Introduction
On the surface of healthy vascular endothelium resides a structure, the endothelial glycocalyx, that consists of extracellular domains of receptor, adhesion and channel proteins and, foremost, of molecules such as transmembrane syndecan 1 (bearing covalently bound, highly negatively charged glycosaminoglycans, such as heparan and chondroitin sulfates) and the receptor-bound, long-chained hyaluronic acid molecule [
1],[
2]. Together with bound plasma proteins and glycosaminoglycans, the glycocalyx forms the endothelial surface layer with a functional thickness of more than 1 μm [
3],[
4]. Disruption of the glycocalyx has been shown to increase capillary permeability and firm attachment of leukocytes and blood platelets, leading to tissue edema, suggesting that the glycocalyx acts as a competent permeability barrier and antiadhesive interface with blood [
5]. In patients in septic shock, glycocalyx shedding has been found to be associated with increased mortality and to be an independent predictor of mortality in trauma patients [
6]-[
8].
Traditional perioperative fluid therapy is often performed in a liberal manner, leading to fluid overload and tissue edema. In clinical studies, hypervolemia has been shown to have detrimental influences on several aspects of patient outcome, including cardiopulmonary complications, anastomotic insufficiency, length of hospital stay, duration of mechanical ventilation and mortality [
9]-[
11]. One possible underlying trigger may be the release of atrial natriuretic peptide (ANP) from the cardiac atria invoked by mechanical wall stress [
12]. ANP is known to induce rapid shifts of intravascular fluid into the interstitial space and has been shown to cause deterioration of the endothelial glycocalyx. In an isolated heart model, artificially infused ANP induced an increase in vascular permeability, a histologically detectable degradation of the glycocalyx and significant tissue edema [
13]. Furthermore, an increase in plasma ANP has been found to precede shedding of the glycocalyx in patients undergoing coronary bypass surgery [
14].
ANP is released during hypervolemia, which could explain the context sensitivity of volume effects of iso-oncotic colloidal infusions (for example, 6% hydroxyethyl starch or 5% human albumin) [
15],[
16]. The “volume effect” is that part of an infused fluid bolus that remains within the vasculature for a longer period. Direct blood volume measurements have revealed that the presumed volume effect of about 100% for such colloids is realized only in normovolemic patients—that is, during acute normovolemic hemodilution (ANH), a procedure in which blood is withdrawn and simultaneously replaced by equal amounts of colloidal fluid [
16]. During volume loading (VL) (that is, the hypervolemic infusion of colloids into a primarily normovolemic circulation without simultaneous blood withdrawal), about 60% of the infused amount was observed to directly load the interstitial space within 30 minutes, leaving a volume effect of merely 40% [
15]. Also, 60% of the infused fluid was found to leave the intravascular space, and 60% of the administered macromolecules (hydroxyethyl starch (HES) and albumin) were extravasated.
The aim of the present study was to investigate comparatively whether the established blood-sparing procedures VL (hypervolemia) and ANH (normovolemia) are associated with increased ANP levels and shedding of the endothelial glycocalyx.
Material and methods
The study was approved by the independent ethics committee of our institution (Medical Faculty of the Ludwig-Maximilians-University Munich, Germany; trial registration 128-04), and all patients included gave us their written informed consent to participate. Inclusion criteria were patient consent, good cardiopulmonary health, expected blood loss of more than 500 ml, and preoperative indication of the necessity to insert arterial and central venous catheters. The study was performed before the results of the 6S and CHEST trials were published (Scandinavian Starch for Severe Sepsis/Septic Shock trial and Crystalloid versus Hydroxyethyl Starch trial, respectively) [
17],[
18].
