Abstract

The main objective was to show the decrement of serotoninergic brain activity in depressed women, through the analyses of the slope amplitude of N1/P2 components of the auditory-evoked potentials (AEP), and the measurement of the L-tryptophan free fraction in plasma (FFT). This cross-sectional study was carried out in 60 women, 30 depressed and 30 normal controls. Both groups were measured FFT, glucose, and neutral amino acids (NAA) levels; besides performing AEP to analyses the N1/P2 slope amplitude. It was found a lengthening in the slope amplitude of N1/P2 components of AEP in the group of depressed women, and despite that the level of FFT was low, there were no changes between bound fraction and the total L-Trp. The former suggests a decrease in serotonergic brain activity in the group of depressed women. Otherwise, since the auditory cortex response to sound is regulated by serotonergic innervation, it was expected a change in the behavior of AEP in the group of depressed patients. Thus, the slope amplitude of N1/P2 components of the AEP and the measurement of FFT have proved to be a good clinical indicators of the serotonergic neurotransmission state in the brain of depressed patients, and in another clinical conditions where brain serotonin is involved.

Highlights

  • The main objective was to show the decrement of serotoninergic brain activity in depressed women, through the analyses of the slope amplitude of N1/P2 components of the auditory-evoked potentials (AEP), and the measurement of the L-tryptophan free fraction in plasma (FFT)

  • The main objective of this study was to show the decrement of serotoninergic brain activity in depressed women, through the analyses of the slope amplitude of N1/P2 components of the auditory-evoked potentials, and the measurement of the L-tryptophan free fraction in plasma

  • Biochemical results showed a significantly low level of the free fraction of L-Trp in the depressed women group; fact that initially suggests a low transport of tryptophan to the brain and as a result, a low synthesis of serotonin which leads to a serotoninergic activity reduction

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Summary

Introduction

There are some hypotheses related to the dysfunction of some networks and neurotransmission neuronal systems inside the limbic area, and the cortex; which are based on different polymorphisms that may lead to metabolism dysfunction, and transport alterations of monoamines, serotonin, dopamine, norepinephrine, glutamate, and gamma-amino-butyric acid (GABA) along these systems (Nestler et al, 2002; Meltzer, 1990; Dunlop & Nemeroff, 2007; Nutt, 2006; Sullivan et al, 2000; Lohoff, 2010; Pehrson & Sanchez, 2014). Depression must not be viewed as a single disease, but as a syndrome triggered by different causes and physiopathology (Nestler et al, 2002). Different attempts have been made to establish several subtypes of depression, based on certain groups of symptoms (Akiskal, 2000; Blazer, 2000); these subtypes are based solely on symptomatic differences, and there is as yet no evidence that they reflect different underlying disease states

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