Invitro Advances in Tendon Cell Biology: Tenosan® as a Potential Nutraceutical Tool for Tendon Care

Tendinopathies are chronic, multifactorial conditions marked by inflammation, Extracellular Matrix (ECM) degradation, and impaired healing. Nutraceuticals are increasingly explored as adjunctive therapies to modulate these processes. This study evaluates the biological effects of Tenosan®, a dietary supplement, on human tenocytes under both physiological and inflammatory conditions. An In vitro model of tendinopathy was established by stimulating human tenocytes with interleukin-1β. The effect of Tenosan® in improving tendon wellness was evaluated by analyzing matrix and inflammatory markers. Results shows that Tenosan® significantly increased the type I/III collagen ratio, reduced Vascular Endothelial Growth Factor (VEGF) secretion, and enhanced nitric oxide production, indicating improved extracellular matrix remodeling and pro-regenerative activity. These findings demonstrate that Tenosan® positively modulates key pathways involved in tendon healing, supporting its potential use as part of a multimodal strategy for managing tendinopathies.

Tendons are highly organized, dense connective tissues primarily composed of collagen fibers, predominantly type I collagen (~95%), along with proteoglycans and elastin, which confer tensile strength and elasticity essential for tendon function [1,2]. Tendons play a crucial role in the musculoskeletal system by connecting muscles to bones, enabling the transmission of force necessary for joint movement, stability, and postural control [3].

Tendinopathy refers to a heterogeneous and widespread group of chronic, often painful disorders, characterized by tendon tissue degeneration and impaired function. These conditions are particularly prevalent in athletes and individuals engaged in repetitive mechanical activities; however, they also affect the general population, with an increasing incidence linked to aging and lifestyle-related factors [4]. Metabolic factors such as hypoxia, chronic inflammation, oxidative stress, apoptosis, and hormonal imbalances play a critical role in tendinopathy pathogenesis. Key histological and molecular characteristics of tendinopathy include collagen fiber disorganization, increased neovascularization and innervation, enhanced inflammation, and elevated cellular apoptosis [5].

In particular, growing evidence highlights the active involvement of inflammation in the progression of tendinopathies [6], characterized by the increased levels of pro-inflammatory cytokines (e.g., IL-1b, TNF-a), immune cell infiltration, and activation of inflammatory pathways such as NF-kB and MAPK [7,8]. Moreover, pathological stimuli induce a dysregulation of collagen turnover in tenocytes, which contributes to tendon degeneration [9,10]. In addition, angiogenesis plays an essential role in tendon dysregulation and repair and must be finely regulated in the context of tendinopathies. VEGF expression peaks after the initial inflammatory phase and acts as a potent stimulator of neovascularization [11]. While this process is critical in the early stages of healing, persistent VEGF overexpression has been associated with pathological angiogenesis, characterized by disorganized collagen deposition, excessive scar formation, and impaired biomechanical properties of the tendon [12].

In this context, novel therapeutic strategies targeting the inflammatory microenvironment of tendinopathies are increasingly being explored. Current therapeutic approaches advocate for a comprehensive, multimodal strategy that combines therapeutic exercise, targeted physical therapies (e.g., shockwave therapy), and specific nutritional support aimed at enhancing tendon healing processes [13-15]. Specifically, recent studies on patients with calcific shoulder tendinopathy treated with Radial Shockwave Therapy (RSWT) have demonstrated that adjunctive nutraceutical supplementation significantly reduced pain, inflammation, and intratendinous calcifications, while improving range of motion, muscle strength, and quality of life. These benefits were maintained over time, with no relapses observed at the 3-month follow-up and superior outcomes compared with control groups [16]. Moreover, in the postoperative setting, prolonged supplementation has been shown to reduce pain and enhance structural integrity following rotator cuff repair, supporting faster recovery and lower recurrence rates [17]. Likewise, the combination of nutraceutical supplementation with Extracorporeal Shockwave Therapy (ESWT) has shown promise in the treatment of insertional Achilles tendinopathy, suggesting a synergistic effect that warrants further investigation [18].

