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Severe burn and disuse in the rat independently adversely impact body composition and adipokines

Critical Care volume 17, Article number: R225 (2013) Cite this article

Abstract

Introduction

Severe trauma is accompanied by a period of hypermetabolism and disuse. In this study, a rat model was used to determine the effects of burn and disuse independently and in combination on body composition, food intake and adipokines.

Methods

Male rats were assigned to four groups 1) sham ambulatory (SA), 2) sham hindlimb unloaded (SH), 3) 40% total body surface area full thickness scald burn ambulatory (BA) and 4) burn and hindlimb unloaded (BH). Animals designated to the SH and BH groups were placed in a tail traction system and their hindlimbs unloaded. Animals were followed for 14 days. Plasma, urine, fecal and tissue samples were analyzed.

Results

SA had a progressive increase in body mass (BM), SH and BA no change and BH a reduction. Compared to SA, BM was reduced by 10% in both SH and BA and by 17% when combined in BH. Compared to SA, all groups had reductions in lean and fat body mass with BH being greater. The decrease in lean mass was associated with the rate of urinary corticosterone excretion. The loss in fat mass was associated with decreases in plasma leptin and adiponectin and an increase in ghrelin. Following the acute response to injury, BH had a greater food intake per 100 g BM. Food intake was associated with the levels of leptin, adiponectin and ghrelin.

Conclusions

The effects of the combination of burn and disuse in this animal model were additive, therefore in assessing metabolic changes with severe trauma both injury and disuse should be considered. Furthermore, the observed changes in adipokines, corticosterone and ghrelin provide insights for interventions to attenuate the hypermetabolic state following injury, possibly reducing catabolism and muscle loss and subsequent adverse effects on recovery and function.

Introduction

A major factor that impacts the treatment and recovery of patients with severe traumatic injuries is a pronounced increase in metabolism. Injury induces a systemic catabolic response characterized by increased energy expenditure and massive loss of body mass (BM). This substantial loss is due to reductions in both lean (LBM) and fat mass (FM) [1–7]. The loss of LBM subsequently compromises the patient’s ability to resume normal activities and has been attributed, in part, to prolonged inactivity associated with bed rest, as well as a response to injury [8]. Burns are suggested to induce the greatest increase in metabolic demand as a result of loss of the insulation properties of skin and the increased demands of wound healing. Hypermetabolism is evident immediately after injury, and peaks days after injury when oxygen and nutrient delivery to tissue increases, allowing for a further increase in metabolic activity [1]. The burn-induced imbalance of protein synthesis and breakdown is sustained from the time of hospital admission to discharge, when wounds are 95% or more healed. In some cases, catabolism persists for up to one year after discharge, resulting in substantial muscle wasting and atrophy during convalescence [2, 3, 6, 9]. Patients with severe burns usually require long-term bed rest during hospitalization, and have limited mobility once leaving the hospital. Inactivity, coupled with increased metabolic demands, clearly contributes to a multitude of issues limiting and/or prolonging recovery from injury [10, 11].

We, along with others, have recently reported alterations in plasma adipokines (leptin, adiponection and resistin) concentrations in burns and severe illness. Adipokines are derived from fat and have been associated with the inflammatory response to injury, insulin resistance, and the severity of illness. Adipokines have been extensively studied in metabolic diseases that have led to interest in their role in metabolic disorders observed with severe injury [12–16].

It has been observed that rats with full thickness burn ≥30% total body surface area (TBSA) have an acute hypermetabolic response similar to that reported in humans [7, 17, 18], persisting for over 14 days post injury [17–19]. The increase in metabolism was associated with a reduction in body protein and fat content when animals were held on a restricted diet [20, 21]. When they were provided access to food ad libitum, their intake was increased [22, 23]. This increased intake may alter the responses reported in body composition, and attenuate shifts in metabolic substrates. Furthermore, the question must be raised as to the possible role of disuse in these changes.

Hindlimb unloading (HLU) in rats has been commonly used to study the effect of inactivity on muscle metabolism and physiological changes of muscle due to disuse and the microgravity environment of space flight [24–27]. Importantly, HLU mimics the physiologic change of long term bed rest [24]. In addition, immunological alterations with inactivity may contribute to delayed wound healing, as well as potentiating the catabolic state [28, 29]. Because of this, it is thought that HLU, in addition to burns, will more closely resemble the clinical condition in patients with severe burns.

To determine whether disuse is an additional or associate factor contributing to burn-induced hypermetabolism, and the loss of lean and fat body mass, we employed a rat model combining hindlimb unloading and severe burn.

Material and methods

Animals

All procedures were reviewed and approved by the US Army Institute for Surgical Research and University of Texas Health Science Center San Antonio Institutional Animal Care and Use Committees. Data from these experiments in regards to muscle function and bone health have been previously published [30, 31].

Male Sprague-Dawley rats (250 to 275 g on arrival) were used for this study (Charles Rivers, Wilmington, MA, USA). Animals weighed approximately 300 g at the start of the experiment. All animals were given food and water ad lib. Light cycle 12:12 hr (0600, on:1800, off).

Housing

Upon arrival, animals were housed in standard vivarium cages and then housed in specialized metabolic/unloading HLU cages (144 in2 usable floor area) one week before injury to allow for acclimation [32]. Animals were fed a certified diet (Harlan Teklad #2018), in powder-form, while housed in the HLU cages. Room temperature was maintained at 26 ± 2°C with 30 to 80% relative humidity to simulate, as closely as possible, the ambient temperature maintained in a standard burn unit.

Experimental group assignments

Following 24 hours of data collection (Day 0), rats were randomly assigned to one of four experimental groups: Sham Ambulatory (SA; n = 10); Burn Ambulatory (BA; n = 9); Sham Hindlimb Unloading (SH; n = 10); Burn Hindlimb Unloading (BH; n = 10). A block design was used for this study where four animals were weight-matched to each other and then each animal was randomly assigned to one of the four treatment groups. This assignment was carried out prior to any experimental manipulations. Following the experimental treatments, animals were followed for 14 days.

