Open Access

Renal haemodynamic, microcirculatory, metabolic and histopathological responses to peritonitis-induced septic shock in pigs

  • Jiri Chvojka1,
  • Roman Sykora1,
  • Ales Krouzecky1,
  • Jaroslav Radej1,
  • Veronika Varnerova1,
  • Thomas Karvunidis1,
  • Ondrej Hes2,
  • Ivan Novak1,
  • Peter Radermacher3 and
  • Martin Matejovic1Email author
Critical Care200812:R164

https://doi.org/10.1186/cc7164

Received: 15 September 2008

Accepted: 24 December 2008

Published: 24 December 2008

Abstract

Introduction

Our understanding of septic acute kidney injury (AKI) remains incomplete. A fundamental step is the use of animal models designed to meet the criteria of human sepsis. Therefore, we dynamically assessed renal haemodynamic, microvascular and metabolic responses to, and ultrastructural sequelae of, sepsis in a porcine model of faecal peritonitis-induced progressive hyperdynamic sepsis.

Methods

In eight anaesthetised and mechanically ventilated pigs, faecal peritonitis was induced by inoculating autologous faeces. Six sham-operated animals served as time-matched controls. Noradrenaline was administered to maintain mean arterial pressure (MAP) greater than or equal to 65 mmHg. Before and at 12, 18 and 22 hours of peritonitis systemic haemodynamics, total renal (ultrasound Doppler) and cortex microvascular (laser Doppler) blood flow, oxygen transport and renal venous pressure, acid base balance and lactate/pyruvate ratios were measured. Postmortem histological analysis of kidney tissue was performed.

Results

All septic pigs developed hyperdynamic shock with AKI as evidenced by a 30% increase in plasma creatinine levels. Kidney blood flow remained well-preserved and renal vascular resistance did not change either. Renal perfusion pressure significantly decreased in the AKI group as a result of gradually increased renal venous pressure. In parallel with a significant decrease in renal cortex microvascular perfusion, progressive renal venous acidosis and an increase in lactate/pyruvate ratio developed, while renal oxygen consumption remained unchanged. Renal histology revealed only subtle changes without signs of acute tubular necrosis.

Conclusion

The results of this experimental study argue against the concept of renal vasoconstriction and tubular necrosis as physiological and morphological substrates of early septic AKI. Renal venous congestion might be a hidden and clinically unrecognised contributor to the development of kidney dysfunction.

Introduction

Despite the fact that acute kidney injury (AKI) in critically ill patients is predominantly caused by sepsis and septic shock [1], the pathophysiology of septic AKI is still poorly understood [2]. Although renal vasoconstriction and consequent renal ischaemia and acute tubular necrosis (ATN) occupy a central role in AKI development in hypodynamic states, during sepsis the role and character of haemodynamic alterations within the kidney still remain controversial [24].

It must be stressed that the majority of studies reporting a reduction in renal blood flow were derived from fairly heterogenous, short-term and mostly hypodynamic models characterised by a reduced cardiac output, which therefore only have a limited resemblance with human pathophysiology [2, 3]. By contrast, utilising clinically more relevant models of hyperdynamic sepsis in sheep, Langenberg and colleagues have recently challenged the conventional presumption of renal vasoconstriction as a prerequisite for the development of AKI during hyperdynamic bacteraemia in a sheep model [58]. As suggested earlier [9], the authors provided 'proof of concept' that septic AKI may represent a unique form of hyperaemic AKI [2]. However, further research is needed to establish whether this concept is valid in other clinically relevant models of sepsis-induced AKI. [8, 10].

In addition, the vast amount of experimental studies report on haemodynamic changes only, without providing their relationship to microcirculatory, metabolic and histopathological responses. Prompted by these facts, we dynamically assessed the pattern of renal haemodynamics in a long-term porcine model of progressive hyperdynamic sepsis induced by faecal peritonitis. Furthermore, a potential link between renal haemodynamics and renal cortex microcirculatory, metabolic and histological changes was simultaneously analysed.

Materials and methods

Animal handling was in accordance with the European Directive for the Protection of Vertebrate Animals Used for Experimental and Other Scientific Purposes (86/609/EU). The experiments were approved by the Committee for Experiments on Animals of the Charles University Medical School, Plzen, Czech Republic.

