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Pulmonary delivery of d-methionine is associated with an increase in ALCAR and glutathione in cochlear fluids.
KTH, Centres, Science for Life Laboratory, SciLifeLab.ORCID iD: 0000-0002-4720-2756
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2013 (English)In: Hearing Research, ISSN 0378-5955, E-ISSN 1878-5891, Vol. 298, 93-103 p.Article in journal (Refereed) Published
Abstract [en]

In animals, hearing loss resulting from cochlear mechanosensory cell damage can be mitigated by antioxidants such as d-methionine (d-met) and acetyl-l-carnitine (ALCAR). The systemic routes of administration of these compounds, that must of necessity transit trough the cochlear fluids, may affect the antioxidant levels in the cochlea and the resulting oto-protective effect. In this study, we analyzed the pharmacokinetics of [C]d-met in the cochlea and four other tissues after intratracheal (IT), intranasal (IN), and oral by gavage (OG) administration and compared it to intravenous administration (IV). We then analyzed the effect of these four routes on the antioxidant content of the cochlear fluids after d-met or ALCAR administration, by liquid chromatography/mass spectrometry. Our results showed that the concentration of methionine and ALCAR in cochlear fluids significantly increased after their respective systemic administration. Interestingly, d-met administration also contributed to an increase of ALCAR. Our results also showed that the delivery routes differently affected the bioavailability of administered [C]d-met as well as the concentrations of methionine, ALCAR and the ratio of oxidized to reduced glutathione. Overall, pulmonary delivery via IT administration achieved high concentrations of methionine, ALCAR, and oxidative-related metabolites in cochlear fluids, in some cases surpassing IV administration, while IN route appeared to be the least efficacious. To our knowledge, this is the first report of the direct measurements of antioxidant levels in cochlear fluids after their systemic administration. This report also demonstrates the validity of the pulmonary administration of antioxidants and highlights the different contributions of d-met and ALCAR allowing to further investigate their impact on oxidative stress in the cochlear microenvironment.

Place, publisher, year, edition, pages
2013. Vol. 298, 93-103 p.
National Category
Pharmacology and Toxicology
URN: urn:nbn:se:kth:diva-119785DOI: 10.1016/j.heares.2012.12.011ISI: 000317159100010PubMedID: 23296212OAI: diva2:612546

QC 20130603

Available from: 2013-03-22 Created: 2013-03-22 Last updated: 2013-06-03Bibliographically approved

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