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Background:
Systematic Review

Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review

by
Pedro Augusto Querido Inacio
1,
Felipe Augusto Chaluppe
2,
Gerson Ferreira Aguiar
1,
Carly de Faria Coelho
1 and
Rodolfo P. Vieira
1,3,*
1
Laboratory of Pulmonary and Exercise Immunology (LABPEI), Evangelical University of Goias (Unievangelica), Avenida Universitária Km 3.5, Anápolis 75083-515, GO, Brazil
2
Peptech Colagen from Brazil, 1500 North Halsted Street—Floor 2, Chicago, IL 60642-2517, USA
3
Brazilian Institute of Teaching and Research in Pulmonary and Exercise Immunology (IBEPIPE), Rua Pedro Ernesto 240, São José dos Campos 12245-520, SP, Brazil
*
Author to whom correspondence should be addressed.
Nutrients 2024, 16(11), 1543; https://doi.org/10.3390/nu16111543
Submission received: 26 February 2024 / Revised: 7 May 2024 / Accepted: 15 May 2024 / Published: 21 May 2024
(This article belongs to the Special Issue Food-Derived Bioactive Peptides, Efficacy, Metabolic Fate, and Mechanisms of Action)
Browse Figure
Versions Notes

Abstract

:
Background: Our objective was to conduct a systematic review of the effects of hydrolyzed collagen supplementation on the proliferation and activation of fibroblasts. Methods: The search was conducted for journals that published articles in the English language, peer-reviewed, meeting the following criteria: (a) randomized clinical trials, (b) randomized studies in animals or humans, (c) in vitro studies, (d) studies using hydrolyzed collagens or collagen peptides, and (e) studies assessing alterations on fibroblasts as the primary or secondary outcome. We utilized the main journal databases PubMed/Web of Science and ongoing reviews by PROSPERO. For bias risk and methodological quality, we used an adaptation of the Downs and Black checklist. Our review followed the PRISMA checklist, conducted from February 2024 to the first week of March 2024, by two independent researchers (P.A.Q.I. and R.P.V.). Results: Eleven studies were included in this review, where our findings reinforce the notion that hydrolyzed collagens or collagen peptides at concentrations of 50–500 μg/mL are sufficient to stimulate fibroblasts in human and animal tissues without inducing toxicity. Different enzymatic processes may confer distinct biological properties to collagens, allowing for scenarios favoring fibroblast promotion or antioxidant effects. Lastly, collagens with lower molecular weights exhibit greater bioavailability to adjacent tissues. Conclusions: Hydrolyzed collagens or collagen peptides with molecular sizes ranging from <3 to 3000 KDa promote the stimulation of fibroblasts in human tissues.

