keyword
https://read.qxmd.com/read/37622283/pgam5-knockout-causes-depressive-like-behaviors-in-mice-via-atp-deficiency-in-the-prefrontal-cortex
#21
JOURNAL ARTICLE
Weiwei Cui, Chunhui Chen, Liya Gong, Junyan Wen, Shanshan Yang, Min Zheng, Baogui Gao, Junxiong You, Xuecong Lin, Yanyu Hao, Zhimin Chen, Ziqi Wu, Liaoming Gao, Jiayu Tang, Zhen Yuan, Xuegang Sun, Linlin Jing, Ge Wen
INTRODUCTION: Major depressive disorder (MDD) affects about 17% population in the world. Although abnormal energy metabolism plays an important role in the pathophysiology of MDD, however, how deficiency of adenosine triphosphate (ATP) products affects emotional circuit and what regulates ATP synthesis are still need to be elaborated. AIMS: Our study aimed to investigate how deficiency of PGAM5-mediated depressive behavior. RESULTS: We firstly discovered that PGAM5 knockout (PGAM5-/- ) mice generated depressive-like behaviors...
August 25, 2023: CNS Neuroscience & Therapeutics
https://read.qxmd.com/read/37603735/intersectin-deficiency-impairs-cortico-striatal-neurotransmission-and-causes-obsessive-compulsive-behaviors-in-mice
#22
JOURNAL ARTICLE
Dennis Vollweiter, Jasmeet Kaur Shergill, Alexandra Hilse, Gaga Kochlamazashvili, Stefan Paul Koch, Susanne Mueller, Philipp Boehm-Sturm, Volker Haucke, Tanja Maritzen
The generation of appropriate behavioral responses involves dedicated neuronal circuits. The cortico-striatal-thalamo-cortical loop is especially important for the expression of motor routines and habits. Defects in this circuitry are closely linked to obsessive stereotypic behaviors, hallmarks of neuropsychiatric diseases including autism spectrum disorders (ASDs) and obsessive-compulsive disorders (OCDs). However, our knowledge of the essential synaptic machinery required to maintain balanced neurotransmission and plasticity within the cortico-striatal circuitry remains fragmentary...
August 29, 2023: Proceedings of the National Academy of Sciences of the United States of America
https://read.qxmd.com/read/37528492/calcineurin-inhibition-protects-against-dopamine-toxicity-and-attenuates-behavioral-decline-in-a-parkinson-s-disease-model
#23
JOURNAL ARTICLE
Rupsha Mondal, Chayan Banerjee, Sumangal Nandy, Moumita Roy, Joy Chakraborty
BACKGROUND: Parkinson's disease (PD), a highly prevalent neuro-motor disorder is caused due to progressive loss of dopaminergic (DAergic) neurons at substantia nigra region of brain. This leads to depleted dopamine (DA) content at striatum, thus affecting the fine tuning of basal ganglia. In patients, this imbalance is manifested by akinesia, catalepsy and tremor. PD associated behavioral dysfunctions are frequently mitigated by l-DOPA (LD) therapy, a precursor for DA synthesis. Due to progressive neurodegeneration, LD eventually loses applicability in PD...
August 1, 2023: Cell & Bioscience
https://read.qxmd.com/read/37527694/recovery-of-motor-function-is-associated-with-rescue-of-glutamate-biomarkers-in-the-striatum-and-motor-cortex-following-treatment-with-mucuna-pruriens-in-a-murine-model-of-parkinsons-disease
#24
JOURNAL ARTICLE
Tanya Denne, Lila C Winfrey, Cindy Moore, Chase Whitner, Theresa D'Silva, Amala Soumyanath, Lynne Shinto, Amie Hiller, Charles K Meshul
There is growing interest in the use of natural products for the treatment of Parkinson's disease (PD). Mucuna pruriens has been used in the treatment of humans with PD. The goal of this study was to determine if daily oral treatment with an extract of Mucuna pruriens, starting after the MPTP-induced loss of nigrostriatal dopamine in male mice, would result in recovery/restoration of motor function, tyrosine hydroxylase (TH) protein expression in the nigrostriatal pathway, or glutamate biomarkers in both the striatum and motor cortex...
