A Single Bout of High Heels Dancing Causes an Increase in Circulating Markers of Muscle Tissue Degradation and MMP-3 in Young Healthy Women

Silva, Jamila; Borges, Leandro; Weimann, Eleine; Belmiro Dias, Beatriz; Gomes Faria, Flavio; Ferreira Salgado, Beatriz; de Freitas, Paulo; Cristina Pithon-Curi, Tania; Hatanaka, Elaine

doi:https://doi.org/10.1155/2023/8852889

Translational Sports Medicine

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Abstract Introduction Methods Results Discussion Conclusion Data Availability Ethical Approval Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2023 | Article ID 8852889 | https://doi.org/10.1155/2023/8852889

A Single Bout of High Heels Dancing Causes an Increase in Circulating Markers of Muscle Tissue Degradation and MMP-3 in Young Healthy Women

Jamila Silva,¹Leandro Borges,¹Eleine Weimann,¹Beatriz Belmiro Dias,¹Flavio Gomes Faria,¹Beatriz Ferreira Salgado,¹Paulo de Freitas,¹Tania Cristina Pithon-Curi,¹and Elaine Hatanaka¹

Academic Editor: Abigail Mackey-Sennels

Received22 Mar 2023

Revised08 May 2023

Accepted26 May 2023

Published01 Jun 2023

Abstract

Prolonged wearing of high heels can cause chronic injury and inflammation. Herein, we investigated the presence of muscle injury, inflammation, and neutrophil function in young women after a single bout of stiletto dance class. Sixteen volunteers (23.4 ± 3.8 years; 61.7 ± 8.1 kg; 23.4 ± 2.3 kg/m²; and 27.2 ± 3.8% body fat) participated in the study. The plasma biomarkers matrix metalloproteinase 3 (MMP-3), muscle damage (myoglobin (Mb), total creatine kinase (CK), and lactate dehydrogenase (LDH)), and inflammation (interleukin 8 (IL-8), tumour necrosis factor-alpha (TNF-α), interleukin (IL]-1β, and IL-6) were quantified before and immediately after a single stiletto class (60 min) of moderate intensity. After class, our data showed that the plasma concentration of MMP-3, Mb, and CK increased by 56% (; d = 0.8), 113% (; d = 1.1), and 21% (; d = 0.4), respectively. Reactive oxygen species produced by neutrophils and the plasma concentration of IL-8, TNF-α, IL-1β, and IL-6 were not affected under the study conditions. We concluded that a single bout of stiletto dance class caused muscle damage but did not alter the plasma concentration of proinflammatory cytokines. These findings are crucial in preventing the progress of chronic injuries that are often noted in dancers with synovitis and arthritis.

1. Introduction

Dancing combines artistic ability and physical fitness. While some recreational dance modalities can improve physiological and immunological capabilities [1, 2], competitive dances usually promote a higher risk for musculoskeletal injuries and inflammation due to excessive movement repetitions and nonanatomical positions [3, 4]. Additionally, inadequate shoes can generate muscle damage, joint impairment, and chronic inflammation [5], which are the events that are the basis for the development of degenerative diseases. Barnish and Barnish [6] developed a systematic review from an epidemiological perspective to investigate the effect of stiletto shoes on musculoskeletal injuries in human participants without prior musculoskeletal conditions. They found that high-heeled shoes were shown to be associated with hallux valgus, musculoskeletal pain, and first-party injury. Moreover, Luximon et al. [7] also found that the use of high-heeled shoes elevates the risk of straining and falling, and these shoes may also cause ankle sprain or ligament ruptures due to fall and bone fractures or permanent damage. In this context, stiletto dance, a dance style performed with high heels that combines movements from urban dances and jazz, imposes joint effort in the execution of the movement from the ankles to the knees, replacing the neuromechanical actions of natural protection [8]. Therefore, the high-heeled shoe affects the biomechanical landing characteristics, leading to the hypothesis that the stiletto dance could generate joint damage and inflammation.

