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 in | Hormones and behavior Vol. 48; no. 3; pp. 291 - 302 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Eugenia surname: Papalexi fullname: Papalexi, Eugenia organization: Laboratory of Histology and Embryology, Athens University Medical School, Mikras Asias 75, Goudi 11527, Athens, Greece – sequence: 2 givenname: Katerina surname: Antoniou fullname: Antoniou, Katerina organization: Department of Pharmacology, Medical School, University of Ioannina, Greece – sequence: 3 givenname: Efthimia surname: Kitraki fullname: Kitraki, Efthimia email: ekitraki@med.uoa.gr organization: Laboratory of Histology and Embryology, Athens University Medical School, Mikras Asias 75, Goudi 11527, Athens, Greece |
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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 |
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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 |
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