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1.
Pharmacol Biochem Behav ; 94(1): 63-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19635494

ABSTRACT

Caffeine is widely consumed in beverages and food, and its consumption in high doses is associated with anxiety increase. Stress situations are often associated to coffee consumption, and have a strong influence on oxidative DNA damage. As there are sex-specific differences in many metabolic, neurochemical and behavioral aspects, the aim of this study is to verify the interaction between chronic consumption of caffeine and chronic stress on anxiety and DNA breaks in the hippocampus on male and female rats. Wistar rats were submitted to restraint stress for at least 50 days. The diet consisted of standard rat chow and caffeine 0.3 or 1 g/L in drinking water "ad libitum" as the only drinking source. Controls received tap water. Anxiety-like behavior and DNA breaks in the hippocampus were evaluated. Caffeine consumption and chronic stress increased anxiety-like behavior as well as DNA breaks in the hippocampus of male rats. No effect on these parameters was observed in females. These results may be related to the presence of estradiol, which may have anxiolytic and neuroprotective properties.


Subject(s)
Anxiety/physiopathology , Caffeine/administration & dosage , Central Nervous System Stimulants/administration & dosage , DNA Breaks , Hippocampus/chemistry , Stress, Physiological , Stress, Psychological/physiopathology , Adrenal Glands/anatomy & histology , Analysis of Variance , Animals , Behavior, Animal , Caffeine/adverse effects , Caffeine/metabolism , Central Nervous System Stimulants/adverse effects , Central Nervous System Stimulants/metabolism , Corticosterone/blood , Exploratory Behavior , Female , Locomotion , Male , Maze Learning , Organ Size , Rats , Rats, Wistar , Restraint, Physical , Sex Characteristics
2.
Neurochem Res ; 34(9): 1568-74, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19283473

ABSTRACT

We studied the effect of chronic caffeine on parameters related to oxidative stress in different brain regions of stressed and non-stressed rats. Wistar rats were divided into three groups: control (receiving water), caffeine 0.3 g/L and caffeine 1.0 g/L (in the drinking water). These groups were subdivided into non-stressed and stressed (repeated restraint stress during 40 days). Lipid peroxide levels and the total radical-trapping potential were assessed, as well as antioxidant enzyme activities superoxide dismutase, gluthatione peroxidase, and catalase in hippocampus, striatum and cerebral cortex. Results showed interactions between stress and caffeine, especially in the cerebral cortex, since caffeine increased the activity of some antioxidant enzymes, but not in stressed animals. We concluded that chronic administration of caffeine led, in some cases, to increased activity of antioxidant enzymes. However, these effects were not observed in the stressed animals.


Subject(s)
Antioxidants/metabolism , Caffeine/pharmacology , Oxidative Stress , Stress, Psychological/metabolism , Animals , Catalase/metabolism , Cerebral Cortex/metabolism , Corpus Striatum/metabolism , Glutathione Peroxidase/metabolism , Hippocampus/metabolism , Oxidative Stress/drug effects , Rats , Rats, Wistar , Restraint, Physical , Superoxide Dismutase/metabolism , Thiobarbituric Acid Reactive Substances/metabolism
3.
Physiol Behav ; 95(3): 295-301, 2008 Oct 20.
Article in English | MEDLINE | ID: mdl-18602935

