Impact of Maillard reaction products on nutrition and health: Current knowledge and need to understand their fate in the human digestive system

The Maillard Reaction (MR) is a non-enzymatic chemical reaction which results in the linkage between the amino group of amino acids and the carbonyl group of reduced sugars. MR products (MRPs) are common components of processed foods, mainly as a result of heating, especially in the Western diet. MRPs are classified as into three stages: initial, intermediate, and final stages, indicative of increased complexity and size, incurring different flavor, aroma, and texture. MRPs presence is known to reduce the nutritional quality of foods, particularly by reducing protein digestibility. Early reports have linked MRPs, especially advanced glycation end-products (AGEs) present in high concentration in the typical Western diet, to health conditions and diseases. However conflicting data has since been reported, and only a few (acrylamide, heterocyclic amines and 5-Hydroxymethylfurfural) MRPs have documented potential toxic or carcinogenic effects. High molecular weight MRPs are not available for direct absorption in the higher gastrointestinal tract, and are thus mostly metabolized by resident colonic microbes. MRPs have been the subject of sparse research interest in comparison with other non-digestible dietary elements. In this review, we outline the state of knowledge on MRPs in nutrition and health, and highlight the need to develop the limited knowledge on their impact on the gut microbiota and which metabolites derive from MRPs fermentation.     

肉制品加工过程中晚期糖基化终产物形成、检测及抑制研究进展

晚期糖基化终产物(advanced glycation end products, AGEs)是还原糖的羰基与蛋白质、脂质或核酸的游离氨基通过美拉德反应等途径产生的一系列结构复杂的化合物总称。目前已有不少研究证明AGEs在体内的积累会导致衰老、糖尿病、阿尔兹海默症等相关慢性疾病的发生, 也会引起肿瘤的发展与恶化。近年来, 随着国民生活水平的不断提高, 肉制品消费的不断增加, 其加工过程中AGEs的生成逐渐引起广泛关注。本文阐述了肉类加工过程中AGEs的结构、分类、形成途径与机制、检测方法, 总结了在不同加工方式下, 采用不同检测方法测量肉类中羧甲基赖氨酸和羧乙基赖氨酸的含量, 并重点介绍了AGEs形成的影响因素及其抑制, 旨在为肉制品加工过程中AGEs的生成控制等深入研究提供理论基础。     

Structural elucidation and analysis of thermal degradation products of the Fusarium mycotoxin nivalenol

The major class of mycotoxins produced by Fusarium moulds are trichothecenes, a large group of sesquiterpenes sharing the same basic chemical structure, a 12,13-epoxytrichothec-9-ene ring system. Their toxic effects range from causing diarrhoea, vomiting and gastro-intestinal inflammation to noncompetitive inhibition of the biosynthesis of proteins in eukaryotic cells. Trichothecenes in general are relatively stable compounds, their degradation is observed only at high temperatures and prolonged heating time. In order to investigate the stability of the trichothecene nivalenol (NIV) under food processing conditions such as cooking or baking, we performed model heating experiments and screened the residue for degradation products using gas chromatography-mass spectrometry (GC-MS). Heating of nivalenol, especially under mild alkaline conditions, gave a mixture of four compounds (norNIV A, norNIV B, norNIV C, and NIV lactone), which where isolated and identified by nuclear magnetic resonance (NMR) and MS experiments. Although their formation was also demonstrated in heating experiments with spiked flour samples, only norNIV B was detectable in a screening of several commercially available samples, possibly due to the very low contamination with nivalenol. Furthermore, cell culture experiments using immortalized human kidney epithelial (IHKE) cells showed that the four compounds are less cytotoxic (formazan dye cytotoxicity assay) compared to nivalenol. Whereas nivalenol revealed an EC50 at 0.9 micromol, all other compounds did not show any significant effect up to 100 micromol.     

Effects of temperature,pH and light on the stability of aloin A and characterisation of its major degradation products

This study explored the stability and degradation products of aloin A under varying pH, temperature and light conditions usually encountered in processing. The stability of aloin A was significantly affected by temperature and pH. The content of aloin A decreased by more than 90% within 12 h at 50 °C and within 6 h at 70 °C, respectively. A significant decrease in stability was also observed at higher pHs. At pH 8.0, less than 2% of aloin A remained within 12 h. However, aloin A exhibited good stability at acidic pH levels with 94% remaining at pH 2.0 for 14 days. Light exerted no influence on the stability during the experimental period (14 days). Aloe‐emodin, elgonica‐dimers A and B were characterised as major degradation products of aloin A at pH 5.0 or below, and elgonica‐dimers were mainly formed at 4 °C as well. 10‐hydroxyaloins A and B were found under any condition except at pH 2.0 and 3.0, and they were mainly formed under high temperature, neutral‐basic and any light conditions.     

