Objective: Arginine supplementation seems logical in situations where this amino acid becomes essential, for example after massive intestinal resection. Arginine is taken up and metabolised by the liver to a large extent and its supplementation is potentially unsafe. Citrulline is not captured by the liver and passes freely to the kidneys where it is metabolised to arginine, and so is a good candidate to generate arginine and thereby improve nutritional status.
Methods: Twenty four rats were assigned to four groups: citrulline, arginine, control, and sham. The sham group underwent transection and the three other groups resection of 80% of the small intestine. All rats were fed by enteral nutrition and its composition was as follows: supplementation with citrulline in the citrulline group, supplementation with arginine in the arginine group, and standard polymeric enteral nutrition in the control and sham groups. All groups received isonitrogenous nutrition and citrulline and arginine intakes were equimolar in their respective groups. After 10 days, the rats were sacrificed.
Results: Arginine concentration was higher (p<0.05) in plasma and muscle in the citrulline group than in the three other groups. Plasma levels of arginine were 110 (12), 79 (7), 167 (22), and 228 (13) μmol/l in the sham, control, arginine, and citrulline groups respectively. Arginine concentrations in the gastrocnemius were: 0.15 (0.02), 0.16 (0.02), 0.40 (0.05), and 0.94 (0.20) μmol/g, respectively. Citrulline preserved nitrogen balance in resected rats but not in arginine supplemented rats (mean J10: 2.27 (0.29), 1.67 (0.15), 1.98 (0.29), and 2.43 (0.41) g/24 hours in the sham, control, arginine, and citrulline groups, respectively).
Conclusion: Supplementing the diet with citrulline is a very efficient means of increasing arginine levels and improving nitrogen balance after massive intestinal resection. The results of this study form a strong rationale for citrulline supplementation in these patients.
- EDL, extensor digitorum longus
- SBS, short bowel syndrome
- short bowel syndrome
- intestinal adaptation
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Arginine is recognised as one of the most versatile amino acids in cells.1 It serves as a precursor for the synthesis not only of proteins but also of nitric oxide,2 polyamines,3 proline,4 and agmatine—a recently discovered decarboxylation product of arginine but whose physiological roles have yet to be established.5 Arginine stimulates the secretion of hormones such as insulin, prolactin, glucagon, and growth hormone,6,7 and plays a key role in the nitrogen homeostasis modulating ureagenesis.8 A balance between arginine intake, arginine production, and its degradation maintains arginine homeostasis.
The liver and gut are two organs that play a major role in the metabolism of arginine. As the activity of arginase is very high in the liver,9 most of the arginine that arrives in the liver is converted into urea. If unregulated, this process would be detrimental in certain situations. This is why arginine flux to the liver is modulated by the intestine, which can convert dietary arginine to citrulline.10 As the activity of the two enzymes that metabolise citrulline (argininosuccinate synthetase and argininosuccinate lyase) is very low in the intestine,11,12 citrulline produced by enterocytes cannot be used in situ and citrulline is released as such into the circulation. It is not taken up by the liver but captured by the kidneys. Renal citrulline uptake is approximately 80% of the amount released by the gut.6 In turn, the kidneys generate arginine, which is released into the blood stream for use by other tissues for protein synthesis and other purposes.13,14 This arginine-citrulline-arginine cycle can be seen as a means of protecting dietary arginine from excessive degradation in the liver,9 especially in situations where the intake of protein is low.
In massive intestinal resection, the main site of citrulline production is greatly reduced, and hypocitrullinaemia proportional to the severity of intestinal disease is observed in patients with short bowel syndrome (SBS).15 This observation has recently been extended to patients with coeliac disease16 and radiation induced small bowel damage.17 As a consequence of the diminished plasma levels of citrulline, decreased levels of arginine are also observed,15,18 suggesting that arginine becomes an essential amino acid after massive intestinal resection (for example, of rat small intestine).18
In this situation, supplementing with arginine would seem logical. However, the fact that arginine is captured and largely metabolised by the liver to yield urea raises questions about the safety of arginine supplementation, which is liable to cause excessive ureagenesis as arginine is the allosteric activator of N-acetylglutamate synthase, which synthesises N-acetylglutamate, which in turn activates carbamoyl-phosphate synthase; hence arginine acts as a catalyst of ureagenesis.19,20 On the other hand, citrulline, which is not taken up by the liver and is the major precursor of arginine, should be a good candidate to generate arginine and improve nutritional status in massive intestinal resection. The aim of this work was to test this hypothesis.
MATERIALS AND METHODS
All chemicals were purchased from Sigma (St-Quentin-Fallavier, France). Citrulline was a gift from Biocodex (Compiègne, France).
