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环氧合酶和脂氧合酶抑制剂替泊沙林对慢性骨关节炎犬类前列腺素和白三烯生成的体内作用

In vivo effects of tepoxalin, an inhibitor of cyclooxygenase and lipoxygenase, on prostanoid and leukotriene production in dogs with chronic osteoarthritis.

作者信息

Agnello Kimberly A, Reynolds Lisa R, Budsberg Steven C

机构信息

Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.

出版信息

Am J Vet Res. 2005 Jun;66(6):966-72. doi: 10.2460/ajvr.2005.66.966.

Abstract

OBJECTIVE

To evaluate in vivo effects of tepoxalin, an inhibitor of cyclooxygenase (COX) and lipoxygenase (LOX), on prostaglandin (PG) and leukotriene production in osteoarthritic dogs.

ANIMALS

7 mixed-breed adult dogs with chronic unilateral arthritis of a stifle joint.

PROCEDURE

Dogs were treated in accordance with a randomized 3-way crossover design. Each dog received an inert substance, meloxicam, or tepoxalin for 10 days. On day 0 (baseline), 3, and 10, dogs were anesthetized and samples of blood, stifle joint synovial fluid, and gastric mucosa were collected. Concentrations of PGE2 were measured in synovial fluid and after lipopolysaccharide stimulation of whole blood; PGE1 and PGE2 synthesis was measured in gastric mucosa. Thromboxane B2 (TxB2) concentration was measured in whole blood. Leukotriene B4 (LTB4) concentration was determined in gastric mucosa and in whole blood after ex vivo stimulation with a calcium ionophore.

RESULTS

Tepoxalin significantly decreased LTB4 concentrations in the blood and gastric mucosa at day 10 and TxB2 concentrations in the blood and PGE2 in the gastric mucosa and synovial fluid at days 3 and 10, compared with baseline values. Meloxicam significantly decreased PGE2 concentrations in the blood at days 3 and 10 and synovial fluid at day 3. Meloxicam also decreased PGE1 and PGE2 synthesis in the gastric mucosa at day 3. Meloxicam did not affect LTB4 synthesis in the blood or LTB4 concentrations in the gastric mucosa.

CONCLUSIONS AND CLINICAL RELEVANCE

Tepoxalin has in vivo inhibitory activity against COX-1, COX-2, and 5-LOX in dogs at the current approved recommended dosage.

摘要

目的

评估环氧合酶(COX)和脂氧合酶(LOX)抑制剂替泊沙林对骨关节炎犬体内前列腺素(PG)和白三烯生成的影响。

动物

7只患有慢性单侧膝关节关节炎的成年杂种犬。

方法

采用随机三交叉设计对犬进行治疗。每只犬接受惰性物质、美洛昔康或替泊沙林治疗10天。在第0天(基线)、第3天和第10天,对犬进行麻醉,并采集血液、膝关节滑液和胃黏膜样本。测定滑液中以及全血经脂多糖刺激后的PGE2浓度;测定胃黏膜中PGE1和PGE2的合成。测定全血中血栓素B2(TxB2)浓度。在用钙离子载体进行体外刺激后,测定胃黏膜和全血中的白三烯B4(LTB4)浓度。

结果

与基线值相比,替泊沙林在第10天时显著降低了血液和胃黏膜中的LTB4浓度,在第3天和第10天时显著降低了血液中的TxB2浓度以及胃黏膜和滑液中的PGE2浓度。美洛昔康在第3天和第10天时显著降低了血液中的PGE2浓度,在第3天时显著降低了滑液中的PGE2浓度。美洛昔康在第3天时还降低了胃黏膜中PGE1和PGE2的合成。美洛昔康不影响血液中LTB4的合成或胃黏膜中LTB4的浓度。

结论及临床意义

在当前批准的推荐剂量下,替泊沙林对犬体内的COX-1、COX-2和5-LOX具有体内抑制活性。

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