کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6262632 1613810 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research ReportNeuroglobin immunoreactivity in the human cochlea
ترجمه فارسی عنوان
گزارش تحقیقاتی ایمونوآرژیتی نوروگلوبین در حلزون انسانی
کلمات کلیدی
نوروگلوبین، استخوان انسانی، استرس اکسیداتیو، گوش داخلی، نورون گانگلیوی اسپیرال،
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
چکیده انگلیسی


- Ngb-IR was detected in the human organ of Corti, and spiral ganglion neurons (SGNs)
- SGNs Ngb-IR was significantly reduced in cochleas with otologic pathologies
- Neuroglobin (Ngb) may protect the inner ear from oxidative stress
- Ngb-IR localization in the human and rodent cochlea was similar

Neuroglobin (Ngb) is an oxygen-binding protein with a demonstrated role in endogenous neuroprotective mechanisms. It has been shown to function as a scavenger for reactive oxidizing species thereby assisting in cellular defense against oxidative stress. In the present study, we characterized the presence of Ngb in the human cochlea. Immunohistochemical staining was performed on formalin fixed celloidin human cochlea sections obtained from human temporal bones, using affinity purified polyclonal antibodies against Ngb. Thirty-six temporal bones were analyzed, 15 with normal otologic histories and 21 diagnosed with different inner ear pathologies. Ngb immunoreactivity (Ngb-IR) was consistently expressed in the neurons of spiral ganglia (SG) and supporting cells of the organ of Corti. There was a significant decrease of Ngb-IR in SGNs from specimens with inner ear pathologies when compared to normal specimens. In contrast, Ngb-IR in the organ of Corti did not show significant changes between pathological and normal specimens. The differential pattern of Ngb expression in these cochlear structures suggests that Ngb may participate in defense mechanisms in inner ear pathologies where oxidative stress is involved.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1630, 1 January 2016, Pages 56-63
نویسندگان
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