间歇性低氧损害阻塞性睡眠呼吸暂停-低通气综合征大鼠模型的认知功能并促进有丝分裂和溶酶体吞噬

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jizu Ling, BoWen Li, XinHui Yuan, WenKai Yang, KeYang Sun
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引用次数: 0

摘要

自噬调节间歇性缺氧(IH)诱发的阻塞性睡眠呼吸暂停-低通气综合征(OSAHS)。我们研究了间歇性低氧及其停用对 OSAHS 的认知功能、自噬和溶噬的影响。我们建立了 OSAHS 大鼠模型,并将大鼠分为五组:常氧对照组、IH-4w 组(4 周 IH)、IH-6w 组(6 周 IH)、IH-8w 组(8 周 IH)和 IH-8w + 4w 组(8 周 IH 和 4 周常氧)。研究评估了大鼠的认知行为;海马组织线粒体和溶酶体形态;线粒体呼吸功能、通透性和膜电位;溶酶体功能;自噬和溶噬相关蛋白水平;以及缺氧相关的自噬基因表达。IH-4w、IH-6w 和 IH-8w 组大鼠的认知功能明显受损。在IH-8w细胞中,线粒体功能受损,形态肿胀,数量、呼吸、通透性和膜电位下降,有丝分裂相关蛋白ATG5和LC3II/LC3水平显著升高,p62水平下降。缺氧相关自噬基因 Becn1、Hif1、Bnip3、Bnip3l 和 Fundc1 的表达在 IH-8w 组明显升高。IH-8w细胞中LAMP2、CTSB和ACP2水平的显著增加进一步表明溶酶体功能受损。IH-8w组溶酶体相关蛋白LAMP1、LC3II/LC3I和TFEB水平显著升高,而p62水平显著降低。上述证据表明,IH 处理的 OSAHS 大鼠模型线粒体和溶酶体受损,并刺激了有丝分裂和溶酶体吞噬。撤除 IH 并在正常条件下培养 4 周后,大鼠的认知功能得到改善,而有丝分裂和溶酶体吞噬功能下降。我们的研究结果表明,IH会损害OSAHS大鼠模型的认知功能,促进有丝分裂和溶酶体吞噬,而停用IH可恢复上述效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermittent Hypoxia Impairs Cognitive Function and Promotes Mitophagy and Lysophagy in Obstructive Sleep Apnea-Hypopnea Syndrome Rat Model.

Autophagy regulates intermittent hypoxia (IH)-induced obstructive sleep apnea-hypopnea syndrome (OSAHS). We investigated the effects of IH and its withdrawal on cognitive function, autophagy, and lysophagy in OSAHS. An OSAHS rat model was established, and rats were divided into five groups: normoxia control, IH-4w (4-week IH), IH-6w (6-week IH), IH-8w (8-week IH), and IH-8w + 4w (8-week IH and 4-week normoxia). The cognitive behavior; mitochondrial and lysosomal morphology of the hippocampal tissue; mitochondrial respiratory function, permeability, and membrane potential; lysosomal function; autophagy- and lysophagy-related protein levels; and hypoxia-associated autophagy gene expression in rats were assessed. The cognitive function of rats in the IH-4w, IH-6w, and IH-8w groups was significantly impaired. In IH-8w cells, mitochondrial function was damaged with swollen morphology and decreased quantity, respiration, permeability, and membrane potential, along with significantly increased mitophagy-related protein ATG5 and LC3II/LC3 levels and decreased p62 levels. Expression of hypoxia-associated autophagy genes Becn1, Hif1, Bnip3, Bnip3l, and Fundc1 was significantly higher in the IH-8w group. Significantly increased LAMP2, CTSB, and ACP2 levels in IH-8w cells further indicated impaired lysosomal function. Lysophagy-related protein LAMP1, LC3II/LC3I, and TFEB levels were significantly increased in the IH-8w group, whereas p62 level was significantly decreased. The above listed evidence indicated damage to the mitochondria and lysosomes, as well as stimulation of mitophagy and lysophagy in IH-treatment OSAHS rat model. After withdrawing IH and culturing for 4 weeks in normal conditions, the cognitive function of rats improved, and mitophagy and lysophagy decreased. Our findings indicate that IH impairs cognitive function and promotes mitophagy and lysophagy in an OSAHS rat model, and IH withdrawal recovered the above effects.

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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