Abstract
This study aimed to in vitro assess the impact of the cooking process of eggs (hard-boiled, poached, and omelet) on nutrients digestibility and vitamins A and D3 bioaccessibility under elderly gastrointestinal (GI) conditions. Three elderly digestion models were mimicked: oral (E1); oral and gastric (E2); and oral, gastric, and intestinal (E3), and a healthy adult model (C). Proteolysis extent reduced after digestion of omelet under the E3 model (p < 0.05) (up to 37% of reduction). Thus, hard-boiled and poached were more recommendable to enhance protein digestibility in elders. Altered GI conditions negatively influence neither the absorbable lipid fraction nor the cholesterol stability. Finally, vitamin A bioaccessibility was not affected but D3 slightly decreased with the elderly (E3). Hence, the digestion of nutrients was dependent on the resulting matrix, poached being the greater supplier of protein and lipid end-digestion products. Poached and omelet, however, offer a high net supply of bioaccessible vitamin D3 for elders.
Keywords: aging, egg, cooking methods, macronutrients digestibility, vitamin bioaccessibility
Introduction
Current prospects confirm that the population continues to considerably grow because of both high fertility and life expectancy. At the same time, it is expected that the number of people aged 65 years or over surpasses infants and youth in number by 2050.1 Consequently, elders wellness is a global concern that involves lifestyle and nutritional issues.2 The European Society for Clinical Nutrition and Metabolism recommends the elders to increase the consumption of rich-protein foods with high amounts of micronutrients,3 and especially those rich in essential amino acids such as leucine or tryptophan.4 Besides, healthy lipids, minerals, and vitamins are also important due to their relevance as immune modulators and their contribution to the bone health of these subjects.5 Physiological functions declining with aging include body composition, brain function, gastrointestinal (GI) tract function, fluid balance, bones and joints, or cardiovascular system, among others.6 Sarcopenia, loss of muscle mass associated with a protein deficit, asthenia, depression, or weakness of the immune system often occur in elderly.7,8 The masticatory deficiency in elderly, i.e., leading to food boluses with larger particle size distribution and more difficult to swallow, has been reported to influence the nutrients digestibility.9 Also, a decline in the GI tract function has been reported to be partially responsible for the protein deficit. The secretion of digestive fluids and enzymes, saliva, peristaltic contractions, and chyme passage rates could be suboptimal, resulting in maldigestion and malabsorption of nutrients, especially proteins and vitamins.10−12
Among the dietary protein and micronutrients sources, egg is considered as a moderate calorie source (about 140 kcal/100 g) and the lowest-cost animal source of proteins, vitamin A, iron, vitamin B12, riboflavin, and choline, as well as the second lowest-cost source for zinc and calcium. Egg proteins are distributed equally between egg white and egg yolk, while lipids, vitamins, and minerals are essentially concentrated in egg yolk.13 Raw egg yolk contains a high amount of vitamin A and D3 (371 and 5.4 μg/100 g, respectively), among others.13 Proteins provide a reasonable supply of amino acids of biological value,14 with a digestible indispensable amino acid score (DIAAS) value of 1.13 in the same high level of the whole milk with 1.14 score.15 The relative amount of mono- and polyunsaturated to saturated fatty acids in yolk is particularly higher than that in other animal-derived foods. Besides, even though egg cholesterol content is high, it has been reported to not negatively contribute to the increase in plasma total cholesterol.13 Therefore, a regular egg consumption of about 6 per week is advisable.16 Thus, egg is one of the most eaten food over the world and is served in such a variety of ways and recipes.17
Egg meal preparation often involves a heating treatment resulting in protein denaturation, greater vitamins, and minerals availability,18 as well as loss and antinutritional factors decrease, among others. The extent of these changes will depend on the way of cooking and the intensity of the heating.14 Additionally, cooking implies a series of structural changes, which could modulate digestion and absorption rates (i.e., amino acid isomerization and desulfurization, reactions with sugars and lipids, etc.), therefore having an impact on health benefits coming from egg consumption.19 Among the most common ways of cooking eggs, hard and soft boiled, hard and soft scrambled, omelet, sunny side up, etc. can be mentioned. The literature reports the impact of the egg protein structure on proteolysis in model systems consisting in white gels. Studies performed at static19−21 and dynamic in vitro systems21,22 clearly evidencing the role of the matrix structure. However, information related to the modulation of egg protein digestibility neither by cooking nor under elderly GI conditions has been previously reported in real foods.
In this context, this study aims at in vitro analyzing the impact of elderly gastrointestinal conditions and egg cooking (hard-boiled, poached, and omelet) on proteolysis, lipolysis, and vitamins A and D3 bioaccessibility.
Materials and Methods
Chemicals
Pepsin from the porcine gastric mucosa (3200–4500 U/mg), pancreatin (8 × USP) from porcine pancreas, bile bovine (dried, unfractionated), analytical-grade salts (potassium chloride, potassium dihydrogen phosphate, sodium bicarbonate, sodium chloride, magnesium chloride, ammonium carbonate, calcium chloride, and potassium sulfate), boric acid, hydrochloric acid (37%), sulfuric acid (95–97%), tetrahydrofuran (HPLC grade), methanol (HPLC grade), retinol (≥99%, HPLC grade), cholecalciferol (≥98%, HPLC grade), and sodium hydroxide were obtained from Sigma-Aldrich (Deisenhofen, Germany). Also, petroleum ether (VWR Chemicals), acetonitrile (HPLC grade, JT Baker), and EZ-Faast amino acid kit (Phenomenex) were used.
Standard eggs were purchased at local stores in Valencia (Spain).
Sample Preparation
Fresh hen eggs were cooked according to Asensio-Grau et al.23 and immediately characterized or in vitro digested. For the hard-boiled whole shell, eggs were boiled with water covering the eggs for 10 min (95 ± 5 °C) and cooled under running tap water for 5 min, and they were immediately peeled. For poached preparation, eggs were broken and wrapped into cling-film before boiling them with boiling water for 4 min (95 ± 5 °C) and cooled under running tap water for 5 min. For omelet, a white/yolk ratio of 70:30 (w:w) was mixed and stirred for 1 min before microwave cooking at 12.5 W/g for 80 s without oil addition. The egg white and yolks resulted from hard-boiling and poaching were separated to be added to the digestion tubes in the same white:yolk ratio as in omelet.
Compositional Analysis
After cooking, moisture, ashes, fat, and protein contents were determined using the official methods to be 934.01, 942.05, 920.39, and 960.52,24 respectively. Carbohydrates were calculated by difference (100 g minus the sum of grams of water, ashes, lipids, and protein, in wet basis).25 Besides, 5 g of samples was subjected to saponification and extraction of vitamins A (retinol) and D3 (cholecalciferol) according to the protocol published by Castaneda and Lee.26 Both liposoluble vitamins were separated by chromatography (RP-HPLC) and detected at 265 and 325 nm for vitamin D3 and vitamin A, respectively.27 Additionally, cold lipid extraction was performed to analyze the egg lipid profile by means of proton nuclear magnetic resonance (1H NMR) (Bruker, model 400/R), according to Nieva-Echevarría et al.28 The molar percentages of triglycerides (TG), diglycerides (1,2-DG and 1,3-DG), monoglycerides (1-MG and 2-MG), and free fatty acids (FFA) were determined in the samples. To assess its stability after the egg cooking and digestion, the cholesterol content was also quantified by 1H NMR, as a minor lipidic component.
Determinations were performed by triplicate in at least three independent eggs for each cooking method.
Static In Vitro Simulation of GI Digestion
Four in vitro models were stated according to Hernández-Olivas et al.27 to determine the contribution of the different alterations and deterioration occurring with aging (i.e., mastication deficiency, secretion of digestive fluids and enzymes, saliva, GI tract contractions, and chyme passage rates)9,12 on the macronutrients digestibility and micronutrients bioaccessibility in the cooked eggs. Figure 1 gathers the specific conditions of each simulation model (Elderly 1 (E1), Elderly 2 (E2), Elderly 3 (E3), and control (C)). GI-altered conditions of elderly models E1, E2, and E3 were based on Shani-Levi et al.,12 while the C model corresponded to Minekus et al.29 Three independent digestion assays were carried out for each C, E1, E2, and E3 GI condition. Cooked eggs (5 g, hard-boiled, poached, and omelet) ensuring a 70:30 white/yolk ratio were digested by triplicate under each GI model (C, E1, E2, and E3). Gastric and intestinal stages were in vitro simulated, while oral stage was in vivo performed by a volunteer with healthy dentition. The number of mastication cycles to reach a bolus with similar physical characteristics to that of a tomato or mustard paste was established at 16.30 Once this parameter was established, chewing cycles were reduced to 50% to mimic suboptimal oral conditions given in elders.27 Before digestion experiments, gastric (SGF) and intestinal (SIF) digestion fluids were prepared fresh daily from stock solutions and the enzymatic activity of digestive enzymes was tested following the protocol proposed by Minekus et al.29
Figure 1.
