Estrogens influence behavioral responses in a kainic acid model of neurotoxicity

The behavioral and neuroprotective effects of 17β-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid (KA), were examined. Estradiol was administered either acutely (150 μg/rat, ip) along with KA, 14 days post-ovariectomy, or chronically (sc capsu...

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Published inHormones and behavior Vol. 48; no. 3; pp. 291 - 302
Main Authors Papalexi, Eugenia, Antoniou, Katerina, Kitraki, Efthimia
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.09.2005
Elsevier
Elsevier BV
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Abstract The behavioral and neuroprotective effects of 17β-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid (KA), were examined. Estradiol was administered either acutely (150 μg/rat, ip) along with KA, 14 days post-ovariectomy, or chronically (sc capsules providing proestrus estrogen levels in serum) starting at ovariectomy. Exploratory behavior, as deduced by sniffing in the open field test, was reduced in KA-treated rats. Both hormonal schemes partially restored sniffing behavior in KA-lesioned subjects. Moreover, acute and chronic E2 administration in KA-treated rats resulted in increased vertical and horizontal activity of these animals in the open field test. Memory for object recognition was reduced following KA and was not restored by hormonal treatments. Acute, but not chronic, E2 coadministration with KA significantly impaired spatial performance in the water maze task, while KA alone had no effect. Both acute and chronic estradiol administration rescued hilar and CA1 neurons from KA-induced cell death. Chronic, but not acute, E2 increased neurofilament immunoreactivity in the mossy fibers of the dentate gyrus neurons, similarly to KA. Our results show that although estradiol administration in KA-treated rats has beneficial effects on cell survival, it has diverse effects on exploratory behavior, object, and spatial memory. Estradiol effects on KA-lesioned animals depended on the duration and timing of exposure to the hormone, implying different mechanisms of hormone actions.
AbstractList The behavioral and neuroprotective effects of 17 beta -estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid (KA), were examined. Estradiol was administered either acutely (150 mu g/rat, ip) along with KA, 14 days post-ovariectomy, or chronically (sc capsules providing proestrus estrogen levels in serum) starting at ovariectomy. Exploratory behavior, as deduced by sniffing in the open field test, was reduced in KA-treated rats. Both hormonal schemes partially restored sniffing behavior in KA-lesioned subjects. Moreover, acute and chronic E2 administration in KA-treated rats resulted in increased vertical and horizontal activity of these animals in the open field test. Memory for object recognition was reduced following KA and was not restored by hormonal treatments. Acute, but not chronic, E2 coadministration with KA significantly impaired spatial performance in the water maze task, while KA alone had no effect. Both acute and chronic estradiol administration rescued hilar and CA1 neurons from KA-induced cell death. Chronic, but not acute, E2 increased neurofilament immunoreactivity in the mossy fibers of the dentate gyrus neurons, similarly to KA. Our results show that although estradiol administration in KA-treated rats has beneficial effects on cell survival, it has diverse effects on exploratory behavior, object, and spatial memory. Estradiol effects on KA-lesioned animals depended on the duration and timing of exposure to the hormone, implying different mechanisms of hormone actions.
The behavioral and neuroprotective effects of 17β-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid (KA), were examined. Estradiol was administered either acutely (150 μg/rat, ip) along with KA, 14 days post-ovariectomy, or chronically (sc capsules providing proestrus estrogen levels in serum) starting at ovariectomy. Exploratory behavior, as deduced by sniffing in the open field test, was reduced in KA-treated rats. Both hormonal schemes partially restored sniffing behavior in KA-lesioned subjects. Moreover, acute and chronic E2 administration in KA-treated rats resulted in increased vertical and horizontal activity of these animals in the open field test. Memory for object recognition was reduced following KA and was not restored by hormonal treatments. Acute, but not chronic, E2 coadministration with KA significantly impaired spatial performance in the water maze task, while KA alone had no effect. Both acute and chronic estradiol administration rescued hilar and CA1 neurons from KA-induced cell death. Chronic, but not acute, E2 increased neurofilament immunoreactivity in the mossy fibers of the dentate gyrus neurons, similarly to KA. Our results show that although estradiol administration in KA-treated rats has beneficial effects on cell survival, it has diverse effects on exploratory behavior, object, and spatial memory. Estradiol effects on KA-lesioned animals depended on the duration and timing of exposure to the hormone, implying different mechanisms of hormone actions.
