Amino acids, antioxidative status and reproduction: methionine and cysteine

In reproducing animals, the hormonal regulation of the ovarian metabolism generates reactive oxygen species and free radicals⁽ Reference Agarwal, Gupta and Sharma ^{5 )} that must be neutralised locally by antioxidants such as vitamin E, vitamin C and by the Se-dependent glutathione peroxidase (GSH-Px) system. A constant and adequate antioxidant status is critical for optimal ovulation both in terms of quantity and quality. This is particularly important in hyperprolific lines of sows, because of the poor quality of oocytes shed by the supplemental follicles⁽ Reference Driancourt, Martinat-Botté and Terqui ^{6 )}.

The metabolism of oxidised and reduced glutathione, as well as the enzymes GSH-Px and glutathione reductase, are closely related to cysteine and methionine via the key metabolite homocysteine. Homocysteine is an intermediate AA that can be metabolised by transmethylation (towards methionine) or transsulfuration (towards cysteine and glutathione, the precursor of GSH-Px). In fact, reactive oxygen species and peroxides up-regulate transsulfuration and down-regulate transmethylation⁽ Reference Mosharov, Cranford and Banerjee ^{7 )}. Therefore, the presence (or the production) of oxidative metabolites stimulates the transsulfuration pathway, which will in turn neutralise these metabolites.

The animal metabolism does not distinguish between sulfur forms of methionine and cysteine and their Se analogues⁽ Reference Daniels ^{8 )}. Under oxidative pressure, both seleno-cysteine and seleno-homocysteine are thus key factors just like their sulfur forms. Seleno-cysteine is either supplied directly by the diet or is derived from seleno-methionine after transsulfuration, a metabolic reaction that is up-regulated by redox changes⁽ Reference Mosharov, Cranford and Banerjee ^{7 )}. Then, it is mineralised to selenide and Se phosphate⁽ Reference Johansson, Gafvelin and Arner ^{9 –} Reference Yasumoto, Iwami and Yoshida ^{11 )} and resynthesised into a seleno-cysteinyl moiety that modulates gene expression and activates Se-dependent enzyme, GSH-Px⁽ Reference Johansson, Gafvelin and Arner ^{9 ,} Reference Flohé, Wingender, Brigelus-Flohé, Forman and Cadenas ^{12 )}. This metabolic control was observed recently in pigs⁽ Reference Fortier, Audet and Giguère ^{13 )} by studying homoeostasis of Se-dependent GSH-Px during the peri-estral period under oxidative pressure (Fig. 1). The Se-dependent GSH-Px activity dropped shortly after ovulation in control gilts, while the synthesis of GSH-Px was maintained and enhanced by dietary supplementation of respectively inorganic and organic Se. This drop in GSH-Px activity of the control gilts is in agreement with the earlier-mentioned transient and local demand for antioxidants at ovulation. In contrast, there was an up-regulation of GSH-Px in gilts supplemented with organic Se in synchrony with the pro-oxidative conditions brought by ovulation. The inorganic source of Se (selenite, the dietary form routinely used in animal nutrition) is rapidly transformed to selenide and Se-phosphate⁽ Reference Johansson, Gafvelin and Arner ^{9 –} Reference Yasumoto, Iwami and Yoshida ^{11 )} and short-circuits the transsulfuration and the regulation of GSH-Px by redox changes. Therefore, it appears that inorganic Se produces a readily and persistent response to GSH-Px, independent of the need for this enzyme, while the response to seleno-AA directs the Se flow through a succession of metabolic steps in response to redox changes.

Fig. 1. Blood Se-dependent glutathione peroxidase (GSH-Px) activity during the peri-estrus period in gilts according to the level and source of dietary Se. Gilts were offered a control diet containing a basal level of 0·2 mg/kg Se, or a diet supplemented with 0·3 mg/kg of either inorganic selenite (MSe) or organic Se (OSe). Day 0=third estrus. One unit (U) of GSH-Px activity equals 1 μmol of NADPH oxidised per minute. Values are Least Squares means and maxima se were 206·5, 123·9, 147·5, 146·8, 129·7, 155·8, 165·1 and 195·6 for days −4, −3, −2, −1, 0, 1, 2 and 3 (adapted from⁽ Reference Fortier, Audet and Giguère ^{13 )}).

