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Eur J Nutr. 2016 Mar;55(2):601-610. doi: 10.1007/s00394-015-0880-7. Epub 2015 Mar 24.

引用本文的文献

1
Hypothalamic DNA 5-hydroxymethylation levels are altered by diet-induced weight gain during the development of obesity in a sex-specific manner.饮食诱导的体重增加会以性别特异性的方式改变肥胖发展过程中下丘脑的 DNA 5-羟甲基化水平。
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2
Controlling hypothalamic DNA methylation at the Pomc promoter does not regulate weight gain during the development of obesity.控制肥胖发生过程中 Pomc 启动子的下丘脑 DNA 甲基化不能调节体重增加。
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本文引用的文献

1
Proteomic Analysis Reveals Sex-Specific Protein Degradation Targets in the Amygdala During Fear Memory Formation.蛋白质组学分析揭示恐惧记忆形成过程中杏仁核内的性别特异性蛋白质降解靶点。
Front Mol Neurosci. 2021 Sep 29;14:716284. doi: 10.3389/fnmol.2021.716284. eCollection 2021.
2
Females, but not males, require protein degradation in the hippocampus for contextual fear memory formation.女性而非男性需要海马体中的蛋白质降解来形成情境性恐惧记忆。
Learn Mem. 2021 Jul 15;28(8):248-253. doi: 10.1101/lm.053429.121. Print 2021 Aug.
3
Ubiquitination of Histone H2B by Proteasome Subunit RPT6 Controls Histone Methylation Chromatin Dynamics During Memory Formation.组蛋白 H2B 的泛素化由蛋白酶体亚基 RPT6 控制,在记忆形成过程中控制组蛋白甲基化染色质动力学。
Biol Psychiatry. 2021 Jun 15;89(12):1176-1187. doi: 10.1016/j.biopsych.2020.12.029. Epub 2021 Jan 9.
4
Age-Related Memory Impairment and Sex-Specific Alterations in Phosphorylation of the Rpt6 Proteasome Subunit and Polyubiquitination in the Basolateral Amygdala and Medial Prefrontal Cortex.年龄相关的记忆障碍以及基底外侧杏仁核和内侧前额叶皮质中Rpt6蛋白酶体亚基磷酸化和多聚泛素化的性别特异性改变
Front Aging Neurosci. 2021 Apr 9;13:656944. doi: 10.3389/fnagi.2021.656944. eCollection 2021.
5
Altered Phosphorylation of the Proteasome Subunit Rpt6 Has Minimal Impact on Synaptic Plasticity and Learning.蛋白酶体亚基 Rpt6 的磷酸化改变对突触可塑性和学习的影响很小。
eNeuro. 2021 May 5;8(3). doi: 10.1523/ENEURO.0073-20.2021. Print 2021 May-Jun.
6
Considering sex as a biological variable will require a global shift in science culture.考虑将性别视为生物学变量将需要在科学文化中进行全球性转变。
Nat Neurosci. 2021 Apr;24(4):457-464. doi: 10.1038/s41593-021-00806-8. Epub 2021 Mar 1.
7
Males and females differ in the regulation and engagement of, but not requirement for, protein degradation in the amygdala during fear memory formation.在恐惧记忆形成过程中,杏仁核中的蛋白质降解的调节和参与存在性别差异,但并非必需。
Neurobiol Learn Mem. 2021 Apr;180:107404. doi: 10.1016/j.nlm.2021.107404. Epub 2021 Feb 18.
8
The diversity of linkage-specific polyubiquitin chains and their role in synaptic plasticity and memory formation.连接特异性多泛素链的多样性及其在突触可塑性和记忆形成中的作用。
Neurobiol Learn Mem. 2020 Oct;174:107286. doi: 10.1016/j.nlm.2020.107286. Epub 2020 Aug 1.
9
Dysregulation of protein degradation in the hippocampus is associated with impaired spatial memory during the development of obesity.海马体中蛋白质降解的失调与肥胖发展过程中空间记忆受损有关。
Behav Brain Res. 2020 Sep 1;393:112787. doi: 10.1016/j.bbr.2020.112787. Epub 2020 Jun 27.
10
Sexual dimorphism in hypothalamic inflammation in the offspring of dams exposed to a diet rich in high fat and branched-chain amino acids.母体高脂支链氨基酸饮食暴露对子代下丘脑炎症的性别二态性。
Am J Physiol Endocrinol Metab. 2019 Sep 1;317(3):E526-E534. doi: 10.1152/ajpendo.00183.2019. Epub 2019 Jul 30.

