Abstract
Objective:
The extracellular matrix is essential for skeletal muscle function, providing structural support and facilitating force transmission from muscle fibers to tendons and the skeletal system. Collagen structures, known for their high plasticity, adapt to various stimuli, including mechanical loading during high-load resistance training. The present study aimed to assess the impact of specific collagen peptide (SCP) supplementation, combined with resistance training, on the levels of intramuscular collagen (COL) types I, III, and IV, and to assess the change in intramuscular fibroblast content.
Methods:
In a randomized, placebo-controlled study, 29 healthy male participants completed 12-week high-load resistance training (70-85% of 1 repetition maximum) with daily supplementation of 15g of SCP or placebo (PLA). Before and after the intervention period, muscle biopsies from the vastus lateralis muscle were obtained to quantify intramuscular collagen amount and fibroblast density.
Results:
SCP supplementation together with exercise led to increased (p = 0.026) collagen type I content (29.8%) compared to training with placebo (9.9%). Collagen types III and IV content increased significantly across the pooled sample (p < 0.05) with no significant group x time interaction. Fibroblast density did not change over the time course of intervention, either within or between groups.
Conclusion:
Endomysial collagen type I content increased in response to resistance training when supplemented with SCP compared to placebo. The observed increase in intramuscular collagen content may contribute to improved structural support of skeletal myofibers.
1 Introduction
Collagen is the most abundant structural protein in humans and accounts for one-third of all protein in the human body (). As a component of the extracellular matrix (ECM), collagens are crucial for the mechanical stability of various tissues, including skeletal muscle ().
In skeletal muscle, extracellular collagen facilitates force transmission from muscle fibers to the tendons and bones (; ), thus playing an important role in the execution of movement. Within skeletal muscle tissue, collagen types I and III are the most abundant of the 28 collagen subtypes (), accounting for approximately 74% of the total collagen content of human skeletal muscle (). The fibril-forming properties of collagen I and III are known to contribute to the tensile strength, stiffness, and elasticity of muscle tissue (; ). In addition, type IV collagen is the main component of the myofiber basement membrane (), where it forms network-forming, interdigitated structures that provide important membrane stability (; ).
Although collagen was previously considered metabolically stable (), it is now well established that intramuscular connective tissue undergoes continuous remodeling in response to mechanical loading and that resistance exercise is a potent stimulus for collagen turnover (; ; ; ). Whether nutritional approaches can enhance exercise-induced collagen remodeling remains unclear. While one study reported an increase in intramuscular connective tissue protein synthesis rates during the later phase of post-exercise recovery following whey protein ingestion (), the majority of studies found no additive effect of leucine-rich protein supplementation on exercise-induced collagen synthesis rates (; ; ).In contrast, collagen peptides may support ECM remodeling by providing targeted amino acid substrates for collagen synthesis (e.g., glycine, proline, hydroxyproline), and through the potential signaling properties of collagen-derived di- and tripeptides such as prolyl-hydroxyproline (Pro-Hyp) and hydroxyprolyl-glycine (Hyp-Gly), which have been shown to stimulate fibroblast proliferation and ECM production in vitro (; )Notably, collagen-derived supplements have been reported to induce structural and/or functional adaptations in collagen-rich tissues such as bone (; ; ), articular cartilage () and tendon (; ; , ; ). In their narrative review, suggest that collagen products high in glycine and proline may stimulate connective tissue synthesis when administered in parallel with concurrent exercise stimuli. Supporting a stimulatory effect of collagen supplementation on intramuscular connective tissue, a greater acute increase in collagen type I synthesis was observed after gelatine (a collagen derivative) compared with placebo in response to a single session of rope-skipping exercise (). In contrast, recent experiments () showed that adding collagen supplementation to one week of high-volume resistance-type exercise (combining resistance and plyometric training) did not lead to a greater increase in intramuscular connective tissue protein synthesis, in the quadriceps muscle, compared to intake of non-caloric placebo. Together, these findings highlight that the effects of collagen peptide supplementation on intramuscular connective tissue remodeling including collagen adaption remain inconclusive, particularly with respect to longer-term resistance training interventions in humans. No study to date has systematically examined whether prolonged collagen peptide supplementation during high-load resistance training leads to changes in specific intramuscular collagen subtypes (types I, III, and IV).
Fibroblasts are the primary ECM producing cells in skeletal muscle, and are responsible for the synthesis and maintenance of interstitial collagens, especially collagen types I and III (), and thus play an important role to muscle fiber structural integrity and ECM remodeling (; ). Through mechanotransduction, fibroblasts are highly sensitive to mechanical loadings, enabling adaptive regulation of ECM remodeling in response to exercise (). As such, fibroblasts may represent a key cellular link through which both mechanical loading and nutritional factors, such as collagen peptide supplementation, influence ECM adaptation in skeletal muscle.
While resistance exercise is one of the most potent stimuli for skeletal muscle ECM remodeling, most research has focused on muscle fiber adaptations, whereas the connective tissue compartment and its primary ECM-producing cells have received comparatively less attention. Data on the effects of protein supplementation in this context are scarce and largely limited to in vitro findings in dermal fibroblasts showing that collagen peptides stimulate proliferation and activation, while in vivo human studies have not assessed fibroblast-related outcomes (). Thus, it remains unknown whether long-term high-load resistance training combined with collagen peptide supplementation modulates intramuscular collagen remodeling at the level of specific subtypes (I, III, and IV) and whether such adaptations are associated with changes in intramuscular fibroblast content.
The present study, therefore, investigated the effect of 12 weeks of high-load resistance training (HLRT) combined with daily SCP on endomysial collagen types I, III, and IV compared with HLRT plus placebo. In addition, intramuscular fibroblast content was assessed to provide cellular-level context for potential ECM remodeling processes. To our knowledge, this is the first study to simultaneously examine intramuscular collagen subtype-specific adaptations and fibroblast-related outcomes in response to long-term collagen peptide supplementation during resistance training in humans. We hypothesized that 12 weeks of HLRT combined with SCP supplementation would increase intramuscular collagen content (type I, III, IV) to a greater extent than HLRT and placebo, potentially accompanied by increased fibroblast density.
2 Materials & methods
2.1 Study design
The present data were obtained as part of a larger ongoing study investigating the effects of a SCP supplementation on general skeletal muscle adaptations induced by resistance training. A randomized, controlled, double-blind study design was employed to examine the effects of daily SCP or placebo supplementation combined with 12 weeks of resistance training on skeletal muscle connective tissue collagen types I, III, and IV content and fibroblast density.
