Research Article

Prenatal stress impairs recognition memory and leads to neurodevelopmental deficits in hippocampus of adolescent rats with early acute pentylenetetrazole-kindling

Volume: 7 Number: 4 July 4, 2021
EN

Prenatal stress impairs recognition memory and leads to neurodevelopmental deficits in hippocampus of adolescent rats with early acute pentylenetetrazole-kindling

Abstract

Objectives: This study aimed to investigate the effects of prenatal stress (PS) on hippocampus of early acute pentylenetetrazole (PTZ)-kindled offspring in adolescence. Recognition memory, morphological changes and synaptophysin levels in hippocampus were evaluated.

Methods: Restraint stress was induced to a group of pregnant dams and non-stressed (NA) group remained undisturbed. Next, male and female offspring were divided as 1. PS-PTZ, 2. PS -control, 3. NA-PTZ and 4. NA-control (n = 12 in each group). The object recognition test was performed following PTZ injection (45 mg/kg) on postnatal day 10 (P10). Brains were collected on postnatal day 35 (P35) to determine neuronal density and synaptophysin expression by immuno/-histological studies. Further, oxidative stress products in hippocampus were analyzed with different biochemical assays.

Results: PS impaired recognition memory in PTZ group significantly (p = 0.03); however, the impairment of PS was reversible in control group compared to PTZ (p = 0.04). Furthermore, PS caused neuronal loss in CA1 (p = 0.01) and decreased synaptophysin expression in the CA3 area of hippocampus in PTZ group (p = 0.03). PS also increased the oxidative stress markers in PTZ group significantly (p < 0.05).

Conclusions: These results suggest that PS causes neurodevelopmental deficits in adolescent hippocampus and recognition memory after early-life seizures prominently. However, the damage of only PS in adolescence can be reversible. Therefore, the effects of PS in the adult hippocampus and other regions of brain need to be further studied.

Keywords

Supporting Institution

The Scientific Research Project Coordination of Ege University

Project Number

18-SBE-004/ 2018

Thanks

We would like to thank Assoc. Prof. Dr. Timur Köse for his support on statistical analysis and The Department of Histology and Embryology staff for their assistance in the laboratory work.

References

  1. 1. Weinstock M. The long-term behavioural consequences of prenatal stress. Neurosci Biobehav Rev 2008;32:1073-86.
  2. 2. Qulu L, Daniels WM, Mabandla M. Exposure to prenatal stress enhances the development of seizures in young rats. Metab Brain Dis 2012;27:399-404.
  3. 3. Lopim GM, Gutierre RC, da Silva, EA, Arida RM. Physical exercise during pregnancy minimizes PTZ-induced behavioral manifestations in prenatally stressed offspring. Dev Psychobiol 2020;62:240-49.
  4. 4. Krugers HJ, Karst H, Joels M. Interactions between noradrenaline and corticosteroids in the brain: from electrical activity to cognitive performance. Front Cell Neurosci 2012;6:15.
  5. 5. Weinstock M. The potential influence of maternal stress hormones on development and mental health of the offspring. Brain Behav Immun 2005;19:296-308.
  6. 6. Jia N, Yang K, Sun Q, Cai Q, Li H, Cheng D, et al. Prenatal stress causes dendritic atrophy of pyramidal neurons in hippocampal CA3 region by glutamate in offspring rats. Dev Neurobiol 2010;70:114-25.
  7. 7. Lai MC, Huang LT. Effects of early life stress on neuroendocrine and neurobehavior: mechanisms and implications. Pediatr Neonatol 2011;52:122-9.
  8. 8. Schoenfeld TJ, McCausland HC, Morris HD, Padmanaban V, Cameron HA. Stress and loss of adult neurogenesis differentially reduce hippocampal volume. Biol Psychiatry 2017;82:914-23.

Details

Primary Language

English

Subjects

Psychiatry , Anatomy , Neurosciences , Medical Physiology

Journal Section

Research Article

Publication Date

July 4, 2021

Submission Date

September 29, 2020

Acceptance Date

March 17, 2021

Published in Issue

Year 1970 Volume: 7 Number: 4

AMA
1.Çelik K, Bilim P, Garip G, Durmaz B, Y. Sözmen E, Baka M. Prenatal stress impairs recognition memory and leads to neurodevelopmental deficits in hippocampus of adolescent rats with early acute pentylenetetrazole-kindling. Eur Res J. 2021;7(4):340-347. doi:10.18621/eurj.801699

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