1. Introduction

Collagen is the primary protein composing the extracellular matrix, formed by a chain of specific amino acids. In its primary form, collagen exhibits a triple-helical structure [1]. The triple-helical structure of collagen molecules is constituted by three α chains, characterized by repeating peptide triplets with the sequence glycine-X-Y. While X and Y represent any amino acid, they typically correspond to proline and hydroxyproline, respectively. Adjacent to the triple-helical regions are non-glycine-X-Y segments known as non-collagenous domains or Col domains. These regions often incorporate identifiable peptide modules found in other extracellular matrix molecules [2].
In addition, the collagen family encompasses 28 types of collagens which are distributed in different proportions in all organs and systems in the human body, constituting an essential component of cellular membranes [3]. Although almost all of the collagens are presented in filamentous or fiber forms, few forms are also presented in soluble structures [3]. In this way, collagens fulfill structural functions and play crucial roles in determining the mechanical characteristics, arrangement, and form of tissues. They engage with cells through various receptor groups, influencing their growth, movement, and specialization. Certain types of collagens exhibit limited distribution within tissues, indicating specialized functions tailored to specific biological processes [3]. The proper functioning of tissues relies on the accurate assembly of molecular aggregates integrated into the matrix. This review underscores the key structural attributes of the collagen types I–XXVIII [2].
Collagens stand as the predominant proteins in mammals, constituting approximately 30% of the total protein mass. The unveiling of collagen II by Miller and Matukas in 1969 marked a pivotal moment, leading to the subsequent identification of 26 additional collagen types. Advances in molecular biology and gene cloning techniques have greatly expedited the pace of discovery in this field [2].
Beyond their physiological and pathophysiological roles, the development of collagen-based proteins and peptides is expanding rapidly [4]. Through a process of heating, the collagen molecule undergoes enzymatic denaturation, partly through the hydrolysis of peptide bonds, resulting in its gelatinous form, commercially known as hydrolyzed collagen or collagen peptides [5,6,7]. Its production occurs through animal skin, bones, connective tissues (tendons), or the skin and scales of saltwater and freshwater fish [8]. The growing interest of the pharmaceutical and cosmetic industries is due to the evidenced effects, mainly on the regeneration of wrinkled cutaneous tissue and dermal hydration, seemingly resulting from the recovery of degraded collagen fibers [9].
Hydrolyzed collagen, also known as collagen peptides, is a popular dietary supplement widely used for its potential health benefits, including improved skin elasticity, joint health, and bone density. The industrial production of hydrolyzed collagen involves several key techniques to extract and process collagen from animal sources, primarily bovine (cow) or porcine (pig) hides, bones, or fish scales. So, the industrial techniques used in the production of commercial hydrolyzed collagen are briefly described as follows:
The extraction of collagen: The first step involves the extraction of collagen from animal tissues. This is typically performed through acid or alkaline treatment to break down the connective tissue and release the collagen fibers. Various studies detail the optimization of extraction parameters such as temperature, pH, and extraction time to maximize collagen yield [10].
Purification: Once extracted, the collagen undergoes purification processes to remove impurities such as fats, proteins, and minerals. Techniques like filtration, centrifugation, and precipitation are employed for this purpose [10].
Hydrolysis: The purified collagen is then subjected to enzymatic hydrolysis, where enzymes such as proteases break down the collagen molecules into smaller peptides. This process increases the bioavailability and solubility of collagen peptides, making them easier to digest and absorb in the body [11].
Fractionation: Fractionation techniques are sometimes employed to isolate the collagen peptides of specific molecular weights or sizes, as different sizes may exhibit different bioactive properties. Fractionation methods include chromatography and ultrafiltration [12].
Drying and packaging: The hydrolyzed collagen solution is then concentrated and dried to obtain a powder form suitable for use as a dietary supplement. Spray-drying is a commonly used technique for this purpose, as it allows for rapid drying while preserving the nutritional and functional properties of collagen peptides. The dried powder is then packaged in airtight containers to maintain its quality and shelf life [13].
Quality control: Throughout the production process, quality control measures are implemented to ensure the safety, purity, and consistency of the final product. This includes testing for contaminants, such as heavy metals and pathogens, as well as monitoring key parameters like collagen content, amino acid profile, and molecular weight distribution [14].
Regulatory compliance: The industrial production of hydrolyzed collagen must comply with the regulatory standards set by organizations such as the Food and Drug Administration (FDA) in the United States or the European Food Safety Authority (EFSA) in Europe. This includes adherence to good manufacturing practices (GMPs) and labeling requirements for dietary supplements [15].
In terms of health implications, collagen supplementation has been implicated in elderly sarcopenic populations, wound healing, and degenerative processes related to tendon and bone structures [1]. Interestingly, Wang et al. (2011), using a low-molecular-weight collagen peptide (800 KDa), tested whether a composite among this collagen peptide and chito-oligosaccharide may have the antibacterial properties and biocompatibility of the composite electrospun with nanofibrous membranes (NFMs) using human skin fibroblasts [1]. New findings also suggest that hydrolyzed collagen possesses properties to reduce inflammatory markers and fibroblast proliferation. This emerging research showing this relationship is justified by the mechanism of action in which collagens are formed by fibroblasts [16], supporting the notion that collagen appears to stimulate fibroblast proliferation. In addition, this study from Brandao-Rangel et al. (2022) showed that collagen peptide at different concentrations 2.5 mg/mL, 5 mg/mL, and 10 mg/mL protected human skin fibroblast (CCD-1072Sk) and human skin keratinocytes (hKT-nh-skp-KT0026) inducing a latent anti-inflammatory response against lipopolysaccharide stimulation (LPS; 10 ng/mL) [16]. Animal studies and cell culture experiments corroborate this rationale [17,18]. In this way, Chotphruethipong et al. (2021) showed that hydrolyzed collagen from the defatted Asian sea bass (Lates calcarifer) (Asbs-HC) presenting high hydrophobic amino acids and imino acids did not cause cytotoxicity at any concentration (25–1000 µg/mL). In addition, the highest concentration (1000 µg/mL) induced high MRC-5 fibroblast cell line (human fetal lung) proliferation and migration suggesting a potential for wound healing, beyond a high antioxidant capacity [17]. In another study, Offengenden et al. (2018), using hydrolyzed collagen obtained from seven different enzymatic processes, compared their effects on inflammation, oxidative stress, type I collagen synthesis, and cell proliferation, using cultured human dermal fibroblasts. In conclusion, the authors stated that different enzymatic treatments may generate hydrolyzed collagen possessing distinct chemical and biological profiles [18]. Fibroblasts were first introduced to the scientific community in 1858 by the German pathologist Rudolf Virchow, and subsequently, the properties of this discovery turned towards their role in tissue repair, implicating fibroblasts in the production of new connective tissues [19]. Broadly, fibroblasts are known as mesenchymal cells, exhibiting various functions such as tissue repair agents in various pathological scenarios, target cells, and modulators for immune functions; the secretion of metabolites and signaling factors to neighboring cells, as well as the regulation of metabolism in various organs; and extracellular matrix remodeling [20].
Based on these findings, we investigated how supplementation with hydrolyzed collagen peptides can induce the proliferation and activation of fibroblasts, which are the cells capable of synthesizing collagen in various organs and tissues. The justification for this literature review stems from the lack of a review that explains the studies corroborating the idea of “hydrolyzed collagen inducing fibroblast stimulation”. The objective of this review is to present possible evidence that brings to light fibroblast proliferation through the ingestion or application of hydrolyzed collagen peptides and their reduced forms, to highlight limitations, and to create a more solid database for the mechanisms adjacent to the use of hydrolyzed collagen.

