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2 Department of Nutritional Sciences, Nagoya University of Arts and Sciences, Nissin 470-0196, Japan; 3 Department of Food and Nutrition, Sugiyama Jogakuen University, Nagoya 464-8662, Japan
* To whom correspondence should be addressed. E-mail: saiko{at}nuas.ac.jp.
The aim of this experiment was to clarify the contribution of the
-tocopherol transfer activity of lipoprotein lipase (LPL) to vitamin E transport to tissues in vivo. We studied the effect of Triton WR1339, which prevents the catabolism of triacylglycerol-rich lipoproteins by LPL on vitamin E distribution in rats. Vitamin E-deficient rats fed a vitamin E-free diet for 4 wk were injected with Triton WR1339 and administered by oral gavage an emulsion containing 10 mg of
-tocopherol, 10 mg of
-tocopherol, or 29.5 mg of a tocotrienol mixture with 200 mg of sodium taurocholate, 200 mg of triolein, and 50 mg of albumin.
-Tocopherol was detected in the serum and other tissues of the vitamin E-deficient rats, but
-tocopherol,
- and
-tocotrienol were not detected. Triton WR1339 injection elevated (P < 0.05) the serum
-tocopherol concentration and inhibited (P < 0.05) the elevation of
-tocopherol concentration in the liver, adrenal gland, and spleen due to the oral administration of
-tocopherol. Neither
-tocopherol administration nor Triton WR1339 injection affected (P
0.05) the
-tocopherol concentration in the perirenal adipose tissue, epididymal fat, and soleus muscle despite a high expression of LPL in the adipose tissue and muscle. These data show that
-tocopherol transfer activity of LPL in adipose tissue and muscle is not important for
-tocopherol transport to the tissue after
-tocopherol intake or that the amount transferred is small relative to the tissue concentration. Furthermore, Triton WR1339 injection tended to elevate the serum
-tocopherol (P = 0.071) and
-tocotrienol (P = 0.053) concentrations and lowered them (P < 0.05) in the liver and adrenal gland of rats administered
-tocopherol or
-tocotrienol. These data suggest that lipolysis of triacylglycerol-rich chylomicron by LPL is necessary for postprandial vitamin E transport to the liver and subsequent transport to the other tissues.