Animals and preparations

Fourteen domestic pigs with a median body weight of 32 kg (range: 27 to 35 kg) were investigated. Anaesthesia was induced with intravenous atropine (0.5 mg), propofol 2% (1 to 2 mg/kg) and ketamine (2.0 mg/kg). Animals were mechanically ventilated (fraction of inspired oxygen 0.4; positive end-expiratory pressure 5 to 10 cm H2O; tidal volume 10 ml/kg; respiratory rate was adjusted to maintain arterial partial pressure of carbon dioxide (PCO2) between 4.0 to 5.0 kPa). Surgical anaesthesia was maintained with continuous intravenous thiopental (10 mg/kg/hour) and fentanyl (10 to 15 μg/kg/hour). Thereafter, continuous thiopental (5 mg/kg/hour) and fentanyl infusions (5 μg/kg/hour) were maintained until the end of the experiment (in total 30 hours of anaesthesia: 8 hours surgery and stabilisation period, 22 hours experiment). Muscle paralysis was achieved with pancuronium (4 to 6 mg/hour). Infusion of Plasma Lyte solution (Baxter Healthcare, Deerfield, IL, United States) 15 ml/kg/hour was administered during surgery and than reduced to 7 ml/kg/hour as a maintenance fluid. To maintain arterial blood glucose levels between 4.5 and 7 mmol/l during the whole experiment, 20% glucose was infused.

Central venous and pulmonary artery catheters for monitoring of systemic haemodynamics, blood sampling and drug infusions were placed via jugular veins. One femoral arterial catheter was placed for blood pressure recording and blood sampling, and a fibre-optic one for thermal-dye double-indicator dilution measurements (only in septic animals). After performing midline laparotomy, a precalibrated ultrasound flow probe (Transonic Systems, Ithaca, NY) was placed around the left renal artery. Renal cortex microcirculation was monitored by placing Laser Doppler probe (PF 404, Suturable angled probe, Perimed, Jarfalla, Sweden) directly over the renal cortex. A double-lumen catheter was inserted into the left renal vein for renal venous pressure measurements and blood sampling. Two drains were used for peritonitis induction and ascites drainage. Then, the abdominal wall was closed and epicystostomy under ultrasound control was performed percutaneously for urine collection. The pigs were allowed to stabilise after the surgery for a period of six hours before baseline data collection and measurements were performed.

Haemodynamic measurements and calculations

The measurement of systemic haemodynamics included cardiac output (CO), systemic vascular resistance (SVR), intrathoracic blood volume (ITBV) and filling pressures of both ventricles (central venous pressure (CVP), pulmonary artery occlusion pressure (PAOP)). Arterial, mixed venous and renal blood samples were analysed for pH, partial pressure of oxygen (pO2), pCO2 and for haemoglobin oxygen saturation. Systemic oxygen delivery, systemic oxygen uptake and renal oxygen delivery and oxygen uptake were derived from the appropriate blood gases and flow measurements. Renal vascular resistance (RVR) was calculated according to the formula:

RVR = mean arterial pressure (MAP; mmHg) – renal venous pressure (mmHg)/renal blood flow (l.min-1)

Blood and tissue samples

Arterial and renal venous lactate (L) and pyruvate (P) concentrations were measured. Arterial blood samples were analysed for plasma creatinine, tumour necrosis factor-α (TNF-α; immunoassay) and interleukin-6 (IL-6; immunoassay) levels [11, 12]. Oxidative and nitrosative stress were evaluated by measuring concentrations of arterial thiobarbituric acid reactive species (TBARS; spectrophotometry) and arterial nitrate/nitrite (NOx; colorimetric assay) [11, 12]. To correct for dilutional effects resulting from volume resuscitation, the levels of NOx, TBARS, IL-6 and TNF-α were normalised with plasma protein content [11, 12]. At the end of the experiment, the left kidney was harvested for H&E staining and semiquantitative analysis of the kidney tissue damage was performed in a blinded fashion by a certified nephropathologist.

Protocol

Following a recovery period of six hours, baseline measurements were recorded and pigs were randomised to sham operated (control, n = 6) or to septic group (AKI, n = 8). In the septic group, faecal peritonitis was induced by inoculating 0.5 g/kg of autologous faeces suspended in 200 ml saline through the drains into the abdomen. After 12, 18 and 22 hours after the induction of peritonitis the next set of measurements and data collection were performed. In addition to an infusion of the Plasma Lyte solution, 6% hydroxyethylstarch 130 kD/0.4 (Voluven 6%, Fresenius Kabi Deutschland GmbH, Bad Homburg, Germany) was infused at a rate of 10 ml/kg/hour (7 ml/kg/hour if CVP or PAOP ≥ 18 mmHg) to maintain cardiac filling pressures at 12 mmHg or above. Continuous intravenous noradrenaline was administered if MAP fell below 70 mmHg and titrated to maintain MAP above 65 mmHg. When the last set of data had been obtained, the animals were euthanased by potassium chloride injection under deep anaesthesia and section was performed.

