Effect of dietary protein level and origin on the redox status in the digestive tract of mice.

The present study was undertaken to evaluate the effects of high protein (soybean protein or casein) on the balance between production of free radicals and antioxidant level in digestive organs of mice. For this purpose, male (C57BL/6J) mice were adapted to experimental diets containing soybean protein or casein with 20% (normal protein diets, NPDs) or 60% (high protein diets, HPDs), and HPDs supplemented with 0.06 g/kg cysteamine. After two weeks of feeding, oxidative and antioxidative parameters in duodenum, liver and pancreas were measured. The results show that ingestion of high protein markedly increased contents of superoxide anion and malondialdehyde (MDA), decreased activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and Na(+) K(+)-ATPase, and content of reduced glutathione (GSH) in digestive organs of mice (P<0.05). Levels of oxidative parameters were lower and antioxidant capacity of both enzyme and non-enzyme was higher in mice fed with soybean protein than those fed with casein. In groups fed HPDs supplemented with cysteamine, oxidative stress was mitigated. However, oxidative parameter levels were still higher than those of NPD-fed groups. The present study indicates that ingestion of high protein diets could result in an imbalance between oxidant and antioxidant, and thus induce oxidative stress in digestive organs of mice. The oxidative damage was smaller in mice fed with high level of soy protein in comparison with casein.

1. Introduction

The scientific literature on whether ingestion of high protein can cause adverse effects to the healthy population is controversial. High protein diets are suspected to be detrimental to the renal and hepatic functions, calcium balance and insulin sensitivity, such as increased urinary nitrogen excretion, glomerular filtration rate, kidney hypertrophy, renal hemodynamics and eicosanoid production in renal tubules [1-3]. In addition, increased risk of renal cell cancer [4] and a higher incidence of noninsulin-dependent diabetes (NIDDM) [5,6] have been linked to high-protein intake. Furthermore, Vlajinac et al. [7] and Holmes et al. [8] found a relationship between high-protein intake and prostate cancer and calcium oxalate nephrolithiasis. High protein ingestion increases amino acid oxidation and urea synthesis [9] and decreases the nutritional efficiency of energy utilization [10,11]. However, the reoxidation of reducing equivalents derived from amino acid oxidation is linked to the mitochondrial redox chain [12]. Free radical generation during mitochondrial oxygen reduction may lead to oxidative stress if the antioxidant capacity is insufficient to quench the extra free radical production. Thus, intake of high protein may cause a situation of physiological oxidative stress.

It was reported that dietary-protein origin may influence cholesterol metabolism. Soybean protein, for example, as compared with casein, lowers plasma cholesterol concentrations in rats [13], exhibits anticarcinogenic effects [14], and regulates polyunsaturated fatty acid metabolism [15,16]. In addition, many findings showed that soybean protein had antioxidative activity. Madani et al. [17] reported that rats fed a soybean protein diet were found to have lower concentrations of plasma thiobarbituric acid-reactive substances (TBARS) than rats fed a casein diet. Soybean protein intake has been reported to inhibit oxidative modification of LDL in vitro [18]. Furthermore, Aoki et al. [19] found that intake of soybean protein may reduce paraquat-induced oxidative stress in rats. The present study was designed to investigate whether high protein (soybean protein or casein) could increase generation of free radicals and decrease antioxidant capacity in digestive organs of mice, and the effect of protein origin on the balance between oxidative levels and antioxidative abilities.

2. Materials and Methods

2.1 Animals and diets

The care and use of the mice followed the institutional guideline of Jiangnan University. Male C57BL/6J mice (body weigh, 12–13 g; 3 wk old) were used in this study. All animals were housed under a controlled atmosphere (temperature, 23°C ± 1; relative humidity, 55 ± 5%; and a fixed 12-h light: dark cycle, light 0700 to 1900h). Prior to the feeding experiment they were allowed free access to deionized water and a semipurified diet (Shanghai, China; crude protein 180 g/kg, crude fat 40 g/kg, metabolizable energy 11.9 MJ/kg) for 10 days to allow acclimatization to these conditions. Then all animals were divided randomly into six groups of ten each. Group 1 and 4 (normal protein diets, NPD) received a normal diet containing 20% casein or soy protein, respectively. Group 2 and 5 (high protein diets, HPD) received a high protein diet containing 60% casein or soy protein, respectively. Group 3 and 6 received HPDs supplemented with 0.06g/kg cysteamine. Casein and soy protein was exchanged isoenergetically by corn starch. The composition of the experimental diets is shown in Table 1. All mice were allowed free access to the experimental diets and deionized water throughout the experimental period.

