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首页> 外文期刊>The Journal of Veterinary Medical Science >Effects of Furazolidone on Duration of Righting Reflex Loss Induced with Hexobarbital and Zoxazolamine in the Rat
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Effects of Furazolidone on Duration of Righting Reflex Loss Induced with Hexobarbital and Zoxazolamine in the Rat

机译:呋喃唑酮对己糖巴比妥和唑恶唑胺致大鼠直立反射丧失持续时间的影响

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References(12) Cited-By(9) Effects of furazolidone (FZ) on the sleeping time induced with hexobarbital (HEX) and paralysis time induced by zoxazolamine (ZOX) were investigated by measuring the length of time required to recover from righting reflex loss in rats after oral administration of FZ at doses of 50, 100, 200 and 400 mg/kg/day for 4 successive days. Administration of 50 mg/kg to rats of both sexes induced no effect on the HEX sleeping time, but of 100 mg/kg FZ or more induced prolongation of sleeping time dose-dependently. In female rats, HEX sleeping time of the control gloup was twice that of the male rats, but HEX sleeping time after receiving FZ above 200mg/kg was approximately the same as in the male rats. ZOX paralysis time exhibited no sex differences in the control rats, and it was significantly prolonged by FZ at a dose of 100 mg/kg or more. No significant differences in blood levels of HEX and ZOX at the time of recovery were found between the control and FZ treated rats, suggesting that FZ produced prolongation of the drug effects was due to the maintenance of the blood levels rather than the change in the sensitivities of rats at the receptor sites. Body weight gains were inhibited in the rats treated with FZ at doses over 100 mg/kg. Cytochrome P-450 content in hepatic microsomes in the rats which received 100 mg/kg FZ were slightly increased. It is suggested that successive oral administration of FZ to rats at high doses impaired drug clearance and this resulted in the prolongation of HEX sleeping and ZOX paralysis times.
机译:参考文献(12)引用了(9)呋喃唑酮(FZ)对己糖巴比妥(HEX)诱导的睡眠时间和唑沙唑胺(ZOX)诱导的麻痹时间的影响,方法是测量恢复直立反射力所需的时间长度连续4天以50、100、200和400 mg / kg / day的剂量口服FZ后,在大鼠体内的剂量降低。两种性别的大鼠服用50 mg / kg对HEX睡眠时间无影响,但100 mg / kg FZ或更高剂量会导致剂量依赖的睡眠时间延长。在雌性大鼠中,对照组的HEX睡眠时间是雄性大鼠的两倍,但是接受FZ高于200mg / kg后的HEX睡眠时间与雄性大鼠大致相同。在对照大鼠中,ZOX麻痹时间没有性别差异,并且100 mg / kg或更高剂量的FZ可以显着延长麻痹时间。在对照组和FZ处理的大鼠之间,恢复时的HEX和ZOX的血药浓度没有发现显着差异,这表明FZ产生药物作用的延长是由于维持血药浓度而不是敏感性的改变大鼠在受体部位。在用FZ治疗的大鼠中,体重超过100 mg / kg时,体重增加受到抑制。接受100 mg / kg FZ的大鼠肝微粒体中细胞色素P-450含量略有增加。提示高剂量连续给大鼠口服FZ会损害药物清除率,从而延长HEX睡眠时间和ZOX麻痹时间。

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