Advances in neurobiology最新文献

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Neuroprotective and Neurotrophic Effects of Astaxanthin on the Brain. 虾青素对大脑的神经保护和神经营养作用。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-981-95-0066-6_17
Jang Soo Yook, Hideaki Soya
{"title":"Neuroprotective and Neurotrophic Effects of Astaxanthin on the Brain.","authors":"Jang Soo Yook, Hideaki Soya","doi":"10.1007/978-981-95-0066-6_17","DOIUrl":"10.1007/978-981-95-0066-6_17","url":null,"abstract":"<p><p>Oxidative stress in the brain is associated with the development and progression of neurological disorders, posing antioxidant nutrients as an effective strategy for protecting neuronal cells and potentially slowing cognitive decline. Bioactive compounds from natural sources with antioxidant effects promote brain health. Among various natural compounds, astaxanthin (ASX), a potent red-pigment carotenoid found in various microorganisms and marine animals, is well recognized for its potential health benefits. In this review, we highlight the promising neuroprotective effects of ASX through cellular experiments and animal models. This review can provide novel insights on the therapeutic potential of ASX through its antioxidant, anti-inflammatory, and anti-apoptotic effects against neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. In addition to demonstrating the neurotrophic effects of ASX on structural and functional changes in hippocampal neuronal plasticity, this review also discusses its synergistic potential with other interventions, such as exercise.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"44 ","pages":"317-334"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145147519","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unlocking the Potential of High-Quality Dopamine Transporter Pharmacological Data: Advancing Robust Machine Learning-Based QSAR Modeling. 解锁高质量多巴胺转运体药理学数据的潜力:推进基于机器学习的强大QSAR建模。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-96364-3_3
Kuo Hao Lee, Sung Joon Won, Precious Oyinloye, Lei Shi
{"title":"Unlocking the Potential of High-Quality Dopamine Transporter Pharmacological Data: Advancing Robust Machine Learning-Based QSAR Modeling.","authors":"Kuo Hao Lee, Sung Joon Won, Precious Oyinloye, Lei Shi","doi":"10.1007/978-3-031-96364-3_3","DOIUrl":"10.1007/978-3-031-96364-3_3","url":null,"abstract":"<p><p>The dopamine transporter (DAT) plays a critical role in the central nervous system and has been implicated in numerous psychiatric disorders. The ligand-based approaches are instrumental to decipher the structure-activity relationship (SAR) of DAT ligands, especially the quantitative SAR (QSAR) modeling. By gathering and analyzing data from literature and databases, we systematically assemble a diverse range of ligands binding to DAT, aiming to discern the general features of DAT ligands and uncover the chemical space for potential novel DAT ligand scaffolds. The aggregation of DAT pharmacological activity data, particularly from databases like ChEMBL, provides a foundation for constructing robust QSAR models. The compilation and meticulous filtering of these data, establishing high-quality training data sets with specific divisions of pharmacological assays and data types, along with the application of QSAR modeling, prove to be a promising strategy for navigating the pertinent chemical space. Through a systematic comparison of DAT QSAR models using training data sets from various ChEMBL releases, we underscore the positive impact of enhanced data set quality and increased data set size on the predictive power of DAT QSAR models.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"46 ","pages":"63-94"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145231335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of Oligodendroglia and Myelin. 少突胶质细胞和髓磷脂的发育。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-87919-7_3
Hao Huang, Xiaofeng Xu, Mengsheng Qiu
