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Thirty\u2010two Wistar rats were divided into four groups of eight rats each: Control Group; <jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> Group; <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> Group; <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> Group. In the <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> groups, the pulp chambers of the mandibular first molars were surgically exposed and were left open to the oral environment for 4\u2010weeks to allow the establishment of periapical lesions. The rats in the Control and <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> groups were treated intraperitoneally with saline solution (with a daily dose of 100\u00a0mg\u00a0kg<jats:sup>\u22121<\/jats:sup>, for 28\u00a0days after periapical lesion induction). The rats in the <jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> groups were treated intraperitoneally with <jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> (with a daily dose of 100\u00a0mg\u00a0kg<jats:sup>\u22121<\/jats:sup>, for 28\u00a0days after periapical lesion induction). After decapitation, the trunk blood was collected for the assessment of biochemical parameters. The mandibles were surgically removed and dissected for histopathologic analysis and further scanned with micro\u2010<jats:styled-content style=\"fixed-case\">CT<\/jats:styled-content>. Groups of data were compared with a two\u2010way analysis of variance (two\u2010way <jats:sc>anova<\/jats:sc>) followed by Sidak's multiple comparison tests. Values of <jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05 were regarded as significant.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u2010\u03b1, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2, <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\u20101, <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\u20102 levels were significantly lower in <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> group compared with <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> group (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05). There was a significant difference between the <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> groups according to assessment of the inflammatory scores (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05). The periapical inflammatory infiltrates were significantly more severe (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05) in the <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> group. The <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> group exhibited lower values both in terms of surface area and volume of resorption cavities than the <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content> group and this difference was significant (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>alpha\u2010lipoic acid treatment provided therapeutic effects on the inhibition of periapical bone loss.<\/jats:p><\/jats:sec>","DOI":"10.1111\/iej.13121","type":"journal-article","created":{"date-parts":[[2019,3,22]],"date-time":"2019-03-22T11:54:01Z","timestamp":1553255641000},"page":"1317-1326","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":34,"title":["Effects of alpha\u2010lipoic acid therapy on experimentally induced apical 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