Statistical analysis

All values shown are median and interquartile ranges. After exclusion of normality using Kolmogorov-Smirnov test, differences within each group before and after induction of peritonitis were tested using a Friedman analysis of variance on ranks and, subsequently, a Dunn's test for multiple comparisons with Bonferroni's correction. The Mann-Whitney rank sum test was performed to compare data between treatment groups. A p < 0.05 was regarded as statistically significant.

Results

There were no statistically significant differences in any measured variables between the sham-operated and peritonitis-induced pigs at baseline.

Systemic variables

Haemodynamic and oxygen exchange parameters, inflammatory responses, oxidative and nitrosative stress, and other laboratory parameters are summarised in Table 1. Faecal peritonitis induced a hyperdynamic circulatory state with an increased cardiac output and low SVR. All pigs in the peritonitis group needed noradrenaline (median dose of 1.8 μg/kg/min) to maintain MAP above 65 mmHg. The median time to development of arterial hypotension was 16 hours. Adequate fluid resuscitation was ensured by monitoring cardiac filling pressures that were significantly increased over time in septic animals, while intrathoracic blood volume was well maintained (baseline 23 (22 to 24), 22 hours of sepsis 24 (19 to 34) ml/kg). The increased CO resulted in a significant rise of systemic oxygen delivery, while systemic oxygen consumption remained unchanged. The peritonitis-induced sepsis caused a significant fall of arterial pH and markedly increased plasma levels of TNF-α and IL-6. Overproduction of NOx in this model was documented by a significant increase in arterial NOx levels. These changes were accompanied by a remarkable increase of TBARS levels providing the evidence for oxidative stress.
Table 1

Systemic variables

 

Group

Baseline

12 hours

18 hours

22 hours

MAP

Control

91 (86 to 95)

82.5 (71 to 88)

77 (70 to 81)

77 (64 to 85)

(mmHg)

AKI

94 (89 to 97)

80 (72.5 to 93)

75 (68 to 83)*

72 (66 to 76)*

MPAP

Control

25 (20 to 26)

26 (23 to 27)

25 (24 to 26)

26 (25 to 29)

(mmHg)

AKI

24 (21 to 28)

31 (28 to 37)*§

42 (34 to 46)*§

44 (41 to 47)*§

CO

Control

92 (83 to 110)

98 (88 to 109)

87 (79 to 100)

88 (79 to 102)

(ml/kg)

AKI

79 (64 to 102)

113 (95 to 164)§

140 (116 to 178)*§

174 (120 to 191)*§

SVR

Control

2697 (1508 to 2914)

2007 (1913 to 2093)

1930 (1876 to 1965)

1950 (1670 to 2289)

(dyne.s.cm-5)

AKI

2595 (1972 to 2809)

1523 (968 to 1917)*§

964 (683 to 1263)*§

757 (600 to 852)*§

CVP

Control

8 (8 to 9)

11 (10 to 13)*

13 (12 to 15)*

13 (12 to 15)*

(mmHg)

AKI

10 (9 to 13)

13 (12 to 15)*

16 (14 to 18)*

18 (16 to 19)*§

PAOP

Control

8 (7 to 10)

11 (8 to 12)

12 (10 to 13)

12 (10 to 17)

(mmHg)

AKI

10 (9 to 12)

12 (11 to 15)*

16 (14 to 17)*§

16 (16 to 17)*

DO2

Control

11 (11 to 12)

11 (9 to 12)

10 (9 to 12)

10 (9 to 12)

(ml/min/kg)

AKI

11 (9 to 13)

16 (14 to 27)§

16 (14 to 19)§

19 (11 to 25)

VO2

Control

5 (4 to 6)

6 (5 to 6)

5 (5 to 6)

5 (5 to 5)

(ml/min/kg)

AKI

5 (5 to 6)

6 (5 to 8)

6 (5 to 6)

6 (5 to 8)

pH

Control

7.58 (7.55 to 7.59)

7.56 (7.52 to 7.58)

7.57 (7.54 to 7.60)

7.58 (7.50 to 7.61)

 

AKI

7.54 (7.52 to 7.60)

7.45 (7.43 to 7.49)*§

7.41 (7.20 to 7.47)*§

7.31 (7.08 to 7.36)*§

IL-6

Control

2 (1 to 3)

1 (0 to 1)

1 (0 to 1)

1 (0 to 2)

(pg/ml/g protein)

AKI

4 (1 to 8)

41 (29 to 201)*§

240 (111 to 602)*§

384 (163 to 1405)*§

TNF-α

Control

0 (0 to 0)

1 (1 to 2)

2 (1 to 2)

1 (1 to 2)

(pg/ml/g protein)

AKI

1 (1 to 2)

