van der Heijden Jaap, Kolliopoulos Constantinos, Skorup Paul, Sallisalmi Marko, Heldin Paraskevi, Hultström Michael, Tenhunen Jyrki
Department of Surgical Sciences, Anesthesiology and Intensive Care, Uppsala University, 75185, Uppsala, Sweden.
Department Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Intensive Care Med Exp. 2021 Oct 11;9(1):53. doi: 10.1186/s40635-021-00418-3.
Plasma hyaluronan concentrations are increased during sepsis but underlying mechanisms leading to high plasma hyaluronan concentration are poorly understood. In this study we evaluate the roles of plasma hyaluronan, effective plasma hyaluronidase (HYAL) activity and its endogenous plasma inhibition in clinical and experimental sepsis. We specifically hypothesized that plasma HYAL acts as endothelial glycocalyx shedding enzyme, sheddase.
Plasma hyaluronan, effective HYAL activity and HYAL inhibition were measured in healthy volunteers (n = 20), in patients with septic shock (n = 17, day 1 and day 4), in patients with acute pancreatitis (n = 7, day 1 and day 4) and in anesthetized and mechanically ventilated pigs (n = 16). Sixteen pigs were allocated (unblinded, open label) into three groups: Sepsis-1 with infusion of live Escherichia coli (E. coli) 1 × 10 CFU/h of 12 h (n = 5), Sepsis-2 with infusion of E. coli 1 × 10 CFU/h of 6 h followed by 1 × 10 CFU/h of the remaining 6 h (n = 5) or Control with no E. coli infusion (n = 6).
In experimental E. coli porcine sepsis and in time controls, plasma hyaluronan increases with concomitant decrease in effective plasma HYAL activity and increase of endogenous HYAL inhibition. Plasma hyaluronan increased in patients with septic shock but not in acute pancreatitis. Effective plasma HYAL was lower in septic shock and acute pancreatitis as compared to healthy volunteers, while plasma HYAL inhibition was only increased in septic shock.
Elevated plasma hyaluronan levels coincided with a concomitant decrease in effective plasma HYAL activity and increase of endogenous plasma HYAL inhibition both in experimental and clinical sepsis. In acute pancreatitis, effective plasma HYAL activity was decreased which was not associated with increased plasma hyaluronan concentrations or endogenous HYAL inhibition. The results suggest that plasma HYAL does not act as sheddase in sepsis or pancreatitis.
脓毒症期间血浆透明质酸浓度会升高,但导致血浆透明质酸浓度升高的潜在机制尚不清楚。在本研究中,我们评估了血浆透明质酸、有效血浆透明质酸酶(HYAL)活性及其内源性血浆抑制在临床和实验性脓毒症中的作用。我们特别假设血浆HYAL作为内皮糖萼脱落酶,即脱落酶。
在健康志愿者(n = 20)、感染性休克患者(n = 17,第1天和第4天)、急性胰腺炎患者(n = 7,第1天和第4天)以及麻醉并机械通气的猪(n = 16)中测量血浆透明质酸、有效HYAL活性和HYAL抑制。16头猪(非盲法、开放标签)被分为三组:脓毒症-1组,以1×10⁹CFU/h的速度输注活大肠杆菌(E. coli)12小时(n = 5);脓毒症-2组,以1×10⁹CFU/h的速度输注大肠杆菌6小时,然后在剩余6小时以1×10⁹CFU/h的速度输注(n = 5);对照组,不输注大肠杆菌(n = 6)。
在实验性大肠杆菌猪脓毒症和时间对照组中,血浆透明质酸增加,同时有效血浆HYAL活性降低,内源性HYAL抑制增加。感染性休克患者的血浆透明质酸升高,但急性胰腺炎患者未升高。与健康志愿者相比,感染性休克和急性胰腺炎患者的有效血浆HYAL较低,而血浆HYAL抑制仅在感染性休克中增加。
在实验性和临床脓毒症中,血浆透明质酸水平升高与有效血浆HYAL活性同时降低以及内源性血浆HYAL抑制增加相一致。在急性胰腺炎中,有效血浆HYAL活性降低,但这与血浆透明质酸浓度升高或内源性HYAL抑制增加无关。结果表明,血浆HYAL在脓毒症或胰腺炎中不作为脱落酶起作用。