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Beneficial Effects of Collagen Hydrolysate: A Review on Recent Developments

Authors:
1/4
Research Article Open Access


11,2*
1Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, China
2Beijing Higher Institution Engineering Research Center of Animal Product, China
 July 15, 2017;  July 24, 2017
 Bo Li, Beijing Higher Institution Engineering Research Center of Animal Product, Beijing Advanced Innovation Center for Food
Nutrition and Human Health, 17, Qinghua East Road, Haidian District, Beijing 100083, China, Tel: ; Email:
Introduction
Collagen is the main structural protein of the different
connective tissues, such as skin, bone, cartilage and tendons, and
comprises about one-third of total proteins in mammals. Collagen
extracted from collagen-rich materials with hot water is known
as gelatin. The common materials used for extracting gelatin
include pig skin (46%), bovine hide (29.4%), bones (23.1%)
         
great attention in recent years due to the religions, cultures and
health concerns. The further enzymatic hydrolysis of gelatin
results in collagen hydrolysate (CH). CH has long been used in
pharmaceuticals and foods in many countries and regions, such
as United States, Europe, China and Japan. Approved as Generally
 
the Food and Drug Administration (FDA) Center for Food Safety and
Nutrition. The bioavailability and absorption of CH have also been
widely studied. It has been reported that CH is more easily absorbed
and has higher bioavailability than gelatin [2,3]. Besides free amino
acids, small peptides especially dipeptide and tripeptide are also
absorbed into body by peptide transporter 1 (PepT1) [4]. To date,
more than30 peptides (mainly dipeptides and tripeptides) have

the most abundant collagen-derived peptide [5-7]. These peptides
         
studies reported [8-9]. In this paper, we will mainly focus on the

CH in animal experiments and clinical trials (Figure 1). The possible

Figure 1: The benecial effects of CH in animal experiments
and clinical trials.

Tech Res 1(2)-2017. BJSTR. MS.ID.0002017.DOI: 10.26717/BJSTR.2017.01.000217
Abstract
Collagen hydrolysate (CH) has received increasing attention in recent decades. This review mainly summarizes the recent developments

 
anti obesity and hypoglycemic effects. We also make comments on the current researches and give suggestions for future studies in this review.
       
guidance to develop CH-based health care supplements for disease prevention and/or treatment.
 
DOI: 10.26717/BJSTR.2017.01.000217
Bo Li.

2/4
Submission Link: http://biomedres.us/submit-manuscript.php
Bo Li. Biomed J Sci & Tech Res Volume 1- Issue 2: 2017
Benecial Eects

CH itself has good antioxidant activity as demonstrated by
in vitro assays [10,11]. CH intake also increases the activities of
antioxidant enzymes in body, including SOD, GSH-Px and CAT
[3,12]. Nuclear factor E2-related factor 2 (Nrf2)-antioxidant
response element (ARE) pathway plays a central role in regulating
antioxidant enzymes. Therefore, we speculate that CH exerts it
antioxidant effect in a direct and/or indirect manner. More work is
needed to investigate the effect of CH on Nrf2-AREsignaling.

Anti aging effect of CH has been widely investigated in several
animal models, including photo aged model, chronologically aged
model and acetone-induced dry skin model [3,12-15]. General
      
the formation of deep wrinkles and improving skin elasticity, are
also observed in clinical trials after taking 10g of CH once a day
for more than 6 weeks [16]. It should be noted that anti aging
effect of CH is more obvious on women aged more than 30 years.
       
the dual effects of CH on skin collagen synthesis and degradation,
as previous study reported [13].

Anti osteoporotic and anti osteoarthritis effects of CH have been


the symptoms of osteoarthritis and osteoporosis [18]. Combined
CH with other nutritional ingredients has received much interest.
It has been reported that combined oral administration of CH with
calcium and vitamin D has better effects on bone health than alone
administration of CH or calcium and vitamin D [19-21]. Future
studies are needed to determine the optimal form and optimal dose
of CH.

Oral administration of marine CH is reported to enhance
cutaneous wound healing and angiogenesis in rats [22-23]. In
addition to elevated VEGF and FGF-2 expression, the effect of CH
 
wound healing, as previous study reported that Pro-Hyp, a collagen-
        


Glycine is one of the major structural units of collagen,
accounting for one-third of the amino acids.CH has the ability
        
      
cytokine via glycine-gated chloride channels (GlyR).