One week before the intervention period, participants completed a preliminary screening involving a full medical history and general medical examination confirm eligibility with the study-specific inclusion criteria (see: “Participants”). Afterwards, participants were randomly assigned to the intervention or control group supplemented with either SCP or placebo, respectively. The order of allocation was determined by a computerized random number generator (Microsoft Excel; Version 365; Microsoft Corporation, Redmond, WA, USA). All outcome assessors, the statistical analysis group, exercise instructors and participants were blinded to group assignments. Before and after the 12-week intervention, a muscle biopsy was taken from the right VL muscle of each participant.
2.2 Participants
A total of 30 male participants were included in the study, with an age range of 18 to 29 years and a body mass index (BMI) between 18.5 kg/m2 and 25 kg/m2. This study was part of a larger research project on the effects of SCP supplementation on skeletal muscle adaptations to resistance training, from which acute gene expression responses to a single bout of HLRT have been reported previously (). The a priori sample size calculation was performed for the overarching project based on effect sizes from related functional and molecular outcomes, rather than for the histological endpoints presented here. Prior to the intervention, all participants were found to be moderately active (~150 min/week of moderate or 75 min/week of vigorous exercise [e.g., team sports, cycling]) with no regular participation in strength training during the last 12 months. Participants diagnosed with acute or chronic diseases, cardiac problems, or metabolic disorders were excluded from the study. All study procedures were approved by the local Ethics Committee of the University of Freiburg (study code: 380/19) in accordance with the Declaration of Helsinki and registered in the German Clinical Trials Register (DRKS00027112). All participants were informed about the study procedures and the potential risks of the study before giving their written informed consent.
Dietary intake three days prior to pre and post biopsy samplings was recorded by all participants using a standardized dietary registration protocol (). All participants were instructed to maintain their usual diet until the evening before the experiment, and to refrain from any exercise as well as alcohol and caffeine intake 48 hours prior to arrival at the laboratory (). For the final food intake 12 hours before the experimental trial, participants received a pre-packed meal. The protein content of the final meal was set at 0.4 g per kg body mass. This amount is aligned with current recommendations for trained male athletes () and was derived from a targeted total daily protein intake of approximately 1.2–1.4 g per kg body mass (; ). The quantity of calories in the meal was adjusted to meet the estimated total caloric requirement according to the Benedict-Harris equation using a physical activity level (PAL) value of 1.6 (). This combined approach of habitual dietary monitoring, randomization, and short-term pre-biopsy standardization reflects established methodological practice to reduce systematic bias in group comparisons in exercise–nutrition trials where full dietary control is not feasible. Under these conditions, remaining dietary variability is not expected to differentially affect group comparisons and is therefore unlikely to induce systematic bias between groups (; ).
2.3 Supplementation procedures
The interventional supplement consisted of 15 g SCP (BODYBALANCE®, Gelita AG, Eberbach, Germany). The placebo consisted of non-caloric silicon dioxide adjusted to a volume-equivalent amount of the active supplement to ensure comparable appearance and mouthfeel, thereby maintaining blinding conditions. A non-caloric, inert placebo was used to isolate the additive effects of collagen peptide supplementation on resistance training–induced adaptations. The exact amino acid composition of the interventional supplement is listed in Table 1. All participants were advised to consume the test product dissolved in 250 ml of water directly after exercise on training days, and at the same time of day on non-training days. The daily intake of the supplements was either directly monitored or queried by the trainer and recorded in participants’ training protocol. A minimum adherence rate of 80% (supplement intake on ≥80% of intervention days) was required for inclusion in the final analyses. Both supplements consisted of white, tasteless powders that could not be differentiated by flavor, color or solubility.
Table 1
| Amino acid | Weight [%] | Mol [%] |
|---|---|---|
| Hydroxyproline | 11.3 | 9.6 |
| Aspartic Acid | 5.8 | 4.8 |
| Serine | 3.2 | 3.4 |
| Glutamic acid | 10.1 | 7.5 |
| Glycine | 22.1 | 32.3 |
| Histidine | 1.2 | 0.8 |
| Arginine | 7.8 | 5.0 |
| Threonine | 1.8 | 1.7 |
| Alanine | 8.5 | 10.5 |
| Proline | 12.3 | 11.8 |
| Tyrosine | 0.9 | 0.5 |
| Hydroxylysine | 1.7 | 1.2 |
| Valine | 2.4 | 2.3 |
| Methionine | 0.9 | 0.9 |
| Lysine | 3.8 | 2.9 |
| Isoleucine | 1.3 | 1.1 |
| Leucine | 2.7 | 2.3 |
| Phenylalanine | 2.1 | 1.4 |
Amino acid composition of the SCP supplement.
SCP, specific collagen peptides.
2.4 Training protocol
The training intervention consisted of 12 weeks of 3 weekly exercise sessions. Successive exercise sessions were separated by at least 36 hours of rest to allow adequate recovery. Each exercise session was preceded by a 10-minute warm-up on a stationary cycle ergometer (50–80 Watts). The training protocol included three sets of knee extension and leg press exercises, respectively. In week 1-2, an exercise load of 70% of 1 repetition maximum (1RM) was employed, with loads progressing to 75, 80 and 85%-1RM in weeks 3-4, 5–8 and 9-12, respectively. At the same time points, the number of repetitions decreased from 15 to 12, 10 and 8 repetitions per set. Individual 1RM tests were performed before the intervention and after week 2, 4 and 8 to ensure progressive load increments throughout the study. Standardized resting periods were one minute between sets and three minutes between exercises. Leg press and knee extension were performed from 90° knee angle to nearly full extension. In addition, upper body exercises in the form of latissimus pull, supine bench press, and sit-ups were included in the exercise protocol with the aim of to increasing exercise compliance. A minimum training adherence of 80% was required for inclusion, defined as the full completion of ≥ 29 of the prescribed training sessions.
2.5 Muscle tissue sampling and handling
One week before and within one week after completing the intervention period, all participants arrived at the laboratory between 7.00 and 8.00 a.m. after an overnight fast (). After a 30-min resting period, a muscle biopsy was obtained from the VL muscle of the right leg. For this purpose, a 5-mm Bergström needle with manual aspiration was used after local anesthesia (2% xylocitin) (; ). The tissue sample was cleaned of excess blood using blotting paper. Afterwards, the sample was frozen in isopentane pre-cooled in liquid nitrogen. All samples were stored at -80 °C for later analysis (; ).
