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1.
Exp Physiol ; 98(1): 290-303, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22707502

ABSTRACT

The antistress effect of theanine (γ-glutamylethylamide), an amino acid in tea, was investigated using mice that were psychosocially stressed from a conflict among male mice in conditions of confrontational housing. Two male mice were housed in the same cage separated by a partition to establish a territorial imperative. When the partition was removed, the mice were co-housed confrontationally. As a marker for the stress response, changes in the adrenal gland were studied in comparison to group-housed control mice (six mice in a cage). Significant adrenal hypertrophy was observed in mice during confrontational housing, which was developed within 24 h and persisted for at least 1 week. The size of cells in the zona fasciculata of the adrenal gland, from which glucocorticoid is mainly secreted, increased (∼1.11-fold) in mice during confrontational housing, which was accompanied by a flattened diurnal rhythm of corticosterone and ACTH in blood. The ingestion of theanine (>5 µg ml(-1)) prior to confrontational housing significantly suppressed adrenal hypertrophy. An antidepressant, paroxetin, suppressed adrenal hypertrophy in a similar manner in mice during confrontational housing. In mice that ingested theanine, behavioural depression was also suppressed, and a diurnal rhythm of corticosterone and ACTH was observed, even in mice that were undergoing confrontational housing. Furthermore, the daily dose of theanine (40 µg ml(-1)) blocked the counteracting effects of caffeine (30 µg ml(-1)) and catechin (200 µg ml(-1)). The present study demonstrated that theanine prevents and relieves psychosocial stress through the modulation of hypothalamic-pituitary-adrenal axis activity.


Subject(s)
Glutamates/pharmacology , Social Dominance , Stress, Psychological/drug therapy , Adrenal Glands/anatomy & histology , Adrenal Glands/drug effects , Adrenocorticotropic Hormone/blood , Animals , Antidepressive Agents/pharmacology , Caffeine/pharmacology , Circadian Rhythm , Corticosterone/blood , Housing, Animal , Hypertrophy , Hypothalamo-Hypophyseal System/drug effects , Hypothalamo-Hypophyseal System/physiology , Male , Mice , Organ Size/drug effects , Paroxetine/pharmacology , Pituitary-Adrenal System/drug effects , Pituitary-Adrenal System/physiology , Tea/chemistry
2.
Biol Pharm Bull ; 34(3): 311-7, 2011.
Article in English | MEDLINE | ID: mdl-21372377

ABSTRACT

Increased oxidative stress is known to accelerate age-related pathologies. Beta-cryptoxanthin (ß-CRX, (3R)-ß,ß-caroten-3-ol) is a potent antioxidant that is highly rich in Satsuma mandarin orange (mandarin), which is the most popular fruit in Japan. We investigated the antioxidative and anti-aging effects of ß-CRX and mandarin using senescence-accelerated mice (SAMP10), which were characterized by a short lifespan, high generation of superoxide anions in the brain and poor learning ability with aging. ß-CRX (0.5-5.0 µg/ml) or mandarin juice (3.8-38.0%) was added to drinking water of SAMP10 one to 12 months of age. ß-CRX was dose-dependently incorporated into the cerebral cortex and the contents were similar to the concentration of ß-CRX in the human frontal lobe. These mice also had higher learning ability. The level of DNA oxidative damage was significantly lower in the cerebral cortex of mice that ingested ß-CRX and mandarin than control mice. In addition, the mice that ingested ß-CRX (>1.5 µg/ml) and mandarin (>11.3%) exhibited a higher survival when 12 month-old, the presenile age of SAMP10, than control mice. These results suggest that ß-CRX is incorporated into the brain and has an important antioxidative role and anti-aging effect.


Subject(s)
Aging/physiology , Antioxidants/therapeutic use , Brain/drug effects , Citrus/chemistry , Cognition Disorders/prevention & control , Oxidative Stress/drug effects , Xanthophylls/therapeutic use , Animals , Antioxidants/pharmacology , Brain/physiology , Cognition Disorders/etiology , Cryptoxanthins , DNA Damage , Dose-Response Relationship, Drug , Fruit , Learning/drug effects , Longevity/drug effects , Male , Mice , Mice, Inbred Strains , Oxidative Stress/physiology , Phytotherapy , Plant Preparations/pharmacology , Plant Preparations/therapeutic use , Xanthophylls/pharmacology
3.
Free Radic Res ; 45(8): 966-74, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21425911

ABSTRACT

To evaluate the psychosocial effect on lifespan and cognitive function, this study investigated the effect of confrontational housing on mice because conflict among male mice is a psychosocial stress. In addition, it investigated the anti-stress effect of theanine (γ-glutamylethylamide), an amino acid in tea. Mice were housed under confrontation. That is, two male mice were separately housed in the same cage with a partition for establishing the territorial imperative in each mouse. Then, the partition was removed and mice were co-housed confrontationally (confront-housing) using a model mouse of accelerated-senescence (SAMP10) that exhibited cerebral atrophy and cognitive dysfunction with ageing. It was found that mice began to die earlier under confront-housing than group-housed control mice. Additionally, it was found that cerebral atrophy, learning impairment and behavioural depression were higher in mice under the stressed condition of confront-housing than age-matched mice under group-housing. Furthermore, the level of oxidative damage in cerebral DNA was higher in mice housed confrontationally than group-housed control mice. On the other hand, the consumption of purified theanine (20 µg/ml, 5-6 mg/kg) suppressed the shortened lifespan, cerebral atrophy, learning impairment, behavioural depression and oxidative damage in cerebral DNA. These results suggest that psychosocial stress accelerates age-related alterations such as oxidative damage, lifespan, cognitive dysfunction and behavioural depression. The intake of theanine might be a potential candidate for suppression of disadvantage under psychosocial stress.


Subject(s)
Cognition Disorders/drug therapy , Depressive Disorder/drug therapy , Glutamates/pharmacology , Glutamates/therapeutic use , Longevity/drug effects , Stress, Psychological/complications , Animals , Chronic Disease , Cognition Disorders/etiology , Corticosterone/blood , Depressive Disorder/etiology , Glutamates/administration & dosage , Male , Mice , Mice, Inbred Strains
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