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Brain-Derived Neurotrophic Factor in Neuronal Survival and Behavior-Related Plasticity

机译:神经元生存和行为相关可塑性脑源性神经营养因子

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Neurotrophins are critical to the development and maintenance of the mammalian central nervous system. Among them is brainderived neurotrophic factor (BDNF), whose synthesis and release is targeted by activation of glutamate receptors. Perturbation of this process probably underlies neurodegenerative and psychiatric disorders. A naturally occurring variation in humans, in the form of a common singlenucleotide polymorphism in the pro region of the polypeptide at codon 66 (Va166u Met), affects processing of the pro-BDNF polypeptide and its activation-dependent release. This variant is associated with differences in the volume of the hippocampal formation and with anxiety and depression-related phenotypes. Convergent findings supporting a role for BDNF in alterations to hippocampal structure and behavior are found in a "humanized" BDNF trausgenic mouse. Also, recent human genetic studies have supported a role of BDNF signaling in addictive behaviors by allele-, genotype-, and haplotype-based association of the TrkB gene, which encodes the cognate receptor for BDNF, with alcohol dependence. A better understanding of the influence of BDNF-mediated pathways in cell survival and plasticity will aid in developing new approaches to restoring normal function in disease states.
机译:神经营养素对哺乳动物中枢神经系统的开发和维持至关重要。其中是脑的神经营养因子(BDNF),其合成和释放是通过谷氨酸受体的活化来靶向。这种过程的扰动可能是神经退行性和精神病疾病的基础。人类的天然存在于多肽的常见单核苷酸多态性的形式,在密码子66(Va166U MET)的Pro区域中的常见单核苷酸多态性的形式影响Pro-BDNF多肽的处理及其活化依赖性释放。该变体与海马形成的体积和焦虑和抑郁相关表型相关的差异有关。在“人源化”BDNF Trausgenic小鼠中发现支持对海马结构和行为改变的BDNF作用的收敛调查结果。此外,最近的人类遗传学研究支持BDNF信号传导通过等位基因,基因型和单倍型的基因组合的成瘾性行为中的作用,其编码BDNF的同源受体,具有醇依赖性。更好地了解BDNF介导的途径在细胞存活和塑性中的影响将有助于开发恢复疾病状态正常功能的新方法。

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