Home LiteratureArticle Details
PMID: 2065918 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Circadian rhythm of cellular proliferation in the human rectal mucosa.

Gastroenterology ·Vol. 101 ·No. 2 ·1991-08-00 ·Pages 410-5

Buchi KN, Moore JG, Hrushesky WJ, Sothern RB, Rubin NH

Abstract

Circadian rhythms of DNA synthesis and cellular proliferation in the gastrointestinal mucosa have been well documented in animal models. This investigation was designed to determine whether similar rhythms could be demonstrated in the human rectal epithelium: 24 studies were performed in 16 healthy men under fasting (n = 14) and fed (n = 10) conditions. Rectal mucosal biopsy specimens were obtained through a proctoscope every 2 or 3 hours for a 24-hour span. Ex vivo measurements of tritiated thymidine incorporation into DNA were made on the mucosal samples. Feeding and time of day were each found to have an effect on the rate of thymidine incorporation into the DNA of rectal mucosal cells. Both fasted and fed subjects showed significant circadian rhythms in thymidine incorporation, which peaked at about 7 AM. Fasting lowered the overall mean thymidine uptake without altering the rhythm. Thymidine uptake generally reflects the amount of DNA synthesis in the sampled tissue. Therefore, these data may be important in the design of cancer chemotherapeutic regimens that use drugs specifically active during DNA synthesis.

MeSH Terms
Adult Analysis of Variance Biopsy Cell Division/physiology Circadian Rhythm/physiology DNA/biosynthesis Humans Intestinal Mucosa/cytology Male Rectum/cytology,pathology
Chemicals
DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Buchi K N
Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City.
Moore J G
Hrushesky W J
Sothern R B
Rubin N H
Article Info
Journal
Gastroenterology
Abbr.
Gastroenterology
ISSN
0016-5085
Published
1991-08-00
Pages
410-5
Language
English
Region
United States
NLM ID
0374630
Subset
IM
Grants
PHS HHS · R01-31635-06 · United States
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