Liang et al. reported CH intake inhibited spontaneous tumor
incidence and increase life spanin sprague-dawley (SD) rats
[26]. Our previous study found that CH intake inhibited platelet
release and down regulated proangiogenic factors in blood [27].
Considering angiogenesis is of key importance in the process of
tumorprogression. Our results provide a possible mechanism
underlying antitumor effect of CH.

Antihypertensive effect of CH has been reported in animal
experiments and clinical trials [28,29]. Oral administration of
  
pressure by inhibiting angiotensin I converting enzyme (ACE)
[28]. Tang et al. [30]found that oral administration of collagen
tripeptide had an inhibitory effect on atherosclerosis development
in hypercholesterol emic rabbits [30]. Platelets are involved in the
patho physiology of atherosclerosis and thrombosis.CH has an
inhibitory activity on platelet release and platelet aggregation, which
may justify potential application of CH as a health care supplement
to prevent and/or treat atherosclerosis and thrombosis-related
cardiovascular diseases [27].

CH intake has an effect on the absorption and metabolism of

weight gain and down regulates serum levels of total cholesterol,
triglyceride and low-density lipoprotein [31]. Further, CH could
alter lipid metabolism-related gene expression and the unfolded
protein response in mouse liver [32]. The hypoglycemic effects
of CH have also been reported [33,34]. It has been reported that
CHcan improve glucose tolerance by inhibiting intestinal glucose
uptake and enhancing insulin secretion [34], suggesting the anti
diabetic property of CH.
Conclusion and Perspective

effects on body health. Those effects make CH new and potential
healthcare supplement for disease prevention and/or treatment
in pharmaceuticals and foods. However, several issues should be
noted and need to be further explored. First, many in vitro studies
only focus on the biological activities of CH, neglecting its tolerance
in gastrointestinal tract. Certain collagen peptides isolated in in
vitro studies may be hydrolyzed by gastrointestinal enzymes and
exert no biological activity in body as expected in in vitro studies.
In vitro simulated GI digestion and Caco-2 mono layers have been
widely used and allow the prediction of oral compounds digestion
       
effects of CH have been reported, what is the peptide sequence
       
activity relationship will guide the application of CH. Third, the
biological activities of protein hydrolysates are highly affected by
their molecular structure and weight, which are greatly impacted
by their processing conditions. Therefore, processing conditions