Tenosan® is a commercially available dietary supplement designed to support tendon, joint, and muscle health, particularly in individuals exposed to increased mechanical stress or affected by tendinopathies. Its composition includes bioactive compounds with antioxidant, anti-inflammatory, and structural support properties: L-Arginine Alpha-Ketoglutarate (AAKG), optimized methylsulfonylmethane (OptiMSM®), beetroot extract (TruBeet®), polyphenols from Vitis vinifera (ViNitrox®), hydrolyzed collagen type I, Vitamin D (Vit D), and Vitamin C (Vit C).

In particular, hydrolyzed collagen type I has garnered attention as a nutritional intervention for tendon health, thanks to its specific activity on tendon structure, since its positive effects on connective tissue are well documented [19-21]. AAKG is commonly marketed as an ergogenic aid due to its potential to enhance vasodilation through the upregulation of the endothelial L-arginine–nitric oxide pathway [22]. Methylsulfonylmethane (MSM) is a sulfur-based nutritional supplement reported to exert analgesic and anti-inflammatory effects. In addition, as a sulfur donor, it is essential for supporting protein synthesis, including collagen [23].

Beetroot is rich in dietary nitrates and betalains, pigments with antioxidant and anti-inflammatory properties. As a natural source of nitrate, beetroot consumption increases Nitric Oxide (NO) availability and is emerging as a potential strategy to prevent and manage pathologies associated with diminished NO bioavailability [24]. Similarly, Vitis vinifera, a compound rich in polyphenols, increases the synthesis and bioavailability of NO, which is widely recognized as a key mediator of vasodilation. ViNitrox™ is a purified extract with more than 60% total polyphenols [25].

Vitamin D exerts pleiotropic biological effects, including tendon protection, partly mediated through the stimulation of tenocyte proliferation [26]. Vitamin C plays a crucial role in preventing and managing oxidative stress-related conditions, including those affecting the musculoskeletal system [27-29]. In vitro studies have demonstrated that vitamin C stimulates collagen synthesis in human tenocytes, while In vivo evidence supports its role in promoting tendon healing by enhancing angiogenesis, increasing collagen production, and reducing fibrosis and adhesion formation [30-33]. Furthermore, vitamin C may enhance the efficacy of stem cell-based regenerative approaches and has shown clinical benefits in improving recovery in patients with tendinopathies [34].

The effectiveness of Tenosan® in supporting tendon health under tendinopathy conditions has already been demonstrated by several preclinical and clinical studies. Specifically, supplementation with Tenosan®, particularly when combined with low-frequency focused shockwave therapy, has been shown to significantly improve pain and functional scores in patients with plantar fasciopathy, with sustained benefits in the medium to long term [13]. Similar findings have been reported in the management of calcific tendon diseases, where supplementation facilitates the reduction of inflammatory catabolites and promotes connective tissue remodeling [35].

In the present study, the biological effects of Tenosan® on primary human tenocytes were investigated under both physiological and inflammatory conditions, thus simulating an In vitro model of tendinopathy. The impact of Tenosan® on key markers of tendon health, including collagen types I and III, VEGF, and NO production, was assessed. The obtained results demonstrate that Tenosan® promotes a favorable collagen I/III ratio, reduces VEGF secretion, and enhances NO levels. Collectively, these findings support the rationale for integrating nutraceutical supplementation, such as Tenosan®, into a comprehensive treatment paradigm for tendinopathies, particularly in cases with underlying metabolic or inflammatory contributors.

Tenosan® preparation

Tenosan® was provided in powder form, packaged in individual sachets. Fresh preparations were obtained by dissolving the powder in sterile distilled water (dH₂O) according to the manufacturer's instructions. The resulting solution was sterilized by filtration through 0.22 µm pore-size filters.

Cells cultures

Primary human tenocytes, isolated from the Achilles tendon of a healthy 74-year-old male donor, were purchased from Zen-Bio Inc. (Durham, NC, USA). Cells were maintained in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% Fetal Bovine Serum (FBS), 1% L-glutamine, and 1% Penicillin/Streptomycin (P/S). Cultures were incubated at 37°C in a humidified atmosphere containing 5% CO2. Only cells at passages ≤ 5 were used for experiments, to ensure phenotypic consistency.

