Dietary Supplementation with Tocotrienols Enhances Immune Function in C57BL/6 Mice  

Oleh:

Ren, Zhihong ; Pae, Munkyong ; Dao, Maria Carlota

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: JN: The Journal of Nutrition vol. 140 no. 07 (Jul. 2010), page 1335-1341.
Topik: IMMUNE FUNCTION; DIETARY SUPPLEMENTATION; TOCOTRIENOLS

Ketersediaan

Perpustakaan FK Nomor Panggil: J42.K.2010.02 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

{alpha}-Tocopherol ({alpha}-Toc) enhances T cell function, whereas little is known in this regard for tocotrienols (T3), the less-known members of the vitamin E family. We pair-fed young (4 mo) and old (23 mo) C57BL/6 mice 0.1% Tocomin 50%, a mixture of T3 and {alpha}-Toc or a control diet containing an equal amount of {alpha}-Toc for 6 wk. As expected, lymphocyte proliferation was lower in the old mice compared with the young mice. Lymphocyte proliferation in the old T3 group was significantly higher than that in the old control group, whereas no significant difference was found in young mice. Splenocytes from old mice produced less interleukin (IL)-2, IL-4, IL-6, and IL-10 compared with young mice, whereas no significant age-related difference was found in IL-1ß, tumor necrosis factor-{alpha}, and interferon-{gamma}. T3 feeding was associated with a higher IL-1ß production in old mice but not in young mice. Peritoneal macrophages from old mice produced significantly more IL-1ß, IL-6, IL-10, and prostaglandin E2 (PGE2) compared with those from young mice. Mice of both ages fed T3 had higher production of IL-1ß but not PGE2 or other cytokines. In the in vitro study, splenocytes isolated from young and old mice were supplemented with the purified form of each individual T3 (0.01–10 µmol/L) and mitogen-stimulated cell proliferation was determined. All T3 enhanced lymphocyte proliferation in old but not young mice with a potency order of {alpha}- > {gamma}- > {delta}-T3. Together, these results suggest a beneficial effect of T3 in improving the age-related decline in T cell function.

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