10 (5 to 16)*§

17 (8 to 28)*§

21 (8 to 33)*§

TBARS

Control

17 (16 to 19)

19 (17 to 28)

22 (19 to 30)

23 (16 to 25)

(nmol/g protein)

AKI

18 (15 to 24)

63 (44 to 93)*§

90 (71 to 117)*§

78 (68 to 108)*§

Plasma nitrate+nitrite levels

Control

1 (1 to 1)

1 (0 to 1)*

1 (0 to 1)*

1 (1 to 1)

(μmol/g protein)

AKI

1 (1 to 1)

1 (1 to 2)*§

2 (1 to 2)*§

1 (1 to 2)*

CO = cardiac output, CVP = central venous pressure, DO2 = oxygen delivery, IL = interleukin, MAP = mean arterial pressure, MPAP = mean pulmonary artery pressure, PAOP = pulmonary artery occlusion pressure, SVR = systemic vascular resistance, TBARS = thiobarbituric acid reactive species, TNF = tumour necrosis factor, VO2 = oxygen uptake.

Control = sham operated group; AKI = peritonitis induced group

* significant difference within each group versus baseline (p < 0.05); §significant difference between groups (p < 0.05). Data are median and 25th and 75th quartiles.

Renal haemodynamics, microcirculation, metabolism, function and histology

The parameters of renal haemodynamics, oxygen exchange, cortex microcirculation, metabolic and acid-base status, as well as kidney function and histomorphology are presented in Table 2 and in Figures 1 to 5. Renal blood flow remained unchanged during hyperdynamic sepsis, with only minor decline at the end of the experiment compared with baseline values. Nevertheless, there were no intergroup differences throughout the whole experiment. RVR did not change either and even decreased at 18 hours of sepsis compared with the control group. Although renal artery pressure was maintained with noradrenaline, renal perfusion pressure significantly decreased in the AKI group as a result of gradually increased renal venous pressure. Despite maintained renal blood flow, renal cortex microcirculation decreased early and this deterioration persisted until the end of the experiment (Figure 1).
Figure 1

Renal cortex microcirculation during the time course of sepsis showing early deterioration of microcirculation perfusion in the peritonitis group (AKI). * significant difference within each group versus baseline (p < 0.05); §significant difference between groups (p < 0.05).

Figure 2

Progressive renal venous acidosis during the time course of sepsis. * significant difference within each group versus baseline (p < 0.05); §significant difference between groups (p < 0.05). AKI = peritonitis induced group.

Figure 3

Gradual worsening of lactate/pyruvate ratio during the time course of sepsis. * significant difference within each group versus baseline (p < 0.05); §significant difference between groups (p < 0.05). AKI = peritonitis induced group.

Figure 4

Representative histological image of a control kidney.

Figure 5

Representative histological image of a septic kidney. Arrows showing epithelial cells vacuolisation with damage of brush border.

Table 2

Renal haemodynamics, oxygen exchange and acid base balance

 

Group

Baseline

12 hours

18 hours

22 hours

Delta creatinine

Control

0 (0 to 0)

-1.5 (-7 to 0)

0.5 (-4 to 11)

2 (-1 to 11)

(μmol/l)

AKI

0 (0 to 0)

8 (-12 to 27)

23 (-3 to 46)

31 (18 to 60)*§

RBF

Control

5 (5 to 9)

4 (4 to 6)

4 (3 to 6)

4 (3 to 6)

(ml/kg)

AKI

6 (4 to 8)

5 (4 to 8)

7 (5 to 7)

4 (3 to 4)*

RVP

Control

9 (8 to 10)

15 (12 to 16)

13 (12 to 14)

12 (11 to 20)

(mmHg)

AKI

13 (11 to 15)

14 (12 to 16)

16 (15 to 19)*§

21 (18 to 25)*

RPP

Control

82 (77 to 89)

68 (59 to 72)

65 (58 to 70)

70 (44 to 75)

(mmHg)

AKI

84 (76 to 87)

71 (59 to 78)*

63 (55 to 65)*

51 (48 to 58)*

Renal DO2

Control

0.63 (0.55 to 0.93)

0.48 (0.42 to 0.68)

0.47 (0.39 to 0.70)

0.40 (0.34 to 0.63)

(ml/min/kg)

AKI

0.81 (0.59 to 0.97)

0.87 (0.46 to 1.16)

0.8 (0.53 to 0.87)

0.50 (0.22 to 0.58)

Renal VO2

Control

0.17 (0.13 to 0.22)

0.14 (0.13 to 0,24)

0.18 (0.13 to 0.21)

0.19 (0.14 to 0.22)

(ml/min/kg)

AKI

0.21 (0.14 to 0.24)

0.17 (0.08 to 0.23)

