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限制蛋氨酸通过 H19 减轻中年胰岛素抵抗小鼠海马神经元凋亡改善认知能力。

Methionine Restriction Improves Cognitive Ability by Alleviating Hippocampal Neuronal Apoptosis through H19 in Middle-Aged Insulin-Resistant Mice.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China.

Center for Food Nutrition and Functional Food Engineering, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China.

出版信息

Nutrients. 2022 Oct 26;14(21):4503. doi: 10.3390/nu14214503.

Abstract

LncRNA H19 has been reported to regulate apoptosis and neurological diseases. Hippocampal neuron apoptosis damages cognitive ability. Methionine restriction (MR) can improve cognitive impairment. However, the effect of MR on hippocampal neuronal apoptosis induced by a high-fat diet (HFD) in middle-aged mice remains unclear. For 25 weeks, middle-aged mice (C57BL/6J) were given a control diet (CON, 0.86% methionine + 4.2% fat), a high-fat diet (HFD, 0.86% methionine + 24% fat), or an HFD + MR diet (HFMR, 0.17% methionine + 24% fat). The HT22 cells were used to establish the early apoptosis model induced by high glucose (HG). In vitro, the results showed that MR significantly improved cell viability, suppressed the generation of ROS, and rescued HT22 cell apoptosis in a gradient-dependent manner. In Vivo, MR inhibited the damage and apoptosis of hippocampal neurons caused by a high-fat diet, reduced hippocampal oxidative stress, improved hippocampal glucose metabolism, relieved insulin resistance, and enhanced cognitive ability. Furthermore, MR could inhibit the overexpression of H19 and caspase-3 induced by HFD, HG, or HO in vivo and in vitro, and promoted let-7a, b, e expression. These results indicate that MR can protect neurons from HFD-, HG-, or HO-induced injury and apoptosis by inhibiting H19.

摘要

长链非编码 RNA H19 已被报道可调节细胞凋亡和神经疾病。海马神经元凋亡损伤认知能力。蛋氨酸限制(MR)可以改善认知障碍。然而,MR 对中年小鼠高脂肪饮食(HFD)诱导的海马神经元凋亡的影响尚不清楚。在 25 周的时间里,中年小鼠(C57BL/6J)给予对照饮食(CON,0.86%蛋氨酸+4.2%脂肪)、高脂肪饮食(HFD,0.86%蛋氨酸+24%脂肪)或高脂肪饮食+蛋氨酸限制饮食(HFMR,0.17%蛋氨酸+24%脂肪)。用 HT22 细胞建立高糖(HG)诱导的早期细胞凋亡模型。在体外,结果表明,MR 显著提高细胞活力,以梯度依赖的方式抑制 ROS 的产生,并挽救 HT22 细胞凋亡。在体内,MR 抑制高脂肪饮食引起的海马神经元损伤和凋亡,减少海马氧化应激,改善海马糖代谢,缓解胰岛素抵抗,增强认知能力。此外,MR 可以抑制 HFD、HG 或 HO 体内和体外诱导的 H19 和 caspase-3 的过表达,并促进 let-7a、b、e 的表达。这些结果表明,MR 可以通过抑制 H19 来保护神经元免受 HFD、HG 或 HO 诱导的损伤和凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c642/9653609/8be294703156/nutrients-14-04503-g001.jpg

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