2. Methods

2.1. Inclusion and Exclusion Criteria

Our analyses were limited to journals that published articles in the English language, peer-reviewed, meeting the following criteria: (a) randomized clinical trials, (b) randomized studies in animals or humans, (c) in vitro studies, (d) studies using hydrolyzed collagens or collagen peptides, and (e) studies assessing alterations on fibroblasts as the primary or secondary outcome. Review articles, brief reviews, opinion articles, case reports, or observational studies, as well as research utilizing forms of non-hydrolyzed collagens, were considered ineligible for the construction of this review.

2.2. Search Strategy

The search for articles, as well as the construction of this review, was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [21]. Our primary search was performed in the main databases PubMed/MEDLINE and Web of Science/Clarivate, which publish articles in the English language. We also consulted the ongoing review database (PROSPERO). The search was conducted from February 2024 to the first week of March 2024. The following syntax was used for the search: hydrolyzed collagen peptides AND fibroblast, low molecular weight collagen peptides AND fibroblast. Articles that included any of the following terms in their title or abstract: collagen hydrolyzed, fibroblast, and low-molecular-weight collagen, were included for further analysis. From these selected articles, the reference lists were subsequently consulted to identify possible additional publications [22]. To avoid selection bias, the search was conducted by two researchers who independently analyzed the articles (P.I. and R.P.V.). If any article was deemed divergent for inclusion and exclusion, a third, fourth, and fifth researcher (F.A.C., G.F.A., and C.F.C.) was consulted, with the final decision resting with them.

