Abstract
Four episodes of immobilization stress induced a decrease in the sensitivity of rats to glucocorticoid hormones, which was accompanied by anxiogenic behavior, increased MAO-B activity, and a parallel increase in lipid peroxidation (LPO) in brain tissues. There was a simultaneous increase in MAO-B activity in the kidneys and accumulation of LPO products in the liver and kidneys. Administration of Kenalog (2 mg/kg), a pharmacological analog of glucocorticoid hormones, prevented the poststress activation of MAO-B and LPO and decreased the extent of anxiogenic behavioral abnormalities in rats.
MeSH terms
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Animals
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Behavior, Animal / drug effects*
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Behavior, Animal / physiology
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Brain / drug effects
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Brain / enzymology
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Female
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Glucocorticoids / pharmacology*
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Kidney / drug effects
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Kidney / enzymology
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Lipid Peroxidation / drug effects*
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Lipid Peroxidation / physiology
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Liver / drug effects
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Liver / enzymology
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Locomotion / drug effects
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Locomotion / physiology
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Male
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Monoamine Oxidase / metabolism*
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Motor Activity / drug effects
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Rats
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Restraint, Physical / methods
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Statistics, Nonparametric
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Stress, Physiological* / enzymology
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Stress, Physiological* / physiopathology
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Triamcinolone Acetonide / pharmacology
Substances
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Glucocorticoids
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Monoamine Oxidase
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Triamcinolone Acetonide