Animal husbandry measurements

Body masses of all animals were measured daily from the time of arrival until the end of the study. Animals assigned to SH and BH treatment groups were weighed using a hook attached to a ring-stand placed on the balance to avoid any type of weight-bearing on the hindlimbs during the weighing procedure [24]. Food and water intake were measured daily in all groups.

Urine collection

Housing in the metabolic cages allowed for the collection of uncontaminated urine samples. Beginning one day before injury, 24-hour urine volumes were measured. Urine was aliquoted and samples were stored at -80°C for future analysis.

Scald injury

Rats randomly assigned to either burn treatment group (that is, BA or BH) received a 40% total body surface area, full-thickness scald burn as described by Walker-Mason [33]. Rats were anesthetized with isoflurane (2 to 3% in 100% O2) throughout the procedure and administered buprenorphine (0.05 mg/kg s.c) prior to injury. Each rat was shaved and secured in a plexiglass mold exposing 20% of the total body surface area of the dorsal side. The dorsal surface was submerged in 100°C water for 10 seconds. The animal was removed from the mold, administered 20 cc of Lactated Ringer’s intraperitoneally, which was based on the modified Brooke Formula for resuscitation fluids in burn patients [34], placed back in the mold exposing the ventral (belly) surface and submerged in 100°C water for two seconds. Sham groups (SA and SH) were exposed to the anesthesia procedure, shaved and submerged in water at room temperature. All animals were administered additional analgesics (buprenorphine; 0.05 mg/kg s.c) 6 to 8 hours following the scald procedure and every 24 hours thereafter for 72 hours.

Hindlimb unloading

Following the scald procedure described above, animals randomly assigned to the HLU group were placed in a tail traction system using an established HLU model [24]. Briefly, the tail was prepared for HLU by cleaning with alcohol wipes, tincture of benzoin was then applied, allowing it to become tacky to the touch. A half-inch strip of Skin Trac© (Zimmer, San Jose, CA, USA) was secured on the tail, it was then wrapped in Stockinette, and three one-inch strips of filament fiber tape were applied (base, middle, top). Animals were allowed to completely recover from anesthesia, approximately 20 to 30 minutes, before being placed in HLU cages and their hindlimbs were unloaded at approximately 30° using a hook and pulley system. The pulley system allowed the animals to have 360° access within the cage environment without applying load to their hindlimbs. Animals were observed immediately after unloading for any apparent signs of distress and were monitored several times during the day throughout the study following the burn/HLU procedure.

Tissue collection and body composition

At the conclusion of the study on Day 14, animals were deeply anesthetized with isoflurane (1 to 3% in 100% O2) and blood was collected via cardiac puncture. Animals were euthanized by exsanguination and predetermined tissues were harvested, weighed and minimal tissue samples obtained. Tissues measured were visceral fat (epididymal), liver and hindlimb muscles (tibialis anterior, extensor digitorum longus, plantaris, soleus, medial gastrocnemius, lateral gastrocnemius). Data as to individual hindlimb muscle masses have been previously presented [31]. Excess tissues were returned to the carcass prior to dual-energy X-ray absorptiometry (DEXA) measurements. DEXA scans were taken using Encore 2005 software (GE Lunar Prodigy, Madison, WI, USA) of all carcasses at the conclusion of the tissue collection to assess total body fat and lean body mass.

Plasma assay

Plasma collected from whole blood samples were stored at -80°C for later analysis. Commercial plasma enzyme-linked-immunosorbent assays (ELISA; Linco Research, St. Charles, MO, USA; Neogen Corp, Lexington, KY, USA) were used to measure leptin (L), ghrelin (G), adiponectin (A), and resistin (R). Additional plasma samples were analyzed for blood urea nitrogen (BUN) and total protein (TP).

Urine assay

Urine was collected daily, aliquoted and stored at -80°C for later analysis. Using commercial urinary ELISAs (Neogen Corp), daily urine samples were analyzed for corticosterone (CORT) and testosterone.

Nitrogen balance

For nitrogen balance calculations, urinary urea nitrogen (UUN) was analyzed using a Dade Dimension Chemistry Analyzer® (Deerfield, IL, USA). Urinary nitrogen (N) was calculated for rats using duplicate determinations of UUN; urinary N (mg/mL) = (UUN (mg/mL) × 1.067) -0.302. Nitrogen intake was calculated as food intake x dietary protein content divided by 6.25. Fecal nitrogen was assumed to be a constant value of 60 mg/day. Nitrogen balance was calculated as the difference between N intake and N excretion (urinary + fecal) [35, 36].

Statistics

Two distinct patterns of metabolic change over the course of time have been identified in patients with burns and in animal models of injury [37, 38]. Therefore, in the analysis of data over time, two periods were considered, the initial response to injury, the “ebb phase” lasting over three days and the compensatory “flow phase” after the initial response, days 3 to 14. Discontinuous data were compared using a Chi-square test. Continuous data were compared between groups using ANOVA and, where appropriate, adjusted for repeated measurements over time. A Tukey’s test was used for post-hoc analyses. Values in the text are reported as mean ± SEM and differences determined at P <0.05.

Results

Body mass

There were no differences in initial body mass between the treatment groups; however, differences were apparent by Day 14 (Figure 1; Table 1). BA and SH showed similar reductions in body mass and BH had the most dramatic decrease over time, accentuated by an additive effect from the combination of burn and disuse. The percent changes in body mass over the 14 days were +10%, -2%, - 3% and -10% for SA, BA, SH and BH, respectively.

Figure 1
figure 1

Mean body mass over time. No differences were observed between groups on Day 0. Significant differences were observed between treatment groups after Day 3 through Day 14; SA >BA = SH >BH, P <0.01 treatment effect. Sham-ambulatory (SA; closed circles); Burn-ambulatory (BA; open circles); Sham-hindlimb (SH; closed triangles); Burn-hindlimb (BH; open triangles).

