کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2568990 1128502 2012 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cerebroside D, a glycoceramide compound, improves experimental colitis in mice with multiple targets against activated T lymphocytes
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Cerebroside D, a glycoceramide compound, improves experimental colitis in mice with multiple targets against activated T lymphocytes
چکیده انگلیسی

In the present paper, we aimed to examine the novel effects of cerebroside D, a glycoceramide compound, on murine experimental colitis. Cerebroside D significantly reduced the weight loss, mortality rate and alleviated the macroscopic and microscopic appearances of colitis induced by dexran sulfate sodium. This compound also decreased the levels of TNF-α, IFN-γ and IL-1β in intestinal tissue of mice with experimental colitis in a concentration-dependent manner, accompanied with markedly increased serum level of IL-10. Cerebroside D inhibited proliferation and induced apoptosis of T cells activated by concanavalin A or anti-CD3 plus anti-CD28 antibodies. The compound did not show an effect on naive lymphocytes but prevented cells from entering S phase and G2/M phase during T cells activation. Moreover, the treatment of cerebroside D led to apoptosis of activated T cells with the cleavage of caspase 3, 9, 12 and PARP. These results showed multiple effects of cerebroside D against activated T cells for a novel approach to treatment of colonic inflammation.

Figure optionsDownload high-quality image (141 K)Download as PowerPoint slideHighlights
► Cerebroside D, a glycoceramide compound, alleviated DSS induced colitis.
► The mechanism of the compound involved multiple effects against activated T cells.
► It regulated cytokine profiles in mice with experimental colitis.
► It prevented T cells from entering S and G2/M phases during activation.
► It led to apoptosis of activated T cells with the cleavage of caspases and PARP.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology and Applied Pharmacology - Volume 263, Issue 3, 15 September 2012, Pages 296–302
نویسندگان
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