0.23 (0.21 to 0.23)

0.17 (0.12 to 0.24)

Renal ER

Control

28 (22 to 33)

33 (31 to 39)

33 (31 to 39)

32 (30 to 52)

(%)

AKI

26 (22 to 27)

26 (16 to 32)

25 (21 to 45)

37 (34 to 58)*

Renal venous pH

Control

7.54 (7.53 to 7.55)

7.5 (7.48 to 7.53)

7.53 (7.51 to 7.56)

7.50 (7.47 to 7.57)

 

AKI

7.53 (7.5 to 7.57)

7.42 (7.42 to 7.47)*§

7.4 (7.21 to 7.47)*§

7.31 (7.01 to 7.35) §

UO

Control

4 (3 to 6)

3 (2 to 6)

4 (3 to 6)

4 (3 to 5)

(ml/kg/h)

AKI

2 (2 to 3)§

2 (1 to 4)

2 (1 to 2)§

1 (1 to 2)*§

DO2 = oxygen delivery, ER = extraction ratio, RBF = renal blood flow, RPP = renal perfusion pressure, RVP = renal venous pressure, UO = urine output, VO2 = oxygen uptake.

Control = sham operated group; AKI = peritonitis induced group

* significant difference within each group vs. baseline (p < 0.05); §significant diference between groups (p < 0.05) Data are median and 25th and 75th quartiles.

Microvascular alterations were associated with a marked metabolic stress of the kidney as documented by a significant development of renal venous metabolic acidosis and progressively increased L/P ratio (Figures 2 and 3). The renal oxygen extraction increased at the end of the experiment in septic animals, without changes in renal oxygen consumption. Progressive sepsis caused renal dysfunction as evidenced by significant changes in serum creatinine levels (Table 2). In addition, urine output significantly decreased in the AKI group over time. Only minor histological changes encompassing mild brush-border loss and vacuolisation of tubular cells were present at 22 hours of the experiment on kidney histology. No signs of ATN or tubular cast formation were found. Representative images of control and septic kidney are shown in Figures 4 and 5.

Discussion

In this clinically relevant model of hyperdynamic septic shock AKI developed without apparent renal vasoconstriction, renal oxygen consumption did not change and renal histology revealed only subtle changes despite significant kidney cortex microvascular and metabolic stress. Renal venous congestion might contribute to the pathogenesis of septic AKI.

The renal haemodynamic, microvascular and metabolic responses to and morphological sequelae of sepsis remain inconsistent because of marked heterogeneity attributable to the use of different species, models of sepsis, experimental settings and supportive treatment. Hence, the next fundamental step to understand the pathophysiology of septic AKI is the use of animal models designed to meet the criteria of human sepsis/septic shock [13, 14]. However, the majority of studies have been derived from very heterogenous, short-term and mostly hypodynamic models characterised by a reduced CO. By contrast, the sepsis model used in our study replicates many of the features of adequately resuscitated human septic shock (i.e. hyperdynamic circulation, inflammatory response accompanying with nitrosative, oxidative and metabolic stress). The substantial instrumentalisation used offers a broad insight into organ haemodynamic and metabolic pathways, thereby making it an appealing sepsis model in studies of AKI. Moreover, this is underpinned by the fact that the pig kidney is more similar to the human kidney than that of dog, rat or mice because of similar renal anatomy, architecture and lymphatic pattern, urinary concentrating ability, tolerance to ischaemia and medullary thickness [15, 16].

To our knowledge, our study is the first to tackle the issue of directly measured renal venous pressure allowing both the determination of RVR and true renal perfusion pressure in a large animal sepsis model. In keeping with recent reports [5, 6, 8], our study provides further evidence against the widely held concept that sepsis increases RVR [1]. Importantly, it is apparent from the present study that, at least in this model, renal venous congestion leading to decreased renal perfusion pressure might play an important role in mediating fall in glomerular filtration despite clinically acceptable MAP and CO.

It is amazing that there are no animal studies that provide information on the behaviour of renal venous pressure in their sepsis models. The combined impact of both venous congestion due to elevated right atrial pressure and sepsis-induced capillary leak promoting the development of tissue oedema and abdominal hypertension could explain the elevated renal venous pressure and associated reduction in the filtration gradient. Of note, our data suggests that the assumption that renal perfusion pressure is essentially equal to MAP might not be valid under conditions of severe capillary leak and aggressive fluid resuscitation.