Estimation of ruminal and intestinal digestion profiles,hourly effective degradation ratio and potential N to energy synchronization of co‐products from bioethanol processing

BACKGROUND: Little research has been conducted to determine the magnitude of the differences in nutritive value among wheat dried distillers' grains with solubles (DDGS), corn DDGS and blend DDGS, or between different bioethanol plants. The objectives of this study were to compare different types of DDGS and different bioethanol plants in terms of: (1) rumen degradation kinetics profile of each DDGS component and rumen availability; (2) intestinal digestion profile of rumen undegraded protein; (3) hourly effective rumen degradation ratio and potential N‐to‐energy synchronization; (4) the role of acid detergent insoluble nitrogen in the determination of nutrient availability of DDGS. In addition, these parameters were compared in DDGS as opposed to parental grain. RESULTS: (1) The effective degradability of dry matter in DDGS samples increased as the content of feedstock wheat increased. DDGS are a good source of rumen‐undegradable protein. The protein content of DDGS derived from wheat is higher relative to that derived from corn; however, the undegradability of the protein fraction increases as the proportion of corn in the feedstock augments. (2) In addition, DDGS provide significant amounts of rumen‐degradable protein, which increased as the content of wheat in the feedstock increased. This indicates a potential loss of N when high levels of DDGS are included in the diet. (3) Acid detergent insoluble crude protein (ADICP) levels were low across DDGS samples, revealing no effect on ruminal and intestinal disappearance of protein. However, consideration should be given to the numerical differences in digestibility of rumen‐undegradable protein and the relation to ADICP content. (4) Further research with a higher number of samples and higher variability in the ADICP content should be undertaken to investigate the effect of ADICP on rumen and intestinal disappearance of DDGS protein. CONCLUSION: The digestive characteristics of each DDGS component (dry matter, organic matter, crude protein and neutral detergent fiber), the hourly effective degradation ratio between N and organic matter, and the intestinal availability of rumen‐undegradable protein differed significantly (P < 0.05) among wheat DDGS, blend DDGS and corn DDGS, and to a lesser extent between the different bioethanol plants. These results indicate that it is inappropriate to assume fixed rumen and intestinal degradation characteristics for DDGS without considering factors such as DDGS type and bioethanol plant origin. Copyright © 2010 Society of Chemical Industry     

The impact of the various chemical and physical factors on the degradation rate of bronopol

Bronopol (2‐bromo‐2‐nitropropane‐1,3‐diol) is used as preservative in cosmetic industry. Its main role in commercial products consists in protection of the cosmetic composition stability by inhibiting the development of micro‐organisms. Unfortunately, preservatives can also undergo the degradation processes. The aim of examinations was to prove that bronopol decomposes in aqueous solutions and storage conditions have a significance influence on its degradation rate. High‐performance liquid chromatography method (methanol/water with hydrochloric acid 5:95 v/v) with spectrophotometric detection (210 nm) was used for examining the decomposition rate of bronopol. The impact of chemical (addition of cosmetics components: citric acid and/or sodium dodecylsulfate) and physical (elevated and ambient temperature, sunlight or ultraviolet radiation and air access) factors has been elaborated. Bronopol decomposes most rapidly (independently on the sample surrounding conditions) when it is in solution with sodium dodecylsulfate, the inverse dependence is observed in the presence of two compounds – citric acid and sodium dodecylsulfate. Additionally, the elevated temperature causes the acceleration of decomposition. Bronopol degradation by‐products were also identified as methanol, formic acid, tris(hydroxymethyl)methane and 2‐bromo‐2‐nitroethanol.     

Microbial degradation of normal maize and bm3 maize in the rumen observed by scanning electron microscopy

Samples of internodes and leaf blades from normal and bm3 maize (Zea mays L) harvested at dough to glazing stage were studied separately to determine their dry matter content, wall composition (NDF, ADF and ADL) and digestibility in sacco. For examination by light and scanning electron microscope, fragments 0·5 cm long were cut halfway along the internode beneath the female ear and on the corresponding blade. The wall and lignin contents of the bm3 maize were lower than in normal maize. The bm3 maize had a greater extent and faster rate of internode and blade disappearance in the rumen than normal maize samples. The histological structure of the two maizes was the same, but after 24 h in the rumen the parenchyma of the bm3 maize had degraded faster and the secondary walls of the fibres of its vascular bundles were degraded whereas those of normal maize had remained intact. After 72 h in the rumen the sclerenchyma of normal maize had changed little whereas that of the bm3 maize had much thinner walls and was abundantly colonised by rumen bacteria.     