Cytotoxicity assay

The cytotoxic profile of Tenosan® was evaluated with MTT assay. Tenocytes were seeded in 96-well plates at a density of 1 × 10⁴ cells/well. After 24 h, cells were treated with serial dilutions of Tenosan®, starting from concentration of 25 mg/ml, in starvation condition. Following 24 h of exposure, cell viability was assessed by incubating the cultures with 0.5 mg/ml MTT (3-(4,5-dimethyltiazol-2-yl)-2,5-diphenyltetrazolium bromide) solution for 2 h at 37°C. Formazan crystals formed by metabolically active cells were solubilized in isopropanol, and absorbance was measured at 550 nm using an Infinite M Nano+ plate reader (Tecan).

Tendinopathy In vitro model

To mimic the pathological environment characteristic of tendinopathy, an In vitro inflammatory model was established by stimulating human tenocytes with IL-1β [36]. To define the optimal pro-inflammatory concentration, cells were treated with a range of IL-1β doses (1-50 ng/ml), and the inflammatory response was assessed by quantifying IL-6 secretion using ELISA assay (Ref. 88-7066-88, ThermoFisher Scientific).

Cells treatment

The effects of Tenosan® in tendinopathy healing was evaluated on an In vitro healthy model, made by human primary tenocytes, and an inflammatory model, obtained by treating cells with IL-1β. Specifically, tenocytes were seeded in 48-well plates at a density of 1.5 × 105cells/well. After 24 h, inflammation was induced using IL-1β 10 ng/ml. Simultaneously, cells of healthy and inflammatory model were treated with Tenosan® at three non-cytotoxic concentrations: 0.8, 0.4, and 0.2 mg/ml, as determined in preliminary viability assays. Negative Control (CTR) consisted of untreated cells. Following 24 h of treatment, cell culture supernatants were collected and analyzed to assess the expression of key markers involved in tendon matrix remodeling, angiogenesis and NO production.

Detection of collagen, VEGF and NO levels

As indicative of tissue remodeling processes, ELISA assays was performed on the supernatants of all the tested condition, in order to measure the secreted amount of collagen type I (Ref.AB285250, Abcam), collagen type III (Ref.LS-F26725, LSBio) and VEGF (Ref.KHG0111, ThermoFisher Scientific). Moreover, the amount of total NO produced following treatments was estimated using Nitric Oxide Assay Kit (Ref.EMSNO, ThermoFisher Scientific), providing further insight into the inflammatory modulation exerted by Tenosan®.

Each experimental group included at least three replicates, and data were plotted as replicates means ± standard error. Statistical analysis was performed thought analysis of variance, using one way ANOVA, and statistical significance was set at p < 0.05. Graph were generated using GraphPad Prism 10 (GraphPad Software, San Diego, CA, USA).

Effects of Tenosan® on tenocyte viability and tendinopathy In vitro model

The cytotoxic effect on Tenosan®, tested at different concentrations, was evaluated on human tenocytes. Cell viability following treatment was assessed using the MTT assay. Results (Figure 1A) showed that Tenosan® did not affect cell viability at concentrations equal or lower than 0.8 mg/ml, whereas a cytotoxic effect was observed at concentrations from 1.5 mg/ml upwards. Therefore, the concentrations chosen for cell treatment were: 0.8, 0.4, and 0.2 mg/ml.

Figure 1 (A) Cell viability of human tenocytes treated with decreasing concentrations of Tenosan® (1.5 to 0.1 mg/ml) for 24 h, assessed via MTT assay.
(A) cytotoxic effect was observed at doses ≥ 1.5 mg/ml, while lower concentrations (≤ 0.8 mg/ml) did not affect cell viability.
(B) Quantification of IL-6 secretion in tenocytes treated with increasing concentrations of IL-1β (1-50 ng/ml) for 24 h. IL-1β induced a dose-dependent increase in IL-6 release, confirming the establishment of an in vitro inflammatory model. Data represent mean ± SD of replicates. ****p < 0.0001, ***p < 0.001, **p < 0.01.

