Sivam S P
Department of Pharmacology and Toxicology, Northwest Center for Medical Education, Indiana University School of Medicine, Gary 46408, USA.
Brain Res. 1995 Sep 4;690(2):259-63. doi: 10.1016/0006-8993(95)00604-o.
A regimen of repeated administration of GBR (10 or 20 mg/kg/day, i.p., for 4 days) to female Sprague-Dawley rats induced a dose-and time-related increase in the incidence of self-injurious behavior (SIB) that consisted of injury to body areas, paws and tail. The treatment regimen decreased striatal DA and DOPAC levels. Dopaminergic denervation with 6-hydroxydopamine (6-OHDA) or D1 DA antagonist, SCH-23390 or D2 DA antagonist, spiperone, blocked the GBR-induced SIB. Male rats were less sensitive than female rats to exhibit a comparable incidence of SIB. Taken together, the study reveals that repeated administration of GBR induces SIB that is dependent on the integrity of nigrostriatal dopaminergic system and the presence of D1 and/or D2 DA receptors.
对雌性斯普拉格-道利大鼠重复给予GBR(10或20毫克/千克/天,腹腔注射,共4天)的方案导致自伤行为(SIB)发生率出现剂量和时间相关的增加,自伤行为包括身体部位、爪子和尾巴受伤。该治疗方案降低了纹状体多巴胺(DA)和3,4-二羟基苯乙酸(DOPAC)水平。用6-羟基多巴胺(6-OHDA)进行多巴胺能去神经支配或使用D1多巴胺拮抗剂SCH-23390或D2多巴胺拮抗剂螺哌隆可阻断GBR诱导的自伤行为。雄性大鼠表现出与自伤行为相当发生率的敏感性低于雌性大鼠。综上所述,该研究表明重复给予GBR会诱导自伤行为,这种自伤行为依赖于黑质纹状体多巴胺能系统的完整性以及D1和/或D2多巴胺受体的存在。