题名 | Effects of Fibroblast Growth Factor 21 on Lactate Uptake and Usage in Mice with Diabetes-Associated Cognitive Decline |
作者 | |
发表日期 | 2022-09 |
发表期刊 | MOLECULAR NEUROBIOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article ; Early Access |
关键词 | Diabetes mellitus Fibroblast growth factor 21 Monocarboxylate transporter Lactate Learning and memory |
其他关键词 | NEURONAL MONOCARBOXYLATE TRANSPORTER ; MITOCHONDRIAL-FUNCTION ; METABOLIC ALTERATIONS ; BRAIN ; EXPRESSION ; FGF21 ; ASTROCYTES ; MCT2 ; INSULIN ; SYSTEM |
摘要 | Fibroblast growth factor 21 (FGF21) is an endocrine hormone that exerts beneficial effects on glucose and lipid metabolic homeostasis. However, the impact of FGF21 on type 1 diabetes-associated cognitive decline (DACD) and its mechanisms of action remain unclear. In this study, we aimed to evaluate the effects of FGF21 on lactate uptake and usage in a mouse model of streptozotocin-induced DACD. Six-week-old male C57BL/6 mice were divided into the control, diabetic, and FGF21 (which received 2 mg/kg recombinant human FGF21) groups. At the end of the treatment period, learning and memory performance, nuclear magnetic resonance-based metabonomics, and expressions of various hippocampal protein were analyzed to determine the efficacy of FGF21. The results showed that compared to the control mice, the diabetic mice had reduced long-term memory performance after the hyperglycemic insult; decreased hippocampal levels of lactate dehydrogenase-B (LDH-B) activity, bioenergy metabolites, and monocarboxylate transporter 2 (MCT2); and increased lactate levels. Impaired phosphoinositide 3-kinase (PI3K) signaling was also observed in the diabetic mice. However, FGF21 treatment improved LDH-B activity, beta-nicotinamide adenine dinucleotide, and ATP levels, and increased MCT2 expression and PI3K signaling pathway, which in turn improved the learning and memory defects. These findings demonstrated that the effects of FGF21 on DACD were associated with its ability to improve LDH-B-mediated lactate usage and MCT2-dependent lactate uptake. Further, these beneficial effects of FGF21 in the hippocampus were mediated by the PI3K signaling pathways. |
资助项目 | Natural Science Foundation of Zhejiang Province [LY22H070003]; National Natural Science Foundation of China [81770830, 21974096, 81771386] |
出版者 | SPRINGER |
出版地 | NEW YORK |
ISSN | 0893-7648 |
EISSN | 1559-1182 |
卷号 | 59期号:9页码:5656-5672 |
DOI | 10.1007/s12035-022-02926-z |
页数 | 17 |
WOS类目 | Neurosciences |
WOS研究方向 | Neurosciences & Neurology |
WOS记录号 | WOS:000816998400001 |
收录类别 | SCIE ; SCOPUS ; PUBMED |
URL | 查看原文 |
PubMed ID | 35761156 |
SCOPUSEID | 2-s2.0-85132936025 |
通讯作者地址 | [Zhao, Liangcai]School of Pharmaceutical Sciences,Wenzhou Medical University,Zhejiang,Wenzhou,325035,China ; [Gao, Hongchang]School of Pharmaceutical Sciences,Wenzhou Medical University,Zhejiang,Wenzhou,325035,China |
Scopus学科分类 | Neuroscience (miscellaneous);Neurology;Cellular and Molecular Neuroscience |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/148317 |
专题 | 药学院(分析测试中心) 卓越中心_老年研究院 |
通讯作者 | Zhao, Liangcai; Gao, Hongchang |
作者单位 | 1.School of Pharmaceutical Sciences,Wenzhou Medical University,Zhejiang,Wenzhou,325035,China; 2.Institute of Aging,Key Laboratory of Alzheimer’s Disease of Zhejiang Province,Wenzhou Medical University,Wenzhou,China |
第一作者单位 | 药学院(分析测试中心) |
通讯作者单位 | 药学院(分析测试中心) |
第一作者的第一单位 | 药学院(分析测试中心) |
推荐引用方式 GB/T 7714 | Zhao, Liangcai,Jiang, Haowei,Xie, Jiaojiao,et al. Effects of Fibroblast Growth Factor 21 on Lactate Uptake and Usage in Mice with Diabetes-Associated Cognitive Decline[J]. MOLECULAR NEUROBIOLOGY,2022,59(9):5656-5672. |
APA | Zhao, Liangcai., Jiang, Haowei., Xie, Jiaojiao., Shen, Danjie., Yi, Qingqing., ... & Gao, Hongchang. (2022). Effects of Fibroblast Growth Factor 21 on Lactate Uptake and Usage in Mice with Diabetes-Associated Cognitive Decline. MOLECULAR NEUROBIOLOGY, 59(9), 5656-5672. |
MLA | Zhao, Liangcai,et al."Effects of Fibroblast Growth Factor 21 on Lactate Uptake and Usage in Mice with Diabetes-Associated Cognitive Decline".MOLECULAR NEUROBIOLOGY 59.9(2022):5656-5672. |
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