{"title":"Development of Oligodendroglia and Myelin.","authors":"Hao Huang, Xiaofeng Xu, Mengsheng Qiu","doi":"10.1007/978-3-031-87919-7_3","DOIUrl":"https://doi.org/10.1007/978-3-031-87919-7_3","url":null,"abstract":"<p><p>Myelin sheaths formed by oligodendrocytes (OLs) wrap around neuronal axons and allow for saltatory conduction of nerve impulses, significantly increasing the speed of electrical signal transmission. The development of oligodendrocyte lineage consists of several coordinated steps. Briefly, oligodendrocyte precursor cells (OPCs) are first generated from neural precursor cells of certain neuroepithelial regions, and then they proliferate and migrate to other regions of the central nervous system (CNS), where they differentiate into oligodendrocytes and form myelin sheaths around the axons of neurons. These developmental processes are tightly and precisely regulated during animal development by a cohort of intracellular molecular and extracellular signals.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"43 ","pages":"61-79"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144273872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oligodendroglia in Neuromyelitis Optica Spectrum Disorder. 神经脊髓炎中的少突胶质细胞。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-87919-7_16
Ai Guo, Yuzhen Wei, Alexei Verkhratsky, Fu-Dong Shi
{"title":"Oligodendroglia in Neuromyelitis Optica Spectrum Disorder.","authors":"Ai Guo, Yuzhen Wei, Alexei Verkhratsky, Fu-Dong Shi","doi":"10.1007/978-3-031-87919-7_16","DOIUrl":"https://doi.org/10.1007/978-3-031-87919-7_16","url":null,"abstract":"<p><p>Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease of the central nervous system, in which aquaporin-4 immunoglobulin G (AQP4-IgG) targets the water channel aquaporin-4 (AQP4) localized at astrocytic endfeet, thus triggering inflammatory lesions and tissue damage. The pathological characteristics of NMOSD are early loss of oligodendrocytes, extensive demyelination, and axonal injury. The pathogenesis of oligodendrocyte damage in NMOSD includes complement-dependent bystander effect, antibody-dependent cell-mediated cytotoxicity bystander effect, glutamate toxicity, connexin dysregulation, and blood-brain barrier disruption. Remyelination levels in acute NMOSD lesions are low.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"43 ","pages":"457-472"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144273962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oligodendroglia and Myelin: Supporting the Connectome. 少突胶质细胞和髓磷脂:支持连接组。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-87919-7_1
Jianqin Niu, Alexei Verkhratsky, Arthur Butt, Chenju Yi
{"title":"Oligodendroglia and Myelin: Supporting the Connectome.","authors":"Jianqin Niu, Alexei Verkhratsky, Arthur Butt, Chenju Yi","doi":"10.1007/978-3-031-87919-7_1","DOIUrl":"https://doi.org/10.1007/978-3-031-87919-7_1","url":null,"abstract":"<p><p>Oligodendroglia are the only cell lineage of the central nervous system (CNS) responsible for producing myelin. They originate from precursor cells known as oligodendrocyte precursor cells (OPCs), which are born around the ventricular zones of the brain and spinal cord and migrate throughout the developing CNS, and many of them ultimately differentiate into mature myelinating oligodendrocytes. Recent research has shown that OPCs and oligodendrocytes possess distinct characteristics when compared either to other types of glial cells in the CNS or to each other. Under different physiological and pathophysiological conditions, the processes of development or regeneration, the features, and, in some cases, even the functions of oligodendroglia can be modified. These changes can contribute to disease progression and affect the functional status of the nervous system. For instance, experience-dependent \"adaptive\" myelination plays a crucial role in the plasticity of neuronal circuits and influences learning processes; additionally, the non-myelinating functions of oligodendroglia expand their pathological potential, allowing them to regulate neuronal development and activity, angiogenesis, astrocyte maturation, and neuroinflammation. This chapter serves as a comprehensive introduction to oligodendroglia by presenting evidence from fundamental studies and fresh insights into their development, physiological and pathophysiological attributes, as well as the newly discovered non-myelinating functions.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"43 ","pages":"1-37"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144273960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Effects of Exercise on Hippocampus-Based Cognitive Dysfunction in Type 2 Diabetes Mellitus: A Possible Involvement of Hippocampal Monocarboxylate Transporter 2. 运动对2型糖尿病海马认知功能障碍的影响:海马单羧酸转运蛋白2的可能参与
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-981-95-0066-6_15
