Perconditioning combined with postconditioning on kidney ischemia and reperfusion¹

Abstract

Purpose:

To evaluate if combination of perconditioning and postconditioning provides improved renal protection compared to perconditioning alone in a model of renal reperfusion injury.

Methods:

Thirty rats were assigned into 6 groups: normality; sham; ischemia and reperfusion; postconditioning; perconditioning; perconditioning + postconditioning. Animals were subjected to right nephrectomy and left renal ischemia for 30 minutes. Postconditioning consisted of 3 cycles of 5 min renal perfusion followed by 5 min of renal ischemia after major ischemic period. Perconditioning consisted of 3 cycles of 5 min hindlimb ischemia followed by 5 min of hindlimb perfusion contemporaneously to renal major ischemic period. After 24 hours, kidney was harvested and blood collected to measure urea and creatinine.

Results:

Perconditioning obtained better values for creatinine and urea level than only postconditioning (p<0.01); performing both techniques contemporaneously had no increased results (p>0.05). Regarding tissue structure, perconditioning was the only technique to protect the glomerulus and tubules (p<0.05), while postconditioning protected only the glomerulus (p<0.05). Combination of both techniques shows no effect on glomerulus or tubules (p>0.05).

Conclusions:

Perconditioning had promising results on ischemia and reperfusion induced kidney injury, enhanced kidney function and protected glomerulus and tubules. There was no additive protection when postconditioning and perconditioning were combined.

Key words:
Ischemic Postconditioning; Ischemia; Reperfusion; Rats.

Introduction

After tissue ischemia is resolved and blood flow is restored, the reperfusion injury has been identified as an important mechanism contributing to tissue injury; being even more deleterious than ischemia^1,2. The clinical syndrome of ischemia and reperfusion (IR) is associated with deleterious consequences for several organs. This syndrome contributes to morbidity and mortality in up to 60-70% of all cases of acute kidney injury syndrome which constitutes a serious clinical problem that, despite being common, lacks a truly effective treatment^3,4.

The most critical factor that determines the severity of tissue damage caused by IR appears to be the duration of ischemia^5,6. In addition to early reperfusion, “tissue conditioning” by a series of alternating intervals of brief episodes of ischemia and reperfusion is currently the most promising approach to limit tissue damage caused by prolonged ischemia^7-9.

In a setting of kidney transplantation or contrast induced nephropathy, where the renal intervention or damage is planned, the ischemic preconditioning, that consist of performing short cycles of ischemia and reperfusion before a major period of ischemia, could easily be applied and showed great results and applicability^10,11. However, in kidney transplantation when the organ is from a deceased donor and in a setting of renal artery thrombosis, the preconditioning is not feasible. In such situations, the local ischemic postconditioning (POS) stands pronounced importance. It consists of short cycles of reperfusion and ischemia before the free reperfusion of a tissue that has been under ischemia¹². POS has been demonstrated to be similarly effective as preconditioning^13,14.

Schmidt et al.¹⁵ demonstrated the concept of remote ischemic perconditioning (PER). They applied a tourniquet to a porcine limb to produce alternating periods of occlusion and reperfusion while the myocardium was under ischemia. This technique led to a pronounced protection to the myocardium against the deleterious effects of the ischemia and reperfusion. Since then, this technique has been demonstrated to protect brain, liver, myocardium and kidney from the IR syndrome in various animal models and in clinical settings^16-21.

PER might be even more practical than POS, because it is performed in a distant tissue and is a non-invasive procedure, thus does not require direct access to the artery and could be easily applied during endovascular revascularization^18,22. Mechanisms underlying the remote ischemic conditioning are barely understood. It is known that its protective effects are mediated through potassium channels¹⁵, and through the cellular activation of reperfusion injury salvage kinase pathway and of the survivor activating factor enhancement²³. The connection between the tissue where the intermittent ischemia is performed and the tissue that is under permanent ischemia appears to occur through a neurogenic pathway, mediated by the parasympathetic system²⁴.

PER and POS appear to share similar pathways, such as the activation of the reperfusion injury salvage kinase pathway^21,23. However, previous studies demonstrated that they might also have unique mechanisms. Moreover, their combination might increase the outcome protection against ischemia and reperfusion injury. Thus, we tested the hypothesis that the combination of PER and POS provides improved renal protection compared to PER alone in a well-established rat model of renal reperfusion injury.

Methods

The project was previously approved by the Animal Use and Care Committee, UEPA.

Thirty (8-10 weeks) male Wistar rats (Rattus norvergicus), weighing 250-300 g, were used in this study. The animals were kept in a vivarium of the Experimental Surgery Laboratory, UEPA with a controlled environment; water and the food were provided ad libitum. The research followed the rules of Brazilian Law for Animal Care (Law: 11.794/08) that is based on NIH guidelines, and followed the rules of Council for International Organization of Medical Sciences ethical code for animal experimentation.