After muscle injury as a result of the muscular effort, the breakdown of muscle fibers leads to a serum increase in muscle enzymes, such as myoglobin (Mb), creatine kinase (CK), and lactate dehydrogenase (LDH) [9, 10]. Subsequently, the inflammatory response to cellular injuries is started by the infiltration of leukocytes, such as neutrophils, into the damaged tissue. At inflammatory focus, neutrophils produce inflammatory cytokines and reactive oxygen species (ROS). This production needs to be fast and self-controlled to avoid tissue destruction. If not controlled properly, acute inflammation can generate chronic inflammation, decreased strength, and consequent degenerative joint damage.

Among the potential cartilage biomarkers, members of proteoglycan metabolism, such as matrix metalloproteinase (MMP)-3 and others, are included as promising ones. The literature shows that MMP-3 is in part responsible for the degradation of no collagenous matrix proteins in cartilage in rheumatoid arthritis and osteoarthritis [11]. Besides, structural molecules of the joint, or fragments thereof, are understood to be the most promising biomarkers for use following acute and chronic exercise as well as with joint degradation [12], and MMP-3 is considered an adequate tool to evaluate the intense sport’s response [13]. A broader discussion on the mechanisms of change in biomarkers of joint metabolism in response to exercise training in physiologic and pathological conditions has been reviewed elsewhere [14].

Although wearing high heels is an imminent risk for muscle injury and joint damage, there is no study on the physiological and immunological consequences imparted by stiletto dance and the resulting implications on dancers’ health. Herein, we aimed to quantify the biomarkers MMP-3, muscular injury (CK, LDH, and Mb), neutrophils activation (ROS), and the levels of cytokines (IL-8, TNF-α, IL-1β, and IL-6) in the plasma of young women before and after a single bout of stiletto dance class.

2. Methods

2.1. Subjects

After approval by the Ethics Committee of the local university, sixteen women agreed to participate in the research. All dancers had provided written consent before enrolling in the research, and the study followed the Declaration of Helsinki. Inclusion criteria were nonobese women (BMI 18.5 to 24.9 kg/m²) aged between 18 to 35 years. Participants were excluded from the research if they had chronic noncontagious degenerative diseases, used anti-inflammatories medication, or were declared to be smokers or to have acute inflammation on the day of collection. Moreover, all participants reported having no history of previous surgery or major injury to weight-bearing joints. The participants did not perform any exercise for 48 hours before the dance class.

2.2. Stiletto Class Protocol

The class consisted of three phases, namely, warm-up, the technical part, and the choreographic sequence. The initial part lasted 10 minutes and consisted of muscle and joint warming. The second part of the class lasted 20 minutes and consisted of walking exercises with high heels and exercises for specific movements for hands and arms, posture, and hips. The final 30 minutes of class were devoted to composing a choreographic sequence. The class was monitored using heart rate (HR) monitors (FT7, PolarSP, Brazil), and the class intensity was defined according to the following HR reserve values (mean ± standard deviation of the mean (SD)): 101 ± 20.9 at the beginning of class, 137 ± 17.2 after 10 minutes, 147 ± 22 after 30 min, and 164 ± 16.4 at the end of class.

2.3. Sample Collection

Twenty milliliters of venous blood were collected before and immediately after the stiletto dance class. The blood samples were drawn from one of three main veins at the antecubital fossa (the cephalic, basilica, and median cubitals). In each case, the vein was chosen based on the identification of an optimal site by both visual and tactile exploration. The blood samples were drawn into BD Vacutainer® tubes, which were used for plasma collection and neutrophils separation. After collecting the samples, the blood was centrifuged (400 g, 10 minutes), and the serum and plasma were separated from the cell components. Neutrophils were immediately isolated, and cellular function was assessed.

2.4. Determination of Creatine Kinase (CK) and Lactate Dehydrogenase (LDH) Activities

Plasma CK and LDH activities were measured according to the methods established by Zammit and Newsholme [15] no later than 24 hours after the collection of the plasma. For the LDH assay, there was a loss of five samples.

