Dipeptidyl peptidase-4 inhibitors enhance memory retention via neuropeptide Y

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Iulia Zoicas , Stephan von Hörsten , Anne-Christine Plank , Johannes Kornhuber
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引用次数: 0

Abstract

We have previously shown that neuropeptide Y (NPY) prolongs the retention of memory in the object discrimination test in mice. In this study, we investigated the potential memory-enhancing effects of dipeptidyl peptidase-4 (DPP4) inhibitors, commonly referred to as gliptins, which are known to prevent the degradation of NPY, thereby increasing its concentration. We show that administration of sitagliptin (50 and 100 mg/kg/day) and linagliptin (5 and 10 mg/kg/day) via the drinking water facilitates the retention of object memory in male CD1 mice, extending memory retention to time points when control mice no longer retain memory. Similar to gliptin-treated mice, male and female homozygous and heterozygous DPP4 deficient mice displayed intact object memory at time points when wild-type littermates showed no memory. Sitagliptin treatment, however, did not facilitate the retention of memory in male and female homozygous NPY deficient mice, indicating that NPY is essential for the memory-enhancing effects of sitagliptin. These results indicate that sitagliptin exerts memory-enhancing effects through an NPY-dependent mechanism and highlight the potential of gliptins as cognitive enhancers in healthy individuals.

Abstract Image

二肽基肽酶-4抑制剂通过神经肽Y增强记忆保留。
我们之前已经在小鼠的物体辨别测试中证明神经肽Y (NPY)延长了记忆的保留。在这项研究中,我们研究了二肽基肽酶-4 (DPP4)抑制剂的潜在记忆增强作用,通常被称为gliptin,已知它可以阻止NPY的降解,从而增加其浓度。我们发现,通过饮用水给药西格列汀(50和100 mg/kg/天)和利格列汀(5和10 mg/kg/天)有助于雄性CD1小鼠对物体记忆的保留,将记忆保留延长到对照组小鼠不再保留记忆的时间点。与gliptin处理的小鼠类似,雄性和雌性纯合子和杂合子DPP4缺陷小鼠在野生型幼崽没有记忆的时间点上表现出完整的物体记忆。然而,西格列汀治疗并不能促进雄性和雌性纯合子NPY缺陷小鼠的记忆保留,这表明NPY对西格列汀的记忆增强作用至关重要。这些结果表明西格列汀通过npy依赖机制发挥记忆增强作用,并强调了西格列汀在健康个体中作为认知增强剂的潜力。
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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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