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- W2897763649 abstract "Recent progress in hearing loss research has provided strong evidence for the imbalance of cellular redox status and inflammation as common predominant mechanisms of damage affecting the organ of Corti including noise induced hearing loss. The discovery of a protective molecule acting on both mechanisms is challenging. The thiazolidinediones, a class of antidiabetic drugs including pioglitazone and rosiglitazone, have demonstrated diverse pleiotrophic effects in many tissues where they exhibit anti-inflammatory, anti-proliferative, tissue protective effects and regulators of redox balance acting as agonist of peroxisome proliferator-activated receptors (PPARs). They are members of the family of ligand regulated nuclear hormone receptors that are also expressed in several cochlear cell types, including the outer hair cells. In this study, we investigated the protective capacity of the, pioglitazone, in a model of noise-induced hearing loss in Wistar rats and the molecular mechanisms underlying this protective effects. Specifically, we employed a formulation of pioglitazone in a biocompatible thermogel providing rapid, uniform and sustained inner ear drug delivery via transtympanic injection. Following noise exposure (120 dB, 10 kHz, 1h), different time schedules of treatment were employed: we explored the efficacy of pioglitazone given immediately (1h) or at delayed time points (24h and 48h) after noise exposure and the time course and extent of hearing recovery were assessed. We found that pioglitazone was able to protect auditory function at the mid-high frequencies and to limit cell death in the cochlear basal/middle turn, damaged by noise exposure. Immunofluorescence and western blot analysis provided evidence that pioglitazone mediates both anti-inflammatory and anti-oxidant effects by decreasing NF-B and IL-1 expression in the cochlea and opposing the oxidative damage induced by noise insult. These results suggest that intratympanic pioglitazone can be considered a valid therapeutic strategy for attenuating noise-induced hearing loss and cochlear damage, reducing inflammatory signaling and restoring cochlear redox balance." @default.
- W2897763649 created "2018-10-26" @default.
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- W2897763649 date "2018-10-08" @default.
- W2897763649 modified "2023-09-30" @default.
- W2897763649 title "Pioglitazone Represents an Effective Therapeutic Target in Preventing Oxidative/Inflammatory Cochlear Damage Induced by Noise Exposure" @default.
- W2897763649 cites W1516068437 @default.
- W2897763649 cites W1647126819 @default.
- W2897763649 cites W1967291007 @default.
- W2897763649 cites W1974168061 @default.
- W2897763649 cites W1975786243 @default.
- W2897763649 cites W1976072714 @default.
- W2897763649 cites W1978302160 @default.
- W2897763649 cites W1978700067 @default.
- W2897763649 cites W1979120081 @default.
- W2897763649 cites W1980260792 @default.
- W2897763649 cites W1991695417 @default.
- W2897763649 cites W1993288470 @default.
- W2897763649 cites W1993979020 @default.
- W2897763649 cites W1994976931 @default.
- W2897763649 cites W1998812648 @default.
- W2897763649 cites W1999902482 @default.
- W2897763649 cites W2003836413 @default.
- W2897763649 cites W2011785430 @default.
- W2897763649 cites W2014354706 @default.
- W2897763649 cites W2014941838 @default.
- W2897763649 cites W2020766314 @default.
- W2897763649 cites W2022116094 @default.
- W2897763649 cites W2025742167 @default.
- W2897763649 cites W2030626033 @default.
- W2897763649 cites W2032995646 @default.
- W2897763649 cites W2043046748 @default.
- W2897763649 cites W2043287342 @default.
- W2897763649 cites W2046983778 @default.
- W2897763649 cites W2047591801 @default.
- W2897763649 cites W2048034726 @default.
- W2897763649 cites W2057259086 @default.
- W2897763649 cites W2059552796 @default.
- W2897763649 cites W2060462930 @default.
- W2897763649 cites W2060610804 @default.
- W2897763649 cites W2064270413 @default.
- W2897763649 cites W2065953416 @default.
- W2897763649 cites W2066092624 @default.
- W2897763649 cites W2068264180 @default.
- W2897763649 cites W2069141048 @default.
- W2897763649 cites W2073578030 @default.
- W2897763649 cites W2073583479 @default.
- W2897763649 cites W2073976306 @default.
- W2897763649 cites W2074437959 @default.
- W2897763649 cites W2075639702 @default.
- W2897763649 cites W2085284136 @default.
- W2897763649 cites W2086667809 @default.
- W2897763649 cites W2088880784 @default.
- W2897763649 cites W2094328405 @default.
- W2897763649 cites W2094863064 @default.
- W2897763649 cites W2097041552 @default.
- W2897763649 cites W2097511872 @default.
- W2897763649 cites W2100750761 @default.
- W2897763649 cites W2105681613 @default.
- W2897763649 cites W2111464898 @default.
- W2897763649 cites W2111790428 @default.
- W2897763649 cites W2113328569 @default.
- W2897763649 cites W2122044177 @default.
- W2897763649 cites W2124605635 @default.
- W2897763649 cites W2125276264 @default.
- W2897763649 cites W2128900735 @default.
- W2897763649 cites W2131847074 @default.
- W2897763649 cites W2138934663 @default.
- W2897763649 cites W2140871354 @default.
- W2897763649 cites W2144473903 @default.
- W2897763649 cites W2148119611 @default.
- W2897763649 cites W2168374306 @default.
- W2897763649 cites W2183389059 @default.
- W2897763649 cites W2236270374 @default.
- W2897763649 cites W2344245973 @default.
- W2897763649 cites W2536806286 @default.
- W2897763649 cites W2559725989 @default.
- W2897763649 cites W2751111792 @default.
- W2897763649 cites W2770062105 @default.
- W2897763649 cites W2787930551 @default.
- W2897763649 cites W3022611142 @default.
- W2897763649 doi "https://doi.org/10.3389/fphar.2018.01103" @default.
- W2897763649 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6187064" @default.
- W2897763649 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30349478" @default.
- W2897763649 hasPublicationYear "2018" @default.
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