September 2023: Molecular and Cellular Neurosciences
https://read.qxmd.com/read/37464153/significant-functional-differences-between-dopamine-d-4-receptor-polymorphic-variants-upon-heteromerization-with-%C3%AE-1a-adrenoreceptors
#25
JOURNAL ARTICLE
Patricia Homar-Ruano, Ning-Sheng Cai, Verònica Casadó-Anguera, Vicent Casadó, Sergi Ferré, Estefanía Moreno, Enric I Canela
The functional role of the dopamine D4 receptor (D4 R) and its main polymorphic variants has become more evident with the demonstration of heteromers of D4 R that control the function of frontal cortico-striatal neurons. Those include heteromers with the α2A adrenoceptor (α2A R) and with the D2 R, localized in their cortical somato-dendritic region and striatal nerve terminals, respectively. By using biophysical and cell-signaling methods and heteromer-disrupting peptides in mammalian transfected cells and rat brain slice preparations, here we provide evidence for a new functionally relevant D4 R heteromer, the α1A R-D4 R heteromer, which is also preferentially localized in cortico-striatal glutamatergic terminals...
July 18, 2023: Molecular Neurobiology
https://read.qxmd.com/read/37253589/differential-development-of-dendritic-spines-in-striatal-projection-neurons-of-direct-and-indirect-pathways-in-the-caudoputamen-and-nucleus-accumbens
#26
JOURNAL ARTICLE
Hsiao-Ying Kuo, Ya-Hui Yang, Shih-Yun Chen, Tzu-Hsin Kuo, Wan-Ting Lin, Fu-Chin Liu
Synaptic modification in postnatal development is essential for the maturation of neural networks. Developmental maturation of excitatory synapses occurs at the loci of dendritic spines that are dynamically regulated by growth and pruning. Striatal spiny projection neurons (SPNs) receive excitatory input from the cerebral cortex and thalamus. SPNs of the striatonigral direct pathway (dSPNs) and SPNs of the striatopallidal indirect pathway (iSPNs) have different developmental roots and functions. The spatial and temporal dynamics of dendritic spine maturation of these two types of SPNs remain elusive...
May 30, 2023: ENeuro
https://read.qxmd.com/read/37236391/plasticity-of-cortico-striatal-neurons-of-the-caudal-anterior-cingulate-cortex-during-experimental-neuropathic-pain
#27
JOURNAL ARTICLE
María Jesús Trujillo, Constanza Ilarraz, Fernando Kasanetz
Maladaptive neuronal plasticity is a main mechanism for the development and maintenance of pathological pain. Affective, motivational and cognitive deficits that are comorbid with pain involve cellular and synaptic modifications in the anterior cingulate cortex (ACC), a major brain mediator of pain perception. Here we use a model of neuropathic pain (NP) in male mice and ex-vivo electrophysiology to investigate whether layer 5 caudal ACC (cACC) neurons projecting to the dorsomedial striatum (DMS), a critical region for motivational regulation of behavior, are involved in aberrant neuronal plasticity...
May 24, 2023: Neuroscience
https://read.qxmd.com/read/37169859/arg1-expressing-microglia-show-a-distinct-molecular-signature-and-modulate-postnatal-development-and-function-of-the-mouse-brain
#28
JOURNAL ARTICLE
Vassilis Stratoulias, Rocío Ruiz, Shigeaki Kanatani, Ahmed M Osman, Lily Keane, Jose A Armengol, Antonio Rodríguez-Moreno, Adriana-Natalia Murgoci, Irene García-Domínguez, Isabel Alonso-Bellido, Fernando González Ibáñez, Katherine Picard, Guillermo Vázquez-Cabrera, Mercedes Posada-Pérez, Nathalie Vernoux, Dario Tejera, Kathleen Grabert, Mathilde Cheray, Patricia González-Rodríguez, Eva M Pérez-Villegas, Irene Martínez-Gallego, Alejandro Lastra-Romero, David Brodin, Javier Avila-Cariño, Yang Cao, Mikko Airavaara, Per Uhlén, Michael T Heneka, Marie-Ève Tremblay, Klas Blomgren, Jose L Venero, Bertrand Joseph
Molecular diversity of microglia, the resident immune cells in the CNS, is reported. Whether microglial subsets characterized by the expression of specific proteins constitute subtypes with distinct functions has not been fully elucidated. Here we describe a microglial subtype expressing the enzyme arginase-1 (ARG1; that is, ARG1+ microglia) that is found predominantly in the basal forebrain and ventral striatum during early postnatal mouse development. ARG1+ microglia are enriched in phagocytic inclusions and exhibit a distinct molecular signature, including upregulation of genes such as Apoe, Clec7a, Igf1, Lgals3 and Mgl2, compared to ARG1- microglia...