短期暴露于致肥胖饮食会导致雌性大鼠下丘脑中蛋白酶体介导的蛋白质降解的动态失调。

Short-term exposure to an obesogenic diet causes dynamic dysregulation of proteasome-mediated protein degradation in the hypothalamus of female rats.

机构信息

Department of Animal and Poultry Science, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.

School of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.

出版信息

Nutr Neurosci. 2023 Apr;26(4):290-302. doi: 10.1080/1028415X.2022.2046965. Epub 2022 Mar 13.

DOI:10.1080/1028415X.2022.2046965
PMID:35282800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9468187/
Abstract

OBJECTIVES

Previous work has shown that exposure to a high fat diet dysregulates the protein degradation process in the hypothalamus of male rodents. However, whether this occurs in a sex-independent manner is unknown. The objective of this study was to determine the effects of a short-term obesogenic diet on the ubiquitin-proteasome mediated protein degradation process in the hypothalamus of female rats.

METHODS

We fed young adult female rats a high fat diet or standard rat chow for 7 weeks. At the end of the 7th week, animals were euthanized and hypothalamus nuclear and cytoplasmic fractions were collected. Proteasome activity and degradation-specific (K48) ubiquitin signaling were assessed. Additionally, we transfected female rats with CRISPR-dCas9-VP64 plasmids in the hypothalamus prior to exposure to the high fat diet in order to increase proteasome activity and determine the role of reduced proteasome function on weight gain from the obesogenic diet.

RESULTS

We found that across the diet period, females gained weight significantly faster on the high fat diet than controls and showed dynamic downregulation of proteasome activity, decreases in proteasome subunit expression and an accumulation of degradation-specific K48 polyubiquitinated proteins in the hypothalamus. Notably, while our CRISPR-dCas9 manipulation was able to selectively increase some forms of proteasome activity, it was unable to prevent diet-induced proteasome downregulation or abnormal weight gain.

CONCLUSIONS

Collectively, these results reveal that acute exposure to an obesogenic diet causes reductions in the protein degradation process in the hypothalamus of females.

摘要

目的

先前的研究表明,高脂肪饮食会使雄性啮齿动物下丘脑的蛋白质降解过程失调。然而,这种情况是否具有性别独立性尚不清楚。本研究的目的是确定短期致肥胖饮食对雌性大鼠下丘脑泛素-蛋白酶体介导的蛋白质降解过程的影响。

方法

我们用高脂肪饮食或标准大鼠饲料喂养年轻成年雌性大鼠 7 周。在第 7 周结束时,处死动物并收集下丘脑核和细胞质部分。评估蛋白酶体活性和降解特异性(K48)泛素信号。此外,我们在雌性大鼠暴露于高脂肪饮食之前,用 CRISPR-dCas9-VP64 质粒转染下丘脑,以增加蛋白酶体活性,并确定降低蛋白酶体功能对肥胖饮食引起的体重增加的作用。

结果

我们发现,在整个饮食期间,高脂肪饮食组的雌性大鼠体重增加速度明显快于对照组,并表现出蛋白酶体活性的动态下调、蛋白酶体亚基表达降低以及下丘脑降解特异性 K48 多聚泛素化蛋白的积累。值得注意的是,虽然我们的 CRISPR-dCas9 操作能够选择性地增加某些形式的蛋白酶体活性,但它不能防止饮食引起的蛋白酶体下调或异常体重增加。

结论

总之,这些结果表明,急性暴露于致肥胖饮食会导致雌性大鼠下丘脑蛋白质降解过程减少。