The experimental protocol is illustrated in Figure 1. The animals were randomly assigned into the following 6 groups (N=5 for each group):

Figure 1
The experimental protocol of each group.

• (1) In the Normality group (N) no intervention was performed. This group served to establish physiologic values for the outcome parameters for the rat strain/colony used in our study;

• (2) In the sham Group (SHAM) the same surgical procedure as in the remaining groups was performed but no renal ischemia was induced;

• (3) In the ischemia and reperfusion group (IR) renal ischemia was induced for 30 min followed by reperfusion without any form of conditioning;

• (4) In the local ischemic postconditioning group (POS) 30 min of renal ischemia was followed by 30 min of autologous postconditioning (3 cycles of 5 min renal perfusion followed by 5 min of renal ischemia);

• (5) In the remote ischemic perconditioning group (PER) renal ischemia was simultaneously accompanied by remote ischemic conditioning. Remote ischemic conditioning consisted of 3 cycles of 5 min hindlimb ischemia followed by 5 min of hindlimb perfusion²²;

• (6) In the ischemic remote ischemic perconditioning group + local postconditioning group (PER+POS) renal ischemia was simultaneously accompanied by remote ischemic conditioning in the left hindlimb followed by autologous ischemic post-conditioning (3 cycles of 5 min renal perfusion followed by 5 min of renal ischemia).

Surgical procedures

Renal ischemia and remote and/or autologous per- and/or post-conditioning was performed in anesthesia (ketamine and xylazine 70 mg/kg and 10 mg/kg, respectively, IP). Briefly, a right nephrectomy was performed and the left renal artery was exposed through a midline laparotomy. Renal ischemia was induced by applying a microsurgical clip on the renal artery. Hindlimb ischemia was achieved using an elastic rubber band tied around the thigh of the left leg, through a non-invasive method that was successfully used in previous studies^18,22.

Following the renal ischemia/conditioning protocols, rats were allowed to recover from anesthesia for 24 hours. Then rats were anesthetized and a 3 ml blood sample was obtained via puncture of the abdominal vena cava and the left kidney was harvested for histological analysis. Subsequently, the animals were euthanized by lethal anesthetic doses.

Parameters evaluation

Blood samples were immediately sent to laboratory analysis. Urea and creatinine levels were measured on Selectra-E auto analyzer. The left kidney was cut longitudinally in two halves, fixed in 10% formaldehyde, embedded in paraffin, and stained using hematoxyline/eosine. Multiple sections were analyzed with regard to the glomerulus and tubules injury.

Total number of glomeruli per field as well as damaged glomeruli has been accounted for. Glomeruli were considered normal whenever capillary loops were open, with thin walls and whenever there was no content inside the Bowman’s capsule. On the other hand, glomeruli were considered as damaged whenever they presented a contraction of glomerular tuft with approximation of structures, contents inside the Bowman’s capsule or vacuolization of endothelial cells. The degree of glomerular lesion has been characterized as: 0- No damage; 1-light (up to 25% of damaged glomeruli); 2-moderate (26% to 50% of damaged glomeruli); 3-sharp (51% to 75% of damaged glomeruli); severe (above 75% of damaged glomeruli)²⁵.

Tubules were considered damaged when there was either severe tubular lysis, loss of brush border, and sloughed debris in tubular lumen space. Tubular damage was graded at: 0: no damage; 1: 0-25% damaged tubules; 2: 25-50% damaged tubules; 3: 50-75% damaged tubules; 4: >75% damaged tubules²⁵.

Statistics

Analysis of variance (ANOVA), followed by Tukey post-hoc tests correction, was performed to analyze urea and creatinine. Kruskal-Wallis, followed by Student-Newman-Keuls correction, was used to analyze the histological parameters. Statistical significance was assumed at p<0.05.

Results

During the procedure, no animal died or were performed resuscitation maneuvers. Table 1 shows the mean of urea and creatinine serum levels. From the urea serum level, IR showed the highest level when compared to all groups. PER and PER+POS obtained better results than IR and POS groups (p<0.05), and not show difference in comparison to SHAM. POS obtained better results than IR (p<0.05). PER and PER + POS groups obtained similar values (p=0.49).

Table 1
Mean urea and creatinine serum level of each group.

Group		Urea	Creatinine
Normality		72.16 ±7.13	0.30 ±0.30
Sham		86.18 ±11.95	1.14 ±0.34
Ischemia-Reperfusion		216.30 ±7.17	2.06 ±0.34
Postconditioning		137.84 ±6.81	1.38 ±0.21
Perconditioning		83.74 ±14.58	0.72 ±0.11
Per+Postconditioning		100.24 ±12.40	0.71 ±0.10

• p<0.01 Ischemia-Reperfusion vs. all groups
• p>0.05 Perconditioning vs. Per+Postconditioning

The IR group had the highest creatinine levels compared to all other groups (p<0.001); POS group obtained worse results than the PER and PER + POS group (p<0.01); PER and PER + POS groups obtained similar values (p=0.88).