Several reactions of the transsulfuration pathway, which is involved in the fate of organic Se for the control of the GSH-Px system, are pyridoxine (vitamin B₆)-dependent⁽ Reference Yasumoto, Iwami and Yoshida ^{11 )}. In a recent experiment, the importance of pyridoxine for an adequate flow of organic Se (Se-cysteine) towards the GSH-Px system was demonstrated in response to oxidative pressure induced by the peri-estrus period in sows⁽ Reference Roy, Audet and Palin ^{14 )}. Indeed, gene expressions of GSH-Px and Se-cysteine oxidase (control of the flow of Se-cysteine to the GSH-Px system) in the cytosol of both liver and kidney cells were 50–70% greater in gilts supplemented with an organic source of Se and vitamin B₆ as compared with the other groups, either unsupplemented, supplemented with inorganic Se (with or without vitamin B₆), or with organic Se without vitamin B₆. In terms of reproductive performance, ovulation rate was approximately 23% greater in gilts supplemented with organic Se and vitamin B₆ ⁽ Reference Roy, Audet and Palin ^{14 )}. These last two effects highlight the crucial role of micronutrients modulating the metabolic pathways of AA, such as seleno-analogues of methionine and cysteine, towards regulation of antioxidation and eventually optimal ovulation conditions.

Fetus development and lactation: l-arginine

A moderate to extensive dietary supplementation with specific AA can have important physiological effects on reproduction. l-Arginine is the common precursor for NO and polyamines, which are key regulators of angiogenesis, embryogenesis, and placental and fetal growth. Arginine is particularly abundant in porcine allantoic fluid, and associated with high rates of synthesis of NO and polyamines in the placenta during the first half of pregnancy⁽ Reference Wu, Bazer and Wallace ^{15 )}. This led to the hypothesis that dietary supplementation with l-arginine to sows may stimulate placental growth to promote conceptus survival, growth and development of some tissues (Fig. 2). Studies have consistently shown an effect of l-arginine supplementation during gestation on reproductive performance; however, the effects vary according to treatment period and dose. When given during early gestation (0–25 d of gestation)⁽ Reference Li, Bazer and Johnson ^{16 )}, l-arginine improved placental vascularity regardless of the dose. However, it had no effect on survival and weight of the embryos at a dose of 8 g/d supplemented arginine but had an adverse effect on these traits at a dose of 16 g/d. When supplementation started during embryonic implantation and lasted for 2 weeks (from 14 to 28 d of gestation) at a dose of 25 g/d supplemented arginine, a positive effect was observed on placental vascularity⁽ Reference Hazeleger, Ramaekers, Smits, Wiseman, Varley, McOrist and Kemp ^{17 )}. Additionally, it resulted in an increased number of fetuses (+1 to +3 fetuses)⁽ Reference Hazeleger, Ramaekers, Smits, Wiseman, Varley, McOrist and Kemp ^{17 ,} Reference Berard and Bee ^{18 )} or in an increased number of piglets born alive (+1 piglet)⁽ Reference Ramaekers, Kemp and van der Lende ^{19 )}. Importantly, this treatment did not reduce within-litter birth weight⁽ Reference Ramaekers, Kemp and van der Lende ^{19 )}. When given from 30 d of gestation to term at the dose of 20 g/d supplemented arginine, a positive effect on litter size was still observed (+2 piglets born alive) without detrimental effects on within-litter birth weight and variation in birth weight⁽ Reference Mateo, Wu and Bazer ^{20 )}.

Fig. 2. Schematic involvement of arginine, NO and polyamines in fetal development (adapted from⁽ Reference Wu, Bazer and Wallace ^{15 )}).