Specific gastrointestinal conditions set for the four in vitro digestion models of this study.
After in vitro digestion, sample pH was adjusted to 5 and kept in an ice bath for 10 min to inhibit the enzymatic reactions before fraction separation. Separation of the bioaccessible fraction (liquid phase) from the remaining solid phase was performed by centrifuging at 4000g for 5 min at 10 °C, and the supernatant was collected as a bioaccessible fraction. Aliquots of the bioaccessible fraction were immediately frozen and stored until their use for the analytical determinations.
Analytical Determinations in Digesta
Free Amino Acids
Free amino acids (essential and nonessential amino acids (EAA and NEAA)) resulting from protein digestion were determined through the protocol published by Peinado et al.31 with some amendments. The resulted amino acids were classified into groups according to their chemical structure (hydrophobic amino acids (HAA = Ala, Val, Ile, Leu, Tyr, Phe, Trp, Pro, Met, Cys); positively charged amino acids (PCAA = Lys, His); negatively charged amino acids (NCAA = Asp, Asn, Glu, Gln); aromatic amino acids (AAA = Phe, Trp, Tyr); and sulfur-containing amino acids (SCAA = Cys, Met)).32 Briefly, 100 μL of bioaccessible fraction was derivatized using the EZ-Faast amino acid kit and analyzed using gas chromatography–mass spectrometry (GC–MS) (Agilent Technologies, Injector 7683B series, Network GC System 6890N series, Inert Mass Selective Detector 5975 series, MSD ChemStation software). Norvaline was used as internal standard. The extent of proteolysis based on free amino acids was calculated according to eq 1
![]() |
1 |
where the FAA released corresponds to the sum of the free amino acids in the bioaccessible fraction.
Lipidic End-Digestion Products
Digesta samples were subjected to cold liquid–liquid extraction, and the composition of the lipid phase, including cholesterol, was determined by 1H NMR following the same procedure described in the Compositional Analysis section. Thus, absorbable and nonabsorbable lipid fractions, as well as the lipolysis extent, were calculated according to eqs 2–4
![]() |
2 |
![]() |
3 |
![]() |
4 |
where 1,2-DG and 1,3-DG correspond to diglycerides; 1-MG and 2-MG to monoglycerides; and FFA to free fatty acids obtained in the digested samples.
Vitamin A and D3 Bioaccessibility
Bioaccessible fraction (20 mL) was subjected to saponification and extraction to determine the bioaccessibility of vitamin A and D3 following the same protocol as for total vitamin content in undigested cooked eggs (Compositional Analysis section). Vitamin bioaccessibility was calculated according to eq 5
![]() |
5 |
where the amount of released vitamin represents the recovered part in the bioaccessible fraction after in vitro digestion and the total amount of vitamin found in the cooked eggs before in vitro digestion.
Statistical Analysis
An analysis of variance (multivariate ANOVA) was performed and multiple-range test was determined by the less significant difference (LSD) of Fisher’s test to identify homogeneous groups between models and cooked eggs using Statgraphics Centurion XVII software with a confidence level of 95% (p < 0.05). Also, a principal component analysis (PCA) was applied to find the relationship among the experimental data (EAA/NEAA ratio, total, HAA, PCAA, NCAA, AAA, and SCAA proteolysis extents; absorbable and nonabsorbable lipid fractions; lipolysis extent; cholesterol content; and vitamin A and D3 bioaccessibility) obtained from in vitro digestion studies carried out in cooked eggs under elderly (E1, E2, and E3) or standard (C) GI conditions.
Results and Discussion
Effect of Cooking on Egg Composition
The nutritional composition of eggs was evaluated immediately after being cooked, and the values are presented in Table 1. Even though the egg nutritional contents are highly dependent on the hen feed composition,33 macronutrients content (protein and fat) were close to those reported for noncooked egg.34−37 Therefore, no losses of protein or fat were observed during cooking. Regarding the water content, the shell (in hard-boiled egg) and the plastic film used during poaching avoided the sample dehydration compared with the open-air preparation of omelet. Concerning the analyzed vitamins, cooked eggs presented lower values of vitamin A but similar to D3 compared to the contents reported in fresh egg.34,35,37 A decrease of yolk hydrophobic micronutrients has been previously reported after cooking,38 vitamin A being more sensitive to light, oxygen, and temperature than other liposoluble vitamins.39 In addition, Hemery et al.40 report a greater effect of photolysis than oxidation on vitamin A. Reasonably, the lower vitamin A content found in omelet, compared to hard-boiled and poached egg, can be due to a greater yolk exposure to light and oxygen than during the other cooking ways. In omelet preparation, the shell is removed and the yolk and egg white were mixed, stirred, and placed in a plate, resulting in a larger interphase surface to thermal heating than in boiled or poached. With respect to vitamin D3, omelet presented higher content than hard-boiled or poached eggs. Hemery et al.40 report that the impact of light or oxygen exposure on vitamin D3 is not as severe as for vitamin A. Vitamin D3 seems to be sensible to heat and decrease as long as the processing time increases.41,42 Thus, the lower cooking time involved in the microwave preparation of omelet (80 s compared to 4 and 10 min, respectively) could be associated with the better preservation of vitamin D3 compared to boiling and poaching.
Table 1. Total Contents (per 100 g Dry Basis) of Water, Protein, Fat, Ashes, Carbohydrates, Vitamin A and Vitamin D3 of Hard-boiled, Poached and Omelet Eggse.
nutrient content | rawd | hard-boiled | poached | omelet |
---|---|---|---|---|
water (g) | 292–308 | 310 ± 3b | 319 ± 3c | 154 ± 2a |
protein (g) | 47–52 | 51.6 ± 0.2b | 49.5 ± 0.6a | 51.8 ± 0.3b |
fat (g) | 35–48 | 35.4 ± 0.6a | 35.0 ± 1.0a | 33.4 ± 1.7a |
ashes (g) | 3.4–3.6 | 5.9 ± 0.1a | 5.9 ± 0.1a | 5.8 ± 0.1a |
carbohydrates (g) | 0.7–3.8 | 4.9 ± 0.1b | 4.6 ± 0.1a | 5.1 ± 0.1c |
vitamin A (μg) | 560–1112 | 690 ± 30b | 700 ± 30b | 376 ± 18a |
vitamin D3 (μg) | 5–12 | 6.3 ± 0.3a | 6.5 ± 0.3a | 11.2 ± 0.4b |
Effect of Egg Cooking on Gastrointestinal Proteolysis in Elders
Figure 2A shows the proteolysis extent (%) obtained from the free amino acid profile (Table 2) achieved after in vitro gastrointestinal digestion of boiled, poached, and omelet eggs simulating different models (standardized (C) and elderly (E1, E2, and E3)). It can be noted that proteolysis extent was much higher in boiled eggs (79%) than in poached and omelet ones (60 and 56%, respectively) under control GI conditions. Apparently, trypsin inhibitors present in white eggs seem to be inactivated as long as the food is exposed to 100 °C as well as a greater protein denaturation,13,14 leading to a greater extent in hard-boiled eggs than in poached and omelet eggs. It is well known that the different ways of egg cooking lead to different matrix structures, physical behavior, sensorial quality, and composition of eggs.43 Therefore, an impact of cooking eggs on digestibility was expected. In the case of omelet, the mixing and stirring of yolk with white egg seem to generate new protein–lipid organization that, together with the solid structure resulting from the heat treatment, would hinder the access of gastric and pancreatic proteases to the substrate and result in lower protein digestion.23 It is important to highlight that the extent of proteolysis achieved by the samples could be even higher than reported because the extent of proteolysis calculation has been just based on FAA without considering the possible short-chain peptides which are also bioabsorbable.
Figure 2.
