CN112914104B - Nutritional composition for preventing obesity in infants - Google Patents
Nutritional composition for preventing obesity in infants Download PDFInfo
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- CN112914104B CN112914104B CN202110250194.0A CN202110250194A CN112914104B CN 112914104 B CN112914104 B CN 112914104B CN 202110250194 A CN202110250194 A CN 202110250194A CN 112914104 B CN112914104 B CN 112914104B
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- lactobacillus
- nutritional composition
- weight
- oligosaccharide
- oligosaccharides
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- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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Abstract
The present invention relates to a nutritional composition comprising Osteopontin (OPN) and lacto-oligosaccharides, said nutritional composition comprising at least a high concentration of osteopontin, one sialylated oligosaccharide and at least one N-acetylated oligosaccharide, which may be used for the prevention of obesity in infants and young children.
Description
Technical Field
The present invention relates to a nutritional composition comprising osteopontin and specific breast milk oligosaccharides, said nutritional composition comprising at least a high concentration of osteopontin, one sialylated oligosaccharide and at least one N-acetylated oligosaccharide, for use in preventing obesity and promoting healthy growth of infants.
Background
Obesity is a chronic metabolic disease characterized by excessive accumulation of body fat and excess body weight, and is caused by interaction of various factors such as genetic factors and environmental factors. Obesity can lead to an increase in the incidence of metabolic syndrome as well as cardiovascular disease, type 2 diabetes, retinal and renal complications, nonalcoholic fatty liver disease, sleep apnea, polycystic ovary syndrome, infertility, asthma, orthopedic complications, psychiatric disorders and cancer. Earlier obesity may lead to earlier onset of the associated disease. Factors causing obesity in infants are very complex and are related to heredity, nutrition, ethnicity, socioeconomic conditions, caesarean delivery, antibiotics, etc.
Human Milk Oligosaccharides (HMOs) are the third largest solid nutritional component in human milk that is inferior to lactose and lipids. Concentrations in colostrum and mature milk are 22-24g/L and 12-13g/L, respectively, and recently nearly 200 structures have been identified. The core structure of the compound is composed of 5 monomers of N-acetylneuraminic acid (Neu5Ac) derived from galactose (Gal), glucose (Glc), N-acetylglucosamide (GlcNac), fucose (Fuc) and sialic acid (Sia), and the monomers are connected with different groups to generate different effects. The breast milk oligosaccharide can be used as prebiotics, for regulating intestinal flora, as anti-adhesion agent, for resisting pathogen adhesion, and as immune response regulator and for regulating cell inflammatory reaction. The breast milk oligosaccharide can affect various aspects of the growth and development of infants through the mechanism, improve diarrhea, prevent respiratory tract infection, relieve allergy and intervene obesity.
Breast milk HMOs stimulate the growth of certain intestinal flora, which play a role in the childhood obesity pathogenesis by regulating energy absorption, altering metabolic pathways, inducing inflammatory reactions, etc. E.g. butyric acid in short chain fatty acids, which are metabolites of the flora, is an energy source for 70% of the intestinal epithelial cells. Therefore, the infant obesity can be prevented by supplementing breast milk oligosaccharide.
Osteopontin (OPN) is one of the important immunostimulating factors in breast milk, and can promote the maturation of the immune system of infants and protect breast-fed infants from pathogen infection. The OPN can promote the accumulation of macrophages in adipose tissues by mediating the chemotaxis of the macrophages and enhancing the action of Monocyte Chemotactic Protein (MCP) -1, can also cause the increase of adipose tissue inflammatory response factors related to obesity, and plays an important role in the development process of obesity and insulin resistance. However, the regulation effect of OPN on obesity has less published research results, and particularly, the influence on the body weight of infants is not reported.
Disclosure of Invention
It was surprisingly found that a nutritional composition comprising OPN and specific breast milk oligosaccharides has a synergistic effect on the body weight of infants compared to infants fed with conventional nutritional compositions and can be used for preventing obesity in infants.
Accordingly, the present invention provides a nutritional composition comprising OPN and specific breast milk oligosaccharides, said specific breast milk oligosaccharides comprising at least one sialylated oligosaccharide and at least one N-acetylated oligosaccharide.
