Division of Neurology, Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, OH 45229-3039, USA.
Genes Brain Behav. 2012 Jul;11(5):614-22. doi: 10.1111/j.1601-183X.2012.00796.x. Epub 2012 May 8.
Phosphodiesterases (PDEs) are a superfamily of intracellular second messenger cyclic nucleotide hydrolyzing enzymes composed of 12 families. The Pde4 family has been implicated in depression and cognition, and PDE4 inhibitors have been evaluated as antidepressants and possible cognitive enhancers. Pde4d(-/-) mice show an antidepressant phenotype and learning enhancement on some tests, but not others as do mice treated with PDE4 inhibitors. Here, we report for the first time the behavioral phenotype of a new Pde4d knock-down (KD) rat model of PDE4D deficiency. Consistent with other data on PDE4D deficiency, Pde4d KD rats showed depression resistance in the Porsolt forced swim test and hyperreactivity of the acoustic startle response with no differential response on prepulse inhibition, suggesting no sensorimotor gating defect. Pde4d KD rats also exhibited a small exploratory activity reduction but no difference following habituation, and no enhanced spatial learning or reference memory in the Morris water maze. A selective improvement in route-based learning in the Cincinnati water maze was seen as well as enhanced contextual and cued fear conditioning and a more rapid rate of cued extinction from their higher freezing level that declined to wild-type (WT) levels only after ∼20 extinction trials. The rat model confirms Pde4d's role in depression but not in spatial learning or memory enhancement and shows for the first time higher fear conditioning and altered extinction compared with controls. The new model provides a tool by which to better understand the role of PDE4D in neuropsychiatric disorders and for the development of alternate treatment approaches.
磷酸二酯酶(PDEs)是细胞内第二信使环核苷酸水解酶的超家族,由 12 个家族组成。Pde4 家族与抑郁症和认知有关,PDE4 抑制剂已被评估为抗抑郁药和潜在的认知增强剂。Pde4d(-/-) 小鼠在某些测试中表现出抗抑郁表型和学习增强,但其他测试则没有,而接受 PDE4 抑制剂治疗的小鼠则没有。在这里,我们首次报道了 PDE4D 缺乏的新 Pde4d 敲低(KD)大鼠模型的行为表型。与其他 PDE4D 缺乏数据一致,Pde4d KD 大鼠在强迫游泳试验中表现出抗抑郁作用,在声起始反应中表现出高反应性,而在预脉冲抑制中没有差异反应,表明没有感觉运动门控缺陷。Pde4d KD 大鼠也表现出轻微的探索性活动减少,但在习惯化后没有差异,在 Morris 水迷宫中也没有增强的空间学习或参考记忆。在辛辛那提水迷宫中观察到基于路线的学习得到了改善,以及增强的情境和线索恐惧条件反射,以及从较高的冻结水平更快地从线索中消退,而只有在大约 20 次消退试验后,才会下降到野生型(WT)水平。大鼠模型证实了 Pde4d 在抑郁症中的作用,但不在空间学习或记忆增强中,并且首次显示出与对照组相比,更高的恐惧条件反射和改变的消退。该新模型为更好地理解 PDE4D 在神经精神疾病中的作用以及开发替代治疗方法提供了工具。