Ordway Gregory A, Szebeni Attila, Hernandez Liza J, Crawford Jessica D, Szebeni Katalin, Chandley Michelle J, Burgess Katherine C, Miller Corwin, Bakkalbasi Erol, Brown Russell W
Department of Biomedical Sciences and Department of Psychiatry and Behavioral Sciences, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee; Department of Health Sciences, College of Public Health, East Tennessee State University, Johnson City, Tennessee; DS Therapeutics, Houston, Texas.
Int J Neuropsychopharmacol. 2017 Dec 1;20(12):994-1004. doi: 10.1093/ijnp/pyx068.
Many patients suffering from depressive disorders are refractory to treatment with currently available antidepressant medications, while many more exhibit only a partial response. These factors drive research to discover new pharmacological approaches to treat depression. Numerous studies demonstrate evidence of inflammation and elevated oxidative stress in major depression. Recently, major depression has been shown to be associated with elevated levels of DNA oxidation in brain cells, accompanied by increased gene expression of the nuclear base excision repair enzyme, poly(ADP-ribose) polymerase-1. Given these findings and evidence that drugs that inhibit poly(ADP-ribose) polymerase-1 activity have antiinflammatory and neuroprotective properties, the present study was undertaken to examine the potential antidepressant properties of poly(ADP-ribose) polymerase inhibitors.
Two rodent models, the Porsolt swim test and repeated exposure to psychological stressors, were used to test the poly(ADP-ribose) polymerase inhibitor, 3-aminobenzamide, for potential antidepressant activity. Another poly(ADP-ribose) polymerase inhibitor, 5-aminoisoquinolinone, was also tested.
Poly(ADP-ribose) polymerase inhibitors produced antidepressant-like effects in the Porsolt swim test, decreasing immobility time, and increasing latency to immobility, similar to the effects of fluoxetine. In addition, 3-aminobenzamide treatment increased sucrose preference and social interaction times relative to vehicle-treated control rats following repeated exposure to combined social defeat and unpredictable stress, mediating effects similar to fluoxetine treatment.
The poly(ADP-ribose) polymerase inhibitors 3-aminobenzamide and 5-aminoisoquinolinone exhibit antidepressant-like activity in 2 rodent stress models and uncover poly(ADP-ribose) polymerase as a unique molecular target for the potential development of a novel class of antidepressants.
许多患有抑郁症的患者对目前可用的抗抑郁药物治疗无效,而更多患者仅表现出部分反应。这些因素推动了对治疗抑郁症新药理学方法的研究。大量研究表明,重度抑郁症存在炎症和氧化应激升高的证据。最近发现,重度抑郁症与脑细胞中DNA氧化水平升高有关,同时伴有核碱基切除修复酶聚(ADP - 核糖)聚合酶 - 1的基因表达增加。鉴于这些发现以及抑制聚(ADP - 核糖)聚合酶 - 1活性的药物具有抗炎和神经保护特性的证据,本研究旨在探讨聚(ADP - 核糖)聚合酶抑制剂的潜在抗抑郁特性。
使用两种啮齿动物模型,即波索尔特游泳试验和反复暴露于心理应激源,来测试聚(ADP - 核糖)聚合酶抑制剂3 - 氨基苯甲酰胺的潜在抗抑郁活性。另一种聚(ADP - 核糖)聚合酶抑制剂5 - 氨基异喹啉酮也进行了测试。
聚(ADP - 核糖)聚合酶抑制剂在波索尔特游泳试验中产生了类似抗抑郁的效果,减少了不动时间,并增加了不动潜伏期,类似于氟西汀的效果。此外,与反复暴露于联合社交挫败和不可预测应激后的载体处理对照大鼠相比,3 - 氨基苯甲酰胺治疗增加了蔗糖偏好和社交互动时间,介导了类似于氟西汀治疗的效果。
聚(ADP - 核糖)聚合酶抑制剂3 - 氨基苯甲酰胺和5 - 氨基异喹啉酮在两种啮齿动物应激模型中表现出类似抗抑郁的活性,并揭示聚(ADP - 核糖)聚合酶是一类新型抗抑郁药潜在开发的独特分子靶点。