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Table 1 Physiological measurements
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Food consumption

Over the course of the 14 days, there was no difference in total food consumption. However, there were significant differences in the food intake patterns, characteristic of the ebb and flow phases following injury. There was a significant reduction in absolute food consumption, even when corrected by body mass, on Day 1 in all treatment groups as compared to SA. After Day 1, food consumption slowly increased over time in all groups. When food consumption was corrected for body mass, a significant difference was observed between SA and the other treatment groups from Day 1 and Day 3. By Day 7 after injury, BH corrected food consumption was greater than the other treatment groups and from Day 9 on was significantly greater (P <0.001) than all treatment groups (Figure 2). Groups BA, SH and BH cumulative food intake corrected for body mass between days 3 to 14 was significantly changed from SA by 9.4%, 1.7% and 12.3%, respectively There were no differences observed between BA and SH.

Figure 2
figure 2

Mean food consumption per 100 g of daily body mass over 14 days. Independent analyzes were conducted during the “ebb phase” days 0 to 3, and the “flow phase” days 3 to 14. Significant differences were observed between SA and other treatment groups between Day 1 and Day 3 (SA >SH >BA = BH, P <0.01), and then from Day 9 until the end of the study (SA >SH = BA >BH, P <0.01). No differences were observed between BA and SH. Sham-ambulatory (SA; closed circles); Burn-ambulatory (BA; open circles); Sham-hindlimb (SH; closed triangles); Burn-hindlimb (BH; open triangles). * indicates significant differences between groups, P <0.05.

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Lean body mass, fat mass, visceral fat mass, liver mass and total muscle mass

Using DEXA, there were significant differences in LBM measured between BH and all other treatment groups (Table 1). However, when LBM was corrected for body mass obtained on Day 14, there were no differences observed in percent LBM. There was a significant decrease in fat mass and percent fat mass in all treatment groups from SA (P <0.001), with the most dramatic reduction, 48%, being in BH group (Table 1). BH was significantly different from SH, but there were no differences observed between either of the HLU groups from BA, indicating that the burn injury may cause a physiological change that overwhelms the effect of the disuse.

There were significant reductions in visceral fat mass and visceral fat mass per 100 g BM in all groups as compared to SA. In addition, BA and SH were significantly different from BH, indicating that the loss in fat is independent in each manipulation, and additive when in combination (Table 1).

Liver mass was significantly reduced in all groups compared to SA. SH was significantly lower than BA, but BH was not different from BA or SH. When corrected for body mass, there were no differences between either of the burn groups, suggesting that in terms of liver mass, disuse alone has more of an overall effect than burn (Table 1).

Total hindlimb muscle mass, (the sum of mass of tibialis anterior, extensor digitorum longus, plantaris, soleus, medial gastrocnemius, lateral gastrocnemius), was significantly reduced in BH compared to all other groups. In addition, BA and SH were different from SA, but, were not different from each other, suggesting an additive effect on muscle mass.

Urinary corticosterone and nitrogen balance over 14 days

Urinary CORT and testosterone concentrations were measured daily throughout the study. No differences in urinary CORT excretion rates were observed between any of the groups before the initiation of injury and HLU. A significant increase in CORT was observed between all groups from SA the day immediately following injury (P <0.001), with the most dramatic increase in BH. A steady decline was observed after Day 3; however, BH continued to be significantly higher than all other treatment groups. By Day 14, all groups remained significantly higher than SA (P <0.001); however, BA and SH showed similar responses by the end of the study (Figure 3). When average daily urinary CORT excretion was calculated, there were significant differences between BH and all treatment groups (P <0.001) (Table 2). There were no differences between BA and SH, indicating that in terms of total urinary CORT, the additive response had much more of an overall effect than each treatment alone. Average urinary testosterone was not different between groups (Table 2).

Figure 3
figure 3

Mean urinary corticosterone (CORT) over 14 days. A significant increase in CORT was observed initially after treatment (BH >BA = SH >SA, P <0.001), but steadily declined by Day 14. Significant differences (P <0.001) were still apparent between BH and other treatment groups through Day 14. Sham-ambulatory (SA; closed circles); Burn-ambulatory (BA; open circles); Sham-hindlimb (SH; closed triangles); Burn-hindlimb (BH; open triangles). * indicates significant differences between groups, P <0.05.

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Table 2 Protein metabolism
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Daily nitrogen balance was calculated for the duration of the study. No differences were observed between groups prior to injury. A significant reduction in nitrogen balance was observed within all groups the day following treatment, with both burn-treated groups showing the most dramatic response (P <0.001). Average daily nitrogen balance was different between groups (SA = 540.4 ± 9.2; BA = 515.0 ± 13.4; SH = 474.6 ± 7.5; BH = 478.4 ± 16.4 mg/day (P <0.001). There was a steady increase over the following seven days in all treatment groups. The increase in SH was not as great as the other treatment groups and was significantly lower than the other groups until the conclusion of the study (P <0.001) (Figure 4). The mean daily nitrogen balance was associated with the increases in average urinary CORT excretion over the same time (Figure 5a). A lower lean body mass on Day 14 was associated with a reduced daily nitrogen balance (Figure 5b). BUN concentrations were increased in all burn groups, while plasma total protein levels were not significantly altered (Table 2).

Figure 4
figure 4

Mean urinary nitrogen balance over 14 days. The three treatment groups went into negative nitrogen balance after initial treatment (SA >SH = BA = BH, P <0.001), but a steady increase was observed over time. Significant differences were observed until Day 8 and then on the final day after treatment (SA >SH, P <0.001). Sham-ambulatory (SA; closed circles); Burn-ambulatory (BA; open circles); Sham-hindlimb (SH; closed triangles); Burn-hindlimb (BH; open triangles). * indicates significant differences between groups, P <0.05.

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Figure 5
figure 5

Mean daily urinary nitrogen balance vs mean corticosterone and lean body mass. (a) Mean daily urinary nitrogen balance from control vs mean daily urinary corticosterone. A correlation was observed between control vs daily urinary corticosterone (r = 0.47; P <0.003; n = 39). (b) Mean lean body mass (LBM) vs urinary nitrogen balance. A positive correlation was observed (r = 0.61; P <0.001; n = 39). Sham-ambulatory (SA; closed triangles); Burn-ambulatory (BA; closed circles); Sham-hindlimb (SH; open triangles); Burn-hindlimb (BH;, open circles).

