Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-05T14:41:26.192Z Has data issue: false hasContentIssue false

Protein hydrolysates and tissue repair

Published online by Cambridge University Press:  21 November 2011

Rebecca L. Thomson*
Affiliation:
Nutritional Physiology Research Centre, Sansom Institute for Health Research, University of South Australia, Adelaide, South Australia5001, Australia
Jonathan D. Buckley
Affiliation:
Nutritional Physiology Research Centre, Sansom Institute for Health Research, University of South Australia, Adelaide, South Australia5001, Australia
*
*Corresponding author: Dr Rebecca Thomson, fax +61 8 8302 2178, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Protein hydrolysates provide a rich source of protein which is useful in situations where excess protein is needed, such as during repair of tissue damage. The consumption of protein hydrolysates has been shown to result in more rapid uptake of amino acids compared with whole proteins or free-form amino acid mixtures and some peptides in hydrolysates exhibit biological activity. Early studies showed that protein hydrolysates are more effectively utilised than intact proteins or amino acids. In addition, they promote a strong insulinotropic effect, which reduces protein breakdown and enhances muscle and tissue uptake of branched-chain amino acids. These effects contribute to benefits of protein hydrolysates for enhancing repair of tissue damage caused by surgery, ulcers, burns and muscle-damaging exercise. While there is evidence that protein hydrolysates may be useful for facilitating tissue repair, additional research is needed to further examine various roles of protein hydrolysates in this process.

Type
Review Article
Copyright
Copyright © The Authors 2011

Introduction

Protein is a major structural and functional component of tissue and dietary sources supply essential amino acids which are necessary for protein synthesis. Changes in protein turnover following tissue damage are critical to tissue repair and advancing knowledge of dietary protein requirements has emphasised the need for increased protein intake during tissue repair. Tissue repair involves four phases – haemostasis, inflammation, repair and remodelling – and adequate protein intake has three important roles in this process: promoting wound healing, maintenance of tissue integrity, and speeding convalescence(Reference Tui1). Indeed, while an adequate protein intake is essential for rapid wound healing and recovery(Reference Levy2), an inadequate protein intake can delay wound healing and reduce the integrity of the repaired tissue(Reference Harvey and Howes3). Following moderate to severe injury, protein depletion occurs due to an increased metabolic loss of N (due to loss of actual tissue, blood or exudates from the damaged area, loss due to excessive protein catabolism which follows injury or infection, and disuse or reflex atrophy)(Reference Learmonth and Cuthbertson4). By counteracting the negative N balance that occurs after injury, supplementation that can increase protein intake and enhance protein synthesis may be useful. For this reason there has been considerable interest in the use of nutritional interventions to promote tissue repair, in particular the use of protein hydrolysates.

Protein hydrolysates

The hydrolysis of protein results in the production of a range of peptides. The nature of the peptides produced depends on the method and duration of the hydrolytic process, and the conditions (for example, temperature, pH) under which the hydrolysis is performed. During hydrolysis, as a result of the cleavage of peptide bonds, proteins are broken down into peptides of different sizes and free amino acids(Reference Sinha, Radha and Prakash5) but typically contain mostly di- and tri-peptides. The hydrolytic process can be performed using enzymes, acids or alkali and the hydrolysates are produced from purified sources of heating with acid or the addition of proteolytic enzymes, followed by purification procedures(Reference Bucci, Unlu, Wolinsky and Driskell6Reference Clemente8). Enzymic hydrolysis is the preferred method, as acid and alkaline hydrolysis methods tend to be difficult to control and can yield variable products with reduced protein quality and biological value(Reference Bucci, Unlu, Wolinsky and Driskell6, Reference Clemente8).

The consumption of protein hydrolysates has been shown to result in a more rapid uptake of amino acids compared with whole proteins or free-form amino acid mixtures(Reference Bucci, Unlu, Wolinsky and Driskell6, Reference Di Pasquale9) and some peptides exhibit biological activity. The more rapid availability of amino acids and the presence of biologically active peptides have resulted in protein hydrolysates being used as therapeutic substances and incorporated into clinical nutrition products, such as geriatric dietary supplements, weight-control and therapeutic diets, or for clinical treatments in patients with digestion or absorption disorders, or malnutrition associated with cancer, trauma and burns(Reference Clemente8).

Potential effects on tissue repair

Early studies in rats showed that protein hydrolysates are more effectively utilised than intact proteins or amino acids(Reference Poullain, Cezard and Roger10). In addition, they were shown to promote a strong insulinotropic effect(Reference Power, Hallihan and Jakeman11, Reference Manninen12), which is important given that insulin is an anabolic hormone that reduces protein breakdown(Reference Woolfson, Heatley and Allison13, Reference Odessey and Parr14) and enhances muscle and tissue uptake of branched-chain amino acids (BCAA). As a result, protein hydrolysates, in particular casein and whey protein hydrolysates, have been used extensively to promote post-surgical healing and to assist with the repair of tissue damage(Reference Bucci, Unlu, Wolinsky and Driskell6).

