Effects of vitamin restriction and supplementation on rat intestinal epithelial cell apoptosis
- 作者：Vijayalakshhmi ; Bodiga ; Sesikeran ; Boindala ; Udaykumar ; Putcha ; Kalyanasundaram ; Subramaniam ; et. al.
- 关键词：Vitamin restriction ; Riboflavin ; Folic acid ; Vitamin E ; Oxidative stress ; Intestinal apoptosis ; Free radicals
- 刊名：Free Radical Biology and Medicine
- 出版年：2005
- 期刊代码：105_08915849
- 类别：med
- 出版时间：June 15, 2005
- 卷：38
- 期：12
- 页码：1614-1624
- 文件大小：1.59 M
摘要
Diet influences intestinal growth and function and vitamins modulate intestinal cell turnover. We have assessed the effects of chronic, moderate (50%of control) vitamin restriction and supplementation on intestinal epithelial cell (IEC) apoptosis and the relevance of this to alterations in tissue oxidative stress and antioxidant status. Feeding a vitamin-restricted diet to male, weanling WNIN rats for 20 weeks significantly increased IEC apoptosis, but only in the villi region, as evident from increased annexin V staining, M30 positivity, histological observations, DNA ladder formation, and reduced expression of Bcl-2. This was associated with elevated levels of lipid peroxides and protein carbonyls in the intestinal mucosa despite the increased activities of superoxide dismutase, catalase, and glutathione peroxidase. Consistent with the increased oxidative stress and apoptosis, structural and functional integrity of the villi were compromised as evident from the lowered ratio of villus height:crypt depth and the decreased activities of the membrane marker enzymes alkaline phosphatase and Lys-Ala dipeptidyl aminopeptidase. These changes were reversed by supplementation with a vitamin mixture or vitamin E alone, whereas riboflavin or folic acid supplementation reduced the apoptotic rates, but only partially. Further, oxidative stress was the least in vitamin E- or vitamin mixture-supplemented rats and correlated well with their IEC apoptotic rates. Increased tissue oxidative stress seems to mediate the vitamin-restriction-induced apoptosis of the IECs in rats.