Cholesterol for synthesis of myelin is made locally, not imported into brain
Abstract
We examined whether cholesterol needed for myelin formation is locally synthesized or whether it comes from the circulation. The experimental design was to inject [3H]water and to use incorporation of label into brain cholesterol as a measure of the rate of accumulation of newly synthesized cholesterol in brain. The contribution of the circulation to this labeled cholesterol pool was minimized by repressing liver synthesis of cholesterol with a high cholesterol diet. The rate of accumulation of total cholesterol was calculated from the increasing amounts of sterol in brain regions at successive time intervals during development. Thus, accumulating cholesterol not explained as being newly synthesized (radioactive) could be assumed to have come from the circulation. Long-Evans rats, ranging in age from birth to 35 days, were injected intraperitoneally with [3H]water (0.3-1.0 mCi/g of body weight) and killed 2 h later. The brain was dissected into brainstem, cerebellum, and cerebral hemispheres, and total lipids were extracted. Cholesterol and its precursors were quantified by HPLC. The radioactivity associated with the sterol fractions and the specific activity of body water determined from serum were used to calculate the absolute amount of newly synthesized sterol. The rates of cholesterol synthesis were compared with the rates of accumulation of total cholesterol in each brain region. The rate of accumulation of total sterol (cholesterol and desmosterol) closely followed tha…
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Once myelin formation begins to reach completion, the requirement for locally synthesized cholesterol falls dramatically.
“Once this process begins to reach completion, the requirement for locally synthesized cholesterol falls dramatically (Jurevics and Morell, 1995; Quan et al., 2003).”
From Suppression of brain cholesterol synthesis in male Mecp2-deficient mice is age dependent and not accompanied by a concurrent change in the rate of fatty acid synthesis (2017) · cites this paper as Jurevics and Morell, 1995
In mice of both genotypes, the rate of cholesterol synthesis declined markedly after 21 days.
“In mice of both genotypes, the rate of cholesterol synthesis declined markedly after 21 days, in keeping with what has been well documented for the developing brain in several species (Jurevics and Morell, 1995; Quan et al., 2003).”
From Suppression of brain cholesterol synthesis in male Mecp2-deficient mice is age dependent and not accompanied by a concurrent change in the rate of fatty acid synthesis (2017) · cites this paper as Jurevics and Morell, 1995
The fine balance between synthesis and degradation prevents accumulation of excess unesterified cholesterol while ensuring that the supply of newly synthesized cholesterol for myelin formation is not disrupted.
“This fine balance between synthesis and degradation prevents the accumulation of excess unesterified cholesterol, while at the same time ensuring that the supply of newly synthesized cholesterol for myelin formation is not disrupted (Jurevics and Morell, 1995; Snipes and Suter, 1997).”
From Suppression of brain cholesterol synthesis in male Mecp2-deficient mice is age dependent and not accompanied by a concurrent change in the rate of fatty acid synthesis (2017) · cites this paper as Jurevics and Morell, 1995
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Cited by 302
- Authors
- Jurevics, H., & Morell, P.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Morell, Pierre
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 1995-02
- Volume
- 64
- Issue
- 2
- Pages
- 895-901
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- OpenAlex
- W2045942675
- Cited by
- 302
- References
- 0
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 5 · 2023: 7 · 2022: 8 · 2021: 7 · 2020: 3 · 2019: 11 · 2018: 9 · 2017: 8 · 2016: 10 · 2015: 7 · 2014: 19 · 2013: 8 · 2012: 16
- FWCI
- 6.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ns011615-29)
- National Institute of Neurological Disorders and Stroke (NS-11615)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (#HD03110, P30HD003110)
- Topics
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- myelination, circulating cholesterol, postnatal brain development, desmosterol, hepatic cholesterol synthesis, high-cholesterol diet, brainstem, cerebellum, cerebral hemispheres, Long-Evans rats
- MeSH terms
- Aging, Animals, Animals, Newborn, Blood, Brain, Cholesterol, Desmosterol, Myelin Sheath, Rats
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