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Prenatal exposure to interleukin-6 results in inflammatory neurodegeneration in hippocampus with NMDA/GABA(A) dysregulation and impaired spatial learning

Samuelsson, Anne-Maj, 1977 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
Jennische, Eva, 1949 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Hansson, Hans-Arne, 1939 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
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Holmäng, Agneta, 1959 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
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 (creator_code:org_t)
2006
2006
English.
In: Am J Physiol Regul Integr Comp Physiol. ; 290:5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • During pregnancy, infection or immune responses induce cytokine release, which might influence fetal neurodevelopment, leading to neurodegenerative disease in adulthood. Because the hippocampus is a key area for learning and memory, we evaluated 4- and 24-wk-old rats for the effects of early and late prenatal exposure to interleukin-6 (IL-6) on hippocampal morphology, expression of mRNA for IL-6, the gamma-aminobutyric acid receptor (GABA(Aalpha5)), the NR1 subunit of the N-methyl-D-aspartate receptor, and glial fibrillary acidic protein (GFAP), caspase-3 protein and mRNA levels, and learning abilities. Late exposure increased serum IL-6 and hippocampal expression of IL-6 mRNA at 4 and 24 wk. All adult rats showed neuronal loss in the hilus and astrogliosis; males had losses mainly in the CA2 and CA3 regions, and females in CA1. Expression of GABA(Aalpha5), NR1, and GFAP mRNA increased in late-exposed males and females at 4 and 24 wk. mRNA and protein levels of the apoptosis marker caspase-3 were increased in all late-exposed rats except males at 4 wk. Evaluation of hippocampus-dependent working memory in the Morris water maze at 20 wk of age showed increases in escape latency and time spent near the pool wall in all IL-6 adult rats, especially females. These findings suggest that fetal IL-6 exposure, especially in late pregnancy, leads to increased IL-6 levels in the circulation and hippocampus, abnormalities of hippocampal structural and morphology, and decreased learning during adulthood.

Keyword

Adrenocorticotropic Hormone/blood
Aging/metabolism/psychology
Animals
Apoptosis/drug effects
Astrocytes/pathology
Blotting
Western
Body Weight/physiology
Caspase 3
Caspases/metabolism
DNA
Complementary/biosynthesis/genetics
Female
Glial Fibrillary Acidic Protein/metabolism
Gliosis/chemically induced/pathology
Hippocampus/*pathology
Hydrocortisone/blood
Immunohistochemistry
Inflammation/*pathology
Interleukin-6/*pharmacology
Maze Learning/*physiology
Nerve Degeneration/*pathology
Pregnancy
Prenatal Exposure Delayed Effects
Rats
Rats
Wistar
Receptors
GABA-A/*physiology
Receptors
N-Methyl-D-Aspartate/drug effects/*physiology
Reverse Transcriptase Polymerase Chain Reaction

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