To establish an appropriate In vitro model of cellular inflammation, tenocytes were treated with IL-1b at concentrations ranging from 50 to 1 ng/ml for 24 h. IL-6 levels in the culture medium were measured by ELISA and compared with the untreated Control (CTR) (Figure1B). Results showed that IL-1b significantly increased IL-6 production in a dose-dependent manner, triggering an inflammatory response. In contrast, untreated control cells displayed IL-6 levels close to 0. The dose selected for subsequent experiments and for establishing the inflamed tendon model was 10 ng/ml: this concentration elicits a clear inflammatory response without compromise cell viability.

Quantification of collagen I and III levels

To evaluate the efficacy of Tenosan® in matrix remodeling, in healthy model and tendinopathy-like condition, collagen production was assessed. Indeed, collagen plays a fundamental role in the reparative response following tissue injury [37]. Specifically, collagen type I is essential for structural repair and proper connective tissue organization, contributing to tissue strength, whereas collagen type III, characterized by more flexible fibers, is primarily involved in the early stages of healing and leads to the formation of a more disorganized and elastic scar tissue [38,39]. Based on this, collagen type I, collagen type III and their ratio of was investigated, after treating human tenocytes with Tenosan®, in presence or absence of IL-1b 10 ng/ml.

To this end, ELISA assays were performed to quantify the levels of collagen type I and type III in human tenocytes treated with different concentrations of Tenosan®, in the presence or absence of IL-1b (10 ng/ml). The results showed that collagen III levels remained unchanged between treated and untreated groups under both healthy and inflammatory conditions. In contrast, collagen I levels were significantly upregulated following Tenosan® treatment, as shown in (Figures 2A-D). Specifically, the product exhibited a dose dependent effect, statistically significant for doses of 0,8 and 0,4 mg/ml, in both analysed conditions. The selective increase in collagen I, without a corresponding rise in collagen III, results in a higher collagen I/III ratio, both in healthy (Figure 2E) and inflammatory models (Figure 2F). Notably, this effect aligns with the expected activity of the product, which is specifically formulated to enhance collagen I synthesis, with the aim of promote the formation of stronger and more organized tendon matrix. Indeed, higher levels of collagen I in relation to collagen III allows the formation solid structure, suggesting the beneficial effects of the product in strengthen tendon structure in healthy condition. Moreover, Tenosan® could have a crucial role in supporting the structural tendons repair, by the synthesis of a proper matrix, in response to stress and inflammatory conditions.

Figure 2 Effect of Tenosan® treatment in the modulation of levels of collagen type I (A,B), collagen type III (C,D) and their ratio (E,F) in human tenocytes. Left panel shows results under healthy conditions; right panel refers to the inflammatory model induced by IL-1β (10 ng/ml). In both models, Tenosan® modulated collagen I secretion in a dose-dependent manner, with an effect in increasing collagen I/III ratio, suggesting enhanced extracellular matrix remodeling. Data represent mean ± SD of replicates. ****p < 0.0001, ***p < 0.001, **p < 0.01, *p < 0.05.

Quantification of VEGF levels

VEGF plays a crucial role in angiogenesis during tendon healing, but its effects are complex and time dependent. In early stages, VEGF facilitates repair by promoting blood vessel formation, delivering nutrients and regulating immune responses. However, persistent high VEGF expression may impair tendon repair in later stages [40]. For this reason, VEGF production in human tenocytes subjected to Tenosan® treatment, in both healthy (Figure 3A) and inflammatory model (Figure 3B), was evaluated using ELISA assay. Results showed the effect of the product in reducing VEGF secretion, in both In vitro models. Specifically, a statistically significant effect was displayed following the treatment with all the tested concentrations.