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Adipokines and ghrelin

To determine the effects of injury and disuse on fat metabolism, the primary adipokines, namely leptin, resistin and adiponectin, were analyzed, as well as the gut derived hormone ghrelin. Leptin, which plays a role in the regulation of energy intake and energy expenditure, had a profound effect due to injury and disuse after 14 days (Table 3). A significant decrease in plasma leptin was observed in all groups from SA (Table 3). A significant positive correlation was observed between plasma leptin and total body fat mass (r = 0.74, P <0.00001, n = 35) (Figure 6a).

Table 3 Fat metabolism
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Figure 6
figure 6

Association of plasma leptin (a), adiponectin (b) and ghrelin (c) concentrations with body fat mass on Day 14. (a) A positive correlation was observed between plasma leptin and total fat mass (r = 0.74; P <0.00001; n = 35). (b) A positive correlation was observed between plasma adiponectin and total fat mass (r = 0.61; P <0.0002; n = 36), (c) A negative correlation was observed between plasma ghrelin and total fat mass (r = -0.57; P <0.0002; n = 37). Sham-ambulatory (SA; closed triangles); Burn-ambulatory (BA; closed circles); Sham-hindlimb (SH; open triangles); Burn-hindlimb (BH; open circles).

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Adiponectin, a protein hormone, modulates glucose regulation and fatty acid catabolism. Significant differences were observed between the burn treatment groups from SA (Table 3). The disuse group was not different from SA, indicating that the burn injury component has significant effects on adiponectin, rather than the disuse component. Like leptin, there was a significant positive correlation between adiponectin and total body fat mass (r = 0.61, P <0.0002, n = 35) (Figure 6b).

Plasma resistin was increased only in the SH group compared to the burn groups (Table 3).

Ghrelin, considered the counterpart of leptin, stimulates appetite rather than causing an increase in metabolism. A significant increase in plasma ghrelin was observed in the BH group compared to the other groups (Table 3). No significant differences were observed between SA, BA or SH. A negative relationship was observed between plasma ghrelin and total body fat mass (r = -0.57, P <0.0002, n = 35) (Figure 6c).

Food intake adjusted for body mass on Day 14 was associated with changes in leptin, adiponectin and ghrelin. Lower levels of leptin (r = -0.47; P <0.004; n = 37) and adiponectin (r = -0.49; P <0.002; n = 37) were moderately associated with increased food intake. In contrast, food intake was related to increased concentrations of ghrelin (r = 0.46; P <0.001; n = 36).

Discussion

Hypermetabolism and catabolism are an on-going concern in the care of patients with severe injuries that necessitate bed rest [1, 4, 7, 37, 39–42]. Several factors associated with injury are a result of the hypermetabolic response. In the present study of burn and disuse, there was a reduction in body mass with an increase in food consumption three days after injury, obvious indices of a hypermetabolic state associated with the flow phase. We employed an animal model incorporating severe burn and disuse independently and in combination. In the majority of metabolic parameters measured, the effects were additive, suggesting independent contributions of burn and disuse to the shifts observed in patients (Table 4). Burn and disuse independently decreased body mass on Day 14 by 10.7% and 10.2%, respectively, but resulted in a 17.3% decrease when in combination (Table 4). Similar observations were made for lean and fat mass; however, the proportional decrease in fat mass was greater, representing a larger contribution to the reduction in body mass. This disproportionally greater decrease in fat mass is similar to that observed in severely burned patients. Additionally of interest, was the additive effect noted in corticosterone. Previous studies have shown that the response to additive stresses does not result in higher levels, but persistently elevated levels, which is in contrast to the additive effect observed in the present study. Historically, studies of burn in rat models do not usually account for the effects of disuse. Shangraw and Turinsky conducted studies of combine burn and disuse in rats by casting the hind legs, but noted no effect of disuse [43, 44]. Wolfe and colleagues have conducted extensive metabolic studies in humans during bed rest and inferred effects of the patient with traumatic injuries [42]. Our study is the first to demonstrate the effects in combination and shows the lack of interaction between the two treatments and that in many cases their effects are additive. Thus, as proposed by Wolfe et al., injury and disuse need to be considered independently in the evaluation of interventions for the treatment of the critically injured patient [42, 45].

Table 4 Percent change from control (SA)
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The loss of lean body mass was associated with a net negative nitrogen balance, increased BUN and decreases in hindlimb muscle mass, which are greatest in the combination of burn and disuse. A catabolic state was persistent in animals with BH with both injury and disuse contributing. Shangraw and Turinsky evaluated protein turnover in the soleus muscles of burned (6 to 7% TBSA) rats whose hindlimbs were casted [43, 44]. In contrast to the present study, they found disuse to be only a minor contributor. However, they reported no change to disuse alone, while we and others have demonstrated extensive reductions in our HLU model, as well as bed rest in humans [24, 46, 47]. The overall catabolism, associated with a reduction in lean mass that we observed is similar to that in a patient in negative nitrogen balance, with decreased immunologic function and all of the wound-healing problems associated with protein loss and malnutrition. In the present study, the decrease in lean mass was related to corticosterone in the absence of a change in testosterone. Ferrando and colleagues found that bed rest sensitized skeletal muscles to the catabolic effects of cortisol [40, 48]. However, in the present study of injury and/or disuse, the effect of increased corticosterone levels was linear with an additive effect of the two manipulations noted indicative of no change in sensitivity.

Decreases in body and visceral fat masses were associated with significant decreases in plasma leptin and adiponectin concentrations. Both leptin and adiponectin have recently been shown to be reduced in critically ill patients and associated with stress related parameters [15, 49, 50]. We have recently seen similar changes in adipokines in patients with severe burns [16]. These adipokines have been suggested to play important roles in tissue inflammation; however, a role in critically ill patients has yet to be elucidated [51–53]. In the present study, reduced adipokine levels were observed in the presence of injury rather than disuse, suggesting a greater influence of the injury component. Administration of leptin in burned rats has been shown to increase angiogenesis in injured tissues and decrease multiple organ damage [54, 55]. Resistin was not altered in the present studies, but has been reported to be decreased in children with burns [56]. In contrast, an increase in resistin is noted in patients in the intensive care unit who are septic [13]. Recently, days after burn injury resistin levels have been reported to be increased and associated with plasma cortisol concentration and with the level of insulin resistance [16, 57].