2.3. Methodological Quality

We assessed the methodological quality of the included studies using the Downs and Black checklist with 27 items [22]. This checklist addresses different aspects of study design, including reporting (items 1–10), external validity (items 11–13), internal validity (items 14–26), and statistical power (item 27). Given the specificity of the included studies, we used the checklist as a reference and listed 10 items to be considered to evaluate the methodological quality of the studies. If the item was present, a value of 1 was assigned, otherwise a value of 0, similar to the Downs and Black checklist. Studies were classified as good quality if they scored 8–10, moderate quality if they scored 6–7, and poor quality if they scored 5 or below. The studies were independently evaluated by the 2 reviewers (P.I. and R.P.V.).

3. Results

From the studies searched in the databases, we obtained a total of 220 articles, of which 184 articles were listed for the initial analysis. However, these were subsequently excluded due to ineligibilities identified by automation tools, resulting in the exclusion of a total of 172 documents, including duplicates (n = 8) and articles published in languages other than English (n = 4), leaving 36 articles. After summarization, those that did not meet criteria (a); (b); (c); (d), or were not considered relevant for the review construct, in agreement between the two researchers (P.I. and R.P.V.), were excluded (n = 21), totaling 15. Three articles were evaluated by the third, fourth, and fifth researcher (F.A.C. and C.F.C.), who made the final decision regarding their inclusion or exclusion in the present review. Two articles proceeded for analysis, and one document was excluded. Subsequently, the articles were read in full, and the references were re-evaluated to retrieve possible documents not found in the initial data searches. During the full-text reading of the articles, three articles were excluded: one as it was a review, and the other two documents did not demonstrate in their results the effects of hydrolyzed collagen on fibroblast proliferation. Eleven articles were included in the final review. Figure 1 presents the flowchart of the literature search. In summary, the studies included for analysis are as follows.

3.1. Study Coding

The studies were individually read and coded by the two researchers (P.I. and R.P.V.) using the PICO tool for the following variables: (a) population, (b) intervention, (c) comparison/control, and (d) outcomes. Population refers to the type of hydrolyzed collagen used and, if reported, its molecular weight in kilodalton KDa. Intervention on fibroblasts identifies the types of fibroblastic cells used, whether human or animal. For comparison and control, we listed the controls used as well as the dosages. Lastly, outcomes present the results exclusively regarding fibroblast cell proliferation. Table 1 presents an overview of the studies that met all inclusion criteria.

3.2. Article Retrieval

Throughout the process of reading and summarizing the articles, their references and citations were independently reviewed to find articles that were not reached in our initial searches. However, no articles that had not already been identified during the review process were found. From all references, the researcher (P.I.) listed one document that addressed the outcome of fibroblast proliferation by collagens. Upon reading the document in its entirety, it became evident that the document aimed to evaluate the effects of collagen that did not undergo hydrolysis processes, thus disqualifying it as hydrolyzed collagen or collagen peptides. Therefore, it was not included.

3.3. Characteristics of the Studies

Eleven studies were included in this review [16,17,18,23,24,25,26,27,28,29,30] for the outcome of the stimulation or proliferation of fibroblasts by the application or ingestion of hydrolyzed collagen supplements or collagen peptides. Three studies used rat fibroblast cell lines as the intervention method, while the remaining articles used human fibroblast cells. The types of collagens used varied among the selected articles, including animal, fish, and chicken origins, with one study utilizing a collagen-enriched beverage [29], and two studies combining hydrolyzed collagen with vitamin C applications [28,30]. When reported, the molecular weight of all hydrolyzed collagens was stated in Daltons, with all studies presenting low molecular weights, with the lowest being reported in the work of Rangel et al., 2022 (see Table 1). The studies used control cells without interventions or with the additions of various concentrations of hydrolyzed collagen (25, 50, 100, 500, and 1000 μg/mL).