Proteolysis extent (%) (g FAAs released/100 g protein) (A); essential and nonessential amino acids ratio (EAA/NEAA ratio) (B); and amino acid quantities (g/100 g of protein) classified by chemical structure (HHA (C), PCAA (D), NCAA (E), AAA (F), and SCAA (G)) found in hard-boiled, poached, and omelet eggs in vitro digested under C (control), E1 (Elderly 1), E2 (Elderly 2), and E3 (Elderly 3) GI conditions. EAA = (Val, Leu, Ile, Thr, Met, Phe, Lys, His, Trp); NEAA = (Ala, Gly, Ser, Pro, Asn, Asp, Glu, Tyr, Cys). Hydrophobic amino acids (HAA = Ala, Val, Ile, Leu, Tyr, Phe, Trp, Pro, Met, Cys); positively charged amino acids (PCAA = Lys, His); negatively charged amino acids (NCAA = Asp, Asn, Glu, Gln); aromatic amino acids (AAA = Phe, Trp, Tyr); and sulfur-containing amino acids (SCAA = Cys, Met). Data shown are mean values from triplicates and the standard deviation. Different lowercase letters indicate significant differences between models, and different capital letters indicate significant differences between cooking methods, with a significance level of 95% (p < 0.05).
Table 2. Amino Acids Profile (g/100 g Initial Protein) Resulting from In Vitro Digestion of Hard-boiled, Poached and Omelet Eggs under Different Simulated GI Conditions (Control (C), Elderly 1 (E1), Elderly 2 (E2), Elderly 3 (E3) Models)d.
hard-boiled |
poached |
omelet |
||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
amino acid | C | E1 | E2 | E3 | C | E1 | E2 | E3 | C | E1 | E2 | E3 |
alanine (Ala) | 4.39 ± 0.15cB | 3.68 ± 0.28bC | 3.67 ± 0.37bB | 2.50 ± 0.12aB | 3.05 ± 0.42aA | 3.21 ± 0.09aB | 3.00 ± 0.34aB | 2.63 ± 0.18aB | 2.65 ± 0.34bA | 2.23 ± 0.09bA | 2.42 ± 0.13bA | 1.76 ± 0.12aA |
glycine (Gly) | 1.48 ± 0.25bB | 1.50 ± 0.24bB | 1.53 ± 0.16bC | 0.48 ± 0.12aAB | 1.24 ± 0.26bB | 1.16 ± 0.10bB | 1.14 ± 0.04bB | 0.51 ± 0.02aB | 0.83 ± 0.12bA | 0.66 ± 0.02bA | 0.70 ± 0.08bA | 0.33 ± 0.07aA |
valine (Val) | 5.77 ± 0.01bB | 5.77 ± 0.64bB | 6.07 ± 0.58bC | 4.18 ± 0.34aB | 4.78 ± 0.38aA | 5.20 ± 0.09aB | 4.52 ± 0.25aB | 4.72 ± 0.38aB | 4.49 ± 0.52bA | 3.77 ± 0.10abA | 3.94 ± 0.19abA | 3.15 ± 0.49aA |
leucine (Leu) | 10.37 ± 0.26bB | 10.08 ± 1.28bB | 10.86 ± 1.08bB | 7.49 ± 0.58aAB | 8.72 ± 0.47aA | 8.65 ± 0.26aB | 7.88 ± 0.12aA | 8.13 ± 0.46aB | 8.91 ± 0.88bA | 7.46 ± 0.37aA | 7.60 ± 0.40aA | 6.81 ± 0.30aA |
isoleucine (Ile) | 4.29 ± 0.07bB | 4.24 ± 0.28abB | 4.01 ± 0.92abA | 3.12 ± 0.22aAB | 3.63 ± 0.32aA | 3.87 ± 0.12aB | 3.10 ± 0.51aA | 3.45 ± 0.40aB | 3.51 ± 0.32bA | 2.92 ± 0.17aA | 3.01 ± 0.19abA | 2.78 ± 0.18aA |
threonine (Thr) | 3.25 ± 0.26bB | 2.96 ± 0.20bC | 3.12 ± 0.34bC | 1.77 ± 0.15aB | 2.22 ±0.28abA | 2.61 ± 0.06cB | 2.19 ± 0.13bcB | 1.88 ± 0.20aB | 2.02 ± 0.33bA | 1.79 ± 0.04bA | 1.91 ± 0.05bA | 1.39 ± 0.08aA |
serine (Ser) | 3.71 ± 0.18bB | 3.43 ± 0.33bB | 3.65 ± 0.38bC | 1.40 ± 0.10aB | 2.29 ± 0.21abA | 2.96 ± 0.30bB | 2.62 ± 0.19abB | 1.87 ± 0.28aC | 2.21 ± 0.39bA | 1.97 ± 0.14bA | 2.15 ± 0.12bA | 1.13 ± 0.07aA |
proline (Pro) | 1.24 ± 0.05bC | 1.15 ± 0.15bB | 1.27 ± 0.16bC | 0.67 ± 0.06aB | 1.01 ± 0.10abB | 1.15 ± 0.01bB | 0.98 ± 0.11abB | 0.76 ± 0.12aC | 0.77 ± 0.06bA | 0.67 ± 0.04bA | 0.72 ± 0.05bA | 0.46 ± 0.06aA |
asparagine (Asn) | 2.73 ± 0.56aB | 2.48 ± 0.23aB | 2.65 ± 0.28aB | 2.00 ± 0.40aAB | 2.74 ± 0.24aB | 2.11 ± 0.38aAB | 1.68 ± 0.22bA | 1.42 ± 0.02bA | 1.60 ± 0.19bA | 0.40 ± 0.18a | ||
aspartic acid (Asp) | 2.40 ± 0.10bB | 2.31 ± 0.32bB | 2.32 ± 0.28bB | 0.19 ± 0.06aA | 1.83 ± 0.13bA | 2.27 ± 0.08bB | 2.10 ± 0.16bB | 1.17 ± 0.26aC | 1.55 ± 0.20bA | 1.38 ± 0.09bA | 1.38 ± 0.09bA | 0.72 ± 0.03aB |
methionine (Met) | 3.24 ± 0.12abB | 3.06 ± 0.53abAB | 3.39 ± 0.39bB | 2.57 ± 0.11aA | 2.80 ± 0.24aA | 3.00 ± 0.03aB | 2.60 ± 0.10aA | 2.58 ± 0.46aA | 2.95 ± 0.27bAB | 2.58 ± 0.17abA | 2.56 ± 0.19abA | 2.40 ± 0.17aA |
glutamic acid (Glu) | 3.20 ± 0.42bB | 3.10 ± 0.18abB | 3.12 ± 0.15abB | 2.54 ± 0.18aB | 3.02 ± 0.10bB | 3.32 ± 0.10cB | 2.97 ± 0.10bB | 2.66 ± 0.07aB | 2.20 ± 0.20bA | 1.98 ± 0.05bA | 1.99 ± 0.05bA | 1.56 ± 0.05aA |
phenylalanine (Phe) | 6.56 ± 0.15bB | 6.66 ± 1.10bB | 7.35 ± 0.77bB | 4.91 ± 0.27aA | 5.90 ± 0.21cA | 5.63 ± 0.30bcAB | 4.84 ± 0.09aA | 5.01 ± 0.44abA | 6.27 ± 0.49bAB | 5.18 ± 0.31aA | 5.10 ± 0.27aA | 4.64 ± 0.34aA |
glutamine (Gln) | 6.60 ± 0.11bC | 5.85 ± 0.93bC | 6.49 ± 0.77bC | 4.20 ± 0.24aB | 4.58 ± 0.41aB | 4.48 ± 0.43aB | 4.97 ± 0.84aB | 4.22 ± 0.36aB | 3.61 ± 0.22cA | 3.42 ± 0.20bcA | 3.10 ± 0.10bA | 2.18 ± 0.12aA |
lysine (Lys) | 7.87 ± 1.18bB | 7.36 ± 0.26bB | 8.52 ± 0.31bC | 4.33 ± 0.71aB | 4.43 ± 0.43aA | 6.37 ± 0.75bB | 5.97 ± 0.21bB | 5.17 ± 0.05aC | 5.05 ± 0.84bA | 4.36 ± 0.13bA | 5.12 ± 0.60bA | 3.08 ± 0.10aA |
histidine (His) | 2.32 ± 0.14bB | 2.60 ± 0.43bB | 2.85 ± 0.31bC | 1.60 ± 0.09aB | 2.19 ± 0.08bB | 1.99 ± 0.20abB | 2.03 ± 0.08abB | 1.92 ± 0.11aC | 1.76 ± 0.19bA | 1.60 ± 0.07abA | 1.71 ± 0.06bA | 1.36 ± 0.07aA |
tyrosine (Tyr) | 6.96 ± 0.25bC | 7.14 ± 0.72bB | 7.62 ± 0.95bC | 4.88 ± 0.16aC | 3.48 ± 0.09abA | 3.56 ± 0.06abA | 3.12 ± 0.01aA | 3.81 ± 0.41bB | 4.77 ± 0.40cB | 3.88 ± 0.22bA | 3.64 ± 0.14abB | 3.10 ± 0.25aA |
tryptophan (Trp) | 2.75 ± 0.06abA | 3.01 ± 0.34bcB | 3.53 ± 0.36cB | 2.18 ± 0.12aB | 2.65 ± 0.18bA | 2.37 ± 0.27abA | 2.18 ± 0.18aA | 2.29 ± 0.06abB | 2.66 ± 0.27bA | 2.21 ± 0.17aA | 2.18 ± 0.12aA | 1.90 ± 0.14aA |
cystine (Cys) | 0.97 ± 0.26a | 1.01 ± 0.02a | 1.02 ± 0.12a | 0.82 ± 0.05a |
Different lowercase letters indicate significant differences between models, with a significance level of 95% (p < 0.05).