Dietary supplementation with l-arginine may also benefit piglets, irrespective of the l-arginine given to the lactation sow⁽ Reference Mateo, Wu and Moon ^{21 )} or directly to the piglet⁽ Reference Kim, McPherson and Wu ^{22 ,} Reference Yao, Yin and Chu ^{23 )}. Supplementing the lactation diet with 1% l-arginine has been shown to increase the concentration of most AA in milk compared with the control group⁽ Reference Mateo, Wu and Moon ^{21 )}. This greater transfer of AA in the milk could be related to the positive effects of l-arginine on vascularity and blood flow to the mammary gland⁽ Reference Kim and Wu ^{24 )}. In support of this hypothesis, a short-term infusion of a NO donor has been shown to increase the blood flow to the mammary gland in goats⁽ Reference Lacasse and Prosser ^{25 )}. Supplementing l-arginine to the diets of primiparous sows may also increase milk production⁽ Reference Mateo, Wu and Moon ^{21 )}. Moreover, piglets receiving milk-based diet supplemented with 0·4% l-arginine had greater plasma concentrations of insulin and growth hormone⁽ Reference Kim, McPherson and Wu ^{22 ,} Reference Yao, Yin and Chu ^{23 )}. All these studies reported an increase in weight gain of the piglets during the treatment period that may be due, at least partly, to an increase in protein synthesis and the signalling activity of the mammalian target of rapamycin in skeletal muscle⁽ Reference Kim and Wu ^{24 )}. Direct effects of l-arginine on tissue development have been reported in vivo and in vitro. In growing–finishing pigs, dietary l-arginine supplementation increased muscle gain by enhancing muscle protein, glycogen and fat content, while decreasing carcass fat content⁽ Reference Tan, Yin and Liu ^{26 )}. This is consistent with the finding that l-arginine supplementation favoured lipogenesis in muscle and lipolysis in adipose tissue⁽ Reference Tan, Yin and Liu ^{27 )}. Less consistent effects of arginine and NO have been reported in vitro. Arginine-induced pre-adipocyte differentiation in rats⁽ Reference Yan, Aziz and Shillabeer ^{28 )}, whereas NO suppressed some markers of differentiation in 3T3-L1 murine cell line through suppressing the transcriptional activity of the key regulator PPARγ⁽ Reference Kawachi, Moriya and Korai ^{29 )}. These results suggest that the l-arginine supply may affect the balance between fat and muscle development in pigs, but specific studies are required to identify the most critical periods.

Control of feed intake by amino acids: tryptophan and valine

An inadequate or imbalanced AA supply implies that one (or more) AA is provided in disproportionate amount compared with the others. Many species are able to detect a dietary AA imbalance⁽ Reference Harper and Rogers ^{31 )} and react by reducing feed intake. This is particularly the case for two essential AA, tryptophan and valine. In pigs, the effect of tryptophan and valine deficiencies on growth are mainly associated with a reduction in appetite and feed intake⁽ Reference Ettle and Roth ^{32 –} Reference Wiltafsky, Pfaffl and Roth ^{35 )}. In growing pigs, the depressive effect of a tryptophan deficiency on feed intake was enhanced by increasing the level of protein and thus the level of large neutral AA (valine, isoleucine, leucine, tyrosine, phenylalanine and methionine). These AA compete with tryptophan for transport across the blood–brain barrier⁽ Reference Henry, Sève and Mounier ^{34 ,} Reference Leathwood ^{36 )} because they share the same transport system. The depressive effect of valine deficiency on feed intake was enhanced by an excess supply of leucine known to stimulate the activity of the branched-chain keto acid dehydrogenase complex, thereby increasing the catabolism of valine in rats and pigs⁽ Reference Wiltafsky, Pfaffl and Roth ^{35 ,} Reference May, Piepenbrock and Kelly ^{37 )}. Recent data showed that pigs rejected a valine-imbalanced diet within 2 d of exposure to the diet by reducing the daily number of meals⁽ Reference Gloaguen, Le Floc'h and Corrent ^{38 )}. This behavioural response suggests that the response to a valine imbalance results from post-absorptive feedback signals.

The physiological mechanisms involved in the rejection of an AA imbalanced diet are probably different among AA and have not been clearly identified in pigs. In rats, an AA imbalance is detected by the brain in the cortex piriform anterior⁽ Reference Hao, Sharp and Ross-Inta ^{39 )}. An AA deficiency results in an accumulation of its uncharged tRNA, which activates the general control of non-depressible-2 kinase in the cortex piriform anterior. A valine deficiency increased the expression of somatostatin mRNA in the hypothalamus in the anorectic mice, and intracerebroventricular administration of somatostatin reduced the feed intake of mice⁽ Reference Nakahara, Takata and Ishii ^{40 )}. Moreover, because tryptophan is a precursor of serotonin, a brain neuromediator involved in the control of feed intake in pigs, this pathway might be involved in the rejection effect of a tryptophan-deficient diet. Serotonin manipulation is known to affect meal size⁽ Reference Henry, Sève and Mounier ^{34 ,} Reference Blundell ^{41 )}. Tryptophan could be also involved in the peripheric control of appetite through a modulation of the rate of gastric emptying⁽ Reference Ponter, Cortamira and Sève ^{42 )}, insulin secretion and sensitivity⁽ Reference Ponter, Cortamira and Sève ^{42 ,} Reference Ponter, Cortamira and Sève ^{43 )}. Tryptophan effect on appetite could be mediated by ghrelin⁽ Reference Zhang, Yin and Defa ^{44 )}, a gut hormone involved in the regulation of feed intake. Indeed, tryptophan supplementation to low-tryptophan diets induced ghrelin secretion, expression of ghrelin mRNA in the stomach and duodenum of piglets, and increased feed intake. Tryptophan also stimulates the release of cholecystokinin, a hormone that decreases meal size⁽ Reference Wang, Chandra and Samsa ^{45 )}.

