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Tackling mental health disorders in females

Grant number: 14/50829-4
Support type:Regular Research Grants
Duration: April 01, 2015 - March 31, 2016
Field of knowledge:Biological Sciences - Pharmacology - Neuropsychopharmacology
Cooperation agreement: CONFAP ; Newton Fund, with FAPESP as a partner institution in Brazil ; MRC, UKRI
Principal researcher:Marcus Lira Brandão
Grantee:Marcus Lira Brandão
Principal researcher abroad: Thelma Anderson Lovick
Institution abroad: University of Bristol, England
Home Institution: Instituto de Neurociências e Comportamento (INEC). Ribeirão Preto , SP, Brazil

Abstract

The medial hypothalamus, amygdala and dorsal periaqueductal gray (dPAG) and the inferior colliculus (I C) have been grouped together as an "encephalic aversion system" (EAS). The neural substrates responsible for fear and anxiety of these structures translate information of aversive nature in behavioral and emotional adaptive output reactions. Nowadays, it is believed that the EAS possess a sensorimotor filter that functions as a gating for the threatening stimuli. Malfunctioning of this filter results in maladaptive processing that may lead to anxiety. The understanding of the neurochemical, anatomical and genetic substrates of fear and anxiety must take into account the chemistry of the "defense-system" in a broader approach and prospect. It has been proposed that GABAergic mechanisms are involved in the gating of distinct sensory information of aversive nature depending on the midbrain structure which is activated. The prefrontal cortex and the core and shell subregions of the nucleus accumbens (NAC) may also contribute to the organization of defensive reactions to threatening and dangerous situations. Besides GABA, 5-HT, opioids, dopamine, neurokinins and excitatory amino acids have ali been implicated in the regulation of anxiety-related behaviors induced by stimulation of the EAS. However, little is known on how they regulate the processing of aversive information. This project will tackle on how these neurochemical mechanisms modulate the sensory information input and the behavioral output underlying the defensive responses associated with fear and anxiety. It is also our purpose to determine the extent to which the combined activity of the hypothalamic-pituitary-adrenal (HPA) axis and the neurochemical systems involved in the expression of conditioned and unconditioned fear responseswork together in the modulation of the defense reaction. The challenge will be to establish an integrative approach (behavioral, pharmacological, electrophysiological, neurochemical and imunohistochemical) that enable us to characterize the whole stimulus-defensive behavior process instead of treating the defense reaction in relative isolation, and secondly, the neurochemical and anatomical systems that subserve the consequences of aversive information to the organism so as to produce knowledge that might lead to therapeutic change using novel behavioral and drug therapy. This project also dedicate part of its financial resources for diffusing the acquired knowledge in the neurobiology of anxiety and depression to the general public. In this respect we act in partnership with the Institute of Neurosciences and Behavior (INeC), which is a non-profit private organization of public interest, with infrastructure set up for the organization of courses and scientific meetings, as well as for the elaboration of educational material that is available at its homepage (www.inec-usp.org). (AU)

Articles published in Agência FAPESP Newsletter about the research grant:

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
FIGUEIREDO, REBECA MACHADO; DE CARVALHO, MILENE CRISTINA; BRANDAO, MARCUS LIRA; LOVICK, THELMA ANDERSON. Short-term, low-dose fluoxetine prevents oestrous cycle-linked increase in anxiety-like behaviour in female rats. JOURNAL OF PSYCHOPHARMACOLOGY, v. 33, n. 5, p. 548-557, MAY 2019. Web of Science Citations: 0.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.