Takeru Shima, Hideaki Soya
{"title":"The Effects of Exercise on Hippocampus-Based Cognitive Dysfunction in Type 2 Diabetes Mellitus: A Possible Involvement of Hippocampal Monocarboxylate Transporter 2.","authors":"Takeru Shima, Hideaki Soya","doi":"10.1007/978-981-95-0066-6_15","DOIUrl":"10.1007/978-981-95-0066-6_15","url":null,"abstract":"<p><p>Cognitive dysfunction in type 2 diabetes mellitus (T2DM) poses a significant peril not only to compromised human well-being but also to the onset of dementia, Alzheimer's disease, and depression. Given the present research findings utilizing animal models, various potential biochemical mechanisms have been reported for hippocampus-based cognitive dysfunction in T2DM. This chapter focuses on the relationship between cognitive dysfunction in T2DM and dysregulation of the hippocampal astrocyte-neuron lactate shuttle, with specific emphasis on monocarboxylate transporter 2 (MCT2). Furthermore, it provides a summary of the evidence suggesting the potentiality of exercise as a viable therapeutic intervention, encompassing not solely glycemic control but also the amelioration of cognitive dysfunction in T2DM.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"44 ","pages":"281-296"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145147499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dopamine-Glutamate and Dopamine-GABA Co-release. 多巴胺-谷氨酸和多巴胺- gaba共释放。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-96364-3_8
Annalisa Scimemi
{"title":"Dopamine-Glutamate and Dopamine-GABA Co-release.","authors":"Annalisa Scimemi","doi":"10.1007/978-3-031-96364-3_8","DOIUrl":"10.1007/978-3-031-96364-3_8","url":null,"abstract":"<p><p>Some neuronal populations in the brain have the ability to release multiple neurotransmitters, which may be packaged in the same vesicle, or released by distinct subsets of vesicles. Here, we review current knowledge on the molecular mechanisms by which multiple neurotransmitters can be stored in the same cell and the functional implications that this has for information processing throughout the brain and the control of movement execution by basal ganglia and cortical motor circuits.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"46 ","pages":"197-214"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145231193","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Causal Mechanisms of Monoamine Transporter Phosphorylation. 单胺转运蛋白磷酸化的致病机制。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-96364-3_5
Sammanda Ramamoorthy, Durairaj Ragu Varman, Lankupalle D Jayanthi
{"title":"Causal Mechanisms of Monoamine Transporter Phosphorylation.","authors":"Sammanda Ramamoorthy, Durairaj Ragu Varman, Lankupalle D Jayanthi","doi":"10.1007/978-3-031-96364-3_5","DOIUrl":"10.1007/978-3-031-96364-3_5","url":null,"abstract":"<p><p>Monoamine transporters are essential proteins located at presynaptic terminals that play a crucial role in regulating neurotransmission of serotonin, dopamine, and norepinephrine by rapid reuptake of released amines from the synapse. Clinically used antidepressants and widely abused psychostimulants exhibit a high affinity for amine transporters. Function and expression of biogenic amine transporter are altered in subjects suffering from psychiatric diseases such as depression and in psychostimulant use disorder. Therefore, proper functional regulation of monoamine transporters is critical in maintaining normal amine homeostasis. Monoamine transporters possess several potential phosphorylation sites/motifs and exist in a phosphorylated state. Various cellular protein kinases and phosphatases are known to regulate the phosphorylation dynamics of amine transporters, which in turn influences subcellular expression and trafficking, microdomain-specific protein-protein interactions, transporter protein degradation, and overall transport capacity. Dysfunctional amine transporter function, phosphorylation, and association with interacting proteins are evident in neuropsychiatric disease states, including psychostimulant use disorder. However, the neurobiological consequences of in vivo amine transporter phosphorylation and its regulation remain unclear. Recent studies utilizing intact animal models are beginning to connect these molecular mechanisms with observed animal behaviors. This review summarizes current knowledge on the causal role of amine transporter phosphorylation in regulating amine transport and its relevance to animal behavior. Further understanding of phosphorylation-dependent molecular mechanisms governing amine transporter regulation potentially identifies regulatory motif(s) as potential therapeutic targets for treating neuropsychiatric disorders.