Male Wistar rats (n = 24, body weight 220–230 g) from Iffa Credo (L’Arbresle, France) were used. They were acclimatised in metabolic cages for five days before surgery, with free access to standard laboratory chow (17% protein, 3% fat, 59% carbohydrate, 21% water, vitamins and minerals—A04; Usine d’Alimentation Rationnelle, Villemoisson-sur-Orge, France) and water.
Animals were fasted for 12 hours before surgery. They were anaesthetised by isoflurane inhalation (3% isoflurane) using a regulated airflow apparatus (Minerve, Esternay, France). Enterectomy was performed on rats in the citrulline, arginine, and control groups (see below for definition) by removing 80% of the small intestine, leaving 10% of the proximal jejunum and 10% of the distal ileum. Six rats were sham operated (transection). For both resected and transected animals, continuity was restored with end to end anastomosis using a single running silk 6-0 suture. Placement of the gastrostomy tube immediately followed intestinal resection or transection. A silicone tube (Tygon, size 0.51 mm; Fisher Bioblock Scientific, Illkirch, France) was introduced into the lumen of the stomach and the remaining end of the catheter was tunnelled subcutaneously to the back of the neck and attached to a spring coil-swivel mechanism (Harvard Apparatus, Les Ulis, France) allowing free movement of the rat in the cage.
One of the authors (CM) is authorised by the French government (No 75522) to use this experimental model of surgery. Animal care complied with French regulations for the protection of animals used for experimental and other scientific purposes (D 2001-486) and with European Community regulations (Official Journal of the European Community, L538 12:18:1986).
Rats were housed individually in metabolic cages. They were allowed a five day recovery period. On the first two days they had free access to a 5% glucose solution. On day 3 glucose was withdrawn and rats had access to standard laboratory chow and water. On day 4 enteral nutrition was introduced at a flow rate of 0.5 ml/h using a Harvard infusion pump (pump 11; Harvard Apparatus). The rats also had free access to chow food and water. The flow rate was gradually increased to a maximum on day 5 corresponding to intake of 2 g N/kg/day. From day 5 until the end of the experiment, rats received only enteral nutrition and had free access to water.
The rats were randomly assigned to one of four groups (table 1).
The citrulline group (n = 6) consisted of rats receiving standard enteral nutrition (Sondalis; Nestlé Clinical Nutrition, 1 kcal/ml) supplemented with citrulline at a dose of 1 g/kg/day (5.708 mM/kg/day).
The arginine group (n = 6) consisted of rats receiving standard enteral nutrition supplemented with arginine at a dose of 0.994 g/kg/day, which was equimolar to the citrulline group.
The control group (n = 6) and the sham group (n = 6) consisted of rats receiving standard enteral nutrition.
The standard enteral diet contained 5.8 g of arginine/100 g protein, providing an intake of 0.746 g of arginine/kg/day.
To keep all groups isonitrogenous, standard enteral nutrition in the citrulline, control, and sham groups were supplemented with a mixture of non-essential amino acids consisting of alanine, asparagine, glycine, serine, histidine, and proline in equimolar amounts. All groups were isonitrogenous (2 g N/kg/day) and isocaloric (200 kcal/kg/day) (see table 1).
Rats were weighed and urine was collected daily. Total enteral nutrition was administered for 10 days. Enteral nutrition was stopped two hours before decapitation.
Blood was sampled in heparinised tubes, which were rapidly centrifuged.
The abdominal cavity was opened. The liver was immediately removed and weighed, and a sample was cut off, frozen in liquid nitrogen, and stored at −80°C.
Jejunum and ileum
The intestinal mucosa was washed with cold NaCl (0.9%), reverted and scraped, rapidly frozen in liquid nitrogen, and stored at −80°C until analysis.
Three muscles of the hindlimbs (extensor digitorum longus (EDL), gastrocnemius, and soleus) were rapidly removed, weighed, frozen in liquid nitrogen, and stored at −80°C until analysis. These three muscles were selected because they differ widely in their function and fibre type21 and have different metabolic responses to stress.22,23
Parameters studied and analytical methods
Nitrogen was quantified by chemiluminescence24 using an Antek 9000 apparatus (Antek, Houston, Texas, USA) and nitrogen balance was calculated as the difference between nitrogen intake and nitrogen urinary output.
Amino acid concentrations in plasma and tissues (muscles, liver, and intestinal mucosa).
Plasma was deproteinised with a 30% (w/v) sulphosalicylic acid solution. Supernatants were stored at −80°C until analysis. Tissues were ground and deproteinised with 10% trichloroacetic acid containing 0.5 mM EDTA.25 Supernatants were stored at −80°C until analysis. Amino acids were measured by ion exchange chromatography using an amino acid auto analyser (model Aminotac; Jeol, Tokyo, Japan). The results of our participation in the European Quality Control Scheme (ERNDIM) indicate the accuracy of our amino acid determinations.