In a specific embodiment, the specific breast milk oligosaccharides comprise at least two or more of LDFT (lacto-difucotetraose), 3' SL (3 ' sialyllactose), LNT (lacto-N-neotetraose), 2' FL (2-fucosyllactose), and LNnT (lacto-N-neotetraose).
In a specific embodiment, the nutritional composition comprises at least two or more of OPN, LSTc (sialyl-lacto-N-tetraose c), LNT (lacto-N-tetraose), 2 'FL (2' -fucosyllactose), and LNnT (lacto-N-neotetraose).
In a particular embodiment, the mass ratio of Osteopontin (OPN) to total oligosaccharides in the nutritional composition is 1: 20-200.
In a particular embodiment, the sialylated oligosaccharide is present in the nutritional composition in an amount of from 10 to 20% by weight, more preferably the sialylated oligosaccharide comprises sialylated-lacto-N-tetraose c (lstc) in an amount of from 0.2% to 20% by weight of the total weight of the nutritional composition.
In a particular embodiment, the nutritional composition comprises 25% to 50% fucosylated neutral oligosaccharides by weight percentage, more preferably 2-fucosyllactose (2' -FL) comprised in the fucosylated neutral oligosaccharides represents 25% to 50% of the total weight of the nutritional composition.
In a particular embodiment, the nutritional composition comprises 5-35 wt% of neutral oligosaccharides of N-acetylated oligosaccharides, more preferably, the neutral oligosaccharides of N-acetylated oligosaccharides comprise 5-35 wt% of lacto-N-neotetraose (LNnT) and 5-25 wt% of LNT (lacto-N-tetraose) based on the total weight of the nutritional composition.
In a specific embodiment, the nutritional composition is a personalized nutritional composition comprising oligosaccharides at a concentration of 10-10000mg oligosaccharide per 100g nutritional composition.
Another object of the present invention relates to the use of the above nutritional composition.
In a particular embodiment, the nutritional composition is for use in preventing obesity in an infant.
Drawings
The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention and not to limit the invention. In the drawings:
FIG. 1T 1 graph comparing breast milk oligosaccharide content in the low and high weight groups over three periods;
FIG. 2T 2 graph comparing breast milk oligosaccharide content in the low and high weight groups over three periods;
FIG. 3T 3 graph comparing breast milk oligosaccharide content in the low and high weight groups over three periods.
Detailed Description
The preferred embodiments of the present invention will be described in conjunction with the accompanying drawings, and it will be understood that they are described herein for the purpose of illustration and explanation and not limitation.
Example 1 relationship between specific types of Breast milk oligosaccharides and infant weight
1 recruiting 28 infant volunteers from hospital, wherein the selection criteria are healthy, term infant (gestational age is more than or equal to 37 weeks), and vaginal delivery; medically proven to be healthy infants: no symptoms and no signs of disease. The mothers of the infants who participated in the experiment will all be informed protocol and guaranteed to be purely breast-fed during the experiment.
2 by collecting mother's milk samples and measuring the weight of the infant during the first month T1(30d + -2 d), the second month T2(60d + -2 d), the third month T3(90d + -2 d) of the infant's age. 28 infants are divided into high-body recombination and low-body weight groups for analysis, the content of 22 oligosaccharides in breast milk of mothers in three periods is measured, and statistics shows that the content of specific types of oligosaccharides in breast milk is related to the weight of the infants.
TABLE 1 infants T1 with significantly different breast milk oligosaccharide species content
TABLE 2 infants T2 have significantly different breast milk oligosaccharide species content
TABLE 3 significantly different Breast milk oligosaccharide species content for infant T3
TABLE 4 significant differences in HMO content in the high and low body weight groups at different periods in breast milk
As can be seen from table 1 and fig. 1, at T1, the three breast milk oligosaccharides DSLNT, LSTc, LNT all showed significant differences (p < 0.05) between the low and high body weight groups, and the three breast milk oligosaccharides were higher in the low body weight group than in the high body weight group. As can be seen from table 2 and fig. 2, three breast milk oligosaccharides LDFT,3 '-SL and LNT were significantly different (p < 0.05) between the low and high body weight groups at time T2, and wherein LDFT and 3' -SL were higher in the high body weight group than in the low body weight group and LNT was higher in the low body weight group than in the high body weight group. As can be seen from table 3 and fig. 3, there were four breast milk oligosaccharides LDFT,3 '-SL, LSTc, LNT at time T3 that were significantly different (p < 0.05) between the low and high weight groups, where LDFT and 3' -SL were higher in the high weight group than in the low weight group, and LSTc and LNT were higher in the low weight group than in the high weight group. In summary, the high breast milk oligosaccharides in the high body recombination were LDFT and 3' -SL, and the high breast milk oligosaccharides in the low body weight group were DSLNT, LSTc and LNT.