2.6 Immunofluorescence analysis
In brief, transverse cut serial sections (8 µm) of the muscle tissue biopsies were fixed (4% formaldehyde, Triton-X buffer) for 10 min, washed in PBS (3x3 min), and subsequently blocked (X0909, Dako, Glostrup, Denmark) for 10 min (; ). A staining was performed to visualize collagen I (Sigma-Aldrich (SA), C2456) and IV (SA, MAB3303). A second analysis was performed to visualize collagen III (SA, C7805) and fibroblasts (anti-transcription factor 4 (TCF‐4) recognizing transcription factor 7‐like 2 (TCF7L2, Cell Signalling, 2569) (). The following secondary antibodies were used (order listed: Goat anti-Rabbit (SA, A21424) Goat Anti-mouse 488 (SA, A21121), biotinylated anti-rabbit (Vector)/DyLight-549 (Vector, SA-5549). Sections were initially incubated with primary antibodies for 60 minutes at room temperature, followed by a wash step (PBS, 3x3 min), while subsequently incubated with secondary antibodies for 60 minutes. Finally, sections were washed in PBS, stained with 4’,6-diamidino-2-phenylindole (DAPI) and mounted in medium (Vector, H-5700) and stored protected from light at 5 °C. Sections in which primary antibodies were omitted served as negative controls.
Stained sections were visualized using fluorescent microscopy (Axio Imager M1, Carl Zeiss, Germany) and a high-resolution AxioCam (Carl Zeiss). Images were obtained using standardized settings (cf. x10, exposure). All analyses were performed manually in AxioVision image analysis software (AxioVision 4.6, Carl Zeiss). Endomysial collagen flourescence density was quantified as mean signal intensity per area using a standardized grid of circular regions of interest (ROIs, radius 6 µm). For each myofiber, only the most centrally positioned ROI was kept and systematically translated such that its center aligned with the sarcolemmal region, thereby ensuring consistent endomysial sampling and minimizing selection bias across images. Any immunoreactive areas were excluded only if predefined criteria were met, including presence of imaging artifacts (e.g., tissue folds) or inclusion of non-representative structures (e.g., vessels) with disproportionally high signal intensity. These criteria were applied uniformly across all images using identical analysis settings. All density measures were background corrected and expressed in arbitrary units. Fibroblasts were identified as TCF7L2-positive nuclei, defined by co-localization of TCF7L2 immunostaining with DAPI (TCF7L2+/DAPI+). Only TCF7L2+-nuclei with clear spatial localization within the endomysium were classified as fibroblasts, in accordance with established criteria (). Fibroblast abundance was quantified and expressed relative to the number of analyzed myofibers. An average of 319 ± 139, 188 ± 92 and 247 ± 129 myofibers were analyzed per muscle biopsy for collagen I/IV, collagen III, and fibroblasts, respectively. A minimum of 50 analyzed myofibers was set for analyses to be representative, resulting in two participants being withdrawn from the fibroblast analysis (final analyses involved SCP/PLA: 14/13). All analyses, including ROI placement and signal quantification, were performed by an investigator blinded to participant ID, group allocation, and time point.
2.7 Lifestyle parameters
The self-reported physical activity performed beyond the intervention program was assessed using the Freiburg Questionnaire of Physical Activity () before the beginning of the intervention.
Additionally, dietary intake was assessed using three-day dietary records (two weekdays and one weekend day) collected from all participants during the week before and after the intervention period. From this, macronutrient and total energy intake were analyzed using Nutriguide 4.6 [Nutri Science GmbH; Hausach, Germany]. To exclusively assess the impact of the intervention, all participants were instructed to maintain their habitual diet and habitual physical activity (aside from the standardized training intervention) throughout the entire study period.
2.8 Statistical analysis
All statistical analyses were performed blinded to group allocation and participant identity. Statistical analyses were conducted using SPSS [version 27.0, IBM]. All results are presented as group mean ± SD if not otherwise indicated. Since all variables showed normal distribution according to Shapiro-Wilk testing, parametric (i.e. Gaussian) tests were used for statistical analysis. Baseline group differences were assessed using unpaired t-tests. After confirming homogeneity of variances by Levene’s test, repeated measurement ANOVA (rmANOVA) was used to assess group x time interaction effects. Paired t-tests were applied for within-group comparisons. The level of significance was set to p < 0.05. Effect sizes are presented by the partial eta squared (ƞp²) with ƞp² > 0.01 indicating small, ƞp² > 0.06 indicating medium and ƞp² > 0.14 indicating large effect sizes (), and are reported with 95% confidence intervals.
3 Results
3.1 Participant characteristics
In total, n = 29 of the n = 30 participants completed all study procedures, with n = 14 in the SCP group and n = 15 in the PLA group. One participant dropped out due to relocation during the intervention period. Table 2 shows the anthropometric characteristics at baseline for all participants included in the analysis.
Table 2
| Variable | SCP | PLA |
|---|---|---|
| Age (years) | 25.4 ± 2.4 | 24.0 ± 2.6 |
| Height (cm) | 177.9 ± 8.1 | 178.5 ± 7.3 |
| Weight (kg) | 72.5 ± 9.9 | 71.2 ± 7.8 |
| BMI (kg/m²) | 22.9 ± 2.2 | 22.4 ± 2.4 |
Baseline anthropometric characteristics.
SCP, specific collagen peptides; PLA, placebo; BMI, body mass index. Data are [mean ± SD] (n = 29).
The groups were similar at baseline with respect to age, height, weight and BMI (p > 0.05). There were no significant between-group differences in exercise or supplementation compliance (p > 0.05). All included participants completed 100% (36/36) of the prescribed training sessions and mean self-reported supplement compliance was 99.3 ± 1.4% in SCP and 98.7 ± 1.4% in PLA.
3.2 Collagen content
For collagen type I, significantly greater increases were observed in SCP (+ 29.8%) compared with PLA (+ 9.9%), as indicated by a significant group × time interaction (p = 0.003) and a large effect size (hp2 = 0.170, 95 % CI [0.05, 0.31]) (Figure 1A). Group × time interactions for collagen type III and IV were not statistically significant (p = 0.648 and p = 0.393, respectively), indicating no evidence of differential changes between groups over time for these outcomes. The estimated effect size of the between-group differences in change was small for collagen type IV [ηp² = 0.027, 95% CI (0.00, 0.11)] and trivial for collagen type III [ηp² = 0.008, 95% CI (0.00, 0.06)]. A significant main effect of time was observed for collagen type I (p < 0.001; ηp² = 0.397), collagen type III (p = 0.016; ηp² = 0.195), and collagen type IV (p < 0.001; ηp² = 0.385). No significant baseline differences were observed between groups for any outcome measure (all p > 0.05). Within-group pre–post comparisons indicated increases are reported for descriptive purposes only, and are not part of the inferential analysis of the treatment effects. These analyses show increases in SCPfor all three collagen types (COL I: p < 0.001; COL III: p = 0.028; COL IV: p = 0.001; Figures 1A–C), whereas in PLA, collagen content increased for COL IV and remained unchanged for COL I (p = 0.137) and COL III (p = 0.077). These within-condition analyses are reported solely to illustrate the direction of changes within each condition, and to complement the interpretation of the group × time interaction effects, which constitute the basis for between-group inference.
