Paulo Leonardo Morais

Dr. Paulo Leonardo Morais


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 November 2019 in Journal of Comparative Neurology
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PMPaulo Leonardo Morais
Paulo Leonardo Morais
RLRuthnaldo R. M. de Lima
Ruthnaldo R. M. de Lima
JRJorge Alexander Ríos-Flórez
Jorge Alexander Ríos-Flórez
TMTúlio F. V. Melo
Túlio F. V. Melo
FCFrancisco Clascá
Francisco Clascá
EJExpedito S. Nascimento Junior
Expedito S. Nascimento Junior

12 June 2025 in Life
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Journal Article
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FGFrancisca Tayná da Silva Gomes
Francisca Tayná da Silva Gomes
AAAntônio Vicente Dias de Andrade
Antônio Vicente Dias de Andrade
PMPaloma Paloma Melo
Paloma Paloma Melo
Roque Ribeiro da Silva JúniorRoque Ribeiro da Silva Júnior
Roque Ribeiro da Silva Júnior
DSDébora de Souza
Débora de Souza
JCJose Rodolfo Lopes de Paiva Cavalcanti
Jose Rodolfo Lopes de Paiva Cavalcanti
High-fat diets, characterised by their high lipid content, have been associated with structural and functional alterations in the hippocampus of rodents, including a reduction in the expression of brain-derived neurotrophic factor (BDNF), which negatively impacts learning and memory. Evidence suggests that these impairments may be attenuated by regular physical exercise. This review aimed to gather relevant scientific evidence available on the effects of the association between high-fat diets and physical exercise on BDNF expression levels in the hippocampus of rats. The studies analysed highlight a neuroprotective effect of exercise, capable of positively modulating BDNF levels and, consequently, improving the cognitive functions of these animals.

27 March 2019 in Frontiers in Neuroanatomy
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Journal Article
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PMPaulo Leonardo Morais
Paulo Leonardo Morais
MGMaría García-Amado
María García-Amado
RLRuthnaldo Rodrigues Melo Lima
Ruthnaldo Rodrigues Melo Lima
ACAngélica Córdoba-Claros
Angélica Córdoba-Claros
JCJeferson Souza Cavalcante
Jeferson Souza Cavalcante
ENExpedito Silva Nascimento
Expedito Silva Nascimento
The amygdaloid complex (AC) is a heterogeneous aggregate of nuclei located in the rostromedial region of the temporal lobe. In addition to being partly connected among themselves, the AC nuclei are strongly interconnected with the cerebral cortex, striatum, basal forebrain, hypothalamus and brainstem. Animal and human functional studies have established that the AC is a central hub of the neuronal networks supporting emotional responsivity, particularly its negative/aversive components. Dysfunction of AC circuits in humans has been implicated in anxiety, depression, schizophrenia and bipolar disorder. The small New-World marmoset monkey (Callithrix jacchus) has recently become a key model for neuroscience research. However, the nuclear and fiber tract organization of marmoset AC has not been examined in detail. Thus, the extent to which it can be compared to the AC of Old-World (human and macaque) primates is yet unclear. Here, using Nissl and acetylcholinesterase (AChE) histochemical stains as a reference, we analyzed the cytoarchitecture and nuclear parcellation of the marmoset AC. In addition, given the increasing relevance of tractographic localization for high-resolution in vivo imaging studies in non-human primates, we also identified the myelin fiber tracts present within and around the AC as revealed by the Gallyas method. The present study provides a detailed atlas of marmoset AC. Moreover, it reveals that, despite phylogenetic distance and brain size differences, every nucleus and myelinated axon bundle described in human and macaque studies can be confidently recognized in marmosets.

7 June 2023 in Clinical Psychopharmacology and Neuroscience
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DSDébora de Souza
Débora de Souza
HCHosana Mirelle Goes e Silva Costa
Hosana Mirelle Goes e Silva Costa
FNFrancisca Idalina Neta
Francisca Idalina Neta
PMPaulo Leonardo Morais
Paulo Leonardo Morais
LGLuís Marcos de Medeiros Guerra
Luís Marcos de Medeiros Guerra
CVClaudio Lopes de Vasconcelos
Claudio Lopes de Vasconcelos
Débora Lopes Silva de Souza, Hosana Mirelle Goes e Silva Costa, Francisca Idalina Neta, Paulo Leonardo Araujo de Gois Morais, Luís Marcos de Medeiros Guerra, Fausto Pierdoná Guzen, Lucídio Clebeson de Oliveira, José Rodolfo Lopes de Paiva Cavalcanti, Cynthia Cavalcanti de Albuquerque, Claudio Lopes de Vasconcelos. Clin Psychopharmacol Neurosci -0001;0:. https://doi.org/10.9758/cpn.23.1058

1 December 2014 in Neuroscience Research
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PMPaulo Leonardo Morais
Paulo Leonardo Morais
MSMelquisedec Santana
Melquisedec Santana
JCJudney Cley Cavalcante
Judney Cley Cavalcante
MCMiriam Stela Maris de Oliveira Costa
Miriam Stela Maris de Oliveira Costa
JCJeferson Sousa Cavalcante
Jeferson Sousa Cavalcante
ENExpedito Silva Do Nascimento
Expedito Silva Do Nascimento

15 May 2018 in Frontiers in Neuroanatomy
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Journal Article
Open access
NSNelyane N. M. Santana
Nelyane N. M. Santana
MBMarília A. S. Barros
Marília A. S. Barros
HMHelder H. A. Medeiros
Helder H. A. Medeiros
MSMelquisedec A. D. Santana
Melquisedec A. D. Santana
LSLara L. Silva
Lara L. Silva
ENExpedito S. Nascimento
Expedito S. Nascimento
In mammals, the suprachiasmatic nucleus (SCN) and the intergeniculate leaflet (IGL) are the main components of the circadian timing system. The SCN, classically known as the master circadian clock, generates rhythms and synchronizes them to environmental cues. The IGL is a key structure that modulates SCN activity. Strategies on the use of time by animals can provide important clues about how some species are adapted to competitive process in nature. Few studies have provided information about temporal niche in bats with special attention on the neural substrate underlies circadian rhythms. The aim of this study was to investigate these circadian centers with respect to their cytoarchitecture, chemical content and retinal projections in the flat-faced fruit-eating bat (Artibeus planirostris), a chiropteran endemic to South America. Unlike other species of phyllostomid bats, the flat-faced fruit-eating bat’s peak of activity occurs five hours after sunset. This raises several questions about the structure and function of the SCN and IGL in this species. We carried out a mapping of the retinal projections and cytoarchitectural study of the nuclei using qualitative and quantitative approaches. Based on relative optical density findings, the SCN and IGL of the flat-faced fruit-eating bat receive bilaterally symmetric retinal innervation. The SCN contains vasopressin (VP) and vasoactive intestinal polypeptide (VIP) neurons with neuropeptide Y (NPY), serotonin (5-HT) and glutamic acid decarboxylase (GAD) immunopositive fibers/terminals and is marked by intense glial fibrillary acidic protein (GFAP) immunoreactivity. The IGL contains NPY perikarya as well as GAD and 5-HT immunopositive terminals and is characterized by dense GFAP immunostaining. In addition, stereological tools were combined with Nissl stained sections to estimate the volumes of the circadian centers. Taken together, the present results in the flat-faced fruit-eating bat reveal some differences compared to other bat species which might explain the divergence in the hourly activity among bats in order to reduce the competitive potential and resource partitioning in nature.