烧伤两周后大鼠中枢神经系统的转录重编程:肾素治疗对氧化应激相关基因表达的影响。

Scars, burns & healing Pub Date : 2020-08-11 eCollection Date: 2020-01-01 DOI:10.1177/2059513120939443
Desmond D Mascarenhas
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摘要

简介严重烧伤的幸存者终生都会受到神经炎症的影响,表现为重度抑郁症和神经退行性疾病的发病率较高。在烫伤模型中,Nephrilin 肽曾被证明能保护大鼠免受瘦体重、肾功能和血糖控制能力下降的影响,这些并发症在烧伤患者群体中也被证明会持续存在。Nephrilin的作用机制被认为是防止过度氧化应激:我们使用定量逆转录酶聚合酶链反应(qRT-PCR)扩增从雄性大鼠背根神经节中提取的总 RNA 中的转录物,在暴露于热损伤 14 天后,我们查询了 34 个被认为与中枢神经系统(CNS)氧化应激生物学相关的基因的相对表达水平。我们利用这些数据来探讨氧化应激在星形胶质细胞病变、免疫抑制和线粒体稳态中的核心作用:接受肾素治疗的大鼠(烫伤后每天一次皮下注射,每次 4 毫克/千克)显示,一些关键基因(如 NOX2、GFAP、AQP4 和 RAC1)的基因表达升高显著降低,而其他基因(如 NOX4、STEAP4、ARG1 和 CCL2)的基因表达升高则没有降低:结论:本文讨论了这些数据对 Nephrilin 在减轻烧伤创伤对中枢神经系统的持久影响方面的潜在临床用途的影响。Nephrilin能降低烧伤后神经变性相关基因的表达。本研究通过在大鼠烫伤模型中观察中枢神经系统中基因的表达,来衡量奈普利林治疗创伤后神经退行性疾病的能力。Nephrilin似乎能减少一些已知与神经退行性病变过程相关的关键基因的表达,而不是其他基因的表达,从而产生有益的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Transcriptional re-programming in rat central nervous system two weeks after burn trauma: the impact of nephrilin treatment on the expression of oxidative stress-related genes.

Introduction: Survivors of severe burns suffer lifetime neuroinflammatory consequences manifested by higher incidence of major depression and neurodegenerative disease. In a scald model, nephrilin peptide has previously been shown to protect rats from loss of lean body mass, kidney function and glycaemic control, complications that have also been shown to endure in burn patient populations. Nephrilin's mechanism of action has been suggested to involve protection from excessive oxidative stress.

Methods: Using quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) amplification of transcripts in total RNA extracted from dorsal root ganglia of male rats 14 days after exposure to thermal insult, we query the relative levels of expression of 34 genes believed to be associated with oxidative stress biology in the central nervous system (CNS). We use these data to explore the central role of oxidative stress in astrogliosis, immunosuppression and mitochondrial homeostasis.

Results and discussion: Rats that received nephrilin treatment (4 mg/kg by subcutaneous bolus injection once daily for seven days after scald injury) showed significantly reduced elevations in gene expression of some key genes such as NOX2, GFAP, AQP4 and RAC1, but not of others such as NOX4, STEAP4, ARG1 and CCL2.

Conclusion: The implications of these data with reference to nephrilin's potential clinical utility for mitigating the enduring effects of burn trauma on the CNS are discussed. Nephrilin reduces the expression of some genes implicated in neurodegeneration after burn insult.

Lay summary: Nephrilin peptide is a novel treatment for short- and long-term systemic effects of burn trauma. This study measures the capability of nephrilin to address post-traumatic neurodegenerative disease by looking at the expression of genes in the central nervous system, in a rat scald model. Nephrilin appears to have beneficial effects by reducing the expression of some key genes known to be relevant in neurodegenerative processes, but not others.

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