Evaluation of immunological safety of topiramate, an anti-epileptic drug, in a murine model

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dc.contributor.authorS B Han-
dc.contributor.authorJ Y Kim-
dc.contributor.authorS W Kwon-
dc.contributor.authorJong Soon Kang-
dc.contributor.authorHwan Mook Kim-
dc.contributor.authorS Song-
dc.contributor.authorJ T Hong-
dc.contributor.authorY Kim-
dc.contributor.authorW S Kim-
dc.date.accessioned2017-04-19T09:13:45Z-
dc.date.available2017-04-19T09:13:45Z-
dc.date.issued2009-
dc.identifier.issn1976-9148-
dc.identifier.uri10.4062/biomolther.2009.17.2.168ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8947-
dc.description.abstractEpilepsy is one of the most common neurological disorders, and topiramate (TPM) is one of the most effective drugs that can render patients seizure-free. The focus of the present study was to evaluate the immunological safety of TPM in a mouse model. We examined the in vitro effect of TPM on immune functions of BV2 microglial cells, RAW 264.7 macrophages, B cells, T cells, and dendritic cells. We also examined the in vivo effect of TPM on mouse immune organs, such as lymph node, spleen, and thymus. When cells were directly treated with TPM at concentrations from 1 to 30 μg/ml, TPM did not affect nitrite production by BV2 cells and macrophages, proliferation of B cells and T cells, or maturation of dendritic cells. In addition, TPM did not change the weight and cellularity of lymph nodes, spleen, and thymus in vivo at doses from 3 to 100 mg/kg injected i.p. into mice once a day for 4 consecutive days. These data showed that TPM, which is widely used as an anti-epileptic drug, is immunologically safe.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleEvaluation of immunological safety of topiramate, an anti-epileptic drug, in a murine model-
dc.title.alternativeEvaluation of immunological safety of topiramate, an anti-epileptic drug, in a murine model-
dc.typeArticle-
dc.citation.titleBiomolecules & Therapeutics-
dc.citation.number2-
dc.citation.endPage174-
dc.citation.startPage168-
dc.citation.volume17-
dc.contributor.affiliatedAuthorJong Soon Kang-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.alternativeName한상배-
dc.contributor.alternativeName김지윤-
dc.contributor.alternativeName권순우-
dc.contributor.alternativeName강종순-
dc.contributor.alternativeName김환묵-
dc.contributor.alternativeName송석길-
dc.contributor.alternativeName홍진태-
dc.contributor.alternativeName김영수-
dc.contributor.alternativeName김원섭-
dc.identifier.bibliographicCitationBiomolecules & Therapeutics, vol. 17, no. 2, pp. 168-174-
dc.identifier.doi10.4062/biomolther.2009.17.2.168-
dc.subject.keywordTopiramate-
dc.subject.keywordAnti-epileptic drug-
dc.subject.keywordAdverse effect-
dc.subject.keywordImmune functions-
dc.subject.localTopiramate-
dc.subject.localAnti-epileptic drug-
dc.subject.localAdverse effect-
dc.subject.localImmune function-
dc.subject.localImmune functions-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
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