Protein hydrolysates have also been investigated for their value in tissue repair in conditions where natural food cannot be ingested or ingested in sufficient quantities to replace N loss, such as burns, gastrectomy, cholecystectomy and herniotomy. Hydrolysates are also better tolerated by diseased gastrointestinal tracts than natural food; they not only neutralise the acid, relieve the stomach of digestive effort due to the pre-digested nature of the hydrolysate, but also provide the body with a rich source of nutrients to assist in repair(Reference Tui15).

Effect on post-surgical recovery

The typical daily protein intake requirement of an adult is 70 g/d, but this is increased considerably in post-surgical patients who require a protein intake of up to 300–400 g/d(Reference Levenson and Lund16). Surgical trauma leads to an increase in whole-body protein degradation(Reference Clague, Keir and Wright17), with the extent depending on the severity of the insult(Reference Tashiro, Yamamori and Takagi18Reference Yamamori, Tashiro and Mashima20). These changes in whole-body protein turnover result in a period of negative N balance. Due to the importance of protein nutrition in tissue repair, high-protein diets have been shown to accelerate the rate of tissue regeneration and increase tensile strength of the wound(Reference Harvey and Howes3). Protein hydrolysates have also been investigated and a study by Ziegler et al. (Reference Ziegler, Ollivier and Cynober21) followed twelve intensive care patients after abdominal surgery and compared the effect of two enteral diets with identical N and energy supply – a lactoserum protein hydrolysate diet and a non-degraded protein diet (control). Compared with the control diet, the protein hydrolysate diet was more effective at restoring plasma amino acid and protein levels; in particular it significantly increased plasma concentrations of thirteen amino acids (including all essential amino acids and BCAA) compared with only two in the non-degraded protein diet(Reference Ziegler, Ollivier and Cynober21). There was also a significantly greater increase in plasma insulin concentrations 1 h after consumption with the protein hydrolysate diet(Reference Ziegler, Ollivier and Cynober21). Thus, compared with consuming native protein, the consumption of hydrolysed protein post-surgery may promote greater increases is plasma concentrations of essential amino acids, resulting in an environment that is more conducive to tissue repair, and thus result in a more rapid repair of damaged tissue. However, additional well-controlled human trials are required to confirm this finding.

Effect on severe burn recovery

The stress response to severe burn injury initiates a catabolic cascade that rapidly decreases lean body mass(Reference Bessey, Jiang and Johnson22, Reference Jahoor, Desai and Herndon23) and the associated depletion of protein stores leads to altered immune function and impaired wound healing(Reference Bessey, Jiang and Johnson22, Reference Jahoor, Desai and Herndon23). Considerable attention has focused on attenuating this response with early nutritional support, with one study involving the administration of a protein hydrolysate. Demling & DeSanti(Reference Demling and DeSanti24) compared the effect of two diets – a standard nutrient supplement (protein intake 1·3–1·5 g/kg per d) and a high-protein diet plus protein hydrolysate (70 g/d; protein intake 1·7–2 g/kg per d) on the recovery of fifteen patients with severe burns. While both groups gained weight and improved muscle strength and endurance, the increase in protein intake with the high-protein/hydrolysate diet increased the rate of restoration of body weight and muscle function(Reference Demling and DeSanti24). However, the design of this study did not allow for determination of whether the more rapid recovery was due to either the high protein content of the diet or to the inclusion of the hydrolysate into the diet.

Effect on gastric repair

The benefits of providing hydrolysed protein preparations has been studied in patients with peptic ulcers or gastric haemorrhages who require additional protein intake without adding dietary bulk(Reference Levy2). In a group of patients with hypoproteinaemia following gastrointestinal haemorrhage, compared with a standard diet, patients who consumed the standard diet and an additional 150–200 g of protein hydrolysate returned to normal circulating protein levels in 10·2 d, where as those on the standard diet only returned to normal protein levels in 19·5 d(Reference Levy2). The patients consuming hydrolysed protein also reported feeling better and stronger, and experienced an improved sense of well-being compared with controls(Reference Levy2). Tui(Reference Tui15) also observed improved symptoms and ulcer healing in 164 patients with previously intractable peptic ulcers who were given very high-protein diets in the form of partially hydrolysed protein (0·6 g N/kg/d) in an uncontrolled study.

There are several suggestions regarding how protein hydrolysates might promote the healing of peptic ulcers. The prompt recovery response is thought to be due to a combination of the neutralisation of the acidity of the gastric juice by the strong buffer action of protein hydrolysates, reduced work of digestion due to the protein already being partially digested, and the rapid provision of essential protein components and amino acids for tissue repair(Reference Tui15). Hence the action of neutralisation of the gastric acid in addition to a rich nutrient supply is believed to promote a more rapid tissue repair(Reference Tui1).