2.5. Determination of Cytokines

Plasma cytokines were evaluated by enzyme-linked immunosorbent assay (ELISA). The concentration of IL-8, TNF-α, IL-1β, and IL-6 was determined according to the manufacturer’s instructions (DuoSet Kit; Quantikine, R&D Systems, Minneapolis, MN, USA), and the samples were stored for no longer than 3 months.

2.6. Neutrophils Purification

The experiments were performed within 1 h of venipuncture. Human neutrophil (>98%) was isolated from the peripheral blood of human donors under endotoxin-free conditions using Histopaque® (Sigma Chemical Co.) according to the manufacturer’s instructions. The purity of the cell preparation was higher than 98%.

2.7. Flow Cytometric Measurement of Reactive Oxygen Metabolites Using Hydroethidine

To evaluate ROS release, hydroethidine (1 μM) was added to the neutrophil (2.5 × 10⁶ cells/mL) incubation medium and the cells were treated with PMA (54 ng/mL). ROS release was monitored for 30 minutes. The assays were run in PBS buffer supplemented with CaCl₂ (1 mM), MgCl₂ (1.5 mM), and glucose (10 mM) at 37°C in a final volume of 0.3 mL. Fluorescence was measured using the FL3 channel of a FACS Accuri C6 cytometer (Becton Dickinson, CA, USA). Ten thousand events were analyzed per experiment [16].

2.8. Statistical Analysis

Data are expressed as mean ± SD of the participants. The characterization of outliers was determined by limiting to two SD, plus or minus, and adjusting the values. After applying the normality test (Shapiro–Wilk test), the statistical analysis consisted of parametric (paired t-test) and nonparametric tests (Wilcoxon test) using the software GraphPad Prism (INStat; Graph Pad Software, San Diego, CA, USA). For the comparison between conditions with and without PMA stimulus, the Friedman test was used for nonparametric data. Significance was accepted at , and the effect size was calculated and interpreted using Cohen’s d.

3. Results

The participants were characterized by (mean ± SD) weight 61.7 ± 8.1 kg, height 1.6 ± 0.0 m, age 23.4 ± 3.8 years, body mass index (BMI) 23.4 ± 2.3 kg/m², body fat 27.2 ± 3.8% (measured by the tetrapolar bioimpedance device: Biodynamics Corporation, 310, EUA), waist circumference 74.1 ± 4.8 cm, hip circumference 98.4 ± 6.5 cm, and waist-hip ratio 0.8 ± 0.1 cm (Table 1).

Figure 1 shows the plasma concentration of MMP-3 in the pre and poststiletto class. There was a 56% increase (; d = 0.8) in the levels of MMP-3 after class, and the effect size was considered large. Figure 2 illustrates the change in plasma protein concentration and activity of muscle enzymes in the pre and postclass moments. The plasma level of Mb (Figure 2(a)) increased by 113% (; d = 1.1), while CK activity (Figure 2(b)) increased by 21% (; d = 0.3) after class with the effect size considered large and medium, respectively. LDH (Figure 2(c)), under the conditions studied, did not show difference, and the effect size was considered medium (d = 0.3).

(a)

(b)

(c)

The plasma levels of proinflammatory cytokines are shown in Figure 3. There was no difference between the moments before and after the class for IL-8, TNF-α, IL-1β, and IL-6. The effect size was considered small for IL-8 (Figure 3(a)) and TNF-α (Figure 3(b)) (d = 0.2 and d = 0.3, respectively), while for IL-1β (Figure 3(c)) and IL-6 (Figure 3(d)), the effect size was insignificant (d = 0.04 and d = 0.1, respectively).

(a)

(b)

(c)

(d)

Figure 4 presents the production of ROS by neutrophils (with and without PMA stimulation) in the moments before and after a stiletto dance class. As internal quality control of the assay, the difference between conditions was confirmed (with vs. without PMA stimulus) (). However, there was no difference between the moments’ pre and postclass, and the effect size was considered medium (d = 0.4).

