Methamphetamine‐induced loss of striatal dopamine innervation in BDNF heterozygote mice does not further reduce D3 receptor concentrations

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Abstract
Depletion of dopamine (DA) reduces D3 receptor number, but D3 receptor expression is also regulated by brain-derived neurotrophic factor (BDNF). We took advantage of transgenic heterozygous BDNF mutant mice (+/−) to determine if reduced BDNF and loss of DA fibers produced by methamphetamine were additive in their impact on D3 receptor number. We assessed selective markers of the dopaminergic system including caudate-putamen DA concentrations and quantitative autoradiographic measurement of tyrosine hydroxylase (TH) levels, DA transporter (DAT), and DA D3 receptor binding between vehicle and methamphetamine-treated BDNF +/− and their wildtype (WT) littermate control mice. Caudate-putamen DA concentrations, TH and DAT levels were significantly reduced following methamphetamine treatment in both WT and BDNF +/− mice. The extent of methamphetamine-induced reduction in TH and DAT was greater for the WT than BDNF +/− mice and DAT levels were also decreased to a greater extent in nucleus accumbens of WT as compared to BDNF +/− mice. Lower D3 receptor existed in caudate-putamen and nucleus accumbens in BDNF +/− mice and these differences were not affected by methamphetamine treatment. Taken together, these results not only substantiate the importance of BDNF in controlling D3 receptor expression, but also indicate that a methamphetamine-induced depletion of DA fibers fails to produce an additive effect with lowered BDNF for control of D3 receptor expression. In addition, the reduction of D3 receptor expression is associated with a decreased neurotoxic response to methamphetamine in BDNF +/− mice. Synapse 52:11–19, 2004.