Inhibition of the carbachol-evoked synthesis of inositol phosphates by ototoxic drugs in the rat cochlea - HAL Accéder directement au contenu
Article dans une revue Hearing Research Année : 1993

Inhibition of the carbachol-evoked synthesis of inositol phosphates by ototoxic drugs in the rat cochlea

Résumé

The ability of amikacin, neomycin, ethacrynate, mercuric chloride and cisplatin to alter the inositol phosphate (IP) signalling pathway was assessed in the 12-day-old rat cochlea, where the turnover of IPs is coupled to muscarinic receptors. This study was motivated by: (1) the demonstration of neomycin binding to phosphatidylinositol 4,Sbiphosphate, the precursor of IPs, and (2) the fact that ototoxic drugs induce some common symptoms in outer hair cells. At concentrations below 1 mM, none of the compounds changed the control 'H-IP formation. Mercuric chloride, cisplatin and ethacrynate inhibited the carbachol-induced formation of IPs in a dose-dependent manner with IC?,, values of 74, 340 and 430 /LM. respectively. The aminoglycosides were less efficient in reducing the carbachol-stimulated accumulation of IPs, since neither amikacin nor neomycin. both at 1 mM, had any significant effect. However. neomycin applied at 15 and 30 PM induced 29% and 43% of inhibition of the stimulated IP response. Finally, additive effects are obtained between some of the toxic drugs. The results suggest that a block of the IP transduction system, associated with the cholinergic efferent innervation of the organ of Corti, is a feature that may he involved in some types of ototoxicity. The inefficiency of aminoglycosides and the putative targets of the ototoxic agents are discussed.
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hal-02163282, version 1 (24-06-2019)

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  • HAL Id : hal-02163282 , version 1

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Sylvain Bartolami, Myriam Planche, Rémy Pujol. Inhibition of the carbachol-evoked synthesis of inositol phosphates by ototoxic drugs in the rat cochlea. Hearing Research, 1993, 67, pp.203 - 210. ⟨hal-02163282⟩

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