A unique observation in the present study is the negative association of adiponectin and leptin with body fat mass. In normal subjects, these adipokines are inversely associated with body fat, as body fat decreases, adiponectin levels increase and leptin concentrations are reduced [51, 58–60]. The decrease in both adipokines associated with the reduction in body fat mass in animals with burns and disuse raises questions as to secondary mediation possibly via cytokines or catecholamines. Lower levels of adiponectin are also associated with insulin insensitivity and increased hepatic fat content which are often reported in patients with severe burns [51].

Of note is the increase in food intake in the presence of an elevation in ghrelin in animals with both burn and disuse. The increase in this orexigenic hormone again is reflective of the hypermetabolic state post injury [60]. Recent work has suggested ghrelin administration during the acute or “ebb” phase in burned rats improves outcome by increasing growth hormone, inhibiting protein breakdown and attenuating inflammatory processes [61–63]. In the present study, measurements were taken on Day 14 after injury during the late or “flow phase”. The alteration of ghrelin and adipokines with burn and disuse offers possibilities for interventions to attenuate the persistent hypermetabolism of patients with severe traumatic injuries.

The present animal model incorporates burn injury and disuse; however, in patients there are additional manipulations affecting outcomes. These include early excision and grafting. The impact of these procedures and other clinical manipulations, such as wound care, could exasperate and prolong the findings observed in the present study during the ebb phase, necessitating a greater compensatory response during the flow phase. Another limitation in the inference of these data to the human condition is metabolic differences. For example, in rats the rate of muscle protein synthesis is approximately 2.5-fold greater than that of humans. That said, the dynamic changes in response to burn appear to be similar between the present animal model and the patient with severe burns [64].

Conclusions

Clinically, our animal model of injury and disuse allows examination of the dramatic metabolic changes that occur due to trauma. Independently, burn injury and disuse had similar body mass reductions from control; however, when combined, additive effects were apparent. We have previously demonstrated, using this model, a similar response of an additive effect of burn and disuse on muscle function and bone health [30, 31]. Thus, in assessing metabolic changes with severe trauma both injury and disuse should be considered. Furthermore, the observed changes in corticosterone, adipokines and ghrelin provide insights for interventions to attenuate the hypermetabolic state following injury, possibly reducing catabolism and muscle loss and the subsequent adverse effects on recovery and function.

Key messages

  • We evaluated independent and combined effects of burn and disuse on metabolism in a rat model.

  • Lean and fat body mass was reduced in all groups compared to sham ambulatory animals.

  • Decrease in lean body mass was associated with the rate of urinary corticosterone excretion.

  • Loss of fat body mass was associated with decreased plasma leptin and adiponectin levels, and increased ghrelin levels.

  • Burn and disuse produced additive effects on metabolic changes in this animal model.

Abbreviations

A:

Adiponectin

BA:

Burn ambulatory

BH:

Burn hindlimb unloading

BM:

Body mass

BUN:

Blood urea nitrogen

CORT:

Corticosterone

DEXA:

Dual energy x-ray absorptiometry

ELISA:

Enzyme linked immunosorbent assay

FM:

Fat mass

G:

Ghrelin

HLU:

Hindlimb unloading

L:

Leptin

LBM:

Lean body mass

N:

Nitrogen

R:

Resistin

SA:

Sham ambulatory

SH:

Sham hindlimb unloading

TBSA:

Total body surface area

TP:

Total protein

UUN:

Urinary urea nitrogen.

References

  1. Demling RH, Seigne P: Metabolic management of patients with severe burns. World J Surg 2000, 24: 673-680. 10.1007/s002689910109

    Article  CAS  PubMed  Google Scholar 

  2. Hart DW, Wolf SE, Chinkes DL, Gore DC, Mlcak RP, Beauford RB, Obeng MK, Lal S, Gold WF, Wolfe RR, Herndon DN: Determinants of skeletal muscle catabolism after severe burn. Ann Surg 2000, 232: 455-465. 10.1097/00000658-200010000-00001

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Klein GL, Herndon DN, Goodman WG, Langman CB, Phillips WA, Dickson IR, Eastell R, Naylor KE, Maloney NA, Desai M, et al.: Histomorphometric and biochemical characterization of bone following acute severe burns in children. Bone 1995, 17: 455-460. 10.1016/8756-3282(95)00279-1

    Article  CAS  PubMed  Google Scholar 

  4. Caldwell FT Jr: Energy metabolism following thermal burns. Arch Surg 1976, 111: 181-185. 10.1001/archsurg.1976.01360200087017

    Article  PubMed  Google Scholar 

  5. Hart DW, Wolf SE, Chinkes DL, Beauford RB, Mlcak RP, Heggers JP, Wolfe RR, Herndon DN: Effects of early excision and aggressive enteral feeding on hypermetabolism, catabolism, and sepsis after severe burn. J Trauma 2003, 54: 755-761. discussion 761–764 10.1097/01.TA.0000060260.61478.A7

    Article  CAS  PubMed  Google Scholar 

  6. Long C: Energy expenditure of major burns. J Trauma 1979, 19: 904-906.

    CAS  PubMed  Google Scholar 

  7. Herndon DN, Wilmore DW, Mason AD Jr: Development and analysis of a small animal model simulating the human postburn hypermetabolic response. J Surg Res 1978, 25: 394-403. 10.1016/S0022-4804(78)80003-1

    Article  CAS  PubMed  Google Scholar 

  8. Ferrando AA: Effects of inactivity and hormonal mediators on skeletal muscle during recovery from trauma. Curr Opin Clin Nutr Metab Care 2000, 3: 171-175. 10.1097/00075197-200005000-00002

    Article  CAS  PubMed  Google Scholar 

  9. Hart DW, Herndon DN, Klein G, Lee SB, Celis M, Mohan S, Chinkes DL, Wolf SE: Attenuation of posttraumatic muscle catabolism and osteopenia by long-term growth hormone therapy. Ann Surg 2001, 233: 827-834. 10.1097/00000658-200106000-00013

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  10. Herridge MS: Legacy of intensive care unit-acquired weakness. Crit Care Med 2009, 37: S457-S461.