儿童肠道中乳酸菌的分离、鉴定及其降解3-甲基吲哚的功能研究

为研究从人体肠道分离、筛选的乳酸菌(lactic acid bacteria,LAB),其体外降解3-甲基吲哚的功能.采用MRS培养基从3～8岁健康儿童肠道中筛选乳酸菌,提取细菌总DNA,扩增16S rRNA序列,构建系统发育树.在以3-甲基吲哚为唯一碳源、氮源的无机盐培养基中胁迫培养乳酸菌,紫外分光光度计测定吸光度值...     

Variation in the carotenoid composition of acerola and its processed products

Acerola is now commercially produced and processed in Brazil. Known for its very high vitamin C content, this fruit is also a good source of β‐carotene. The present study was carried out to verify variation in the carotenoid composition along the food chain. Neoxanthin, violaxanthin, lutein, β‐cryptoxanthin, α‐carotene and β‐carotene were found in the acerola fruit. β‐Carotene predominated with mean concentrations of 12.4 and 38.1 µg g^?1 in the ripe fruit, 8.8 and 30.1 µg g^?1 in the peeled ripe fruit and 5.4 and 12.0 µg g^?1 in the partially ripe fruit of an undefined variety taken from home gardens and the commercial cultivar Olivier, respectively. Aside from β‐carotene, β‐cryptoxanthin increased significantly in both garden and commercial fruits and violaxanthin in the latter fruits during ripening. Peeling reduced β‐carotene in both garden and commercial lots, violaxanthin decreased in the commercial fruits, and the other carotenoids remained virtually unchanged. Four brands of frozen pulp and three brands of processed juice had variable and markedly lower carotenoid levels than those of the fresh fruit, indicating that the processing should be improved. Copyright © 2006 Society of Chemical Industry     

Content of anthocyanins and glycoalkaloids in blue‐fleshed potatoes and changes in the content of α‐solanine and α‐chaconine during manufacture of fried and dried products

In the last ten or so years, potatoes with purple or blue‐flesh and derivative products, for example chips, have appeared on the European markets. The interest in this raw material and these products is increasing among both producers and consumers searching for novel and attractive choices. The anthocyanin content of the analysed potato varieties differed; a higher content of these pigments was determined in Blaue Elise var. potatoes. In blue‐flesh varieties, the prevailing anthocyanins were acylated glycosides: petunidin and malvidin. The production process of French fries, chips and puree caused a decrease in the content of glycoalkaloids in semi‐products and finished products, compared to the raw material. The greatest losses of α‐chaconine and α‐solanine were observed after tuber peeling (ca. 70%) and after frying (ca. 90%). French fries contained 3%, chips 16% and puree 17% of the initial amount of total glycoalkaloids. The losses of α‐chaconine and α‐solanine in the analysed semi‐products and finished products were at the same level, regardless of the processing technology applied.     

Modulation of the postprandial phase by beta-glucan in overweight subjects: effects on glucose and insulin kinetics

Decreasing the postprandial glucose response is potentially of major importance to public health when low-glycemic index or high-fibre content foods are associated with a decreased risk of diabetes. We investigated in overweight subjects the effect of adding beta-glucan (BG) to a polenta (Pol) meal on postprandial metabolism and glucose bioavailability using stable isotopes. In this single-blind, randomized, crossover trial, 12 subjects ate two meals containing Pol with (Pol + BG) or without (Pol) 5 g BG. Concentrations of glucose, insulin, C-peptide, nonesterified fatty acids, triacylglycerol, total and exogenous glucose kinetics were assessed for 6 h postprandially. The kinetics of total and exogenous glucose importantly differed between the meals, but not the quantity of total and exogenous glucose appearing in plasma. Less total and exogenous glucose appeared during the first 120 min after the Pol + BG meal; the phenomenon was then reversed (both p < 0.0001). After 120 min, glucose and insulin responses declined, but remained higher after the Pol + BG meal (p < 0.05) in parallel to the inhibition of lipolysis. The endogenous glucose production (EGP) was significantly more inhibited after the Pol + BG meal. The addition of BG slowed the appearance of glucose in plasma, resulting in longer-lasting insulin secretion which exerted a prolonged inhibition of EGP and lipolysis.     

