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甘丙肽与神经肽Y的相互作用增强大鼠海马颗粒前体细胞的增殖及神经保护因子的表达,从而增强空间记忆。

Galanin and Neuropeptide Y Interaction Enhances Proliferation of Granule Precursor Cells and Expression of Neuroprotective Factors in the Rat Hippocampus with Consequent Augmented Spatial Memory.

作者信息

Mirchandani-Duque Marina, Barbancho Miguel A, López-Salas Alexander, Alvarez-Contino Jose Erik, García-Casares Natalia, Fuxe Kjell, Borroto-Escuela Dasiel O, Narváez Manuel

机构信息

Instituto de Investigación Biomédica de Málaga, Facultad de Medicina, Universidad de Málaga, 29071 Malaga, Spain.

Department of Neuroscience, Karolinska Institute, 17177 Stockholm, Sweden.

出版信息

Biomedicines. 2022 Jun 1;10(6):1297. doi: 10.3390/biomedicines10061297.

Abstract

Dysregulation of hippocampal neurogenesis is linked to several neurodegenereative diseases, where boosting hippocampal neurogenesis in these patients emerges as a potential therapeutic approach. Accumulating evidence for a neuropeptide Y (NPY) and galanin (GAL) interaction was shown in various limbic system regions at molecular-, cellular-, and behavioral-specific levels. The purpose of the current work was to evaluate the role of the NPY and GAL interaction in the neurogenic actions on the dorsal hippocampus. We studied the Y1R agonist and GAL effects on: hippocampal cell proliferation through the proliferating cell nuclear antigen (PCNA), the expression of neuroprotective and anti-apoptotic factors, and the survival of neurons and neurite outgrowth on hippocampal neuronal cells. The functional outcome was evaluated in the object-in-place task. We demonstrated that the Y1R agonist and GAL promote cell proliferation and the induction of neuroprotective factors. These effects were mediated by the interaction of NPYY1 (Y1R) and GAL2 (GALR2) receptors, which mediate the increased survival and neurites' outgrowth observed on neuronal hippocampal cells. These cellular effects are linked to the improved spatial-memory effects after the Y1R agonist and GAL co-injection at 24 h in the object-in-place task. Our results suggest the development of heterobivalent agonist pharmacophores, targeting Y1R-GALR2 heterocomplexes, therefore acting on the neuronal precursor cells of the DG in the dorsal hippocampus for the novel therapy of neurodegenerative cognitive-affecting diseases.

摘要

海马神经发生的失调与多种神经退行性疾病有关,在这些患者中促进海马神经发生成为一种潜在的治疗方法。越来越多的证据表明,神经肽Y(NPY)和甘丙肽(GAL)在分子、细胞和行为特定水平上在边缘系统的各个区域存在相互作用。当前研究的目的是评估NPY和GAL相互作用在背侧海马神经发生作用中的作用。我们研究了Y1R激动剂和GAL对以下方面的影响:通过增殖细胞核抗原(PCNA)检测海马细胞增殖、神经保护和抗凋亡因子的表达,以及海马神经元细胞上神经元的存活和神经突生长。在位置辨别任务中评估功能结果。我们证明Y1R激动剂和GAL促进细胞增殖并诱导神经保护因子。这些作用是由NPYY1(Y1R)和GAL2(GALR2)受体的相互作用介导的,它们介导了在海马神经元细胞上观察到的存活率增加和神经突生长。这些细胞效应与在位置辨别任务中24小时后Y1R激动剂和GAL共同注射后空间记忆效应的改善有关。我们的结果表明,开发针对Y1R-GALR2异源复合物的异二价激动剂药效团,从而作用于背侧海马齿状回的神经元前体细胞,用于治疗影响认知的神经退行性疾病的新疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5657/9219743/5444d751f74d/biomedicines-10-01297-g001.jpg

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