Antimicrobial activities of ethanol and butanol fractions of white rose petal extract

被引:19
作者
Park, Dongsun [1 ]
Shin, Kyungha [1 ]
Choi, Youngjin [1 ]
Guo, Haiyu [1 ]
Cha, Yeseul [1 ]
Kim, Sa-Hyun [2 ]
Han, Nam Soo [3 ]
Joo, Seong Soo [4 ]
Choi, Jae Kwon [5 ]
Lee, Yoon Bok [5 ]
Choi, Ehn-Kyoung [1 ]
Kim, Jong Bae [6 ]
Kim, Yun-Bae [1 ]
机构
[1] Chungbuk Natl Univ, Coll Vet Med, 1 Chungdaero Gaesin Dong, Cheongju 28644, Chungbuk, South Korea
[2] Semyung Univ, Dept Biomed Lab Sci, Jecheon, South Korea
[3] Chungbuk Natl Univ, Dept Food Sci & Technol, Cheongju 28644, Chungbuk, South Korea
[4] Gangneung Wonju Natl Univ, Dept Marine Mol Biotechnol, Kangnung, South Korea
[5] Dr Chungs Food Co Ltd, Cent Res Inst, Cheongju, South Korea
[6] Yonsei Univ, Dept Biomed Lab Sci, Wonju, South Korea
基金
新加坡国家研究基金会;
关键词
White rose petal extract; Ethanol fraction; Butanol fraction; Antimicrobial activity; Helicobacter pylori; Propionibacterium acnes; GASTRIC-MUCOSAL INJURY; HELICOBACTER-PYLORI; ANTIFUNGAL ACTIVITY; HEXANE FRACTION; SECONDARY METABOLITES; CAMPYLOBACTER-PYLORI; FATTY-ACIDS; ANTIOXIDANT; FLOWER; FLUOROFAMIDE;
D O I
10.1016/j.yrtph.2016.01.011
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
White rose (Rosa hybrida) petals were extracted with ethanol (EtOH) or butanol (BuOH), and tested for their antimicrobial activities against two species of Gram-positive bacteria, six species of Gram-negative bacteria, and two species of fungi. On in vitro antimicrobial assays, Helicobacter pylori and Propionibacterium acnes were highly susceptible to white rose petal extract (WRPE)-EtOH and WRPE-BuOH, leading to minimal inhibitory concentrations of 100 and 10 mu g/mL for H. pylori and 400 and 40 mu g/mL for P. acnes, respectively. In in vivo experiments, C57BL/6 mice were infected with H. pylori by intragastric inoculation (1 x 10(8) CFU/mouse) 3 times, and orally treated twice a day for 14 days with WRPE-EtOH and WRPE-BuOH. On a CLO kit assay, 200 mg/kg of WRPE-EtOH fully eliminated the bacteria from the gastric mucosa, and the effect of 100 mg/kg of ethanol fraction was similar to pantoprazole (30 mg/kg), displaying 75% elimination. WRPE-BuOH was more effective, exhibiting 75% elimination at 20 mg/kg. The CLO test results were confirmed by bacterial identification. WRPE-EtOH and WRPE-BuOH inhibited the growth of various bacteria and fungi, and in particular, they effectively killed H. pylori and eliminated the bacteria from the mouse stomach. The results indicate that WRPE-EtOH and WRPE-BuOH could be good candidates for the elimination of H. pylori. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 47 条
[1]   Antifungal activity of fatty acids and their monoglycerides against Fusarium spp. in a laboratory medium [J].
Altieri, Clelia ;
Bevilacqua, Antonio ;
Cardillo, Daniela ;
Sinigaglia, Milena .
INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY, 2009, 44 (02) :242-245
[2]  
Borchardt JR, 2008, J MED PLANTS RES, V2, P81
[3]   Adrenomedullin modulates COX-2 and HGF expression in reserpine-injuried gastric mucosa in the rat [J].
Cantarella, G ;
Martinez, G ;
Cutuli, VM ;
Loreto, C ;
D'Alcamo, M ;
Prato, A ;
Amico-Roxas, M ;
Bernardini, R ;
Clementi, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 518 (2-3) :221-226
[4]   Protective effects of amylin on reserpine-induced gastric damage in the rat [J].
Cantarella, Gluseppina ;
Martinez, Giuseppa ;
Di Benedetto, Giulia ;
Loreto, Carla ;
Musumeci, Giuseppe ;
Prato, Agata ;
Lempereur, Laurence ;
Matera, Mario ;
Amico-Roxas, Matilde ;
Bernardini, Renato ;
Clementi, Giuseppe .
PHARMACOLOGICAL RESEARCH, 2007, 56 (01) :27-34
[5]   Comparison of the effects of pantoprazole enantiomers on gastric mucosal lesions and gastric epithelial cells in rats [J].
Cao, H ;
Wang, MW ;
Jia, JH ;
Wang, QH ;
Cheng, MS .
JOURNAL OF HEALTH SCIENCE, 2004, 50 (01) :1-8
[6]  
COGHLAN JG, 1987, LANCET, V2, P1109
[7]   HELICOBACTER-PYLORI AND GASTRODUODENAL DISEASE [J].
COVER, TL ;
BLASER, MJ .
ANNUAL REVIEW OF MEDICINE, 1992, 43 :135-145
[8]  
Dias PC, 2000, J ETHNOPHARMACOL, V69, P57, DOI 10.1016/S0378-8741(99)00133-6
[9]   Mechanisms by which endogenous glucocorticoid protects against indomethacin-induced gastric injury in rats [J].
Filaretova, L ;
Tanaka, A ;
Miyazawa, T ;
Kato, S ;
Takeuchi, K .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 283 (05) :G1082-G1089
[10]  
GRAHAM DY, 1989, J CLIN GASTROENTEROL, V11, pS43