Figure 1
3.3 Fibroblast density
For fibroblast density, there was no significant group × time interaction (p = 0.124, ηp² = 0.092) and no main effect of time (p = 0.706, ηp² = 0.006). In addition, no changes from pre- to post-measurements were observed in SCP (+24.6%, p = 0.177) and PLA (-17.8%, p = 0.121; Figure 2).
Figure 2
3.4 Dietary intake and physical activity
Before start of the intervention, no between-group differences were observed in self-reported physical activity–related energy expenditure (SCP: 538 ± 421 kcal/day; PLA: 382 ± 183 kcal/day; unpaired t-test p > 0.05). Likewise, average daily total energy intake and macronutrient distribution did not differ between groups at baseline (p > 0.05) and remained comparable over the course of the intervention, with no significant time x group interaction for any of the examined parameters (p > 0.05; Table 3).
Table 3
| Variable | SCP | PLA | |
|---|---|---|---|
| Caloric intake [kcal/day] | Pre | 2283 ± 521 | 2208 ± 648 |
| Post | 2416 ± 681 | 2487 ± 856 | |
| Protein [g/day] | Pre | 85.2 ± 20.5 | 88.8 ± 29.5 |
| Post | 87.7 ± 25.6 | 91.7 ± 29.0 | |
| Fat [g/day] | Pre | 80.3 ± 30.1 | 78.6 ± 34.1 |
| Post | 88.6 ± 34.6 | 83.3 ± 31.8 | |
| Carbohydrate [g/day] | Pre | 282 ± 71 | 259 ± 103 |
| Post | 288 ± 103 | 318 ± 137 | |
Dietary intake.
SCP, collagen peptides; PLA, placebo. Data are [Mean ± SD] (n = 29).
4 Discussion
The objective of the present double-blind randomized controlled trial was to determine whether supplementation with SCP during resistance training increases collagen content in intramuscular connective tissue in healthy, moderately active men. The present findings report for the first time an increase in intramuscular type I collagen content after 12 weeks of resistance training and concomitant daily supplementation of 15g of specific collagen peptides compared to the same training regimen combined with placebo.
4.1 Collagen content
The SCP group showed a ~3.5-fold greater increase in collagen type I content in comparison to HLRT combined with placebo. This effect was supported by a significant group x time interaction and a large effect size. Thus, the present results indicate that ingestion of SCP during resistance exercise is associated with a greater increase in intramuscular collagen type I accretion of healthy male individuals compared by HLRT and placebo.
Collagen types III and IV did not show statistically significant group × time interactions, indicating that no additional effect of SCP supplementation beyond training alone was observed for these outcomes. A significant main effect of time was present for all collagen types, reflecting an overall increase during the intervention period in both groups. These findings suggest that 12 weeks of HLRT, irrespective of supplementation, were sufficient to elicit measurable changes in the intramuscular collagen content, while no additive effect of SCP could be demonstrated for COL III and IV. Given the limited sample size, small effects cannot be entirely ruled out, and adequately powered studies will be needed to clarify whether nutritional strategies can meaningfully modulate intramuscular collagen remodeling beyond the stimulus provided by resistance training alone.
Recently, it has been discussed whether protein supplementation has an additive effect on exercise-related adaptations of intramuscular connective tissue. reported a time-dependent effect of ingestion of 18 g whey protein on intramuscular collagen synthesis, with higher fractional synthesis rates observed for whey protein compared with carbohydrate during the late (3–5 h) post-exercise recovery period, whereas no overall effect across the entire recovery period was detected (). However, although amino acids from dietary proteins seems to be incorporated in newly synthesized intramuscular connective tissue proteins, reflecting de novo collagen synthesis () most studies have not observed an additive effect of high-quality protein supplementation (whey, casein) either with or without exercise (; ; ).
Interestingly, a recent study that supplemented participants with hydrolyzed collagen peptides failed to demonstrate an effect on intramuscular connective tissue protein synthesis in response to a one-week training intervention consisting of ~70% of 1RM RT, drop jumping, and rope skipping (). Despite significantly elevated concentrations of circulating glycine, proline, and hydroxyproline in the collagen group, no differences in connective or myofibrillar protein synthesis were observed compared to placebo. These divergent outcomes may be explained by differences in training duration and exercise stimuli, respectively. The present study involved 12 weeks of resistance training involving leg press, knee extension at intensities of up to 85% of 1RM. Within tendon research, it is well established that structural adaptations in collagen-rich connective tissues require prolonged intervention durations, combined with sustained high mechanical loading and extended time under tension (; ). Similarly, the training stimulus employed in the present study may have been more effective in inducing the adaptive processes underlying increased intramuscular type I collagen synthesis than a shorter training period (one week) and a protocol imposing different mechanical demands due to the inclusion of plyometric exercises (e.g., rope skipping, drop jumps).
Based on the present observations, collagen peptides may support increases in intramuscular collagen type I accretion when combined with resistance exercise. This effect may be attributable to the specific amino acid profile of collagen peptides (Table 1), rich in amino acids (i.e., glycine and proline) with importance for collagen synthesis. Notably, previous metabolic flux analysis revealed that endogenous glycine synthesis is stoichiometrically limited and the glycine content of a typical dietary intake is often insufficient to meet the total daily requirement for metabolic processes, including diurnal collagen production (~10 g per day for a 70 kg adult) (). With only ~3 g/day endogenously synthesized and 1.5–3 g/day typically consumed via the diet (), the resulting glycine deficit has been proposed as a potential limiting factor for collagen synthesis, especially under conditions of increased demand associated with i.e. resistance training. It is possible that supplementation with collagen peptides may help bridge this potential gap and promote more effective intramuscular connective tissue remodeling during periods of HLRT in line with recent suggestions (). Beyond substrate provision, collagen-derived peptides have been shown in previous studies to act as bioactive signaling molecules by activating receptor-mediated pathways-integrin-, DDR-, and TGF-β-dependent signaling cascades- that regulate collagen synthesis and extracellular matrix remodeling. These pathways have been implicated in the regulation of collagen synthesis and extracellular matrix remodeling, and are considered to be relevant under conditions of increased mechanical loading (; ; ; ; Zhang et al., 2025). In the same cohort as the present study, reported an up−regulation of the MAPK and PI3K−Akt pathways (), which in other experimental contexts have been associated with the regulation of collagen synthesis (; ).
