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    고양이 전농화 실험을 통한 Ethacrynic Acid와 체중 간의 상관성 고찰 = Correlation between Dose of Ethacrynic Acid and Weight of Cat in the Cat Deafening Procedure

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    https://www.riss.kr/link?id=A101610180

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    Background and Objectives Co-administration of kanamycin (KM) with the loop diuretic ethacrynic acid (EA) has been known to produce a rapid and profound hearing loss in adult animals. The objective of this study was to see if monitoring the hearing status during intravenous infusion of EA could minimalize individual variability and to evaluate the correlation between the dose of EA and the body weight (wt).
    Materials and Method Twenty cats with the mean age of 24 weeks±3.7 (range, 20.6-28.3 weeks) and the mean weight of 3.27 kg±0.75 (range 2.4-4.75 kg) received a subcutaneous injection of KM (300 mg/kg) followed by an intravenous infusion of EA (1 mg/min). Click evoked auditory brainstem responses (ABRs) were recorded to monitor the hearing during the infusion. When the ABR thresholds rose to levels in excess of 90 dB SPL, the infusion of EA was stopped. The histopathologies for sections of apex, middle, base of cochlea were examined after 6 months.
    Results There was a significant positive correlation (p<.001, r2=.583) between the EA dose and body weight. Cochlear histopathology showed an absence of organ of Corti and decrease of spiral ganglion cells in the majority of cochleas, especially in the basal turn. The extent of loss of spiral ganglion cells was dependent on their distance from the round window.
    Conclusion Monitoring the animal’s hearing status during the procedure ensured that the dose of EA was optimized for individual animals. Thus, the positive correlation between the EA dose and body weight should be considered should in designing the animal models of controlled high frequency hearing loss.
    Korean J Otorhinolaryngol-Head Neck Surg 2010;53:749-54
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    Background and Objectives Co-administration of kanamycin (KM) with the loop diuretic ethacrynic acid (EA) has been known to produce a rapid and profound hearing loss in adult animals. The objective of this study was to see if monitoring the hearing st...

    Background and Objectives Co-administration of kanamycin (KM) with the loop diuretic ethacrynic acid (EA) has been known to produce a rapid and profound hearing loss in adult animals. The objective of this study was to see if monitoring the hearing status during intravenous infusion of EA could minimalize individual variability and to evaluate the correlation between the dose of EA and the body weight (wt).
    Materials and Method Twenty cats with the mean age of 24 weeks±3.7 (range, 20.6-28.3 weeks) and the mean weight of 3.27 kg±0.75 (range 2.4-4.75 kg) received a subcutaneous injection of KM (300 mg/kg) followed by an intravenous infusion of EA (1 mg/min). Click evoked auditory brainstem responses (ABRs) were recorded to monitor the hearing during the infusion. When the ABR thresholds rose to levels in excess of 90 dB SPL, the infusion of EA was stopped. The histopathologies for sections of apex, middle, base of cochlea were examined after 6 months.
    Results There was a significant positive correlation (p<.001, r2=.583) between the EA dose and body weight. Cochlear histopathology showed an absence of organ of Corti and decrease of spiral ganglion cells in the majority of cochleas, especially in the basal turn. The extent of loss of spiral ganglion cells was dependent on their distance from the round window.
    Conclusion Monitoring the animal’s hearing status during the procedure ensured that the dose of EA was optimized for individual animals. Thus, the positive correlation between the EA dose and body weight should be considered should in designing the animal models of controlled high frequency hearing loss.
    Korean J Otorhinolaryngol-Head Neck Surg 2010;53:749-54

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    참고문헌 (Reference)

    1 Cody AR, "Variability of noise-induced damage in the guinea pig cochlea: electrophysiological and morphological correlates after strictly controlled exposures" 9 (9): 55-70, 1983

    2 Brugge JF, "Signs of functional maturation of peripheral auditory system in discharge patterns of neurons in anteroventral cochlear nucleus of kitten" 41 (41): 1557-1559, 1978