    Article  PubMed  Google Scholar 

  11. Cheung AM, Tansey CM, Tomlinson G, Diaz-Granados N, Matte A, Barr A, Mehta S, Mazer CD, Guest CB, Stewart TE, Al-Saidi F, Cooper AB, Cook D, Slutsky AS, Herridge MS: Two-year outcomes, health care use, and costs of survivors of acute respiratory distress syndrome. Am J Respir Crit Care Med 2006, 174: 538-544. 10.1164/rccm.200505-693OC

    Article  PubMed  Google Scholar 

  12. Alberda C, Gramlich L, Jones N, Jeejeebhoy K, Day AG, Dhaliwal R, Heyland DK: The relationship between nutritional intake and clinical outcomes in critically ill patients: results of an international multicenter observational study. Intensive Care Med 2009, 35: 1728-1737. 10.1007/s00134-009-1567-4

    Article  PubMed  Google Scholar 

  13. Koch A, Gressner OA, Sanson E, Tacke F, Trautwein C: Serum resistin levels in critically ill patients are associated with inflammation, organ dysfunction and metabolism and may predict survival of non-septic patients. Crit Care 2009, 13: R95. 10.1186/cc7925

    Article  PubMed Central  PubMed  Google Scholar 

  14. Langouche L, Vander Perre S, Frystyk J, Flyvbjerg A, Hansen TK, Van den Berghe G: Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin. Crit Care 2009, 13: R112. 10.1186/cc7956

    Article  PubMed Central  PubMed  Google Scholar 

  15. Venkatesh B, Hickman I, Nisbet J, Cohen J, Prins J: Changes in serum adiponectin concentrations in critical illness: a preliminary investigation. Crit Care 2009, 13: R105. 10.1186/cc7941

    Article  PubMed Central  PubMed  Google Scholar 

  16. Wade CE, Mora AG, Shields BA, Pidcoke HF, Baer LA, Chung KK, Wolf SE: Signals from fat after injury: plasma adipokines and ghrelin concentrations in the severely burned. Cytokine 2013, 61: 78-83. 10.1016/j.cyto.2012.08.031

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. Barrow RE, Meyer NA, Jeschke MG: Effect of varying burn sizes and ambient temperature on the hypermetabolic rate in thermally injured rats. J Surg Res 2001, 99: 253-257. 10.1006/jsre.2001.6183

    Article  CAS  PubMed  Google Scholar 

  18. Izamis ML, Uygun K, Uygun B, Yarmush ML, Berthiaume F: Effects of burn injury on markers of hypermetabolism in rats. J Burn Care Res 2009, 30: 993-1001. 10.1097/BCR.0b013e3181bfb7b4

    Article  PubMed Central  PubMed  Google Scholar 

  19. Caldwell FT Jr, Osterholm JL, Sower ND, Moyer CA: Metabolic response to thermal trauma of normal and thyroprivic rats at three environmental temperatures. Ann Surg 1959, 150: 976-988. 10.1097/00000658-195912000-00003

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  20. Al Shamma GA, Goll CC, Baird TB, Broom J, Nicholas GA, Richards JR: Changes in body composition after thermal injury in the rat. Br J Nutr 1979, 42: 267-275. 10.1079/BJN19790113

    Article  CAS  PubMed  Google Scholar 

  21. Gedeon GS, Goll C, Shenkin A, Al-Shamma G, Richards JR, Fleck A, Cuthbertson DP, Fell GS: The effect of environmental temperature on protein and energy changes following burn injury in the rat. Clin Nutr 1983, 2: 13-24.

    Article  CAS  PubMed  Google Scholar 

  22. Chance WT, Nelson JL, Kim M, Foley-Nelson T, Chen MH, Fischer JE: Burn-induced alterations in feeding, energy expenditure, and brain amine neurotransmitters in rats. J Trauma 1987, 27: 503-509. 10.1097/00005373-198705000-00008

    Article  CAS  PubMed  Google Scholar 

  23. Wood RH, Caldwell FT Jr, Wallace BH: Effect of early feeding on the postburn hypermetabolic response in rats. J Trauma 1990, 30: S24-S30.

    Article  CAS  PubMed  Google Scholar 

  24. Morey-Holton ER, Globus RK: Hindlimb unloading rodent model: technical aspects. J Appl Physiol 2002, 92: 1367-1377. 10.1063/1.1492860

    Article  PubMed  Google Scholar 

  25. Ohira Y, Yoshinaga T, Nomura T, Kawano F, Ishihara A, Nonaka I, Roy RR, Edgerton VR: Gravitational unloading effects on muscle fiber size, phenotype and myonuclear number. Adv Space Res 2002, 30: 777-781. 10.1016/S0273-1177(02)00395-2

    Article  CAS  PubMed  Google Scholar 

  26. Sonnenfeld G: Use of animal models for space flight physiology studies, with special focus on the immune system. Gravit Space Biol Bull 2005, 18: 31-35.

    PubMed  Google Scholar 

  27. Stein T, Schluter M, Galante A, Soteropoulos P, Tolias P, Grindeland R, Moran M, Wang T, Polansky M, Wade C: Energy metabolism pathways in rat muscle under conditions of simulated microgravity. J Nutr Biochem 2002, 13: 471. 10.1016/S0955-2863(02)00195-X

    Article  CAS  PubMed  Google Scholar 

  28. Aviles H, Belay T, Fountain K, Vance M, Sonnenfeld G: Increased susceptibility to Pseudomonas aeruginosa infection under hindlimb-unloading conditions. J Appl Physiol 2003, 95: 73-80.