Effect on pressure ulcer recovery

Nutritional supplements, specifically high-protein diets, are often used for the treatment and/or prevention of pressure ulcers (bed sores), although the research supporting this use is limited. An association between protein nutrition status and the maintenance of tissue integrity was observed by Mulholland et al. (Reference Mulholland, Tui and Wright25) as long ago as 1943 when they found that low plasma protein levels were associated with the occurrence of bed sores and that the ulcers healed promptly when N balance was restored. This finding was interpreted as suggesting that protein-deficient tissues undergo pressure necrosis more readily than normal tissue(Reference Mulholland, Tui and Wright25).

More recently, a study which examined the effect of a collagen protein hydrolysate supplement on pressure ulcer healing demonstrated more rapid healing compared with standard treatment(Reference Lee, Posthauer and Dorner26). Seventy-one long-term care residents with pressure ulcers were given standard care plus either a concentrated fortified collagen protein hydrolysate supplement or placebo. Residents who received the supplement and standard care had significantly better healing (combined score for parameters of exudate, wound surface area and tissue type) compared with standard care with the placebo after 8 weeks of treatment(Reference Lee, Posthauer and Dorner26). While both groups had decreased scores, indicating healing, the protein hydrolysate group had approximately twice the rate of healing compared with the standard care-only group, indicating that the collagen hydrolysate enhanced the recovery process. However, the mechanism by which the more rapid tissue repair occurred was not identified in this study.

Effect on preventing the development of atopic dermatitis-like skin lesions

Whey protein hydrolysates have also been investigated for their effect on the development of atopic dermatitis-like skin lesions. Shimizu et al. (Reference Shimizu, Dairiki and Ogawa27) compared the effect of a whey protein hydrolysate, casein and a casein protein hydrolysate diet on the development of atopic dermatitis-like skin lesions induced by mite antigen in NC/Nga mice. Thirty-five mice were fed one of the diets for 2 weeks before and during 4 weeks of mite antigen application. Whey protein hydrolysate-fed mice showed significantly less atopic dermatitis-like skin lesions at 2 and 4 weeks, whereas both casein protein hydrolysate- and casein-fed mice manifested in a similar manner, with no inhibitory effect(Reference Shimizu, Dairiki and Ogawa27). Serum soluble E-selectin was significantly lower with the whey protein hydrolysate diet and correlated with skin scores (the degree of erythema/haemorrhage, oedema, excoriation/erosion and dryness)(Reference Shimizu, Dairiki and Ogawa27). The pathologic tissue of the whey protein hydrolysate-fed mice had less infiltration of inflammatory cells, such as neutrophils than the casein protein hydrolysate-fed mice(Reference Shimizu, Dairiki and Ogawa27). IgE levels were similarly elevated in all groups, suggesting that the mechanism for the suppressive effect of whey protein hydrolysate on atopic dermatitis-like skin lesions is independent of IgE production(Reference Shimizu, Dairiki and Ogawa27). There was also no difference in cell proliferation or cytokine production from cervical lymph nodes, suggesting that the suppressive effect of whey protein hydrolysate on atopic dermatitis-like skin lesions did not involve T cells(Reference Shimizu, Dairiki and Ogawa27). The authors proposed that it was probably due to different effects on macrophages at the inflammation site through the different peptides resulting from whey and casein protein digestion(Reference Shimizu, Dairiki and Ogawa27); however, further research is needed to investigate these mechanisms.

Effect on recovery from muscle damage

Muscle protein synthesis is depressed for several hours following tissue injury(Reference Lowe, Warren and Ingalls28) and exercise(Reference Rennie and Tipton29) while the rate of protein degradation is increased for days. This results in a net loss of total protein and limits the rate of restoration of function(Reference Lowe, Warren and Ingalls28). By counteracting the negative N balance that occurs after muscle injury, supplementation that can attenuate functional losses or accelerate recovery may be useful. It is possible that protein hydrolysates may be useful for enhancing the recovery from exercise, specifically recovery of muscle damage induced by exhaustive exercise(Reference Saunders, Moore and Kies30Reference Cooke, Rybalka and Stathis32).

Eccentric exercise is associated with skeletal muscle damage and the more rapid repair of this damage would facilitate a more rapid recovery of contractile function and may be accelerated by protein hydrolysates. Buckley et al. (Reference Buckley, Thomson and Coates31) observed that a single dose of a whey protein isolate hydrolysate (25 g) resulted in a more rapid recovery of muscle force-generating capacity following eccentric exercise compared with flavoured water or a non-hydrolysed whey protein isolate. Participants consuming the whey protein hydrolysate had complete muscle strength recovery by 6 h post-exercise while muscle strength in the other groups was still suppressed at 24 h. The mechanism underlying the enhanced recovery was not apparent but was thought to be due to the supplement accelerating tissue repair. Despite the more rapid recovery of muscle strength the whey protein hydrolysate had no effect on muscle soreness or blood markers of muscle damage and inflammation(Reference Buckley, Thomson and Coates31), although the authors argued that the relatively short time period (i.e. 24 h) over which the assessments were conducted may have been too short for changes in blood markers to manifest.

