AI Article Synopsis

  • The reticular lamina in the cochlea protects the organ of Corti from endolymph in the scala media, and changes to its endothelial nitric oxide synthase (eNOS) levels were observed after noise exposure.
  • In a study with guinea pigs, the application of nitric oxide donor SNAP increased eNOS expression by 176% in specific cellular areas compared to control animals.
  • SNAP treatment shifted the cellular associations in the cochlea, indicating that nitric oxide plays a role in protecting cochlear structures after noise exposure.

Article Abstract

In the vertebrate cochlea, the reticular lamina seals the organ of Corti against the endolymph filled scala media. After noise exposure, fast alterations in the endothelial nitric oxide synthase (eNOS) expression level were identified in this cochlear structure. Minor amounts of nitric oxide (NO) produced by eNOS or applied by NO donors such as S-nitroso--acetyl-penicillamine (SNAP) might protect this vulnerable part of the organ of Corti, on the line of gap junctions of supporting cells and cochlear microcirculation. In =5 anesthetized guinea pigs, SNAP was intravenously applied in two concentrations. Six untreated animals served as controls. The cochleae were removed and prepared for immunoelectron microscopy using specific gold-labeled anti-eNOS antibodies. The density of the gold particles was quantified for seven cellular regions in the reticular lamina at the ultrastructural level. Following SNAP application, a significant increase in eNOS expression (+176%) was detected compared with controls (=0.012). The increase occurred mainly in actin-rich cuticular structures and the prominent microtubules bundles. Correlation analysis revealed three clear and five moderate cellular associations for controls, whereas only one clear and one moderate after SNAP application. Thus, application of the NO donor SNAP resulted in an increase in eNOS expression in distinct regions of the reticular lamina.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554578PMC
http://dx.doi.org/10.1369/00221554211054642DOI Listing

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