June 2023: Nature Neuroscience
https://read.qxmd.com/read/37137515/speech-and-language-linked-foxp2-mutation-targets-protein-motors-in-striatal-neurons
#29
JOURNAL ARTICLE
Hsiao-Ying Kuo, Shih-Yun Chen, Rui-Chi Huang, Hiroshi Takahashi, Yen-Hui Lee, Hao-Yu Pang, Cheng-Hsi Wu, Ann M Graybiel, Fu-Chin Liu
Human speech and language are among the most complex motor and cognitive abilities. The discovery of a mutation in the transcription factor FOXP2 in KE family members with speech disturbances has been a landmark example of the genetic control of vocal communication in humans. Cellular mechanisms underlying this control have remained unclear. By leveraging FOXP2 mutation/deletion mouse models, we found that the KE family FOXP2R553H mutation directly disables intracellular dynein-dynactin 'protein motors' in the striatum by induction of a disruptive high level of dynactin1 that impairs TrkB endosome trafficking, microtubule dynamics, dendritic outgrowth and electrophysiological activity in striatal neurons alongside vocalization deficits...
May 4, 2023: Brain
https://read.qxmd.com/read/37091877/early-life-adversity-impaired-dorsal-striatal-synaptic-transmission-and-behavioral-adaptability-to-appropriate-action-selection-in-a-sex-dependent-manner
#30
JOURNAL ARTICLE
Gregory de Carvalho, Sheraz Khoja, Mulatwa T Haile, Lulu Y Chen
Early life adversity (ELA) is a major health burden in the United States, with 62% of adults reporting at least one adverse childhood experience. These experiences during critical stages of brain development can perturb the development of neural circuits that mediate sensory cue processing and behavioral regulation. Recent studies have reported that ELA impaired the maturation of dendritic spines on neurons in the dorsolateral striatum (DLS) but not in the dorsomedial striatum (DMS). The DMS and DLS are part of two distinct corticostriatal circuits that have been extensively implicated in behavioral flexibility by regulating and integrating action selection with the reward value of those actions...
2023: Frontiers in Synaptic Neuroscience
https://read.qxmd.com/read/37086722/compartment-specific-dendritic-information-processing-in-striatal-cholinergic-interneurons-is-reconfigured-by-peptide-neuromodulation
#31
JOURNAL ARTICLE
Stephen R Williams, Xiangyu Zhou, Lee Norman Fletcher
Cholinergic interneurons are central hubs of the striatal neuronal network, controlling information processing in a behavioral-state-dependent manner. It remains unknown, however, how such state transitions influence the integrative properties of these neurons. To address this, we made simultaneous somato-dendritic recordings from identified rodent cholinergic interneurons, revealing that action potentials are initiated at dendritic sites because of a dendritic axonal origin. Functionally, this anatomical arrangement ensured that the action potential initiation threshold was lowest at axon-bearing dendritic sites, a privilege efficacy powerfully accentuated at the hyperpolarized membrane potentials achieved in cholinergic interneurons following salient behavioral stimuli...
June 21, 2023: Neuron
https://read.qxmd.com/read/37061023/altered-amantadine-effects-after-repetitive-treatment-for-l-dopa-induced-involuntary-movements-in-a-rat-model-of-parkinson-s-disease
#32
JOURNAL ARTICLE
Yoshiki Murakami, Haruo Nishijima, Takashi Nakamura, Tomonori Furukawa, Iku Kinoshita, Tomoya Kon, Chieko Suzuki, Masahiko Tomiyama
BACKGROUND: l-3,4-dihydroxyphenylalanine (l-dopa) is the most effective drug for Parkinson's disease (PD); however, most PD patients develop motor fluctuations including wearing-off and l-dopa-induced dyskinesia (LID). Amantadine is beneficial for improving the motor symptoms, reducing "off" time, and ameliorating LID, although its long-term efficacy remains unknown. OBJECTIVES: To investigate the effects of amantadine on PD and LID using a rat model with repetitive drug treatment...
