X. Alterations in the BDNF-mTOR Signaling Pathway in the Spinal Cord Contribute to Hyperalgesia in a Rodent Model of Chronic Restraint Stress. Neuroscience. vol 409. 2020-01-09. PMID:30940563. |
crs significantly altered bdnf and mtor phosphorylation in the anterior cingulate cortex and spinal cord but not in the hippocampus. |
2020-01-09 |
2023-08-13 |
Not clear |
| Antonio Caretta, Daniela Cevolani, Giuseppe Luppino, Massimo Matelli, Roberto Tirindell. Characterization and Regional Distribution of a Class of Synapses with Highly Concentrated cAMP Binding Sites in the Rat Brain. The European journal of neuroscience. vol 3. issue 7. 2019-11-20. PMID:12106475. |
saf-camp labelling is prominent in well defined regions of the rat brain: (i) the frontal and entorhinal areas of the cortex; (ii) the field ca1 of the hippocampus; (iii) the olfactory system; (iv) the medial nuclei of the thalamus; (v) the parabrachial nuclei and other less defined regions of the reticular substance; (vi) the substantia gelatinosa of rolando in the spinal cord; and (vii) the neo- and paleocerebellum in the purkinje cell layer, the archicerebellum in the granular cell layer. |
2019-11-20 |
2023-08-12 |
rat |
| Carlos Gonzalez-Islas, Pernille Bülow, Peter Wenne. Regulation of synaptic scaling by action potential-independent miniature neurotransmission. Journal of neuroscience research. vol 96. issue 3. 2019-11-18. PMID:28782263. |
this class of homeostatic synaptic plasticity is compared in studies using hippocampal and cortical cultures, as well as in vivo work in the embryonic chick spinal cord. |
2019-11-18 |
2023-08-13 |
chicken |
| U A Gutner, M A Shupik, O A Maloshitskaya, S A Sokolov, A P Rezvykh, S Yu Funikov, A T Lebedev, A A Ustyugov, A V Alessenk. Changes in the Metabolism of Sphingoid Bases in the Brain and Spinal Cord of Transgenic FUS(1-359) Mice, a Model of Amyotrophic Lateral Sclerosis. Biochemistry. Biokhimiia. vol 84. issue 10. 2019-11-14. PMID:31694512. |
the aim of this study was to evaluate changes in the content of sphingoid bases - sphingosine (sph), sphinganine, and sphingosine-1-phosphate (sph-1-p) - and in expression of genes encoding enzymes involved in their metabolism in the brain structures (hippocampus, cortex, and cerebellum) and spinal cord of transgenic fus(1-359) mice. |
2019-11-14 |
2023-08-13 |
mouse |
| Inken Waltl, Christopher Käufer, Ingo Gerhauser, Chintan Chhatbar, Luca Ghita, Ulrich Kalinke, Wolfgang Lösche. Microglia have a protective role in viral encephalitis-induced seizure development and hippocampal damage. Brain, behavior, and immunity. vol 74. 2019-09-10. PMID:30217535. |
microglia depletion accelerated the occurrence of seizures, exacerbated hippocampal damage, and led to neurodegeneration in the spinal cord, which is normally not observed in this mouse strain. |
2019-09-10 |
2023-08-13 |
mouse |
| Shaofeng Pu, Shuangyue Li, Yongming Xu, Junzhen Wu, Yingying Lv, Dongping D. Role of receptor-interacting protein 1/receptor-interacting protein 3 in inflammation and necrosis following chronic constriction injury of the sciatic nerve. Neuroreport. vol 29. issue 16. 2019-04-10. PMID:30192300. |
the mrna expression and protein levels of inflammatory factors rip1 and rip3 in the dorsal root ganglion (drg), spinal cord (sc) and hippocampus (hip) were also determined. |
2019-04-10 |
2023-08-13 |
mouse |
| Gabriela Riego, Alejandro Redondo, Sergi Leánez, Olga Po. Mechanism implicated in the anti-allodynic and anti-hyperalgesic effects induced by the activation of heme oxygenase 1/carbon monoxide signaling pathway in the central nervous system of mice with neuropathic pain. Biochemical pharmacology. vol 148. 2018-12-17. PMID:29247614. |