Control of protein synthesis by amino acids: leucine

The role of leucine, one of the three branched-chain AA, has been known for a long time for its ability to stimulate muscle protein synthesis and inhibit protein degradation in rodents⁽ Reference Dardevet, Sornet and Balage ^{46 ,} Reference Dardevet, Sornet and Bayle ^{47 )} and young piglets⁽ Reference Escobar, Frank and Suryawan ^{48 –} Reference Torrazza, Suryawan and Gazzaneo ^{50 )}. The role of leucine as a signal molecule for the intracellular pathway leading to activation of the first step of protein synthesis has been widely explored. Leucine is known to activate mammalian target of rapamycin leading to activation of the translation initiation factor and then to the aggregation of ribosome and mRNA translation⁽ Reference Stipanuk ^{51 )}. Recently, this effect has been reported in young growing pigs fed a low-protein diet supplemented with leucine up to 30% higher than the recommendations for maximum growth rate⁽ Reference Yin, Yao and Liu ^{52 )}. After 2 weeks of treatment, growth rate and tissue protein synthesis were increased in pigs fed the leucine-supplemented diet and this effect was independent of feed intake. This result opens new ways to improve feed efficiency and growth rate through nutrition.

Preservation of gut homoeostasis: threonine

In young piglets, threonine has been shown to be indispensable for gut development and physiology. Threonine is extracted from the small intestine in greater proportion than the other essential AA⁽ Reference Le Floc'h and Sève ^{53 )}. In orally fed piglets, the threonine requirement, evaluated by the indicator AA oxidation technique, is twice that of parenterally fed piglets⁽ Reference Bertolo, Chen and Law ^{54 )}. The high rate of intestinal threonine extraction is not explained by threonine catabolism⁽ Reference Le Floc'h and Sève ^{53 ,} Reference Le Floc'h, Thibault and Sève ^{55 )} but is associated with intestinal protein synthesis, especially for the synthesis of mucins⁽ Reference Law, Bertolo and Adjiri-Awere ^{56 ,} Reference Wang, Qiao and Yin ^{57 )}. The threonine content in mucin ranges from 13 to 26% of total constituting AA⁽ Reference Lien, Sauer and Fenton ^{58 ,} Reference Mantle and Allen ^{59 )}. Mucins are excreted in the lumen, and their constituting AA are poorly re-absorbed. Therefore threonine is found in high concentrations in ileal endogenous protein losses⁽ Reference Hess and Sève ^{60 )}. This questions the impact of dietary threonine supply on gut homoeostasis. In piglets, a threonine deficiency impaired total protein and mucin synthesis⁽ Reference Wang, Qiao and Yin ^{61 ,} Reference Wang, Zeng and Mao ^{62 )} and also had an impact on other functions of the small intestine. In piglets, a low threonine supply (70% of recommendations) for 2 weeks induced atrophy of the villi associated with a reduction in aminopeptidase N activity in the ileum⁽ Reference Hamard, Sève and Le Floc'h ^{63 )}. It also increased paracellular permeability and glucose absorption capacity⁽ Reference Hamard, Mazurais and Boudry ^{64 )}, and modified ileal gene expression profiles. Notably, the increase in the expression of genes involved in immune and defence functions associated with the increased paracellular permeability suggests that threonine is essential to preserve intestinal integrity. These morphological and functional disturbances are also observed during starvation or malnutrition (e.g. after weaning) and are frequently associated with an increased risk of gut disorders⁽ Reference Boza, Möennoz and Vuichoud ^{65 –} Reference Boudry, Péron and Le Huërou-Luron ^{67 )}. The impact of dietary threonine on weaning diet as a strategy to minimise gut disorders deserves further attention⁽ Reference de Lange, Pluske and Gong ^{68 )}.

Control of inflammatory response: tryptophan

In pig farms, permanent exposure to antigens, unfavourable sanitary conditions and moderate infectious diseases induce an inflammatory status that limits growth by reducing feed intake⁽ Reference Sandberg, Emmans and Kyriazakis ^{69 )} and affecting nutrient metabolism⁽ Reference Le Floc'h, Jondreville and Matte ^{70 ,} Reference Pastorelli, van Milgen and Lovatto ^{71 )}. Indeed, AA are partitioned from body protein deposition towards tissues and functions involved in the animal's defence system⁽ Reference Klasing ^{72 )}. If an AA is supplied in limited amount, this partition is not necessary fully compensated by endogenous supplies. The consequence could be a reduction of AA available for protein deposition, the defence system, or for both. The impact of an inflammatory challenge on AA metabolism has been demonstrated in several species for dispensable AA such as cysteine involved in glutathione synthesis⁽ Reference Malmezat, Breuillé and Pouyet ^{73 )}, glutamine used as a fuel for rapidly dividing cells such as enterocytes and lymphocytes⁽ Reference Yoo, Field and McBurney ^{74 )}, and tryptophan and its metabolites implied in the inflammatory response.

