Evidence map›Paper›PMID 25101489›Full record

ArticleJournal of periodontology2015

Periodontitis in rats induces systemic oxidative stress that is controlled by bone-targeted antiresorptives.

Sehkar Oktay, Sasanka S Chukkapalli, Mercedes F Rivera-Kweh, Irina M Velsko, L Shannon Holliday, Lakshmyya Kesavalu

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of periodontology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Sehkar OktayDepartment of Periodontology, College of Dentistry, University of Florida, Gainesville, FL.
Sasanka S Chukkapalli
Mercedes F Rivera-Kweh
Irina M Velsko
L Shannon Holliday
Lakshmyya Kesavalu
University of Florida · US

Funding

Dental applications for a novel osteoclast inhibitorR21DE019862 · NIDCR · UNIVERSITY OF FLORIDA · PI HOLLIDAY, LEXIE SHANNON · 2010 to 2011
$401k
NIDCR NIH HHS R21 DE019862
6 · The paper itself

Abstract

backgroundPeriodontitis is a chronic, polymicrobial inflammatory disease that degrades connective tissue and alveolar bone and results in tooth loss. Oxidative stress has been linked to the onset of periodontal tissue breakdown and systemic inflammation, and the success of antiresorptive treatments will rely on how effectively they can ameliorate periodontal disease-induced oxidative stress during oral infection.

methodsRats were infected with polybacterial inoculum consisting of Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia, as an oral lavage every other week for 12 weeks. Daily subcutaneous injections of enoxacin, bis-enoxacin, alendronate, or doxycycline were administered for 6 weeks after 6 weeks of polybacterial infection in rats. The serum levels of oxidative stress parameters and antioxidant enzymes, including glutathione peroxidase, superoxide dismutase, and catalase, were evaluated in each of the infected, treated, and sham-infected rats.

resultsRats infected with the periodontal pathogens displayed a five-fold increase in the oxidative stress index compared with controls as a result of increased levels of serum oxidants and decreases in total antioxidant activity. The overall decrease in antioxidant activity occurred despite increases in three important antioxidant enzymes, suggesting an imbalance between antioxidant macromolecules/small molecules production and antioxidant enzyme levels. Surprisingly, the bone-targeted antiresorptives bis-enoxacin and alendronate inhibited increases in oxidative stress caused by periodontitis. Bis-enoxacin, which has both antiresorptive and antibiotic activities, was more effective than alendronate, which acts only as an antiresorptive.

conclusionTo the best of the authors' knowledge, this is the first study to demonstrate that the increased oxidative stress induced by periodontal infection in rats can be ameliorated by bone-targeted antiresorptives.

Indexed as

AlendronateAnimalsAnti-Bacterial AgentsAntioxidantsBacteroidaceae InfectionsBacteroides InfectionsBone Density Conservation AgentsCatalaseCoinfectionDoxycyclineEnoxacinFemaleFree Radical ScavengersGlutathione PeroxidaseGram-Negative Bacterial InfectionsLipid PeroxidationAlendronateAnti-Bacterial AgentsAntioxidantsBone Density Conservation AgentsCatalaseDoxycyclineEnoxacinFree Radical ScavengersGlutathione PeroxidaseOxidantsSuperoxide DismutaseAlendronatebacteriaenoxacinlipid peroxidationoxidative stressperiodontalperiodontal diseases

Identifiers

PMID25101489
PMCPMC4557732
OpenAlexW1979521647

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.