effect.
Acknowledgement
This study was supported by the grants from China Agriculture
Research System (CARS-46) and National Natural Science
Foundation of China (NSFC,No. 31271846).
3/4
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Bo Li. Biomed J Sci & Tech Res Volume 1- Issue 2: 2017
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... Previous studies have demonstrated that oral intake of enzymatically hydrolyzed collagen peptides can have positive effects on skin health, such as dermal ECM generation, fibroblast growth, antioxidation, recovery, elasticity, and wrinkle reduction [6][7][8][9][10] . Particularly, gelatin-and collagenoriented hydrolysates are widely applied these days and produced in a variety of fields, such as the fields of functional foods, nutraceuticals, medical supplies, and the biotech industry [11][12][13] . The molecular weight of gelatin, a water-soluble polymer, is considerably higher than that of collagen hydrolysates, and it is produced by enzymatically hydrolyzing collagen that is normally used as a food ingredient and delivery carrier for the regulated distribution of bioactivities [14][15][16][17] . ...
... The molecular weight of gelatin, a water-soluble polymer, is considerably higher than that of collagen hydrolysates, and it is produced by enzymatically hydrolyzing collagen that is normally used as a food ingredient and delivery carrier for the regulated distribution of bioactivities [14][15][16][17] . When the high molecular weight of gelatin is hydrolyzed by treating a particular fungal or bacterial protease, the outputs, small molecular weight peptides, are conveniently called collagen hydrolysate 11,12,18 . There is growing evidence indicating that collagen peptides improve not only human skin indicators associated with aging, such as hydration, wrinkles, and elasticity, but also the antihypertensive effect in spontaneously hypertensive rats (SHRs) 19 . ...
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Collagen hydrolysate, which contains bioactive peptides, is used as a dietary supplement for the refinement of elasticity, hydration, desquamation, and wrinkling of aging human skin. Here, we conducted a double-blind, randomized, and placebo-controlled oral administration study on the effects of a collagen peptide (CPNS) containing dipeptides, including Gly-Pro and Pro-Hyp, on skin wrinkling, desquamation, elasticity, and hydration. Our results show that an intake of 1650 mg per day of CPNS for 12 weeks had beneficial effects on skin health in a cohort of women aged from 30 to 60 years (n = 100). Compared with the placebo group, skin desquamation, hydration, skin wrinkling, and elasticity were significantly improved after 4, 4, 12, and 12 weeks of administration, respectively. In a safety test of CPNS ingestion, none of the participants showed any side effects during the clinical study period. These results demonstrate that the low molecular weight bioactive peptides contained in CPNS, such as Gly-Pro and Pro-Hyp, exert positive effects on skin hydration, elasticity, desquamation, and wrinkling.
... It has been reported that CH is more easily absorbed and has higher bioavailability than gelatin (Oesser et al., 1999 andSong et al., 2017). Ohara et al., (2010), Hatanaka et al., 2014 andHongdong andBo, 2017) reported that Collagen hydrolysate (CH) has many beneficial effects include antioxidant, anti aging, anti osteoporotic , anti osteoarthritis, anti-inflammatory, anti tumor, anti hypertensive, anti atherosclerotic, anti obesity and hypoglycemic effects. ...
... It has been reported that CH is more easily absorbed and has higher bioavailability than gelatin (Oesser et al., 1999 andSong et al., 2017). Ohara et al., (2010), Hatanaka et al., 2014 andHongdong andBo, 2017) reported that Collagen hydrolysate (CH) has many beneficial effects include antioxidant, anti aging, anti osteoporotic , anti osteoarthritis, anti-inflammatory, anti tumor, anti hypertensive, anti atherosclerotic, anti obesity and hypoglycemic effects. ...
... Recently, the study of the therapeutic effect of some di-and tripeptides has become important, because some di-and tripeptides have been related to a better rate of absorption, and their presence in the blood has been identified after the consumption of sources rich in proteins and peptides. Also, some di-and tripeptides can present specific biological activities [34][35][36]. Additionally, it has been reported that the dipeptides of CAR and Hannaneh (Leu-Gly) generate a protective effect, presenting a decrease in enzymatic activities (AST, ALT, and FA) in the kidney related to cell lesions. ...
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... Collagen has long been used as a medical material because it promotes tissue regeneration by stimulating major cells in collagen-rich tissues [8]. In recent years, it was reported that the oral administration of collagen hydrolysate (CH) obtained by hydrolyzing collagen through enzyme engineering has various health benefits in humans including the prevention of skin aging and stimulation of bone formation and cartilage regeneration through ECM synthesis in cells [9]. Tsuruoka et al. [10] confirmed that CH stimulates bone fracture healing by promoting type I collagen synthesis in osteoblastic cells. ...
