Literature DB >> 6333551

An analysis of creatine phosphokinase in the mucosa and the muscularis of the gastrointestinal tract.

G M Graeber, P J Cafferty, R E Wolf, J W Harmon.   

Abstract

Previous work has shown that mesenteric infarction causes elevation of total serum creatine phosphokinase (CPK) and each of its three isoenzymes. The exact origin of the CPK has not been determined. Little is known about the actual tissue distribution of CPK in bowel. Experiments were performed to confirm the expectation that CPK was present in the bowel wall and to determine its concentration and the distribution of CPK isoenzymes in the muscularis and mucosa, respectively. Multiple segments were resected from the esophagus, stomach, duodenum, jejunum, ileum, and the proximal and distal colon of normal dogs. The mucosa (MUC) was separated from the seromuscular (MSL) tissue in each of the segments and 1-g samples were analyzed individually for total CPK activity by spectrophotometric analysis and for isoenzyme distribution by agarose gel electrophoresis. The results show that all three isoenzymes of CPK are present throughout the GI tract and that the majority of CPK found is in the MSL. Hence, elevations in serum CPK associated with injuries to the GI tract suggest seromuscular injury. While no isoenzyme is located specifically in the bowel, certain associations were seen. CPK-MM, presumably from striated muscles, was most prevalent in the esophagus. In other portions of the bowel all three isoenzymes were present almost equally. In the mucosa the levels of CPK-MM and CPK-BB always exceeded the level of CPK-MB. Knowledge of the distribution of CPK and its isoenzymes in bowel provides a framework for studying and interpreting serum levels of CPK during bowel injury.

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Year:  1984        PMID: 6333551     DOI: 10.1016/0022-4804(84)90203-8

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  4 in total

1.  Potential of magnetic resonance spectroscopy in assessing the effect of fatty acids on inflammatory bowel disease in an animal model.

Authors:  Sonal Varma; Michael N A Eskin; Ranjana Bird; Brion Dolenko; Jayadev Raju; Omkar B Ijare; Tedros Bezabeh
Journal:  Lipids       Date:  2010-08-19       Impact factor: 1.880

2.  Serum enzyme levels during intestinal ischemia.

Authors:  J S Thompson; L E Bragg; W W West
Journal:  Ann Surg       Date:  1990-03       Impact factor: 12.969

3.  Creatine kinase isoenzymes in the diagnosis of intestinal infarction.

Authors:  M W Fried; U K Murthy; S R Hassig; J Woo; R P Oates
Journal:  Dig Dis Sci       Date:  1991-11       Impact factor: 3.199

4.  Detection of inflammatory bowel disease by proton magnetic resonance spectroscopy (1H MRS) using an animal model.

Authors:  Sonal Varma; Ranjana Bird; Michael Eskin; Brion Dolenko; Jayadev Raju; Tedros Bezabeh
Journal:  J Inflamm (Lond)       Date:  2007-11-26       Impact factor: 4.981

  4 in total

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