Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 9 von 217

Details

Autor(en) / Beteiligte
Titel
Transcriptional-profile changes in the medial geniculate body after noise-induced tinnitus
Ist Teil von
  • Experimental biology and medicine (Maywood, N.J.), 2024, Vol.249, p.10057-10057
Ort / Verlag
Switzerland: Frontiers Media S.A
Erscheinungsjahr
2024
Link zum Volltext
Quelle
Elektronische Zeitschriftenbibliothek - Freely accessible e-journals
Beschreibungen/Notizen
  • Tinnitus is a disturbing condition defined as the occurrence of acoustic hallucinations with no actual sound. Although the mechanisms underlying tinnitus have been explored extensively, the pathophysiology of the disease is not completely understood. Moreover, genes and potential treatment targets related to auditory hallucinations remain unknown. In this study, we examined transcriptional-profile changes in the medial geniculate body after noise-induced tinnitus in rats by performing RNA sequencing and validated differentially expressed genes via quantitative polymerase chain reaction analysis. The rat model of tinnitus was established by analyzing startle behavior based on gap-pre-pulse inhibition of acoustic startles. We identified 87 differently expressed genes, of which 40 were upregulated and 47 were downregulated. Pathway-enrichment analysis revealed that the differentially enriched genes in the tinnitus group were associated with pathway terms, such as coronavirus disease COVID-19, neuroactive ligand-receptor interaction. Protein-protein-interaction networks were established, and two hub genes (Rpl7a and AC136661.1) were identified among the selected genes. Further studies focusing on targeting and modulating these genes are required for developing potential treatments for noise-induced tinnitus in patients.
Sprache
Englisch
Identifikatoren
ISSN: 1535-3702
eISSN: 1535-3699
DOI: 10.3389/ebm.2024.10057
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10984379

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX