1. Effects of selective and combined serotonin and dopamine depletion on the loudness dependence of the auditory evoked potential (LDAEP) in humans
- Author
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Rodney J. Croft, Barry V. O'Neill, Pradeep J. Nathan, Valérie Guille, Kirsty Elizabeth Scholes, K. Luan Phan, and Sumie Leung
- Subjects
Adult ,Male ,Serotonin ,medicine.medical_specialty ,Dopamine ,Loudness Perception ,Phenylalanine ,Serotonergic ,Double-Blind Method ,Internal medicine ,medicine ,Humans ,Pharmacology (medical) ,Tyrosine ,Evoked potential ,Cross-Over Studies ,Electromyography ,Chemistry ,Tryptophan ,Electroencephalography ,Psychiatry and Mental health ,Endocrinology ,Monoamine neurotransmitter ,Acoustic Stimulation ,Neurology ,Evoked Potentials, Auditory ,Neurology (clinical) ,medicine.drug - Abstract
Background The loudness dependence of the auditory evoked potential (LDAEP) has been suggested as a possible in vivo measure of central serotonin function. However, more recent studies suggest that the LDAEP may be modulated by multiple neuromodulatory systems in addition to the serotonergic system. Accordingly we further examined the effects of selective serotonin, dopamine and simultaneous serotonin and dopamine depletion on the LDAEP in healthy subjects. Methods The study employed a placebo-controlled, double-blind, cross over design. Fourteen subjects were tested under four acute treatment conditions: placebo (balanced amino acid drink), tryptophan (serotonin) depletion (ATD), tyrosine/phenylalanine (dopamine) depletion (ATPD) and combined tryptophan/tyrosine/phenylalanine (serotonin and dopamine) depletion (CMD). Testing was conducted 5.5 h post-depletion and changes in the amplitude of the N1/P2 at varying intensities (60, 70, 80, 90, 100 dB) were examined at CZ. Results Greater than 80% plasma precursor depletion was achieved across all conditions. Despite significant depletion of monoamine precursors, ATD, (p = 0.318), ATPD (p = 0.061) and CMD (p = 0.104) had no effects on the LDAEP (60–100 dB). Conclusion Acute serotonin and dopamine depletion did not modulate the LDAEP. This finding adds support to growing evidence that the LDAEP is insensitive to acute changes in serotonin and dopamine neurotransmission. Copyright © 2008 John Wiley & Sons, Ltd.
- Published
- 2008