Table 1.

Composition of dietsa.

Ingredient	Casein (g/kg diet)			Soybean protein (g/kg diet)
	Group1	Group2	Group3	Group4	Group5	Group6
Caseinb	200	600	600
soybean proteinb				200	600	600
Corn starchc	580	220	220	580	220	220
Sucrose	60	20	20	60	20	20
Soybean oild	50	50	50	50	50	50
Cellulose powdera	50	50	50	50	50	50
Mineral mixturee	40	40	40	40	40	40
Vitamin mixturef	20	20	20	20	20	20
Cysteaminec			0.06			0.06

The diets were semipurified, isoenergetic (16.20 MJ/kg);

Shanghai, China;

Wuxi, China;

The commercial product (50 g/kg) provides 11.81% of energy. The soybean oil provides the following fatty acids: 14:0, traces; C16:0, 10.3; C16:1 ω-7, 0.1; C18:0, 3.9; C18:1 ω-7 +ω-9, 22.1; C18:2 ω-6, 54.8; C18:3 ω-3, 7.5; C20:0, 0.4; C20:1 ω-9 + ω-11, 0.2; C22:0, 0.4; C22:5 ω-3, traces; C24:0, traces; sum of saturated fatty acids (S), 15; sum of monounsaturated, 22.4; sum of polyunsaturated fatty acids (P), 84.7; P/S, 5.65; Σω-6/Σω-3, 7.3;

The salt mixture provides the following amounts (g/kg diet–1): Ca, 4; K, 2.4; Na, 1.6; Mg, 0.4; Fe, 0.12; trace elements: Mn, 0.032; Cu, 0.005; Zn, 0.018; Co, 0.00004; I, 0.00002;

The vitamin mixture provides the following amounts (mg/kg diet–1): retinol, 12; cholecalciferol, 0.125; thiamin, 40; riboflavin, 30; pantothenic acid, 140; pyridoxine, 20; inositol, 300; cyanocobalamine, 0.1; ascorbic acid, 1600; (dL) α-tocopherol, 340; menadione, 80; nicotinic acid, 200; paraaminobenzoic acid, 100; folic acid, 10; biotin, 0.6; choline, 2720. Group 1and 4 (normal protein diets [NPD]), a normal diet containing 20% casein or soy protein, respectively; Group 2 and 5 (high protein diets [HPD]), a high protein diet containing 60% casein or soy protein, respectively; Group 3 and 6, high protein diets plus 0.06g/kg cysteamine.

2.2 Sampling procedures

At the end of the experimental period, mice were deprived of food overnight but had free access to deionized water. Mice were sacrificed by decapitation and the whole duodenum, liver and pancreas were removed immediately, gently rinsed in ice-cold PBS and then were cut into 50-to 100-mg portions as tissue samples. They were frozen in liquid nitrogen and stored at –80°C for further treatment. After thawed, tissue samples were homogenized with ice-cold 0.9% NaCl solution and then were centrifuged at 4000g for 15 min at 4 °C. The supernates were used to determined protein content and antioxidant defense and lipid peroxidation.

2.3 Analytical methods

2.3.1 Superoxide anion determination

The level of oxidative stress was determined by specifically measuring superoxide anion, as described byPick [20].

2.3.2 Lipid peroxidation determination

Lipid peroxidation products, thiobarbituric acid reactive substances (TBARS), were measured by a standard method and are expressed as the content of malondialdehyde (MDA) in nanomoles per milligram of protein [21].

2.3.3 Glutathione peroxidase assay

Glutathione peroxidase (GSH-Px) activity was measured according to the method of Hafeman et al. [22]. One unit of GSH-Px was defined as a decrease in the log of mmol GSH per minute and was expressed in unit per milligram protein. The automatically decrease of GSH without enzyme (control reaction under same condition) was subtracted from calculation.

2.3.4 Superoxide dismutase assay

Total superoxide dismutase (SOD) activity was assayed using hypoxanthine–xanthine oxidase-generated O2− to reduce nitrotetrazolium (NBT) monitored spectrophotometrically at 550 nm. Inhibition of NBT reduction to 50% of maximal is defined as 1U of SOD activity and enzyme activity was expressed in units per milligram protein [23].

