Carruba M O, Ricciardi S, Negreanu J, Calogero M, Mantegazza P
Psychopharmacology (Berl). 1980;70(3):223-9. doi: 10.1007/BF00427878.
In rats, lisuride, either administered systemically or intracerebroventricularly induced a dose-related hypothermia. This effect was selectively antagonized by blockade of DA receptors in the CNS but not by inhibition of catecholamine synthesis or blockade of serotoninergic receptors. Also a blocker of "peripheral" DA receptors failed to antagonize the hypothermic effect of lisuride in rats. Induction of rat liver microsomal drug-metabolizing enzymes by phenobarbital counteracted lisuride-induced hypothermia. In rabbits lisuride induced a hyperthermic response which was sensitive to both pimozide and metergoline pretreatment. These findings indicate that stimulation of brain DA receptors involved in thermoregulation is responsible for the changes in body temperature indiced by lisuride in rats and rabbits and that these effects are caused by the drug itself and do not require previous biotransformation into an active metabolite.
在大鼠中,利苏瑞ide经全身给药或脑室内给药均可诱导剂量相关的体温过低。这种效应可被中枢神经系统中多巴胺(DA)受体的阻断选择性拮抗,但不能被儿茶酚胺合成的抑制或5-羟色胺能受体的阻断所拮抗。此外,一种“外周”DA受体阻滞剂未能拮抗利苏瑞ide对大鼠的体温过低效应。苯巴比妥诱导大鼠肝脏微粒体药物代谢酶可抵消利苏瑞ide诱导的体温过低。在兔子中,利苏瑞ide诱导了一种对匹莫齐特和麦角苄酯预处理均敏感的体温过高反应。这些发现表明,参与体温调节的脑DA受体的刺激是利苏瑞ide在大鼠和兔子中引起体温变化的原因,并且这些效应是由药物本身引起的,不需要预先生物转化为活性代谢物。