Different capital letters indicate significant differences between cooking methods, with a significance level of 95% (p < 0.05).
Data shown are mean values from triplicates and the standard deviation.
Concerning the effect of GI alterations of elders on egg digestion, results also show that neither oral nor gastric alterations (E1 and E2) negatively impacted in vitro proteolysis extent (sum of the FAA released). Nevertheless, suboptimal intestinal conditions with reduced pancreatic and bile salts concentration coupled with an increase of residence time (E3) significantly reduced protein digestibility in both hard-boiled and omelet eggs. Proteolysis experimented reduction of 38 and 32% of the FAA released in hard-boiled and omelet eggs, respectively, under E3 GI conditions and compared to C. This result evidences the role of matrix organization, the proteins from solid matrices (hard-boiled and omelet) hinder to a greater extent than semiliquid matrices, the release and hydrolysis of proteins under suboptimal intestinal conditions.44 Poached egg resulted in a liquid yolk and semisolid white, which can be easily mixed with digestive fluids. In hard-boiled egg, both white and yolk acquired a solid structure, making the matrix degradation harder for its consequent hydrolyzation. In turn, omelet presents an emulsion-like structure of medium moisture in which protein network embeds lipid molecules and proteolysis has to occur before lipids can be made accessible to lipases.45 The intrinsic molecular properties of the egg proteins might determine enzyme accessibility, these properties being modified according to processing such as heat gelation. In fact, products with the same composition but different matrix structures can lead to different digestion patterns.20 In turn, Asensio-Grau et al.23 reported a higher impact of egg cooking methods on the digestibility of proteins, lipids, and xanthophylls bioaccessibility under exocrine pancreatic insufficiency (EPI) conditions than under healthy ones. Thus, poaching favored egg protein digestion under EPI conditions compared to other methods, mainly due to its semiliquid structure and lower degree of protein denaturation.
The essential amino acids (EAA)/nonessential amino acids (NEAA) ratio is also shown in Figure 2B. The EAA/NEAA ratio of cooked eggs digested under C model ranged from 1.78 to 2.14, this value being significantly lower in hard-boiled than in poached egg and omelet. A similar EAA/NEAA ratio was obtained from egg samples digested under E1 (oral alteration) and E2 (oral and gastric alterations) GI conditions. However, a considerable increase was found in samples digested mimicking the most suboptimal GI conditions given in elders (E3 model). According to this result, elderly intestinal conditions might favor the essential amino acids release to a greater extent than the nonessential ones, even if the total proteolysis extent was reduced under the E3 model. The predominant release of EAA than NEAA might be due to pancreatic enzymes specificity for certain peptide bonds,46 this effect being more relevant under a low enzymatic concentration (E3 model). The importance of EAA lies in muscle protein synthesis, as they are highly involved in this process.47 Therefore, even if the total FAA achieved under the most critical scenery resulted in reductions, this result would be especially relevant for elders suffering from sarcopenia, especially for the qualitative (referred to more EAA than NEAA) more than quantitative (total FAA extent) protein consumption point of view.
Complementarily, Figure 2 shows the amino acidic contents (g amino acids/100 g of initial protein) of hydrophobic amino acids (HAA), positively charged amino acids (PCAA), negatively charged amino acids (NCAA), aromatic amino acids (AAA), and sulfur-containing amino acids (SCAA). The presence of HAA and PCAA in the samples, especially Tyr, Met, His, and Lys, has been found to improve the antioxidant properties of peptides. In turn, amino acids with a large side group such as tryptophan (AAA with an indolic group) and histidine (PCAA with an imidazole group) contribute to the antioxidant potential of peptides but in the case as hydrogen donors. Additionally, peptide–lipid interactions can promote, or even improve, the antioxidant effects of peptides as a consequence of their hydrophobic properties.46 Moreover, some of the PCAAs are involved in upregulation of genes involved in mitochondrial biogenesis, offering another mechanism for increased oxidation of long-chain fatty acids and glucose in insulin-sensitive tissues.48 Likewise, methionine (with an SCAA character) besides histidine, serine, and glycine are the major donors of 1-carbon groups.48 In fact, diet supplementation with some NCAA, PCAA, and SCAA (e.g., glutamine, arginine, and N-acetyl-cysteine, respectively) are proposed for contributing to oxidative defense and immune function.48 After digestion under C conditions, the higher presence of amino acids with hydrophobic character (HAA) (sum of alanine, valine, isoleucine, leucine, tyrosine, phenylalanine, tryptophan, proline, methionine, and cysteine) in the amino acid profile (between 36 and 45.6 g HAA/100 g protein) is notable, corresponding to hard-boiled the greatest content compared to the other chemical groups. HAA content experimented, however, a notable decrease under E3 GI conditions in hard-boiled and omelet. On the contrary, sulfur-containing amino acid (SCAA) (sum of cysteine and methionine) was the least present chemical group (between 3.2 and 3.9 g/100 g protein under C model), regardless of the cooking methods or GI conditions. Slight reductions in SCAA content in the three cooking methods were shown, but only a statistical effect of elderly GI conditions was found in poached and omelet. Regarding the positively (PCAA) and negatively (NCAA) charged as well as the aromatic (AAA) amino acid contents, values obtained under E3 model were significantly lower than those found in the amino acid profile under C model in hard-boiled eggs and omelet. However, the hard-boiled egg seems to provide greater amounts of almost all of the chemical groups (excepting of SCAA) and also was the most affected sample by elderly alterations, with reductions up to 53% for NCAA under E3 GI conditions.
Besides the nutritional point of view, protein hydrolysates exert a positive impact on human health such as radical scavenging and reducing potential when large amounts of hydrophobic sulfur-containing amino acids such as cysteine, histidine, tryptophan, tyrosine, and phenylalanine are released.32,49 The contribution of scavenging free radicals to human health promotion has been stated as delayers of associated oxidative damage to the physiological macromolecules. They play, therefore, a crucial role against cardiovascular, inflammatory, and aging-induced degenerative diseases as well as cancers.50
Effect of Egg Cooking on Lipid Digestibility in Elders
The molar percentages of acyl groups (AG) of the products derived from triglyceride hydrolysis (TG) after digestion are presented in Table 3. As expected, 90% of the total fat in cooked eggs was present as TG before digestion. After GI digestion under C conditions, lipolysis extent achieves values of 99.7, 95.6, and 94.9% for hard-boiled eggs, poached eggs, and omelet, respectively. The conversion due to the hydrolytic action of pancreatic lipase of TG was mainly into FFA with values of 77.23, 80.92, and 71.18% in hard-boiled eggs, poached eggs, and omelet, respectively; followed by 1,2-DG, 2-MG, 1-MG, and 1,3-DG. In omelet samples, fat globules could be trapped in a well-stable protein network resulting from mixing and the posterior thermal treatment. Thus, the protein enzymatic breakdown occurs before lipids can be made accessible to lipases.45 These lipid–protein interactions slow down the accessibility of enzymes to the substrate, leading to lower conversion of TG into FFA together with lower matrix degradation compared to other methods.23
Table 3. Molar Percentages of Acyl Groups (AG) Supported on the Different Glyceryl Backbone Structures (TG, 1,2-DG, 1,3-DG, 2-MG, 1-MG) and Free Fatty Acids (FFA) and Cholesterol Content (mg/g Fat), Present in Non-digested (ND) and Digested Hard-boiled, Poached and Omelet Eggs; In Vitro GI Models: Control (C), Elderly 1 (E1), Elderly 2 (E2), Elderly 3 (E3)e.