    3 Hutchin T, "Proposed molecular and cellular mechanism for aminoglycoside ototoxicity" 38 (38): 2517-2520, 1994

    4 Xu SA, "Profound hearing loss in the cat following the single co-administration of kanamycin and ethacrynic acid" 70 (70): 205-215, 1993

    5 Shepherd RK, "Onset of ototoxicity in the cat is related to onset of auditory function" 92 (92): 131-142, 1995

    6 Bowes T, "Novel mitochondrial extensions provide evidence for a link between microtubule-directed movement and mito chondrial fission" 376 (376): 40-45, 2008

    7 Leake-Jones PA, "Neomycin ototoxicity: ultrastructural surface pathology of the organ of Corti" 3 : 427-434, 1980

    8 Duckert LG, "Morphological changes in the normal and neomycin-perfused guinea pig cochlea following chronic prosthetic implantation" 93 (93): 841-855, 1983

    9 Ding D, "Mechanisms of rapid sensory hair-cell death following co-administration of gentamicin and ethacrynic acid" 259 (259): 16-23, 2010

    10 West BA, "Interaction of kanamycin and ethacrynic acid. Severe cochlear damage in guinea pigs" 98 (98): 32-37, 1973

    1 Cody AR, "Variability of noise-induced damage in the guinea pig cochlea: electrophysiological and morphological correlates after strictly controlled exposures" 9 (9): 55-70, 1983

    2 Brugge JF, "Signs of functional maturation of peripheral auditory system in discharge patterns of neurons in anteroventral cochlear nucleus of kitten" 41 (41): 1557-1559, 1978

    3 Hutchin T, "Proposed molecular and cellular mechanism for aminoglycoside ototoxicity" 38 (38): 2517-2520, 1994

    4 Xu SA, "Profound hearing loss in the cat following the single co-administration of kanamycin and ethacrynic acid" 70 (70): 205-215, 1993

    5 Shepherd RK, "Onset of ototoxicity in the cat is related to onset of auditory function" 92 (92): 131-142, 1995

    6 Bowes T, "Novel mitochondrial extensions provide evidence for a link between microtubule-directed movement and mito chondrial fission" 376 (376): 40-45, 2008

    7 Leake-Jones PA, "Neomycin ototoxicity: ultrastructural surface pathology of the organ of Corti" 3 : 427-434, 1980

    8 Duckert LG, "Morphological changes in the normal and neomycin-perfused guinea pig cochlea following chronic prosthetic implantation" 93 (93): 841-855, 1983

    9 Ding D, "Mechanisms of rapid sensory hair-cell death following co-administration of gentamicin and ethacrynic acid" 259 (259): 16-23, 2010

    10 West BA, "Interaction of kanamycin and ethacrynic acid. Severe cochlear damage in guinea pigs" 98 (98): 32-37, 1973

    11 Tran Ba Huy P, "Ethacrynic acid facilitates gentamicin entry into endolymph of the rat" 11 (11): 191-202, 1983

    12 Tew KD, "Coordinate changes in expression of protective genes in drug-resistant cells" 111 (111): 199-211, 1998

    13 Brummett RE, "Comparative ototoxicity of bumetanide and furosemide when used in combination with kanamycin" 21 (21): 628-636, 1981

    14 Hiel H, "Cellular and subcellular localization of tritiated gentamicin in the guinea pig cochlea following combined treatment with ethacrynic acid" 57 (57): 157-165, 1992

    15 Nishida I, "Attenuation of aminoglycoside ototoxicity by glutathione" 58 (58): 68-73, 1996

    16 Schuknecht HF, "Atrophy of the stria vascularis, a common cause for hearing loss" 84 (84): 1777-1821, 1974

    17 Begg EJ, "Aminoglycosides--50 years on" 39 (39): 597-603, 1995

    18 Schacht J, "Aminoglycoside ototoxicity: prevention in sight?" 118 (118): 674-677, 1998

    19 Strupp M, "Acute vestibulopathy" 14 (14): 11-20, 2001

    20 Orsulakova A, "A biochemical mechanism of the ototoxic interaction between neomycin and ethacrynic acid" 93 (93): 43-48, 1982

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