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"46 ","pages":"121-142"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13247851/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145231124","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Monoamine Transporters in Drugs of Abuse: Insights from Fast Scan Cyclic Voltammetry. 滥用药物中的单胺转运体:快速扫描循环伏安法的见解。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-3-031-96364-3_7
Shanna B Samels, Pelin Yuksel, Rodrigo A España
{"title":"Monoamine Transporters in Drugs of Abuse: Insights from Fast Scan Cyclic Voltammetry.","authors":"Shanna B Samels, Pelin Yuksel, Rodrigo A España","doi":"10.1007/978-3-031-96364-3_7","DOIUrl":"10.1007/978-3-031-96364-3_7","url":null,"abstract":"<p><p>Monoamine transmission is critical for regulating numerous physiological processes, including stress, learning, motor activity, and reward. Over the past few decades, the adoption of fast scan cyclic voltammetry has unveiled an intricate interplay between monoamine release and uptake dynamics, particularly concerning monoamine transporter involvement in reward and reinforcement processes for drugs of abuse. This review discusses how fast scan cyclic voltammetry has revolutionized our understanding of the processes that govern monoamine release and uptake, emphasizing the heterogeneity in transporter function across terminal regions, the influence of autoreceptors on monoamine transmission, and the complex interactions between drugs of abuse and monoamine transporters. While much of the review focuses on what is known about dopamine transporters-due to the wealth of evidence on dopamine transmission-we also emphasize significant gaps in knowledge regarding the serotonin and norepinephrine transporters. Finally, we highlight remaining questions about the dynamic nature of monoaminergic transporter efficiency and suggest new areas of investigation to gain a more comprehensive understanding of the biochemical mechanisms through which monoamine transporters regulate behavior.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"46 ","pages":"163-196"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145231298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Dual Role of Lactate in the Exercising Brain: Fueling Energy and Signaling Fatigue. 乳酸在运动大脑中的双重作用:补充能量和发出疲劳信号。
Advances in neurobiology Pub Date : 2025-01-01 DOI: 10.1007/978-981-95-0066-6_11
Takashi Matsui, Hideaki Soya
{"title":"The Dual Role of Lactate in the Exercising Brain: Fueling Energy and Signaling Fatigue.","authors":"Takashi Matsui, Hideaki Soya","doi":"10.1007/978-981-95-0066-6_11","DOIUrl":"10.1007/978-981-95-0066-6_11","url":null,"abstract":"<p><p>Historically regarded as a \"fatigue substance\" that impedes muscle contraction, lactate has undergone a paradigm shift in its scientific perception. Currently, it is acknowledged as an indispensable substrate for aerobic ATP synthesis, functioning as a pivotal intermediate in the glycolysis pathway. Within the brain context, lactate derived from glycogen in astrocytes is instrumental in augmenting exercise endurance and enhancing memory formation via the astrocyte-neuron lactate shuttle. This glia-neuron interaction mechanism underscores the expansive influence of lactate beyond mere muscular physiology. Contemporary investigations have pivoted toward elucidating a novel hypothesis: the role of lactate as a ligand for the G protein-coupled receptor (GPR) 81, posited to orchestrate a \"fatigue signal\" amid exercise capabilities. This hypothesized function in neural inhibition underscores the comprehensive impact of lactate on physiological responses to prolonged exercise. This evolving perspective of lactate not only accentuates its central role in metabolic processes but also paves the way for advanced exploration into the whole-body's sophisticated mechanisms for managing and adapting to physical exhaustion and central fatigue.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"44 ","pages":"207-216"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145147435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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