4. Discussion

Walking in high heels can be challenging with the usual cause of venous complaints, such as fatigue, pain, and heavy-feeling legs, yet they remain a part of many women’s attire [17]. The main findings of this research were that stiletto dancing, lasting 60 minutes, increased circulating markers of muscle tissue degradation and MMP-3 after a single class at moderate intensity.

In recent years, CK and Mb serve as biomarkers used to indicate degradation in muscle fibers [18]. After the increase of markers of muscle damage, the symptoms and loss of function during the next hours (respectively days) following these peak values usually involve the conditions of exercise-induced muscle damage: delayed onset of muscle soreness, loss of muscle strength and power, decreased range of motion and systemic increases of myocellular enzymes and proteins, swelling, or an association of these [19]. Commonly, these symptoms last for at least up to 72 h, depending on the extent of disruption of subcellular structures and the volume of muscle-damaging exercise [20]. Our data showed that a single stiletto dancing class increased the plasma level of MMP-3, CK, and Mb. To date, studies have found an increase in these biomarkers in high-intensity exercises [21, 22], which highlights the peculiar character of the use of high heels during moderate-intensity physical exercise.

Given the role of inflammation and synovitis in the progress of degenerative diseases, MMPs may help our understanding of the role of loading on joint health [23]. MMPs in the circulation are thought to regulate the activation of cytokines, growth factors, and angiogenesis, favoring physiological changes to exercise training, and research suggests that the response of catalyzers, such as MMPs, may explain the response of serum joint biomarkers after exercise [14]. Similar to our findings, the MMP-3 level in the blood has been shown to elevate from baseline following a multistage ultramarathon [24]. Curiously, this effect was correlated with the elevation in cartilage oligomeric matrix protein (COMP), implying that MMP-3 may play a function in the degradation of noncollagenous matrix proteins [24]. In this context, an acute bout of high-intensity resistance exercise (6 sets of 10 repetitions at ∼75% 1-RM (one repetition maximum)) has also been demonstrated to acutely elevate MMP-3 in a group of healthy untrained participants [13]; nevertheless, this effect was not noted after an 8-week training program, indicating that training status may impact the response of MMP-3. It is also important to emphasize that outcomes in this field are still preliminary and it is prudent to the development of robust research that investigates the effects of exercise training programs on transcriptional and translational adaptations in the MMP system in skeletal muscle.

Subsequent inflammatory processes are closely associated with muscular damage with a relevant impact on physiological repair mechanisms, as indicated by an elevated invasion of immune cells, such as neutrophils, and usual patterns of pro- and anti-inflammatory cytokines [18]. Moreover, despite the function of matrix metalloproteinases in the degradation of extracellular matrix proteins and tissue remodeling [25], they also influence inflammatory processes through their functional inactivation of cytokines and chemokines [26]. The plasma levels of IL-8, TNF-α, IL-1β, and IL-6 are associated with the severity of inflammatory processes [27]. In our study, we did not find a difference between these biomarkers before and after the stiletto dance class. The intensity, type, and duration of the exercise can impact the inflammatory response [28], thus, the moderate intensity of the stiletto class (101–164 of the mean HR reserve) may be associated with the permanent concentration of the biomarkers after the proposed class. Besides, the stiletto protocol had a short time duration (60 min), and even if there was a local tissue increase of cytokines, this was not found in the systemic circulation. Therefore, research that targets local tissue concentrations of inflammatory biomarkers associated with the effect of stiletto training could exhibit a promising path in future studies.

Similar to plasma cytokine data, ROS production change can also be related to the intensity of the training. Furthermore, it is important to mention that methodological differences in the assay of ROS, as well as differences in fiber types between the muscles studied, could also be contributory factors to the differences reported in the science sports literature [29]. Studies of our group show that high-intensity exercise in dancers from different styles, such as street dance and classical ballet, can induce a relevant dysfunction of the peripheral blood leukocytes, which is followed by an elevation in proinflammatory mediators [4, 30, 31].