Anesthesiological procedure
The mandatory fasting period after consumption of solid food, milk and milk-containing fluids was 6 hours, and clear fluids were allowed up to 2 hours before induction of anesthesia. After each patient arrived in the operating theatre, monitoring with electrocardiography and pulse oximetry was implemented. General anesthesia was induced with 0.5 μg/kg sufentanil, 2 mg/kg propofol and 0.1 mg/kg cisatracurium, and, after tracheal intubation, anesthesia was maintained with 1.6% to 2.0% sevoflurane. Radial artery and central venous catheters were inserted. Mechanical ventilation was performed to maintain partial pressure of arterial oxygen at 100 to 150 mmHg and partial pressure of carbon dioxide at 40 ± 5 mmHg. No intravenous infusions were applied, except for negligible amounts required to inject the intravenous drugs. After a steady state was achieved, the patients were assigned to receive either VL or ANH.
Acute normovolemic hemodilution
Blood was removed at a rate of about 60 ml/min via the arterial line and simultaneously replaced with iso-oncotic HES colloid solution (6% HES 130/0.4 (Volulyte); Fresenius Kabi, Bad Homburg, Germany) at almost the same rate through the central venous line. At first, a quantity of approximately 500 ml/m2 of blood was removed. The hemodilution bags were weighed on a precision scale so that the volume of withdrawn blood could be evaluated immediately. For fine-tuning, frequent determinations of hematocrit were carried out to reach a target hematocrit level of 24 ± 2%. The hemodilution procedure took about 30 minutes.
Volume loading
VL was initiated by infusing 20 ml/kg of an iso-oncotic HES colloid solution (6% HES 130/0.4, Volulyte) within 15 minutes at a rate of approximately 90 ml/min.
Blood sampling
In all patients, blood and urine samples were taken directly after induction of anesthesia (pre) to determine basal values. Both VL and ANH procedures were initiated immediately thereafter and lasted for 30 minutes, followed by the second blood and urine sampling (post). The time window for the present study was chosen because we knew from previous direct double-tracer blood volume measurements that, after VL with 5% human albumin or 6% HES administration, the total volume of the endothelial surface layer (glycocalyx and bound plasma proteins) would be significantly reduced 30 minutes after the procedure [
15]. The patients were kept strictly in supine position during the whole investigation period. All measurements were performed before surgical incisions were made.
Determination of glycocalyx constituents
Immediately after withdrawal into serum vials, blood samples were centrifuged at 2,000 g for 10 minutes. The serum fraction was frozen and stored at -80°C until assayed. Urine samples were also frozen at -80°C until assayed.
Syndecan concentration
Syndecan 1 concentrations in serum and urine were determined directly as previously reported by using an enzyme-linked immunosorbent assay kit (Diaclone Research, Besancon, France) [
14],[
19],[
20]. In this kit, a solid-phase monoclonal B-B4 antibody against an extracellular domain of syndecan 1 is employed.
Heparan sulfate concentration
Serum and urinary heparan sulfate concentrations were quantified using a special enzyme-linked immunosorbent assay kit (Seikagaku, Tokyo, Japan) as previously reported [
14],[
19],[
21]-[
23]. Serum was pretreated with protease from
Streptomyces griseus (Actinase E; Sigma-Aldrich, St Louis, MO, USA). This kit employs two monoclonal antibodies specific for heparan sulfate-related epitopes.
Hyaluronan concentration
Hyaluronan concentrations were measured in serum using an enzyme-linked immunosorbent assay kit (Echelon Biosciences, Salt Lake City, UT, USA) designed to detect human hyaluronic acid, as previously described [
14],[
23]. Hyaluronan concentrations were not measured in urine, because renal excretion plays a negligible part in clearance. The major part of the elimination of hyaluronan (about 90%) from the systemic circulation occurs in the liver via receptor-mediated endocytosis in the sinusoidal liver endothelial cells [
24],[
25].
Atrial natriuretic peptide concentration
Blood was sampled into ethylenediaminetetraacetic acid in vials and centrifuged immediately (2,000
g, 10 minutes). The plasma was directly frozen and stored at ?80°C until assayed. Plasma levels of ANP were measured with a sandwich enzyme-linked immunosorbent assay kit (Uscn Life Science, Wuhan, China) with an antibody specific to human ANP as performed previously [
14]. The kit did not require a preliminary step for extraction or purification of plasma samples.
