» Articles » PMID: 25279334

Location of α-tocopherol and α-tocotrienol to Heterogeneous Cell Membranes and Inhibition of Production of Peroxidized Cholesterol in Mouse Fibroblasts

Overview
Journal Springerplus
Date 2014 Oct 4
PMID 25279334
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: α-Tocopherol (α-T) and α-tocotrienol (α-T3) are well recognized as lipophilic antioxidants. Nevertheless, there is limited knowledge on their location in heterogeneous cell membranes. We first investigated the distribution of α-T and α-T3 to the cholesterol-rich microdomains (lipid rafts and caveolae) of heterogeneous cell membranes by incubating these antioxidants with cultured mouse fibroblasts.

Findings: Levels of cellular uptake for α-T and α-T3 were adjusted to the same order, as that of the latter was much more efficient than that of the former in the cultured cells. After ultracentrifugation, α-T and α-T3 were partitioned to the microdomain fractions. When the distribution of α-T and α-T3 was further confirmed by using methyl-β-cyclodextrin (which removes cholesterol from membranes), α-T was suggested to be distributed to the microdomains (approx. 9% of the total uptake). The same treatment did not affect α-T3 content in the microdomain fractions, indicating that α-T3 is not located in these cholesterol-rich domains. However, α-T and α-T3 significantly inhibited the production of peroxidized cholesterol when cells were exposed to ultraviolet-A light.

Conclusions: These results suggest that α-T and α-T3 can act as membranous antioxidants against photo-irradiated cholesterol peroxidation irrespective of their distribution to cholesterol-rich microdomains.

Citing Articles

The difference in the cellular uptake of tocopherol and tocotrienol is influenced by their affinities to albumin.

Nakatomi T, Itaya-Takahashi M, Horikoshi Y, Shimizu N, Parida I, Jutanom M Sci Rep. 2023; 13(1):7392.

PMID: 37149706 PMC: 10164177. DOI: 10.1038/s41598-023-34584-z.


Deregulation of Lipid Homeostasis: A Fa(c)t in the Development of Metabolic Diseases.

Cisa-Wieczorek S, Hernandez-Alvarez M Cells. 2020; 9(12).

PMID: 33291746 PMC: 7761975. DOI: 10.3390/cells9122605.


Palm vitamin E reduces locomotor dysfunction and morphological changes induced by spinal cord injury and protects against oxidative damage.

Zadeh-Ardabili P, Rad S, Rad S, Khazaai H, Sanusi J, Zadeh M Sci Rep. 2017; 7(1):14365.

PMID: 29085045 PMC: 5662565. DOI: 10.1038/s41598-017-14765-3.

References
1.
Serbinova E, Kagan V, Han D, Packer L . Free radical recycling and intramembrane mobility in the antioxidant properties of alpha-tocopherol and alpha-tocotrienol. Free Radic Biol Med. 1991; 10(5):263-75. DOI: 10.1016/0891-5849(91)90033-y. View

2.
Lemaire-Ewing S, Desrumaux C, Neel D, Lagrost L . Vitamin E transport, membrane incorporation and cell metabolism: Is alpha-tocopherol in lipid rafts an oar in the lifeboat?. Mol Nutr Food Res. 2010; 54(5):631-40. DOI: 10.1002/mnfr.200900445. View

3.
Nishio K, Horie M, Akazawa Y, Shichiri M, Iwahashi H, Hagihara Y . Attenuation of lipopolysaccharide (LPS)-induced cytotoxicity by tocopherols and tocotrienols. Redox Biol. 2013; 1:97-103. PMC: 3757666. DOI: 10.1016/j.redox.2012.10.002. View

4.
Gruszka J, Pawlak A, Kruk J . Tocochromanols, plastoquinol, and other biological prenyllipids as singlet oxygen quenchers-determination of singlet oxygen quenching rate constants and oxidation products. Free Radic Biol Med. 2008; 45(6):920-8. DOI: 10.1016/j.freeradbiomed.2008.06.025. View

5.
Royer M, Lemaire-Ewing S, Desrumaux C, Monier S, Pais de Barros J, Athias A . 7-ketocholesterol incorporation into sphingolipid/cholesterol-enriched (lipid raft) domains is impaired by vitamin E: a specific role for alpha-tocopherol with consequences on cell death. J Biol Chem. 2009; 284(23):15826-34. PMC: 2708879. DOI: 10.1074/jbc.M808641200. View