The implications of this research should be interpreted in light of some limitations. First, this is a convenience sample of dancers, and the sample size was small with study participants acting as self-controls, which may limit the generalizability of the findings. Second, the current literature has a scarcity of studies that investigate health parameters in practitioners of the stiletto dance, which makes it hard to compare and discuss the data from the present study with the findings of other dancers. Third, future research could also investigate the effect of a dance class in heels on different biomarkers related to components of cartilage. Regarding the last issue, Bjerre–Bastos et al. recently developed a randomized, cross-over, and exploratory clinical study to assess acute alterations in biochemical markers of bone and cartilage turnover (markers of type I (CTX-I), II (C2M, CTX-II), and VI (C6M) collagen degradation, COMP, and procollagen C-2 (PRO-C2)) in response to moderate intensity and duration (with and without joint impact) in healthy human subjects. They found that running, but not cycling, induced acute changes in biomarkers of bone and cartilage extracellular matrix turnover [32]. Thus, new controlled studies with a larger number of participants are suggested to investigate the effect of stiletto dancers on other joint biomarkers, and the interpretation of these findings should be interpreted with caution.

5. Conclusion

In conclusion, an acute bout of stiletto dancing induces an increase in markers of muscle tissue turnover and MMP-3 in young, healthy women. Our data did not indicate changes in markers of inflammation or neutrophil function after the stiletto dancing class. These findings may represent a useful tool to design new studies and strategies to improve the dancer’s health.

Data Availability

The data that support the findings of this study are available from the corresponding author upon request.

Ethical Approval

This study was approved by the Ethics Committee of the Cruzeiro do Sul University (3096402).

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

E.H. and J.S. contributed to conception and design of research; L.B., E.W., B.B.D, F.G.F., and B.F. performed experiments; J.S., L.B., P.B.F.J., and E.H. analyzed data; J.S., L.B., P.B.F.J., T.C.P.C., and E.H. interpreted results of experiments; J.S. prepared figures; J.S. and L.B. drafted the manuscript; all authors edited and revised the manuscript and approved the final version.

Acknowledgments

This research was supported by the Brazilian research funding agencies Fundacão de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (Grant no. 20/12267-5; 14/21185-1; 11/21441-0), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) (Grant no. 88882.314890/2013-01, finance code 1), and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Grant no. 308700/2017-1). The authors acknowledge the support of Aline Morais and Bianca Palmeira who assisted with data collection and organization.