    Article  PubMed  Google Scholar 

  29. Radek KA, Baer LA, Eckhardt J, DiPietro LA, Wade CE: Mechanical unloading impairs keratinocyte migration and angiogenesis during cutaneous wound healing. J Appl Physiol 2008, 104: 1295-1303. 10.1152/japplphysiol.00977.2007

    Article  PubMed  Google Scholar 

  30. Baer LA, Wu X, Tou JC, Johnson E, Wolf SE, Wade CE: Contributions of severe burn and disuse to bone structure and strength in rats. Bone 2012, 52: 644-650.

    Article  PubMed Central  PubMed  Google Scholar 

  31. Wu X, Baer LA, Wolf SE, Wade CE, Walters TJ: The impact of muscle disuse on muscle atrophy in severely burned rats. J Surg Res 2010, 164: e243-e251. 10.1016/j.jss.2010.08.032

    Article  PubMed Central  PubMed  Google Scholar 

  32. Harper JS, Mulenburg GM, Evans J, Navidi M, Wolinsky I, Arnaud SB: Metabolic cages for a space flight model in the rat. Lab Anim Sci 1994, 44: 645-647.

    CAS  PubMed  Google Scholar 

  33. Walker HL, Mason AD Jr: A standard animal burn. J Trauma 1968, 8: 1049-1051. 10.1097/00005373-196811000-00006

    Article  CAS  PubMed  Google Scholar 

  34. Pruitt BA: Fluid resuscitation of the extensively burned patients. Ann Chir Plast 1979, 24: 268-272.

    CAS  PubMed  Google Scholar 

  35. Lintault LM, Zakrzewska EI, Maple RL, Baer LA, Casey TM, Ronca AE, Wade CE, Plaut K: In a hypergravity environment neonatal survival is adversely affected by alterations in dam tissue metabolism rather than reduced food intake. J Appl Physiol 2007, 102: 2186-2193. 10.1152/japplphysiol.01015.2006

    Article  CAS  PubMed  Google Scholar 

  36. Stein TP, Leskiw MJ, Schluter MD: Diet and nitrogen metabolism during spaceflight on the shuttle. J Appl Physiol 1996, 81: 82-97.

    CAS  PubMed  Google Scholar 

  37. Cree MG, Wolfe RR: Postburn trauma insulin resistance and fat metabolism. Am J Physiol Endocrinol Metab 2008, 294: E1-E9.

    Article  CAS  PubMed  Google Scholar 

  38. Wolfe RR: Review: acute versus chronic response to burn injury. Circ Shock 1981, 8: 105-115.

    CAS  PubMed  Google Scholar 

  39. Atiyeh BS, Gunn SW, Dibo SA: Metabolic implications of severe burn injuries and their management: a systematic review of the literature. World J Surg 2008, 32: 1857-1869. 10.1007/s00268-008-9587-8

    Article  PubMed  Google Scholar 

  40. Ferrando AA, Paddon-Jones D, Wolfe RR: Bed rest and myopathies. Curr Opin Clin Nutr Metab Care 2006, 9: 410-415. 10.1097/01.mco.0000232901.59168.e9

    Article  PubMed  Google Scholar 

  41. Jeschke MG, Chinkes DL, Finnerty CC, Kulp G, Suman OE, Norbury WB, Branski LK, Gauglitz GG, Mlcak RP, Herndon DN: Pathophysiologic response to severe burn injury. Ann Surg 2008, 248: 387-401.

    Article  PubMed Central  PubMed  Google Scholar 

  42. Wolfe RR: The underappreciated role of muscle in health and disease. Am J Clin Nutr 2006, 84: 475-482.

    CAS  PubMed  Google Scholar 

  43. Shangraw RE, Turinsky J: Effect of disuse and thermal injury on protein turnover in skeletal muscle. J Surg Res 1982, 33: 345-355. 10.1016/0022-4804(82)90048-8

    Article  CAS  PubMed  Google Scholar 

  44. Shangraw RE, Turinsky J: Altered protein kinetics in vivo after single-limb burn injury. Biochem J 1984, 223: 747-753.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  45. Paddon-Jones D: Interplay of stress and physical inactivity on muscle loss: nutritional countermeasures. J Nutr 2006, 136: 2123-2126.

    CAS  PubMed  Google Scholar 

  46. Stein TP, Wade CE: Protein turnover in atrophying muscle: from nutritional intervention to microarray expression analysis. Curr Opin Clin Nutr Metab Care 2003, 6: 95-102. 10.1097/00075197-200301000-00014

    Article  PubMed  Google Scholar 

  47. Stein TP, Schluter MD, Galante AT, Soteropoulos P, Ramirez M, Bigbee A, Grindeland RE, Wade CE: Effect of hind limb muscle unloading on liver metabolism of rats. J Nutr Biochem 2005, 16: 9-16. 10.1016/j.jnutbio.2004.07.003

    Article  CAS  PubMed  Google Scholar 

  48. Ferrando AA, Stuart CA, Sheffield-Moore M, Wolfe RR: Inactivity amplifies the catabolic response of skeletal muscle to cortisol. J Clin Endocrinol Metab 1999, 84: 3515-3521. 10.1210/jc.84.10.3515

    CAS  PubMed  Google Scholar 

  49. Steiner AA, Romanovsky AA: Leptin: at the crossroads of energy balance and systemic inflammation. Prog Lipid Res 2007, 46: 89-107. 10.1016/j.plipres.2006.11.001

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  50. Robinson K, Prins J, Venkatesh B: Clinical review: adiponectin biology and its role in inflammation and critical illness. Crit Care 2011, 15: 221. 10.1186/cc10021

    Article  PubMed Central  PubMed  Google Scholar 

  51. Lihn AS, Pedersen SB, Richelsen B: Adiponectin: action, regulation and association to insulin sensitivity. Obes Rev 2005, 6: 13-21. 10.1111/j.1467-789X.2005.00159.x

    Article  CAS  PubMed  Google Scholar 

  52. Tsuchihashi H, Yamamoto H, Maeda K, Ugi S, Mori T, Shimizu T, Endo Y, Hanasawa K, Tani T: Circulating concentrations of adiponectin, an endogenous lipopolysaccharide neutralizing protein, decrease in rats with polymicrobial sepsis. J Surg Res 2006, 134: 348-353. 10.1016/j.jss.2006.01.001

