Introduction
Flexibility is a component of physical fitness, and various studies have been conducted
to research ways to improve flexibility [1]. There are many methods of improving flexibility, dermal suction being one of them. In a traditional Chinese medicine-based therapy, dermal suction is known as cupping therapy. Cupping therapy is a treatment method that involves application of a vacuum to a localized area of the skin [2]. The mechanism of action of cupping therapy is not clear [3]; however, cupping has been reported to be beneficial for pain, herpes zoster, and other diseases [4]. Regarding flexibility, some studies have reported that cupping therapy increases the joint range of motion (ROM) [5–8], whereas another study demonstrated no significant change in the joint ROM after cupping therapy [9].
As above-mentioned, previous studies evaluated the influence of cupping therapy
on joint flexibility using joint ROM as an index of joint flexibility [5–9]. However, all the structures located around the joint including the muscles, tendons, skin, subcutaneous tissue, joint capsule, and cartilage, contribute to joint flexibility [10]. In previous experiments involving only joint flexibility [5–9], it was unclear what the changes in the joint ROM can be attributed.
Ultrasound elastography is a technique that can localize stiffness or hardness of a
muscle [11]. Muscle stiffness has been defined as the ratio of change in force to change in length along the long axis of a muscle (proximal to distal direction of the muscle belly) [12], whereas muscle hardness has been defined as the resistance offered by the muscle against perpendicular pressure [13]. Several different ultrasound elastography methods including shear wave elastography and strain elastography are currently used [11]. Each of them uses a different physical principle to measure the mechanical properties of the target tissue [14]. Shear wave elastography and strain elastography assess the muscle stiffness and muscle hardness, respectively [11].
Recently, to examine whether cupping therapy could change mechanical properties
of muscle, Jan et al. [15] investigated the effect of cupping therapy on muscle hardness
in the triceps of 12 healthy subjects using strain elastography and reported that cupping
therapy significantly reduces muscle hardness. However, the ROM of a joint is considered to be influenced by the longitudinal mechanical property of a muscle (i.e., muscle stiffness). Thus, in the context of the mechanism underlying the improvement of joint flexibility caused by dermal suction, muscle stiffness needs to be examined. Elucidation of the dermal suction effects on passive muscle stiffness using shear wave elastography may aid in our understanding of the mechanisms of improvement in joint flexibility achieved using dermal suction, and provide useful information for physical therapists and conditioning professionals who use dermal suction on muscles or joints in their clinical practice. The aim of our study, therefore, was to examine the acute effects of dermal suction on the passive mechanical properties of specific muscles and joints to verify the hypothesis that dermal suction decreases passive muscle stiffness and improves joint flexibility.
Materials and Methods
Subjects
We enrolled 12 men and 12 women who were recreationally active in this study. None
of the subjects reported any ongoing neuromuscular diseases or musculoskeletal injuries
specific to the ankle joint. In addition, no subject complained about poor physical condition on the measurement day. The age and physical characteristics of the subjects are shown in Table 1. Before the survey, we explained the purpose, content, methods, and risks of the study to the subjects. We obtained written informed consent from each participant. The present study was approved by the local ethics committee.
Table 1. Age and physical characteristics of the enrolled subjects.
Procedure
This study was a single-arm study designed to examine the acute effects of dermal
suction on passive muscle and joint stiffness. After measuring ankle joint stiffness using
a dynamometer and the passive stiffness of the medial head of the gastrocnemius of the
right leg using ultrasound shear wave elastography, dermal suction was applied to the right calf of the subjects for 8 min, and the same measurements were taken immediately
after the application.
Passive Ankle Joint Stiffness
Passive plantar flexion torque was measured using a specially designed dynamometer
(Vine, Tokyo, Japan), which has previously been used by other investigators to measure the plantar flexion torque [16–18]. The subjects were seated on the bench of the dynamometer with the knee fully extended while the right ankle was set on the footplate and fastened and restricted to relax the muscles at each joint position (Figure 1). The footplate was fixed with the ankle positioned at 20 degree, 10 degree , 0 degree (neutral position), and −10 degree. The positive and negative values corresponded to the plantar flexion and dorsiflexion angles, respectively. The footplate was passively and manually dorsiflexed at a low speed. The ankle was returned to the 20 degree position before testing the next position. For testing, each joint position was maintained for
approximately 10 s. The torque data were imported into a personal computer at a sampling frequency of 1000 Hz using an A/D converter (PowerLab 16/35, AD Instruments, Australia). The relationship between the joint angle and passive torque at each 10 degree was defined as passive joint stiffness. Four training plates of different weights were used to investigate the reliability and validity of the dynamometer. Loads of 12.25 Nm, 24.5 Nm, 36.75 Nm, and 49 Nm were applied, and each load was measured 10 times. The coefficient of variations (CV), standard error of the mean (SEM), and intraclass correlation coefficients (ICC) were calculated. Pearson’s correlation coefficient was used to test the significance of the relationship between torque values measured by the dynamometer and the loads. Torque values measured by the dynamometer were 12.27 (0.31) Nm, 24.83 (0.38) Nm, 36.85 (0.28) Nm, and 49.01 (0.14)
Nm. CV for loads of 12.25 Nm, 24.5 Nm, 36.75 Nm, and 49 Nm were 2.54%, 1.53%, 0.76%, and 0.28%, respectively. The SEM for four loads were 0.10, 0.12, 0.09, 0.04 (Nm), respectively. ICC (1,1) was 1.000 [95% confidence interval, 0.999 to 1.000]. The correlation coefficient between torque values measured by the dynamometer and the loads was 0.999.
