MacKay R J, Clark C K, Logdberg L, Lake P
Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610, USA.
Am J Vet Res. 1999 Jan;60(1):68-75.
To determine the efficacy of polymyxin B-dextran 70 (PBD) for treatment of endotoxemic horses.
15 horses during study 1 and 6 horses during study 2.
3 groups were used in study 1. Horses in groups 1 and 2 were given 30 ng of lipopolysaccharide (LPS)/kg of body weight, IV, over 60 minutes. Horses in group 3 were given saline (0.9% NaCl) solution. Beginning 15 minutes before LPS infusion and continuing for 75 minutes, horses in groups 1 and 3 were given PBD, IV. Horses in group 2 were given dextran 70. Blood samples were obtained for hemograms and determination of cytokine, lactate, and prostanoid concentrations. In study 2, horses were given ketoprofen (2.2 mg/kg) or saline solution 15 minutes before infusion of PBD. Fourteen days later, treatments were reversed, using a crossover design. Blood samples were obtained for measurement of thromboxane B2 (TXB2) concentration.
For study 1, prior treatment with PBD completely blocked endotoxin-induced changes for heart and respiratory rates, rectal temperature, WBC count, and plasma tumor necrosis factor, interleukin 6, TXB2, and prostaglandin F1 concentrations. There was transient tachypnea, sweating, and increased plasma TXB2 concentration in horses given PBD (with or without LPS). Prior treatment with ketoprofen eliminated all PBD-induced signs and prevented the increase in plasma TXB2 concentration.
Signs of endotoxemia were prevented in horses by treatment with PBD, although its use was associated with mild adverse effects.
When used in combination with a cyclooxygenase-inhibiting drug, PBD has potential for treatment of horses with endotoxemia.
确定多粘菌素B-葡聚糖70(PBD)治疗内毒素血症马匹的疗效。
研究1中有15匹马,研究2中有6匹马。
研究1中使用3组。第1组和第2组的马匹静脉注射30 ng脂多糖(LPS)/千克体重,持续60分钟。第3组的马匹给予生理盐水(0.9%氯化钠)溶液。在LPS输注前15分钟开始并持续75分钟,第1组和第3组的马匹静脉注射PBD。第2组的马匹给予葡聚糖70。采集血样进行血常规检查以及测定细胞因子、乳酸和前列腺素浓度。在研究2中,马匹在输注PBD前15分钟给予酮洛芬(2.2 mg/kg)或生理盐水溶液。14天后,采用交叉设计更换治疗方法。采集血样测量血栓素B2(TXB2)浓度。
对于研究1,预先使用PBD完全阻断了内毒素诱导的心率、呼吸频率、直肠温度、白细胞计数以及血浆肿瘤坏死因子、白细胞介素6、TXB2和前列腺素F1浓度的变化。给予PBD的马匹(无论是否给予LPS)出现短暂的呼吸急促、出汗以及血浆TXB2浓度升高。预先使用酮洛芬消除了所有PBD诱导的体征,并防止了血浆TXB2浓度升高。
PBD治疗可预防马匹内毒素血症的体征,尽管其使用会伴有轻微不良反应。
与环氧化酶抑制药物联合使用时,PBD有治疗内毒素血症马匹的潜力。