ABSTRACT

Anorectic effects of caffeine are controversial in the literature, while stress and obesity are growing problems in our society. Since many stressed people are coffee drinkers, the objective of the present study was to evaluate the effect of stress and chronic administration of caffeine on feeding behavior and body weight in male and female rats. Wistar rats (both males and females) were divided into 3 groups: control (receiving water), caffeine 0.3 g/L and caffeine 1.0 g/L (in the drinking water). These groups were subdivided into non-stressed and stressed (repeated-restraint stress for 40 days). During the entire treatment, chow consumption was monitored and rats were weighed monthly. Afterwards, feeding behavior was evaluated during 3-min trials in food-deprived and ad libitum fed animals and also in repeated exposures, using palatable food (Froot Loops and Cheetos). Chronic administration of caffeine did not affect rat chow consumption or body weight gain, but diminished the consumption of both salty (Cheetos) and sweet (Froot Loops) palatable food. In the repeated trial tests, stress diminished savory snack consumption in the later exposures [I.S. Racotta, J. Leblanc, D. Richard The effect of caffeine on food intake in rats: involvement of corticotropin-releasing factor and the sympatho-adrenal system. Pharmacol Biochem Behav. 1994, 48:887-892; S.D. Comer, M. Haney, R.W. Foltin, M.W. Fischman Effects of caffeine withdrawal on humans living in a residential laboratory. Exp Clin Psychopharmacol. 1997, 5:399-403; A. Jessen, B. Buemann, S. Toubro, I.M. Skovgaard, A. Astrup The appetite-suppressant effect of nicotine is enhanced by caffeine. Diab Ob Metab. 2005, 7:327-333; J.M. Carney Effects of caffeine, theophylline and theobromine on scheduled controlled responding in rats. Br J Pharmacol. 1982, 75:451-454] and caffeine diminished consumption of both palatable foods (savory and sweet) during the early and later exposures. Most responses to caffeine were stronger in females, and stress exposure influenced the effect. Neither chronic caffeine nor stress affected adrenal weight and plasma corticosterone levels of the rats. These observations suggest that chronic caffeine consumption may have sex-specific effects on palatable food ingestion.


Subject(s)
Caffeine/administration & dosage , Central Nervous System Stimulants/administration & dosage , Feeding Behavior/drug effects , Feeding Behavior/physiology , Stress, Psychological/physiopathology , Adrenalectomy/methods , Analysis of Variance , Animals , Behavior, Animal/drug effects , Body Composition/drug effects , Body Weight/drug effects , Body Weight/physiology , Corticosterone/blood , Dose-Response Relationship, Drug , Eating/drug effects , Enzyme-Linked Immunosorbent Assay/methods , Female , Male , Rats , Rats, Wistar , Reaction Time/drug effects , Reaction Time/physiology , Restraint, Physical/methods , Salts/metabolism , Sex Factors
4.
Appetite ; 51(3): 592-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18524415

ABSTRACT

The stress response is known to lead to behavioral and metabolic changes. Exposure to chronic stress can promote the development of physiological and behavioral dysfunctions, including alterations in feeding behavior. The aim of this study was to verify whether chronic restraint stress alters the consumption of a highly palatable, highly caloric diet (chocolate), chronically offered to the animals. Male rats ate more chocolate than females, and they also exhibited a higher weight gain, abdominal fat deposition, and higher plasma levels of total cholesterol, LDL-cholesterol and glucose. The stress exposure decreased body weight, increased adrenal weight and decreased plasma insulin levels. Overall, female rats had lower plasma insulin levels and chocolate consumption prevented the increased adrenal gland weight after exposure to chronic stress, suggesting a reduction of stress effects induced by palatable food consumption. Taken together, these results suggest a peculiar metabolic pattern, related to energy store and expenditure, in stressed animals receiving a palatable diet. Since these effects were sex-specific, we may also propose that females and males subjected to restraint stress and chocolate consumption are differentially affected.


Subject(s)
Cacao , Energy Metabolism/physiology , Handling, Psychological , Stress, Psychological/psychology , Weight Gain/drug effects , Abdominal Fat/metabolism , Adrenal Glands/growth & development , Animals , Behavior, Animal , Blood Glucose/metabolism , Energy Intake/physiology , Female , Habituation, Psychophysiologic/physiology , Insulin/blood , Leptin/blood , Lipids/blood , Male , Organ Size , Random Allocation , Rats , Rats, Wistar , Sex Factors , Stress, Psychological/blood , Stress, Psychological/metabolism , Time Factors , Weight Gain/physiology
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