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Editorial [Hot Topic: Drug Metabolisms Associated with Human Microbiome (Guest Editor: Chun-Ming Huang) ]

机译:社论[热门话题:与人类微生物组有关的药物代谢(来宾编辑:黄春明)]

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摘要

The human microbiome contains all of the genomes or proteomes, of all the microorganisms present in or on the human body [1, 2]. With increasing interest in the understanding of the association of human microbome with diseases, this special issue is focused specifically on diseases caused by the alteration in human microbiome. The biological mechanisms and pharmacokinetics of various drugs are also included. In addition, this issue also introduces some novel modalities or concepts for treatments of human microbome-related diseases.nnTwo papers, by Matthew E. Falagas and his colleagues, in this issue exemplify the pharmacokinetic/pharmacodynamic aspects of linezolid and tigecycline, two antibiotics for human bacterial infections including community-acquired and nosocomial pneumonia, skin and soft tissue infections, and infections due to vancomycin-resistant enterococci. The paper, by Anja Sandek and coworkers, discusses the gut and intestinal bacteria in chronic heart failure and suggest that the gut may pose a potential target for therapeutic interventions in patients with chronic heart failure. The paper, by Minoru Fukuda and his coworkers, demonstrated their recent findings of inhibition of cholesterol alphaglucosyltransferase by mucin-type O-glycans. The finding illustrates that a battery of carbohydrates expressed in the stomach is closely associated with pathogenesis and prevention of Helicobacter pylori-related diseases. The paper, by Doris M. Jacobs and coworkers, reviews the metabolomics studies with a focus on microbe-host mutualism and concludes that metabolomics holds great potential to better understand the fate of non-digestible food ingredients on gut health and immunity.nnKeith L. Kirkwood and Carlos Rossa, Jr. discuss the importance of the p38 MAPK pathway in periodontal disease progression and the potential therapeutic consequences of pharmacological antagonism of this pathway in the treatment of periodontal diseases. The paper, by Maria Carmen Collado and coworkers, introduces new evidences support the use of probiotics in the prevention and treatment of many human diseases including atopic diseases, immune disorders, obesity, and diabetes. Andrea M Stringer and his colleagues explore the potentially vital connection between intestinal microflora and the subsequent development of chemotherapy-induced mucositis. Benjamin J. Vesper and his colleagues summarize current advancements in the interactions between the proton pump inhibitors and the natural human microbiota. In this paper of Huang Chun-Ming Eric and his coworkers, novel modalities using vaccination and photodynamic therapies for oral microbialrelated diseases are introduced. The advantages of novel modalities are highlighted and compared with antimicrobial agents and traditional periodontal surgery.nnWe hope you enjoy reading these papers as we did. Special thanks must go to our reviewers for this special issue.
机译:人类微生物组包含存在于人体中或人体上的所有微生物的所有基因组或蛋白质组[1、2]。随着人们对人类微生物组与疾病之间关系的理解的兴趣日益浓厚,这个特殊问题专门针对人类微生物组变化引起的疾病。还包括各种药物的生物学机制和药代动力学。此外,本期还介绍了一些治疗人类微生物相关疾病的新颖方法或概念。nnMatthew E. Falagas和他的同事发表的两篇论文举例说明了利奈唑胺和替加环素这两种抗生素的药代动力学/药效学方面。人类细菌感染,包括社区获得性和医院内肺炎,皮肤和软组织感染以及耐万古霉素的肠球菌引起的感染。由Anja Sandek及其同事共同撰写的论文讨论了慢性心力衰竭中的肠道和肠道细菌,并建议肠道可能成为慢性心力衰竭患者治疗干预的潜在目标。 Minoru Fukuda及其同事的论文证明了他们最近对粘蛋白型O聚糖抑制胆固醇α-葡萄糖基转移酶的发现。这一发现说明,胃中表达的一系列碳水化合物与幽门螺杆菌相关疾病的发病机理和预防密切相关。多里斯·雅各布斯(Doris M.Jacobs)及其同事撰写的这篇论文回顾了以代谢物组学为研究重点的微生物与宿主的共生关系,并得出结论认为,代谢组学具有巨大的潜力,可以更好地理解不可消化食品成分对肠道健康和免疫力的影响。 Kirkwood和Carlos Rossa,Jr.讨论了p38 MAPK途径在牙周疾病进展中的重要性以及该途径的药理拮抗作用在牙周疾病治疗中的潜在治疗后果。玛丽亚·卡门·科拉多(Maria Carmen Collado)及其同事撰写的这篇论文介绍了新的证据,证明了益生菌在预防和治疗许多人类疾病中的应用,包括特应性疾病,免疫疾病,肥胖症和糖尿病。安德里亚·斯特林格(Andrea M Stringer)和他的同事们探索了肠道菌群与化学疗法诱发的粘膜炎随后发展之间潜在的重要联系。本杰明·韦斯珀(Benjamin J. Vesper)和他的同事总结了质子泵抑制剂与天然人类微生物群之间相互作用的最新进展。在黄春明和他的同事的论文中,介绍了使用疫苗和光动力疗法治疗口腔微生物相关疾病的新方法。我们强调了新型方法的优势,并将其与抗菌剂和传统的牙周手术进行了比较。nn我们希望您像我们一样喜欢阅读这些论文。对于这个特殊问题,必须特别感谢我们的审稿人。

著录项

  • 来源
    《Current Drug Metabolism》 |2009年第1期|p.1-1|共1页
  • 作者

    Huang Chun-Ming;

  • 作者单位

    Department of Medicine, Division of Dermatology University of California San Diego, Rm2317A 3350 La Jolla Village San Diego, CA, 92161 USA.;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
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