Notably, reported a greater increase in fat-free mass after 12 weeks of resistance training in young, recreationally active men who received collagen peptides compared with those receiving placebo. The authors attributed part of this effect to an increase in intramuscular connective tissue (). Although this hypothesis cannot be verified directly, it is indirectly supported by the present findings of increased collagen type I density. Although collagen represents only a small fraction of total skeletal muscle protein (), supplementation may nonetheless enhance the extracellular matrix at a structural level and thereby contribute, at least in part, to the greater gains in fat-free mass previously observed with collagen peptides compared with placebo (; ; ; ).
Given the established role of intramuscular connective tissue in the mechanical behavior of skeletal muscle, such changes may be relevant to tissue-level properties involved in force transmission and load distribution (; ). However, as the present analysis focused on structural outcome parameters, no conclusions can be drawn regarding effects on functional outcomes such as muscle performance, strength, or neuromuscular function. Accordingly, functional implications remain theoretical and require confirmation in future studies incorporating evaluation of physical performance or mechanical muscle function.
4.2 Fibroblast density
The present analysis of intracellular fibroblasts content in the knee extensor muscle (VL) did not show any response to resistance training or additional supplementation (SCP or Placebo). Given that fibroblasts are the primary cellular source of extracellular matrix proteins, including (pro)collagen (; ), an increase in collagen accretion could potentially require changes in fibroblast abundance. In the present study, increased intramuscular collagen content occurred over the course of the intervention in the absence of detectable changes in fibroblast density. This suggests that collagen accretion can occur without parallel alterations in fibroblast content under the applied conditions. These data are consistent with prior studies indicating that SCP supplementation may enhance the activity of existing fibroblasts and promote ECM remodeling (; ). To date, it is largely unknown to what extent different exercise modalities influence fibroblast content in human skeletal muscle tissue. There is evidence that HLRT increases circulating levels of fibroblast growth factors (), which are known to play a role in fibroblast cell proliferation ().
Notably, a specific exercise protocol designed to induce focalized myofiber injury resulted in a four-fold increase in the number of fibroblasts in human VL muscle, with fibroblasts preferentially localized in the proximity of regenerating muscle fibers () while accompanied by a 2-fold increase in collagen gene expression (). In contrast, although strenuous, the present resistance training protocol did not appear to provide sufficient mechanical or regenerative stimuli to increase fibroblast content, suggesting that stronger collagen protein synthesis stimuli and/or more pronounced muscle regeneration may be required to stimulate intramuscular fibroblast proliferation.
4.3 Methodological considerations
The trial has some limitations that should be considered when interpreting the findings. The sample size was determined as part of pre-specified randomized controlled trial investigating skeletal muscle adaptations to resistance training combined with collagen peptide supplementation, and was therefore not specifically powered for the present histological outcomes. Accordingly, the relatively small sample size may have limited the ability to detect small, albeit physiological relevant within- and between-group differences in intramuscular outcomes. Future studies, specifically powered for the outcomes of interest, are needed to determine whether supplementation affects ECM properties and the tissue microenvironment, including expression of interstitial collagens and fibroblast content.
Immunofluorescence intensity analysis is inherently semi-quantitative and may be influenced by imaging conditions and ROI selection. Although acquisition settings were kept constant across samples, and ROIs were defined using consistent criteria, a degree of observer-dependent bias cannot be fully excluded.
The present findings should be interpreted within the context of a cohort of young, healthy, recreationally active males without recent resistance training experience. Accordingly, extension of these findings to trained individuals, females, older adults, or clinical populations represents relevant topics for future research.
It is important to note that collagen peptide preparations can vary in composition and pharmacological effects (), meaning the efficacy of one formulation cannot be generalized to others. Therefore, the results of this study are specific to the collagen peptide product tested and cannot necessarily be extrapolated to other formulations.
5 Conclusion
The findings of the present study demonstrated an increased formation of type I collagen in intramuscular connective tissue in response to 12 weeks of HLRT when combined with daily supplementation of 15 grams of bioactive collagen peptides and compared to placebo. Additionally, collagen types III and IV increased significantly from pre to post in SCP, while only collagen type IV increased in PLA, with no significant between-group differences. No changes in intramuscular fibroblast content were observed following training.
Statements
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by Ethics Committee of the University of Freiburg, Germany. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
SJ: Data curation, Formal analysis, Investigation, Software, Visualization, Writing – original draft, Writing – review & editing, Project administration. JN: Data curation, Formal analysis, Investigation, Methodology, Project administration, Validation, Visualization, Writing – original draft, Writing – review & editing. CC: Data curation, Formal analysis, Investigation, Methodology, Project administration, Software, Visualization, Writing – original draft, Writing – review & editing. JM: Data curation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing. CS: Data curation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing. SO: Funding acquisition, Writing – original draft, Writing – review & editing. AG: Supervision, Writing – original draft, Writing – review & editing. PA: Supervision, Writing – original draft, Writing – review & editing. DK: Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Software, Supervision, Writing – original draft, Writing – review & editing.
Funding
The author(s) declared that financial support was received for this work and/or its publication. Part of the study costs were supported by Gelita AG, Uferstraße 7, Eberbach, Germany. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article, or the decision to submit it for publication.
Acknowledgments
We like to thank all participants who volunteered for this study.
Conflict of interest
SO has received honoraria for speaking at symposia related to the effects of collagen peptides. He is also co-inventor of patents related to collagen peptide supplementation.
The remaining author(s) declared that this work 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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The author(s) declared that generative AI was not used in the creation of this manuscript.
