Effect of peritoneal dialysis solution with different pyruvate concentrations on intestinal injury

To investigate the effects of direct peritoneal resuscitation with pyruvate-peritoneal dialysis solution (Pyr-PDS) of different concentrations combined with intravenous resuscitation on acid–base imbalance and intestinal ischemia reperfusion injury in rats with hemorrhagic shock. Sixty rats were randomly assigned to group SHAM, group intravenous resuscitation, and four direct peritoneal resuscitation groups combined with intravenous resuscitation: group NS, LA, PY1, and PY2, that is, normal saline, lactate-PDS (Lac-PDS), lower concentration Pyr-PDS (Pyr-PDS1), and higher concentration Pyr-PDS (Pyr-PDS2), respectively. Two hours after hemorrhagic shock and resuscitation, the pH, oxygen partial pressure, carbon dioxide partial pressure (PCO2), base excess, and bicarbonate ion concentration (HCO3−) of the arterial blood were measured. The intestinal mucosal damage index and intercellular adhesion molecule 1 (ICAM-1), tumor necrosis factor-α, interleukin-6, zonula occludens-1, claudin-1, and occludin levels in intestinal issues were detected. Two hours after resuscitation, group PY2 had higher mean arterial pressure, pH, oxygen partial pressure, and base excess and lower PCO2 of arterial blood than group PY1 (P < 0.05). Tumor necrosis factor-α and interleukin-6 levels in group PY2 were significantly lower than those in group PY1 (P < 0.05). Zonula occludens-1, claudin-1, and occludin expression levels were significantly higher in group PY2 than in group PY1 (P < 0.05). Direct peritoneal resuscitation with Pyr-PDS2 combined with intravenous resuscitation enhanced the hemodynamics, improved the acid–base balance, and alleviated intestinal ischemia reperfusion injury from hemorrhagic shock and resuscitation in rats. The mechanisms might include correction of acidosis, inhibition of inflammatory response, enhancement of systemic immune status, regulation of intestinal epithelial permeability, and maintenance of intestinal mucosal barrier function. Impact statement Hemorrhagic shock is a life-threatening condition after trauma or during surgery. Acid–base imbalance and intestinal ischemia reperfusion injury are two significant causes in the pathogenetic process and multiple organ dysfunction. As a result, it is urgent and necessary to find an effective method of resuscitation in order to reverse the acid–base imbalance and protect organ function. This current study confirmed the protection against hypoxic acidosis and intestinal ischemia reperfusion injury by peritoneal resuscitation with pyruvate combined with intravenous resuscitation in rats with hemorrhagic shock. And the peritoneal dialysis solution with pyruvate of high concentration plays a crucial role in the process. It provided a new idea and possible direction of fluid resuscitation for alleviating organ injuries, protecting organ functions, and improving clinical prognosis after hemorrhagic shock and resuscitation.

[1]  Sheng Liu,et al.  Sodium butyrate inhibits the production of HMGB1 and attenuates severe burn plus delayed resuscitation-induced intestine injury via the p38 signaling pathway. , 2019, Burns : journal of the International Society for Burn Injuries.

[2]  Ching-Yi Cheng,et al.  Anti‐inflammatory property of quercetin through downregulation of ICAM‐1 and MMP‐9 in TNF‐&agr;‐activated retinal pigment epithelial cells , 2019, Cytokine.

[3]  Nancy J. Denke,et al.  Resuscitative Strategies in the Trauma Patient: The Past, the Present, and the Future , 2018, Journal of trauma nursing : the official journal of the Society of Trauma Nurses.

[4]  B. Harbrecht,et al.  Direct peritoneal resuscitation reduces intestinal permeability after brain death , 2017, The journal of trauma and acute care surgery.

[5]  T. Markel,et al.  Direct peritoneal resuscitation improves mesenteric perfusion by nitric oxide dependent pathways. , 2017, The Journal of surgical research.

[6]  S. Bhoi,et al.  Gender-based Assessment of Survival in Trauma-hemorrhagic Shock: A Retrospective Analysis of Indian Population , 2017, Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine.

[7]  Jason W. Smith,et al.  Direct Peritoneal Resuscitation: A review. , 2016, International journal of surgery.

[8]  Xiang-Hu He,et al.  EFFECT OF INTRAPERITONEAL RESUSCITATION WITH DIFFERENT CONCENTRATIONS OF SODIUM PYRUVATE ON INTESTINAL ISCHEMIA REPERFUSION INJURY IN HEMORRHAGIC SHOCK RAT , 2015, Shock.

[9]  J. Bravo,et al.  Intestinal Barrier and Behavior. , 2016, International review of neurobiology.

