Skarda David E, Putt Karson S, Hergenrother Paul J, Mulier Kristine E, Beilman Greg J
Department of Surgery, University of Minnesota, Minneapolis, MN 55433, USA.
Resuscitation. 2007 Oct;75(1):135-44. doi: 10.1016/j.resuscitation.2007.02.020. Epub 2007 Apr 30.
The aim of our study was to compare poly(ADP-ribose) polymerase (PARP) activity levels in a porcine model of hemorrhagic shock and resuscitation.
We designed a prospective, comparative randomized survival study of hemorrhagic shock using 20 male Yorkshire-Landrace pigs (15-25 kg). In 16 pigs after splenectomy, we induced hemorrhagic shock to a mean arterial pressure of 50 mm Hg ( approximately 35% bleed). Pigs were randomized to receive normotensive resuscitation (SBP 90 mm Hg), mild hypotensive resuscitation (SBP 80 mm Hg), moderate hypotensive resuscitation (SBP 65 mm Hg), or no resuscitation (n=4 in each group). We also included a group of sham animals that were instrumented and had a splenectomy but not bled (n=4). Muscle and liver biopsies were taken prior to hemorrhage, after 45 min of shock, and 8, 24, and 48 h after resuscitation. PARP activity levels in biopsies were measured using chemical quantitation of NAD+.
Irrespective of our resuscitation strategy or outcome, both muscle and liver PARP activity levels rose after 45 min of shock and then returned to baseline. Excluding our control animals, PARP activity levels were significantly higher during shock in non-survivors compared to survivors.
In our model of porcine hemorrhagic shock, PARP activity levels increased during hemorrhagic shock. However, this increase in PARP activity levels was transient as they returned to baseline regardless of resuscitation strategy. Interestingly, PARP activity levels were significantly higher during hemorrhagic shock in non-survivors compared to survivors. These findings suggest that PARP activity may be a part of initial pathways leading from hemorrhagic shock to death.
我们研究的目的是比较出血性休克及复苏猪模型中聚(ADP - 核糖)聚合酶(PARP)的活性水平。
我们设计了一项前瞻性、比较性随机生存研究,使用20头雄性约克夏 - 长白猪(15 - 25千克)进行出血性休克研究。在16头脾切除术后的猪中,我们将平均动脉血压诱导至50毫米汞柱(约35%失血)以引发出血性休克。猪被随机分为接受正常血压复苏(收缩压90毫米汞柱)、轻度低血压复苏(收缩压80毫米汞柱)、中度低血压复苏(收缩压65毫米汞柱)或不进行复苏(每组n = 4)。我们还纳入了一组假手术动物,这些动物接受了仪器植入和脾切除术但未出血(n = 4)。在出血前、休克45分钟后以及复苏后8、24和48小时采集肌肉和肝脏活检样本。使用NAD + 的化学定量法测量活检样本中的PARP活性水平。
无论我们的复苏策略或结果如何,休克45分钟后肌肉和肝脏的PARP活性水平均升高,然后恢复至基线。排除我们的对照动物,与存活者相比,非存活者在休克期间的PARP活性水平显著更高。
在我们的猪出血性休克模型中,出血性休克期间PARP活性水平升高。然而,PARP活性水平的这种升高是短暂的,因为无论复苏策略如何,它们都会恢复至基线。有趣的是,与存活者相比,非存活者在出血性休克期间的PARP活性水平显著更高。这些发现表明PARP活性可能是从出血性休克到死亡的初始通路的一部分。