Wan F J, Swerdlow N R
Department of Neuroscience and Psychiatry, UCSD School of Medicine, La Jolla, CA 92093-0804.
Psychopharmacology (Berl). 1993;113(1):103-9. doi: 10.1007/BF02244341.
Prepulse inhibition (PPI) of the startle reflex is reduced by systemic administration of dopamine (DA) agonists. Since PPI is impaired in patients with schizophrenia, the DA agonist-induced disruption of PPI in rats may be a useful model for studying the pathophysiology of impaired sensorimotor gating in schizophrenia. In the present study, we replicated the observation that PPI is disrupted by systemic administration of the D2 agonist quinpirole, but not by the D1 agonist SKF 38393. PPI caused by weak [1-5 dB(A)] or more intense [10 dB(A)] prepulses was also disrupted by quinpirole infusion into the nucleus accumbens (NAC). The effects of intraaccumbens quinpirole on PPI were blocked by pretreatment with the D2 antagonist haloperidol. These results support the notion that the reduction of PPI after systemic administration of DA agonists is mediated via stimulation of NAC D2 receptors.
全身给予多巴胺(DA)激动剂会降低惊吓反射的前脉冲抑制(PPI)。由于精神分裂症患者的PPI受损,DA激动剂诱导的大鼠PPI破坏可能是研究精神分裂症感觉运动门控受损病理生理学的有用模型。在本研究中,我们重复了以下观察结果:全身给予D2激动剂喹吡罗会破坏PPI,但D1激动剂SKF 38393不会。向伏隔核(NAC)注射喹吡罗也会破坏由弱[1-5 dB(A)]或更强[10 dB(A)]前脉冲引起的PPI。D2拮抗剂氟哌啶醇预处理可阻断伏隔核内喹吡罗对PPI的影响。这些结果支持以下观点:全身给予DA激动剂后PPI的降低是通过刺激NAC D2受体介导的。