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Chemically modified tetracyclines: The novel host modulating agents

Periodontal pathogens and destructive host responses are involved in the initiation and progression of periodontitis. The emergence of host response modulation as a treatment concept has resulted from our improved understanding of the pathogenesis of periodontal disease. A variety of drugs have been...

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Autores principales: Swamy, Devulapalli Narasimha, Sanivarapu, Sahitya, Moogla, Srinivas, Kapalavai, Vasavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555791/
https://www.ncbi.nlm.nih.gov/pubmed/26392682
http://dx.doi.org/10.4103/0972-124X.149934
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author Swamy, Devulapalli Narasimha
Sanivarapu, Sahitya
Moogla, Srinivas
Kapalavai, Vasavi
author_facet Swamy, Devulapalli Narasimha
Sanivarapu, Sahitya
Moogla, Srinivas
Kapalavai, Vasavi
author_sort Swamy, Devulapalli Narasimha
collection PubMed
description Periodontal pathogens and destructive host responses are involved in the initiation and progression of periodontitis. The emergence of host response modulation as a treatment concept has resulted from our improved understanding of the pathogenesis of periodontal disease. A variety of drugs have been evaluated as host modulation agents (HMA), including Non Steroidal Anti Inflammatory Drugs (NSAIDS), bisphosphonates, tetracyclines, enamel matrix proteins and bone morphogenetic proteins. Chemically modified tetracyclines (CMTs) are one such group of drugs which have been viewed as potential host modulating agents by their anticollagenolytic property. The CMTs are designed to be more potent inhibitors of pro inflammatory mediators and can increase the levels of anti inflammatory mediators.
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spelling pubmed-45557912015-09-21 Chemically modified tetracyclines: The novel host modulating agents Swamy, Devulapalli Narasimha Sanivarapu, Sahitya Moogla, Srinivas Kapalavai, Vasavi J Indian Soc Periodontol Review Article Periodontal pathogens and destructive host responses are involved in the initiation and progression of periodontitis. The emergence of host response modulation as a treatment concept has resulted from our improved understanding of the pathogenesis of periodontal disease. A variety of drugs have been evaluated as host modulation agents (HMA), including Non Steroidal Anti Inflammatory Drugs (NSAIDS), bisphosphonates, tetracyclines, enamel matrix proteins and bone morphogenetic proteins. Chemically modified tetracyclines (CMTs) are one such group of drugs which have been viewed as potential host modulating agents by their anticollagenolytic property. The CMTs are designed to be more potent inhibitors of pro inflammatory mediators and can increase the levels of anti inflammatory mediators. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4555791/ /pubmed/26392682 http://dx.doi.org/10.4103/0972-124X.149934 Text en Copyright: © Journal of Indian Society of Periodontology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Swamy, Devulapalli Narasimha
Sanivarapu, Sahitya
Moogla, Srinivas
Kapalavai, Vasavi
Chemically modified tetracyclines: The novel host modulating agents
title Chemically modified tetracyclines: The novel host modulating agents
title_full Chemically modified tetracyclines: The novel host modulating agents
title_fullStr Chemically modified tetracyclines: The novel host modulating agents
title_full_unstemmed Chemically modified tetracyclines: The novel host modulating agents
title_short Chemically modified tetracyclines: The novel host modulating agents
title_sort chemically modified tetracyclines: the novel host modulating agents
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555791/
https://www.ncbi.nlm.nih.gov/pubmed/26392682
http://dx.doi.org/10.4103/0972-124X.149934
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