cooking method | GI conditions | AGTg(%) | AG1,2DG(%) | AG1,3-DG (%) | AG2-MG(%) | AG1-MG(%) | FFA (%) | absorbable fraction (%)f | non-absorbable fraction (%)g | lipolysis extent (%)h | cholesterol (mg/g fat) |
---|---|---|---|---|---|---|---|---|---|---|---|
hard-boiled | ND | 89.57 ± 2.10 | 10.42 ± 2.08 | 10.43 ± 2.10 | 10.43 ± 2.10 | 54.14 ± 2.92bA | |||||
C | 0.32 ± 0.26aA | 12.84 ± 0.44cA | 1.021 ± 0.002cB | 5.61 ± 0.18bB | 3.00 ± 0.31aB | 77.23 ± 0.06aB | 85.83 ± 0.18aC | 13.86 ± 0.44cB | 99.68 ± 0.27bC | 50.91 ± 4.91abAB | |
E1 | 0.30 ± 0.07aA | 11.81 ± 0.06bA | 0.84 ± 0.09bB | 5.70 ± 0.10bB | 2.87 ± 0.20aB | 78.97 ± 1.04aB | 87.55 ± 0.74aC | 12.66 ± 0.03bA | 100.20 ± 0.78bC | 47.82 ± 4.22abA | |
E2 | 0.96 ± 0.22aA | 11.88 ± 0.23bcB | 0.53 ± 0.06aB | 6.15 ± 0.27bB | 3.12 ± 0.02aB | 78.09 ± 1.16aB | 87.36 ± 1.41aB | 12.41 ± 0.17bA | 99.77 ± 1.24bB | 46.65 ± 7.18abA | |
E3 | 4.73 ± 2.69bAB | 6.53 ± 0.49aA | 2.63 ± 0.04dB | 1.35 ± 0.21aA | 3.68 ± 0.05bB | 81.09 ± 3.41aB | 86.12 ± 3.14aAB | 9.15 ± 0.45aA | 95.27 ± 2.69aAB | 51.19 ± 5.68aA | |
poached | ND | 89.98 ± 0.29 | 9.99 ± 0.30 | 10.02 ± 0.29 | 10.02 ± 0.29 | 56.39 ± 2.81aA | |||||
C | 4.41 ± 0.42bB | 11.16 ± 0.44bcB | 0.91 ± 0.13aB | 1.82 ± 0.02bA | 0.79 ± 0.07bA | 80.92 ± 1.09aC | 83.53 ± 0.99aB | 12.06 ± 0.57bcA | 95.59 ± 0.42aB | 60.31 ± 4.06aB | |
E1 | 2.40 ± 0.19aB | 12.46 ± 0.27cB | 1.00 ± 0.03aC | 1.46 ± 0.06aA | 0.49 ± 0.09aA | 82.19 ± 0.20aC | 84.14 ± 0.05aB | 13.46 ± 0.24cB | 97.60 ± 0.19bB | 63.08 ± 4.48aB | |
E2 | 2.01 ± 0.88aAB | 10.83 ± 0.86bA | 0.81 ± 0.07aC | 1.33 ± 0.20aA | 0.46 ± 0.04aA | 84.56 ± 0.17bC | 86.34 ± 0.06bB | 11.65 ± 0.94bA | 97.99 ± 0.88bAB | 58.69 ± 8.46aA | |
E3 | 2.32 ± 0.39aA | 8.99 ± 0.04aB | 0.82 ± 0.02aA | 1.78 ± 0.04bB | 0.61 ± 0.07abA | 85.47 ± 0.48bC | 87.86 ± 0.37cB | 9.81 ± 0.02aA | 97.68 ± 0.39bB | 56.65 ± 7.39aA | |
omelet | ND | 90.86± 1.01 | 9.63 ± 1.09 | 9.64 ± 1.11 | 9.64 ± 1.11 | 52.27 ± 1.58bA | |||||
C | 5.11 ± 0.24abB | 13.06 ± 0.02abA | 0.30 ± 0.10aA | 7.22 ± 0.13cC | 3.11 ± 0.59aB | 71.18 ± 0.09aA | 81.51 ± 0.37abA | 13.37 ± 0.13aB | 94.89 ± 0.24aA | 45.29 ± 0.86abA | |
E1 | 5.49 ± 0.08bC | 13.61 ± 0.38bC | 0.68 ± 0.02abA | 6.22 ± 0.07bC | 3.10 ± 0.04aB | 71.67 ± 0.50abA | 80.98 ± 0.61aA | 14.29 ± 0.39aC | 95.28 ± 1.00aA | 47.33 ± 1.72abA | |
E2 | 3.90 ± 1.10aB | 11.97 ± 0.37aB | 0.29 ± 0.12aA | 7.03 ± 0.28cC | 3.64 ± 0.12aC | 73.21 ± 1.02abA | 83.87 ± 0.62bA | 12.26 ± 0.49aA | 96.12 ± 1.10aA | 49.83 ± 5.58abA | |
E3 | 4.28 ± 0.09abB | 13.03 ± 1.02abC | 0.93 ± 0.39bA | 4.11 ± 0.38aC | 3.38 ± 0.61aB | 74.27 ± 1.74bA | 81.76 ± 1.50abA | 13.96 ± 1.41aB | 95.72 ± 0.09aA | 47.18 ± 2.25aA |
Different lowercase letters indicate significant differences between models, with a significance level of 95% (p < 0.05).
Different capital letters indicate significant differences between cooking methods, with a significance level of 95% (p < 0.05).
Data shown are mean values from triplicates and the standard deviation.
Absorbable fraction includes AG2-MG% + AG1-MG% + FFA%.
Nonabsorbable fraction AG1,2-DG% + AG1,3-DG%.
Lipolysis extent represent the summarize.
Regarding the elderly GI conditions and their effect on lipid digestion, oral, gastric, and intestinal alterations negatively impact the absorbable fraction of hard-boiled, poached, and omelet eggs. In fact, a significant increase (p < 0.05) was noted in E3 with respect to C in poached egg. Nevertheless, the nonabsorbable fraction was slightly, but significantly, reduced in hard-boiled and poached eggs, and therefore the total lipolysis extent. Therefore, a longer intestinal transit time would be responsible for exerting a positive effect on lipid digestion,51 even under reduced pancreatic lipase and bile concentrations (E3 model).
Finally, the cholesterol contents (Table 3) of hard-boiled, poached, and omelet eggs before digestion were similar. These results are in agreement with those reported by Hur et al.,52 where the cholesterol content in pork patties was not affected by different cooking methods. However, cholesterol stability was slightly reduced in hard-boiled and omelet eggs after in vitro digestion. The decrease of cholesterol could be attributed to the higher formation of cholesterol oxidation products during in vitro digestion,53 being both physicochemical and enzymatic conditions the oxidation promoters.54 Also, microwave cooking52 might be co-responsible for the higher oxidative damage of cholesterol during the posterior GI digestion.
Vitamins A and D3 Bioaccessibility in Eggs: Impact of Cooking and GI Alterations in Elders
Figure 3 shows the vitamin A and D3 bioaccessibility (%) of hard-boiled, poached, and omelet eggs. Similarly to macronutrient digestibility, the structure matrix seems to be responsible, to a certain extent, for to the differences found in terms of solubilization and micellar incorporation of the micronutrients. Hence, it was found that the higher the complexity of structured food matrices (i.e., omelet), the minor the fat-soluble vitamin bioaccessibility present in the yolk.23,55 Vitamin D3 bioaccessibility values under standardized GI conditions (C) agree with this behavior. Nevertheless, vitamin A bioaccessibility was higher in omelet than in hard-boiled or poached eggs. Vitamin A has been reported to experiment oxidation along digestion, leading to a reduced final concentration but increasing the presence of other compounds such as β-ionone, 2,2,6-trimethylcyclohexanone,β-cyclocitral,(E)-5,6-epoxy-β-ionone, ionene, β-homocyclocytral, and dihydroactinidiolide.56 Hence, omelet structure could exert a protective effect on vitamin A against oxidation reactions and explain a higher vitamin A bioaccessibility in omelet than in hard-boiled and poached eggs.