Similarly, Cooke et al. (Reference Cooke, Rybalka and Stathis32) compared a carbohydrate supplement with a hydrolysed whey protein isolate (about 120 g/d) following muscle-damaging exercise. The hydrolysed whey protein isolate resulted in an attenuation of the exercise-induced force reduction during the recovery period(Reference Cooke, Rybalka and Stathis32). It was suggested this was due to an increase in protein synthesis from the essential amino acids contained in the whey protein hydrolysate supplement and also attributed to a reduction in the extent of muscle damage as suggested by a trend for lower plasma lactate dehydrogenase(Reference Cooke, Rybalka and Stathis32).

Intense and prolonged exercise causes a decrease in glutamine levels, which may lead to immunosuppression and consequently a higher incidence of infection and illness and delayed wound healing(Reference Parry-Billings, Budgett and Koutedakis33). Thus, an increase in glutamine status is required for muscle restoration. Protein hydrolysates, specifically hydrolysed whey protein isolate, contain high concentrations of essential amino acids, including BCAA which are the major precursors for glutamine synthesis. The consumption of whey protein hydrolysates has been shown to increase plasma and muscle glutamine stores(Reference Castell and Newsholme34) and, thus, supplementation with a rich source of BCAA, such as whey protein hydrolysates, may attenuate the decline in plasma glutamine levels seen after intense endurance exercise(Reference Bassit, Sawada and Bacurau35) and thus contribute to the maintenance of tissue integrity or promote tissue repair.

Proposed mechanisms of action

Enhanced availability

The absorption of amino acids by the intestine can have a critical influence on their availability to peripheral tissues and therefore the kinetics of amino acid absorption can largely mediate their subsequent effects on wound healing and muscle protein anabolism(Reference Manninen7). It has been suggested that the ingestion of a fast-acting protein hydrolysate (i.e. one which is rapidly broken down and absorbed) results in a less efficient uptake by the splanchnic bed, resulting in a more rapid increase in circulating amino acid concentrations(Reference Manninen7) and thus maximises tissue amino acid delivery.

It is generally accepted that protein hydrolysates are absorbed faster and utilised more effectively than intact proteins(Reference Bucci, Unlu, Wolinsky and Driskell6, Reference Manninen7, Reference Di Pasquale9, Reference Poullain, Cezard and Roger10, Reference Koopman, Crombach and Gijsen36Reference Manninen38). A number of studies have shown that the same N load is absorbed faster when delivered as hydrolysed protein, or di- and tri-peptides rather than as whole protein or free amino acids(Reference Silk, Chung and Berger37Reference Morifuji, Ishizaka and Baba39) and this results in significantly greater increases in plasma concentrations of amino acids and dipeptides(Reference Morifuji, Ishizaka and Baba39). These greater increases in absorption and appearance of amino acids in plasma have also been associated with greater incorporation of N into protein, with a number of studies demonstrating greater N incorporation into tissue protein in animals fed hydrolysed whey peptides compared with intact protein(Reference Poullain, Cezard and Roger10, Reference Boza, Moënnoz and Vuichoud40). However, some studies have failed to demonstrate a greater increase in circulating amino acid concentrations following consumption of hydrolysed protein. Farnfield et al. (Reference Farnfield, Trenerry and Carey41) reported that compared with consuming 25 g of whey protein isolate, the consumption of 25 g hydrolysed whey protein isolate led to a slower rate of increase in plasma amino acid concentrations over the 2 h period immediately post-consumption. Power et al. (Reference Power, Hallihan and Jakeman11) also found no difference in the rate of increase of BCAA in the circulation and no difference in the estimated rate of gastric emptying over 3 h following the ingestion of 45 g of intact whey protein or whey protein hydrolysate. The rate of increase in plasma amino acid concentration also appears to be related to the type of protein consumed, as plasma amino acid concentrations have been shown to increase more when a whey protein hydrolysate was consumed compared with a soya protein hydrolysate(Reference Morifuji, Ishizaka and Baba39). The effects on circulating amino acid concentrations, and the mechanisms regulating the magnitude of increase in concentration, might be specific to the particular protein or protein hydrolysate consumed, which in turn might be related to the manufacturing processes to which the protein has been subjected. Hydrolysates can be produced by fermentation or by enzymic hydrolysis. The endproduct depends to a great extent on the duration of hydrolysis and, for enzymic methods, on the pH and enzymes used, which can alter the composition of different proteins in protein isolates and the level of hydrolysis in protein hydrolysates(Reference Manninen7, Reference Clemente8, Reference Neklyudov, Ivankin and Berdutina42). Additional research is required to allow us to better understand the factors that influence amino acid bioavailability as this can make an impact substantially on protein synthesis rates, and therefore potentially influence tissue repair. In particular, effects on the bioavailability of the BCAA leucine, as well as valine and isoleucine, are important to study given the important role of these amino acids in stimulating protein synthesis(Reference Buse and Reid43).

