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Geranylgeranylacetone ameliorates acute cochlear damage caused by 3-nitropropionic acid.
- Source :
-
Neurotoxicology [Neurotoxicology] 2010 Jun; Vol. 31 (3), pp. 317-25. Date of Electronic Publication: 2010 Mar 10. - Publication Year :
- 2010
-
Abstract
- 3-Nitropropionic acid (3-NP) induces hearing loss by impairing mitochondrial energy generation. Geranylgeranylacetone (GGA) is known to protect the cochlea from various injuries. The present study was designed to investigate the protective effect of GGA against acute 3-NP-induced damage to the cochlear mitochondria. Female Hartley guinea pigs were divided into 4 groups. The 3-NP vehicle was injected to control animals and in animals receiving GGA alone, only GGA was administered for 7 days. 3-NP (500 mM, 4 microl) was administered with (animals receiving both GGA and 3-NP) or without (animals receiving 3-NP alone) GGA pretreatment (800 mg/kg, 7 days). The auditory brainstem response (ABR) was recorded at click and at 8, 16 and 32 kHz before and after injection, respectively. After cochlear harvest, hematoxylin/eosin staining and immunohistochemistry for anti-HSP70 antibody were done. 3-NP exposure resulted in elevated ABR thresholds that exceeded the maximum recording limit, while GGA pretreatment before 3-NP exposure led to a significant decrease in hearing threshold shift. Histological analysis of above former group revealed loss of type II fibrocytes in the spiral ligament, hair cells in the organ of Corti, stellate fibrocytes in the spiral limbus and spiral ganglion cells, while in above latter group, these cells were preserved. Control animals revealed weak HSP70 expression in the nuclei of some supporting cells (pillar cells, Deiters' cells and Hensen's cells) and interdental cells. Animals receiving GGA alone showed strong HSP70 expression in the same area as in control animals, while animals receiving both GGA and 3-NP demonstrated slightly decreased HSP70 expression in that area. These results suggest that GGA may protect the cochlea against acute injury resulting from mitochondrial dysfunction.<br /> (Copyright 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Acoustic Stimulation methods
Animals
Auditory Threshold drug effects
Cochlear Diseases physiopathology
Disease Models, Animal
Drug Interactions
Electroencephalography methods
Evoked Potentials, Auditory, Brain Stem drug effects
Female
Gene Expression Regulation drug effects
Guinea Pigs
HSP72 Heat-Shock Proteins metabolism
Organ of Corti metabolism
Organ of Corti pathology
Organ of Corti ultrastructure
Cochlear Diseases chemically induced
Cochlear Diseases drug therapy
Diterpenes therapeutic use
Histamine H2 Antagonists therapeutic use
Nitro Compounds
Propionates
Subjects
Details
- Language :
- English
- ISSN :
- 1872-9711
- Volume :
- 31
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Neurotoxicology
- Publication Type :
- Academic Journal
- Accession number :
- 20226206
- Full Text :
- https://doi.org/10.1016/j.neuro.2010.03.001