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References
1
Abreu-VelezA. M.HowardM. S. (2012). Collagen IV in normal skin and in pathological processes. N. Am. J. Med. Sci.4, 1–8. doi: 10.4103/1947-2714.92892
2
AussiekerT.HilkensL.HolwerdaA. M.FuchsC. J.HoubenL. H. P.SendenJ. M.et al. (2023). Collagen protein ingestion during recovery from exercise does not increase muscle connective protein synthesis rates. Med. Sci. Sports Exerc55, 1792–1802. doi: 10.1249/mss.0000000000003214
3
BaarK. (2019). Stress relaxation and targeted nutrition to treat patellar tendinopathy. Int. J. Sport Nutr. Exerc Metab.29, 453–457. doi: 10.1123/ijsnem.2018-0231
4
BabrajJ. A.CuthbertsonD. J.SmithK.LangbergH.MillerB.KrogsgaardM. R.et al. (2005). Collagen synthesis in human musculoskeletal tissues and skin. Am. J. Physiol. Endocrinol. Metab.289, E864–E869. doi: 10.1152/ajpendo.00243.2005
5
BishopJ. E.LaurentG. J. (1995). Collagen turnover and its regulation in the normal and hypertrophying heart. Eur. Heart J.16, 38–44. doi: 10.1093/eurheartj/16.suppl_c.38
6
BohmS.MersmannF.ArampatzisA. (2015). Human tendon adaptation in response to mechanical loading: a systematic review and meta-analysis of exercise intervention studies on healthy adults. Sports Med. - Open1, 7. doi: 10.1186/s40798-015-0009-9
7
BurdN. A.HolwerdaA. M.SelbyK. C.WestD. W.StaplesA. W.CainN. E.et al. (2010). Resistance exercise volume affects myofibrillar protein synthesis and anabolic signalling molecule phosphorylation in young men. J. Physiol.588, 3119–3130. doi: 10.1113/jphysiol.2010.192856
8
CameraD. M.WestD. W.PhillipsS. M.RerecichT.StellingwerffT.HawleyJ. A.et al. (2015). Protein ingestion increases myofibrillar protein synthesis after concurrent exercise. Med. Sci. Sports Exerc47, 82–91. doi: 10.1249/mss.0000000000000390
9
CentnerC.JergerS.MallardA.HerrmannA.VarfolomeevaE.GollhoferS.et al. (2022). Supplementation of specific collagen peptides following high-load resistance exercise upregulates gene expression in pathways involved in skeletal muscle signal transduction. Front. Physiol.13, 838004. doi: 10.3389/fphys.2022.838004
10
ChapmanM. A.MezaR.LieberR. L. (2016). Skeletal muscle fibroblasts in health and disease. Differentiation92, 108–115. doi: 10.1016/j.diff.2016.05.007
11
ChiquetM.GelmanL.LutzR.MaierS. (2009). From mechanotransduction to extracellular matrix gene expression in fibroblasts. Biochim. Biophys. Acta1793, 911–920. doi: 10.1016/j.bbamcr.2009.01.012
12
CohenJ. (1988). Statistical power analysis for the behavioral sciences (New York: Routledge).
13
CsapoR.GumpenbergerM.WessnerB. (2020). Skeletal muscle extracellular matrix - what do we know about its composition, regulation, and physiological roles? A narrative review. Front. Physiol.11, 253. doi: 10.3389/fphys.2020.00253
14
DierckxS.PatriziM.MerinoM.GonzálezS.MullorJ. L.Nergiz-UnalR. (2024). Collagen peptides affect collagen synthesis and the expression of collagen, elastin, and versican genes in cultured human dermal fibroblasts. Front. Med. (Lausanne)11, 1397517. doi: 10.3389/fmed.2024.1397517
15
ElangoJ.HouC.BaoB.WangS.Maté Sánchez de ValJ. E.WenhuiW. (2022). The molecular interaction of collagen with cell receptors for biological function. Polymers (Basel)14. doi: 10.3390/polym14050876
16
ElangoJ.RobinsonJ.ZhangJ.BaoB.MaN.de ValJ.et al. (2019). Collagen peptide upregulates osteoblastogenesis from bone marrow mesenchymal stem cells through MAPK- Runx2. Cells8. doi: 10.3390/cells8050446
17
FinniT.de Brito FontanaH.MaasH. (2023). Force transmission and interactions between synergistic muscles. J. Biomech.152, 111575. doi: 10.1016/j.jbiomech.2023.111575
18
FrantzC.StewartK. M.WeaverV. M. (2010). The extracellular matrix at a glance. J. Cell Sci.123, 4195–4200. doi: 10.1242/jcs.023820
19
FreyI.BergA.GrathwohlD.KeulJ. (1999). Freiburg questionnaire of physical activity--development, evaluation and application. Soz Praventivmed44, 55–64. doi: 10.1007/bf01667127
20
GilliesA. R.LieberR. L. (2011). Structure and function of the skeletal muscle extracellular matrix. Muscle Nerve44, 318–331. doi: 10.1002/mus.22094
21
GuillerminetF.BeaupiedH.Fabien-SouléV.ToméD.BenhamouC. L.RouxC.et al. (2010). Hydrolyzed collagen improves bone metabolism and biomechanical parameters in ovariectomized mice: an in vitro and in vivo study. Bone46, 827–834. doi: 10.1016/j.bone.2009.10.035
22
HaghighiA. H.HajiniaM.AskariR.AbbasianS.GoldfiedG. (2022). Effect of high-intensity interval training and high-intensity resistance training on irisin and fibroblast growth factor 21 in men with overweight and obesity. Can. J. Physiol. Pharmacol.100, 937–944. doi: 10.1139/cjpp-2021-0712
23
HolmL.RahbekS. K.FarupJ.VendelboM. H.VissingK. (2017). Contraction mode and whey protein intake affect the synthesis rate of intramuscular connective tissue. Muscle Nerve55, 128–130. doi: 10.1002/mus.25398
24
HolmL.van HallG.RoseA. J.MillerB. F.DoessingS.RichterE. A.et al. (2009). Contraction intensity and feeding affect collagen and myofibrillar protein synthesis rates differently in human skeletal muscle. Am. J. Physiol. Endocrinol. Metab.298, E257–E269. doi: 10.1152/ajpendo.00609.2009
25
HolwerdaA. M.AussiekerT.SendenJ.BouwmanF. G.van KranenburgJ.OvermanA.et al. (2026). Assessing the composition of myofibrillar and muscle connective protein fractions within skeletal muscle tissue. Crit. Rev. Food Sci. Nutr.66, 248–258. doi: 10.1080/10408398.2025.2522363
26
HolwerdaA. M.van LoonL. J. C. (2022). The impact of collagen protein ingestion on musculoskeletal connective tissue remodeling: a narrative review. Nutr. Rev.80, 1497–1514. doi: 10.1093/nutrit/nuab083
27
HulmiJ. J.TannerstedtJ.SelänneH.KainulainenH.KovanenV.MeroA. A. (2009). Resistance exercise with whey protein ingestion affects mTOR signaling pathway and myostatin in men. J. Appl. Physiol. (1985)106, 1720–1729. doi: 10.1152/japplphysiol.00087.2009
28
