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低碳水化合物、高脂肪饮食对代谢综合征动物模型脑胰岛素抵抗保护作用的分子研究

Molecular Study of the Protective Effect of a Low-Carbohydrate, High-Fat Diet against Brain Insulin Resistance in an Animal Model of Metabolic Syndrome.

作者信息

Bima Abdulhadi, Eldakhakhny Basmah, Alamoudi Aliaa A, Awan Zuhier, Alnami Abrar, Abo-Elkhair Salwa Mohamed, Sakr Hussein, Ghoneim Fatma Mohamed, Elsamanoudy Ayman

机构信息

Clinical Biochemistry Department, Faculty of Medicine, King Abdulaziz University, Jeddah 21465, Saudi Arabia.

Food, Nutrition, and Lifestyle Research Unit, King Fahd for Medical Research Centre, King Abdulaziz University, Jeddah 21465, Saudi Arabia.

出版信息

Brain Sci. 2023 Sep 28;13(10):1383. doi: 10.3390/brainsci13101383.

Abstract

Brain insulin resistance is linked to metabolic syndrome (MetS). A low-carbohydrate, high-fat (LCHF) diet has been proposed to have a protective effect. Therefore, this study aimed to investigate the brain insulin resistance markers in a rat animal model of MetS and the protective effects of the LCHF diet. Four groups of male rats (10/group) were created. Group I (Control) was fed a regular diet. Groups II-IV were injected with dexamethasone (DEX) to induce MetS. Group II received DEX with a regular diet. Group III (DEX + LCHF) rates were fed a low-carbohydrate, high-fat diet, while Group IV (DEX + HCLF) rats were fed a high-carbohydrate, low-fat (HCLF) diet. At the end of the four-week experiment, HOMA-IR was calculated. Moreover, cerebral gene expression analysis of S-100B, BDNF, TNF-α, IGF-1, IGF-1 R, IGFBP-2, IGFBP-5, Bax, Bcl-2, and caspase-3 was carried out. In the DEX group, rats showed a significant increase in the HOMA-IR and a decrease in the gene expression of IGF-1, IGF-1 R, IGFBP-2, IGFBP-5, BDNF, and Bcl2, with a concomitant rise in S100B, TNF-α, Bax, and caspase-3. The LCHF diet group showed a significantly opposite effect on all parameters. In conclusion, MetS is associated with dysregulated cerebral gene expression of BDNF, S100B, and TNF-α and disturbed IGF-1 signaling, with increased apoptosis and neuroinflammation. Moreover, the LCHF diet showed a protective effect, as evidenced by preservation of the investigated biochemical and molecular parameters.

摘要

脑胰岛素抵抗与代谢综合征(MetS)相关。有人提出低碳水化合物、高脂肪(LCHF)饮食具有保护作用。因此,本研究旨在调查MetS大鼠动物模型中的脑胰岛素抵抗标志物以及LCHF饮食的保护作用。创建了四组雄性大鼠(每组10只)。第一组(对照组)喂食常规饮食。第二至四组注射地塞米松(DEX)以诱导MetS。第二组接受DEX并喂食常规饮食。第三组(DEX + LCHF)大鼠喂食低碳水化合物、高脂肪饮食,而第四组(DEX + HCLF)大鼠喂食高碳水化合物、低脂肪(HCLF)饮食。在为期四周的实验结束时,计算了胰岛素抵抗稳态模型评估(HOMA-IR)。此外,还对S-100B、脑源性神经营养因子(BDNF)、肿瘤坏死因子-α(TNF-α)、胰岛素样生长因子-1(IGF-1)、IGF-1受体(IGF-1 R)、胰岛素样生长因子结合蛋白-2(IGFBP-2)、胰岛素样生长因子结合蛋白-5(IGFBP-5)、凋亡蛋白(Bax)、凋亡抑制蛋白(Bcl-2)和半胱天冬酶-3(caspase-3)进行了脑基因表达分析。在DEX组中,大鼠的HOMA-IR显著增加,IGF-1、IGF-1 R、IGFBP-2、IGFBP-5、BDNF和Bcl2的基因表达降低,同时S100B、TNF-α、Bax和caspase-3升高。LCHF饮食组对所有参数显示出明显相反的作用。总之,MetS与BDNF、S100B和TNF-α的脑基因表达失调以及IGF-1信号传导紊乱有关,伴有细胞凋亡增加和神经炎症。此外,LCHF饮食显示出保护作用,所研究的生化和分子参数得以保留证明了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d62b/10605073/bd7bc890dd7b/brainsci-13-01383-g001.jpg

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