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苯基丁氮酮和氟尼辛葡甲胺同时给药对母马药代动力学变量及血栓素B2体外生成的影响。

Effects of concurrent administration of phenylbutazone and flunixin meglumine on pharmacokinetic variables and in vitro generation of thromboxane B2 in mares.

作者信息

Semrad S D, Sams R A, Harris O N, Ashcraft S M

机构信息

Department of Medical Sciences, University of Wisconsin, Madison 53706.

出版信息

Am J Vet Res. 1993 Nov;54(11):1901-5.

PMID:8291770
Abstract

Flunixin meglumine and phenylbutazone are nonsteroidal anti-inflammatory drugs commonly used for the management of colic, endotoxemia, and musculoskeletal disorders in equids. Although it is not usually recommended, there appears to be an increasing trend to use nonsteroid anti-inflammatory drugs in combination to enhance or prolong their effects. Therefore, we studied the effect of concurrent administration of flunixin (1.1 mg/kg of body weight, IV) as flunixin meglumine and phenylbutazone (2.2 mg/kg, IV) on the pharmacokinetics of each drug and on in vitro thromboxane B2 production. Pharmacokinetic variables calculated for each drug when given alone and in combination were similar to those reported. Serum thromboxane B2 production was significantly (P = 0.05) suppressed for 12, 8, and 24 hours after administration of flunixin, phenylbutazone, and the drugs in combination, respectively. These results indicate that although concurrent administration of these drugs at the aforementioned dosages does not alter either drug disposition or clearance, it prolongs their pharmacologic effect.

摘要

氟尼辛葡甲胺和保泰松是常用于治疗马属动物绞痛、内毒素血症和肌肉骨骼疾病的非甾体抗炎药。尽管通常不推荐,但使用非甾体抗炎药联合用药以增强或延长其效果的趋势似乎在增加。因此,我们研究了同时给予氟尼辛(1.1毫克/千克体重,静脉注射)作为氟尼辛葡甲胺和保泰松(2.2毫克/千克,静脉注射)对每种药物药代动力学以及体外血栓素B2产生的影响。单独给药和联合给药时计算出的每种药物的药代动力学变量与报道的相似。分别在给予氟尼辛、保泰松及联合用药后12、8和24小时,血清血栓素B2的产生受到显著抑制(P = 0.05)。这些结果表明,尽管以上述剂量同时给药这些药物不会改变任何一种药物的处置或清除,但会延长它们的药理作用。

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