3.4. Methodological Quality

The quality of each study was assessed by the two researchers (P.I. and R.P.V.), and in case of any discrepancies regarding quality parameters, a third researcher was consulted to ensure agreement. The scale used was adapted from the Downs and Black checklist, listing 10 points as quality criteria, in which eight studies were considered good quality, and three studies were of moderate quality (see Table 2).
Methodological quality criteria adapted from the checklist:
  • Was the study hypothesis/goal/objective clearly described?
  • Were the main results clearly measured and described in the Introduction or Methods section?
  • Were the characteristics of the cell types used and controls described?
  • Were the interventions of interest clearly described? Treatments and placebos (when relevant) to be compared should be clearly described.
  • Was a list of key confounding factors provided, along with how cellular environments and processes were managed, and described clearly?
  • Were the main conclusions of the study clearly described? Simple outcome data (including denominators and numerators) should be reported for all main findings so that the reader can verify the main analyses and conclusions. (This question does not cover statistical test data, which are considered below.)
  • For non-normally distributed data, was the interquartile range of results reported? For normally distributed data, standard error, standard deviation, or confidence intervals should be reported.
  • Did the authors clearly report the limitations of their findings? If yes, consider 1; if not, consider 0.
  • Were appropriate statistical tests used to assess the main results? The statistical techniques used should be appropriate to the data.
  • Were actual probability values reported (e.g., 0.035 instead of <0.05) for the main results, except where the probability value is less than 0.001?

4. Discussion

The results of this systematic review reinforce the concept of hydrolyzed collagen inducing fibroblast stimulation. This effect appears to be mediated by the ingestion of collagen peptides or hydrolyzed collagens. The studies presented here provide a robust body of evidence demonstrating fibroblast cell proliferation through the use of hydrolyzed collagens without alterations in cellular toxicity. This implies that hydrolyzed collagen may have outcomes beyond those already evidenced.
Hydrolyzed collagen supplementation is widely used for aesthetic purposes, primarily to delay skin aging. Part of its effect is attributed to stimulating extracellular matrix proteins, which are directly regulated by dermal fibroblasts (F.Ds.). As shown in our results, hydrolyzed collagens stimulate the specific growth of F.Ds., especially those with lower molecular weights and high proline/hydroxyproline content.
A determinant factor reported in our review leads us to rationalize that molecular weight is directly related to better solubility. Collagen peptides rich in pro-Hdx exhibit significant bioavailability. Peptides with lower molecular weights have properties to reach deeper dermal layers, thus stimulating better tissue repair. Despite not being the focus of this review, it is important to note that, in addition to increasing fibroblasts, hydrolyzed collagens are gaining traction as potential antioxidant supplements. Some studies included here sought to combine hydrolyzed collagens with other types of supplements known for their positive effects on oxidative scenarios, such as vitamin C.
Among the findings, it was also noted that depending on the enzymatic processes on collagens, different hydrolyzed collagens obtain distinct characteristics. Some seem to prefer antioxidant and inflammatory situations, while others induce fibroblast proliferation in human skin. However, this result is presented by only one study, warranting further investigation to identify if indeed specific types of hydrolyzed collagens are tailored to specific fibroblast applications.
According to our findings, hydrolyzed collagens from different sources and with different molecular weights, yet all considered low-weight, ranging between <3 and 3000 Da, are capable of inducing fibroblasts in human and animal skin tissues.
In addition to the findings presented here, this review also serves an important role in scientific production, encouraging new studies to evaluate the effects of hydrolyzed collagens on fibroblasts in relation to the tested dosages. Most studies indexed here used dosages with different concentrations of collagens in fibroblasts to identify minimum and maximum absorption values and possible toxicity. Summarizing all presented results, the concentrations of 50–500 μg/mL are sufficient for fibroblast proliferation without toxicity implications. The concentrations of 800 μg/mL showed toxicity levels in cultured human dermal fibroblasts (HDFs). However, this result should be analyzed cautiously since in MRC-5 fibroblast cell line (human fetal lung) tissues, the doses of 1000 μg/mL did not create such a scenario, and among lower doses compared to higher doses, none of these doses induced toxicity. With these reviewed findings, new research directions do not require further investigation into solutions with different concentrations when the goal is fibroblast stimulation.

