Lee D K, Chau T T, Weichman B M, Wooley P H
Department of Biochemistry, Ayerst Laboratories Research, Inc., Princeton, New Jersey 08543-8000.
Proc Soc Exp Biol Med. 1988 Mar;187(3):273-7. doi: 10.3181/00379727-187-42663.
Using the curative model of adjuvant arthritis, adult male Sprague-Dawley rats were treated with vehicle or etodolac (1, 3, and 8 mg/kg/day, po) for 9 days. Rats were sacrificed after 1, 2, 4, or 9 daily doses, and paw volume, PGE2 concentrations, and N-acetyl-beta-D-glucosaminidase (NAG) activity were determined in the left adjuvant-injected hindpaws. All three doses of etodolac caused a significant decrease in PGE2 concentrations after the first dose, and the decreases persisted for 2, 4, and 9 days of treatment, respectively. In rats given four daily doses of 3 and 8 mg/kg/day of etodolac, the paw volume was significantly decreased by about 50%, compared with that of the arthritic controls. A significant decrease in NAG activity was observed only after nine daily doses of 8 mg/kg/day etodolac. The sequence of anti-inflammatory events manifested following etodolac treatment would appear to be an initial inhibition of PGE2 synthesis, followed by resorption of fluid, and then by a reduction in macrophage infiltration.
采用佐剂性关节炎治疗模型,对成年雄性Sprague-Dawley大鼠分别给予赋形剂或依托度酸(1、3和8毫克/千克/天,口服),持续9天。在每日给药1、2、4或9次后处死大鼠,并测定左后爪佐剂注射部位的爪体积、前列腺素E2(PGE2)浓度和N-乙酰-β-D-氨基葡萄糖苷酶(NAG)活性。所有三种剂量的依托度酸在首次给药后均使PGE2浓度显著降低,且降低情况分别在治疗的第2、4和9天持续存在。在每日给予4次3毫克/千克/天和8毫克/千克/天依托度酸的大鼠中,与关节炎对照组相比,爪体积显著减小约50%。仅在每日给予9次8毫克/千克/天依托度酸后,NAG活性才显著降低。依托度酸治疗后出现的抗炎事件顺序似乎是首先抑制PGE2合成,随后是液体吸收,然后是巨噬细胞浸润减少。