May 29, 2023: Neuroscience Letters
https://read.qxmd.com/read/37009450/detrimental-effects-of-soluble-%C3%AE-synuclein-oligomers-at-excitatory-glutamatergic-synapses
#33
JOURNAL ARTICLE
Elena Ferrari, Michela Salvadè, Elisa Zianni, Marta Brumana, Monica DiLuca, Fabrizio Gardoni
INTRODUCTION: Oligomeric and fibrillar species of the synaptic protein α-synuclein are established key players in the pathophysiology of Parkinson's disease and other synucleinopathies. Increasing evidence in the literature points to prefibrillar oligomers as the main cytotoxic species driving dysfunction in diverse neurotransmitter systems even at early disease stages. Of note, soluble oligomers have recently been shown to alter synaptic plasticity mechanisms at the glutamatergic cortico-striatal synapse...
2023: Frontiers in Aging Neuroscience
https://read.qxmd.com/read/37001611/dopamine-independent-development-and-maintenance-of-mouse-striatal-medium-spiny-neuron-dendritic-spines
#34
JOURNAL ARTICLE
Manli Zhong, Yuhan Wang, Geng Lin, Francesca-Fang Liao, Fu-Ming Zhou
Striatal medium spiny neurons (MSNs) and striatal dopamine (DA) innervation are profoundly important for brain function such as motor control and cognition. A widely accepted theory posits that striatal DA loss causes (or leads to) MSN dendritic atrophy. However, examination of the literature indicates that the data from Parkinson's disease (PD) patients and animal PD models were contradictory among studies and hard to interpret. Here we have re-examined the potential effects of DA activity on MSN morphology or lack thereof...
March 29, 2023: Neurobiology of Disease
https://read.qxmd.com/read/36996810/altered-striatal-actin-dynamics-drives-behavioral-inflexibility-in-a-mouse-model-of-fragile-x-syndrome
#35
JOURNAL ARTICLE
Valentina Mercaldo, Barbora Vidimova, Denise Gastaldo, Esperanza Fernández, Adrian C Lo, Giulia Cencelli, Giorgia Pedini, Silvia De Rubeis, Francesco Longo, Eric Klann, August B Smit, Seth G N Grant, Tilmann Achsel, Claudia Bagni
The proteome of glutamatergic synapses is diverse across the mammalian brain and involved in neurodevelopmental disorders (NDDs). Among those is fragile X syndrome (FXS), an NDD caused by the absence of the functional RNA-binding protein FMRP. Here, we demonstrate how the brain region-specific composition of postsynaptic density (PSD) contributes to FXS. In the striatum, the FXS mouse model shows an altered association of the PSD with the actin cytoskeleton, reflecting immature dendritic spine morphology and reduced synaptic actin dynamics...
June 7, 2023: Neuron
https://read.qxmd.com/read/36968092/synaptic-scaling-of-corticostriatal-circuits-underlies-hyperactivity-in-gaba-transporter-1-deficient-mice
#36
JOURNAL ARTICLE
Yan-Jiao Wu, Xin Yi, Xue Gu, Qi Wang, Qin Jiang, Ying Li, Michael X Zhu, Jianqing Ding, Wei-Guang Li, Tian-Le Xu
Homeostatic synaptic scaling entails adjustment of synaptic strength on a cell to prolonged changes of neuronal activity, which is postulated to participate in neuropsychiatric disorders in vivo . Here, we find that sustained elevation in ambient GABA levels, by either genetic deletion or pharmacological blockade of GABA transporter-1 (GAT1), leads to synaptic scaling up of corticostriatal pathways, which underlies locomotor hyperactivity. Meanwhile, medium spiny neurons of the dorsal striatum exhibit an aberrant increase in excitatory synaptic transmission and corresponding structural changes in dendritic spines...