The well-preserved renal blood flow does not guarantee adequate perfusion to microvascular beds. Indeed, peritonitis-induced sepsis caused significant reduction in cortical microvascular perfusion in our model, supporting the emerging evidence that renal microvascular dysfunction may be a culprit of septic AKI [17]. Within the limitations arising from renal cortex laser Doppler flowmetry measurements, we can unambiguously determine neither the most affected part of the nephron nor the fate of intrarenal distribution of blood flow in deeper cortex layers and medulla in our model. Nevertheless, recent long-term rodent models of sepsis-induced acute renal failure demonstrated marked decline in cortical peritubular capillary perfusion [1820] that was associated with tubular redox stress and preceded the development of renal failure [19]. In addition, the distribution of blood flow from the cortex towards medulla has been suggested by several studies [2123], although contradictory results have also been reported [24].

Only a few studies with conflicting data have been performed investigating simultaneous renal haemodynamics and oxygen [23, 2528]. In our study, the apparent kidney metabolic stress as evidenced by gradually worsened renal venous L/P ratio (a marker of redox state) and acid base status occurred despite unchanged renal oxygen consumption. The design of the present study does not allow conclusions to be drawn about what processes are responsible for altered kidney energy metabolism. Nevertheless, taking into account an increased renal oxygen extraction at the end of the experiment, our results could indicate that these metabolic alterations may be attributable to the deterioration in microcirculatory perfusion and related tissue hypoxia. Of note, highly heterogenous renal tissue perfusion and oxygen consumption within the kidney make any extrapolation of the total oxygen uptake measurement potentially erroneous and regions or energy requiring pathways (e.g. tubular sodium reabsorption) suffering from hypoxia might have been overlooked [29]. In support of this notion, in endotoxaemic rats, Johannes and colleagues recently provided the evidence for the presence of microvascular hypoxic areas, even though renal oxygen consumption was not significantly reduced and no hypoxia was detected in the average microcirculatory pO2 measurements [30]. Finally, Porta and colleagues recently showed that kidney mitochondrial function was preserved in a prolonged porcine endotoxaemia with well-maintained renal blood flow [28], making the disturbed cellular energy machinery independent of tissue oxygen availability a less plausible explanation for the renal metabolic stress.

Analogous to the renal hypoperfusion paradigm in septic AKI, ATN is generally regarded as the most frequent mechanism of renal failure in critically ill patients [1]. However, there is no published study in septic patients, that would provide conclusive histopathological evidence for the presence of ATN in sepsis-induced AKI and very few experimental studies simultaneously evaluate physiological features of AKI and underlying histopathological changes allowing data to be put into the relevant complex picture. In our model, only subtle histological changes without any signs of ATN occurred despite marked microvascular and metabolic changes. Admittedly, a longer duration of the experiment could have been required for the development of more severe kidney dysfunction and corresponding histological changes. On the other hand, our results are consistent with a recently published systematic review showing only mild, non-specific changes in the majority of clinical and experimental studies [31].

Our study has several limitations. Despite a gradual severity of the septic process, the pigs developed relatively mild AKI, probably as a result of early and aggressive haemodynamic management. Nevertheless, even small changes in serum creatinine (delta 30 μmol/l in our study) achieved within 22 hours suggest significant renal injury, confirmed by some histological evidence. One could also argue that fluid resuscitation with a large dose of hydroxyethylstarch could contribute to the renal dysfunction in this model. However, the available data still remains inconclusive and the safety profile of a new colloid generation as used in our study (6% hydroxyethylstarch 130/0.4) needs to be further clarified. Due to logistical limitations, other important variables of renal function, such as creatinine clearance or tubular reabsorption functions, were not measured. In addition, we did not directly measure intra-abdominal pressure and the absence of techniques to precisely assessing intraglomerular and peritubular microvasculature and tissue oxygenation/energetics do not allow any robust conclusions to be drawn. Finally, the long-term effects of sepsis over several days might give different results.

Conclusion

Within the boundaries of the limitations, the results of our study support the recent evidence arguing against the concept of renal vasoconstriction and ATN as physiological and morphological substrates of early septic AKI and show that renal venous congestion might be a hidden and clinically unrecognised factor in the development of kidney dysfunction.

Key messages

  • The results of this experimental study argue against the concept of renal vasoconstriction in early sepsis-induced kidney dysfunction.

  • Despite maintained renal perfusion significant renal cortex microvascular and metabolic stress developed very early in the course of AKI.

  • Kidney oxygen extraction capabilities remained well-maintained during progressive hyperdynamic sepsis.

  • Only subtle histological changes without signs of ATN occurred after 22 hours of peritonitis-induced septic shock.

  • Renal venous congestion might be a hidden and clinically unrecognised factor contributing to the development of septic kidney dysfunction.

Authors' information

Work was performed at the animal research laboratory of the 1st Medical Department at Charles University Medical School.