“水解植物蛋白液 葡萄糖”模型热反应中 3-氯-1,2-丙二醇的研究

通过设计“水解植物蛋白液 葡萄糖”模型热反应,考察了不同3-氯-1,2-丙二醇 (3-MCPD)含量的HVP液、葡萄糖用量、反应温度、反应时间等因素对热反应产物中 3-MCPD 含量的影响。结果表明：模型热反应产物中 3-MCPD 含量随着 HVP 液中 3-MCPD 的含量增加而增加;随着葡萄糖用量增加而减少;随着反应温度的升高,3-MCPD 的量先增加后减少;热反应时间越长,3-MCPD 的含量越高。     

The postmortem μ‐calpain activity,protein degradation and tenderness of sheep meat from Duolang and Hu breeds

This study aimed to investigate the differences in meat tenderisation between two Chinese native sheep breeds, Duolang and Hu. The tenderness of longissimus thoracis (LT) muscle, μ‐calpain autolysis and proteolysis of myofibrillar protein was measured at 1‐ and 7‐days postmortem storage at 4 °C. At 7‐days postmortem ageing, meat from Duolang sheep was more tender compared to that from Hu sheep. The Warner–Bratzler shear force of Duolang and Hu sheep was reduced by 55.20% and 41.51% at 7 days compared with 1 day, respectively. In Duolang LT, a higher proportion of 80‐kDa μ‐calpain was autolyzed than in the Hu samples at 1‐day postmortem ageing, but they did not differ significantly at 7 days. More titin, desmin and troponin‐T were degraded in Duolang sheep compared to Hu sheep. Additionally, pH values at the different ageing time were not significantly different, indicating that pH may be not a determinant factor contributing to the tenderness difference between the two breeds. Our data suggest the earlier activation of μ‐calpain and a larger extent of proteolysis of key structural proteins may contribute to the higher rate of tenderisation of Duolang compared to Hu sheep during postmortem ageing.     

Contribution of cysteine and glutathione conjugates to the formation of the volatile thiols 3‐mercaptohexan‐1‐ol (3MH) and 3‐mercaptohexyl acetate (3MHA) during fermentation by Saccharomyces cerevisiae

Background and Aims: 3‐Mercaptohexan‐1‐ol (3MH) and its ester 3‐mercaptohexyl acetate (3MHA) are potent aromatic thiols that substantially contribute to varietal wine aroma. During fermentation, non‐volatile 3MH conjugates are converted by yeast to volatile 3MH and 3MHA. Two types of 3MH conjugates have been identified, S‐3‐(hexan‐1‐ol)‐L‐cysteine (Cys‐3MH) and S‐3‐(hexan‐1‐ol)‐glutathione (GSH‐3MH). Yeast‐driven formation of 3MH from these precursors has been previously demonstrated, while the relationship between 3MHA and GSH‐3MH remains to be established. This paper aims to investigate yeast conversion of GSH‐3MH to 3MH and 3MHA, and to assess the relative contribution of each individual conjugate to the 3MH/3MHA pool of finished wines. Methods and Results: Fermentation experiments were carried out in model grape juice containing Cys‐3MH and GSH‐3MH. We found 3MH formation from GSH‐3MH to be significantly less efficient than that of Cys‐3MH. Conversely, esterification of 3MH to 3MHA was higher when 3MH was formed from GSH‐3MH. Additional in vitro assays for measuring enzyme cleavage activity suggest the involvement of a different mechanism in 3MH conversion for the two precursors. Conclusions: These results indicate that although both 3MH conjugates can be converted by yeast, the type of precursor affects the rate of formation of 3MH and 3MHA during fermentation. Significance of the Study: Management of the pool of aromatic thiols during fermentation can depend on relative proportions of different 3MH conjugates.     

Effect of heat shock protein 27 on the in vitro degradation of myofibrils by caspase‐3 and μ‐calpain

This study was designed to investigate the effect of heat shock protein 27 (HSP27) on the in vitro degradation of myofibrils induced by caspase‐3 or μ‐calpain. Myofibrillar proteins were prepared from at‐death beef muscles and incubated with caspase‐3 or μ‐calpain with and without HSP27, or with HSP27 alone, at 30 °C for 2 h, and protein degradation was assessed. Results showed that caspase‐3 promoted the degradation of titin, nebulin and troponin‐T, and μ‐calpain promoted the degradation of nebulin, desmin and troponin‐T, observed during normal PM ageing. Moreover, the addition of HSP27 restricted the degradation of troponin‐T in μ‐calpain‐ and caspase‐3‐treated myofilaments, and restricted the degradation of desmin in μ‐calpain‐treated myofilaments. Therefore, HSP27 may indirectly or directly interact with caspase‐3 and μ‐calpain, reducing their activity and mediating PM proteolysis of muscle proteins to affect meat tenderisation.