Statistical analysis
A preliminary sample size calculation was based on a previous study in which researchers investigated ANP concentrations after VL with 500 ml of 6% HES and 1,000 ml of Ringer’s lactate solution in patients before caesarean section [
26]. The difference between mean ANP before and after VL was 17.9 pg/ml. Using this difference and the corresponding standard deviations, we calculated a sample size with a two-sided confidence interval of 0.95 and a desired power of 0.80, which yielded a result that we needed nine patients in each group. Data are given as mean ± SEM. All data were compared by performing Student’s
t-test, with
P <0.05 considered statistically significant (SigmaStat; Systat Software, Richmond, VA, USA).
Discussion
The results of the present study reveal that hypervolemia induced by VL is associated with increased plasma concentrations of ANP and raised serum levels of two main constituents of the endothelial glycocalyx. ANH had no comparable effects.
ANH and VL are well-established, frequently used blood-sparing procedures. The main goal of ANH is to withdraw whole blood, which is stored outside the body, and replace this volume with iso-oncotic colloids, thereby diluting the remaining blood whilst retaining a constant normovolemic blood volume [
27]. In this situation, iso-oncotic colloids have a volume effect of nearly 100%, meaning that the entire infused volume remains in the circulation [
16]. In the event of subsequent bleeding, there is a loss of diluted, hemoglobin-reduced blood, which can be replaced with the previously withdrawn hemoglobin-rich blood when the individual transfusion cutoff value is reached. VL, in contrast, dilutes the blood by expanding the blood volume [
27]. In previous studies, direct blood volume measurements have revealed that, during the VL procedure, only 40% of the infused colloids remain within the vasculature [
15]. The other 60% are shifted to the interstitial space, causing tissue edema. The mechanism behind this colloid shifting seems to be an impaired glycocalyx structure, as evidenced by a considerable decrease in the total volume of the endothelial surface layer [
15]. The results of the present study offer an explanation for this phenomenon: ANP is released from human atria during iatrogenic hypervolemia, inducing shedding of constituent parts of the endothelial glycocalyx.
ANP has well-known diuretic, natriuretic and vasodilating effects. Furthermore, this polypeptide hormone also induces rapid shifts of intravascular fluid into the interstitial space [
12],[
28]. Experimental and clinical studies have revealed that elevation of ANP is associated with increased shedding of the endothelial glycocalyx [
13],[
14].
A possible connection between the ability of ANP to acutely shift volume from the intra- to extravascular spaces and its influence on the integrity of the endothelial glycocalyx has been investigated in an experimental setting by our group [
13]. Infusion of ANP in an isolated heart model caused an increase in fluid leak and an accelerated extravasation of colloid. Furthermore, ANP resulted in rapid shedding of the endothelial glycocalyx and histologically detectable destruction of the coronary vascular glycocalyx [
13]. Accordingly, the ANP-induced increase in vascular permeability described
in vivo might be related to changes in the integrity of the glycocalyx. This fragile structure is a crucial part of the vascular barrier, and its deterioration has been shown to cause shifting of fluids and colloids into the interstitial space with concomitant tissue edema.
Indirect evidence for such an effect comes from a recent study of patients undergoing coronary artery bypass surgery [
14]. Three major components of the endothelial glycocalyx were shed from the endothelium and detected in the circulating blood of patients during both on- and off-pump coronary artery bypass surgeries. Comparison of the respective time courses of glycocalyx shedding with release of ANP and various cytokines designated ANP as the mediator that most likely initiated shedding in both surgical procedures [
14].
