Creso E, De Marino V, Donatelli L, Pagnini G
Boll Soc Ital Biol Sper. 1978 Sep 15;54(17):1592-6.
It has been found that TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin), in rats, endoperitoneally or orally administered at dose of 1-10 mcg/kg, provokes irritability, aggressivity and restlessness (increase of spontaneous crossings in the shuttle box). The TCDD does not modify the conditioned avoidance (C.A.) or the conflictual situation. In "vitro" the TCDD stimulates directly the striatal and hypothalamic adenylate cyclase of rat. The TCDD increases the stimulation produced by dopamine on striatal adenylate cyclase. Haloperidol (dopamine antagonist) inhibits the stimulation produced by TCDD. TCDD does not significantly modify the stimulation by hystamine on hypothalamic adenylate cyclase. Cimetidine (H2) antagonist) causes a remarkable increase of the TCDD stimulating effect.
已发现,在大鼠中,以1 - 10微克/千克的剂量腹腔内或口服给予2,3,7,8 - 四氯二苯并 - 对二恶英(TCDD)会引发易怒、攻击性和烦躁不安(穿梭箱中自发交叉次数增加)。TCDD不会改变条件性回避(C.A.)或冲突情境。在“体外”,TCDD直接刺激大鼠的纹状体和下丘脑腺苷酸环化酶。TCDD增加了多巴胺对纹状体腺苷酸环化酶的刺激作用。氟哌啶醇(多巴胺拮抗剂)抑制TCDD产生的刺激。TCDD不会显著改变组胺对下丘脑腺苷酸环化酶的刺激作用。西咪替丁(H2拮抗剂)会使TCDD的刺激作用显著增加。