兔子的体温调节系统。高剂量氟化钠的影响[j]。

Shika gakuho. Dental science reports Pub Date : 1989-03-01
H Machida
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引用次数: 0

摘要

探讨了氟化钠(NaF)致低温的机制,探讨了单胺合成与家兔脑内代谢的关系。本实验选用每组5只公兔,体重约2.5kg,直肠温度38.4 ~ 39.3℃。直肠温度测量采用电体温计,每隔15或30分钟测量5小时。本实验将动物安置在温度为22 ~ 23℃的房间中,实验中使用了以下药物:NaF (40 mg/kg静脉注射)、巴比妥钠(0.1 mg/kg静脉注射)、六甲溴铵(C6, 10 mg/kg静脉注射)、酒石酸麦角胺(30 mg/kg静脉注射)、盐酸苯氧苄胺(15 mg/kg静脉注射)、盐酸普萘洛尔(5 mg/kg静脉注射)、品多洛尔(0.3 mg/kg静脉注射)、硫酸阿托品(30 mg/kg静脉注射)、2,4 -二硝基苯酚(DNP, 20 mg/kg静脉注射)、左旋多巴(20 mg/kg静脉注射)、5-羟色胺(20 mg/kg静脉注射)结果1。静脉注射NaF 30 mg/kg可使直肠温度下降0.66℃。2. 0.1 mg/kg巴比妥钠或10 mg/kg C6预处理显著抑制naff诱导的低温。3.酒石酸麦角胺和苯氧苄胺引起的α -阻断或盐酸心得安和品多洛尔引起的β -阻断对NaF引起的最大体温下降的抑制作用约为50%。然而,酒石酸麦角胺和心得安或苯氧苄胺和品多洛尔引起的α -和β -阻断均对NaF作用有显著的抑制作用。另一方面,硫酸阿托品引起的胆碱能阻断对naff诱导的低温无作用。4. 双侧内脏切开术完全抑制直肠温度下降。5. 静脉注射NaF 40 mg/kg不能抵消DNP 20 mg/kg引起的直肠温度升高。6. 左旋多巴预处理对naff诱导的低温有明显的抑制作用。而5-HTP的抑制作用较弱。7. NaF可显著降低兔下丘脑的去甲肾上腺素水平,但对5-HT水平无影响。
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[The rabbit thermo-regulatory system. Effects of high dose of sodium fluoride].

The mechanism of sodium fluoride (NaF) induced hypothermia was investigated on relations between the monoamine synthesis and metabolism in the rabbit brain. Five male rabbits per a group, weighing about 2.5kg and having rectal temperatures of 38.4 to 39.3 degrees C, were used in this experiment. The rectal temperature measurements were made by means of an electric thermometer for 5 hours at intervals of 15 or 30 minutes. Through this experiment, animals were housed in a room kept at 22 to 23 degrees C. The following drugs were used in this experiment: NaF (40 mg/kg i.v.), barbital sodium (0.1 g/kg s.c.), hexamethonium bromide (C6, 10 mg/kg i.v.), ergotamine tartrate (30 mg/kg s.c.), phenoxybenzamine hydrochloride (15 mg/kg i.v.), propranolol hydrochloride (5 mg/kg s.c.), pindolol (0.3 mg/kg s.c.), atropine sulfate (30 mg/kg s.c.), 2, 4-dinitrophenol (DNP, 20 mg/kg i.v.), l-DOPA (20 mg/kg i.v.), 5-HTP (20 mg/kg i.v.) Results 1. Intravenous injection of 30 mg/kg of NaF induced a drop of 0.66 degrees C in rectal temperature. 2. Pretreatment with 0.1 mg/kg of barbital sodium or 10 mg/kg of C6 prominently inhibited the NaF-induced hypothermia. 3. The alpha-blockade caused by ergotamine tartrate and phenoxybenzamine or the beta blockade by propranolol hydrochloride and pindolol resulted in an approximate 50% inhibition of maximum drop in body temperature induced by NaF administration. Both alpha- and beta-blockades caused by ergotamine tartrate and propranolol or by phenoxybenzamine and pindolol, however, made a remarkable inhibition of the NaF effect. Cholinergic blockade brought on by atropine sulfate, on the other hand, had no effect against NaF-induced hypothermia. 4. Bilateral splanchnicotomy completely inhibited drops in rectal temperature. 5. Intravenous injection of NaF 40 mg/kg failed to counteract the rise of rectal temperature caused by DNP 20 mg/kg. 6. Pretreatment with l-DOPA made a prominent inhibition of NaF-induced hypothermia. The inhibiting effects of 5-HTP, however, were slight. 7. Administration of NaF made a significant decrease in norepinephrine levels in the rabbit hypothalamus, but had no effect on 5-HT levels.

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