References

J. M. McCrary, E. Redding, and E. Altenmüller, “Performing arts as a health resource? An umbrella review of the health impacts of music and dance participation,” PLoS One, vol. 16, no. 6, Article ID e0252956, 2021.
View at: Publisher Site | Google Scholar
Y. Dang, R. Chen, Y. Koutedakis, and M. A. Wyon, “The efficacy of physical fitness training on dance injury: a systematic review,” International Journal of Sports Medicine, vol. 44, no. 2, pp. 108–116, 2023.
View at: Publisher Site | Google Scholar
J. Biernacki, A. Stracciolini, J. Fraser, L. Micheli, and D. Sugimoto, “Risk factors for lower-extremity injuries in female ballet dancers: a systematic review,” Clinical journal of sport medicine: official journal of the Canadian Academy of Sport Medicine, vol. 7, 2018.
View at: Google Scholar
L. Borges, A. Dermargos, S. Gray et al., “Neutrophil migration and adhesion molecule expression after acute high- intensity street dance exercise,” Journal of Immunology Research, vol. 2018, Article ID 1684013, 6 pages, 2018.
View at: Publisher Site | Google Scholar
U. N. Bhatty, S. H. Khan, and A. I. Zubairy, “Managing the patient with heel pain,” British Journal of Hospital Medicine, vol. 80, no. 4, pp. 196–200, 2019.
View at: Publisher Site | Google Scholar
M. S. Barnish and J. Barnish, “High-heeled shoes and musculoskeletal injuries: a narrative systematic review,” BMJ Open, vol. 6, no. 1, Article ID e010053, 2016 Jan.
View at: Publisher Site | Google Scholar
Y. Luximon, Y. Cong, A. Luximon, and M. Zhang, “Effects of heel base size, walking speed, and slope angle on center of pressure trajectory and plantar pressure when wearing high-heeled shoes,” Human Movement Science, vol. 41, pp. 307–319, 2015.
View at: Publisher Site | Google Scholar
D. Han, “Muscle activation of paraspinal muscles in different types of high heels during standing,” Journal of Physical Therapy Science, vol. 27, no. 1, pp. 67–69, 2015.
View at: Publisher Site | Google Scholar
P. Brancaccio, N. Maffulli, and F. M. Limongelli, “Creatine kinase monitoring in sport medicine,” British Medical Bulletin, vol. 81, no. 1, pp. 209–230, 2007.
View at: Publisher Site | Google Scholar
P. Brancaccio, N. Maffulli, R. Buonauro, and F. M. Limongelli, “Serum enzyme monitoring in sports medicine,” Clinics in Sports Medicine, vol. 27, no. 1, pp. 1–18, 2008.
View at: Google Scholar
P. S. Burrage, K. S. Mix, and C. E. Brinckerhoff, “Matrix metalloproteinases: role in arthritis,” Frontiers in Bioscience, vol. 11, no. 1, pp. 529–543, 2006.
View at: Publisher Site | Google Scholar
M. Mazor, T. M. Best, A. Cesaro, E. Lespessailles, and H. Toumi, “Osteoarthritis biomarker responses and cartilage adaptation to exercise: a review of animal and human models,” Scandinavian Journal of Medicine and Science in Sports, vol. 29, no. 8, pp. 1072–1082, 2019.
View at: Publisher Site | Google Scholar
M. L. Urso, J. R. Pierce, J. A. Alemany, E. A. Harman, and B. C. Nindl, “Effects of exercise training on the matrix metalloprotease response to acute exercise,” European Journal of Applied Physiology, vol. 106, no. 5, pp. 655–663, 2009.
View at: Publisher Site | Google Scholar
H. M. Roberts, R.-J. Law, and J. M. Thom, “The time course and mechanisms of change in biomarkers of joint metabolism in response to acute exercise and chronic training in physiologic and pathological conditions,” European Journal of Applied Physiology, vol. 119, no. 11–12, pp. 2401–2420, 2019.
View at: Publisher Site | Google Scholar
V. A. Zammit and E. A. Newsholme, “The maximum activities of hexokinase, phosphorylase, phosphofructokinase, glycerol phosphate dehydrogenases, lactate dehydrogenase, octopine dehydrogenase, phosphoenolpyruvate carboxykinase, nucleoside diphosphatekinase, glutamate-oxaloacetate transaminase and arginine kinase in relation to carbohydrate utilization in muscles from marine invertebrates,” Biochemical Journal, vol. 160, no. 3, pp. 447–462, 1976.
View at: Publisher Site | Google Scholar
M. F. Cury-Boaventura, R. Gorjão, N. R. de Moura et al., “The effect of a competitive futsal match on T Lymphocyte surface receptor signaling and functions,” Frontiers in Physiology, vol. 9, p. 202, 2018.
View at: Publisher Site | Google Scholar
