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轻度镇痛药的药理学评价

Pharmacological evaluation of mild analgesics.

作者信息

Römer D

出版信息

Br J Clin Pharmacol. 1980 Oct;10 Suppl 2(Suppl 2):247S-251S. doi: 10.1111/j.1365-2125.1980.tb01807.x.

Abstract

1 The analgesic, anti-inflammatory, antipyretic and ulcerogenic properties of the non-steroidal agents, acetylsalicylic acid, paracetamol, ibuprofen, propyphenazone and aminophenazone are compared. 2 The results show that ibuprofen has the most potent effect on all four parameters followed in descending order of potency by aminophenazone, propyphenazone, paracetamol and acetylsalicylic acid. 3 The inflamed paw technique and the adjuvant arthritis model, both in the rat and involving pathological (chronic) pain, are the most successful methods of predicting analgesic activity in man. The short-lasting oedema caused by injecting naphthoylheparamine into the rat paw is the most useful method of predicting clinical anti-inflammatory activity.

摘要

1 比较了非甾体类药物乙酰水杨酸、对乙酰氨基酚、布洛芬、保泰松和氨基比林的镇痛、抗炎、解热及致溃疡特性。2 结果表明,布洛芬对所有这四个参数的作用最强,其次按效力递减顺序为氨基比林、保泰松、对乙酰氨基酚和乙酰水杨酸。3 大鼠的炎症足爪技术和佐剂性关节炎模型,二者均涉及病理性(慢性)疼痛,是预测人体镇痛活性最成功的方法。向大鼠足爪注射萘甲酰肝素引起的短暂性水肿是预测临床抗炎活性最有用的方法。

相似文献

1
Pharmacological evaluation of mild analgesics.轻度镇痛药的药理学评价
Br J Clin Pharmacol. 1980 Oct;10 Suppl 2(Suppl 2):247S-251S. doi: 10.1111/j.1365-2125.1980.tb01807.x.

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