5. Limitations and Future Directions

This review focused on only one outcome regarding hydrolyzed collagens, while others such as toxicity and inflammatory levels are recommended for readers to explore in the selected articles. Our aim is to facilitate new research regarding the use of collagens and fibroblasts, as until the present moment, no review with such objectives has been evidenced. Our work is not without limitations; for example, the methodological quality of the listed articles underwent an adaptation process. We encourage future, more robust checklists that include in vitro studies to be developed to facilitate methodological processes for cellular study reviews. Furthermore, studies investigating the molecular mechanisms involved in the collagen peptide-induced fibroblast proliferation and activation must be performed; at the moment, only the study from Brandao-Rangel et al. (2022) has brought some initial pathways about this issue, demonstrating the involvement of nitric oxide and TGF-β and the VEGF pathway in such effects [16]. We chose to limit our searches to articles published in English and peer-reviewed, which may omit data from other sources that would be relevant for a better understanding of the presented findings. However, this choice aims to narrow down the findings to studies with minimal bias and good quality. Finally, this review creates a possible research scenario regarding the specific biological properties of each hydrolyzed collagen, and in the future, identify if specific enzymatic processes substantially alter the action of hydrolyzed collagen on fibroblasts.

6. Conclusions

In conclusion, our review highlights the effectiveness of hydrolyzed collagens and collagen peptides in stimulating and proliferating fibroblast cells, but not for any integral form of collagen. New studies aiming to explore this scenario may consider using dosages ranging between the concentrations of 50 and 500 μg/mL of hydrolyzed collagen. Furthermore, investigations regarding the different enzymatic processes during the collagen hydrolysis process should be conducted to identify if these different processes may affect the biological properties of hydrolyzed collagen or collagen peptides, thus changing their effects on fibroblast stimulation.

Author Contributions

P.A.Q.I.: Conceptualization, investigation, formal analysis. F.A.C.: Conceptualization, investigation, formal analysis. G.F.A.: Conceptualization, investigation, formal analysis, writing—review and editing. C.d.F.C.: Conceptualization, investigation, formal analysis, writing—review and editing. R.P.V.: Conceptualization, investigation, formal analysis, writing—original draft, writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

