Lipid Metabolism and Brain Health

A special issue of Metabolites (ISSN 2218-1989). This special issue belongs to the section "Lipid Metabolism".

Deadline for manuscript submissions: closed (10 January 2024) | Viewed by 583

Special Issue Editors


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Guest Editor
Department of Biology, Faculty of Science, Western University 2025E Biological & Geological Sciences Building, 1151 Richmond Street, London, ON N6A 5B7, Canada
Interests: functional foods; environmental stress; biology; lipid bioinformatics; brain health; agriculture
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Biology, Faculty of Science, Western University 2025E Biological & Geological Sciences Building, 1151 Richmond Street, London, ON N6A 5B7, Canada
Interests: biofunctional foods; nootropic foods; enzymes; drug delivery; nanotechnology; brain health

Special Issue Information

Dear Colleagues,

The brain is the second most lipid-rich organ in the body and lipid metabolism is closely linked to brain energy homeostasis, oxidative stress, neuroinflammation, and imbalances in neuroglial cell lipid metabolism affecting normal neuronal activity (Yang et al., 2022). The brain contains large amounts of sphingolipids, glycerophospholipids, and cholesterol, which are involved in synaptogenesis, neurogenesis, and impulse transmission, and are inextricably linked to the development and maintenance of the brain and the proper conduct of many other cellular processes (Cermenati et al., 2005; Korade and Kenworthy, 2008). However, lipid accumulation production of lipotoxic metabolites induced by impaired lipid metabolism in the brain may further trigger central nervous system diseases and injuries (Han and Kaufman, 2016). Cholesterol, among all the lipids present in astrocytes, may play the most critical role in the structure of these cells. Among the subtypes of glia, oligodendrocytes produce cholesterol for myelin formation, which is involved in brain maturation and neurotransmission, while astrocytes are thought to be the main site of exogenous neuronal cholesterol synthesis (Linetti et al., 2010; Koudinov and Koudinova, 2002). Sphingolipids (SP) are the major lipids that compose the brain and the functional units of neuronal cell membranes and are highly enriched in the nervous system. Although the types of SP that may contribute to neurological dysfunction are unknown, genetic defects in various sphingolipid metabolizing enzymes reveal the importance of sphingolipid metabolism in brain development and health (Astudillo et al., 2015). Lipid droplets (LDs) are first recognized as independent organelles associated with lipid storage and transport, serving as relatively simple storage particles for lipids in the brain (Cermenati et al., 2005). While the brain is under pathological conditions, the content of LDs in glial cells is increased, though to a lesser extent in neurons. It has been controversial whether this lipid accumulation under stress has a protective or detrimental effect on the brain. LDs are highly regulated organelles that contribute to many cellular processes and emerge as metabolic hubs with diverse roles in energy and signalling precursors storage, cell stress management, and protein handling (Linetti et al., 2010; Boyles et al., 1989).

PUFAs are incorporated into membrane phospholipids and therefore play a significant role in the structural integrity and function of cell membranes. The lipid metabolism is changed during ageing (Montanini et al., 1983), as shown by a decline in omega-3 fatty acids and an increase in lipid peroxidation (Chen, 2017). Omega-3 fatty acids have antioxidant properties, and a lack of these fatty acids in one’s diet may accelerate neuronal degeneration (Yehuda et al., 2002). Susceptibility of lipids to peroxidation increases with age (Bourre and Vitamin, 1991), which supports the use of the level of oxidative stress as a critical determinant of neuronal health and longevity (Hulbert et al., 2006). Previous studies have suggested that DHA and EPA may protect against peroxidation and the effects of age-related brain pathology (Hasadsri et al., 2013). Lipids are involved in cellular signalling, energy balance, blood–brain barrier (BBB), and inflammation (Song C, et al., 2008), and such age-dependent lipidome changes that disrupt these functions may contribute to neurodegenerative diseases (Arnoldussen et al., 2016). Brain lipids confer a myriad of functions to the maintenance of a healthy brain and impaired brain health is the number one global health crisis. This Special Issue is dedicated to collecting the latest research and knowledge present in the scientific community in relation to how the lipid metabolism influences brain health outcomes. We encourage researchers to submit any studies related to the brain lipid metabolism and how this converges to either positively or negatively influence brain health outcomes, as well as any strategies that may be useful as part of a management system aimed at addressing brain health as a global health crisis.  

