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Noise Health ; 7(29): 24-30, 2005.
Article in English | MEDLINE | ID: mdl-17478966

ABSTRACT

Both the antioxidant, n-l-acetyl cysteine (L-NAC) and the Src inhibitor, KX1-004, have been used to protect the cochlea from hazardous noise. To date, KX1-004 has only been used locally on the round window. In the current study, the two drugs were administered systemically. LNAC was delivered intraperitoneally at a dose of 325 mg/kg while KX1-004 was administered subcutaneously at a dose of 50 mg/kg. The noise exposure consisted of a 4 kHz octave band of noise at 100 dB SPL for 6 hours/day for 4 days. The drugs were administered once each day, 30 minutes prior to the onset of the noise exposure. The animals' hearing was estimated using the evoked response records from surgically-implanted chronic electrodes in the inferior colliculi. Animals treated with LNAC and KX1-004 had from 10 to 20 dB less temporary threshold shift at day 1 and an average 10 dB less permanent threshold shift by day 21 when compared to control saline treated animals. There were no significant side effects (i.e.: appetite loss, weight loss, lethargy, etc.) related to either of the drug treatments. KX1-004 produced at least as much protection as L-NAC, but at a significantly lower concentration.


Subject(s)
Acetylcysteine/administration & dosage , Evoked Potentials, Auditory/drug effects , Glutathione/administration & dosage , Hearing Loss, Noise-Induced/prevention & control , Noise/adverse effects , Protein Kinase Inhibitors/administration & dosage , Reactive Oxygen Species/adverse effects , src-Family Kinases/antagonists & inhibitors , Acetylcysteine/pharmacology , Animals , Apoptosis/drug effects , Auditory Threshold/drug effects , Chinchilla , Disease Models, Animal , Electrodes , Environmental Exposure/adverse effects , Glutathione/pharmacology , Hearing Loss, Noise-Induced/drug therapy , Inferior Colliculi/physiology , Injections, Intraperitoneal , Protein Kinase Inhibitors/pharmacology , Time Factors , src-Family Kinases/administration & dosage , src-Family Kinases/pharmacology
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