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This study aimed to determine the function of LINC00511 in NLRP3 inflammasome-mediated chondrocyte pyroptosis via the regulation of miR-9-5p and FUT 1. Chondrocyte inflammatory injury was induced by treating chondrocytes with LPS. Afterwards, the levels of IL-1β and IL-18, the expression of NLRP3, ASC, Caspase-1, and GSDMD, cell viability, and LDH activity in chondrocytes were assessed. LINC00511 expression in LPS-treated chondrocytes was detected, and LINC00511 was subsequently silenced to analyse its role in chondrocyte pyroptosis. The subcellular localization of LINC00511 was predicted and verified. Furthermore, the binding relationships between LINC00511 and miR-9-5p and between miR-9-5p and FUT1 were validated. LINC00511 regulated NLRP3 inflammasome-mediated chondrocyte pyroptosis through the miR-9-5p/FUT1 axis. LPStreated ATDC5 cells exhibited elevated levels of inflammatory injury; increased levels of NLRP3, ASC, Caspase-1, and GSDMD; reduced cell viability; increased LDH activity; and increased LINC00511 expression, while LINC00511 silencing inhibited the NLRP3 inflammasome to restrict LPS-induced chondrocyte pyroptosis. Next, LINC00511 sponged miR-9-5p, which targeted FUT1. Silencing LINC00511 suppressed FUT1 by upregulating miR-9-5p. Additionally, downregulation of miR-9-5p or overexpression of FUT1 neutralized the suppressive effect of LINC00511 knockdown on LPSinduced chondrocyte pyroptosis. Silencing LINC00511 inhibited the NLRP3 inflammasome to quench Caspase-1-dependent chondrocyte pyroptosis in OA by promoting miR-9-5p and downregulating FUT1.
... Gelatin is extracted from collagen in hot water [84]. It shows various beneficial effects like anti-oxidant, anti-aging, antitumor, wound healing, anti-inflammatory, antihypertensive, antiatherosclerotic, anti-obesity, hypoglycemic, antiarthritic etc in different animal and clinical studies [85]. The main mechanism of anti-arthritic action is the formation of new collagen type II and stimulation of proteoglycan synthesis [86]. ...
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The use of nutraceuticals and supplements are increasing day by day due to the drawbacks associated with synthetic drugs. Clinicians are aware of these therapies and prescribing the nutraceuticals in addition to the current choice of therapy. Many scientific studies, meta-analysis, randomised clinical trials have proved the effects of nutraceuticals in arthritis. Arthritis is the inflammatory disorder characterized by pain, swelling and stiffness of one or more joints. Two common types of arthritis are rheumatoid arthritis and osteoarthritis. The review covers all the possible nutraceuticals used in these two types of arthritis with their evidence and mechanism of action. Search engines like PubMed, Scopus, Google scholar, Researchgate and Science Direct are used to collect articles published from
... Collagen has long been used as a medical material because it promotes tissue regeneration by stimulating major cells in collagen-rich tissues [8]. In recent years, it was reported that the oral administration of collagen hydrolysate (CH) obtained by hydrolyzing collagen through enzyme engineering has various health benefits in humans including the prevention of skin aging and stimulation of bone formation and cartilage regeneration through ECM synthesis in cells [9]. Tsuruoka et al. [10] confirmed that CH stimulates bone fracture healing by promoting type I collagen synthesis in osteoblastic cells. ...
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This study reveals that low-molecular-weight collagen peptide (LMWCP) can stimulate the differentiation and the mineralization of MC3T3-E1 cells in vitro and attenuate the bone remodeling process in ovariectomized (OVX) Sprague-Dawley rats in vivo. Moreover, the assessed LMWCP increased the activity of alkaline phosphatase (ALP), synthesis of collagen, and mineralization in MC3T3-E1 cells. Additionally, mRNA levels of bone metabolism-related factors such as the collagen type I alpha 1 chain, osteocalcin (OCN), osterix, bone sialoprotein, and the Runt family-associated transcription factor 2 were increased in cells treated with 1,000 μg/ml of LMWCP. Furthermore, we demonstrated that critical bone morphometric parameters exhibited significant differences between the LMWCP (400 mg/kg)-receiving and vehicle-treated rat groups. Moreover, the expression of type I collagen and the activity of ALP were found to be higher in both the femur and lumbar vertebrae of OVX rats treated with LMWCP. Finally, the administration of LMWCP managed to alleviate osteogenic parameters such as the ALP activity and the levels of the bone alkaline phosphatase, the OCN, and the procollagen type 1 N-terminal propeptide in OVX rats. Thus, our findings suggest that LMWCP is a promising candidate for the development of food-based prevention strategies against osteoporosis.