2.3.5 GSH assay

Reduced glutathione (GSH) was measured by the procedure of Moron et al. [24]. In this procedure, reduced GSH reacts with 5,5-dithiobis-(2-nitrobenzoic acid) to produce a compound that absorbs at 412 nm.

2.3.6 Na+ K+-ATPaseand catalase activity determination

Na+ K+-ATPase and catalase (CAT) activities in digestive organs were determined by Reinila et al. [25] and Aebi [26], respectively, using commercial kits from Nanjing Jiancheng Bioengineering Institute. The protein content was determined using the method of Lowry et al. [27].

2.4 Statistical analysis

Data are reported as means ± SD, n = 10. Differences between mean values were determined by ANOVA followed by comparisons using the Newman-Keuls multiple range test. Differences with P < 0.05 were considered significant.

3. Results

3.1 Superoxide anion content in duodenum, liver and pancreas of mice

Figures 1 to 3 show the effect of high protein on superoxide anion content of soybean protein or casein-fed groups. There was a significant increase (P<0.05) in superoxide anion content in duodenum, liver and pancreas of HPD-fed mice. Superoxide anion content was strikingly lower in duodenum and liver of mice fed soybean protein than those fed casein. Treatment with cysteamine ameliorated the change induced by HPD feeding.

Figure 1.

Superoxide anion content in duodenum of mice. Bars represent means ± SD. Means not sharing the same letter are significantly different within experimental period (P < 0.05, n = 10). NPD, a normal diet containing 20% casein or soy protein; HPD, a high protein diet containing 60% casein or soy protein; HPD + CYS, high protein diets plus 0.06g/kg cysteamine.

Figure 3.

Superoxide anion content in pancreas of mice. Bars represent means ± SD. Means not sharing the same letter are significantly different within experimental week (P < 0.05, n = 10). NPD, a normal diet containing 20% casein or soy protein; HPD, a high protein diet containing 60% casein or soy protein; HPD + CYS, high protein diets plus 0.06g/kg cysteamine.

3.2 MDA contents and SOD activities in duodenum, liver and pancreas of mice

Feeding of the HPDs for 14 d resulted in the development of oxidative stress in experimental mice, as is evident from Table 2. There was a significant (P<0.05) increase in MDA content (78% and 104%, 103% and 75%, 138% and 150%, respectively), whereas lower SOD activity (35% and 29%, 28% and 18%, 31% and 30%, respectively) in duodenum, liver and pancreas of mice fed casein and soybean protein. However, the level of oxidative parameter was lower, and antioxidant activity was higher in groups fed soybean protein diets compared with those fed casein diets. These abnormalities caused by HPDs were considerably reduced on treatment with cysteamine.

Table 2.

MDA contents and SOD activities in duodenum, liver and pancreas of mice.

Groups	MDA(nmol/mg prot)			SOD(U/mg prot)
	Duodenum	Liver	Pancreas	Duodenum	Liver	Pancreas
Group1	2.67±0.12ab	3.91±0.26a	2.09±0.10a	95.04±3.57de	218.55±8.25c	98.92±2.51c
Group2	4.76±0.26d	7.92±0.16c	4.99±0.12c	61.27±4.23a	158.28±4.73a	68.74±0.50a
Group3	3.69± 0.15c	5.84±0.16b	3.36±0.14b	79.66±2.36bc	185.09±4.82b	82.60±1.69b
Group4	2.28±0.13a	4.44±0.41a	1.82±0.09a	98.35±3.46e	204.33±8.83c	101.44±1.78c
Group5	4.66±0.35d	7.77±0.25c	4.55±0.22c	69.50±3.02ab	166.96±3.48ab	70.92±4.05a
Group6	3.17±0.26bc	5.85±0.07b	3.09±0.34b	84.21±5.41cd	182.67±2.61b	85.77±4.34b

Values are means ± SD, n = 10. Within an array, values without a common superscript significantly differ, P < 0.05. MDA, malondialdehyde; SOD, superoxide dismutase; Group 1and 4 (normal protein diets [NPD]), a normal diet containing 20% casein or soy protein, respectively; Group 2 and 5 (high protein diets [HPD]), a high protein diet containing 60% casein or soy protein, respectively; Group 3 and 6, high protein diets plus 0.06g/kg cysteamine.