Figure 3 VEGF levels, expressed as pg/ml, secreted by human tenocytes treated with Tenosan®.
(A) VEGF levels in the supernatant of untreated (CTR) and Tenosan®-treated human tenocytes under healthy conditions.
(B) VEGF levels in tenocytes exposed to IL-1β (10 ng/ml) and co-treated with Tenosan®, to mimic an inflamed condition. In both models, Tenosan® treatment resulted in reduction of VEGF secretion, suggesting a modulatory effect on angiogenesis. Data are expressed as mean ± SD of replicates. ***p < 0.001, **p < 0.01.

Quantification of nitric oxide levels

NO based therapies have well-known effects in enhancing tendon healing [41], for this reason are considered a promising treatment to induce tendons regeneration after injuries [42]. To assess the effect of Tenosan® in NO metabolism, levels of NO and its derivatives were measured in the supernatant of healthy and inflamed human tenocytes, treated with different concentrations of the product. Total NO levels were calculated as the sum of nitrite and nitrate, in accordance with the kit's specifications. The results demonstrated a significant increase in NO levels in the supernatant of cells treated with the product compared to untreated Control (CTR), with a dose-dependent effect (Figure 4A). Notably, the product at 0,8 mg/ml induced increase in NO levels also in inflamed condition (Figure 4B), indicating its potential beneficial effects under tendon damage conditions. These findings suggested that Tenosan® stimulates NO synthesis in tenocytes, both under basal and inflammatory conditions.

Figure 4 NO levels (μM) produced in human tenocytes treated with Tenosan®.
(A) NO levels measured in untreated (CTR) and Tenosan® treated tenocytes under physiological conditions.
(B) NO levels in tenocytes exposed to IL-1β (10 ng/ml) and co-treated with Tenosan®, to simulate an inflamed tendon condition. In both models, Tenosan® induced a dose-dependent increase in NO production, suggesting its pro-regenerative activity. Data represent mean ± SD of replicates. ****p < 0.0001, ***p < 0.001, *p < 0.05.

Tendinopathies are multifactorial disorders characterized by inflammation, matrix degeneration and impaired tendons healing, often exacerbated by metabolic imbalances and oxidative stress. Recent strategies emphasize a multimodal approach that includes nutraceutical supplementation to support tendon repair. Tenosan®, a dietary supplement containing bioactive compounds with a focus on tendon protection, has shown clinical promise in improving outcomes in tendon-related disorders.

The aim of the present study was to investigate biologically relevant effects of Tenosan® on an In vitro model of primary human tenocytes, in order to deeply understand the pathways involved in its tendon regenerative action. In particular, experiments were performed under both physiological and inflammatory conditions, with the purpose of investigate Tenosan® efficacy in healthy condition and as a potential therapy for managing tendinopathies.

Firstly, the cell viability assay allowed to identify a safe concentration range of Tenosan® (0.8 - 0.2 mg/ml), below which no cytotoxic effects were observed. Accordingly, subsequent experiments were conducted using these non-toxic concentrations, to ensure the biological relevance of the results. To mimic tendinopathy-like conditions, an In vitro inflammatory model was established using IL-1b stimulation, which resulted in a dose-dependent increase in IL-6 secretion. The selected concentration of 10 ng/ml induced a robust inflammatory response without compromising cell viability, allowing the investigation of Tenosan® modulatory effects in tendinopathy-like condition.

A key finding of this study was the role of Tenosan® in the modulation of collagen synthesis, specifically through the selective upregulation of type I collagen. While collagen type III levels remained unchanged across treatment conditions, Tenosan® significantly increased collagen type I expression, leading to a higher type I/type III collagen ratio. This ratio is a well-established marker of effective tissue remodeling, as type I collagen is the predominant component of mature tendon tissue, providing tensile strength and structural integrity, whereas type III collagen is more prevalent during the early phases of healing and is associated with less organized Extracellular Matrix (ECM) structures [43]. Therefore, the ability of Tenosan® to selectively enhance type I collagen production suggests a shift toward a more functionally mature and mechanically robust matrix composition, thereby potentially promoting more effective and long-lasting tendon repair.

