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Illuminating the neuropeptide Y receptor and its ligand pancreatic polypeptide from a structural, functional, and therapeutic perspective.从结构、功能和治疗角度阐明神经肽 Y 受体及其配体胰多肽。
Neuropeptides. 2024 Jun;105:102416. doi: 10.1016/j.npep.2024.102416. Epub 2024 Feb 24.
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Illuminating the Path to Enhanced Bioimaging by Phosphole-based Fluorophores.基于膦烯的荧光团照亮增强生物成像之路。
Chembiochem. 2024 Mar 1;25(5):e202300857. doi: 10.1002/cbic.202300857. Epub 2024 Feb 8.
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Development of Radiopharmaceuticals for NPY Receptor-5 (Y5) Nuclear Imaging in Tumors by Synthesis of Specific Agonists and Investigation of Their Binding Mode.通过合成特异性激动剂并研究其结合模式来开发用于肿瘤中神经肽Y受体-5(Y5)核成像的放射性药物。
Bioconjug Chem. 2023 Nov 15;34(11):2014-2021. doi: 10.1021/acs.bioconjchem.3c00313. Epub 2023 Aug 9.
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Rational design of highly stabilized and selective adrenomedullin analogs.高稳定性和高选择性肾上腺髓质素类似物的合理设计。
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Potential benefits of intranasal neuropeptide Y include sustained extinction of fear memory.鼻内神经肽 Y 的潜在益处包括恐惧记忆的持续消退。
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Air-liquid interface (ALI) impact on different respiratory cell cultures.气液界面(ALI)对不同呼吸道细胞培养的影响。
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10
Intranasal administration of neuropeptide Y significantly antagonized stress-induced colonic dysmotility via central GABA receptors in male rats.鼻腔给予神经肽 Y 通过雄性大鼠中枢 GABA 受体显著拮抗应激诱导的结肠动力障碍。
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调节神经肽Y系统的肽的鼻内应用

Intranasal Application of Peptides Modulating the Neuropeptide Y System.

作者信息

Jülke Eva-Maria, Özbay Benginur, Nowicki Marcin, Els-Heindl Sylvia, Immig Kerstin, Mörl Karin, Bechmann Ingo, Beck-Sickinger Annette G

机构信息

Institute of Biochemistry, Faculty of Life Sciences, Leipzig University, Brüderstr. 34, 04103 Leipzig, Germany.

Institute of Anatomy, Faculty of Medicine, Leipzig University, Liebigstraße 13, 04103 Leipzig, Germany.

出版信息

ACS Pharmacol Transl Sci. 2025 Apr 1;8(4):1168-1181. doi: 10.1021/acsptsci.5c00082. eCollection 2025 Apr 11.

DOI:10.1021/acsptsci.5c00082
PMID:40242586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11997893/
Abstract

The neuropeptide Y multireceptor-multiligand system plays an important role in multiple physiological processes. Targeting the neuropeptide Y (YR) and Y (YR) receptors has gained interest in treating weight and mental disorders. Nose-to-brain delivery is an effective tool to overcome the challenges of peptide delivery to cerebral structures. In this study, fluorescently labeled peptides that selectively activate either YR or YR were studied. The permeability of these compounds was evaluated on Calu-3 cells, a model system of the nasal mucosa. Particular attention was paid to the stability of peptides, and translocation of the intact compounds was demonstrated by combining a permeability assay with a receptor activation assay. Two compounds, selectively targeting either YR or YR, were selected, and their uptake after intranasal application was analyzed . Two different imaging systems were compared: whole slide scanning and confocal microscopy. Both methods allow detecting specific signals from the fluorescently labeled peptides. While whole slide scanning provides a comprehensive anatomical overview, confocal microscopy offers an improved signal-to-noise ratio. Finally, peptide-specific signals were quantified over time, displaying rapid peptide uptake within the first 15 min and sustained signals for up to 24 h. Overall, cell-based and assays were combined to select peptides with high pharmacological potential for nasal applications.

摘要

神经肽Y多受体-多配体系统在多种生理过程中发挥重要作用。靶向神经肽Y(Y1R)和Y5R受体在治疗体重和精神障碍方面引起了人们的兴趣。鼻脑给药是克服肽类药物向脑结构递送挑战的有效工具。在本研究中,对选择性激活Y1R或Y5R的荧光标记肽进行了研究。在鼻黏膜模型系统Calu-3细胞上评估了这些化合物的通透性。特别关注了肽的稳定性,并通过将通透性测定与受体激活测定相结合,证明了完整化合物的转运。选择了两种分别选择性靶向Y1R或Y5R的化合物,并分析了它们经鼻给药后的摄取情况。比较了两种不同的成像系统:全玻片扫描和共聚焦显微镜。两种方法都能检测到荧光标记肽的特异性信号。全玻片扫描提供了全面的解剖学概述,而共聚焦显微镜提供了更高的信噪比。最后,随时间对肽特异性信号进行了定量,显示在最初15分钟内肽快速摄取,并持续信号长达24小时。总体而言,结合基于细胞的测定和其他测定来选择具有高药理学潜力的鼻用肽。