3.3 GSH-Px activities and GSH contents in duodenum, liver and pancreas of mice

The HPD-fed groups exhibited strikingly lower activity of GSH-Px and GSH content in digestive organs compared to the NPD-fed groups (Table 3). Levels of antioxidant parameters were higher in soybean protein groups than casein groups. The HPD and treatment with cysteamine groups exhibited a similar GSH-Px activity except for duodenum. GSH contents were significantly lower in the HPD groups than in the treatment with cysteamine groups.

Table 3.

GSH-Px activities and GSH contents in duodenum, liver and pancreas of mice.

Group	GSH-Px(U/mg prot)			GSH(mg/g prot)
	Duodenum	Liver	Pancreas	Duodenum	Liver	Pancreas
Group1	80.828±0.925e	59.963±0.206c	102.196±3.630b	99.22±0.32d	191.29±4.25c	153.02±4.69c
Group2	58.748±1.073a	50.688±2.038a	88.169±4.244a	38.91±2.02a	78.23±1.93a	123.38±2.19a
Group3	70.476±1.497c	53.818±0.306ab	97.560±5.194ab	65.59±1.65b	100.84±1.47b	138.97±2.23b
Group4	82.610±0.324e	61.197±2.009c	100.362±1.224b	116.27±3.98e	184.34±6.07c	165.78±3.09d
Group5	67.190±0.573b	52.718±0.297ab	91.768±2.533ab	44.31±1.58a	84.61±3.23a	130.29±1.73a
Group6	76.610±0.566d	54.930±0.248b	97.689±1.692ab	78.72±6.80c	97.55±4.62b	146.11±1.33bc

Values are means ± SD, n = 10. Within an array, values without a common superscript significantly differ, P < 0.05. GSH-Px, glutathione peroxidase; GSH, reduced glutathione; Group 1and 4 (normal protein diets [NPD]), a normal diet containing 20% casein or soy protein, respectively; Group 2 and 5 (high protein diets [HPD]), a high protein diet containing 60% casein or soy protein, respectively; Group 3 and 6, high protein diets plus 0.06g/kg cysteamine.

3.4 CAT and Na+ K+-ATPase activities in duodenum, liver and pancreas of mice

Table 4 presents the effects of high levels of soybean protein and casein on CAT and Na+ K+-ATPase activities. There was significant decrease (P<0.05) in CAT and Na+ K+-ATPase activities of HPD-fed mice compared with NPD-fed mice. CAT and Na+ K+-ATPase activities were higher in soybean protein-fed mice than casein-fed ones. Supplement with cysteamine increased significantly in CAT and Na+ K+-ATPase activities of HPD-fed mice.

Table 4.

CAT and Na+ K+-ATPase activities in duodenum, liver and pancreas of mice.

Groups	CAT(U/mg prot)			Na+ K+-ATPase(μmolPi/mg prot/hour)
	Duodenum	Liver	Pancreas	Duodenum	Liver	Pancreas
Group1	56.17±0.75e	82.16±0.21d	78.65±0.51c	21.53±0.32d	10.67±0.07c	3.14±0.29c
Group2	25.08±1.10a	54.00±0.58a	56.54±1.65a	13.92±0.21a	1.95±0.23a	0.95±0.01a
Group3	42.44±1.33c	73.13±1.46c	68.32±0.66b	15.97±0.23bc	5.47±0.14b	1.93±0.02b
Group4	57.77±0.85e	82.13±1.48d	78.88±0.35c	22.53±1.02d	10.40±0.18c	3.72±0.44c
Group5	37.54±1.91b	58.98±0.69b	57.16±2.94a	14.79±0.64ab	2.59±0.51a	0.99±0.06a
Group6	46.24±0.77d	72.52±1.14c	70.22±0.45b	17.71±0.68c	5.76±0.61b	2.06±0.05b

Values are means ± SD, n = 10. Within an array, values without a common superscript significantly differ, P < 0.05. CAT, catalase; Group 1 and 4 (normal protein diets [NPD]), a normal diet containing 20% casein or soy protein, respectively; Group 2 and 5 (high protein diets [HPD]), a high protein diet containing 60% casein or soy protein, respectively; Group 3 and 6, high protein diets plus 0.06g/kg cysteamine.

