Myers M J, Farrell D E, Evock-Clover C M, McDonald M W, Steele N C
Animal Biology Branch, USFDA/Center for Veterinary Medicine, Laurel, MD 20708, USA.
Am J Vet Res. 1997 Jun;58(6):594-600.
To determine whether recombinant porcine somatotropin (PST) or chromium picolinate (CrP) affected cytokine production and metabolism in swine after endotoxin challenge exposure.
20 Poland China X Landrace pigs, 5/group.
Pigs were given CrP-supplemented feed at body weight of 20 kg; PST treatment began at 60 kg, and both treatments continued through body weight of 90 kg. At 90 kg, pigs were challenge exposed with 20 micrograms of lipopolysaccharide (LPS)/kg of body weight. Blood samples were obtained at various times through 24 hours after LPS challenge exposure.
In all pigs not given PST, glucose concentration decreased 2 to 4 hours after LPS. In PST-treated pigs, blood glucose concentration was decreased at 6 to 8 hours after LPS. Plasma insulin concentration paralleled changes in glucose concentration. Nonesterified fatty acid concentration was high 2 to 24 hours after LPS in pigs not given PST and at 6 to 24 h in PST-treated pigs. Plasma urea nitrogen concentration was high at 6 to 24 hours after LPS in pigs not given PST. The urea nitrogen values in PST-treated pigs were lower at all times. Serum aspartate transaminase activity was high 6 to 24 hours after LPS in pigs not given PST, whereas PST treatment prevented the increase in this enzyme activity. In untreated (PST) pigs, plasma bilirubin (total and direct) concentrations were high 4 to 8 hours after LPS and returned to normal at 24 hours. The PST- and CrP-treated pigs maintained normal plasma bilirubin concentrations. Interleukin 6 activity was unaffected by CrP and PST treatments. Treatment with CrP and PST decreased the tumor necrosis factor alpha response to LPS, compared with that in control pigs.
PST, and to a lesser extent CrP, provide protection against the adverse metabolic effects of LPS-induced septic shock.
确定重组猪生长激素(PST)或吡啶甲酸铬(CrP)在内毒素攻击暴露后是否会影响猪体内细胞因子的产生和代谢。
20头波中猪×长白猪杂交猪,每组5头。
猪体重达20 kg时开始饲喂添加CrP的饲料;体重达60 kg时开始PST处理,两种处理均持续至体重达90 kg。体重达90 kg时,给猪注射20微克/千克体重的脂多糖(LPS)进行攻击暴露。在LPS攻击暴露后的24小时内不同时间采集血样。
在所有未给予PST的猪中,LPS注射后2至4小时血糖浓度下降。在接受PST处理的猪中,LPS注射后6至8小时血糖浓度下降。血浆胰岛素浓度与血糖浓度变化平行。在未给予PST的猪中,LPS注射后2至24小时非酯化脂肪酸浓度较高,在接受PST处理的猪中,该浓度在6至24小时较高。在未给予PST的猪中,LPS注射后6至24小时血浆尿素氮浓度较高。PST处理组猪的尿素氮值在所有时间均较低。在未给予PST的猪中,LPS注射后6至24小时血清天冬氨酸转氨酶活性较高,而PST处理可防止该酶活性升高。在未接受(PST)处理的猪中,LPS注射后4至8小时血浆胆红素(总胆红素和直接胆红素)浓度较高,24小时时恢复正常。接受PST和CrP处理的猪血浆胆红素浓度维持正常。白细胞介素6活性不受CrP和PST处理的影响。与对照猪相比,CrP和PST处理可降低肿瘤坏死因子α对LPS的反应。
PST以及程度较轻的CrP可预防LPS诱导的脓毒性休克的不良代谢影响。