Example 2 prevention of obesity in infants by Breast milk oligosaccharides
It was found from the above studies that breast milk oligosaccharides with high content in the low body weight group were DSLNT, LSTc and LNT. The breast milk oligosaccharide class is associated with the presence of infant body weight. It is envisaged that obesity in infants can be prevented by supplementation with specific breast milk oligosaccharides. The following formulation was then designed and the efficacy of breast milk oligosaccharides was verified by animal experiments.
The obesity prevention verification formula is divided into the following groups:
group 1: 70mg LNT +120mg 2' -FL +100mg LNnT
Group 2: 70mg LSTc +120mg 2' -FL +100mg LNnT
Group 3: 70mg LNT +70mg LSTc +120mg 2' -FL +100mg LNnT
Group 4: 6mg OPN +70mg LNT +70mg LSTc +120mg 2' -FL +100mg LNnT
Control group: 120mg 2' -FL +100mg LNnT
When in use, the formula is prepared into a mixture solution by using warm normal saline, so that the final concentration of oligosaccharide in the solution is 3.9g/L, and the final concentration of OPN in the solution is 65 mg/L.
Kunming male mice with the age of 4-5 weeks are selected, the weight of the Kunming male mice is 20-22g,50 mice are selected, the mice are divided into a control group and 4 test sample experimental groups, and each group comprises 10 mice. The mice are fed with high-nutrition feed in the experimental process. The high-nutrition feed is prepared by adding 10g of milk powder, 10g of lard oil, 1 egg, 10 drops of concentrated cod liver oil and 250g (cut) of fresh soybean sprouts into 100g of common feed, mixing into solid feed and drying. The experimental animals were specifically grouped as follows:
common feed group mice: feeding normal feed for 30 days, and perfusing stomach with normal saline
Control mice: feeding high nutrition feed for 30d, and perfusing stomach with normal saline dissolved with control group formula.
Experimental group 1 mice: feeding high nutrition feed for 30d, and intragastrically irrigating with normal saline dissolved with formula of group 1.
Experimental group 2 mice: feeding high nutrition formulation for 30 days, and intragastrically administering with normal saline solution of formula 2
Experimental group 3 mice: feeding the high nutrition formulation for 30 days, and intragastrically administering with normal saline containing group 3 formulation
Experimental group 4 mice: feeding high nutrition formulation for 30 days, and intragastrically infusing with normal saline containing group 4 formulation
During the experiment, the food intake, food remaining and food intake of each animal were recorded, the weight of the fasting mice was weighed at the beginning and end of the experiment, respectively, the mice were sacrificed by cervical dislocation at the end of the experiment, the total fat around the genitals was stripped off, the fat weight was weighed, and the fat index (g/100g body weight) was calculated.
TABLE 5 mouse body weight measurement results
Results 1 (as shown in table 5): there was no statistical difference in food intake for each group of mice during the experiment. The weights of experimental groups 1, 2, 3 and 4 after the experiment are obviously smaller than those of a control group (P is less than 0.05), the weights of mice of the experimental group 4 are smaller than those of the experimental group 1, the experimental group 2 and the experimental group 3(P is less than 0.05), and the weight difference of the experimental group 4 and the experimental group 2 is not significant compared with that of a common feed group.
TABLE 6 measurement results of fat index of mouse
Results 2 (as shown in table 6): the fat content of the control group is the most, and the experimental group 1, 2, 3, 4 has uniform and significant difference (P is less than 0.05) with the control group. The fat content of the experimental group 4 is the least, and the experimental group 4 has significant difference (P is less than 0.05) with the control group, the experimental group 1, the experimental group 2 and the experimental group 3, and is close to the common feed feeding group (P is more than 0.05).
