摘要
目的 研究生药厚朴提取物(MOCE)及其主要成分厚朴酚与和厚朴酚对于常见口腔致病菌生长和黏附的影响。方法 选取2种致龋菌和2种牙周病致病菌作为实验菌株,用杯碟法和溶液稀释法分别考察其对4种口腔致病菌的最小抑菌浓度(MIC)和最小杀菌浓度(MBC),并考察杀菌速率;另建立黏附实验模型,考察药物对于致龋菌的黏附抑制作用,及其对已形成黏附的脱附作用。结果 MOCE对于4种实验菌株的MIC、MBC值均小于100 μg·mL-1,而且具有突出的速效杀菌特点:1 mg·mL-1MOCE 30 s内速效杀菌达99%以上,在MBC浓度下仅5 min 即已表现出明显杀菌作用(>90%);对于致龋菌的黏附抑制,最小有效浓度为6.25~25 μg·mL-1(随菌种的不同而不同),且该浓度下对已形成的黏附具有脱附作用。结论 MOCE对4种口腔致病菌的生长具有较强抑制作用,速效杀菌,并对致龋菌的黏附具有抑制形成和促进瓦解的双效作用,在口腔用药和保健领域具有重要价值。
Abstract
OBJECTIVE To evaluate the antimicrobial properties of Magnoliae officinalis(MOCE) Cortex extract and its main components, magnolol and honokiol against two cariogenic bacteria strains and two periodontal pathogens. METHODS The minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) against each strain were determined by both cylinder-plate and broth-microdilution METHODS, and bactericidal rate, bacteria adhesion inhibition and bacteria desorption rates were measured by our experimental models. RESULTS The MIC and MBC of MOCE and its two main components against each strain were all less than 100 μg·mL-1, and the minimum effective concentrations for adhesion inhibition and desorption of two cariogenic bacteria were 6.25 and 25 μg·mL-1, respectively. Incubation of the bacteria with MOCE solution at 1 mg·mL-1 killed more than 99% of the test strains in 30 s. The extract at MBC against each strain also showed significant bacteriocidal effect in 5 min (>90%). CONCLUSION Our studies provided experimental evidence for further development and application of MOCE in the field of oral care.
关键词
厚朴 /
致龋菌 /
牙周病致病菌 /
厚朴酚 /
和厚朴酚
{{custom_keyword}} /
Key words
Magnoliae officinalis Cortex /
cariogenic bacteria /
periodontal pathogens /
magnolol /
honokiol
{{custom_keyword}} /
殷其蕾 刘勇 詹先王 韩南银 李金陆 杨圣辉.
厚朴提取物对于4种常见口腔致病菌生长和黏附的作用[J]. 中国药学杂志, 2011, 46(17): 1356-1361
YIN Qi-lei;LIU Yong;ZHN Xin-wng;HN Nn-yin;LI Jin-lu;YNG Sheng-hui.
Evaluation of the Antimicrobial Properties of Magnoliae officinalis Cortex Extract and Its Main Components Against Four Oral Pathogenic Bacteria[J]. Chinese Pharmaceutical Journal, 2011, 46(17): 1356-1361
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] Ch. P (2010) Vol Ⅰ(中国药典2010版一部) [S]. 2010:235.
[2] WANG Z Q, BING W, LIU X B, et al. The in vitro growth-inhibitory effect of Magnolia officinalis [J].Lishizhen Med Mater Med Res(时珍国医国药), 2007,18(11): 2763.
[3] JI C X, JIAO L, ZHU W J, et al. Study of bacteriostatic effect of Cortex Magnolia officinalis [J].J Henan Agric(河南农业), 2010, 8(4): 50.
[4] PARK J, LEE J, JUNG E, et al. In vitro antibacterial and anti-inflammatory effects of honokiol and magnolol against Propionibacterium sp. [J]. Eur J Pharmacol, 2004, 496(1): 189-195.
[5] WANG L Q, JIANG R G, CHEN H F. Progresses of studies on the pharmacological activities of magnolol and honokiol [J].Chin Tradit Herb Drugs(中草药), 2005, 36(10): 155-158.
[6] LIU Y K, DONG Z, ZHU Y. Review of the studies on the pharmacological activities of magnolol and honokiol [J].Chin Tradit Pat Med(中成药), 2006, 28(5): 716-718.