M. Barnish, H. M. Morgan, and J. Barnish, “The 2016 HIGh Heels: health effects and psychosexual BenefITS (HIGH HABITS) study: systematic review of reviews and additional primary studies,” BMC Public Health, vol. 18, no. 1, p. 37, 2017.
View at: Publisher Site | Google Scholar
M. Teschler and F. C. Mooren, “(Whole-Body) electromyostimulation, muscle damage, and immune system: a mini review,” Frontiers in Physiology, vol. 10, p. 1461, 2019.
View at: Publisher Site | Google Scholar
R. D. Hyldahl and M. J. Hubal, “Lengthening our perspective: morphological, cellular, and molecular responses to eccentric exercise,” Muscle and Nerve, vol. 49, no. 2, pp. 155–170, 2014.
View at: Publisher Site | Google Scholar
I. G. Fatouros and A. Z. Jamurtas, “Insights into the molecular etiology of exercise-induced inflammation: opportunities for optimizing performance,” Journal of Inflammation Research, vol. 9, pp. 175–186, 2016.
View at: Publisher Site | Google Scholar
K. Vuolteenaho, T. Leppänen, R. Kekkonen, R. Korpela, and E. Moilanen, “Running a marathon induces changes in adipokine levels and in markers of cartilage degradation--novel role for resistin,” PLoS One, vol. 9, no. 10, Article ID e110481, 2014.
View at: Publisher Site | Google Scholar
M. Schild, G. Eichner, T. Beiter et al., “Effects of acute endurance exercise on plasma protein profiles of endurance-trained and untrained individuals over time,” Mediators of Inflammation, vol. 2016, Article ID 4851935, 11 pages, 2016.
View at: Publisher Site | Google Scholar
V. B. Kraus, B. Burnett, J. Coindreau et al., “Application of biomarkers in the development of drugs intended for the treatment of osteoarthritis,” Osteoarthritis and Cartilage, vol. 19, no. 5, pp. 515–542, 2011.
View at: Publisher Site | Google Scholar
A. Mündermann, C. Klenk, C. Billich et al., “Changes in cartilage biomarker levels during a transcontinental multistage footrace over 4486 km,” The American Journal of Sports Medicine, vol. 45, no. 11, pp. 2630–2636, 2017.
View at: Publisher Site | Google Scholar
W. S. Yang, C. H. Kim, and I. S. Kim, “Physiological properties, functions, and trends in the matrix metalloproteinase inhibitors in inflammation-mediated human diseases,” Current Medicinal Chemistry, vol. 30, no. 18, pp. 2075–2112, 2023.
View at: Publisher Site | Google Scholar
P. Van Lint and C. Libert, “Chemokine and cytokine processing by matrix metalloproteinases and its effect on leukocyte migration and inflammation,” Journal of Leukocyte Biology, vol. 82, no. 6, pp. 1375–1381, 2007.
View at: Publisher Site | Google Scholar
I. Striz, E. Brabcova, L. Kolesar, and A. Sekerkova, “Cytokine networking of innate immunity cells: a potential target of therapy,” Clinical Science, vol. 126, no. 9, pp. 593–612, 2014.
View at: Publisher Site | Google Scholar
J. M. Peake, K. Suzuki, M. Hordern, G. Wilson, K. Nosaka, and J. S. Coombes, “Plasma cytokine changes in relation to exercise intensity and muscle damage,” European Journal of Applied Physiology, vol. 95, no. 5–6, pp. 514–521, 2005.
View at: Publisher Site | Google Scholar
S. K. Powers and M. J. Jackson, “Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production,” Physiological Reviews, vol. 88, no. 4, pp. 1243–1276, 2008.
View at: Publisher Site | Google Scholar
L. Borges, R. Gorjão, S. R. Gray et al., “Lymphocyte activation after a high-intensity street dance class,” PLoS One, vol. 15, no. 9, Article ID e0239516, 2020.
View at: Publisher Site | Google Scholar
L. D. S. Borges, J. R. Bortolon, V. C. Santos et al., “Chronic inflammation and neutrophil activation as possible causes of joint diseases in ballet dancers,” Mediators of Inflammation, vol. 2014, Article ID 846021, 7 pages, 2014.
View at: Publisher Site | Google Scholar
J. J. Bjerre-Bastos, H. B. Nielsen, J. R. Andersen et al., “A biomarker perspective on the acute effect of exercise with and without impact on joint tissue turnover: an exploratory randomized cross-over study,” European Journal of Applied Physiology, vol. 121, no. 10, pp. 2799–2809, 2021.
View at: Publisher Site | Google Scholar

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Copyright © 2023 Jamila Silva et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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