Sphingolipid metabolism in brain insulin resistance and neurological diseases

被引:21
作者
Mei, Meng [1 ]
Liu, Maochang [1 ]
Mei, Yan [1 ]
Zhao, Jing [2 ]
Li, Yang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Wuhan Maternal & Child Healthcare Hosp, Tongji Med Coll,Dept Pharm, Wuhan, Peoples R China
[2] Beijing Univ Chinese Med, Adm Off, Beijing, Peoples R China
关键词
sphingolipid metabolism; brain insulin resistance; ceramide; sphingosine-1-phosphate; Alzheimer's disease; Parkinson's disease; SPHINGOMYELIN SYNTHASE 2; CENTRAL-NERVOUS-SYSTEM; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; SPHINGOSINE; 1-PHOSPHATE; PLASMA-MEMBRANE; SERINE PALMITOYLTRANSFERASE; GLUCOSYLCERAMIDE SYNTHASE; INTRANASAL INSULIN; GLUCOSE-METABOLISM;
D O I
10.3389/fendo.2023.1243132
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sphingolipids, as members of the large lipid family, are important components of plasma membrane. Sphingolipids participate in biological signal transduction to regulate various important physiological processes such as cell growth, apoptosis, senescence, and differentiation. Numerous studies have demonstrated that sphingolipids are strongly associated with glucose metabolism and insulin resistance. Insulin resistance, including peripheral insulin resistance and brain insulin resistance, is closely related to the occurrence and development of many metabolic diseases. In addition to metabolic diseases, like type 2 diabetes, brain insulin resistance is also involved in the progression of neurodegenerative diseases including Alzheimer's disease and Parkinson's disease. However, the specific mechanism of sphingolipids in brain insulin resistance has not been systematically summarized. This article reviews the involvement of sphingolipids in brain insulin resistance, highlighting the role and molecular biological mechanism of sphingolipid metabolism in cognitive dysfunctions and neuropathological abnormalities of the brain.
引用
收藏
页数:15
相关论文
共 151 条
[51]   Integrated sphingosine-1 phosphate signaling in the central nervous system: From physiological equilibrium to pathological damage [J].
Ghasemi, Rasoul ;
Dargahi, Leila ;
Ahmadiani, Abolhassan .
PHARMACOLOGICAL RESEARCH, 2016, 104 :156-164
[52]   Insulin-stimulated translocation of GLUT4 to the plasma membrane in rat hippocampus is PI3-kinase dependent [J].
Grillo, C. A. ;
Piroli, G. G. ;
Hendry, R. M. ;
Reagan, L. P. .
BRAIN RESEARCH, 2009, 1296 :35-45
[53]   PS Dependent APP Cleavage Regulates Glucosylceramide Synthase and is Affected in Alzheimer's Disease [J].
Grimm, Marcus O. W. ;
Hundsdoerfer, Benjamin ;
Groesgen, Sven ;
Mett, Janine ;
Zimmer, Valerie C. ;
Stahlmann, Christoph P. ;
Haupenthal, Viola J. ;
Rothhaar, Tatjana L. ;
Lehmann, Johannes ;
Paetzold, Andreas ;
Zinser, Eva G. ;
Tanila, Heikki ;
Shen, Jie ;
Mueller, Ulrike ;
Grimm, Heike S. ;
Hartmann, Tobias .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2014, 34 (01) :92-110
[54]   Altering Sphingolipid Metabolism Attenuates Cell Death and Inflammatory Response After Myocardial Infarction [J].
Hadas, Yoav ;
Vincek, Adam S. ;
Youssef, Elias ;
Zak, Magdalena M. ;
Chepurko, Elena ;
Sultana, Nishat ;
Sharkar, Mohammad Tofael Kabir ;
Guo, Ningning ;
Komargodski, Rinat ;
Kurian, Ann Anu ;
Kaur, Keerat ;
Magadum, Ajit ;
Fargnoli, Anthony ;
Katz, Michael G. ;
Hossain, Nadia ;
Kenigsberg, Ephraim ;
Dubois, Nicole C. ;
Schadt, Eric ;
Hajjar, Roger ;
Eliyahu, Efrat ;
Zangi, Lior .
CIRCULATION, 2020, 141 (11) :916-930
[55]   CerS6-Derived Sphingolipids Interact with Mff and Promote Mitochondria! Fragmentation in Obesity [J].
Hammerschmidt, Philipp ;
Ostkotte, Daniela ;
Nolte, Hendrik ;
Gerl, Mathias J. ;
Jais, Alexander ;
Brunner, Hanna L. ;
Sprenger, Hans-Georg ;
Awazawa, Motoharu ;
Nicholls, Hayley T. ;
Turpin-Nolan, Sarah M. ;
Langer, Thomas ;
Krueger, Marcus ;
Bruegger, Britta ;
Bruening, Jens C. .
CELL, 2019, 177 (06) :1536-+
[56]   Metabolomics in Early Alzheimer's Disease: Identification of Altered Plasma Sphingolipidome Using Shotgun Lipidomics [J].
Han, Xianlin ;
Rozen, Steve ;
Boyle, Stephen H. ;
Hellegers, Caroline ;
Cheng, Hua ;
Burke, James R. ;
Welsh-Bohmer, Kathleen A. ;
Doraiswamy, P. Murali ;
Kaddurah-Daouk, Rima .
PLOS ONE, 2011, 6 (07)
[57]   LYSOSPHINGOLIPIDS INHIBIT PROTEIN-KINASE-C - IMPLICATIONS FOR THE SPHINGOLIPIDOSES [J].
HANNUN, YA ;
BELL, RM .
SCIENCE, 1987, 235 (4789) :670-674
[58]   Principles of bioactive lipid signalling: lessons from sphingolipids [J].
Hannun, Yusuf A. ;
Obeid, Lina M. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (02) :139-150
[59]   Sphingolipids and their metabolism in physiology and disease [J].
Hannun, Yusuf A. ;
Obeid, Lina M. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2018, 19 (03) :175-191
[60]   Diversity in sphingolipid metabolism across land plants [J].
Haslam, Tegan M. ;
Feussner, Ivo .
JOURNAL OF EXPERIMENTAL BOTANY, 2022, 73 (09) :2785-2798