Data are expressed as means (SEM). Comparisons between sets of data were made using one way analysis of variance (ANOVA) followed by the Newman-Keuls test. PCSM software was used (Deltasoft, Grenoble, France). Differences at p<0.05 were considered significant.
The body weight gain (the difference between body weight on the first day of total enteral nutrition administration and the last day of the experiment) did not differ significantly in the four groups (data not shown).
Regarding tissue weight (table 2), we found no significant differences in muscle and liver weights in the four groups. As a result of intestinal adaptation, the weight of intestinal mucosa (expressed in g/cm) was significantly higher in the three resected groups than in the sham group (citrulline, arginine, control v sham; p<0.05). However, there was no significant difference in intestinal mucosa weight in the three resected groups.
Amino acid concentrations
Citrulline, arginine, and ornithine were the only amino acids whose profiles were influenced by the different diets.
Plasma (fig 1)
Intestinal resection caused decreased levels of citrulline compared with the sham group (control v sham; p<0.05). Supplementation with arginine raised the concentration of citrulline to levels of the sham group but were still not significantly different from controls. Supplementation with citrulline raised levels of citrulline to significantly higher values than in the other three groups (citrulline v sham, control, arginine; p<0.05). Plasma ornithine concentrations were increased in the arginine and citrulline groups compared with the sham and control groups (citrulline and arginine v sham and control; p<0.05).
The plasma level of arginine decreased (−28%) in controls compared with the sham group but the difference did not reach significance. Addition of arginine to the diet raised its concentration to significantly higher values compared with both controls and the sham group (arginine v sham and control; p<0.05). The concentration of arginine in the citrulline supplemented group was significantly higher than in all other groups (citrulline v arginine, control, and sham; p<0.05).
Intestinal mucosa (table 3)
In the jejunum, arginine concentrations in controls were significantly lower than in the sham group (control v sham; p<0.05). Supplementation of arginine or citrulline raised arginine levels to values comparable with those in the sham group (arginine and citrulline v control; p<0.05).
Jejunal and ileal citrulline concentrations were increased in the citrulline compared with the three other groups (citrulline v sham, control, arginine; p<0.05).
Liver (table 4)
Citrulline supplementation did not result in its accumulation. There was an increase in ornithine in the citrulline supplemented group (citrulline v sham, control; p<0.05). Free arginine was not detected in any group.
Muscles (table 5)
Levels of the three amino acids were unchanged in controls compared with the sham group. Arginine supplementation raised levels of ornithine in the soleus compared with the sham group (arginine v sham; p<0.05) and in the soleus and EDL compared with the control group (arginine v control; p<0.05). The effect on arginine concentration of the arginine supplement was seen only in the soleus where arginine levels were significantly higher than in both the sham and control groups (arginine v sham and control; p<0.05). Citrulline supplementation raised levels of citrulline in the three muscles so that they differed significantly from the other three groups (citrulline v sham, control, and arginine; p<0.05). Levels of ornithine were higher in the gastrocnemius and soleus in the citrulline group compared with the sham and control groups (citrulline v sham and control; p<0.05). Arginine levels in all muscles were significantly higher in the citrulline group than in the other three groups (citrulline v sham, control, and arginine; p<0.05).
Nitrogen balance (fig 2)
For the first four days of the experiment there was no significant change in nitrogen balance in the groups. Starting from day 6, nitrogen balance in the control group fell compared with the sham and citrulline groups (control v sham and citrulline; p<0.05). This value did not change up to the end of the experiment.
Arginine supplementation did not restore nitrogen balance which remained diminished on days 9 and 10 compared with sham and citrulline (arginine v sham and citrulline; p<0.05). On day 10, however, it differed significantly from controls (arginine v control; p<0.05).
The effect of citrulline supplementation was seen very early: starting from day 5 it restored nitrogen balance compared with controls (citrulline v control; p<0.05) and from day 7 compared with the arginine group (citrulline v arginine; p<0.05). It did not differ from the sham group at any time during the experiment.
