The effect of escitalopram, desipramine, electroconvulsive seizures and lithium on brain-derived neurotrophic factor mRNA and protein expression in the rat brain and the correlation to 5-HT and 5-HIAA levels
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作者:
Jacobsen, JPR
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H Lundbeck & Co AS, Dept Neurochem, DK-2500 Copenhagen, DenmarkH Lundbeck & Co AS, Dept Neurochem, DK-2500 Copenhagen, Denmark
Jacobsen, JPR
[1
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Mork, A
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H Lundbeck & Co AS, Dept Neurochem, DK-2500 Copenhagen, DenmarkH Lundbeck & Co AS, Dept Neurochem, DK-2500 Copenhagen, Denmark
Mork, A
[1
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机构:
[1] H Lundbeck & Co AS, Dept Neurochem, DK-2500 Copenhagen, Denmark
The reported increase in brain-derived neurotrophic factor (BDNF) mRNA expression after antidepressant treatment is a cornerstone of the BDNF hypothesis of antidepressant action. However, if this increase becomes manifest on the BDNF protein level is unknown. In the present study we performed parallel measurements of BDNF mRNA and protein expression in the frontal cortex and hippocampus of the rat after chronic treatment. with electroconvulsive seizures (ECS), lithium, desipramine or escitalopram. ECS increased BDNF mRNA and protein in the hippocampus and BDNF protein in the frontal cortex. Desipramine moderately increased BDNF mRNA expression in the dentate gyrus but did not change BDNF protein in neither region. Escitalopram did not affect BDNF mRNA expression, but decreased BDNF protein in the frontal cortex and the hippocampus. Lithium increased BDNF protein levels in the hippocampus and frontal cortex, but overall decreased BDNF mRNA expression. Thus, here we report a striking non-correspondence between changes in BDNF mRNA and protein expression induced by the antidepressant treatments and lithium. Further, increased expression of BDNF mRNA or protein was not a common action of the treatments. We also investigated if treatment-induced modulations of the tissue contents of 5-hydroxytryptamine (5-HT) and its metabolite, 5-hydroxy-indoleacetic acid (5-HIAA), were related to changes in BDNF mRNA or protein expression. No correlation was found. However, all treatments increased 5-HT levels in the hippocampus. (C) 2004 Elsevier B.V. All rights reserved.
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Univ Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, CanadaUniv Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, Canada
Bai, O
Chlan-Fourney, J
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Univ Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, CanadaUniv Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, Canada
Chlan-Fourney, J
Bowen, R
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Univ Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, CanadaUniv Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, Canada
Bowen, R
Keegan, D
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Univ Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, CanadaUniv Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, Canada
Keegan, D
Li, XM
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Univ Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, CanadaUniv Saskatchewan, Neuropsychiat Res Unit, Dept Psychiat, Saskatoon, SK S7N 5EA, Canada