Morphological and physiological changes in the small intestine of the dog after its partial resection

1958 ◽  
Vol 46 (4) ◽  
pp. 1261-1265 ◽  
Author(s):  
N. P. Bochkov
1996 ◽  
Vol 271 (2) ◽  
pp. G347-G356 ◽  
Author(s):  
B. D. Dodson ◽  
J. L. Wang ◽  
E. A. Swietlicki ◽  
D. C. Rubin ◽  
M. S. Levin

After partial resection, the remnant small intestine undergoes an adaptive response. Little is known about the molecular and cellular basis of intestinal adaptation. To identify genes transcriptionally regulated in response to loss of functional bowel surface area, we have isolated cDNAs differentially expressed in the adaptive ileum 48 h after 70% proximal small intestinal resection. A cDNA library constructed from the remnant ileum of rats subjected to resection was screened using subtractive hybridization techniques. Several groups of cDNA clones that were induced during intestinal adaptation were isolated. The first included liver fatty acid binding protein, apolipoprotein A-IV, cellular retinol binding protein II, and ileal lipid binding protein. These all encode proteins involved in the absorption, metabolism, and trafficking of nutrients. A second group included the catalytic subunit of protein phosphatase 1 delta, a 78-kDa glucose-regulated protein (grp 78; a glucose-regulated member of the 70-kDa heat-shock protein family), and several pancreatitis-associated proteins. A third group of induced genes contained novel cDNAs. To better characterize the adaptive response, the temporal, spatial, and cellular patterns of expression of several of these genes were analyzed with the use of immunohistochemical and in situ hybridization techniques. These studies indicate that during early adaptation, genes involved in nutrient trafficking, protein processing, and cell cycle regulation are transcriptionally regulated in the residual small intestine in distinct temporal and regional patterns consistent with a complex multifaceted response to intestinal resection.


2009 ◽  
Vol 87 (12) ◽  
pp. 1255-1267 ◽  
Author(s):  
Cécile Helmstetter ◽  
Robert K. Pope ◽  
Mathieu T’Flachebba ◽  
Stephen M. Secor ◽  
Jean-Hervé Lignot

The gastrointestinal tract of Burmese pythons ( Python molurus (L., 1758)) exhibits large morphological and physiological changes in response to feeding and extended periods of fasting. In this study the mucosa of the stomach, small intestine, and colon were examined for changes in structure and cellular proliferation. The mucosa of fasting pythons exhibited low levels of cellular replication, but after feeding, cellular replication was evident as early as 12 h in the small intestine and colon and 24 h in the stomach. Replication peaked 3 days postfeeding for the small intestine and colon, but was still increasing at 6 days postfeeding in the stomach. Interestingly, cell proliferation was still evident after 45 days in the colon. In these tissues, a stock of “ready-to-use” primary lysosomes is found in the mucosal cells of fasting animals, whereas profound intracellular recycling is typical of animals that have been fed. These findings indicate that during the postprandial period, the intestinal mucosa undergoes extensive remodelling in anticipation of the next fasting and feeding period. One key adaptive factor for the python’s ability to cope with infrequent feeding is a well-prepared digestive system in fasting animals that can quickly start functioning again when food becomes available.


Digestion ◽  
1969 ◽  
Vol 2 (1) ◽  
pp. 23-34 ◽  
Author(s):  
I. Skála ◽  
V. Hromádková ◽  
J. Skála

1958 ◽  
Vol 193 (3) ◽  
pp. 516-520 ◽  
Author(s):  
M. R. Loran ◽  
T. L. Althausen

‘Partial’ resection of the small intestine in rats resulted in a disproportionately great impairment of absorption of vitamin A and several lasting anatomical and enzymatic changes. Anatomical changes consisted of a true hypertrophy of the remaining intestine, indicated by an increase in its wet and dry weight. Simple transection produced some increase in the weight of the intestine, and sham operation resulted in loss of intestinal tissue. Our interpretation of these data is that the stress of the abdominal operation results in loss of intestinal tissue, whereas actual removal of a section of the intestine releases a mechanism for restoration of lost tissue. Enzymatic changes after resection consisted of an increase in cholinesterase activity of the intestine and erythrocytes, which was not observed after simple transection or sham operation. All three groups of rats showed an increase in cholinesterase activity of the plasma. Our tentative conclusions from these data are: a) Regenerated intestinal tissue is capable of synthesizing cholinesterase. b) Disproportionately greater impairment of intestinal absorption of vitamin A after resection may be caused in part by a disequilibrium in the acetylcholine-cholinesterase system in favor of cholinesterase. c) Increase in the specific cholinesterase activity of the erythrocytes may be related to the mechanism responsible for the intestinal hypertrophy. d) Increase in the cholinesterase activity of the plasma is caused by the abdominal operation per se.


1997 ◽  
Vol 127 (7) ◽  
pp. 1297-1303 ◽  
Author(s):  
Joseph L. Wang ◽  
Deborah A. Swartz-Basile ◽  
Deborah C. Rubin ◽  
Marc S. Levin

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