2.In vitro and in vivo anti-Helicobacter pylori activities of FEMY-R7 composed of fucoidan and evening primrose extract.
Jingmei CAI ; Tae Su KIM ; Ja Young JANG ; Jihyun KIM ; Kyungha SHIN ; Sung Pyo LEE ; Ehn Kyoung CHOI ; Sa Hyun KIM ; Min PARK ; Jong Bae KIM ; Yun Bae KIM
Laboratory Animal Research 2014;30(1):28-34
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 (1x10(8) 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 microg/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 microg/mL. In vivo elimination study, male C57BL/6 mice were infected with the bacteria by intragastric inoculation (5x10(9) 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.
Animals
;
Bacteria
;
Gastric Mucosa
;
Helicobacter pylori
;
Homicide
;
Humans
;
Hydrogen-Ion Concentration
;
Male
;
Mice
;
Oenothera biennis*
;
Urease
3.Erratum: In vitro and in vivo anti-Helicobacter pylori activities of FEMY-R7 composed of fucoidan and evening primrose extract.
Jingmei CAI ; Tae Su KIM ; Ja Young JANG ; Jihyun KIM ; Kyungha SHIN ; Sung Pyo LEE ; Ehn Kyoung CHOI ; Sa Hyun KIM ; Min PARK ; Jong Bae KIM ; Yun Bae KIM
Laboratory Animal Research 2015;31(2):99-99
As the request of the authors, Acknowledgments section has been changed.
Oenothera biennis*
4.Physical Activity Patterns and Their Associated Factors Measured by Global Physical Activity Questionnaire Survey among Korean
Kyungha MIN ; Yun Hwan OH ; Sun Woo KIM ; Ho Jun KIM ; Houbuem LEE ; Sung Ha LEE ; Sunyoung KIM ; Jeong Sang LEE ; Jong Seung KIM ; Bumjo OH
The Korean Journal of Sports Medicine 2020;38(1):1-11
Research on physical activity and health is actively being conducted. In the Korea National Health and Nutrition Examination Survey (KNHANES), the Global Physical Activity Questionnaire (GPAQ) was newly introduced in 2014. The purpose of this study was to investigate the levels of physical activity and related factors in Koreans who were assessed through the GPAQ by dividing the physical activity by occupation, leisure, and transport domain. This study used data from the KNHANES (2014–2016), the study population of which included 17,357 participants aged 12 to 80 years. We compared the differences in physical activity by sociodemographic factors, health-related factors, and psychological health-related factors. Moreover, we also compared the mean metabolic equivalent of task and daily sitting time according to physical activity domain by sex and age group. Finally, we investigated the sociodemographic factors, health-related factors, and psychological health-related factors that significantly affect the average physical activity per week. The various factors were found to differ in the frequency of physical activity levels. In addition, there was a difference in the amount of physical activity per occupation, leisure, and transport domain in each age group. Finally, age, sex, high-density lipoprotein cholesterol levels, arthritis, allergic rhinitis and sinusitis, sleeping time, and perceived health status significantly affected physical activity. The levels of physical activity significantly differed by sociodemographic factors, health-related factors, and psychological health-related factors. There was also a difference in the physical activity levels according to the age and sex per each domain of physical activity.
Arthritis
;
Cholesterol
;
Humans
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Korea
;
Leisure Activities
;
Lipoproteins
;
Metabolic Equivalent
;
Motor Activity
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Nutrition Surveys
;
Occupations
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Physical Fitness
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Public Health
;
Rhinitis, Allergic
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Risk Factors
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Sinusitis
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Social Determinants of Health
;
Surveys and Questionnaires
5.Anti-atherosclerotic effects of perilla oil in rabbits fed a high-cholesterol diet.
Yeseul CHA ; Ja Young JANG ; Young Hwan BAN ; Haiyu GUO ; Kyungha SHIN ; Tae Su KIM ; Sung Pyo LEE ; Jieun CHOI ; Eun Suk AN ; Da Woom SEO ; Jung Min YON ; Ehn Kyoung CHOI ; Yun Bae KIM
Laboratory Animal Research 2016;32(3):171-179
Anti-atherosclerosis effects of perilla oil were investigated, in comparison with lovastatin, in rabbits fed a high-cholesterol diet (HCD). Hypercholesterolemia was induced in rabbits by feeding the HCD containing 0.5% cholesterol and 1% corn oil, and perilla oil (0.1 or 0.3%) was added to the diet containing 0.5% cholesterol for 10 weeks. HCD greatly increased blood total cholesterol and low-density lipoproteins, and caused thick atheromatous plaques, covering 74% of the aortic wall. Hyper-cholesterolemia also induced lipid accumulation in the liver and kidneys, leading to lipid peroxidation. Perilla oil not only attenuated hypercholesterolemia and atheroma formation, but also reduced fat accumulation and lipid peroxidation in hepatic and renal tissues. The results indicate that perilla oil prevents atherosclerosis and fatty liver by controlling lipid metabolism, and that it could be the first choice oil to improve diet-induced metabolic syndrome.
Atherosclerosis
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Cholesterol
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Corn Oil
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Diet*
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Fatty Liver
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Hypercholesterolemia
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Kidney
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Lipid Metabolism
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Lipid Peroxidation
;
Lipoproteins, LDL
;
Liver
;
Lovastatin
;
Perilla*
;
Plaque, Atherosclerotic
;
Rabbits*