Programmed cell death in rat intestine: Effect of feeding and fasting

Citation
R. Iwakiri et al., Programmed cell death in rat intestine: Effect of feeding and fasting, SC J GASTR, 36(1), 2001, pp. 39-47
Citations number
32
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
ISSN journal
00365521 → ACNP
Volume
36
Issue
1
Year of publication
2001
Pages
39 - 47
Database
ISI
SICI code
0036-5521(200101)36:1<39:PCDIRI>2.0.ZU;2-N
Abstract
Background: The regulation of intestinal cell death by luminal factors is p oorly understood. The objectives of this study were to determine whether a diurnal rhythm of intestinal apoptosis exists, and to determine the role th at feeding and fasting play in this process. Methods: Mucosal apoptotic dea th was measured in fed and 24-h fasted rats and at various times after feed ing by DNA fragmentation and in situ immunohistochemical staining (TUNEL). Results: In 24-h fasted rats, 32% of total mucosal DNA was fragmented as co mpared to 9% in fed animals. In both jejunal and ileal segments, the fragme nted DNA exhibited characteristic apoptotic DNA ladders on agarose gels. Im munohistochemical staining revealed significant location of apoptotic cells at the upper third of the intestinal villus. In the duodenum, DNA fragment ation at 6-12h post feeding was 20% and decreased to 4% at 24 h. In compari son, DNA fragmentation in the jejunum and ileum was low from 0 to 6 h post feeding (2%-9%) and significantly increased at 12 h (18% versus 12%) and 24 h (30% versus 32%), respectively. These results are consistent with a temp oral relationship between percent fragmented DNA and time after feeding wit h greater cell death at longer fasting period. A postprandial rhythm of DNA fragmentation was evident in the jejunum and ileum, in which fragmentation was at a peak between 0900 h and 1200 h. Conclusion: Collectively, the dat a show that initiation of apoptosis in apical enterocytes is coincident wit h cessation of feeding and commencement of fasting, and is consistent with a rhythm of programmed cell death in these cells that parallels the cyclica l pattern of feeding and fasting.