Figure 3.
Vitamin A and D3 bioaccessibility achieved in hard-boiled, poached, and omelet eggs in vitro digested under different GI conditions (control (C), Elderly 1 (E1), Elderly 2 (E2), and Elderly 3 (E3) models). Different lowercase letters indicate significant differences between models, and different capital letters indicate significant differences between cooking methods, with a significance level of 95% (p < 0.05).
With respect to vitamin bioaccessibility under GI conditions of elders (E1, E2, and E3), vitamin D3 release from all egg products was significantly reduced under E3 model conditions. However, no statistically significant differences were found in vitamin A bioaccessibility values achieved under C and E3 digestion conditions. Only vitamin A release from poached eggs seems to be negatively affected when oral and gastric conditions were suboptimal as in E1 and E2 simulations.
Liposoluble compounds release is dependent on their solubilization favored by bile acids presence. Thus, it was expected to obtain lower bioaccessibility values of both vitamins under reduced bile salts concentration occurring in the E3 model. Nevertheless, only vitamin D3 was affected by this suboptimal intestinal condition.57
Descriptive Relationship Among Digestibility, Egg Cooking Methods, and Elderly GI Conditions
A PCA was performed to assess the relationship between digestion end products from a descriptive point of view (Figure 4). Also, the component weights and the scores of hard-boiled, poached, and omelet eggs digested under the simulated GI conditions (C, E1, E2, and E3) are included. The first two principal components of the analysis explain 79.179% of the total variance of the digestibility in the samples (PC1: 57.105% and PC2: 22.074%). Using the number of factor loads for two main components, it was identified which variables significantly affect the components C1 and C2. Vitamin bioaccessibility, lipolysis extent, as well as the HHA, PCAA, NCAA, and total (sum of the FAA released) proteolysis extents have the most significant impact on the value of the PC1. On the other hand, absorbable and nonabsorbable lipid fractions, SCAA, and EAA/NEAA ratio presented the most significant impact on the PC2 value. As a result, this procedure allows the analysis of the two-dimensional space that was created based on the main components. In the score plot, the proximity between samples indicates similar behavior in terms of digestibility. In PC1, it is noted that omelet, located at the upper right side of the plot, exhibits a digestion pattern different from those of hard-boiled and poached eggs, located at the left side of the plot. PC2 seems to distinguish vitamin A bioaccessibility (higher in omelet) and samples with a higher EAA/NEAA ratio after digestion. Overall, PCA shows the narrow relationship between: proteolysis and lipolysis extents; the amino acids chemical classifications (excepting SCAA) with the proteolysis extent and the vitamin D3 bioaccessibility; and the absorbable lipid fraction and the cholesterol content with the lipolysis extent.
Figure 4.
Biplot and component weights of the different end-digestion products of proteins (proteolysis extent, EAA/NEAA ratio, HAA, PCAA, NCAA, AAA, and SCAA contents), lipids (cholesterol content, absorbable, nonabsorbable, and total lipolysis extents), and micronutrients (vitamin A and D3 bioaccessibility) and their association with the binomial cooked eggs (hard-boiled, poached, and omelet) under GI conditions (Control (C), Elderly 1 (E1), Elderly 2 (E2), Elderly 3 (E3)) obtained by means of a principal components analysis (PCA).
In sum, GI alterations appearing with aging negatively affect the ovo-protein digestibility with a reduction of up to 37% in the FAA released, compared with total FAA extents obtained under control conditions. Hard-boiled or poached method was more advisable than omelet preparation to maximize the proteolysis extent (sum of FAA released) under elderly conditions. A notable increase in the release of essential amino acids, compared with the nonessential ones, was also noted under simulated elderly GI conditions. Neither total lipolysis extent nor lipidic absorbable fraction is compromised with aging. Nevertheless, omelet preparation plays a significant role against the absorbable lipid fraction, mainly in free fatty acid release. Finally, vitamin D3, lipolysis, and proteolysis extents seem to be positively linked, especially in hard-boiled and poached eggs under elderly GI conditions. It could be stated that poached and omelet preparations might be more advisable than hard-boiled in terms of net supply of bioaccessible vitamin A for elders, while the bioaccessible vitamin D3 contents provided are very similar regardless of the cooking method. Therefore, this study provides a better understanding of egg protein and lipid hydrolysis, together with liposoluble vitamin bioaccessibility, under GI conditions of elderlies and as a function of cooking method. This information tries to contribute to establishing accurate dietary recommendations addressed to this population group.
Glossary
Abbreviations
- GI
gastrointestinal
- C
standardized gastrointestinal condition
- E1
elderly oral alteration
- E2
elderly oral and gastric alterations
- E3
elderly oral, gastric, and intestinal alterations
- DIAAS
digestible indispensable amino acid score
- U
enzymatic units
- HPLC
high-performance liquid chromatography
- SGF
simulated gastric fluid
- SIF
simulated intestinal fluid
- 1H NMR
proton nuclear magnetic resonance
- FAA
free amino acids
- EAA
essential amino acids
- NEAA
nonessential amino acids
- HAA
hydrophobic amino acids
- PCAA
positively charged amino acids
- NCAA
negatively charged amino acids
- AAA
aromatic amino acids
- SCAA
sulfur-containing amino acids
- GC–MS
gas chromatography–mass spectrometry
- AG
acyl groups
- MG
monoglycerides
- DG
diglycerides
- TG
triglycerides
- FFA
free fatty acids
- ANOVA
analysis of variance
- LSD
less significant difference
- PC
principal component
- PCA
principal component analysis
- Ala
alanine
- Gly
glycine
- Val
valine
- Leu
leucine
- Ile
isoleucine
- Thr
threonine
- Ser
serine
- Pro
proline
- Asn
asparagine
- Asp
aspartic acid
- Met
methionine
- Glu
glutamic acid
- Phe
phenylalanine
- Gln
glutamine
- Lys
lysine
- His
histidine
- Tyr
tyrosine
- Trp
tryptophan
- Cys
cystine
- ND
nondigested
This study was performed with financial support by Generalitat Valenciana (AICO/2018/289). Also, E.H.-O. is a beneficiary of a predoctoral grant (no. 306682) from the Mexican National Council of Science and Technology (CONACyT).
The authors declare no competing financial interest.
References
- UN. World Population Prospects 2019: Highlights (St/Esa/Ser. A/423), 2019.