The above results indicate that the nutritional composition containing LNT and LSTc can prevent obesity and promote healthy growth of infants; the nutritional composition containing two breast milk oligosaccharides, namely OPN, LNT and LSTc, has synergistic effect on preventing obesity of infants and promoting healthy growth of infants.
It will be apparent to those skilled in the art that various changes and modifications may be made in the present invention without departing from the spirit and scope of the invention. Thus, if such modifications and variations of the present invention fall within the scope of the claims of the present invention and their equivalents, the present invention is also intended to include such modifications and variations.
Claims (6)
1. A nutritional composition for preventing obesity in infants and young children comprising Osteopontin (OPN) and specific breast milk oligosaccharides, wherein the specific breast milk oligosaccharides comprise at least one sialylated oligosaccharide, one fucosylated oligosaccharide, and two N-acetylated oligosaccharides, wherein the sialylated oligosaccharides comprise sialyl-lacto-N-tetraose c (LSTc) and/or 6 '-sialyllactose (6' -SL), the fucosylated oligosaccharide comprises 2 '-fucosyllactose (2' -FL), and the N-acetylated oligosaccharide comprises lacto-N-neotetraose (LNnT) and lacto-N-tetraose (LNT);
the nutritional composition comprises the following components in percentage by weight:
(1) 10-20% sialylated oligosaccharide in weight percent, wherein sialylated-lacto-N-tetraose c (lstc) comprised in the sialylated oligosaccharide comprises 0.2-20% by weight of the total weight of the nutritional composition;
(2) 25% -50% fucosylated oligosaccharides by weight percentage, wherein the 2 '-fucosyllactose (2' -FL) comprised in said fucosylated oligosaccharides represents 25% -50% of the total weight of the nutritional composition;
(3) 5-35% by weight of N-acetylated oligosaccharides, wherein the N-acetylated oligosaccharides comprise lacto-N-neotetraose (LNnT) in an amount comprised between 5% and 35% by weight of the total weight of the nutritional composition, lacto-N-tetraose (LNT) in an amount comprised between 5% and 25% by weight of the total weight of the nutritional composition;
the mass ratio of the Osteopontin (OPN) to the specific breast milk oligosaccharide is 1: 20-200.
2. The nutritional composition according to claim 1, wherein the total oligosaccharide concentration in the nutritional composition is 10-10000mg oligosaccharide per 100g nutritional composition.
3. The nutritional composition of claim 1, wherein the composition further comprises a prebiotic selected from the group consisting of fructooligosaccharides, inulin, xylooligosaccharides, polydextrose, and any combination thereof.
4. The nutritional composition of claim 3, further comprising a probiotic.
5. The nutritional composition of claim 4, wherein the probiotic is a probiotic strain selected from the group consisting of: lactobacillus acidophilus (Lactobacillus acidophilus), Lactobacillus salivarius (Lactobacillus salivarius), Lactobacillus rhamnosus (Lactobacillus rhamnosus), Lactobacillus paracasei (Lactobacillus paracasei), Lactobacillus casei (Lactobacillus casei), Lactobacillus johnsonii (Lactobacillus johnsonii), Lactobacillus plantarum (Lactobacillus plantarum), Lactobacillus fermentum (Lactobacillus fermentum), Lactobacillus lactis (Lactobacillus lactis), Lactobacillus delbrueckii), Lactobacillus helveticus (Lactobacillus helveticus), Lactobacillus bulgaricus (Lactobacillus helveticus), Lactobacillus lactis (Lactobacillus bulgaricus), Lactobacillus lactis (Lactobacillus lactis), Lactobacillus bifidus (Lactobacillus bifidus), Lactobacillus bifidus (Lactobacillus), Lactobacillus acidophilus (Lactobacillus acidophilus), Lactobacillus thermophilus (Lactobacillus bulgaricus), Bifidobacterium lactis (Bifidobacterium lactis), Bifidobacterium bifidum (Bifidobacterium lactis), Bifidobacterium lactis (Bifidobacterium lactis), and Bifidobacterium lactis (Bifidobacterium).
6. The nutritional composition according to any one of claims 1 to 5, wherein the composition is a solid or liquid formulation.
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