... Collagen is one of the animal proteins from bovine connective tissues which is used as a nutraceutical, since it has antioxidant, antiaging, anti-tumor, anti-inflammatory, and anti-obesity properties in humans (Song and Li 2017). The role of collagen and collagen peptide (CP) in improving skin elasticity (Kim et al. 2018;Bolke et al. 2019) was reported. ...
Chapter
Nutraceuticals are bioactive compounds used to enhance health-supporting effects and to treat and prevent various diseases. They are largely used to control and prevent chronic diseases like diabetes, cardiovascular diseases, respiratory diseases, cancer, and gastrointestinal and neurological disorders. Thus, the nutraceutical market is increasing at a fast rate. Nutraceuticals can be prescribed by a qulified health professional based on a patient’s health issues or can be used without a prescription. While nutraceuticals are good for health in general and have various advantages including antioxidant, anti-inflammatory, anticancer, etc., the significant disadvantages are underreported as available literature expresses concerns over the authentic source of their raw materials, purity of the compound, presence of other active compounds, quality, lack of experimental evidence, false advertising, contamination with heavy metals, and interactions between supplements and drugs. One of the major limitations of nutraceuticals is questionable drug bioavailability, which is the accessibility of the nutrients by the body after digestion, absorption, and transportation. Poor bioavailability may result in little or no effect in lessening the advantage of nutraceuticals. People with underlying diseases requiring multidrug regimens often simultaneously self-prescribe nutraceuticals. Meanwhile, they are unaware of drug–drug interactions that not only diminish the efficacy of nutraceuticals but also lead to potentially toxic side effects. Side effects of nutraceuticals due to misuse or overuse may vary from mild to moderate and severe. Therefore, it is important to understand the bioavailability, toxicity, and side effect profile of nutraceuticals before use. This review focuses on highlighting the advantages and disadvantages of some commonly used nutraceuticals in various conditions related to heart, liver, kidney, gastrointestinal, and pulmonary disorders. We also explore the potential advantages and disadvantages of nutraceuticals in various neurological conditions, and the mechanisms of their action, particularly their role in the blood–brain barrier in transporting these nutraceuticals into the brain to regulate brain homeostasis and thereby other organs.
... H-collagen has an extremely low molecular weight as compared to gelatine. It is water-soluble and biodegradable (Song and Li, 2017). H-collagen has long been used in medicines and foods in many countries and regions including the US, Europe, China, and Japan. ...
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Hide trimming waste is a by-product of tannery. Collagen is the main structural protein in hide trimming waste (70%), and extensively utilised in numerous industries including food, non-food, cosmetics, and medical. Research related to the development of hydrolysed collagen (h-collagen) extraction methods from cowhide, especially from the hide trimming waste, is still limited. The present work thus aimed to develop a four-step method for extracting h-collagen from hide trimming waste, and examine the product's properties. The present work successfully developed a method for extracting h-collagen from trimming waste with a 20.35% yield. Analysis of molecular weight, FTIR, and amino acid composition confirmed that the product was h-collagen with a molecular weight of 16-23 kDa. This h-collagen had higher antioxidant activity than commercial h-collagen, with an IC50 value of 238.5 ppm.
... Hydrolysed collagen (HC) has received considerable interest because of its gastroprotective, anti-inflammatory and cutaneous wound healing effects [33][34][35]. Properties that could make HC suitable for the treatment and/or prevention of ESGD are its enhancing effects on wound healing and combatting inflammation, as well as its suggested antioxidant properties [35,36]. Ingestion of HC results in the release of short glycine-and proline-containing peptides into the bloodstream [37,38]. ...
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Equine squamous gastric disease (ESGD) is common in horses and poses a serious welfare problem. Several risk factors have been identified and ESGD is routinely treated with omeprazole. Fourteen mares, previously used as embryo recipients and diagnosed with ESGD, were selected. Horses were confined to individual stalls, exercised once daily, and fed ad libitum hay, 1 kg of a low starch compound complementary feed and a mineral supplement. Half of the horses received a compound containing hydrolysed collagen (supplement) and the other half did not (control). At the start of the study, ESGD scores were 3.57 and 3.36 for the supplement and control group, respectively. After 4 weeks, the ESGD grades were significantly reduced in both groups (1.89 and 1.43, respectively, p < 0.01), and healing (ESGD < 2) occurred in 7 out of 14 horses. No treatment effect was observed (p = 0.75), and it was concluded that the change in husbandry overshadowed any potential effect of the compound. Severe ESGD can improve, and even heal, with the provision of a diet of ad libitum forage and a small amount of a compound complementary feed, without the use of omeprazole. A predictable daily routine, with a limited number of dedicated caretakers, may have contributed to the improvement of gastric health.