in male c57bl6 mice with neuropathic pain induced by the chronic constriction of sciatic nerve (cci), we evaluated the effects of corm-2 and copp on the expression of the nuclear factor erythroid 2-related factor 2 (nrf2), ho-1 and nad(p)h:quinone oxidoreductase-1 (nqo1), the microglial marker (cd11b/c), and the mitogen-activated protein kinases (mapk) (jnk, erk½ and p38) in the amygdala, prefrontal cortex, hippocampus, hypothalamus and spinal cord, by using western blot assay. |
2018-12-17 |
2023-08-13 |
mouse |
| Carlos G Martínez-Moreno, Denisse Calderón-Vallejo, Steve Harvey, Carlos Arámburo, José Luis Quintana. Growth Hormone (GH) and Gonadotropin-Releasing Hormone (GnRH) in the Central Nervous System: A Potential Neurological Combinatory Therapy? International journal of molecular sciences. vol 19. issue 2. 2018-08-01. PMID:29373545. |
this brief review of the neurological effects of growth hormone (gh) and gonadotropin-releasing hormone (gnrh) in the brain, particularly in the cerebral cortex, hypothalamus, hippocampus, cerebellum, spinal cord, neural retina, and brain tumors, summarizes recent information about their therapeutic potential as treatments for different neuropathologies and neurodegenerative processes. |
2018-08-01 |
2023-08-13 |
Not clear |
| Xiqian Wang, Xiejia Jiao, Zhonghao Liu, Yixin L. Crocetin Potentiates Neurite Growth in Hippocampal Neurons and Facilitates Functional Recovery in Rats with Spinal Cord Injury. Neuroscience bulletin. vol 33. issue 6. 2018-07-24. PMID:28770439. |
we found that crocetin (1) did not alter the viability of cultured hippocampal neurons; (2) accelerated neurite growth with preference for the longest process in individual hippocampal neurons; (3) reversed the inhibition of neurite growth by chondroitin sulfate proteoglycan and nogoa; (4) facilitated the recovery of motor and sensorimotor functions after spinal cord injury; and (5) did not inhibit pro-inflammatory responses, but restored the innervation of the descending 5-ht system in injured spinal cord. |
2018-07-24 |
2023-08-13 |
rat |
| Janet Best, H F Nijhout, Srimal Samaranayake, Parastoo Hashemi, Michael Ree. A mathematical model for histamine synthesis, release, and control in varicosities. Theoretical biology & medical modelling. vol 14. issue 1. 2018-07-24. PMID:29228949. |
the histamine neuron cell bodies are in the tuberomammillary (tm) nucleus of the hypothalamus and these neurons send projections throughout the central nervous system (cns), in particular to the cerebral cortex, amygdala, basal ganglia, hippocampus, thalamus, retina, and spinal cord. |
2018-07-24 |
2023-08-13 |
Not clear |
| Sheng Yang, Zhiyu Ma, Chuan Suo, Ling Cheng, Juan Su, Zhihai Le. Cloning and mRNA expression of NPB and its effect on hormone secretion of the reproductive cells in the pig. General and comparative endocrinology. vol 261. 2018-07-17. PMID:29481768. |
the results showed that npb mrna expression was higher in hippocampus, cerebellum, spinal cord, thymus, tonsil, duodenum, cecum, colon, ovary and testis. |
2018-07-17 |
2023-08-13 |
Not clear |
| Xi Jiang, Qizhi Yan, Fuhe Liu, Changfeng Jing, Lianshu Ding, Lijin Zhang, Cong Pan. Chronic trans-astaxanthin treatment exerts antihyperalgesic effect and corrects co-morbid depressive like behaviors in mice with chronic pain. Neuroscience letters. vol 662. 2018-07-02. PMID:28982597. |
subsequent study indicated that indoleamine 2,3-dioxygenase (ido) expression increased after cci surgery in hippocampus and spinal cord, accompanied by increase of kynurenine (kyn)/tryptophan (try) ratio, decrease of serotonin (5-ht)/try ratio and decrease of 5-ht/5-hiaa ratio. |
2018-07-02 |
2023-08-13 |
mouse |
| Hong-Bo Jiang, Ai-Lin Du, Hai-Yang Luo, Jun Yang, Xiao-Qiu Luo, Rui-Qing Ma, Chang-He Shi, Yu-Ming X. Arginine vasopressin relates with spatial learning and memory in a mouse model of spinocerebellar ataxia type 3. Neuropeptides. vol 65. 2018-06-14. PMID:28619276. |