IdeK.TakahashiS.SakaiK.TagaY.UenoT.DickensD.et al. (2021). The dipeptide prolyl-hydroxyproline promotes cellular homeostasis and lamellipodia-driven motility via active β1-integrin in adult tendon cells. J. Biol. Chem.297, 100819. doi: 10.1016/j.jbc.2021.100819
29
InacioP. A. Q.ChaluppeF. A.AguiarG. F.CoelhoC. F.VieiraR. P. (2024). Effects of hydrolyzed collagen as a dietary supplement on fibroblast activation: a systematic review. Nutrients16. doi: 10.3390/nu16111543
30
JendrickeP.CentnerC.ZdzieblikD.GollhoferA.KönigD. (2019). Specific collagen peptides in combination with resistance training improve body composition and regional muscle strength in premenopausal women: a randomized controlled trial. Nutrients11. doi: 10.3390/nu11040892
31
JergerS.CentnerC.LauberB.SeynnesO.FriedrichT.LolliD.et al. (2023). Specific collagen peptides increase adaptions of patellar tendon morphology following 14-weeks of high-load resistance training: a randomized-controlled trial. Eur. J. Sport Sci.23, 2329–2339. doi: 10.1080/17461391.2023.2232758
32
JergerS.CentnerC.LauberB.SeynnesO.SohniusT.JendrickeP.et al. (2022). Effects of specific collagen peptide supplementation combined with resistance training on Achilles tendon properties. Scand. J. Med. Sci. Sports32, 1131–1141. doi: 10.1111/sms.14164
33
KhatriM.NaughtonR. J.CliffordT.HarperL. D.CorrL. (2021). The effects of collagen peptide supplementation on body composition, collagen synthesis, and recovery from joint injury and exercise: a systematic review. Amino Acids53, 1493–1506. doi: 10.1007/s00726-021-03072-x
34
KimotoK.NakatsukaK.MatsuoN.YoshiokaH. (2004). p38 MAPK mediates the expression of type I collagen induced by TGF-beta 2 in human retinal pigment epithelial cells ARPE-19. Invest. Ophthalmol. Vis. Sci.45, 2431–2437. doi: 10.1167/iovs.03-1276
35
KirmseM.LottmannT. M.VolkN. R.MaréesD. E. M.HolwerdaA. M.LJCV. A. N. L.et al. (2024). Collagen peptide supplementation during training does not further increase connective tissue protein synthesis rates. Med. Sci. Sports Exerc56, 2296–2304. doi: 10.1249/mss.0000000000003519
36
KirmseM.Oertzen-HagemannV.de MaréesM.BlochW.PlatenP. (2019). Prolonged collagen peptide supplementation and resistance exercise training affects body composition in recreationally active men. Nutrients11. doi: 10.3390/nu11051154
37
KjaerM. (2004). Role of extracellular matrix in adaptation of tendon and skeletal muscle to mechanical loading. Physiol. Rev.84, 649–698. doi: 10.1152/physrev.00031.2003
38
KönigD.OesserS.ScharlaS.ZdzieblikD.GollhoferA. (2018). Specific collagen peptides improve bone mineral density and bone markers in postmenopausal women-a randomized controlled study. Nutrients10. doi: 10.3390/nu10010097
39
KönigD.BraunH.CarlsohnA.GrosshauserM.LampenA.MoslerS.et al. (2020). Position of the working group sports nutrition of the German Nutrition Society (DGE): carbohydrates in sports nutrition. Deutsche Z. Fr. Sportmedizin71, 185–191. doi: 10.5960/dzsm.2020.456
40
KovanenV. (2002). Intramuscular extracellular matrix: complex environment of muscle cells. Exerc Sport Sci. Rev.30, 20–25. doi: 10.1097/00003677-200201000-00005
41
KrishnanS.LeeF.BurnettD. J.KanA.BonnelE. L.AllenL. H.et al. (2020). Challenges in designing and delivering diets and assessing adherence: a randomized controlled trial evaluating the 2010 dietary guidelines for Americans. Curr. Dev. Nutr.4, nzaa022. doi: 10.1093/cdn/nzaa022
42
LeeJ.BridgeJ. E.ClarkD. R.StewartC. E.ErskineR. M. (2023). Collagen supplementation augments changes in patellar tendon properties in female soccer players. Front. Physiol.14, 1089971. doi: 10.3389/fphys.2023.1089971
43
LiuZ.LiY.SongH.HeJ.LiG.ZhengY.et al. (2019). Collagen peptides promote photoaging skin cell repair by activating the TGF-β/Smad pathway and depressing collagen degradation. Food Funct.10, 6121–6134. doi: 10.1039/c9fo00610a
44
MackeyA. L.MagnanM.ChazaudB.KjaerM. (2017). Human skeletal muscle fibroblasts stimulate in vitro myogenesis and in vivo muscle regeneration. J. Physiol.595, 5115–5127. doi: 10.1113/jp273997
45
MackeyA. L.RasmussenL. K.KadiF.SchjerlingP.HelmarkI. C.PonsotE.et al. (2016). Activation of satellite cells and the regeneration of human skeletal muscle are expedited by ingestion of nonsteroidal anti-inflammatory medication. FASEB J.30, 2266–2281. doi: 10.1096/fj.201500198R
46
Martínez-LópezE.Pérez-GuerreroE. E.Torres-CarrilloN. M.López-QuinteroA.Betancourt-NúñezA.Gutiérrez-HurtadoI. A. (2022). Methodological aspects in randomized clinical trials of nutritional interventions. Nutrients14. doi: 10.3390/nu14122365
47
MavropaliasG.BoppartM.UsherK. M.GroundsM. D.NosakaK.BlazevichA. J. (2022). Exercise builds the scaffold of life: muscle extracellular matrix biomarker responses to physical activity, inactivity, and aging. Biol. Rev. Camb Philos. Soc.98, 481–519. doi: 10.1111/brv.12916
48
McAlindonT. E.NuiteM.KrishnanN.RuthazerR.PriceL. L.BursteinD.et al. (2011). Change in knee osteoarthritis cartilage detected by delayed gadolinium enhanced magnetic resonance imaging following treatment with collagen hydrolysate: a pilot randomized controlled trial. Osteoarthritis Cartilage19, 399–405. doi: 10.1016/j.joca.2011.01.001
49
McKeeT. J.PerlmanG.MorrisM.KomarovaS. V. (2019). Extracellular matrix composition of connective tissues: a systematic review and meta-analysis. Sci. Rep.9, 10542. doi: 10.1038/s41598-019-46896-0
50
Meléndez-HeviaE.De Paz-LugoP.Cornish-BowdenA.CárdenasM. L. (2009). A weak link in metabolism: the metabolic capacity for glycine biosynthesis does not satisfy the need for collagen synthesis. J. Biosci.34, 853–872. doi: 10.1007/s12038-009-0100-9
51
MooreD. R.PhillipsS. M.BabrajJ. A.SmithK.RennieM. J. (2005). Myofibrillar and collagen protein synthesis in human skeletal muscle in young men after maximal shortening and lengthening contractions. Am. J. Physiol. Endocrinol. Metab.288, E1153–E1159. doi: 10.1152/ajpendo.00387.2004
52
MooreD. R.RobinsonM. J.FryJ. L.TangJ. E.GloverE. I.WilkinsonS. B.et al. (2009). Ingested protein dose response of muscle and albumin protein synthesis after resistance exercise in young men. Am. J. Clin. Nutr.89, 161–168. doi: 10.3945/ajcn.2008.26401
