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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.

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。

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