April 21, 2023: IScience
https://read.qxmd.com/read/36958627/proteomic-analysis-of-huntington-s-disease-medium-spiny-neurons-identifies-alterations-in-lipid-droplets
#37
JOURNAL ARTICLE
Kizito-Tshitoko Tshilenge, Carlos Galicia Aguirre, Joanna Bons, Akos A Gerencser, Nathan Basisty, Sicheng Song, Jacob Rose, Alejandro Lopez-Ramirez, Swati Naphade, Ashley Loureiro, Elena Battistoni, Mateus Milani, Cameron Wehrfritz, Anja Holtz, Claudio Hetz, Sean D Mooney, Birgit Schilling, Lisa M Ellerby
Huntington's disease (HD) is a neurodegenerative disease caused by a CAG repeat expansion in the Huntingtin (HTT) gene. The resulting polyglutamine (polyQ) tract alters the function of the HTT protein. Although HTT is expressed in different tissues, the medium spiny projection neurons (MSNs) in the striatum are particularly vulnerable in HD. Thus, we sought to define the proteome of human HD patient-derived MSNs. We differentiated HD72 induced pluripotent stem cells and isogenic controls into MSNs and carried out quantitative proteomic analysis...
March 21, 2023: Molecular & Cellular Proteomics: MCP
https://read.qxmd.com/read/36863527/peripheral-nerve-injury-elicits-microstructural-and-neurochemical-changes-in-the-striatum-and-substantia-nigra-of-a-dyt-tor1a-mouse-model-with-dystonia-like-movements
#38
JOURNAL ARTICLE
Lisa Rauschenberger, Esther-Marie Krenig, Alea Stengl, Susanne Knorr, Tristan H Harder, Felix Steeg, Maximilian U Friedrich, Kathrin Grundmann-Hauser, Jens Volkmann, Chi Wang Ip
The relationship between genotype and phenotype in DYT-TOR1A dystonia as well as the associated motor circuit alterations are still insufficiently understood. DYT-TOR1A dystonia has a remarkably reduced penetrance of 20-30%, which has led to the second-hit hypothesis emphasizing an important role of extragenetic factors in the symptomatogenesis of TOR1A mutation carriers. To analyze whether recovery from a peripheral nerve injury can trigger a dystonic phenotype in asymptomatic hΔGAG3 mice, which overexpress human mutated TorsinA, a sciatic nerve crush was applied...
February 28, 2023: Neurobiology of Disease
https://read.qxmd.com/read/36640913/domain-and-cell-type-specific-immunolocalisation-of-voltage-gated-potassium-channels-in-the-mouse-striatum
#39
JOURNAL ARTICLE
Babajide Otuyemi, Torquil Jackson, Ruolin Ma, Ana Rita Monteiro, Mohsen Seifi, Jerome D Swinny
Diverse classes of voltage-gated potassium channels (Kv) are integral to the variety of electrical activity patterns that distinguish different classes of neurons in the brain. A feature of their heterogenous expression patterns is the highly precise manner in which specific cell types target their location within functionally specialised sub-cellular domains. Although Kv expression profiles in cortical brain regions are widely reported, their immunolocalisation in sub-cortical areas such as the striatum, and in associated diseases such as Parkinson's disease (PD), remain less well described...
January 11, 2023: Journal of Chemical Neuroanatomy
https://read.qxmd.com/read/36638871/exposure-to-enriched-environment-ameliorated-chronic-unpredictable-mild-stress-induced-depression-like-symptoms-in-rats-via-regulating-the-mir-92a-3p-kruppel-like-factor-2-klf2-pathway
#40
JOURNAL ARTICLE
Xiao Ji, Zhenwu Zhao
BACKGROUND: Silencing of miR-92a-3p may be beneficial in relieving depression of chronically stressed rats. The level of kruppel-like factor 2 (KLF2) was increased in the striatum of depressed rats after ketamine treatment. Enriched environment (EE) ameliorated depression-like behaviors in rats. However, the specific mechanism of EE treatment on depression induced by chronic unpredictable mild stress (CUMS) remains unclear. METHODS: After CUMS-induced male Sprague Dawley rats were treated under EE or/and Adeno-Associated Virus (AAV)-miR-92a-3p, depression-like behaviors, cognitive ability, dendritic spine density, as well as levels of miR-92a-3p and KLF2 were detected by the behavioral tests, morris water maze test, Golgi staining, and quantitative real-time polymerase chain reaction (qRT-PCR) as needed...
January 10, 2023: Brain Research Bulletin
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