- Carew H. T.; Zhang W.; Rea T. D. Chronic Health Conditions and Survival after Out-of-Hospital Ventricular Fibrillation Cardiac Arrest. Heart 2007, 93, 728–731. 10.1136/hrt.2006.103895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Volkert D.; Beck A. M.; Cederholm T.; Cruz-Jentoft A.; Goisser S.; Hooper L.; Kiesswetter E.; Maggio M.; Raynaud-Simon A.; Sieber C. C.; Sobotka L.; Van Asselt D.; Wirth R.; Bischoff S. C. ESPEN Guideline ESPEN Guideline on Clinical Nutrition and Hydration in Geriatrics. Clin. Nutr. 2018, 38, 10–47. 10.1016/j.clnu.2018.05.024. [DOI] [PubMed] [Google Scholar]
- Morley J. E. Frailty and Sarcopenia: The New Geriatric Giants. Rev. Invest. Clin. 2016, 68, 59–67. [PubMed] [Google Scholar]
- Shlisky J.; Bloom D. E.; Beaudreault A. R.; Tucker K. L.; Keller H. H.; Freund-Levi Y.; Fielding R. A.; Cheng F. W.; Jensen G. L.; Wu D.; Meydani S. N. Nutritional Considerations for Healthy Aging and Reduction in Age-Related Chronic Disease. Adv. Nutr. 2017, 8, 17–26. 10.3945/an.116.013474. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rémond D.; Shahar D. R.; Gille D.; Pinto P.; Kachal J.; Peyron M. A.; Dos Santos C. N.; Walther B.; Bordoni A.; Dupont D.; Tomás-Cobos L.; Vergères G. Understanding the Gastrointestinal Tract of the Elderly to Develop Dietary Solutions That Prevent Malnutrition. Oncotarget 2015, 6, 13858–13898. 10.18632/oncotarget.4030. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rashid I.; Tiwari P.; Lehl S. S. Malnutrition among Elderly a Multifactorial Condition to Flourish: Evidence from a Cross-Sectional Study. Clin. Epidemiol. Global Health 2020, 8, 91–95. 10.1016/j.cegh.2019.05.001. [DOI] [Google Scholar]
- Gilmartin S.; O’Brien N.; Giblin L. Whey for Sarcopenia; Can Whey Peptides, Hydrolysates or Proteins Play a Beneficial Role?. Foods 2020, 9, 750 10.3390/foods9060750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peyron M. A.; Santé-Lhoutellier V.; François O.; Hennequin M. Oral Declines and Mastication Deficiencies Cause Alteration of Food Bolus Properties. Food Funct. 2018, 9, 1112–1122. 10.1039/c7fo01628j. [DOI] [PubMed] [Google Scholar]
- Nagler R. M.; Hershkovich O. Age-Related Changes in Unstimulated Salivary Function and Composition and Its Relations to Medications and Oral Sensorial Complaints. Aging Clin. Exp. Res. 2005, 17, 358–366. 10.1007/BF03324623. [DOI] [PubMed] [Google Scholar]
- Salles N. Basic Mechanisms of the Aging Gastrointestinal Tract. Dig. Dis. 2007, 25, 112–117. 10.1159/000099474. [DOI] [PubMed] [Google Scholar]
- Shani-Levi C.; Alvito P.; Andrés A.; Assunção R.; Barberá R.; Blanquet-Diot S.; Bourlieu C.; Brodkorb A.; Cilla A.; Deglaire A.; Denis S.; Dupont D.; Heredia A.; Karakaya S.; Giosafatto C. V. L.; Mariniello L.; Martins C.; Ménard O.; El S. N.; Vegarud G. E.; Ulleberg E.; Lesmes U. Extending in Vitro Digestion Models to Specific Human Populations: Perspectives, Practical Tools and Bio-Relevant Information. Trends Food Sci. Technol. 2017, 60, 52–63. 10.1016/j.tifs.2016.10.017. [DOI] [Google Scholar]
- Réhault-Godbert S.; Guyot N.; Nys Y. The Golden Egg: Nutritional Value, Bioactivities, and Emerging Benefits for Human Health. Nutrients 2019, 11, 684 10.3390/nu11030684. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang X.; Qiu N.; Liu Y. Effect of Different Heat Treatments on In Vitro Digestion of Egg White Proteins and Identification of Bioactive Peptides in Digested Products. J. Food Sci. 2018, 83, 1140–1148. 10.1111/1750-3841.14107. [DOI] [PubMed] [Google Scholar]
- Phillips S. M. Current Concepts and Unresolved Questions in Dietary Protein Requirements and Supplements in Adults. Front. Nutr. 2017, 4, 13 10.3389/fnut.2017.00013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qureshi A. I.; Suri M. F. K.; Ahmed S.; Nasar A.; Divani A. A.; Kirmani J. F. Regular Egg Consumption Does Not Increase the Risk of Stroke and Cardiovascular Diseases. Med. Sci. Monit. 2006, 13, CR1–CR8. [PubMed] [Google Scholar]
- Mattioli S.; Dal Bosco A.; Martino M.; Ruggeri S.; Marconi O.; Sileoni V.; Falcinelli B.; Castellini C.; Benincasa P. Alfalfa and Flax Sprouts Supplementation Enriches the Content of Bioactive Compounds and Lowers the Cholesterol in Hen Egg. J. Funct. Foods 2016, 22, 454–462. 10.1016/j.jff.2016.02.007. [DOI] [Google Scholar]
- Bernhardt S.; Schlich E. Impact of Different Cooking Methods on Food Quality: Retention of Lipophilic Vitamins in Fresh and Frozen Vegetables. J. Food Eng. 2006, 77, 327–333. 10.1016/j.jfoodeng.2005.06.040. [DOI] [Google Scholar]
- Nyemb K.; Guérin-Dubiard C.; Pézennec S.; Jardin J.; Briard-Bion V.; Cauty C.; Rutherfurd S. M.; Dupont D.; Nau F. The Structural Properties of Egg White Gels Impact the Extent of in Vitro Protein Digestion and the Nature of Peptides Generated. Food Hydrocolloids 2016, 54, 315–327. 10.1016/j.foodhyd.2015.10.011. [DOI] [Google Scholar]
- Nyemb-Diop K.; Causeur D.; Jardin J.; Briard-Bion V.; Guérin-Dubiard C.; Rutherfurd S. M.; Dupont D.; Nau F. Investigating the Impact of Egg White Gel Structure on Peptide Kinetics Profile during in Vitro Digestion. Food Res. Int. 2016, 88, 302–309. 10.1016/j.foodres.2016.01.004. [DOI] [Google Scholar]
- Somaratne G.; Ye A.; Nau F.; Ferrua M. J.; Dupont D.; Paul Singh R.; Singh J. Egg White Gel Structure Determines Biochemical Digestion with Consequences on Softening and Mechanical Disintegration during in Vitro Gastric Digestion. Food Res. Int. 2020, 138, 109782 10.1016/j.foodres.2020.109782. [DOI] [PubMed] [Google Scholar]
- Luo Q.; Boom R. M.; Janssen A. E. M. Digestion of Protein and Protein Gels in Simulated Gastric Environment. LWT – Food. Sci. Technol. 2015, 63, 161–168. 10.1016/j.lwt.2015.03.087. [DOI] [Google Scholar]
- Asensio-Grau A.; Peinado I.; Heredia A.; Andrés A. Effect of Cooking Methods and Intestinal Conditions on Lipolysis, Proteolysis and Xanthophylls Bioaccessibility of Eggs. J. Funct. Foods 2018, 46, 579–586. 10.1016/j.jff.2018.05.025. [DOI] [Google Scholar]
- Official Methods of Análisis, 15th ed.; Association of Official Analytical Chemists, 2000. [Google Scholar]
- Menezes E. W.; de Melo A. T.; Lima G. H.; Lajolo F. M. Measurement of Carbohydrate Components and Their Impact on Energy Value of Foods. J. Food Compos. Anal. 2004, 17, 331–338. 10.1016/j.jfca.2004.03.018. [DOI] [Google Scholar]
- Castaneda N.; Lee Y. Microstructure of a Model Fresh Cheese and Bioaccessibility of Vitamin D3 Using in Vitro Digestion. Gels 2019, 5, 16 10.3390/gels5010016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hernández-Olivas E.; Muñoz-Pina S.; Andrés A.; Heredia A. Impact of Elderly Gastrointestinal Alterations on in Vitro Digestion of Salmon, Sardine, Sea Bass and Hake: Proteolysis, Lipolysis and Bioaccesibility of Calcium and Vitamins. Food Chem. 2020, 326, 127024 10.1016/j.foodchem.2020.127024. [DOI] [PubMed] [Google Scholar]
- Nieva-Echevarría B.; Goicoechea E.; Manzanos M. J.; Guillén M. D. Effects of Different Cooking Methods on the Lipids and Volatile Components of Farmed and Wild European Sea Bass (Dicentrarchus labrax). Food Res. Int. 2018, 103, 48–58. 10.1016/j.foodres.2017.10.029. [DOI] [PubMed] [Google Scholar]
- Minekus M.; Alminger M.; Alvito P.; Ballance S.; Bohn T.; Bourlieu C.; Carrière F.; Boutrou R.; Corredig M.; Dupont D.; Dufour C.; Egger L.; Golding M.; Karakaya S.; Kirkhus B.; Le Feunteun S.; Lesmes U.; MacIerzanka A.; MacKie A.; Marze S.; McClements D. J.; Ménard O.; Recio I.; Santos C. N.; Singh R. P.; Vegarud G. E.; Wickham M. S. J.; Weitschies W.; Brodkorb A. A Standardised Static in Vitro Digestion Method Suitable for Food-an International Consensus. Food Funct. 2014, 5, 1113–1124. 10.1039/c3fo60702j. [DOI] [PubMed] [Google Scholar]
- Jalabert-Malbos M. L.; Mishellany-Dutour A.; Woda A.; Peyron M. A. Particle Size Distribution in the Food Bolus after Mastication of Natural Foods. Food Qual. Preference 2007, 18, 803–812. 10.1016/j.foodqual.2007.01.010. [DOI] [Google Scholar]
- Peinado I.; Koutsidis G.; Ames J. Production of Seafood Flavour Formulations from Enzymatic Hydrolysates of Fish By-Products. LWT – Food Sci. Technol. 2016, 66, 444–452. 10.1016/j.lwt.2015.09.025. [DOI] [Google Scholar]
- Uluko H.; Zhang S.; Liu L.; Tsakama M.; Lu J.; Lv J. Effects of Thermal, Microwave, and Ultrasound Pretreatments on Antioxidative Capacity of Enzymatic Milk Protein Concentrate Hydrolysates. J. Funct. Foods 2015, 18, 1138–1146. 10.1016/j.jff.2014.11.024. [DOI] [Google Scholar]
- Matt D.; Veromann E.; Luik A. Effect of Housing Systems on Biochemical Composition. Agron. Res. 2009, 7, 662–667. [Google Scholar]
- Miranda J. M.; Anton X.; Redondo-Valbuena C.; Roca-Saavedra P.; Rodriguez J. A.; Lamas A.; Franco C. M.; Cepeda A. Egg and Egg-Derived Foods: Effects on Human Health and Use as Functional Foods. Nutrients 2015, 7, 706 10.3390/nu7010706. [DOI] [PMC free article] [PubMed] [Google Scholar]
- U.S. Department of Agriculture, Agricultural Research Service. FoodData Central https://fdc.nal.usda.gov/fdc-app.html#/food-details/169230/nutrients. accessed on January 2020.