Abbreviations

AKI: 

acute kidney injury

ATN: 

acute tubular necrosis

CO: 

cardiac output

CVP: 

central venous pressure

H&E: 

haematoxylin and eosin

IL: 

interleukin

ITBV: 

intrathoracic blood volume

MAP: 

mean arterial pressure

NOx: 

nitrate/nitrite

PAOP: 

pulmonary artery occlusion pressure

PCO2: 

partial pressure of carbon dioxide

PO2: 

partial pressure of oxygen

RVR: 

renal venous resistance

SVR: 

systemic vascular resistance

TBARS: 

thiobarbituric acid reactive species

TNF-α: 

tumour necrosis factor-α.

Declarations

Acknowledgements

This work was supported by the research project MSM 0021620819 (Replacement of and support to some vital organs). It was presented in part at the 28th International Symposium on Intensive Care and Emergency Medicine, Brussels, 18 to 21 March, 2008.

Authors’ Affiliations

(1)
Intensive care unit,Medical Department, Charles University Medical School and Teaching Hospital Plzen
(2)
Department of Pathology, Charles University Medical School and Teaching Hospital Plzen
(3)
Sektion Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Parkstraße 11, Universitätsklinikum

References

  1. Schrier RW, Wang W: Acute renal failure and sepsis. N Engl J Med 2004, 351: 159-169.View ArticlePubMedGoogle Scholar
  2. Wan L, Bagshaw SM, Langenberg C, Saotome T, May C, Bellomo R: Pathophysiology of septic acute kidney injury: what do we really know? Crit Care Med 2008,36(4 Suppl):198-203.View ArticleGoogle Scholar
  3. Langenberg C, Bellomo R, May CN, Wan L, Moritoki E, Morgera S: Renal blood flow in sepsis. Crit Care 2005, 9: 363-374.View ArticleGoogle Scholar
  4. Molitoris BA: Renal blood flow in sepsis: a complex issue. Crit Care 2005, 9: 327-328.PubMed CentralView ArticlePubMedGoogle Scholar
  5. Langenberg C, Wan L, Egi M, May CN, Bellomo R: Renal blood flow in experimental septic acute renal failure. Kidney Int 2006, 69: 1996-2002.View ArticlePubMedGoogle Scholar
  6. Langenberg C, Bellomo R, May CN, Egi M, Wan L, Morgera S: Renal vascular resistance in sepsis. Nephron Physiol 2006, 104: 1-11.View ArticleGoogle Scholar
  7. Langenberg C, Wan L, Bagshaw SM, Egi M, May CN, Bellomo R: Urinary biochemistry in experimental septic acute renal failure. Nephrol Dial Transplant 2006, 21: 3389-3397.View ArticlePubMedGoogle Scholar
  8. Langenberg C, Wan L, Egi M, May CN, Bellomo R: Renal blood flow and function during recovery from experimental septic acute kidney injury. Intensive Care Med 2007, 33: 1614-1618.View ArticlePubMedGoogle Scholar
  9. Rector F, Goyal S, Rosenberg IK, Lucas CE: Sepsis: a mechanism for vasodilatation in the kidney. Ann Surg 1973, 178: 222-226.PubMed CentralView ArticlePubMedGoogle Scholar
  10. Matejovic M, Radermacher P, Joannidis M: Acute kidney injury in sepsis: is renal blood flow more than just an innocent bystander? Intensive Care Med 2007, 33: 1498-1500.View ArticlePubMedGoogle Scholar
  11. Matejovic M, Krouzecky A, Martinkova V, Rokyta R Jr, Radej J, Kralova H, Treska V, Radermacher P, Novak I: Effects of tempol, a free radical scavenger, on long-term hyperdynamic porcine bacteremia. Crit Care Med 2005, 33: 1057-1063.View ArticlePubMedGoogle Scholar
  12. Matejovic M, Krouzecky A, Martinkova V, Rokyta R Jr, Radej J, Kralova H, Treska V, Radermacher P, Novak I: Effects of combining inducible nitric oxide synthase inhibitor and radical scavenger during porcine bacteremia. Shock 2007, 27: 61-68.View ArticlePubMedGoogle Scholar
  13. Heyman SN, Lieberthal W, Rogiers P, Bonventre JV: Animal models of acute tubular necrosis. Curr Opin Crit Care 2002, 8: 526-534.View ArticlePubMedGoogle Scholar
  14. Bellomo R, Ronco C, Kellum JA, Mehta RL, Palevsky P: Acute Dialysis Quality Initiative workgroup Acute renal failure – definition, outcome measures, animal models, fluid therapy and information technology needs: the Second International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group. Crit Care 2004, 8: 204-212.View ArticleGoogle Scholar