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Today, food supplements have become an indispensable part of a healthy and balanced life, and one of them, collagen supplements especially support the healthy skin structure and have many positive effects on it. The present study is aimed that evaluating the effects of PROFIN® Collagen on healthy skin conditions such as skin hydration, wrinkles, and elasticity. With this aim, we conducted a prospective, single-center, double-blind, randomized, placebo-controlled, 2-arm, parallel-design study to evaluate the effect of 12-week consumption of PROFIN® Collagen Hydrolysate on skin health. A total of 72 healthy female adults, aged between 40 and 65 with at least moderate eye wrinkles were randomized to receive 10 g of PROFIN® Collagen or placebo, once daily for 12 weeks. The majority (73(%)) of participants who took ‘Profin Collagen Hydrolysate’ had a statistical improvement (decrease) (p<0,05) in mean wrinkle length at Day 42, this improvement continued at the end of the intervention. Furthermore, compared with the placebo group, in placebo group transepidermal water loss results show that there was a significant increase after 6, and 12 weeks of administration, but not in PROFIN® Collagen group. In conclusion, this study demonstrates that PROFIN® Collagen has a positive effect on skin wrinkles and water loss.
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Action mechanisms underlying various biological activities of collagen peptides (CPs) remained to be elucidated. Cytokines may play an important role in mediating these health benefits of CPs. This study aimed to systemically examine the cytokines in skin and blood regulated by CPs intake. Thirteen-month-old female Kunming mice were administered with CPs for 2 months (0 or 400 mg/kg bodyweight/day). The cytokines in skin and plasma were analysed using a 53-cytokine array and corresponding ELISA kits. In skin, CPs intake significantly down-regulated placenta growth factor (PIGF-2), insulin-like growth factor (IGF)-binding protein (IGFBP) -2 and IGFBP-3, and up-regulated platelet factor 4 (PF4), serpin E1 and transforming growth factor (TGF)-β1. CPs treatment also increased the type I collagen mRNA and protein levels and improved the aged skin collagen fibres. In plasma, nine cytokines were significantly down-regulated by CPs intake compared to the model group: fibroblast growth factor (FGF)-2, heparin-binding (HB) epidermal growth factor (EGF)-like growth factor (HB-EGF), hepatocyte growth factor (HGF), platelet-derived growth factor (PDGF)-AB/BB, vascular endothelial growth factor (VEGF), chemokine (C-X-C motif) ligand 1 (KC), matrix metalloproteinase (MMP)-9, interleukin (IL)-1α and IL-10; 2 cytokines were significantly up-regulated, including TGF-β1 and serpin F1. Furthermore, CPs intake significantly decreased the level of platelet release indicators in the plasma and washed platelets, including PF4, granule membrane protein (GMP)-140, β-thromboglobulin and serotonin. These results provide a mechanism underlying anti-skin ageing by CPs intake and highlight potential application of CPs as a healthcare supplement to combat cancer and cardiovascular disease by inhibiting platelet release.
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The use of collagen hydrolysates (CHs) as a nutraceutical agent in skin aging has gained increasing attention. Here, the effects of various doses and molecular weights of CH from silver carp skin on photoaging in mice were investigated. The ingestion of CH at 50, 100 and 200 mg per kg body weight led to a dose-dependent increase in the hydroxyproline, hyaluronic acid and moisture contents of the skin, but it had no significant effect on the mice body weight, or on the spleen or thymus index. Furthermore, ingesting CH with lower (LMCH, 200-1000 Da, 65%) and higher molecular weight (HMCH, >1000 Da, 72%) significantly increased the skin components and improved the antioxidative enzyme activities in both serum and skin (p < 0.05); LMCH performed better than HMCH. By contrast, gelatin (>120 kDa) ingestion did not bring a significant change compared to model mice. These results indicated that LMCH exerted a stronger beneficial effect on the skin than did either HMCH and gelatin, which supported the feasibility of using LMCH as a dietary supplement from silver carp skin to combat photoaging.
