Miró Xavier, Pérez-Torres Silvia, Artigas Francesc, Puigdomènech Pere, Palacios José M, Mengod Guadalupe
Department of Molecular Genetics, Instituto de Biología Molecular de Barcelona, CID-CSIC 08034, Barcelona, Spain.
Neuropharmacology. 2002 Dec;43(7):1148-57. doi: 10.1016/s0028-3908(02)00220-4.
Changes in brain cyclic AMP (cAMP) have been suggested to underlie the clinical action of antidepressant treatments. Also, a regionally-selective regulation of cAMP-specific phosphodiesterases (PDEs) has been demonstrated for some antidepressants. To further investigate the effects of antidepressant treatments on PDEs, we examined the expression of different cAMP-specific PDEs in the brain of rats treated (1 and 14 days) with fluoxetine 3 mg/kg day. The mRNAs coding for PDE4A, PDE4B, PDE4D, and the five known PDE4D splice variants were analyzed by in situ hybridization on 45 brain structures of acute and chronic fluoxetine-treated rats. We also examined the binding sites for the putative antidepressant drug [(3)H]rolipram, a PDE4-selective inhibitor. In some brain areas single fluoxetine administration increased the density of the mRNA of all PDE4 isozymes, except PDE4D and PDE4D5. Chronic fluoxetine treatment increased PDE4A mRNA levels and decreased those for PDE4B, PDE4D and PDE4D1 mRNAs in some brain regions. The study was complemented with the analysis of the expression of the transcripts of BDNF. Chronic fluoxetine treatment down-regulated the expression of BDNF. These results show that the expression of PDE4 isozymes is modulated by a clinically relevant fluoxetine dose. The significance of these changes in PDE4 expression to the antidepressant effect of fluoxetine is discussed.
脑内环磷酸腺苷(cAMP)的变化被认为是抗抑郁治疗临床作用的基础。此外,已证实某些抗抑郁药对cAMP特异性磷酸二酯酶(PDEs)具有区域选择性调节作用。为了进一步研究抗抑郁治疗对PDEs的影响,我们检测了用3mg/kg·天氟西汀治疗(1天和14天)的大鼠脑内不同cAMP特异性PDEs的表达。通过对急性和慢性氟西汀治疗大鼠的45个脑结构进行原位杂交,分析了编码PDE4A、PDE4B、PDE4D以及五个已知PDE4D剪接变体的mRNA。我们还检测了假定的抗抑郁药物[(3)H]咯利普兰(一种PDE4选择性抑制剂)的结合位点。在一些脑区,单次给予氟西汀增加了除PDE4D和PDE4D5外所有PDE4同工酶mRNA的密度。慢性氟西汀治疗在一些脑区增加了PDE4A mRNA水平,降低了PDE4B、PDE4D和PDE4D1 mRNA水平。该研究还补充了脑源性神经营养因子(BDNF)转录本表达的分析。慢性氟西汀治疗下调了BDNF的表达。这些结果表明,PDE4同工酶的表达受到临床上相关剂量氟西汀的调节。讨论了PDE4表达的这些变化对氟西汀抗抑郁作用的意义。