    Article  CAS  PubMed  Google Scholar 

  53. Lu YQ, Cai XJ, Gu LH, Wang Q, Huang WD, Bao DG: Experimental study of controlled fluid resuscitation in the treatment of severe and uncontrolled hemorrhagic shock. J Trauma 2007, 63: 798-804. 10.1097/TA.0b013e31815202c9

    Article  PubMed  Google Scholar 

  54. Cakir B, Cevik H, Contuk G, Ercan F, Eksioglu-Demiralp E, Yegen BC: Leptin ameliorates burn-induced multiple organ damage and modulates postburn immune response in rats. Regul Pept 2005, 125: 135-144. 10.1016/j.regpep.2004.08.032

    Article  CAS  PubMed  Google Scholar 

  55. Liapaki I, Anagnostoulis S, Karayiannakis A, Korkolis D, Labropoulou M, Matarasso A, Simopoulos C: Burn wound angiogenesis is increased by exogenously administered recombinant leptin in rats. Acta Cir Bras 2008, 23: 118-124.

    Article  PubMed  Google Scholar 

  56. Duffy SL, Lagrone L, Herndon DN, Mileski WJ: Resistin and postburn insulin dysfunction. J Trauma 2009, 66: 250-254. 10.1097/TA.0b013e31815ebad4

    Article  CAS  PubMed  Google Scholar 

  57. Dasu MR, LaGrone L, Mileski WJ: Alterations in resistin expression after thermal injury. J Trauma 2004, 56: 118-122. 10.1097/01.TA.0000053195.32115.9C

    Article  CAS  PubMed  Google Scholar 

  58. Considine RV, Sinha MK, Heiman ML, Kriauciunas A, Stephens TW, Nyce MR, Ohannesian JP, Marco CC, McKee LJ, Bauer TL, et al.: Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J Med 1996, 334: 292-295. 10.1056/NEJM199602013340503

    Article  CAS  PubMed  Google Scholar 

  59. Staiger H, Tschritter O, Machann J, Thamer C, Fritsche A, Maerker E, Schick F, Haring HU, Stumvoll M: Relationship of serum adiponectin and leptin concentrations with body fat distribution in humans. Obes Res 2003, 11: 368-372. 10.1038/oby.2003.48

    Article  CAS  PubMed  Google Scholar 

  60. Tschop M, Weyer C, Tataranni PA, Devanarayan V, Ravussin E, Heiman ML: Circulating ghrelin levels are decreased in human obesity. Diabetes 2001, 50: 707-709. 10.2337/diabetes.50.4.707

    Article  CAS  PubMed  Google Scholar 

  61. Balasubramaniam A, Joshi R, Su C, Friend LA, Sheriff S, Kagan RJ, James JH: Ghrelin inhibits skeletal muscle protein breakdown in rats with thermal injury through normalizing elevated expression of E3 ubiquitin ligases MuRF1 and MAFbx. Am J Physiol Regul Integr Comp Physiol 2009, 296: R893-R901. 10.1152/ajpregu.00015.2008

    Article  CAS  PubMed  Google Scholar 

  62. Balasubramaniam A, Wood S, Joshi R, Su C, Friend LA, Sheriff S, James JH: Ghrelin stimulates food intake and growth hormone release in rats with thermal injury: synthesis of ghrelin. Peptides 2006, 27: 1624-1631. 10.1016/j.peptides.2006.02.005

    Article  CAS  PubMed  Google Scholar 

  63. Sehirli O, Sener E, Sener G, Cetinel S, Erzik C, Yegen BC: Ghrelin improves burn-induced multiple organ injury by depressing neutrophil infiltration and the release of pro-inflammatory cytokines. Peptides 2008, 29: 1231-1240. 10.1016/j.peptides.2008.02.012

    Article  CAS  PubMed  Google Scholar 

  64. Phillips SM, Glover EI, Rennie MJ: Alterations of protein turnover underlying disuse atrophy in human skeletal muscle. J Appl Physiol 2009, 107: 645-654.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

The authors would like to thank Angela Beeler for her editorial assistance. Funding for this project was provided by the National Institutes of Health (1 R01 GM063120-04); The Technologies for Metabolic Monitoring (TMM)/Julia Weaver Fund, A Congressionally Directed Program Jointly Managed by the USA MRMC, NIH, NASA and the Juvenile Diabetes Research Foundation; Combat Casualty Care Division, United States Army Medical Research and Materiel Command. The funding sources played no role in the design of the study, collection, analysis, and interpretation of data, in writing the manuscript or the decision to submit for publication.

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Authors and Affiliations

  1. US Army Institute of Surgical Research, Fort Sam Houston, TX, 78234, USA

    Charles E Wade, Lisa A Baer, Xiaowu Wu, David T Silliman, Thomas J Walters & Steven E Wolf

  2. Department of Surgery, University of Texas Health Science Center, Fort Sam Houston, San Antonio, TX, 78229, USA

    Charles E Wade, Xiaowu Wu & Steven E Wolf

  3. Department of Surgery and Center for Translational Injury Research, University of Texas Health Science Center, 6431 Fannin St.MSB 5.204, Houston, TX, 77030, USA

    Charles E Wade & Lisa A Baer

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  1. Charles E Wade
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Correspondence to Charles E Wade.

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The authors have no competing interests to declare. The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or reflecting the views of the US Department of Defense or the US Government. Some of the authors are employees of the US Government. This work was prepared as part of their official duties and, as such, there is no copyright to be transferred.

Authors’ contributions

CEW, LAB, XW, TJW and SEW designed the study. CEW, LAB, XW and DTS performed animal work and adipokine measurements. CEW, LAB, XW and SEW analyzed the data. CEW, LAB, XW, DTS, TJW and SEW drafted the manuscript. All authors critically revised the manuscript and approved the manuscript for submission.

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Wade, C.E., Baer, L.A., Wu, X. et al. Severe burn and disuse in the rat independently adversely impact body composition and adipokines. Crit Care 17, R225 (2013). https://doi.org/10.1186/cc13048

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Keywords

Critical Care

ISSN: 1364-8535