[10]  M. Vicario,et al.  The intestinal barrier function and its involvement in digestive disease. , 2015, Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva.

[11]  J. Schulzke,et al.  Claudin-related intestinal diseases. , 2015, Seminars in cell & developmental biology.

[12]  A. Blikslager,et al.  Animal models of ischemia-reperfusion-induced intestinal injury: progress and promise for translational research. , 2015, American journal of physiology. Gastrointestinal and liver physiology.

[13]  Sung Hee Lee,et al.  Intestinal Permeability Regulation by Tight Junction: Implication on Inflammatory Bowel Diseases , 2015, Intestinal research.

[14]  J. Zhan,et al.  Protection Against Intestinal Injury from Hemorrhagic Shock by Direct Peritoneal Resuscitation with Pyruvate in Rats , 2014, Shock.

[15]  B. Harbrecht,et al.  Adjunctive treatment of abdominal catastrophes and sepsis with direct peritoneal resuscitation: Indications for use in acute care surgery , 2014, The journal of trauma and acute care surgery.

[16]  Fang-Qiang Zhou,et al.  Pyruvate Is Superior to Reverse Visceral Hypoperfusion in Peritoneal Resuscitation From Hemorrhagic Shock in Rats , 2014, Shock.

[17]  Lina Yang,et al.  Protective Effect of Crocetin on Hemorrhagic Shock–Induced Acute Renal Failure in Rats , 2012, Shock.

[18]  F. Petrat,et al.  Protection by pyruvate infusion in a rat model of severe intestinal ischemia-reperfusion injury. , 2011, The Journal of surgical research.

[19]  D. Ye,et al.  Occludin regulates macromolecule flux across the intestinal epithelial tight junction barrier. , 2011, American journal of physiology. Gastrointestinal and liver physiology.

[20]  M. Fink The therapeutic potential of pyruvate. , 2010, The Journal of surgical research.

[21]  E. Mazzon,et al.  GW0742, a selective PPAR‐β/δ agonist, contributes to the resolution of inflammation after gut ischemia/reperfusion injury , 2010, Journal of leukocyte biology.

[22]  J. Richardson,et al.  Direct peritoneal resuscitation accelerates primary abdominal wall closure after damage control surgery. , 2010, Journal of the American College of Surgeons.

[23]  P. Mongan,et al.  HYPERTONIC SODIUM PYRUVATE SOLUTION IS MORE EFFECTIVE THAN RINGER'S ETHYL PYRUVATE IN THE TREATMENT OF HEMORRHAGIC SHOCK , 2009, Shock.

[24]  C. V. Van Itallie,et al.  Claudins and epithelial paracellular transport. , 2006, Annual review of physiology.

[25]  E. Deitch,et al.  Role of the gut in the development of injury- and shock induced SIRS and MODS: the gut-lymph hypothesis, a review. , 2006, Frontiers in bioscience : a journal and virtual library.

[26]  R. N. Garrison,et al.  Direct peritoneal resuscitation from hemorrhagic shock: effect of time delay in therapy initiation. , 2005, The Journal of trauma.

[27]  R. N. Garrison,et al.  Peritoneal resuscitation. , 2005, American journal of surgery.

[28]  R. N. Garrison,et al.  Direct peritoneal resuscitation as adjunct to conventional resuscitation from hemorrhagic shock: a better outcome. , 2004, Surgery.

[29]  R. Hurt,et al.  A novel method of peritoneal resuscitation improves organ perfusion after hemorrhagic shock. , 2003, American journal of surgery.

[30]  P. Mongan,et al.  Pyruvate improves redox status and decreases indicators of hepatic apoptosis during hemorrhagic shock in swine. , 2002, American journal of physiology. Heart and circulatory physiology.

[31]  S. Tsukita,et al.  Manner of Interaction of Heterogeneous Claudin Species within and between Tight Junction Strands , 1999, The Journal of cell biology.

[32]  M. Itoh,et al.  Occludin: a novel integral membrane protein localizing at tight junctions , 1993, The Journal of cell biology.

[33]  L. Deboer,et al.  Pyruvate enhances recovery of rat hearts after ischemia and reperfusion by preventing free radical generation. , 1993, The American journal of physiology.

[34]  B. Sumpio,et al.  Common pathway of endothelial-leukocyte interaction in shock, ischemia, and reperfusion. , 1993, American journal of surgery.

[35]  H. Scott,et al.  Intestinal mucosal lesion in low-flow states. I. A morphological, hemodynamic, and metabolic reappraisal. , 1970, Archives of surgery.