High-fat diet impairs intermediate-term memory by autophagic-lysosomal dysfunction in Drosophila.

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-08-18 eCollection Date: 2025-08-01 DOI:10.1371/journal.pgen.1011818
Tong Yue, Minrui Jiang, Kotomi Onuki, Motoyuki Itoh, Ayako Tonoki
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引用次数: 0

Abstract

High-fat diet (HFD) is considered a risk factor for age-related memory impairments such as Alzheimer's disease. However, how HFD affects memory formation remains unclear. In this study, we established a model of memory defects caused by HFD in Drosophila. Our results revealed that the HFD impaired intermediate-term memory (ITM), but not short-term memory (STM), produced by classical aversive olfactory conditioning, and decreased autophagic activity in the heads of the HFD-fed flies. Transient reduction in autophagic activity also impaired ITM, but not STM. Genetic enhancement of autophagic activity in neurons effectively restored ITM performance in the HFD-fed flies. Mechanistically, HFD impairs lysosomal function by downregulating the expression of lysosome-related genes, leading to impaired fusion of autophagosomes with lysosomes. These findings suggest that HFD impairs ITM by reducing autophagic activity and lysosomal dysfunction in the neurons.

高脂肪饮食通过自噬-溶酶体功能障碍损害果蝇中期记忆。
高脂肪饮食(HFD)被认为是与年龄相关的记忆障碍(如阿尔茨海默病(AD))的危险因素。然而,HFD如何影响记忆形成仍不清楚。在本研究中,我们建立了由HFD引起的果蝇记忆缺陷模型。我们的研究结果表明,HFD损害了由经典厌恶嗅觉条件反射产生的中期记忆(ITM),但没有损害短期记忆(STM),并降低了HFD喂养的果蝇头部的自噬活性。自噬活性的短暂性降低也会损害ITM,但不会损害STM。基因增强神经元的自噬活性可以有效地恢复饲喂hfd的果蝇的ITM表现。从机制上讲,HFD通过下调溶酶体相关基因的表达来损害溶酶体的功能,导致自噬体与溶酶体的融合受损。这些发现表明,HFD通过降低神经元的自噬活性和溶酶体功能障碍来损害ITM。
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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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