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EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats

BACKGROUND: Our previous research showed that 4 h of maternal anesthesia with isoflurane during early gestation in pregnant rats leads to a deficit in spatial memory of adult male offspring. Because spatial memory is predominantly a hippocampally-mediated task, we asked the question if early gestati...

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Autores principales: Palanisamy, Arvind, Crosby, Gregory, Culley, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744391/
https://www.ncbi.nlm.nih.gov/pubmed/29279051
http://dx.doi.org/10.1186/s12993-017-0132-5
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author Palanisamy, Arvind
Crosby, Gregory
Culley, Deborah J.
author_facet Palanisamy, Arvind
Crosby, Gregory
Culley, Deborah J.
author_sort Palanisamy, Arvind
collection PubMed
description BACKGROUND: Our previous research showed that 4 h of maternal anesthesia with isoflurane during early gestation in pregnant rats leads to a deficit in spatial memory of adult male offspring. Because spatial memory is predominantly a hippocampally-mediated task, we asked the question if early gestational exposure to isoflurane affects development of the hippocampus in the offspring. FINDINGS: Previously behaviorally characterized adult male rats that were exposed to isoflurane during second trimester were sacrificed at 4 months of age (N = 10 and 13, control and isoflurane groups, respectively) for quantitative histology of hippocampal subregions. Sections were stained with cresyl violet and the total number of cells in the granular layer of the dentate gyrus and the pyramidal cell layer in the CA1 region were determined by a blinded observer using unbiased stereological principles and the optical fractionator method. Data were analyzed using Student’s t test; P < 0.05 was accorded statistical significance. Stereological examination revealed 9% fewer cells in the granular layer of the dentate gyrus of isoflurane-exposed adult rats compared to controls (1,002,122 ± 84,870 vs. 1,091,829 ± 65,791, respectively; Mean ± S.D, *P = 0.01). In contrast, there were no changes in the cell number in the CA1 region, nor were there changes in the volumes of both regions. CONCLUSIONS: Our results show that maternal isoflurane anesthesia in rodents causes region-specific cell loss in the hippocampus of adult male offspring. These changes may, in part, account for the behavioral deficits reported in adult rats exposed to isoflurane in utero.
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spelling pubmed-57443912018-01-03 EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats Palanisamy, Arvind Crosby, Gregory Culley, Deborah J. Behav Brain Funct Short Paper BACKGROUND: Our previous research showed that 4 h of maternal anesthesia with isoflurane during early gestation in pregnant rats leads to a deficit in spatial memory of adult male offspring. Because spatial memory is predominantly a hippocampally-mediated task, we asked the question if early gestational exposure to isoflurane affects development of the hippocampus in the offspring. FINDINGS: Previously behaviorally characterized adult male rats that were exposed to isoflurane during second trimester were sacrificed at 4 months of age (N = 10 and 13, control and isoflurane groups, respectively) for quantitative histology of hippocampal subregions. Sections were stained with cresyl violet and the total number of cells in the granular layer of the dentate gyrus and the pyramidal cell layer in the CA1 region were determined by a blinded observer using unbiased stereological principles and the optical fractionator method. Data were analyzed using Student’s t test; P < 0.05 was accorded statistical significance. Stereological examination revealed 9% fewer cells in the granular layer of the dentate gyrus of isoflurane-exposed adult rats compared to controls (1,002,122 ± 84,870 vs. 1,091,829 ± 65,791, respectively; Mean ± S.D, *P = 0.01). In contrast, there were no changes in the cell number in the CA1 region, nor were there changes in the volumes of both regions. CONCLUSIONS: Our results show that maternal isoflurane anesthesia in rodents causes region-specific cell loss in the hippocampus of adult male offspring. These changes may, in part, account for the behavioral deficits reported in adult rats exposed to isoflurane in utero. BioMed Central 2017-12-26 /pmc/articles/PMC5744391/ /pubmed/29279051 http://dx.doi.org/10.1186/s12993-017-0132-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Paper
Palanisamy, Arvind
Crosby, Gregory
Culley, Deborah J.
EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title_full EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title_fullStr EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title_full_unstemmed EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title_short EARLY gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
title_sort early gestational exposure to isoflurane causes persistent cell loss in the dentate gyrus of adult male rats
topic Short Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744391/
https://www.ncbi.nlm.nih.gov/pubmed/29279051
http://dx.doi.org/10.1186/s12993-017-0132-5
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