References

  1. Yang D, et al. 2022. Lipid metabolism and storage in neuroglia: role in brain development and neurodegenerative diseases. Cell & Bioscience volume. 2022; 106.
  2. Cermenati G, et al. Lipids in the nervous system: from biochemistry and molecular biology to patho-physiology. Biochim Biophys Acta. 2005;1851(1):51–60.
  3. Korade Z, Kenworthy AK. Lipid rafts, cholesterol, and the brain. Neuropharmacology. 2008;55(8):1265–73.
  4. Han J, and Kaufman RJ. The role of ER stress in lipid metabolism and lipotoxicity. J Lipid Res. 2016 Aug; 57(8): 1329–1338.
  5. Linetti A, et al. Cholesterol reduction impairs exocytosis of synaptic vesicles. J Cell Sci. 2010;123(Pt 4):595–605.
  6. Koudinov AR, Koudinova NV. Cholesterol’s role in synapse formation. Science. 2002;295(5563):2213.
  7. Astudillo L, et al. Human genetic disorders of sphingolipid biosynthesis. J Inherit Metab Dis. 2015;38(1):65–76.
  8. Linetti A, et al. Cholesterol reduction impairs exocytosis of synaptic vesicles. J Cell Sci. 2010;123(Pt 4):595–605.
  9. Boyles JK, et al. A role for apolipoprotein E, apolipoprotein A-I, and low density lipoprotein receptors in cholesterol transport during regeneration and remyelination of the rat sciatic nerve. J Clin Invest. 1989;83(3):1015–31.
  10. Montanini I, et al. The influence of polyunsaturated phosphatidylcholine on brain lipid synthesis during aging. Farmaco. Sci. 1983; 38, 376–382.
  11. Chen J. Polyunsaturated fatty acids ameliorate aging via redox-telomere-antioncogene axis. Oncotarget, 2017; 8, 7301–7314. doi: 10.18632/oncotarget.14236.
  12. Yehuda S, et al. The role of polyunsaturated fatty acids in restoring the aging neuronal membrane. Neurobiol. Aging. 2002; 23, 843–853. doi: 10.1016/s0197-4580(02)00074-x
  13. Bourre JM. Vitamin E: protection of membrane polyunsaturated fatty acids against radical peroxidation in the course of cerebral aging, particularly in cerebral capillaries and microvessels. Bull. Acad. Natl. Med. 1991; 175, 1305–1317.
  14. Hulbert AJ, et al. Extended longevity of wild-derived mice is associated with peroxidation-resistant membranes. Mech. Ageing Dev. 2006; 127, 653–657. doi: 10.1016/j.mad.2006.03.002
  15. Hasadsri L, et al. Omega-3 fatty acids as a putative treatment for traumatic brain injury. J. Neurotrauma. 2013; 30, 897–906. doi: 10.1089/neu.2012.2672.
  16. Song C, et al. Long-chain polyunsaturated fatty acids modulate interleukin-1beta-induced changes in behavior, monoaminergic neurotransmitters, and brain inflammation in rats. J. Nutr. 2008; 138, 954–963. doi: 10.1093/jn/138.5.954.
  17. Arnoldussen IA, et al. Early intake of long-chain polyunsaturated fatty acids preserves brain structure and function in diet-induced obesity. J. Nutr. Biochem. 2016; 30, 177–188. doi: 10.1016/j.jnutbio.2015.12.011.

Dr. Raymond H. Thomas
Dr. Elham Momeny
Guest Editors

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