The behavioral and neuroprotective effects of 17beta-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid (KA), were examined. Estradiol was administered either acutely (150 mug/rat, ip) along with KA, 14 days post-ovariectomy, or chronically (sc capsules providing proestrus estrogen levels in serum) starting at ovariectomy. Exploratory behavior, as deduced by sniffing in the open field test, was reduced in KA-treated rats. Both hormonal schemes partially restored sniffing behavior in KA-lesioned subjects. Moreover, acute and chronic E2 administration in KA-treated rats resulted in increased vertical and horizontal activity of these animals in the open field test. Memory for object recognition was reduced following KA and was not restored by hormonal treatments. Acute, but not chronic, E2 coadministration with KA significantly impaired spatial performance in the water maze task, while KA alone had no effect. Both acute and chronic estradiol administration rescued hilar and CA1 neurons from KA-induced cell death. Chronic, but not acute, E2 increased neurofilament immunoreactivity in the mossy fibers of the dentate gyrus neurons, similarly to KA. Our results show that although estradiol administration in KA-treated rats has beneficial effects on cell survival, it has diverse effects on exploratory behavior, object, and spatial memory. Estradiol effects on KA-lesioned animals depended on the duration and timing of exposure to the hormone, implying different mechanisms of hormone actions.
Author Antoniou, Katerina
Kitraki, Efthimia
Papalexi, Eugenia
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Issue 3
Keywords Rat
Water maze
Open field
Object recognition
Estradiol
Kainic acid
Hippocampus
Agonist
Memory
Central nervous system
Estrogen
17β-Estradiol
Glutamate receptor
Encephalon
Kainate receptor
Neurotoxicity
Rodentia
Ovarian hormone
Open field behavior
Vertebrata
Mammalia
Animal
Models
Sex steroid hormone
Recognition
Language English
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Snippet The behavioral and neuroprotective effects of 17β-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid...
The behavioral and neuroprotective effects of 17beta-estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid...
The behavioral and neuroprotective effects of 17 beta -estradiol (E2), on ovariectomized rats treated with a subconvulsive dose (7 mg/kg bw, ip) of kainic acid...
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SubjectTerms Analysis of Variance
Animal ethology
Animals
Behavioral psychophysiology
Biological and medical sciences
Brain Injuries - chemically induced
Brain Injuries - drug therapy
Brain Injuries - physiopathology
Estradiol
Estradiol - metabolism
Estradiol - pharmacology
Exploratory Behavior - drug effects
Exploratory Behavior - physiology
Female
Fundamental and applied biological sciences. Psychology
Hippocampus
Hippocampus - drug effects
Hippocampus - pathology
Hippocampus - physiology
Hormones and behavior
Kainic Acid
Mammalia
Maze Learning - drug effects
Maze Learning - physiology
Models, Animal
Neurons - drug effects
Neurons - pathology
Neurons - physiology
Neuroprotective Agents - metabolism
Neuroprotective Agents - pharmacology
Neurotoxicity Syndromes - drug therapy
Neurotoxicity Syndromes - physiopathology
Neurotoxins
Object recognition
Open field
Ovariectomy
Psychology. Psychoanalysis. Psychiatry
Psychology. Psychophysiology
Rat
Rats
Rats, Wistar
Recognition (Psychology) - drug effects
Recognition (Psychology) - physiology
Space Perception - drug effects
Space Perception - physiology
Vertebrata
Water maze
Title Estrogens influence behavioral responses in a kainic acid model of neurotoxicity
URI https://dx.doi.org/10.1016/j.yhbeh.2005.03.009
https://www.ncbi.nlm.nih.gov/pubmed/15907329
https://www.proquest.com/docview/194896228
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https://search.proquest.com/docview/20822867
Volume 48
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