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-Tocopherol Concentration
Manuscript received 25 March 1996. Initial reviews completed 25 July 1996. Revision accepted 28 February 1997.
Graduate Nutritional Sciences Program and Department of Animal Sciences, University of Missouri, Columbia, MO 65211
We have previously reported that both the source of dietary fish oil and the chemical form of vitamin E supplied in the diet affect the vitamin E status of immune cells in rats. The purpose of this study was to investigate further the effect of fish oil source on immune cell vitamin E status using free
-tocopherol (
-T) at the AIN recommended level as the sole source of vitamin E. Sixty weanling female rats were fed semipurified, high fat (20 g/100 g) diets containing either tocopherol-stripped lard (LRD), menhaden fish oil (MFO), sardine fish oil (SRD) or cod liver oil (CLO) as the primary lipid source. Endogenous
-T concentration was measured and equalized to 150 mg/kg oil by addition of free RRR-
-T to each lipid source, allowing for a final concentration of
-T in the mixed diet of 30 mg/kg. An additional group of rats was fed LRD without supplemental vitamin E (LRD
) as a negative control. After feeding experimental diets for 5 or 10 wk, tissues were collected for
-T analysis by HPLC. After 5 wk, plasma and liver
-T (µmol
-T/g lipid) were significantly lower in SRD- and CLO-fed rats compared with LRD-fed rats. At 10 wk, only plasma
-T in CLO-fed rats remained significantly depressed. Plasma and liver
-T concentrations (µmol
-T/g lipid) were not significantly lower in MFO-fed rats than LRD-fed rats at either time point. Compared with LRD, feeding MFO to rats for 5 or 10 wk resulted in significantly greater
-T content of immune cells. In similar fashion, SRD-fed rats, compared with LRD-fed rats, also had significantly greater
-T content in splenocytes at both time points and greater thymocyte
-T at 10 wk. In all instances, the
-T status of rats fed CLO was indistinguishable from that of rats fed the vitamin E-free diet (LRD
). These data further demonstrate the complexity of the relationship between vitamin E status and dietary (n-3) polyunsaturated fatty acids (PUFA).
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