2022
DOI: 10.1016/j.jbior.2022.100900
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Sphingolipids and their role in health and disease in the central nervous system

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Cited by 5 publications
(5 citation statements)
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“…It is widely known that SLs are involved in brain development, changes in lipids metabolism might results in altered lipid composition that can lead to the development of neurological and psychiatric diseases (Hussain et al, 2019; Leal et al, 2022; D. Yang et al, 2022). Furthermore, exposure to an HFD formula during the early stages of development also increases the risk of developing mental and behavioral disorders in offspring after birth (Cortés‐Albornoz et al, 2021; Gawlińska et al, 2021; Mitchell et al, 2022).…”
Section: Diet Modulates Ceramides Metabolism and Susceptibility To Ps...mentioning
confidence: 99%
See 1 more Smart Citation
“…It is widely known that SLs are involved in brain development, changes in lipids metabolism might results in altered lipid composition that can lead to the development of neurological and psychiatric diseases (Hussain et al, 2019; Leal et al, 2022; D. Yang et al, 2022). Furthermore, exposure to an HFD formula during the early stages of development also increases the risk of developing mental and behavioral disorders in offspring after birth (Cortés‐Albornoz et al, 2021; Gawlińska et al, 2021; Mitchell et al, 2022).…”
Section: Diet Modulates Ceramides Metabolism and Susceptibility To Ps...mentioning
confidence: 99%
“…It is widely known that SLs are involved in brain development, changes in lipids metabolism might results in altered lipid composition that can lead to the development of neurological and psychiatric diseases(Hussain et al, 2019;Leal et al, 2022;D. Yang et al, 2022).…”
mentioning
confidence: 99%
“…On the other hand, the contribution of other lipid types such as glycolipids or sphingolipids must not be underestimated and would deserve a dedicated study. For example, sphingolipids have been shown to be key in the formation of highly rigid gel domains, are involved in important physiological processes and may contribute to the action of several antifungal agents (F. C. Santos et al, 2020 ; Aresta-Branco et al, 2011 ; Vecer et al, 2014 ; Körner and Fröhlich, 2022 ; Olsen and Færgeman, 2017 ; Leal and Suarez. 2022 ).…”
Section: Introductionmentioning
confidence: 99%
“…Sphingolipidoses are a group of inherited lysosomal storage disorders caused by deficiency of lysosomal enzymes, such as β-galactosylcerebrosidase in Krabbe disease, β-glucocerebrosidase in Gaucher disease, Globotriaosylceramidase in Fabry disease and acid sphingomyelinase in Niemann Pick type A&B [ 14 , 15 ]. Patients deficient in these enzymes show significant accumulation of its immediate sphingolipid precursor such as β-galactosylceramide and its corresponding metabolic deacylated lyso-form, galactosylsphingosine (psychosine) in Krabbe disease.…”
Section: Introductionmentioning
confidence: 99%