Studies have investigated the acute response of muscle protein synthesis to the ingestion of protein hydrolysates. One study compared the effects of rapidly digested (whey hydrolysate and soya protein) and slowly digested protein (casein) on muscle protein synthesis at rest and after resistance exercise and found that the consumption of whey protein hydrolysates stimulated the greatest degree of muscle protein synthesis(Reference Tang, Moore and Kujbida44). Another study compared carbohydrate with and without a casein protein hydrolysate during a 2 h resistance exercise session(Reference Beelen, Koopman and Gijsen45). Protein co-ingestion led to higher plasma amino acid concentrations, higher protein oxidation and synthesis rates, and lower whole-body protein breakdown, which promoted a positive whole-body net protein balance(Reference Beelen, Koopman and Gijsen45).

Another study found that a whey protein hydrolysate, compared with a free amino acid formula, led to higher N retention and glutamine stores (plasma and muscle concentrations), despite higher glutamine intake with the amino acid formula(Reference Boza, Moënnoz and Vuichoud40). The whey protein hydrolysate formula also showed significantly higher energy conversion efficiency, protein efficiency ratio, N protein utilisation (retention) and biological value than the amino acid formula(Reference Boza, Moënnoz and Vuichoud40). These effects might have been due, at least in part, to the amino acid composition and higher digestibility of the hydrolysate formula (i.e. absorbed N/ingested N) promoting higher plasma essential amino acid concentrations and essential/non-essential amino acid ratios than those fed with the amino acid formula, despite the amino acid formula providing a higher intake of essential amino acids(Reference Boza, Moënnoz and Vuichoud40). The greater increase in glutamine stores with the whey protein hydrolysate diet may have important implications for tissue recovery. Glutamine, an important fuel for some cells of the immune system, may have specific immunostimulatory effects(Reference Castell and Newsholme34) and is known to be depleted after severe tissue injury. Rats that were fed the whey protein hydrolysate diet restored their plasma and muscle glutamine pools whereas the rats fed with the amino acid formula, which was richer in glutamine, did not(Reference Boza, Moënnoz and Vuichoud40). During tissue injury and inflammation immune cells increase their glutamine consumption(Reference Wilmore and Shabert46). If tissue glutamine requirements are not met by dietary intake or endogenous production, this leads to a state of glutamine deficiency. During glutamine deficiency, tissue stores become depleted and plasma and whole blood glutamine concentrations decrease, which limits the ability to achieve optimal responses to catabolism, inflammation and infection(Reference Wilmore and Shabert46, Reference Lacey and Wilmore47) and can lead to a negative protein balance(Reference Hall, Heel and McCauley48).

Increase in levels of insulin

Protein hydrolysates have been shown to produce greater insulinotropic effects compared with intact proteins(Reference Power, Hallihan and Jakeman11, Reference Calbet and MacLean49) and it has been suggested that this enhanced insulin response contributes to protein anabolism(Reference Calbet and MacLean49). Increasing plasma insulin levels stimulate muscle protein synthesis and attenuate protein catabolism after injury(Reference Woolfson, Heatley and Allison13, Reference Odessey and Parr14) and enhance muscle and tissue uptake of BCAA. It has been suggested that the extent of the insulinotropic response is dependent on both the source and degree of hydrolysis of the protein(Reference Claessens, Saris and van Baak50) and different amino acids/peptides have been shown to have varying insulinotropic responses. A recent study found that whey protein hydrolysates caused significantly greater increases in insulin compared with whey protein, soya protein and soya protein hydrolysates(Reference Morifuji, Ishizaka and Baba39). Another study found that peak plasma insulin concentrations were 28 % higher following the ingestion of hydrolysed whey protein compared with intact whey protein isolate(Reference Power, Hallihan and Jakeman11) and this was independent of blood glucose concentrations. Both pea and whey protein hydrolysates have also elicited a peak insulin response two to four times greater than cows' milk (control) and this was closely related to a greater increase in plasma amino acid levels, especially leucine, isoleucine, valine, phenylalanine and arginine(Reference Calbet and MacLean49). On the other hand, it has been shown that despite no differences in gastric emptying rates and amino acid absorption, peptide hydrolysates (casein and whey) elicited about 50 % more gastric secretion than their corresponding whole proteins(Reference Calbet and Holst51). This consequently led to higher plasma levels of glucose-dependent insulinotropic polypeptide, an incretin hormone during the first 20 min of the gastric-emptying process(Reference Calbet and Holst51). However, some studies have shown no difference in insulin and glucagon concentrations after the ingestion of intact whey protein and its hydrolysate(Reference Claessens, Saris and van Baak50). Differences in insulinotropic potential between various protein hydrolysates are probably associated with amino acid composition and/or the average amino acid chain length of the protein hydrolysate.

The mechanism by which the ingestion of protein increases circulating insulin is still uncertain. Several postulated mechanisms include a change in gastric emptying(Reference Calbet and MacLean49), the magnitude of change in circulating essential amino acids and the secretion of incretin hormones from the gut(Reference Holst and Gromada52). However, Power et al. (Reference Power, Hallihan and Jakeman11) found no significant difference in gastric emptying time and rate of appearance of BCAA over a 3 h period following the ingestion of hydrolysed whey protein and whey protein isolate. Postprandial increases in circulating essential amino acids stimulate a marked rise in protein synthesis(Reference Tipton, Ferrando and Phillips53, Reference Fujita, Dreyer and Drummond54), and this effect appears to be due to amino acids themselves acting as the stimulus and not an effect due to the modest increases in insulin that result from amino acid ingestion(Reference Greenhaff, Karagounis and Peirce55).

