Literature DB >> 1403576

Modulation of human gingival fibroblast cell metabolism by methyl mercaptan.

P W Johnson1, W Ng, J Tonzetich.   

Abstract

Methyl mercaptan (CH3SH) is a malodorous compound whose levels are elevated in mouth and crevicular air of individuals with active periodontal disease. Since it may play a role in the disease process, its effects were evaluated using human gingival fibroblast cultures and viable porcine unkeratinized oral mucosal tissue sections. Results showed that the protein content of CH3SH-exposed cell cultures pulsed with [14C]-labelled glycine and proline was decreased by approximately 25%. Furthermore, this deleterious effect was irreversible in test cultures subsequently incubated for 24 h in a control 95% air/5% CO2 mercaptan-free environment. The supporting slab-gel electrophoresis profiles yielded evidence that exposure to CH3SH caused an alteration in collagen metabolism and a pooling of Type I procollagens. In addition, DNA synthesis was suppressed in CH3SH-exposed cultures by 44.1% at the 24 to 26 h peak of DNA synthesis. This is a true inhibition and not a shift in peak of maximum DNA synthesis as the shape and location of time-course curves of control and test systems is very similar. Proline transport study using [14C]-proline indicated a reduction in proline transport in the range of 40 to 50% in cultures exposed for 24 to 30 h to CH3SH. Significantly even 15 min exposure to 6.7 ng CH3SH/ml of incubating atmosphere suppressed proline transport by approximately 24%. This indicates that even brief exposure to low concentrations of CH3SH has a significant adverse effect on proline transport. Fluorescent staining of tissue sections exposed to mercaptan indicated that the agent elevated the number of cells stained with vital dye.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1403576     DOI: 10.1111/j.1600-0765.1992.tb01820.x

Source DB:  PubMed          Journal:  J Periodontal Res        ISSN: 0022-3484            Impact factor:   4.419


  6 in total

Review 1.  Virulence factors of the oral spirochete Treponema denticola.

Authors:  S G Dashper; C A Seers; K H Tan; E C Reynolds
Journal:  J Dent Res       Date:  2010-10-12       Impact factor: 6.116

2.  Porphyromonas gingivalis virulence in a Drosophila melanogaster model.

Authors:  Christina O Igboin; Melvin L Moeschberger; Ann L Griffen; Eugene J Leys
Journal:  Infect Immun       Date:  2010-11-01       Impact factor: 3.441

3.  Formation of methyl mercaptan from L-methionine by Porphyromonas gingivalis.

Authors:  M Yoshimura; Y Nakano; Y Yamashita; T Oho; T Saito; T Koga
Journal:  Infect Immun       Date:  2000-12       Impact factor: 3.441

4.  Pilot evaluation of a novel test strip for the assessment of dissolved thiol levels, as an indicator of canine gingival health and periodontal status.

Authors:  Sandra Manfra Marretta; Maureen Leesman; Anthony Burgess-Cassler; G David McClure; Mary Buelow; Misty Finn
Journal:  Can Vet J       Date:  2012-12       Impact factor: 1.008

5.  Oral malodorous compound activates mitochondrial pathway inducing apoptosis in human gingival fibroblasts.

Authors:  Maiko Fujimura; Bogdan Calenic; Ken Yaegaki; Takatoshi Murata; Hisataka Ii; Toshio Imai; Tutomu Sato; Yuichi Izumi
Journal:  Clin Oral Investig       Date:  2009-06-23       Impact factor: 3.573

6.  Relationship between the concentration of volatile sulphur compound and periodontal disease severity in Nigerian young adults.

Authors:  Adebola O Ehizele; Patrick I Ojehanon
Journal:  Niger Med J       Date:  2013-05
  6 in total

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