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In this study, tilapia collagen peptide (TCP) was prepared by alcalase hydrolysis of tilapia skin, and the antioxidant and hypoglycaemic effects of TCP were investigated. The results showed that TCP possessed DPPH and ABTS+ free radicals-scavenging activities. In diabetic mice in which diabetes was induced by injection of alloxan (50 mg kg−1 bw), high-dose TCP (1.7 g kg−1 bw) and the drug metformin (1.0 g kg−1 bw) were found to reduce 31.8% and 30.3% of blood glucose levels in 25 days, respectively. Moreover, in diabetic mice receiving high-dose TCP, antioxidant enzymes SOD and CAT were increased by 23% and 59.2%, respectively, and MDA was decreased by 39.1%. Comparing the treated high-dose TCP group with the metformin group, there were similar SOD (61.5 U mg−1 vs. 60.2 U mg−1) and MDA (1.4 nmol mg−1 vs. 1.3 nmol mg−1), but more (~7%) CAT (359.8 U g−1 vs. 336.1 U g−1). Together, the present data, for the first time, demonstrated that TCP possessed hypoglycaemic effects in mice.
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Introduction Collagen hydrolysate is recognized as a safe nutraceutical, whose combination of amino acids stimulates the synthesis of collagen in the extracellular matrix of cartilage and other tissues. Objective to conduct a systematic review of literature on the action of collagen hydrolysate in bone and cartilaginous tissue and its therapeutic use against osteoporosis and osteoarthritis. Method a study of the PubMed, MEDLINE, LILACS, and SciELO databases was performed. Articles published in English and Portuguese in the period of 1994 to 2014 were considered. Results: the sample comprised nine experimental articles with in vivo (animals and humans) andin vitro (human cells) models, which found that the use of different doses of collagen hydrolysate were associated with the maintenance of bone composition and strength, and the proliferation and cell growth of cartilage. Conclusion hydrolyzed collagen has a positive therapeutic effect on osteoporosis and osteoarthritis with a potential increase in bone mineral density, a protective effect on articular cartilage, and especially in the symptomatic relief of pain.
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Purpose: Collagen peptides (CPs) and calcium citrate are commonly used as bone health supplements for treating osteoporosis. However, it remains unknown whether the combination of oral bovine CPs with calcium citrate is more effective than administration of either agent alone. Methods: Forty 12-week-old Sprague-Dawley rats were randomly divided into five groups (n = 8) for once-daily intragastric administration of different treatments for 3 months at 3 months after ovariectomy (OVX) as follows: sham + vehicle; OVX + vehicle; OVX + 750 mg/kg CP; OVX + CP-calcium citrate (75 mg/kg); OVX + calcium citrate (75 mg/kg). After euthanasia, the femurs were removed and analyzed by dual energy X-ray absorptiometry and micro-computed tomography, and serum samples were analyzed for bone metabolic markers. Results: OVX rats supplemented with CPs or CP-calcium citrate showed osteoprotective effects, with reductions in the OVX-induced decreases in their femoral bone mineral density. Moreover, CP-calcium citrate prevented trabecular bone loss, improved the microarchitecture of the distal femur, and significantly inhibited bone loss with increased bone volume, connectivity density, and trabecular number compared with OVX control rats. CP or CP-calcium citrate administration significantly increased serum procollagen type I N-terminal propeptide levels and reduced serum bone-specific alkaline phosphatase, osteocalcin, and C-telopeptide of type I collagen levels. Conclusions: Our data indicate that combined oral administration of bovine CPs with calcium citrate inhibits bone loss in OVX rats. The present findings suggest that combined oral administration of bovine CPs with calcium citrate is a promising alternative for reducing bone loss in osteopenic postmenopausal women.
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Bioactivities of fish collagen peptide are now being elucidated in diverse biological systems. Here, we investigated the effect of fish collagen peptide on the adipogenic differentiation of 3T3-L1 preadipocytes and in obese mice fed a high fat diet (HFD). Subcritical water-hydrolyzed fish collagen peptide (SWFCP) significantly inhibited lipid accumulation during the differentiation of 3T3-L1 preadipocytes, which was accompanied by decreased expression of CCAAT-enhancer-binding protein-α (C/EBP-α), peroxisome proliferator-activated receptor-γ (PPAR-γ), and adipocyte protein 2 (aP2) genes, key regulators of differentiation and maintenance of adipocytes. SWFCP was also found to suppress the palmitate-induced accumulation of lipid vacuoles in hepatocytes. Oral administration of SWFCP significantly reduced HFD-induced body weight gain without a significant difference in food intake. Consistent with its effects in 3T3-L1 preadipocytes, SWFCP inhibited the expression of C/EBP-α, PPAR-γ, and aP2 in epididymal adipose tissue of mice fed a HFD, leading to a significant reduction in adipocyte size. Furthermore, SWFCP significantly reduced serum levels of total cholesterol, triglyceride, and low-density lipoprotein, and increased serum high-density lipoprotein. These observations suggest that SWFCP inhibits adipocyte differentiation through a mechanism involving transcriptional repression of the major adipogenic regulators C/EBP-α and PPAR-γ, thereby reducing body weight gain and adipogenesis in an animal model of obesity.
