Boyle E A, Freeman P C, Mangan F R, Thomson M J
J Pharm Pharmacol. 1982 Sep;34(9):562-9. doi: 10.1111/j.2042-7158.1982.tb04794.x.
Nabumetone is a compound of novel structure which displays acute anti-inflammatory activity in the carrageenan-induced oedema model in rats and the ultraviolet-induced erythema model in guinea-pigs. Its activity in these tests is greater than that of aspirin but less than that of naproxen and indomethacin. In the cotton pellet-induced granuloma model in the rat, the compound is active and produces no signs of toxicity at doses much greater than the lowest effective dose, unlike aspirin, naproxen or indomethacin. Nabumetone is also active in the adjuvant-induced arthritis test in rats. In contrast to aspirin, indomethacin and naproxen, the compound is well tolerated by the stomach of fasted rats at doses in excess of those with anti-inflammatory activity. These findings could be linked to the relatively poor ability of nabumetone to inhibit the synthesis of prostaglandins in vitro and to its non-acidic structure. The compound has greater mild analgesic activity than paracetamol, is equi-active with phenylbutazone, but less active than aspirin, naproxen and indomethacin. Nabumetone also has antipyretic activity in the rabbit. No interactions with the hypothalamic-pituitary-adrenal axis have been found.
萘丁美酮是一种结构新颖的化合物,在角叉菜胶诱导的大鼠水肿模型和紫外线诱导的豚鼠红斑模型中显示出急性抗炎活性。在这些试验中,其活性大于阿司匹林,但小于萘普生和吲哚美辛。在大鼠棉球诱导的肉芽肿模型中,该化合物具有活性,在远高于最低有效剂量的情况下未产生毒性迹象,这与阿司匹林、萘普生或吲哚美辛不同。萘丁美酮在大鼠佐剂诱导的关节炎试验中也具有活性。与阿司匹林、吲哚美辛和萘普生相反,该化合物在空腹大鼠胃中以超过抗炎活性剂量给药时耐受性良好。这些发现可能与萘丁美酮在体外抑制前列腺素合成的能力相对较差及其非酸性结构有关。该化合物的轻度镇痛活性比扑热息痛强,与保泰松活性相当,但比阿司匹林、萘普生和吲哚美辛弱。萘丁美酮在兔中也有解热活性。未发现与下丘脑 - 垂体 - 肾上腺轴有相互作用。