[7] ZHU C L, LI Y M. Inhibition of extracts from 17 Chinese herbs on periodontal pathogenic microbes [J].Shanghai J Stomatology(上海口腔医学), 2006,15(4): 434-436.
[8] TANAKA K, HASEWAKA J, ASAMITSU K, et al. Magnolia ovovata extract and its active component magnolol prevent skin photoaging via inhibition of nuclear factor kappa B [J].Eur J Pharmacol, 2007, 565(1-3): 212-219.
[9] LIN Y R, CHEN H H, KO C H, et al. Effects of honokiol and magnolol on acute and inflammatory pain models in mice [J].Life Sci, 2007, 81(13): 1071-1078.
[10] YI L T, XU Q, LI Y C, et al. Antidepressant-like synergism of extracts from magnolia bark and ginger rhizome alone and in combination in mice [J].Prog Neuro Psycho Pharmacol Biol Psychiatry, 2009, 33(4): 616-624.
[11] SHEN C C, NI C L, SHEN Y C, et al. Phenolic constituents from the stem bark of Magnolia officinalis [J].J Nat Prod, 2009, 72(1): 168-171.
[12] LI N, SONG Y, ZHANG W, et al. Evaluation of the in vitro and in vivo genotoxicity of magnolia bark extract [J].Regul Toxicol Pharmaco, 2007, 49(3): 154-159.
[13] UENG T H, KANG J J, WANG H W, et al. An overview of the toxicology of commonly used traditional Chinese medicine [J]J Food Drug Anal, 1997, 5(14): 241-264.
[14] KUO L C, POLSON A M, KANG T. Associations between periodontal diseases and systemic diseases: a review of the inter-relationships and interactions with diabetes, respiratory diseases, cardiovascular diseases and osteoporosis [J]. Public Health, 2008, 122(4): 417-433.
[15] KU L B, ZHU J H. Relationship between postmenopausal osteoporosis and periodontitis [J]. Heilongjiang J Med Pharm(黑龙江医药科学), 2008, 31(6): 59-60.
[16] MENG H X. Association between periodontitis and diabetesmellitus [J].J Peking Univ(Heal Sci)(北京大学学报:医学版), 2007, 39(1): 18-20.
[17] REN L, YANG S H, GUO M Y. Bacteriostasis of tea to oral commen pathogenic bacteria [J]. Beijing J Dent(北京口腔医学), 2003, 11(2):91-94.
[18] HAMADA S, TORII M, KOTANI S, et al. Adherence of streptococcus sanguis clinical isolates to smooth surfaces and interactions of the isolates with streptococcus mutans glucosyltransferase [J].Infect Immun, 1981, 32(1): 364-372.
[19] ZHANG H Y, DONG L Y, YANG L, et al. Rubrus Suarissimus S. Lee Saponin effects on adhering of streptococcus mutans[J]. J Clin Stomatol(中国微生态学杂志), 2009, 21(2):251-253.
[20] ZHAO J, LI Y, SUN Y L, et al. The effects of turkish gall on adherence of Streptococcus mutans and Actinomyces viscosus to salivary acquired pellicle[J]. J Xinjiang Med Uni(新疆医科大学学报), 2009, 32(1): 6-8.
[21] WANG S H, FAN M W, BIAN Z. Experimental study of bacteriostatic activity of Chinese herbal medicines on primary cariogenic bacteria in vitro[J].Chin J Stomatol(中华口腔医学杂志), 2001, 36(5): 68-70.
[22] HUANG B B, FAN M W, YANG X L, et al. Effects of Chinese traditional herbs on growth of periodontopathic bacteria[J]. J Fourth Mil Med Univ(第四军医大学学报), 2003, 24(5): 424-426.
[23] FENG J, LI J Y, ZHOU X D. Effects of the active compounds of M. officinalis on cariogenic bacteria [J]. J Sichuan Univ (Med Sci Edi)(四川大学学报:医学版), 2007, 38(3): 456-458.
[24] GREENGERG M, DODDS M, TIAN M. Naturally occurring phenolic antibacterial compounds show effectiveness against oral bacteria by a quantitative structure-activity relationship study[J]. J Agric Food Chem, 2008, 56(23): 11151-11156.
[25] ZHOU X D, SHI W Y. Human oral microbial community and dental plaque biofilm [J]. West Chin J Stomatol(华西口腔医学杂志), 2010, 28(2): 115-118.
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}