Although arginine is considered a non-essential amino acid, certain situations lead to increased needs for this amino acid, and de novo synthesis of arginine may not be sufficient to meet these needs. Arginine then becomes an essential amino acid. Such situations include growth,26 hypermetabolic situations such as burn injury,27,28 and SBS.18
The work of Wakabayashi and colleagues18,29 recognised arginine as an essential amino acid by showing that removing arginine from the diet after resection led to diminished levels of muscle arginine and negative nitrogen balance. Our experimental conditions were different, as the standard enteral nutrition formula used contained arginine (see materials and methods) and differences between groups were due to supplementation. To our knowledge, use of an arginine supplemented diet in SBS has not previously been studied and our work is therefore the first to show how it influences nitrogen balance and plasma and muscle levels of arginine. In our study, the arginine supplement raised arginine levels in plasma by 38% compared with the sham group. In healthy animals, a 2% arginine supplement in drinking water raises arginine levels to twice those of non-supplemented animals.30,31 This suggests that the body demand for arginine in the situation of intestinal resection is elevated, and this demand is only partially met by arginine supplementation. Similarly, nitrogen balance was also only partially restored by arginine supplementation and it differed from the control group only on the last day of the experiment. It remained however diminished compared with the sham group throughout the experiment.
A large part of dietary arginine is metabolised in enterocytes to yield citrulline. It has been shown that the intestine is the main site of citrulline synthesis10 and this was confirmed in our work by decreased plasma citrulline concentrations in the resected group of rats fed the non-supplemented diet. Unlike arginine, which is extensively taken up by the liver and metabolised to urea, intestine derived citrulline passes freely through the liver. This is well supported in the present study by the fact that citrulline content in the liver did not vary in the citrulline supplemented group whereas there was large accumulation of citrulline in all of the other tissues under study. Citrulline is then captured by the kidneys. Eighty per cent of citrulline synthesised by the intestine is converted into arginine,6 which is released into the blood stream for use by other tissues for protein synthesis and other purposes.13,14 Considering the metabolic features of arginine (partial restoration of nitrogen balance, low increase in plasma arginine, and lack of increase in gastrocnemius and EDL after arginine supplement) we conclude that the remnant intestine is unable to convert dietary arginine to citrulline adequately, and that a large part of arginine supplementation is taken up and metabolised by the liver. This limits the efficacy of arginine supplementation in intestinal resection. Inefficiency of an arginine supplement in a situation where the intestinal synthesis of citrulline was inhibited was studied by Hoogenraad and colleagues.32 Using a selective inhibitor of intestinal ornithine transcarbamylase, an enzyme that synthesises citrulline from ornithine and carbamoyl-phosphate, they showed that rats fed on normal rat chow, with presumably a sufficient intake of arginine, lost weight. Addition of arginine only partially restored weight gain. Serum arginine levels were also reduced by 25% and restored by addition of 1% citrulline.
The fact that citrulline is not taken up by the liver suggests that it may be a good means of increasing arginine levels in intestinal resection. Our experiment shows that citrulline raises arginine levels in plasma and all muscles much more effectively than arginine itself. Even at the intestinal level, citrulline can generate the same amounts of arginine as arginine itself. The effect of arginine or citrulline supplementation on the structure of the intestine of the resected rats was not studied here, but may be of major importance as it has been shown that arginine supplementation has a positive effect resulting in increased villus height and crypt cell mitoses.33 This point deserves further research.
Unlike arginine supplementation, which had no positive effect on nitrogen balance, citrulline supplement restored nitrogen balance, keeping it at the level of the sham group throughout the experiment. No attempt was made to measure nitrogen in stools, and this may be a limitation of our study, but there is no reason to believe that nitrogen loss in stools would be different in the three groups of rats with SBS. In addition, it is noteworthy that stool volume was measured in rats under enteral nutrition and no rat in any of the groups developed diarrhoea at any time during the experiment.
Although the differences in nitrogen balance between groups were obvious, this was not reflected in body weight gain. In order to solve this apparent conflict, it would be of interest to measure body composition of rats and to evaluate fat free mass.
Taken as a whole, our results show that citrulline, by generating large amounts of arginine and totally restoring nitrogen balance, can be an important supplement to a diet of patients who have undergone massive intestinal resection. It is tempting to speculate whether citrulline, although not a component amino acid of proteins, can influence protein synthesis and become an essential amino acid in intestinal resection. Assessment of protein synthesis would be necessary to determine this. Further work to evaluate the fate of the generated arginine would also be valuable to investigate the beneficial effect of citrulline supplementation more fully.
In addition, it would be of great interest to compare the behaviour and effects of arginine and citrulline when administrated by the parenteral route. Providing arginine by the parenteral route would bypass splanchnic extraction, and in this case arginine could be more efficient than when provided enterally. This point deserves further study as in postoperative care, patients with SBS are fed by the parenteral route.34 Finally, it would be interesting to extend the study of the effects of citrulline to other situations of intestinal insufficiency, such as Crohn’s disease or necrotising enterocolitis.
This work was supported by a contrat quadriennal grant from the French Ministry of Research and Technology. S Osowska was the recipient of a fellowship from Laboratoires Biocodex. We thank Harvard Apparatus and Minerve for providing devices used in this study.
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