Bioactive properties

It has also been proposed that protein hydrolysates may have impacts beyond the simple supply of nutritional requirements for amino acids(Reference Crittenden, Buckley and Cameron-Smith56). The physiological effects of protein hydrolysates, in particular the ability to speed recovery from exercise, may be due to the presence of particular peptide(s) that are produced during the hydrolysis process. This suggestion is supported by that fact that several peptides with known biological activity that are not possessed by the native protein can be produced by the hydrolysis of that protein(Reference Korhonen and Pihlanto57, Reference Meisel58). An example is the production of angiotensin I-converting enzyme-inhibitory peptides from milk protein following enzymic hydrolysis or food processing(Reference Pihlanto-Leppälä59). Further research is needed to identify other bioactive properties of protein hydrolysates that may assist in various types of tissue repair.

Conclusion

Protein hydrolysates show potential for enhancing various types of tissue repair. They provide a rich source of protein which can be useful in situations where excess protein is needed, such as tissue repair. This consequently aids in enhancing recovery from surgery, ulcers, burns, muscle-damaging exercise and even preventing muscle soreness and enhancing exercise performance. Additional research is needed to further examine the various roles and mechanisms behind protein hydrolysates enhancing tissue repair and recovery.

Acknowledgements

This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

R. T. drafted the manuscript and J. B. assisted in revising and interpretation.

There are no conflicts of interest.

