Przegaliński E, Baran L, Palider W, Siwanowicz J
Psychopharmacology (Berl). 1979 Apr 25;62(3):295-300. doi: 10.1007/BF00431961.
The central action of the potential antidepressant drug pizotifen (Sandomigran) was studied in mice, rats and rabbits. Pizotifen in doses up to 10 mg/kg i.p. was ineffective in classic tests for antidepressant activity. It neither antagonized the effects of reserpine in rats (hypothermia, ptosis) nor potentiated the effects of amphetamine (in mice and rats), nialamide or L-dopa (in mice) on locomotor activity. However, its antidepressant activitiy was found in the 'despair test' in rats. On the other hand, pizotifen inhibited the head twitch reaction induced by L-5-hydroxytryptophan in mice (ED50 = 0.009 mg/kg, i.p.) and by 5-methoxytryptamine (+ tranylcypromine) in rats (ED50 = 0.45 mg/kg, i.p.). It also antagonized tryptamine-induced clonic convulsions of fore-paws in rats (ED50 = 0.35 mg/kg, i.p.), and in doses of 5--10 mg/kg s.c. inhibited hyperthermia produced by LSD in rabbits. Finally, pizotifen (0.1--0.3 mg/kg, i.v.) inhibited or abolished LSD- or quipazine-induced stimulation of the hind limb flexor reflex of spinal rats; the above effect was not due to noradrenolytic action of the drug. These results suggest that pizotifen strongly blocks the central postsynaptic serotonin receptors.
对潜在的抗抑郁药匹莫齐特(桑多米格伦)在小鼠、大鼠和兔子身上的中枢作用进行了研究。腹腔注射剂量高达10mg/kg的匹莫齐特在经典的抗抑郁活性测试中无效。它既不能拮抗大鼠中利血平的作用(体温过低、眼睑下垂),也不能增强苯丙胺(在小鼠和大鼠中)、尼亚酰胺或左旋多巴(在小鼠中)对运动活性的作用。然而,在大鼠的“绝望试验”中发现了它的抗抑郁活性。另一方面,匹莫齐特抑制小鼠中由L-5-羟色氨酸诱导的头部抽搐反应(半数有效剂量=0.009mg/kg,腹腔注射)以及大鼠中由5-甲氧基色胺(+反苯环丙胺)诱导的头部抽搐反应(半数有效剂量=0.45mg/kg,腹腔注射)。它还拮抗大鼠中色胺诱导的前爪阵挛性惊厥(半数有效剂量=0.35mg/kg,腹腔注射),并且皮下注射剂量为5-10mg/kg时可抑制兔子中由麦角酸二乙胺引起的体温过高。最后,匹莫齐特(0.1-0.3mg/kg,静脉注射)抑制或消除了麦角酸二乙胺或喹哌嗪诱导的脊髓大鼠后肢屈肌反射的刺激;上述作用并非该药物的去甲肾上腺素能阻断作用所致。这些结果表明,匹莫齐特强烈阻断中枢突触后5-羟色胺受体。