Sano H, Totsuka Y, Furuuchi T, Sakai K, Koshikawa N, Shigehara R, Kobayashi M
Nihon Yakurigaku Zasshi. 1982 Aug;80(2):113-24.
In rats given methamphetamine (MAPT, 10 mg/kg i.p.) 24 hrs--48 hrs after the long term-administration of reserpine (RE), we have previously found such "bizarre-biting behaviour" as persistent and bloody biting activity at their own legs and tails or those of their cage mates. The present investigation examined the effect of a blockade of the dopamine receptor in the brain on MAPT-induced "bizarre-biting behaviour" and hypermotility of RE-pretreated rats. Male albino Wistar rats aged 4 weeks were injected intraperitoneally with RE (1.25 mg/kg) or 0.9% saline solution (1.25 ml/kg) every two days for 13 days. Twenty-three hrs after the last injection, rats received chlorpromazine (CP, 150 micrograms, 250 micrograms, 625 micrograms, or 1 mg/rat) intracerebrally by Valzelli's method; and 1 hr later, MAPT (10 mg/kg i.p.) was injected. MAPT-induced hypermotility was potentiated in the RE-pretreated rats, but it was suppressed dose-dependently by CP. Stereotyped licking and biting activities of saline-pretreated rats were completely suppressed by CP at each dose given, however, the "bizarre-biting behaviour" of RE-pretreated rats was inhibited by CP only at high doses (625 micrograms or 1 mg/rat). It is suggested that the MAPT-induced hypermotility of RE-pretreated rats is mediated by activation of dopamine receptor while their "bizarre-biting behaviour" is partially related to it.
在长期给予利血平(RE)后24小时至48小时,给大鼠腹腔注射甲基苯丙胺(MAPT,10毫克/千克),我们之前发现了诸如持续且血腥地啃咬自己或同笼伙伴的腿部和尾巴等“怪异啃咬行为”。本研究考察了脑内多巴胺受体阻断对MAPT诱导的RE预处理大鼠的“怪异啃咬行为”和运动亢进的影响。4周龄的雄性白化Wistar大鼠每隔一天腹腔注射RE(1.25毫克/千克)或0.9%盐溶液(1.25毫升/千克),共注射13天。最后一次注射后23小时,大鼠通过瓦尔泽利方法脑内注射氯丙嗪(CP,150微克、250微克、625微克或1毫克/只);1小时后,腹腔注射MAPT(10毫克/千克)。MAPT诱导的运动亢进在RE预处理大鼠中增强,但CP可剂量依赖性地抑制这种亢进。给予各剂量CP时,盐溶液预处理大鼠的刻板舔舐和啃咬活动均被完全抑制,然而,RE预处理大鼠的“怪异啃咬行为”仅在高剂量(625微克或1毫克/只)时被CP抑制。提示MAPT诱导的RE预处理大鼠运动亢进是由多巴胺受体激活介导的,而它们的“怪异啃咬行为”与之部分相关。