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KMID : 1204320140300010028
Laboratory Animal Research
2014 Volume.30 No. 1 p.28 ~ p.34
In vitro and in vivo anti-Helicobacter pylori activities of FEMY-R7 composed of fucoidan and evening primrose extract
Cai Jingmei

Kim Tae-Su
Jang Ja-Young
Kim Ji-Hyun
Shin Kyung-Ha
Lee Sung-Pyo
Choi Ehn-Kyoung
Kim Sa-Hyun
Park Min
Kim Jong-Bae
Kim Yun-Bae
Abstract
Effects of FEMY-R7, composed of fucoidan and evening primrose extract, on the bacterial growth and intragastric infection of Helicobacter pylori as well as gastric secretion were investigated in comparison with a proton-pump inhibitor pantoprazole. For in vitro anti-bacterial activity test, H. pylori (1¡¿108 CFU/mL) was incubated with a serially-diluted FEMY-R7 for 3 days. As a result, FEMY-R7 fully inhibited the bacterial growth at 100 ¥ìg/mL, which was determined to be a minimal inhibitory concentration. In addition, 6-hour incubation with H. pylori, FEMY-R7 inhibited urease activity in a concentration-dependent manner, showing a median inhibitory concentration of 1,500 ¥ìg/mL. In vivo elimination study, male C57BL/6 mice were infected with the bacteria by intragastric inoculation (5¡¿109 CFU/mouse) 3 times at 2-day intervals, and simultaneously, orally treated twice a day with 10, 30 or 100 mg/kg FEMY-R7 for 7 days. In Campylobcter-like organism-detection test and bacterial identification, FEMY-R7 exerted a high bacteria-eliminating capacity at 30-100 mg/kg, comparably to 30 mg/kg pantoprazole. In contrast to a strong antacid activity of pantoprazole in a pylorus-ligation study, FEMY-R7 did not significantly affect gastric pH, free HCl, and total acidity, although it significantly decreased fluid volume at a low dose (10 mg/kg). The results indicate that FEMY-R7 eliminate H. pylori from gastric mucosa by directly killing the bacteria and preventing their adhesion and invasion, rather than by inhibiting gastric secretion or mucosal damage.
KEYWORD
Helicobacter pylori, FEMY-R7, fucoidan, evening primrose extract, minimal inhibitory concentration (MIC), CLO test, gastric secretion
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