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Ingestion of collagen peptide (CP) elicits beneficial effects on the body, including improvement in blood lipid profiles, but the underlying mechanisms remain unclear. The purpose of this study was to investigate the effects of CP ingestion on the liver, which controls lipid metabolism in the body. Male BALB/cCrSlc mice were bred with the AIN-93M diet containing 14 % casein or the AIN-93M-based low-protein diet containing 10 % casein or a diet containing 6 % casein+4 % CP for 10 weeks ( n 12/group). Total, free and esterified cholesterol levels in the blood decreased in the CP group. DNA microarray analysis of the liver revealed that expressions of genes related to lipid metabolic processes such as the PPAR signalling pathway and fatty acid metabolism increased in the CP group compared with the 10 % casein group. The expressions of several genes involved in steroid metabolic process, including Cyp7a1 and Cyp8b1 , were decreased, despite being targets of transcriptional regulation by PPAR. These data suggest that lipid metabolism in the liver is altered by CP ingestion, and the decrease in blood cholesterol levels in the CP group is not due to enhancement of the steroid metabolic process. On the other hand, expressions of genes related to the unfolded protein response (UPR) significantly decreased at the mRNA level, suggesting that CP ingestion lowers endoplasmic reticulum stress. Indeed, protein levels of phosphorylated inositol-requiring enzyme 1 decreased after CP ingestion. Taken together, CP affects the broader pathways in the liver – not only lipid metabolism but also UPR.
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Background: Collagen hydrolysates (CHs) has been demonstrated to have positive effect on skin photo-aging by topical application or oral ingestion. However, there's little report about its influence on skin chronological aging so far. Results: Nine-month-old female ICR mice were given normal AIN-93M diets containing the CHs (2.5%, 5% and 10%, respectively) from Nile tilapia scale. After 6 months, the collagen content and antioxidant enzymes (superoxide dismutase and glutathione peroxidase) activities significantly increased (p < 0.05), while the survival rate, viscera indexes and the contents of moisture, fat and non-collagenous protein of skin didn't changed (p > 0.05). The color, luster and quantity of hair were obviously ameliorated. Moreover, the structure of epidermis and dermis, density and distribution of collagen fibers and ratio of type I to type III collagen were obviously improved in a dose-dependent manner showed by histochemical staining. Conclusion: The oral ingestion of CHs increased the collagen content and antioxidant enzymes activities, and improved the appearance and structure of skin. These suggested its potential to be developed into nutraceuticals or functional foods.
Article
The aim of this study was to evaluate the antidiabetic properties of collagen hydrolysates (CHs). CHs exhibited dipeptidyl peptidase-IV inhibitory activity and stimulated glucagon-like-peptide-1 (GLP-1) secretion in vitro. We also determined whether CHs improve glucose tolerance in normal mice. Oral administration of CHs suppressed the glycemic response during the oral and intraperitoneal glucose tolerance tests (OGTT and IPGTT), but the effects were weaker in IPGTT than in OGTT. CHs had no effect on the gastric emptying rate. A pretreatment with the GLP-1 receptor antagonist, exendin 9-39 (Ex9), partially reversed the glucose-lowering effects of CHs, but only when coadministered with glucose. CHs administered 45 min before the glucose load potentiated the glucose-stimulated insulin secretion. This potentiating effect on insulin secretion was not reversed by the pretreatment with Ex9, it appeared to be enhanced. These results suggest that CHs improve glucose tolerance by inhibiting intestinal glucose uptake and enhancing insulin secretion, and also demonstrated that GLP-1 was partially involved in the inhibition of glucose uptake, but not essential for the enhancement of insulin secretion.
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Recent studies have reported that oral intake of gelatin hydrolysate has various beneficial effects, such as reduction of joint pain and lowering of blood sugar levels. In this paper, we produced novel gelatin hydrolysate using cysteine-type ginger protease having unique substrate specificity with preferential peptide cleavage with Pro at the P2 position. Substantial amounts of X-hydroxyproline (Hyp)-Gly-type tripeptides were generated up to 2.5% (w/w) concomitantly with Gly-Pro-Y-type tripeptides (5%; w/w) using ginger powder. The in vivo absorption of the ginger-degraded gelatin hydrolysate was estimated using mice. The plasma levels of collagen-derived oligopeptides, especially X-Hyp-Gly, were significantly high (e.g., 2.3-fold for Glu-Hyp-Gly, p˂0.05) compared with that of the control gelatin hydrolysate, which was prepared using gastrointestinal proteases and did not contain detectable X-Hyp-Gly. This study demonstrated that orally administered X-Hyp-Gly was effectively absorbed into blood probably due to high protease resistance of this type of tripeptides.