Fujikawa M, Nagashima M, Inoue T, Yamada K, Furukawa T
Department of Pharmacology, School of Medicine, Fukuoka University, Japan.
Pharmacol Biochem Behav. 1996 Apr;53(4):903-9. doi: 10.1016/0091-3057(95)02096-9.
The present experiments were performed to examine the behavioral effects of OPC-14597, which acts on dopamine receptors in rats. OPC-14597 administered subcutaneously (SC) at doses of 0.1-5 mg/kg elicited yawning, as did OPC-4392 (0.5-2 mg/kg, SC) and (-)-3-PPP (2.5-10 mg/kg, SC). These yawning responses were blocked by intraperitoneal (IP) pretreatment with haloperidol (0.5 mg/kg) but were increased by pindolol (20 mg/kg, IP) or reserpine (5 mg/kg, IP), which per se did not elicit yawning. The yawning induced by talipexole, a selective dopamine D2 receptor agonist, was inhibited by OPC-14597 (0.5-5 mg/kg, SC) and (-)-3-PPP (10 mg/kg, SC). Apomorphine (0.5 mg/kg, SC), a dopamine D1/D2 receptor agonist, elicited stereotypy such as sniffing and licking but OPC-14597 (5-20 mg/kg, SC) did not induce this behavior. The stereotypy induced by apomorphine was inhibited not only by haloperidol (0.5 mg/kg, IP) and (-)-3-PPP (10 mg/kg, SC) but also by OPC-14597 (5-20 mg/kg, SC), without being affected by OPC-4392 (2 mg/kg, SC). In 6-hydroxydopamine (6-OHDA)-treated rats, apomorphine (0.5 mg/kg, SC) elicited rotation behavior whereas OPC-14597, OPC-4392 and (-)-3-PPP did not produce this behavior. These findings suggest that OPC-14597 provokes yawning without causing stereotypy and rotation but markedly antagonizes the talipexole-induced yawning and apomorphine-induced stereotypy, and that OPC-14597 thus exerts partial agonistic effects on yawning behavior but antagonistic effects on stereotypy in rats.
进行本实验以研究OPC - 14597对大鼠多巴胺受体作用的行为效应。皮下注射(SC)剂量为0.1 - 5mg/kg的OPC - 14597会引发打哈欠,OPC - 4392(0.5 - 2mg/kg,SC)和( - )-3 - PPP(2.5 - 10mg/kg,SC)也会引发打哈欠。这些打哈欠反应可被腹腔注射(IP)氟哌啶醇(0.5mg/kg)预处理阻断,但被吲哚洛尔(20mg/kg,IP)或利血平(5mg/kg,IP)增强,而这两种药物本身不会引发打哈欠。选择性多巴胺D2受体激动剂 talipexole 诱导的打哈欠被OPC - 14597(0.5 - 5mg/kg,SC)和( - )-3 - PPP(10mg/kg,SC)抑制。多巴胺D1/D2受体激动剂阿扑吗啡(0.5mg/kg,SC)引发刻板行为,如嗅闻和舔舐,但OPC - 14597(5 - 20mg/kg,SC)不会诱导这种行为。阿扑吗啡诱导的刻板行为不仅被氟哌啶醇(0.5mg/kg,IP)和( - )-3 - PPP(10mg/kg,SC)抑制,也被OPC - 14597(5 - 20mg/kg,SC)抑制,而不受OPC - 4392(2mg/kg,SC)影响。在6 - 羟基多巴胺(6 - OHDA)处理的大鼠中,阿扑吗啡(0.5mg/kg,SC)引发旋转行为,而OPC - 14597、OPC - 4392和( - )-3 - PPP不会产生这种行为。这些发现表明,OPC - 14597引发打哈欠但不引起刻板行为和旋转,且显著拮抗talipexole诱导的打哈欠和阿扑吗啡诱导的刻板行为,因此OPC - 14597对大鼠的打哈欠行为发挥部分激动作用,但对刻板行为发挥拮抗作用。