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非麻醉性镇痛药合剂在大鼠体内的抗炎、镇痛和解热活性。

The anti-inflammatory, analgesic and antipyretic activities of non-narcotic analgesic drug mixtures in rats.

作者信息

Seegers A J, Jager L P, Zandberg P, van Noordwijk J

出版信息

Arch Int Pharmacodyn Ther. 1981 Jun;251(2):237-54.

PMID:6974544
Abstract

The effects of non-narcotic analgesics have been examined, separately and in admixture, on carrageenan-induced hind paw oedema and on yeast-induced hyperalgesia and hyperthermia in adult rats. The efficacy of the drugs was evaluated using the kinetics of drug-receptor interaction. In addition, the hypothesis was tested that the anti-inflammatory, analgesic and antipyretic activities of the drug mixtures used equal the addition of the activities of the individual drugs and could be predicted from their intrinsic activities and affinities. Dose-dependent inhibition of paw oedema, hyperalgesia and hyperthermia was observed after oral administration of acetylsalicylic acid (aspirin), paracetamol, phenacetin (60, 125, 250 and 500 mg.kg--1), and caffeine (12.5, 25, 50 and 100 mg.kf--1). Over the dose-ranges used, the anti-inflammatory activities of paracetamol, phenacetin and caffeine tended to be smaller than that of aspirin. The dose producing a semi-maximal effect for caffeine was lower than that for aspirin which in turn was comparable to that for paracetamol or phenacetin. The analgesic activities of phenacetin and caffeine were classified as stronger than that of aspirin, whereas the efficacy of paracetamol was similar. Paracetamol and aspirin were comparable as antipyretics. The antipyretic activity of phenacetin was higher but that of caffeine was lower than that of aspirin. For caffeine the dose producing a semi-maximal effect was lower than that of aspirin. Within the dose-ranges used, low doses of mixtures of aspirin with either paracetamol, phenacetin or caffeine exhibited anti-inflammatory, analgesic and antipyretic activities which were not different from the activities expected on the basis of addition. Incidentally, at some of the higher dose levels potentiation of the activity of the drugs was found. Low doses of the triple combinations: aspirin + paracetamol + caffeine and aspirin + phenacetin + caffeine showed anti-inflammatory and antipyretic activities which were not different from those expected on the basis of addition, but the activities observed with higher doses of these combinations indicated potentiation. It is concluded that, in the rat, the anti-inflammatory, analgesic and antipyretic activities of dual and triple combinations of aspirin, paracetamol, phenacetin and caffeine at least equal the activities expected on the basis of addition.

摘要

研究了非麻醉性镇痛药单独及混合使用时,对成年大鼠角叉菜胶诱导的后爪水肿、酵母诱导的痛觉过敏和体温过高的影响。使用药物 - 受体相互作用动力学评估药物的疗效。此外,还检验了以下假设:所用药物混合物的抗炎、镇痛和解热活性等于各单独药物活性之和,并且可以根据其内在活性和亲和力进行预测。口服乙酰水杨酸(阿司匹林)、对乙酰氨基酚、非那西丁(60、125、250和500mg·kg⁻¹)和咖啡因(12.5、25、50和100mg·kg⁻¹)后,观察到爪水肿、痛觉过敏和体温过高呈剂量依赖性抑制。在所使用的剂量范围内,对乙酰氨基酚、非那西丁和咖啡因的抗炎活性往往小于阿司匹林。产生半最大效应的咖啡因剂量低于阿司匹林,而阿司匹林又与对乙酰氨基酚或非那西丁相当。非那西丁和咖啡因的镇痛活性被分类为强于阿司匹林,而对乙酰氨基酚的疗效相似。对乙酰氨基酚和阿司匹林作为退热药相当。非那西丁的解热活性高于阿司匹林,但咖啡因的解热活性低于阿司匹林。对于咖啡因,产生半最大效应的剂量低于阿司匹林。在所使用的剂量范围内,低剂量的阿司匹林与对乙酰氨基酚、非那西丁或咖啡因的混合物表现出的抗炎、镇痛和解热活性与基于相加预期的活性无差异。顺便说一下,在一些较高剂量水平发现了药物活性的增强。低剂量的三联组合:阿司匹林 + 对乙酰氨基酚 + 咖啡因和阿司匹林 + 非那西丁 + 咖啡因显示出的抗炎和解热活性与基于相加预期的活性无差异,但这些组合较高剂量时观察到的活性表明有增强作用。得出的结论是,在大鼠中,阿司匹林、对乙酰氨基酚、非那西丁和咖啡因的二元和三元组合的抗炎、镇痛和解热活性至少等于基于相加预期的活性。

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