Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1990 Oct;54(4):477-86.

A morphometric study of the canine colon: comparison of control dogs and cases of colonic disease

Affiliations
Comparative Study

A morphometric study of the canine colon: comparison of control dogs and cases of colonic disease

M T Spinato et al. Can J Vet Res. 1990 Oct.

Abstract

The microstructure of the canine colon was described morphometrically. The artifacts induced by administration of enemas and biopsy technique were studied by comparing biopsy specimens to tissues obtained at necropsy from 15 normal dogs. Biopsies from control dogs and clinical cases of colonic disease were then evaluated quantitatively, and histological abnormalities which might clarify mechanisms underlying large bowel dysfunction in the dog were sought. In control dogs, gland length and diameter, epithelial, goblet cell and mucosal mast cell numbers, and intraepithelial lymphocyte and mitotic indices were remarkably uniform throughout the colon. Minor variations were found in the proximal and distal regions of the colon. An apparent shortening of glands, and a reduction in mucous goblets and intraepithelial lymphocytes in biopsies were attributed to suboptimal orientation and irritation caused by enemas. The only significant difference from controls identified by morphometric analysis of biopsies from clinical cases was fewer epithelial cells lining longitudinal sections of glands. It was concluded that failure to identify morphometric variations in the colonic mucosa of clinical cases might reflect either a biased, homogeneously mild clinical syndrome in this group, or the possibility that in many of the clinical cases, a functional rather than physical abnormality was involved. The proprial inflammatory cell population was not examined quantitatively; further investigation of this component is merited.

PubMed Disclaimer

Similar articles

References

    1. Gut. 1973 Sep;14(9):701-10 - PubMed
    1. J Anat. 1972 Nov;113(Pt 2):169-78 - PubMed
    1. Am J Dig Dis. 1977 Jun;22(6):485-96 - PubMed
    1. Virchows Arch B Cell Pathol. 1979 Feb 6;29(4):351-61 - PubMed
    1. J Clin Pathol. 1980 Feb;33(2):125-30 - PubMed

Publication types

MeSH terms

LinkOut - more resources