期刊
TOXICOLOGY AND APPLIED PHARMACOLOGY
卷 182, 期 1, 页码 76-83出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1006/taap.2002.9435
关键词
Na+/K+ pump; membrane fluidity; linoleic acid metabolite; fatty acid; patch clamp
资金
- NHLBI NIH HHS [HL60174] Funding Source: Medline
- NIGMS NIH HHS [GM56708] Funding Source: Medline
Metabolic derivatives of linoleic acid, both monoepoxides and diols, have been reported to be toxic in humans and multiple animal tissue preparations. A previous electrophysiological study has shown these compounds produce multiple effects on the electrical activity of rat ventricular myocytes. The hydrophobic nature of these compounds suggests the possibility that these effects may be due to nonspecific lipid interactions, i.e., changes in membrane fluidity. This study investigates membrane fluidity as a possible mechanism by which linoleic acid metabolites inhibit Na+/K+ pump current (I-p). This study showed that positional isomers 9,10-and 12,13-epoxy-octadecenoic acid (EOA) and 9,10- and 12,13-dihydroxy-OA (DHOA) inhibit I-p in a dose-dependent manner in N20.1 mouse oligodendrocytes, with greater inhibition produced by EOAs. These compounds, at 10 muM, inhibited I-p by 4.7 +/- 1.6, 18.2 +/- 0.5, 11.7 +/- 0.5, and 25.1 +/- 0.9% for 12,13-DHOA, 9,10-DHOA, 12,13-EOA, and 9,10-EOA, respectively, in oligodendrocytes. Fluorescence recovery after photobleaching measurements showed that both DHOA isomers produced a 7-8% increase in diffusion coefficient of the probe at 10 muM, whereas the diffusion coefficient was decreased by 5 and 13% by 9,10-EOA and 12,13-EOA, respectively. There was no apparent correlation between membrane fluidity and inhibition of I, by these four linoleic acid metabolites. These results indicate that membrane fluidity alone cannot explain the effects of these compounds on I, and suggest that they have a specific interaction with the Na+/K+ PUMP. (C) 2002 Elsevier Science (USA).
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