Literature DB >> 24082703

Pleiotropy of chemically modified tetracycline in periodontitis.

Ashish Agarwal1.   

Abstract

Entities:  

Year:  2013        PMID: 24082703      PMCID: PMC3778596          DOI: 10.4103/0975-7406.116831

Source DB:  PubMed          Journal:  J Pharm Bioallied Sci        ISSN: 0975-7406


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Sir, The current layout for the biological domain map of chronic periodontitis indicates that the bacterial challenge activates immuno-inflammatory response, due to which a complex interplay of several matrix metalloproteinases (MMPs), cytokines, and prostaglandin (PGE2) activates and appear to destroy extracellular matrix material and activate bone resorption.[1] Host modulation therapy (HMT) is a strategy to reduce tissue destruction and stabilize the periodontium by modifying or downregulating destructive aspects of the host response and upregulating protective or regenerative responses is a recent and novel concept in periodontal therapy.[2] Chemically modified tetracycline (CMT), a non-antimicrobial modified tetracycline with versatile anti-inflammatory properties but potent host-modulating effects, is an excellent agent for the management of periodontitis. CMTs were produced by removing the dimethylamino group from the carbon-4 position of the A ring of the four-ringed (A, B, C, D) tetracycline structure. The resulting compound, 4-de-dimethyl amino tetracycline (CMT-1), did not have antimicrobial property, but the anti-collagenase activity was retained both in vitro and in vivo.[3] The main advantage of CMTs over the conventional tetracyclines is that long-term systemic administration does not cause gastrointestinal toxicity and higher plasma concentrations can be obtained with less frequent administration regimens. CMTs combat to periodontitis via prevention of connective tissue breakdown through inhibition of metal-dependant MMPs, suppression of neutrophils, and inhibition of generation of arachidionic acid metabolites by blocking the phospholipase A2 and PGE2 synthesis, scavenging the reactive oxygen species, enhancing the attachment of fibroblasts and connective tissues to the tooth surface, and hence regenerating lost periodontium.[4] Currently, sub-antimicrobial dose doxycycline (SDD) and minocycline have been established as effective HMT. Various researches in the literature has proposed the beneficial effects of adjunctive HMT without surgery in the management of periodontist.[5] Recent studies have demonstrated superior therapeutic role of SDD in combination with access flap debridement for improvement of post-operative wound healing and periodontal health in chronic periodontitis. Other accumulating evidences revealed successful management of periodontal disease in patients with postmenopausal osteoporosis (decrease bone mass condition). Nevertheless, various biomarkers in gingival cervicular fluid (e.g., collagen telopeptide fragments) were found to reduce in subjects following SDD dosing. The field of “perioceutics,” or the use of pharmacological agents, specifically developed to better manage periodontitis, is emerging to aid in the management of susceptible patients who are sub-optimally responding to the conventional therapy for periodontal disease.
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1.  The pathogenesis of human periodontitis: an introduction.

Authors:  R C Page; K S Kornman
Journal:  Periodontol 2000       Date:  1997-06       Impact factor: 7.589

2.  Inhibition of proteolytic, serpinolytic, and progelatinase-b activation activities of periodontopathogens by doxycycline and the non-antimicrobial chemically modified tetracycline derivatives.

Authors:  D Grenier; P Plamondon; T Sorsa; H M Lee; T McNamara; N S Ramamurthy; L M Golub; O Teronen; D Mayrand
Journal:  J Periodontol       Date:  2002-01       Impact factor: 6.993

Review 3.  Tetracyclines inhibit connective tissue breakdown by multiple non-antimicrobial mechanisms.

Authors:  L M Golub; H M Lee; M E Ryan; W V Giannobile; J Payne; T Sorsa
Journal:  Adv Dent Res       Date:  1998-11

4.  Doxycycline inhibits neutrophil (PMN)-type matrix metalloproteinases in human adult periodontitis gingiva.

Authors:  L M Golub; T Sorsa; H M Lee; S Ciancio; D Sorbi; N S Ramamurthy; B Gruber; T Salo; Y T Konttinen
Journal:  J Clin Periodontol       Date:  1995-02       Impact factor: 8.728

5.  Perioceutics: Matrix metalloproteinase inhibitors as an adjunctive therapy for inflammatory periodontal disease.

Authors:  Esther Nalini Honibald; Sebeena Mathew; Jeyantha Padmanaban; Elanchezhiyan Sundaram; Renuka Devi Ramamoorthy
Journal:  J Pharm Bioallied Sci       Date:  2012-08
  5 in total
  1 in total

1.  A Novel Analysis via Micro-CT Imaging Indicates That Chemically Modified Tetracycline-3 (CMT-3) Inhibits Tooth Relapse after Orthodontic Movement: A Pilot Experimental Study.

Authors:  Giovanni Modesto Vieira; Denise Pinheiro Falcao; Sormani Bento Fernandes de Queiroz; Valthierre Nunes de Lima; Ricardo Bentes de Azevedo; Valdenize Tiziane; Heitor Moreno; Rivadavio Amorim
Journal:  Int J Dent       Date:  2019-04-01
  1 in total

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