Repetitive Noxious Neonatal Stimuli Increases Dentate Gyrus Cell Proliferation and Hippocampal Brain- Derived Neurotrophic Factor Levels

Repetitive Noxious Neonatal Stimuli Increases Dentate Gyrus Cell Proliferation and Hippocampal Brain- Derived Neurotrophic Factor Levels

Author Malheiros, J. M. Autor UNIFESP Google Scholar
Lima, M. Autor UNIFESP Google Scholar
Avanzi, R. D. T. Autor UNIFESP Google Scholar
Gomes da Silva, S. Autor UNIFESP Google Scholar
Suchecki, D. Autor UNIFESP Google Scholar
Guinsburg, Ruth Autor UNIFESP Google Scholar
Covolan, Luciene Autor UNIFESP Google Scholar
Institution Universidade Federal de São Paulo (UNIFESP)
Inst Israelita Ensino & Pesquisa Albert Einstein
Abstract Neonatal noxious stimulation has been proposed to model pain triggered by diagnostic/therapeutic invasive procedures in premature infants. Previous studies have shown that hippocampal neurogenesis rate and the behavioral repertoire of adult rats may be altered by neonatal noxious stimuli. the purpose of this study was to evaluate whether noxious stimulation during neonatal period alters the nociceptive response and dentate gyrus neurogenesis when compared to rats subjected to a single noxious stimulus in late infancy. Plasma corticosterone and hippocampal brain-derived neurotrophic factor (BDNF) levels were measured. Neurogenesis in the dentate gyrus was evaluated in adolescent rats (postnatal day 40; P40) exposed twice to intra-plantar injections of Complete Freund's adjuvant (CFA) on P1 and P21 (group P1P21) or P8 and P21 (P8P21) or exposed once on P21 (pubertal). On P21, one subset of animals received 5-bromo-2-deoxyuridine (BrdU) and was euthanized on P40 for identification of proliferating cells in the dentate gyrus. Another subset was sampled for thermal response or plasma corticosterone measurement and hippocampal BDNF levels. Proliferative cell rate in dentate gyrus was the highest in all re-exposed groups (P<0.001), except for P8 females (P8P21F), revealing also a sex difference, where P8P21 males showed higher rate than females (P<0.001). Stimulated groups took longer than CTL animals to lick the paws (P<0.001), regardless of the age when the noxious stimulus was applied. Re-exposed groups had lower corticosterone plasma level (P1P21 M and F, P8P21M) than controls. On the contrary, hippocampal BDNF was increased in males from both re-exposed groups. These results show that infant noxious stimulation in neonatally previously stimulated rats is related to high proliferation in the DG and this association seems to be modified by the animal's sex. the new generated dentate granule cells in the hippocampus may have a role in the long-term behavioral responses to neonatal nociceptive stimulation. Noxious stimulation in the neonatal period results in sex-dependent neurogenic response. (c) 2013 Wiley Periodicals, Inc.
Keywords nociception
hippocampus
newborn
proliferation
sex difference
Language English
Sponsor Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Grant number FAPESP: 2009/53646-0
Date 2014-04-01
Published in Hippocampus. Hoboken: Wiley-Blackwell, v. 24, n. 4, p. 415-423, 2014.
ISSN 1050-9631 (Sherpa/Romeo, impact factor)
Publisher Wiley-Blackwell
Extent 415-423
Origin http://dx.doi.org/10.1002/hipo.22235
Access rights Closed access
Type Article
Web of Science ID WOS:000332768400006
URI http://repositorio.unifesp.br/handle/11600/37586

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