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 |
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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. |
doi_str_mv | 10.1016/j.pbb.2008.06.001 |
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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.</description><subject>Aged</subject><subject>Aging</subject><subject>Aging - psychology</subject><subject>Alpha-methyl- p-tyrosine</subject><subject>alpha-Methyltyrosine - pharmacology</subject><subject>Amphetamine</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - physiology</subject><subject>Brain Chemistry - drug effects</subject><subject>Conditioning, Operant - drug effects</subject><subject>Conditioning, Operant - physiology</subject><subject>Dextroamphetamine - pharmacology</subject><subject>Dopamine</subject><subject>Dopamine Agents - pharmacology</subject><subject>Dopamine Uptake Inhibitors - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electric Stimulation</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Medical sciences</subject><subject>Rate-frequency curve</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Reinforcement</subject><subject>Reinforcement Schedule</subject><subject>Reward</subject><subject>Rewarding brain stimulation</subject><issn>0091-3057</issn><issn>1873-5177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcuO1DAQRS0EYnoGPoAN8gZ2CeVHbEesYEQPSCPYDGvLrzRuJXFjJ6Dm6_HQDexgZal07lW5DkLPCLQEiHi1bw_WthRAtSBaAPIAbYiSrOmIlA_RBqAnDYNOXqDLUvYAwKmQj9EFUZ2ivIcN-nH3JeAcvpvs47zDYRiiM-6I04BtNnHGZYnTOpolphmb2eO4FDwl_3tkj9ing5niHPIuOuzzuiu45o5prX2mgsuvXBo9fvsRbxnnW4KzWcoT9GgwYwlPz-8V-rx9d3f9vrn9dPPh-s1t4xiVS-NkTzrBZMflYA0D6_vOBB-EF-AF5XRwXAyKMWLr57xyynEWLBeKEuq9YFfo5an3kNPXNZRFT7G4MI5mDmktWvSS9CD5f0HSd6SjqqsgOYEup1JyGPQhx8nkoyag783ova5m9L0ZDUJXMzXz_Fy-2in4v4mzigq8OAOmODMO2cwulj8crRorRyv3-sSFerNvMWRdXAyzCz7m4BbtU_zHGj8Bu3Wq-w</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Sonnenschein, Bonnie</creator><creator>Franklin, Keith B.J.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>200810</creationdate><title>The rewarding efficacy of brain stimulation and its modulation by dopaminergic drugs in young adult and old BN F344F1 rats</title><author>Sonnenschein, Bonnie ; Franklin, Keith B.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-c7915637547fba30bd95aede6d60d6242fc46f8331b267d8c8c43eb468212dd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Aging</topic><topic>Aging - psychology</topic><topic>Alpha-methyl- p-tyrosine</topic><topic>alpha-Methyltyrosine - pharmacology</topic><topic>Amphetamine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - physiology</topic><topic>Brain Chemistry - drug effects</topic><topic>Conditioning, Operant - drug effects</topic><topic>Conditioning, Operant - physiology</topic><topic>Dextroamphetamine - pharmacology</topic><topic>Dopamine</topic><topic>Dopamine Agents - pharmacology</topic><topic>Dopamine Uptake Inhibitors - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electric Stimulation</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Medical sciences</topic><topic>Rate-frequency curve</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Reinforcement</topic><topic>Reinforcement Schedule</topic><topic>Reward</topic><topic>Rewarding brain stimulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sonnenschein, Bonnie</creatorcontrib><creatorcontrib>Franklin, Keith B.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmacology, biochemistry and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sonnenschein, Bonnie</au><au>Franklin, Keith B.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The rewarding efficacy of brain stimulation and its modulation by dopaminergic drugs in young adult and old BN F344F1 rats</atitle><jtitle>Pharmacology, biochemistry and behavior</jtitle><addtitle>Pharmacol Biochem Behav</addtitle><date>2008-10</date><risdate>2008</risdate><volume>90</volume><issue>4</issue><spage>735</spage><epage>741</epage><pages>735-741</pages><issn>0091-3057</issn><eissn>1873-5177</eissn><coden>PBBHAU</coden><abstract>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.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18582490</pmid><doi>10.1016/j.pbb.2008.06.001</doi><tpages>7</tpages></addata></record> |
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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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