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Korean red ginseng ameliorates acute 3-nitropropionic acid-induced cochlear damage in mice.

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dc.contributor.authorTian, C-
dc.contributor.authorKim, YH-
dc.contributor.authorKim, YC-
dc.contributor.authorPark, KT-
dc.contributor.authorKim, SW-
dc.contributor.authorKim, YJ-
dc.contributor.authorLim, HJ-
dc.contributor.authorChoung, YH-
dc.date.accessioned2014-05-29-
dc.date.available2014-05-29-
dc.date.issued2013-
dc.identifier.issn0161-813X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/10240-
dc.description.abstract3-Nitropropionic acid (3-NP), a mitochondrial toxin, has been reported to induce an acute cochlear damage. Korean red ginseng (KRG) is known to have protective effects from some types of hearing loss. This study aimed to observe the protective effect of KRG in an ototoxic animal model using 3-NP intratympanic injection. BALB/c mice were classified into 5 groups (n=15) and dose-dependent toxic effects after intratympanic injection with 3-NP (300-5000 mM) on the left ear were investigated to determine the appropriate toxicity level of 3-NP. For observation of the protective effects of KRG, 23 mice were grouped into 3-NP (500 mM, n=12) and KRG+3-NP groups (300 mg/kg KRG for 7 days before 500 mM 3-NP administration, n=11). Auditory brain response (ABR) and cochlear morphological evaluations were performed before and after drug administration. The ABR thresholds in the 800-5000 mM groups exceeded the maximum recording limit at 16 and 32 kHz 1 day after 3-NP administration. The ABR threshold in the 500 mM 3-NP+KRG group was significantly lower than that in the 500 mM 3-NP group from post 1 week to 1 month. The mean type II fibrocyte counts significantly differed between the control and 3-NP groups and between the 3-NP and 3-NP+KRG groups. Spiral ganglion cell degeneration in the 3-NP group was more severe than that in the 3-NP+KRG group. This animal model exhibited a dose-dependent hearing loss with histological changes. KRG administration ameliorated the deterioration of hearing by 3-NP.-
dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAuditory Threshold-
dc.subject.MESHCochlea-
dc.subject.MESHCochlear Diseases-
dc.subject.MESHCytoprotection-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHEvoked Potentials, Auditory, Brain Stem-
dc.subject.MESHHair Cells, Auditory, Outer-
dc.subject.MESHHearing-
dc.subject.MESHHearing Loss-
dc.subject.MESHMale-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred BALB C-
dc.subject.MESHNitro Compounds-
dc.subject.MESHPanax-
dc.subject.MESHPlant Extracts-
dc.subject.MESHPlant Roots-
dc.subject.MESHPlants, Medicinal-
dc.subject.MESHPropionates-
dc.subject.MESHSpiral Ganglion-
dc.subject.MESHTime Factors-
dc.titleKorean red ginseng ameliorates acute 3-nitropropionic acid-induced cochlear damage in mice.-
dc.typeArticle-
dc.identifier.pmid23164932-
dc.identifier.urlhttp://linkinghub.elsevier.com/retrieve/pii/S0161-813X(12)00251-3-
dc.contributor.affiliatedAuthor임, 혜진-
dc.contributor.affiliatedAuthor정, 연훈-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.neuro.2012.10.008-
dc.citation.titleNeurotoxicology-
dc.citation.volume34-
dc.citation.date2013-
dc.citation.startPage42-
dc.citation.endPage50-
dc.identifier.bibliographicCitationNeurotoxicology, 34. : 42-50, 2013-
dc.identifier.eissn1872-9711-
dc.relation.journalidJ00161813X-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Otolaryngology
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