Author Felipe Augusto Chalupe was employed by the company Peptech Colagen from Brazil. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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  27. Wang, Y.; Zhang, C.L.; Zhang, Q.; Li, P. Composite electrospun nanomembranes of fish scale collagen peptides/chito-oligosaccharides: Antibacterial properties and potential for wound dressing. Int. J. Nanomed. 2011, 6, 667–676. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  28. Chotphruethipong, L.; Hutamekalin, P.; Nilsuwan, K.; Sukketsiri, W.; Aluko, R.E.; Abdul, N.R.; Benjakul, S. Combined Effects of Defatted Hydrolyzed Collagen from Salmon Skin and Vitamin C on Proliferation and Migration of Human Fibroblast Cell. Fishes 2022, 7, 265. [Google Scholar] [CrossRef]
  29. Lin, P.; Hua, N.; Hsu, Y.C.; Kan, K.W.; Chen, J.H.; Lin, Y.H.; Lin, Y.H.; Kuan, C.M. Oral Collagen Drink for Antiaging: Antioxidation, Facilitation of the Increase of Collagen Synthesis, and Improvement of Protein Folding and DNA Repair in Human Skin Fibroblasts. Oxid. Med. Cell Longev. 2020, 2020, 8031795. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  30. Benjakul, S.; Karnjanapratum, S.; Visessanguan, W. Hydrolysed collagen from Lates calcarifer skin: Its acute toxicity and impact on cell proliferation and collagen production of fibroblasts. Food Sci. Technol. 2018, 53, 1871–1879. [Google Scholar] [CrossRef]
Nutrients 16 01543 g001
Figure 1. Flowchart of the search process.
Figure 1. Flowchart of the search process.
Nutrients 16 01543 g001
Table 1. Articles included for review and their outcomes.
Table 1. Articles included for review and their outcomes.
ArticleType of Collagen
and Molecular Weight (MW) in Kda		Intervention on FibroblastControl/ComparasionOutcomes
Chai et al., 2010 [23]Collagen peptides from fish.Human and mouse embryonic skin fibroblast lineage.Fibroblast without collagen stimulation.The doses of 0.4–200 μg/mL induced fibroblast proliferation in a dose-dependent manner.
Chotphruethipong et al., 2019 [24]Sea bass skin hydrolysate and collagen with the application of porcine pancreatic lipase.Mouse fibroblasts from subcutaneous connective tissue lineage (L929).Fibroblasts without the addition of hydrolyzed collagen (HC) and solutions with HC concentrations of 50, 100, 200, and 250 μg/mL.The cellular proliferation of fibroblasts, mainly between concentrations 100 and 250 μg/mL.
Chotphruethipong et al., 2021 [17]Hydrolyzed collagen from defatted sea bass skin. MW = 406 to 16,120 Da.MRC-5 fibroblast cell line (human fetal lung).Fibroblasts with the additions of hydrolyzed collagen at the concentrations of 25, 50, 100, 500, and 1000 μg/mL.Concentration-dependent fibroblast proliferation with no significant difference between the concentrations of 500 and 1000 μg/mL (p > 0.05).
Chotphruethipong et al., 2021 [25]Hydrolyzed collagen (HC)
from degreased sea bass skin and collagen (HC) + EGCG epigallocatechin gallate.		MRC-5 fibroblast cell line (human fetal lung).Fibroblasts without addition and with the additions of hydrolyzed collagen (HC), and HC + EGCG.HC promoted cell proliferation more effectively than HC-conjugated EGCG.
Wauquier et al., 2022 [26]Fish cartilage hydrolysate (FCH).
Low MW (under 3000 Da).		Human primary dermal fibroblastsHuman I seruINAIVE or human serum enriched with circulating metabolites resulting from FCHFCH stimulates human dermal fibroblast growth
Brandao-Rangel et al., 2022 [16]Hydrolyzed collagen (types I and III of hydrolyzed collagen)
Total MW < 3 oderientesibroblasts (CCD72Sk).		(1) odetodernly medium stimulated), (2) lipopolysaccharide (LPS 10 ng/mL), (3) collagen 2.5 mg/mL, (4) collagen 5 mg/mL, (5) collagen 10 mg/mL, (6) LPS + collagen 2.5 mg/mL, (7) LPS + collagen 5 mg/mL, and (8) LPS + collagen 10 mg/mL. LPS was added for 1 h,
with the subsequent addition of collagen.		…Collagen supplementation (2.5 mg/mL, 5 mg/mL, 10 mg/mL) increased the proliferation of human’s fibroblasts. p < 0.001.
Offengenden et al., 2018 [18]Chicken collagen hydrolysate (CCH).Cultured human dermal fibroblasts (HDF).A total of 4 dual-enzyme generated hydrolysates.Only 2 out of the 4 enzyme-hydrolyzed collagen stimulate fibroblast proliferation, p < 0.01, p < 0.001.
Wang et al., 2011 [27]Fish scale collagen peptide (FSCP)