- Seuss-Baum I.; Nau F.; Guérin-Dubiard C.. The Nutritional Quality of Eggs. In Improving the Safety and Quality of Eggs and Egg Products; Elsevier Ltd., 2011; Vol. 2, pp 201–236. [Google Scholar]
- El Gran Libro Del Huevo (in Spanish), 2009th ed.; In del Mar Fernández M.; Lobato A., Eds.; Spanish Institute of Egg Studies: Madrid, Spain, 2009. [Google Scholar]
- Nimalaratne C.; Lopes-Lutz D.; Schieber A.; Wu J. Effect of Domestic Cooking Methods on Egg Yolk Xanthophylls. J. Agric. Food Chem. 2012, 60, 12547–12552. 10.1021/jf303828n. [DOI] [PubMed] [Google Scholar]
- Zasada M.; Budzisz E.; Kolodziejska J.; Kalinowska-Lis U. An Evaluation of the Physicochemical Parameters and the Content of the Active Ingredients in Original Formulas Containing Retinol. J. Cosmet. Dermatol. 2020, 19, 2374–2383. 10.1111/jocd.13286. [DOI] [PubMed] [Google Scholar]
- Hemery Y. M.; Fontan L.; Moench-Pfanner R.; Laillou A.; Berger J.; Renaud C.; Avallone S. Influence of Light Exposure and Oxidative Status on the Stability of Vitamins A and D3 during the Storage of Fortified Soybean Oil. Food Chem. 2015, 184, 90–98. 10.1016/j.foodchem.2015.03.096. [DOI] [PubMed] [Google Scholar]
- Haham M.; Ish-Shalom S.; Nodelman M.; Duek I.; Segal E.; Kustanovich M.; Livney Y. D. Stability and Bioavailability of Vitamin D Nanoencapsulated in Casein Micelles. Food Funct. 2012, 3, 737–744. 10.1039/c2fo10249h. [DOI] [PubMed] [Google Scholar]
- Tsai S. Y.; Lin H. Y.; Hong W. P.; Lin C. P. Evaluation of Preliminary Causes for Vitamin D Series Degradation via DSC and HPLC Analyses. J. Therm. Anal. Calorim. 2017, 130, 1357–1369. 10.1007/s10973-017-6209-4. [DOI] [Google Scholar]
- Domínguez R.; Borrajo P.; Lorenzo J. M. The Effect of Cooking Methods on Nutritional Value of Foal Meat. J. Food Compos. Anal. 2015, 43, 61–67. 10.1016/j.jfca.2015.04.007. [DOI] [Google Scholar]
- Hernández-Olivas E.; Muñoz-Pina S.; Sánchez-García J.; Andrés A.; Heredia A. Understanding the Role of Food Matrix on the Digestibility of Dairy Products under Elderly Gastrointestinal Conditions. Food Res. Int. 2020, 137, 109454 10.1016/j.foodres.2020.109454. [DOI] [PubMed] [Google Scholar]
- Heredia A.; Asensio-Grau A.; Calvo-Lerma J.; Andrés A.. Interactions Among Macronutrients and Their Effect on Lypolisis. In Bioaccessibility and Digestibility of Lipids from Food; Springer International Publishing, 2021; pp 151–168. [Google Scholar]
- Aderinola T. A.; Fagbemi T. N.; Enujiugha V. N.; Alashi A. M.; Aluko R. E. Amino Acid Composition and Antioxidant Properties of Moringa oleifera Seed Protein Isolate and Enzymatic Hydrolysates. Heliyon 2018, 4, e00877 10.1016/j.heliyon.2018.e00877. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Volpi E.; Kobayashi H.; Sheffield-Moore M.; Mittendorfer B.; Wolfe R. R. Essential Amino Acids Are Primarily Responsible for the Amino Acid Stimulation of Muscle Protein Anabolism in Healthy Elderly Adults. Am. J. Clin. Nutr. 2003, 78, 250–258. 10.1093/ajcn/78.2.250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu G. Functional Amino Acids in Growth, Reproduction, and Health. Adv. Nutr. 2010, 1, 31–37. 10.3945/an.110.1008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Udenigwe C. C.; Aluko R. E. Chemometric Analysis of the Amino Acid Requirements of Antioxidant Food Protein Hydrolysates. Int. J. Mol. Sci. 2011, 12, 3148–3161. 10.3390/ijms12053148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quansah J. K.; Udenigwe C. C.; Saalia F. K.; Yada R. Y. The Effect of Thermal and Ultrasonic Treatment on Amino Acid Composition, Radical Scavenging and Reducing Potential of Hydrolysates Obtained from Simulated Gastrointestinal Digestion of Cowpea Proteins. Plant Foods Hum. Nutr. 2013, 68, 31–38. 10.1007/s11130-013-0334-4. [DOI] [PubMed] [Google Scholar]
- Lamothe S.; Corbeil M. M.; Turgeon S. L.; Britten M. Influence of Cheese Matrix on Lipid Digestion in a Simulated Gastro-Intestinal Environment. Food Funct. 2012, 3, 724–731. 10.1039/C2FO10256K. [DOI] [PubMed] [Google Scholar]
- Hur S. J.; Lee S. Y.; Moon S. S.; Lee S. J. In Vitro Effects of Cooking Methods on Digestibility of Lipids and Formation of Cholesterol Oxidation Products in Pork. Korean J. Food Sci. Anim. Resour. 2014, 34, 280–286. 10.5851/kosfa.2014.34.3.280. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nieva-Echevarría B.; Goicoechea E.; Guillén M. D. Food Lipid Oxidation under Gastrointestinal Digestion Conditions: A Review. Crit. Rev. Food Sci. Nutr. 2020, 60, 461–478. 10.1080/10408398.2018.1538931. [DOI] [PubMed] [Google Scholar]
- Hur S.; Min B.; Nam K.; Lee E.; Ahn D. Effect of Dietary Cholesterol and Cholesterol Oxides on Blood Cholesterol, Lipids, and the Development of Atherosclerosis in Rabbits. Int. J. Mol. Sci. 2013, 14, 12593–12606. 10.3390/ijms140612593. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Borel P. Factors Affecting Intestinal Absorption of Highly Lipophilic Food Microconstituents (Fat-Soluble Vitamins, Carotenoids and Phytosterols). Clin. Chem. Lab. Med. 2003, 41, 979–994. 10.1515/CCLM.2003.151. [DOI] [PubMed] [Google Scholar]
- Nieva-Echevarría B.; Goicoechea E.; Guillén M. D. Polyunsaturated Lipids and Vitamin A Oxidation during Cod Liver Oil in Vitro Gastrointestinal Digestion. Antioxidant Effect of Added BHT. Food Chem. 2017, 232, 733–743. 10.1016/j.foodchem.2017.04.057. [DOI] [PubMed] [Google Scholar]
- Werner A.; Kuipers F.; Verkade H. J.. Fat Absorption and Lipid Metabolism in Cholestasis. In Madame Curie Bioscience Database; Landes Bioscience, 2013. [Google Scholar]