Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure
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Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure
Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure
解放军医学杂志(英文版)2007年第5期 页码:293-297
Affiliations:
1. Department of Otorhinolaryngology Changzheng Hospital
2. Second Military Medical University
3. ,China
Author bio:
Funds:
Supported by the“Eleventh Five-Year Plan”Medical Science Research Foundation of the PLA(No.06MA157)
DOI:
中图分类号:R764
纸质出版:2007
Accepted:
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Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure[J]. 解放军医学杂志(英文版), 2007,(5):293-297.
[1]吴建,刘冰,何金,范静平,孙爱华.Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure[J].Journal of Medical Colleges of PLA,2007(05):293-297.
Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure[J]. 解放军医学杂志(英文版), 2007,(5):293-297.DOI:
[1]吴建,刘冰,何金,范静平,孙爱华.Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure[J].Journal of Medical Colleges of PLA,2007(05):293-297.DOI:
Adenovirus-mediated human β-nerve growth factor gene transfer has a protective effect on cochlear spiral ganglion after blast exposure
摘要
Abstract
Objective:To study whether adenovirus-mediated human β-nerve growth factor (Ad-hNGFβ) gene has any protective effect on blast hearing impairment. Methods:Deafness was induced by blast exposure (172.0 dB) in 30 healthy guinea pigs. On day 7 of blast exposure
Ad-hNGFβ was infused into the perilymphatic space of 20 animals as the study group (hNGFβ group)
and artificial perilymph fluid (APF) was infused into the perilymphatic space of the other 10 animals as the control group. At weeks 1
4 and 8 after blast exposure
the animals were sacrificed and the cochleae were removed for immunohistochemical and HE stainings. Results: Expression of Ad-hNGFβ protein was detected in each turn of the cochlea at the 1st week
with almost equal intensity in all turns. At the 4th week
the reactive intensity of the expression of Ad-hNGFβ protein decreased. At the 8th week
no expression was detectable. The results of HE staining showed that the amount of spiral ganglions in hNGFβ group was significantly greater than that of the control group at week 4 (P<0.01). Conclusion: Ad-hNGFβ can be expressed at a high level and for a relatively long period in the blast impaired cochlea
suggesting that Ad-hNGFβ has a protective effect on cochlear spiral ganglion cells after blast exposure and the efficient gene transfer into cochlea had been achieved without toxicity.
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