Overstreet David H, Griebel Guy
Department of Psychiatry, Center for Alcohol Studies, CB #7178, 3009 Thurston-Bowles Bldg., University of North Carolina, Chapel Hill, NC 27599-7178, USA.
Eur J Pharmacol. 2004 Aug 16;497(1):49-53. doi: 10.1016/j.ejphar.2004.06.035.
Much interest has been expressed in the antidepressant potential of nonpeptide, orally active corticotropin-releasing factor (CRF) receptor antagonists in recent years. Therefore, the present investigation examined the antidepressant-like effects of the novel CRF(1) receptor antagonist SSR125543 on the exaggerated swim test immobility in the Flinders Sensitive Line rat, a genetic animal model of depression. Chronic treatment with SSR125543 (3, 10, 20, 30 mg/kg, i.p.) for 14 days significantly increased swimming in the Flinders Sensitive Line rats. The reference serotonin reuptake inhibitor fluoxetine (5 mg/kg, i.p.) and the tricyclic antidepressant desipramine (5 mg/kg, i.p.) also significantly increased swimming, as expected. The higher doses of SSR125543 (20 and 30 mg/kg) also significantly increased the abnormally low level of social interaction behavior in the Flinders Sensitive Line rats. Together, these findings indicate that the CRF(1) receptor antagonist SSR125543 has both antidepressant- and anxiolytic-like effects in the Flinders Sensitive Line rats.
近年来,非肽类、口服活性促肾上腺皮质激素释放因子(CRF)受体拮抗剂的抗抑郁潜力引起了广泛关注。因此,本研究考察了新型CRF(1)受体拮抗剂SSR125543对弗林德斯敏感系大鼠(一种抑郁症遗传动物模型)在强迫游泳试验中过度不动行为的抗抑郁样作用。SSR125543(3、10、20、30mg/kg,腹腔注射)连续治疗14天可显著增加弗林德斯敏感系大鼠的游泳时间。如预期的那样,参比血清素再摄取抑制剂氟西汀(5mg/kg,腹腔注射)和三环类抗抑郁药地昔帕明(5mg/kg,腹腔注射)也显著增加了游泳时间。较高剂量的SSR125543(20和30mg/kg)还显著增加了弗林德斯敏感系大鼠异常低下的社交互动行为水平。这些结果共同表明,CRF(1)受体拮抗剂SSR125543在弗林德斯敏感系大鼠中具有抗抑郁和抗焦虑样作用。