Tryptophan is one of the indispensable AA that is found in low concentration in body proteins and plasma. This relatively low amount of tryptophan is singular considering that this AA is involved in several physiological functions such as the regulation of growth, mood, behaviour and immune responses⁽ Reference Le Floc'h, Otten and Merlot ^{75 )}. Depletion of plasma tryptophan has been reported during experimentally induced inflammation in pigs⁽ Reference Lindberg and Clowes ^{76 ,} Reference Melchior, Sève and Le Floc'h ^{77 )}, mice⁽ Reference Saito, Markey and Heyes ^{78 )} and human subjects⁽ Reference Brown, Ozaki and Datta ^{79 ,} Reference Pfefferkorn ^{80 )}. This decrease can be attributed to the synthesis of acute phase proteins, which have a high tryptophan content⁽ Reference Reeds, Fjeld and Jahoor ^{81 )}, and/or to an increase in tryptophan catabolism. Indoleamine 2,3-dioxygenase (IDO), a rate-limiting enzyme for the catabolism of tryptophan to kynurenine, is induced by interferon-γ⁽ Reference Pfefferkorn ^{80 ,} Reference MacKenzie and Hadding ^{82 )} and by inflammation in pigs⁽ Reference Melchior, Mézière and Sève ^{83 ,} Reference Le Floc'h, Melchior and Sève ^{84 )}.

Increased tryptophan catabolism and IDO activation during inflammation are considered as mechanisms involved in the defence system. Three hypotheses have been proposed (Fig. 3). The first one is that local tryptophan depletion resulting from IDO activation in macrophages would be a mechanism controlling proliferation of bacteria, virus and parasite⁽ Reference Pfefferkorn ^{80 ,} Reference MacKenzie and Hadding ^{82 ,} Reference MacKenzie, Heseler and Müller ^{85 )}. The second one is that IDO regulates T-cell activity. Such a mechanism has been shown during gestation where IDO exerts a protective role by preventing the fetal allograft rejection by maternal T-lymphocytes⁽ Reference Munn, Zhou and Attwood ^{86 )}. Finally, IDO induction during immune activation may protect cells from oxidative damage⁽ Reference Hayaishi ^{87 )}. Indeed, 3-hydroxyanthranilic acid and 3-hydroxykynurenine, produced from tryptophan through the IDO–kynurenine pathway, have antioxidant properties⁽ Reference Christen, Peterhans and Stocker ^{88 )}. This suggests that dietary tryptophan could influence the inflammatory response and the animal health. In support of this hypothesis, pigs suffering from an experimentally induced lung inflammation and offered a diet with tryptophan concentration slightly higher than the recommendations had lower acute phase protein concentration and were healthier compared with pigs offered a diet moderately deficient in tryptophan⁽ Reference Le Floc'h, Melchior and Sève ^{84 )}. In a porcine model of induced colitis, tryptophan supplementation loading down-regulated inflammation, restored local immune response and reduced colitis symptoms⁽ Reference Kim, Kovacs-Nolan and Yang ^{89 )}.

Fig. 3. Roles of tryptophan catabolism by the enzyme indoleamine 2,3-dioxygenase (IDO) on the animal's defence system. , , increase and decrease respectively.

The consequences of inflammation on tryptophan metabolism probably impaired the availability of tryptophan for body protein deposition and growth⁽ Reference Le Floc'h, LeBellego and Matte ^{90 )}. However, additional crystalline tryptophan did not totally prevent growth retardation caused by inflammation. Nevertheless, an improvement in growth rate by additional tryptophan was observed in pigs suffering from a moderate inflammation compared with control pigs⁽ Reference Le Floc'h, Matte and Melchior ^{91 )}. Additional tryptophan allowed pigs to partially compensate for the effects of an Escherichia coli infection by increasing feed intake and maintaining growth⁽ Reference Trevisi, Melchior and Mazzoni ^{92 )}. These results suggest that dietary tryptophan should be maintained at an adequate level to preserve health during critical phases of pig rearing.