The rewarding efficacy of brain stimulation and its modulation by dopaminergic drugs in young adult and old BN F344F1 rats

In old age there is evidence of waning motivation, and possibly lowering of mood. Physiologically there is a decline in the levels of brain neurotransmitters such as acetylcholine and dopamine, and loss of myelin. These changes might be expected to impair the functioning of brain circuitry for reinf...

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Veröffentlicht in:Pharmacology, biochemistry and behavior biochemistry and behavior, 2008-10, Vol.90 (4), p.735-741
Hauptverfasser: Sonnenschein, Bonnie, Franklin, Keith B.J.
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description In old age there is evidence of waning motivation, and possibly lowering of mood. Physiologically there is a decline in the levels of brain neurotransmitters such as acetylcholine and dopamine, and loss of myelin. These changes might be expected to impair the functioning of brain circuitry for reinforcement, and to lead to impaired motivation. To evaluate the function of brain reinforcement mechanisms during aging we examined brain stimulation reward and its modulation by dopaminergic drugs in BN F344F1 rats aged from young adult (5 months) to old (37 months). Brain stimulation directly activates the neural circuitry for reinforcement, and the response rate–frequency tradeoff can be used to characterize the functioning of the system. Both young and old subjects readily learned to lever press for 0.6 s trains of 0.15 ms brain stimulation pulses, and there was no difference in the number of pulses per train required to maintain responding at 50% of the maximum rate (M50). Amphetamine (0.5 mg/kg) significantly reduced the M50, and the dopamine synthesis inhibitor alpha-methyl- p-tyrosine (100 mg/kg) increased the M50, but these effects were not influenced by the age of the subjects. The results suggest that in healthy animals dopaminergic modulation of reinforcement is functionally intact in old age.
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Amphetamine (0.5 mg/kg) significantly reduced the M50, and the dopamine synthesis inhibitor alpha-methyl- p-tyrosine (100 mg/kg) increased the M50, but these effects were not influenced by the age of the subjects. 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Amphetamine (0.5 mg/kg) significantly reduced the M50, and the dopamine synthesis inhibitor alpha-methyl- p-tyrosine (100 mg/kg) increased the M50, but these effects were not influenced by the age of the subjects. 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subjects Aged
Aging
Aging - psychology
Alpha-methyl- p-tyrosine
alpha-Methyltyrosine - pharmacology
Amphetamine
Animals
Biological and medical sciences
Brain - physiology
Brain Chemistry - drug effects
Conditioning, Operant - drug effects
Conditioning, Operant - physiology
Dextroamphetamine - pharmacology
Dopamine
Dopamine Agents - pharmacology
Dopamine Uptake Inhibitors - pharmacology
Dose-Response Relationship, Drug
Electric Stimulation
Enzyme Inhibitors - pharmacology
Medical sciences
Rate-frequency curve
Rats
Rats, Inbred F344
Reinforcement
Reinforcement Schedule
Reward
Rewarding brain stimulation
title The rewarding efficacy of brain stimulation and its modulation by dopaminergic drugs in young adult and old BN F344F1 rats
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