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The GI tract normally hosts tens of
billions of bacteria (1 x 1011) per gram of digesta. When an
oral antimicrobial therapeutic regimen is initiated, the antimicrobial
agent cannot differentiate between gut pathogens and normal beneficial
bacteria in the gut. Consequently, these agents can selectively eliminate
portions of the normal gut bacterial populations.
A member of the lincosamide group of antibiotics, clindamycin is
excreted in the bile, thereby prompting a high concentration of the
drug in the GI tract. This can cause a an ecological disturbance in the
gut microflora, significantly reducing the number of anaerobic
microorganisms. Sullivan et al (2003) studied the impact of a
combination of Lactobacillus
F19, Bifidobacterium lactis,
and Lactobacillus acidophilus
on the gut microflora during oral clindamycin therapy.
In a double-blind study, 24 healthy, adult volunteers were randomized
into 2 groups and all received 150 mg of clindamycin orally, 4 times
daily for 7 days. The control group received 250mL of a yogurt product
twice daily for 14
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days. The treatment
group consumed a similar product containing 100 million (1 x 108)
cfu's per mL of acombination of Lactobacillus F19, Bifidobacterium lactis, and Lactobacillus acidophilus. Thus,
the daily administration of total bacteria equaled 50 billion (5 x 1010)
cfu's. Fecal samples were obtained from all volunteers before and
during the trial. Fecal samples were enumerated for different types of
bacteria.
Significant findings from the trial are shown in Figure 7. In the placebo group, both
the lactobacilli and the Bacteroides populations were
affected by clindamycin therapy. Lactobacilli decreasde 3 log numbers
by day 2 of the trial and Bacteroides
numbers dropped by 6 logs. In the treatment group, lactobacilli numbers
actually increased during clindamycin therapy, eventually decling to
pre-trial levels by the end of 21 days (7 days after the last probiotic
supplementation). Numbers of Bacteroides
remained constant for the treatment group. Thus, Lactobacillus F19 was instrumental
in preventing ecological disturbances of the intestinal Bacteroides fragilis-group species
during clindamycin administration.
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