Research
Beneficial Bacteria
Part 3
Chemopreventive effect of a probiotic preparation on the
development of preneoplastic and neoplastic colonic lesions:
an experimental study
Abstract
Hepato-Gastroenterology
Unit, Medical Science Department S. Giuseppe Hospital, Traditional
Medicine-WHO Center, University of Milan, Milan, Italy.
BACKGROUND/AIMS:
A number of studies have suggested a key role played by
certain resident gut bacteria in the development of large
bowel cancer. The aim of the present study was to test the
effect of a novel symbiotic preparation, which has been
recently shown to beneficially modify gut ecosystem and
systemic immunity, on either preneoplastic and neoplastic
changes in a colon carcinogenesis model. METHODOLOGY: Sprague-Dawley
rats were fed a standard diet for 1 week and then were randomly
assigned to three groups. The control diet was given to
groups A and B, whereas in group C, the same diet plus 2
mL of a probiotic mixture was given throughout the experiment.
Thirty rats (groups B, C) each received a weekly subcutaneous
injection of azoxymethane at a dose of 15 mg/kg of body
weight for 10 weeks. Group A served as a control group and
received a subcutaneous injection of saline for 10 weeks.
Forty-five rats were sacrificed at 3-week observation and
60 rats at 20-week observation for assessing metaphase index
together with aberrant crypt foci and intestinal immune
system markers from one hand and tumor occurrence from the
other, respectively. RESULTS: Group A showed a significantly
increased metaphase index either in aberrant crypt foci
or in "normal appearing" crypts when compared
to group A (p < 0.01). Group B rats caused a significant
decrease at both sites (p < 0.05). The numbers of lymphocytes
derived from the mesenteric lymph nodes in group B rats
were significantly decreased (p < 0.01) as compared to
either control and to group C. The percentage of CD8 lymphocytes
in group C was significantly higher than that in group B.
Group C showed a significantly reduced ratio of aberrant
crypt foci/colon and of aberrant crypt per colon and per
each single focus (p < 0.05). A total of 18 (90%) group
B and 10 (50%) group C rats had colon tumors, this difference
was significant. The mean number of colon tumors per rat
was 2.2 and 1.0 in group B and C, respectively. CONCLUSIONS:
Effective probiotics treatment, through mechanisms still
to be fully elucidated (decreased fecal pH, specific reduction
of carcinogenetic bacterial enzymes, modulation of gut-associated
and systemic immune system etc.) has the potential to exert
significant antimutagenic properties against colon cancer.
Reference:
Hepatogastroenterology.
2003 Nov-Dec;50(54):1914-8
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