the results showed that (alves et al., 2010) the swimming velocity, distance traveled and latency to the platform of mwm in sca3 mice were reduced slower than those in wt mice over 4 training days (p<0.05, 0.01 or 0.001); (antunes and zimmerman, 1978) sca3 mice showed a lower performance of spatial learning and memory of mwm during the fifth day (test day) compared to wt mice; (bao et al., 2014) sca3 mice had a decrease of avp concentration in cerebral cortex (6.3±0.6pg/mg vs. 11.4±1.0pg/mg, p<0.01), hypothalamus (6.1±1.3ng/mg vs. 10.3±2.1ng/mg, p<0.05), hippocampus (3.2±0.5pg/mg vs. 5.2±1.0pg/mg, p<0.01) and cerebellum (4.7±0.9pg/mg vs. 8.3±1.1pg/mg, p<0.01), not in spinal cord, pituitary and serum; and (barberies and tribollet, 1996) intraventricular avp could significantly quicken swimming velocity, cut down distance traveled and reduce latency to the platform of mwm in a dose-dependent manner, but intraventricular avp receptor antagonist weakened the spatial learning and memory of mwm in sca3 mice during the fifth day. |
2018-06-14 |
2023-08-13 |
mouse |
| Panos Theofilas, Christian Steinhäuser, Martin Theis, Amin Derouich. Morphological study of a connexin 43-GFP reporter mouse highlights glial heterogeneity, amacrine cells, and olfactory ensheathing cells. Journal of neuroscience research. vol 95. issue 11. 2018-05-18. PMID:28370142. |
applying anti-gfp, all cell types related to astroglia were positive-namely, protoplasmic astrocytes in the hippocampus, cortex, thalamus, spinal cord, olfactory bulb, cerebellum with bergmann glia and astrocytes also in the molecular layer, and retinal müller cells and astrocytes. |
2018-05-18 |
2023-08-13 |
mouse |
| M Hoshikawa, A Kato, H Hojo, Y Shibata, N Kumamoto, M Watanabe, S Ugaw. Distribution of ASIC4 transcripts in the adult wild-type mouse brain. Neuroscience letters. vol 651. 2018-03-26. PMID:28461138. |
previous studies of asic4 expression in the mammalian central nervous system have shown that asic4 is abundantly expressed in the spinal cord and in various brain regions, such as the cerebral cortex, the hippocampus, and the cerebellum. |
2018-03-26 |
2023-08-13 |
mouse |
| G S Finnie, R Gunnarsson, J Manavis, P C Blumbergs, K A Mander, S Edwards, C Van den Heuvel, J W Finni. Characterization of an 'Amyloid Only' Transgenic (B6C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax) Mouse Model of Alzheimer's Disease. Journal of comparative pathology. vol 156. issue 4. 2018-03-21. PMID:28431735. |
they were most abundant in the cerebral cortices, hippocampus, olfactory bulbs, some white matter tracts and the cerebellar molecular layer; no amyloid aggregates were found in the midbrain, brainstem or spinal cord, or in an equivalent number of brains from wild-type mice. |
2018-03-21 |
2023-08-13 |
mouse |
| Cristina Romei, Tiziana Bonifacino, Marco Milanese, Cesare Usai, Luca Raiter. Colocalization of neurotransmitter transporters on the plasma membrane of the same nerve terminal may reflect cotransmission. Brain research bulletin. vol 127. 2017-11-13. PMID:27565422. |
we could observe that functional transporters for glycine and glutamate are coexpressed on nerve terminals in the cerebellum; transporters for dopamine and gaba coexist on striatal terminals; transporters for glycine and gaba, previously found to coexist as cotransmission markers on nerve terminals of spinal cord and cerebellum, are not coexpressed in neocortex and hippocampus, where cotransmission has not been proposed to occur; transporters for gaba, glycine and glutamate are colocalized on nerve terminals of the spinal cord. |
2017-11-13 |
2023-08-13 |
Not clear |