References

1Tui, C (1945) The value of protein and its chemical components (amino acids) in surgical repair. Bull N Y Acad Med 21, 631655.Google ScholarPubMed
2Levy, JS (1952) The use of protein hydrolysates in the therapy of peptic ulcer. South Med J 45, 59.CrossRefGoogle ScholarPubMed
3Harvey, SC & Howes, EL (1930) Effect of high protein diet on the velocity of growth of fibroblasts in the healing wound. Ann Surg 91, 641650.CrossRefGoogle ScholarPubMed
4Learmonth, JR & Cuthbertson, DP (1946) Nutritional factors affecting wound healing. Proc Nutr Soc 4, 185193.CrossRefGoogle ScholarPubMed
5Sinha, R, Radha, C, Prakash, J, et al. . (2007) Whey protein hydrolysate: functional properties, nutritional quality and utilization in beverage formulation. Food Chem 101, 14841491.CrossRefGoogle Scholar
6Bucci, LR & Unlu, L (2000) Protein and amino acid supplements in exercise and sport. In Energy-Yielding Macronutrients and Energy Metabolism in Sports Nutrition, pp. 191212 [Wolinsky, I and Driskell, JA, editors]. Boca Raton, FL: CRC Press.Google Scholar
7Manninen, A (2009) Protein hydrolysates in sports nutrition. Nutr Metab (Lond) 6, 38.CrossRefGoogle ScholarPubMed
8Clemente, A (2000) Enzymatic protein hydrolysates in human nutrition. Trends Food Sci Technol 11, 254262.CrossRefGoogle Scholar
9Di Pasquale, MG (1997) Amino Acids and Proteins for the Athlete – The Anabolic Edge. Boca Raton, FL: CRC Press.Google Scholar
10Poullain, M-G, Cezard, J-P, Roger, L, et al. . (1989) Effect of whey proteins, their oligopeptide hydrolysates and free amino acid mixtures on growth and nitrogen retention in fed and starved rats. JPEN J Parenter Enteral Nutr 13, 382386.CrossRefGoogle ScholarPubMed
11Power, O, Hallihan, A & Jakeman, P (2009) Human insulinotropic response to oral ingestion of native and hydrolysed whey protein. Amino Acids 37, 333339.CrossRefGoogle ScholarPubMed
12Manninen, AH (2006) Hyperinsulinaemia, hyperaminoacidaemia and post-exercise muscle anabolism: the search for the optimal recovery drink. Br J Sports Med 40, 900905.CrossRefGoogle ScholarPubMed
13Woolfson, AM, Heatley, RV & Allison, SP (1979) Insulin to inhibit protein catabolism after injury. N Engl J Med 300, 1417.CrossRefGoogle ScholarPubMed
14Odessey, R & Parr, B (1982) Effect of insulin and leucine on protein turnover in rat soleus muscle after burn injury. Metabolism 31, 8287.CrossRefGoogle ScholarPubMed
15Tui, C (1947) The ambulatory treatment of peptic ulcers with protein hydrolysates and dextri-maltose. Rev Gastroenterol 14, 108129.Google Scholar
16Levenson, SMMD & Lund, CCMD (1948) Protein metabolism in surgical patients. Am J Nurs 48, 415417.Google ScholarPubMed
17Clague, MB, Keir, MJ, Wright, PD, et al. . (1983) The effects of nutrition and trauma on whole-body protein metabolism in man. Clin Sci (Lond) 65, 165175.CrossRefGoogle ScholarPubMed
18Tashiro, T, Yamamori, H, Takagi, K, et al. . (1996) Effect of severity of stress on whole-body protein kinetics in surgical patients receiving parenteral nutrition. Nutrition 12, 763765.CrossRefGoogle ScholarPubMed
19Tashiro, T, Yamamori, H, Takagi, K, et al. . (1996) Increased contribution by myofibrillar protein to whole-body protein breakdown according to severity of surgical stress. Nutrition 12, 685689.CrossRefGoogle ScholarPubMed
20Yamamori, H, Tashiro, T, Mashima, Y, et al. . (1987) Effects of severity of surgical trauma on whole body protein turnover in patients receiving total parenteral nutrition. JPEN J Parenter Enteral Nutr 11, 454457.CrossRefGoogle ScholarPubMed
21Ziegler, F, Ollivier, JM, Cynober, L, et al. . (1990) Efficiency of enteral nitrogen support in surgical patients: small peptides v non-degraded proteins. Gut 31, 12771283.CrossRefGoogle ScholarPubMed
22Bessey, PQ, Jiang, ZM, Johnson, DJ, et al. . (1989) Posttraumatic skeletal muscle proteolysis: the role of the hormonal environment. World J Surg 13, 465471.CrossRefGoogle ScholarPubMed
23Jahoor, F, Desai, M, Herndon, DN, et al. . (1988) Dynamics of the protein metabolic response to burn injury. Metabolism 37, 330337.CrossRefGoogle ScholarPubMed
24Demling, RH & DeSanti, L (1998) Increased protein intake during the recovery phase after severe burns increases body weight gain and muscle function. J Burn Care Rehabil 19, 161168.CrossRefGoogle ScholarPubMed
25Mulholland, JH, Tui, C, Wright, AM, et al. . (1943) Protein metabolism and bed sores. Ann Surg 118, 10151023.CrossRefGoogle ScholarPubMed
26Lee, SK, Posthauer, ME, Dorner, B, et al. . (2006) Pressure ulcer healing with a concentrated, fortified, collagen protein hydrolysate supplement: a randomized controlled trial. Adv Skin Wound Care 19, 9296.CrossRefGoogle ScholarPubMed
27Shimizu, N, Dairiki, K, Ogawa, S, et al. . (2006) Dietary whey protein hydrolysate suppresses development of atopic dermatitis-like skin lesions induced by mite antigen in NC/Nga mice. Allergol Int 55, 185189.CrossRefGoogle ScholarPubMed
28Lowe, DA, Warren, GL, Ingalls, CP, et al. . (1995) Muscle function and protein metabolism after initiation of eccentric contraction-induced injury. J Appl Physiol 79, 12601270.CrossRefGoogle ScholarPubMed
29Rennie, MJ & Tipton, KD (2000) Protein and amino acid metabolism during and after exercise and the effects of nutrition. Annu Rev Nutr 20, 457483.CrossRefGoogle ScholarPubMed
30Saunders, MJ, Moore, RW, Kies, AK, et al. . (2009) Carbohydrate and protein hydrolysate coingestions improvement of late-exercise time-trial performance. Int J Sport Nutr Exerc Metab 19, 136149.CrossRefGoogle ScholarPubMed