Additionally, a reduction in VEGF secretion was observed after Tenosan® treatment, in both physiological and inflamed conditions, highlighting a regulatory effect of Tenosan® on angiogenesis. While VEGF plays a crucial role in the early stages of tendon healing by promoting neovascularization and nutrient delivery, sustained overexpression has been associated with impaired matrix remodeling and the formation of disorganized scar tissue, potentially compromising the mechanical properties of the repaired tendon [44]. Therefore, modulation of VEGF signaling is increasingly recognized as a strategic therapeutic goal in promoting effective and functional tendon regeneration. For this reason, the effect of Tenosan® in downregulate VEGF could have a crucial role in helping to prevent maladaptive angiogenesis during the later stages of healing.

Furthermore, Tenosan® significantly increased NO production at the maximum dose tested. This effect was evident in both healthy and inflamed tenocytes and showed a dose-dependent trend. Several studies have demonstrated that increased NO production plays a beneficial role in tendon healing. In vitro experiments on human tendon cells [45] have shown that exogenous NO donors and upregulation of inducible Nitric Oxide Synthase (iNOS) enhance collagen synthesis, a key component of tendon matrix repair. In support of this, inhibition of Nitric Oxide Synthase (NOS) activity has been shown to impair tendon healing. Specifically, the competitive NOS inhibitor N^G-Nitro-L-Arginine Methyl Ester (L-NAME) has been employed in animal models to investigate the role of NO in tendon regeneration [46]. Treatment with L-NAME led to a marked reduction in both the cross-sectional area and mechanical strength of healing tendons, underlining the critical role of NO in this process [47]. Collectively, this evidence suggest that upregulation of NO contributes positively to tendon healing by promoting extracellular matrix formation, through direct enhance of collagen synthesis [48], and by improving tendon biomechanics. Moreover, NO signalling leads vasodilation, by inducing smooth muscle relaxation through cyclic GMP pathway [49], increasing blood flow. Furthermore, In vivo studies have reported beneficial effects of L-arginine supplementation, including enhanced blood circulation to tissues, and enhance protein synthesis [50]. Take this into account the combination of Arginine a -ketoglutarate, TruBeet® and Vinitrox® contained in Tenosan® could ensure blood flow to tendons.

In summary, the combined effects of Tenosan® on enhancing the type I/III collagen ratio, increasing NO levels and modulating VEGF expression underscore its potential as a therapeutic strategy for improving tendon healing outcomes. Specifically, results support the role of Tenosan® in promoting tendon reparation in inflammatory condition that mimic the tendinopathy environment, by enhancing the quality of the extracellular matrix and regulating key mediators involved in tissue regeneration. Moreover, the product showed efficacy also in healthy condition, by promoting a more organized ECM and regulating angiogenic responses. For this reason, Tenosan® could have a double effect, with a role both in counteracting and in preventing tendinopathy, by reinforcing tendon structure and function, with a consequent reduction of the risk of injury occurrence and escalation. 

Despite the valuable mechanistic insights provided by this In vitro model, it should be acknowledged that In vitro systems cannot fully recapitulate the complex biological, mechanical, and systemic environment of tendinopathies In vivo. Indeed, the absence of biomechanical loading, and vascular components interactions represents a limitation of cell-based models. Nevertheless, the present findings are supported by previous clinical evidence showing beneficial effects of Tenosan® in patients with different tendinopathies. Taken together, these experimental and clinical data strengthen the translational relevance of Tenosan®, supporting its role as an adjunctive strategy within a multimodal therapeutic approach for tendon disorders.

In conclusion, the present study demonstrates that Tenosan® positively modulates key biological pathways involved in tendon health under both physiological and inflammatory conditions, supporting its potential role as a complementary nutraceutical strategy in tendon care. From a translational perspective, these findings provide mechanistic support for the clinical benefits of Tenosan® previously reported in patients with different tendinopathies. The observed modulation of collagen remodeling, angiogenic signaling, and nitric oxide production offers a biological rationale for the improvements in pain, function, and tendon healing described in existing clinical studies. Future research should build on this integrated experimental and clinical evidence to further explore the synergistic effects of Tenosan® within established multimodal therapeutic approaches.

This research was funded by Agave group.

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