4. Discussion

With the elevation of living standards, the amount of protein ingested by people has increased and is above actual nutritional requirements. However, whether the high protein intake will cause adverse effects to the healthy population is still controversial. Many findings indicate that high protein intakes (more than 40% protein level) increase the thermogenic response, which is accompanied by a lower efficiency of food energy utilization, an increase in oxygen consumption, and impaired oxidative phosphorylation capacities (lower adenosine diphosphate oxygen values for nicotinamide adenine dinucleotide-linked substrates in mitochondria) [28-30]. Thus, we assumed that high protein ingestion could induce oxidative stress. In the present study, results showed that ingestion of high protein diets caused increments in the levels of oxidative parameters and decrease in antioxidative activity in digestive organs of mice. This imbalance between the production of free radicals and the ability of the organism's natural protective mechanisms is due to excessive oxidation of amino acids.

Oxidative stress is one of the causative factors of many diseases such as atherosclerosis [31]. An imbalance between production of free radicals and antioxidant level leads to oxidative stress, which is obvious from the depressed antioxidant defense system in the HPD groups of our study. Cysteamine acts as an antioxidant for its sulfhydryl in relation to effectively scavenging free radicals (e.g., hydroxyl radical) [32]. Moreover, cysteamine can stimulate GSH synthesis [33]. In the present study, administration of cysteamine to HPD-fed mice prevented the buildup of oxidative stress by restoring normal activities of the enzymatic antioxidant SOD, CAT and GSH-Px and normal levels of the non-enzymatic antioxidant GSH in the digestive organs; the concentrations of these antioxidants were decreased in the HPD-fed mice. The diminished antioxidant defense system in HPD-fed mice leads to damage of the so-called lipid peroxidation system. We observed increased concentration of MDA, indices of lipid peroxidation, and superoxide anion, the precursor of most reactive oxygen species (ROS) and a mediator in oxidative chain reactions, in the peptic of HPD-fed animals. Administration of cysteamine decreased significantly the lipid peroxidation. This suggests that cysteamine played an antioxidant role in oxidative stress induced by the HPDs.

Na+K+-ATPase, which is a cell membrane protease maintains the electrochemical potential gradient of Na+ and K+ ions in the membranes of cells, and plays an important role in the transport of substances, energy conversion and information transfer [34-36]. The decrease of its activity indicates substances and energy dysmetabolism [37]. In the present study, the activity of Na+K+-ATPase was markedly lower in mice fed the HPD compared with those fed the NPD, which indicates that oxidative stress induced by the HPD diets impairs biomembrane. Moreover, lesion of biomembrane led to the ion pumping dysfunction of the Na/K-ATPase, which could increase [Ca2+] and open mitochondrial ATP-sensitive K channel (mitoKATP) and further stimulate the production of ROS [37-39].

Dietary-protein origin may influence lipid peroxidations. Chiang and Kimura [40] reported that liver and testis lipid peroxide concentrations are significantly lower in stroke-prone spontaneously hypertensive rats (SHR) fed soybean protein than in those fed casein. In rabbits, the soybean protein diet lowers plasma cholesterol level and causes fewer atherosclerotic lesions compared with rabbits fed the casein diet [41]. Madani et al. [17] reported that concentrations of plasma TBARS were lower in rats fed a soybean protein diet than those in rats fed a casein diet. Aoki et al. [19] demonstrated that soybean protein has antioxidative effects on paraquat-induced oxidative stress in rats. The antioxidative activity of soybean protein can potentially be explained by its amino acid composition or the effects of soybean peptides. L-Arginine is reported to have antioxidative activity [42] and is more abundant in soybean protein than in casein. Suetsuna et al. [43] investigated the antioxidative activity of soybean protein hydrolysate and reported two soybean peptides with strong antioxidative activity. Antioxidative activity of histidine-containing peptides from soybean protein has also been reported [44]. In present study, lower levels of oxidative parameters (MDA and superoxide anion) and higher activities of antioxidant enzymes (SOD, CAT, GSH-Px) in digestive organs were observed in groups fed HPD with soybean protein than those fed HPD with casein. This result may be attributed to the antioxidative activity of soybean protein itself.

In summary, these findings suggest that oxidative stress may occur in digestive organs of mice because intake of high protein diets caused an imbalance between the production of ROS and the capacity of the antioxidant defense system. However, at the same level, the extent of oxidative stress in mice fed-soybean protein was lower than that in mice fed-casein.