Braun Natalie N, Reutiman Teri J, Lee Susanne, Folsom Timothy D, Fatemi S Hossein
Department of Psychiatry, Division of Neuroscience Research, University of Minnesota, Minneapolis, Minnesota, USA.
Neuroreport. 2007 Nov 19;18(17):1841-4. doi: 10.1097/WNR.0b013e3282f16dca.
The cyclic adenosine monophosphate-specific phosphodiesterase-4 (PDE4) gene family is the target of several potential therapeutic inhibitors and the PDE4B gene has been associated with schizophrenia and depression. Little, however, is known of any connection between this gene family and autism, with limited effective treatment being available for autism. We measured the expression of PDE4A and PDE4B by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting in Brodmann's area 40 (BA40, parietal cortex), BA9 (superior frontal cortex), and cerebellum from subjects with autism and matched controls. We observed a lower expression of PDE4A5, PDE4B1, PDE4B3, PDE4B4, and PDE4B2 in the cerebella of subjects with autism when compared with matched controls. In BA9, we observed the opposite: a higher expression of PDE4AX, PDE4A1, and PDE4B2 in subjects with autism. No changes were observed in BA40. Our results demonstrate altered expressions of the PDE4A and PDE4B proteins in the brains of subjects with autism and might provide new therapeutic avenues for the treatment of this debilitating disorder.
环磷酸腺苷特异性磷酸二酯酶4(PDE4)基因家族是几种潜在治疗抑制剂的作用靶点,且PDE4B基因已被证实与精神分裂症和抑郁症有关。然而,对于该基因家族与自闭症之间的联系却知之甚少,目前自闭症的有效治疗方法也很有限。我们通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质免疫印迹法,检测了自闭症患者及匹配对照组在布罗德曼40区(BA40,顶叶皮质)、BA9区(额上回皮质)和小脑区域中PDE4A和PDE4B的表达情况。我们发现,与匹配对照组相比,自闭症患者小脑内PDE4A5、PDE4B1、PDE4B3、PDE4B4和PDE4B2的表达较低。而在BA9区,我们观察到了相反的情况:自闭症患者中PDE4AX、PDE4A1和PDE4B2的表达较高。在BA40区未观察到变化。我们的研究结果表明,自闭症患者大脑中PDE4A和PDE4B蛋白的表达发生了改变,这可能为治疗这种致残性疾病提供新的治疗途径。