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1.
Behav Brain Res ; 306: 71-83, 2016 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-26930174

RESUMO

Magnesium (Mg) has been described to possess an anxiolytic function, but a number of studies present inconsistent results on this matter. In this study the effect of Mg deficiency on anxiety-related behavior, brain and blood plasma Mg in young adult male C57BL/6JOlaHsd and C57BL/6NCrl mice was studied. The animals were put on a control or Mg deficient diet from day 0 and significant hypomagnesaemia was evident from day 12 onwards in the test animals. Housing and test conditions were under either conventional light regime (white light behavioral test conditions) or reverse light regime (red light behavioral test conditions). The animals were tested in three tests for unconditioned anxiety: the modified Hole Board (day 14), the light-dark test (day 21) and the elevated plus maze (day 28). Overall integrated behavioral z-scores were calculated over these three behavioral tests. Mg showed a structure dependent distribution at the level of the brain, that differed between C57BL/6 substrain and light regime (conventional versus reverse), respectively. Likewise, total brain Mg did differ between substrain and light regime, but was not affected by the diet. Animals on the Mg deficient diet housed under conventional light regime had a higher final (day 28) blood plasma corticosterone level as compared to controls. Animals housed under reverse light regime exhibited no diet effect of plasma corticosterone levels. The significant hypomagnesaemia at blood plasma level resulted in an effect of Mg deficiency on avoidance, but not overall anxiety-related behavior. Significant differences regarding avoidance behavior were found between the two substrains and light regimes, respectively.


Assuntos
Adaptação Ocular , Ansiedade/etiologia , Aprendizagem da Esquiva/fisiologia , Comportamento Exploratório/fisiologia , Locomoção/fisiologia , Deficiência de Magnésio/complicações , Animais , Ansiedade/genética , Peso Corporal , Encéfalo/metabolismo , Encéfalo/patologia , Corticosterona/sangue , Modelos Animais de Doenças , Magnésio/sangue , Magnésio/metabolismo , Deficiência de Magnésio/sangue , Deficiência de Magnésio/patologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos , Distribuição Aleatória , Estatísticas não Paramétricas
2.
Neuroscience ; 184: 97-106, 2011 Jun 16.
Artigo em Inglês | MEDLINE | ID: mdl-21420473

RESUMO

In humans, high levels of anxiety are associated with poor performance in the Iowa Gambling Task (IGT). The IGT measures decision-making under conditions of uncertainty. In this study, we investigated the association between anxiety and decision-making in rats. Rats were screened for anxiety on the elevated plus maze (EPM) and subsequently tested in a rat analogue of the IGT (r-IGT). We explored the role of frontostriatal areas related to r-IGT performance using c-fos immunohistochemistry following the last training-session. High levels of anxiety were associated with poor r-IGT performance: high anxious rats made fewer choices for the advantageous option and collected fewer sucrose pellets in the r-IGT than low anxious rats. Analysis of win-stay/lose-shift behaviour of choices for the advantageous option revealed that good performing-low anxious subjects showed an increase in win-stays and a decrease in lose-shifts across trial blocks while poor performing-high anxious subjects did not. Furthermore, decision-making performance and, indirectly, anxiety levels were related to neural activity in parts of the medial prefrontal cortex, that is prelimbic and infralimbic cortex, and in parts of the striatum, that is nucleus accumbens shell and core. These data suggest a similar frontostriatal circuitry underlying affective decision-making in humans and rats.


Assuntos
Ansiedade/fisiopatologia , Corpo Estriado/fisiopatologia , Tomada de Decisões/fisiologia , Lobo Frontal/fisiopatologia , Animais , Ansiedade/metabolismo , Corpo Estriado/metabolismo , Lobo Frontal/metabolismo , Masculino , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos
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