Perioperative fluid therapy is currently being discussed intensively concerning not only the kind of fluid but also the right amount. A further aspect of debate is when to infuse the fluid. The danger of hypovolemia’s causing organ hypoperfusion and increasing the risk of systemic inflammation has been known for decades. However, awareness that hypervolemia can have similar detrimental effects on patient outcomes is relatively new. Fluid overload has been shown to abet anastomotic leakage, pulmonary edema, pneumonia and wound infection, as well as postoperative ileus [
10],[
11],[
29]. Individually, both the surgical impact (inflammation, trauma) and the traditional liberal fluid strategy have the potential to impair the competence of the vascular barrier. The combination of both confounders increases this effect significantly. A breakdown of vascular barrier competence results in capillary leakage and protein-rich interstitial edema, which lead to a significant perioperative increase in body weight. In clinical trials, this has been shown to be associated with increased morbidity and mortality [
9]-[
11]. The data derived from the present study support the need for a rational fluid management strategy to maintain normovolemia by replacing actual losses in an adequate manner and avoid unnecessary fluid boluses.
HES preparations are frequently used in clinical practice because their intravascular volume effect is high and their deposition in tissue is low. Under pathological conditions, however, this might not inevitably be the case. Patients with severe sepsis and in septic shock, for example, need very large amounts of fluid to stabilize cardiac preload. Trials have revealed a significantly decreased volume effect of colloids in this situation, despite remaining superior to crystalloids [
30]-[
33]. This effect not only is associated with severe tissue edema but also can cause serious side effects that have a negative impact on patient outcome. Experimental data support the observation that colloids may be retained insufficiently at the vascular barrier during capillary leakage [
34]. Our experimental findings are in agreement with these clinical observations linking degradation of the glycocalyx to colloid and fluid extravasation.
One key question is whether the renal or the vascular effects of ANP stand in the foreground. In our study, we measured no difference in urinary output between these groups, although patients in the VL group were subjected to hypervolemia. However, our urine-sampling period terminated directly after fluid infusion and thus was probably too short to detect changes in urinary output. Indeed, Drummer
et al. demonstrated that an intravenous volume bolus of 2 L in healthy volunteers required more than 48 hours to be completely excreted [
35]. Nevertheless, the unchanged urine production in our study allowed us to analyze clearly the results obtained for urinary elimination of heparan sulfate and syndecan 1. The urinary concentration of the former did not differ between pre- and postintervention for either the VL or ANH patients, whereas the syndecan 1 concentration increased in the VL group. Thus, urinary elimination directly reflects the alteration in blood level determined for these two glycocalyx constituents, with no masking or simulation of shedding on the basis of renal clearance.
One limitation of this trial is that biomarkers of glycocalyx shedding are only an indirect method of measuring glycocalyx thickness and integrity and do not provide insight into the thickness of the remaining glycocalyx structure. Furthermore, we used a third-generation balanced 6% hydroxyethyl starch 130/0.4 solution, so, despite volume effects similar to those seen with other iso-oncotic colloids (for example, 5% human albumin), the results of this trial are not directly transferable to other colloids.
Surprisingly, we found only two markers of glycocalyx degradation to be elevated in the serum of the VL group: syndecan 1 and hyaluronan. It should be borne in mind that shedding of these two constituents requires the action of proteases, whereas the lyase heparanase is needed for shedding of heparan sulfates in humans. Accordingly, VL cannot lead to any marked activation or release of heparanase in humans. A major store of heparanase in humans is in the tissue mast cells [
36]. Fittingly, there are no receptors for ANP on the human mast cell. Thus, VL-induced liberation of ANP is a realistic mechanism by which to explain our finding of dissociated markers of glycocalyx damage.
Competing interests
DC has delivered lectures funded by, and has received research grants from, B Braun, Grifols and Fresenius Kabi. MJ has delivered lectures funded by, and has received research grants from, Baxter, B Braun, Fresenius Kabi, Grifols and Serumwerk Bernburg, and is a member of the Grifols Albumin Advisory Board. MR has delivered lectures funded by, and has received research grants from, CSL Behring and Fresenius Kabi Serumwerk Bernburg. All of the other authors declare that they have no competing interests.