53
NielsenJ. L.AagaardP.BechR. D.NygaardT.HvidL. G.WernbomM.et al. (2012). Proliferation of myogenic stem cells in human skeletal muscle in response to low-load resistance training with blood flow restriction. J. Physiol.590, 4351–4361. doi: 10.1113/jphysiol.2012.237008
54
Oertzen-HagemannV.KirmseM.EggersB.PfeifferK.MarcusK.de MaréesM.et al. (2019). Effects of 12 weeks of hypertrophy resistance exercise training combined with collagen peptide supplementation on the skeletal muscle proteome in recreationally active men. Nutrients11. doi: 10.3390/nu11051072
55
OharaH.IchikawaS.MatsumotoH.AkiyamaM.FujimotoN.KobayashiT.et al. (2010). Collagen-derived dipeptide, proline-hydroxyproline, stimulates cell proliferation and hyaluronic acid synthesis in cultured human dermal fibroblasts. J. Dermatol.37, 330–338. doi: 10.1111/j.1346-8138.2010.00827.x
56
PlikusM. V.WangX.SinhaS.ForteE.ThompsonS. M.HerzogE. L.et al. (2021). Fibroblasts: origins, definitions, and functions in health and disease. Cell184, 3852–3872. doi: 10.1016/j.cell.2021.06.024
57
PraetS. F. E.PurdamC. R.WelvaertM.VlahovichN.LovellG.BurkeL. M.et al. (2019). Oral supplementation of specific collagen peptides combined with calf-strengthening exercises enhances function and reduces pain in Achilles tendinopathy patients. Nutrients11. doi: 10.3390/nu11010076
58
PurslowP. P. (2020). The structure and role of intramuscular connective tissue in muscle function. Front. Physiol.11, 495. doi: 10.3389/fphys.2020.00495
59
Ricard-BlumS. (2011). The collagen family. Cold Spring Harb. Perspect. Biol.3, a004978. doi: 10.1101/cshperspect.a004978
60
SchadowS.SimonsV. S.LochnitG.KordelleJ.GazovaZ.SiebertH. C.et al. (2017). Metabolic response of human osteoarthritic cartilage to biochemically characterized collagen hydrolysates. Int. J. Mol. Sci.18. doi: 10.3390/ijms18010207
61
SchoenfeldB. J.AragonA. A. (2018). How much protein can the body use in a single meal for muscle-building? Implications for daily protein distribution. J. Int. Soc Sports Nutr.15, 10. doi: 10.1186/s12970-018-0215-1
62
ShawG.Lee-BarthelA.RossM. L.WangB.BaarK. (2017). Vitamin C-enriched gelatin supplementation before intermittent activity augments collagen synthesis. Am. J. Clin. Nutr.105, 136–143. doi: 10.3945/ajcn.116.138594
63
SuettaC.FrandsenU.MackeyA. L.JensenL.HvidL. G.BayerM. L.et al. (2013). Ageing is associated with diminished muscle re-growth and myogenic precursor cell expansion early after immobility-induced atrophy in human skeletal muscle. J. Physiol.591, 3789–3804. doi: 10.1113/jphysiol.2013.257121
64
TangJ. E.MooreD. R.KujbidaG. W.TarnopolskyM. A.PhillipsS. M. (2009). Ingestion of whey hydrolysate, casein, or soy protein isolate: effects on mixed muscle protein synthesis at rest and following resistance exercise in young men. J. Appl. Physiol. (1985)107, 987–992. doi: 10.1152/japplphysiol.00076.2009
65
TrommelenJ.HolwerdaA. M.SendenJ. M.GoessensJ. P. B.JV. A. N. K.GijsenA. P.et al. (2020). Casein ingestion does not increase muscle connective tissue protein synthesis rates. Med. Sci. Sports Exerc52, 1983–1991. doi: 10.1249/mss.0000000000002337
66
Watanabe-KamiyamaM.ShimizuM.KamiyamaS.TaguchiY.SoneH.MorimatsuF.et al. (2010). Absorption and effectiveness of orally administered low molecular weight collagen hydrolysate in rats. J. Agric. Food. Chem.58, 835–841. doi: 10.1021/jf9031487
67
YokoyamaK.KimotoK.ItohY.NakatsukaK.MatsuoN.YoshiokaH.et al. (2012). The PI3K/Akt pathway mediates the expression of type I collagen induced by TGF-β2 in human retinal pigment epithelial cells. Graefe's Arch. For. Clin. Exp. Ophthalmol. = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie250, 15–23. doi: 10.1007/s00417-011-1766-x
68
YunY. R.WonJ. E.JeonE.LeeS.KangW.JoH.et al. (2010). Fibroblast growth factors: biology, function, and application for tissue regeneration. J. Tissue Eng.2010, 218142. doi: 10.4061/2010/218142
69
ZdzieblikD.JendrickeP.OesserS.GollhoferA.KönigD. (2021). The influence of specific bioactive collagen peptides on body composition and muscle strength in middle-aged, untrained men: a randomized controlled trial. Int. J. Environ. Res. Public Health18. doi: 10.3390/ijerph18094837
70
ZdzieblikD.OesserS.BaumstarkM. W.GollhoferA.KonigD. (2015). Collagen peptide supplementation in combination with resistance training improves body composition and increases muscle strength in elderly sarcopenic men: a randomised controlled trial. Br. J. Nutr.114, 1237–1245. doi: 10.1017/S0007114515002810
71
ZhangH.YaoZ.SongY.HuaQ.GengX.ZhouF.et al. (2025). Collagen peptides promote skin collagen synthesis by modulating the gut microbiota and activating the TGF-β pathway. Food Funct.16, 5326–5344. doi: 10.1039/d5fo01649e
Summary
Keywords
collagen, extracellular matrix, intramuscular connective tissue, resistance training, skeletal muscle, specific collagen peptides
Citation
Jerger S, Nielsen JL, Centner C, Mathiesen J, Suetta C, Oesser S, Gollhofer A, Aagaard P and König D (2026) Specific collagen peptides supplementation increases collagen type I content in skeletal muscle after 12 weeks of high-load resistance training: a randomized controlled trial. Front. Physiol. 17:1839695. doi: 10.3389/fphys.2026.1839695
Received
26 March 2026
Revised
23 May 2026
Accepted
25 May 2026
Published
15 June 2026
Volume
17 - 2026
Edited by
Hsiuying Wang, National Yang Ming Chiao Tung University, Taiwan
Reviewed by
Chris Nulty, South East Technological University, Ireland
Péter Fritz, Károli Gáspár University of the Reformed Church in Hungary, Hungary
Updates
Copyright
© 2026 Jerger, Nielsen, Centner, Mathiesen, Suetta, Oesser, Gollhofer, Aagaard and König.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Simon Jerger, simon.jerger@sport.uni-freiburg.de
†These authors have contributed equally to this work and share first authorship
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