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长期给予咖啡因对小鼠吗啡诱导的镇痛、耐受性及依赖性的影响。

The effect of chronic administration of caffeine on morphine-induced analgesia, tolerance and dependence in mice.

作者信息

Ahlijanian M K, Takemori A E

出版信息

Eur J Pharmacol. 1986 Jan 14;120(1):25-32. doi: 10.1016/0014-2999(86)90635-7.

Abstract

Morphine-induced analgesia, and the development of morphine-induced tolerance and dependence was determined in mice which had drunk caffeinated water (1 mg/ml) for 14 days or in mice which had received (-)-N6-(phenylisopropyl)-adenosine (PIA) 1 mg/kg i.p. for 14 days. Analgesia was assessed by the tail flick assay. The development of dependence was assessed by determining the ED50 of naloxone to precipitate withdrawal jumping (3 h after 100 mg/kg morphine pretreatment or 72 h after s.c. implantation of a morphine 75 mg pellet) and by determining the extent of naloxone-precipitated hypothermia in morphine-implanted animals. In mice chronically administered caffeine, the ED50 for morphine-induced analgesia was significantly decreased while the naloxone ED50 for withdrawal jumping increased by 2-fold after both types of morphine pretreatment. In control animals (tap water for 14 days), doses of 1 and 10 mg/kg of naloxone caused significant hypothermia in morphine-implanted animals. Doses of naloxone up to 100 mg/kg did not cause significant hypothermia in morphine-implanted animals which had received chronic caffeine. The development of tolerance was determined by computing the morphine potency ratio for the tail flick assay (tolerant ED50/control ED50). In mice chronically administered caffeine, the potency ratio was decreased significantly in morphine-implanted animals when compared to control. Morphine-induced analgesia, tolerance and dependence was not changed significantly in animals chronically administered PIA. Neither the distribution of morphine to the brain nor the opioid receptor binding parameters for [3H]etorphine and [3H]naltrexone were altered in mice chronically administered caffeine or PIA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在饮用含咖啡因水(1毫克/毫升)14天的小鼠或腹腔注射(-)-N6-(苯异丙基)-腺苷(PIA)1毫克/千克共14天的小鼠中,测定吗啡诱导的镇痛作用以及吗啡诱导的耐受性和依赖性的发展情况。通过甩尾试验评估镇痛作用。通过测定纳洛酮诱发戒断跳跃的半数有效剂量(ED50)(在100毫克/千克吗啡预处理后3小时或皮下植入75毫克吗啡丸剂72小时后)以及测定纳洛酮诱发吗啡植入动物体温过低的程度来评估依赖性的发展。在长期给予咖啡因的小鼠中,吗啡诱导镇痛的ED50显著降低,而在两种类型的吗啡预处理后,纳洛酮诱发戒断跳跃的ED50增加了2倍。在对照动物(饮用自来水14天)中,1和10毫克/千克剂量的纳洛酮会使吗啡植入动物出现显著体温过低。高达100毫克/千克剂量的纳洛酮在长期摄入咖啡因的吗啡植入动物中不会引起显著体温过低。通过计算甩尾试验的吗啡效价比(耐受ED50/对照ED50)来确定耐受性的发展。与对照相比,在长期给予咖啡因的小鼠中,吗啡植入动物的效价比显著降低。在长期给予PIA的动物中,吗啡诱导的镇痛、耐受性和依赖性没有显著变化。在长期给予咖啡因或PIA的小鼠中,吗啡在脑中的分布以及[3H]埃托啡和[3H]纳曲酮的阿片受体结合参数均未改变。(摘要截短于250字)

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