  15. Lieberthal W, Nigam SK: Acute renal failure. II. Experimental models of acute renal failure: imperfect but indispensable. Am J Physiol Renal Physiol 2000, 278: 1-12.Google Scholar
  16. Goldfarb RD, Glock D, Kumar A, McCarthy RJ, Mei J, Guynn T, Matushek M, Trenholme G, Parrillo JE: A porcine model of peritonitis and bacteremia simulates human septic shock. Shock 1996, 6: 442-451.View ArticlePubMedGoogle Scholar
  17. Matejovic M, Radermacher P, Thongboonkerd V: From hemodynamics to proteomics: Unrevealing the komplexity of acute kidney injury in sepsis. In Yearbook of Intensive care and emergency medicine. Edited by: Vincent JL. Berlin Heidelberg: Springer-Verlag; 2008:568-578.View ArticleGoogle Scholar
  18. Tiwari MM, Brock RW, Megyesi JK, Kaushal GP, Mayeux PR: Disruption of peritubular blood flow in lipopolysaccharide-induced renal failure: role f nitric oxide and caspase. Am J Physiol Renal Physiol 2005, 289: 1324-1332.View ArticleGoogle Scholar
  19. Wu L, Tiwari MM, Messer KJ, Holthoff JH, Gokden N, Brock RW, Mayeux PR: Peritubular capillary dysfunction and renal tubular epithelial cell stress following lipopolysaccharide administration in mice. Am J Physiol Renal Physiol 2007, 292: 261-268.View ArticleGoogle Scholar
  20. Wu L, Gokden N, Mayeux PR: Evidence for the role of reactive nitrogen species in polymicrobial sepsis-induced renal peritubular capillary dysfunction and tubular injury. J Am Soc Nephrol 2007, 18: 1807-1815.View ArticlePubMedGoogle Scholar
  21. Miller CG, Thiemermann C: Intrarenal haemodynamics and renal dysfunction in endotoxaemia: effects of nitric oxide synthase inhibition. Br J Pharmacol 1997, 121: 1824-1830.View ArticleGoogle Scholar
  22. Cohen RI, Hassell AM, Marzouk K, Marini C, Liu SF, Scharf SM: Renal effects of nitric oxide in endotoxemia. Am J Respir Crit Care Med 2001, 164: 1890-1895.View ArticlePubMedGoogle Scholar
  23. Gullichsen E, Nelimarkka O, Halkola L, Niinikoski J: Renal oxygenation in endotoxin shock in dogs. Crit Care Med 1989, 17: 547-550.View ArticlePubMedGoogle Scholar
  24. Di Giantomasso D, Morimatsu H, May CN, Bellomo R: Intrarenal blood flow distribution in hyperdynamic septic shock: effect of norepinephrine. Crit Care Med 2003, 31: 2509-2513.View ArticlePubMedGoogle Scholar
  25. Weber A, Schwieger IM, Poinsot O, Klohn M, Gaumann DM, Morel DR: Sequential changes in renal oxygen consumption and sodium transport during hyperdynamic sepsis in sheep. Am J Physiol 1992, 262: 965-971.Google Scholar
  26. Heemskerk AE, Husman E, van Lambalgen AA, Bos GC, Hennekes M, Thijs LG, Tangelder GJ: Renal function and oxygen consumption during bacteraemia and endotoxaemia in rats. Nephrol Dial Transplant 1997, 12: 1586-1594.View ArticlePubMedGoogle Scholar
  27. Johanes T, Mik EG, Nohé B, Raat NJ, Unertl KE, Ince C: Influence of fluid resuscitation on renal microvascular PO2 in a normotensive rat model of endotoxemia. Crit Care 2006, 10: 88.View ArticleGoogle Scholar
  28. Porta F, Takala J, Weikert C, Bracht H, Kolarova A, Lauterburg BH, Borotto E, Jakob SM: Effects of prolonged endotoxemia on liver, skeletal muscle and kidney mitochondrial function. Crit Care 2006, 10: 118.View ArticleGoogle Scholar
  29. O'Connor PM: Renal oxygen delivery: matching delivery to metabolic demand. Clin Exp Pharmacol Physiol 2006, 33: 961-967.View ArticlePubMedGoogle Scholar
  30. Johannes T, Mik EG, Ince C: Nonresuscitated endotoxemia induces microcirculatory hypoxic areas in the renal cortex in the rat. Shock 2009, 31: 97-103.View ArticlePubMedGoogle Scholar
  31. Langenberg C, Bagshaw SM, May CN, Bellomo R: The histopathology of septic acute kidney injury: a systematic review. Crit Care 2008, 12: 38.View ArticleGoogle Scholar

Copyright

© Chvojka et al.; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.