31Buckley, JD, Thomson, RL, Coates, AM, et al. . (2010) Supplementation with a whey protein hydrolysate enhances recovery of muscle force-generating capacity following eccentric exercise. J Sci Med Sport 13, 178181.CrossRefGoogle ScholarPubMed
32Cooke, M, Rybalka, E, Stathis, C, et al. . (2010) Whey protein isolate attenuates strength decline after eccentrically-induced muscle damage in healthy individuals. J Int Soc Sports Nutr 7, 30.CrossRefGoogle ScholarPubMed
33Parry-Billings, M, Budgett, R, Koutedakis, Y, et al. . (1992) Plasma amino acid concentrations in the overtraining syndrome: possible effects on the immune system. Med Sci Sports Exerc 24, 13531358.CrossRefGoogle ScholarPubMed
34Castell, LM & Newsholme, EA (1998) Glutamine and the effects of exhaustive exercise upon the immune response. Can J Physiol Pharmacol 76, 524532.CrossRefGoogle ScholarPubMed
35Bassit, RA, Sawada, LA, Bacurau, RFP, et al. . (2002) Branched-chain amino acid supplementation and the immune response of long-distance athletes. Nutrition 18, 376379.CrossRefGoogle ScholarPubMed
36Koopman, R, Crombach, N, Gijsen, AP, et al. . (2009) Ingestion of a protein hydrolysate is accompanied by an accelerated in vivo digestion and absorption rate when compared with its intact protein. Am J Clin Nutr 90, 106115.CrossRefGoogle ScholarPubMed
37Silk, DB, Chung, YC, Berger, KL, et al. . (1979) Comparison of oral feeding of peptide and amino acid meals to normal human subjects. Gut 20, 291299.CrossRefGoogle ScholarPubMed
38Manninen, AH (2004) Protein hydrolysates in sports and exercise: a brief review. J Sports Sci Med 3, 6063.Google ScholarPubMed
39Morifuji, M, Ishizaka, M, Baba, S, et al. . (2010) Comparison of different sources and degrees of hydrolysis of dietary protein: effect on plasma amino acids, dipeptides, and insulin responses in human subjects. J Agric Food Chem 58, 87888797.CrossRefGoogle ScholarPubMed
40Boza, JJ, Moënnoz, D, Vuichoud, J, et al. . (2000) Protein hydrolysate vs free amino acid-based diets on the nutritional recovery of the starved rat. Eur J Nutr 39, 237243.CrossRefGoogle ScholarPubMed
41Farnfield, MM, Trenerry, C, Carey, KA, et al. . (2009) Plasma amino acid response after ingestion of different whey protein fractions. Int J Food Sci Nutr 60, 476486.CrossRefGoogle ScholarPubMed
42Neklyudov, A, Ivankin, A & Berdutina, A (2000) Properties and uses of protein hydrolysates (Review). Appl Biochem Microbiol 36, 452459.CrossRefGoogle Scholar
43Buse, MG & Reid, SS (1975) Leucine: a possible regulator of protein turnover in muscle. J Clin Invest 56, 12501261.CrossRefGoogle ScholarPubMed
44Tang, JE, Moore, DR, Kujbida, GW, et al. . (2009) Ingestion of whey hydrolysate, casein, or soy protein isolate: effects on mixed muscle protein synthesis at rest and following resistance exercise in young men. J Appl Physiol 107, 987992.CrossRefGoogle ScholarPubMed
45Beelen, M, Koopman, R, Gijsen, AP, et al. . (2008) Protein coingestion stimulates muscle protein synthesis during resistance-type exercise. Am J Physiol Endocrinol Metab 295, E70E77.CrossRefGoogle ScholarPubMed
46Wilmore, DW & Shabert, JK (1998) Role of glutamine in immunologic responses. Nutrition 14, 618626.CrossRefGoogle ScholarPubMed
47Lacey, JM & Wilmore, DW (1990) Is glutamine a conditionally essential amino acid? Nutr Rev 48, 297309.CrossRefGoogle ScholarPubMed
48Hall, JC, Heel, K & McCauley, R (1996) Glutamine. Br J Surg 83, 305312.CrossRefGoogle ScholarPubMed
49Calbet, JAL & MacLean, DA (2002) Plasma glucagon and insulin responses depend on the rate of appearance of amino acids after ingestion of different protein solutions in humans. J Nutr 132, 21742182.CrossRefGoogle ScholarPubMed
50Claessens, M, Saris, WHM & van Baak, MA (2008) Glucagon and insulin responses after ingestion of different amounts of intact and hydrolysed proteins. Br J Nutr 100, 6169.CrossRefGoogle ScholarPubMed
51Calbet, JA & Holst, JJ (2004) Gastric emptying, gastric secretion and enterogastrone response after administration of milk proteins or their peptide hydrolysates in humans. Eur J Nutr 43, 127139.CrossRefGoogle ScholarPubMed
52Holst, JJ & Gromada, J (2004) Role of incretin hormones in the regulation of insulin secretion in diabetic and nondiabetic humans. Am J Physiol Endocrinol Metab 287, E199E206.CrossRefGoogle ScholarPubMed
53Tipton, KD, Ferrando, AA, Phillips, SM, et al. . (1999) Postexercise net protein synthesis in human muscle from orally administered amino acids. Am J Physiol Endocrinol Metab 276, E628E634.CrossRefGoogle ScholarPubMed
54Fujita, S, Dreyer, HC, Drummond, MJ, et al. . (2007) Nutrient signalling in the regulation of human muscle protein synthesis. J Physiol 582, 813823.CrossRefGoogle ScholarPubMed
55Greenhaff, PL, Karagounis, LG, Peirce, N, et al. . (2008) Disassociation between the effects of amino acids and insulin on signaling, ubiquitin ligases, and protein turnover in human muscle. Am J Physiol Endocrinol Metab 295, E595E604.CrossRefGoogle ScholarPubMed
56Crittenden, R, Buckley, JD, Cameron-Smith, D, et al. . (2009) Functional dairy protein supplements for elite athletes. Aust J Dairy Technol 64, 133137.Google Scholar
57Korhonen, H & Pihlanto, A (2003) Food-derived bioactive peptides – opportunities for designing future foods. Curr Pharm Des 9, 12971308.CrossRefGoogle ScholarPubMed
58Meisel, H (2005) Biochemical properties of peptides encrypted in bovine milk proteins. Curr Med Chem 12, 19051919.CrossRefGoogle ScholarPubMed
59Pihlanto-Leppälä, A (2000) Bioactive peptides derived from bovine whey proteins: opioid and ACE-inhibitory peptides. Trends Food Sci Technol 11, 347356.CrossRefGoogle Scholar