Author/Authors :
Bılıcı, Muammer Department of Internal Medicine - Bulent Ecevit University School of Medicine, Esenköy, Kozlu, Zonguldak, Turkey , Ilker Oz, Ibrahim Department of Radiology - Bulent Ecevit University School of Medicine, Esenköy, Kozlu, Zonguldak, Turkey , Ilıkhan, Sevil Uygun Department of Internal Medicine - Bulent Ecevit University School of Medicine, Esenköy, Kozlu, Zonguldak, Turkey , Borazan, Ali Department of Nephrology - Bulent Ecevit University School of Medicine, Esenköy, Kozlu, Zonguldak, Turkey
Abstract :
Introduction. This study aimed to investigate the effects of
erythropoiesis-stimulating agents (ESAs) on intestinal flora in
peritoneal fibrosis.
Methods and Methods. Twenty-four Wistar albino rats were divided
into 3 groups as the control group, which received 0.9% saline
(3 mL/d) intraperitoneally; the chlorhexidine gluconate (CH) group,
which received 3 mL/d injections of 0.1% CH intraperitoneally,
and the ESA group, which received 3 mL/d injections of 0.1%
CH intraperitoneally and epoetin beta (3 doses of 20 IU/kg/wk)
subcutaneously. On the 21st day, the rats were sacrificed and the
visceral peritoneum samples were obtained from left liver bowel.
Blood samples were obtained from abdominal aorta and intestinal
flora samples were obtained from transverse colon.
Results. Histopathologically, the CH, ESA, and control groups had
peritoneal thickness of 135.4 ± 22.2 µm, 48.6 ± 12.8 µm, and 6.0 ± 2.3
µm, respectively. Escherichia coli was the predominant bacterium
in the intestinal flora in the control group. Significant changes in
microbial composition of intestinal flora towards Proteus species
and Enterobacter species was seen among the groups (P < .001).
There was no significant difference between the ESA and CH
groups regarding the isolates from blood cultures. However, the
bacterial isolates from cultures of intestinal flora among these
groups were significantly different (P < .05).
Conclusions. Erythropoiesis-stimulating agents change intestinal
flora by a clinically significant amount in experimental peritoneal
fibrosis. We consider that ESAs achieve this via regulating intestinal
peristaltism.