MW 800 Da.		Cultured human dermal fibroblasts (HDF).PVA (polyvinyl alcohol) and E NFM (lectrospun nanofibrous membranes) served as the control.FSCP treatments both showed good in vitro biocompatibility and supported the proliferation of fibroblasts.
Chotphruethipong et al., 2022 [28]Hydrolyzed collagen from salmon skin and vitamin C (Vit C)
Mw 102 Da to 10,175 Da.		Cultured human dermal fibroblasts (HDF).HC (0, 50, 100, 200, 400, and 800 μg/mL) and Vit C (0.01, 0.1, 1, 10, and 100 μg/mL) control (without any treatment).Hydrolyzed collagen (HC) at various levels on the proliferation of HDF cells, there was no difference in the cell proliferation of HC at the levels of 50 and 100 μg/mL,
p > 0.05, cytotoxicity, and 800 µg/mL which showed a slightly decreased proliferation of the cell as compared to the control p < 0.05. Between the two protocols (hc) and vit c, there was no significant difference in relation to the increase in fibroblast proliferation p > 0.05, and when combined, greater proliferation in relation to the isolated methods p < 0.05.
Lin et al., 2020 [29]Elastin collagen peptide complex juice srink (YAMII, Zhejiang Kazman Biotechnology) ingredients: water, fish collageoderide powder (12% oderana powder, apple essence, cherry essence, γ-aminobutyric acoderape powoderlma powodercai powder, perodereed powder, eoderrry powder, boderice powder, honey, vitamin C, erythritol, citric acid, fructose syrup, sucrose, flavor).Human skin fibroblast.Concentrations of collagen drinks (with/without UVA irradiation). 0.125%, 0.25%, and 0.5%, Control 0%.In comparison with the control group, 0.125%, 0.25%, and 0.5% of the collagen drinks could increase the mitochondrial activities of fibroblasts by 30.6%, 16.4%, and 36.1%, respectively. Regarding photoaging improvement, the mitochondrial activities of the UVA-treated cells were improved by 100.9%, 110.2%, and 105.4%, respectively, followed by treatment with corresponding 0.125%, 0.25%, and 0.5% of the collagen drinks. The collagen drinks slightly enhanced the cell proliferation capability in comparison with the control group.
Benjakul et al., 2018 [30]Hydrolysed collagen from seabass (Lates calcarifer) and HC + Vit C.
Molecular weight ranges from 1050 to 1330 Da.		L929 mouse fibroblast, subcutaneous connective tissue.HC powder was dissolved in distilled water and dosed
orally at 2000 and 5000 mg kg body weight. The treated doses were calculated based on the body
weights of rats after fasting. The rats in the control group were dosed with distilled water at the equivolume to the treatment group.		HC promoted cell growth L929. The greatest proliferation was evidenced in combined models of HC + Vit c in a 2:1 ratio at the dosages of 150–200 μg/mL.
Table 2. Methodological quality criteria.
Table 2. Methodological quality criteria.
Article12345678910Total Score
Chai et al., 2010 [23]11111110108
Chotphruethipong 2019 [24]11111110108
Chotphruethipong 2021 [17]11111110108
Chotphruethipong et al., 2021 [25]11111110108
Wauquier et al., 2022 [26]11111110108
Brandao-Rangel et al., 2022 [16]11111111109
Offengenden et al., 2018 [18]11111010107
Wang et al., 2011 [27]11111010107
Chotphruethipong et al., 2022 [28]11111110108
Lin et al., 2020 [29]11111010107
Benjakul et al., 2018 [30]11111110108
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Inacio, P.A.Q.; Chaluppe, F.A.; Aguiar, G.F.; Coelho, C.d.F.; Vieira, R.P. Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review. Nutrients 2024, 16, 1543. https://doi.org/10.3390/nu16111543

AMA Style

Inacio PAQ, Chaluppe FA, Aguiar GF, Coelho CdF, Vieira RP. Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review. Nutrients. 2024; 16(11):1543. https://doi.org/10.3390/nu16111543

Chicago/Turabian Style

Inacio, Pedro Augusto Querido, Felipe Augusto Chaluppe, Gerson Ferreira Aguiar, Carly de Faria Coelho, and Rodolfo P. Vieira. 2024. "Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review" Nutrients 16, no. 11: 1543. https://doi.org/10.3390/nu16111543

APA Style

Inacio, P. A. Q., Chaluppe, F. A., Aguiar, G. F., Coelho, C. d. F., & Vieira, R. P. (2024). Effects of Hydrolyzed Collagen as a Dietary Supplement on Fibroblast Activation: A Systematic Review. Nutrients, 16(11), 1543. https://doi.org/10.3390/nu16111543

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