Table 2 shows the results of the histopathological analysis (Figure 2). PER showed better glomerulus and tubules structure than the IR group (p<0.01). POS showed only better glomerulus structure than the IR group (p<0.01). PER+POS had no statistical difference when compared to the IR group in both glomerulus (p=0.09) and tubules (p=0.11) grading.

Table 2
Average histopathological scores.

Group	Glomerular lesion	Tubular damage
Normality	0.00 ±0.00	0.00 ±0.00
Sham	0.40 ±0.54	0.40 ±0.89
Ischemia-Reperfusion	3.80 ±0.44	3.60 ±0.54
Postconditioning	2.00 ±0.70	2.80 ±0.83
Perconditioning	1.80 ±0.44	1.60 ±0.89
Per+Postconditioning	2.40 ±0.89	2.80 ±0.83

• p<0.01 Ischemia-Reperfusion and Sham vs all groups
• p>0.05 Perconditioning vs Per+Postconditioning

Discussion

Perconditioning is the newest technique described to mitigate IR injury in many tissues^15,18,20. Our study is the first evaluate of the potential protective effect of PER alone or combined with POS on kidney IR-induced injury, that only be test before in myocardium^15,20, brain^17,26, and liver¹⁸.

Creatinine is a good measurement of kidney filtration being a parameter for glomerular function²⁷. All tissue conditioning techniques were able to protect glomerular function. PER and PER+POS showed similar values. POS shows an urea serum level worse than PER. Since urea excretion occurs through glomerular filtration (40%) and tubular secretion on Henle Loop (60%)²⁸, then we hypothesize that PER is giving protection to both glomerulus and tubules, but POS is only protecting glomerular function. The histological analysis shows results similar to those identified in the analysis of serum urea and creatinine and confirming the initial conclusions, similar data was find by Chen et al.²⁹.

The vascular anatomy of kidney is unique^22,30 where glomerulus receive blood supply prior to medullar area (tubulus), being very different from the heart or liver vascular anatomy; myocites have also different cell biology. Our findings that PER might confer protection to the glomerulus and tubules and POS only to the glomerulus, support that tissue conditioning techniques might work in a tissue dependent manner.

We could clearly detect that there was no additional effects when both techniques were held together. The association had slightly worse outcome that could be of statistical significance in a larger series. We suggest that the complementary postconditioning cycles might lead to additional tissue damage, in opposition to the expected additional protection, or at least act in the same pathway, saturating it¹⁸. So, we can also conclude that PER is the best tissue conditioning for kidney ischemia and reperfusion syndrome.

Mechanisms underlying PER and POS protective effects are barely understood, they probably act in different pathway depending on the target organ. In brain²⁷ and myocardium³¹, the combined of per and postconditioning showing a positive synergism; however, in liver¹⁸ there no additional effect, similar to the find of this study.

The finds of this study show that for kidney IR syndrome the perconditioning have a better protecting effect than postconditioning alone or combined. Based on fact that perconditioning is performed in a distant tissue, is a non-invasive procedure and do not increase the surgical time, thus does not require direct access to the artery and could be easily applied during the surgery or endovascular surgery^15-19; this ischemic conditioning must be test in human IR syndromes^20,31. However, new studies aim to understanding the mechanism are need³².

We tested three cycles of 5 min of reperfusion followed by 5 min ischemia, interval referred to previous literature^18,22,32. Whether, the ischemic per and postconditioning plays its role in an ‘on-off’ style or a ‘dose-dependent’ one^22,32,33 was not fully elucidated in this study. Five min may not afford maximal protective effect against renal IR injury if ischemic conditioning was a ‘dose-dependent’ one; and that can influence direct on the result of the combined effect, mainly if one conditioning is minimized. Thus, the exact number of optimal interval and cycles need to be investigated; and with this interval, new studies combining both techniques could be performed.

Conclusions

Perconditioning had promising results on ischemia and reperfusion induced kidney injury, enhanced kidney function and protected glomerulus and tubules. There was no additive protection when postconditioning and perconditioning were combined.

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• Financial source:

  none

• 1
  Research performed at Laboratório de Cirurgia Experimental, Universidade do Estado do Pará (UEPA), Belem-PA, Brazil.

Publication Dates

• Publication in this collection
  Aug 2017

History

• Received
  13 Apr 2017
• Reviewed
  14 June 2017
• Accepted
  17 July 2017