Passive Muscle Stiffness
The passive muscle stiffness of the medial gastrocnemius (MG) was measured using an ultrasound shear wave elastography scanner Aixplorer (Supersonic Imagine, Aix-en-Provence, France) with a linear array transducer SL15-4 (Supersonic Imagine, Aix-en-Provence, France). The validity of shear wave elastography has been confirmed using phantoms [19] and experimental animals [20]; moreover, the measurement of human muscle stiffness by shear wave elastography has been previously reported [21]. In the present study, shear wave velocity (SWV) (m/s) was used as an index of muscle stiffness. The probe was placed on the MG at 30% of the lower leg length (the distance between the popliteal crease and the center of the lateral malleolus). The SWV was calculated over the largest region of interest from which we excluded the aponeurosis and subcutaneous adipose tissue. SWV analysis was performed using the software (Q-Box) built into the ultrasound shear wave elastography scanner. The average of three images at each joint angle was calculated and used for the analysis. To synchronize the SWV and other data, the computer and ultrasonic diagnostic equipment times were synchronized. We investigated the reliability using eight subjects. The stiffness of MG was measured six times for each subject while keeping the subject seated on the bench of the dynamometer and fixing the footplate with the ankle positioned at 20◦ of plantar flexion. The mean values of CV and SEM for eight subjects were 4.43% and 0.05 (m/s). ICC (1, 1) was 0.767 [95% confidence interval, 0.535 to 0.936].
Dermal Suction
Dermal suction was performed using Medicell (MJ Company. K.K., Okayama, Japan)
(Figure 2), which consists of a part that generates negative pressure and a cup that applies suction onto the skin. The negative pressure is displayed on the screen in real time. The internal and external diameters of the cup were 2.96 cm and 4.60 cm, respectively. The cup sizes in this study were similar to those of cups typically used in cupping treatment, which have diameters in the range of approximately 3.80 cm to 5.08 cm [22]. To improve the sliding of the cup during dermal suction, a roller is present in the cup. Dermal suction using Medicell was performed for a total of 8 min (4 min initially, followed by a 30-s rest period, and then 4 min more) on the right calf (Figure 3). The total treatment time was maintained similar to that in the study by Yim et al. [8]. In our preliminary experiments, treating a dermal suction in a constant rhythm for 8 min was deemed as a technical difficulty. Hence, a rest period was provided. During the treatment, while lying prone on a massage table, the subjects were instructed to relax the muscles. Dermal suction targeted the calf muscles, and the cup was slid between the origin and insertion of the gastrocnemius at approximately 0.5 Hz (Figure 3). The intensity of dermal suction was 20 kPa of negative pressure and was adjusted before each treatment. In cupping therapy, the negative pressure is recommended to be between 225 and 300 mmHg (i.e., 30 to 40 kPa) [15]. In contrast, in our preliminary experiments, some subjects complained of strong pain when dermal suction was performed at this intensity (30 to 40 kPa) using the equipment of this study. Therefore, an intensity of 20 kPa was selected. A baby oil (Johnson & Johnson K. K., Tokyo, Japan) consisting of mineral oil and tocopherol acetate was applied to the skin to improve the sliding of the cup.
Statistics
Statistical analyses were performed using SPSS statistics (Version 26, IBM Corporation, Armonk, New York). In order to verify whether there was a difference in the SWV and the joint stiffness due to dermal suction and changes in the joint angles, a two-way repeated measures analysis of variance (ANOVA) was performed, where the independent variables were time (before and after) and the joint angles, and the dependent variables were the SWV and joint stiffness. When appropriate, post hoc comparisons were performed using the Bonferroni-corrected t-test. The level of significance was set at P < 0.05. We calculated the 95% confidence interval (CI) for the difference between the mean values. partial η 2 was calculated as the effect size for the main effect and interaction in the two-way ANOVA where 0.01, 0.06, and 0.14 indicated small, medium, and high effects [23]. Additionally, the effect size (r) for the post hoc test was calculated [24]. Effect size r was classified as small (<0.10 and <0.30), medium (<0.30 and <0.50), and large (<0.50) [25].
Results
No participant dropped out from the study during the entire study duration. The SWV of the MG for each joint angle before and after dermal suction is shown in Figure 4. The two-way repeated measures ANOVA revealed the significant main effects of time (F value = 11.682, P = 0.002, partial h2 = 0.337) and joint angle (F value = 287.860, P < 0.001, partial h2 = 0.926), and showed a significant interaction between the time and the joint angle (F value = 4.502, P = 0.006, partial h2 = 0.164). The post hoc comparison revealed that the SWV increased when the ankle joint was dorsiflexed (20 vs. 10; r = 0.91, P < 0.001, 95% CI [0.871,0.578], 20 vs. 0; r = 0.95, P < 0.001, 95% CI [2.112,1.508], 20 vs.10; r = 0.96, P < 0.001, 95% CI [3.592,2.620], 10 vs. 0; r = 0.93, P < 0.001, 95% CI [1.311, 0.860], 10 vs.10; r = 0.95, P < 0.001, 95% CI [2.799,1.964], 0 vs.10; r = 0.92, P < 0.001, 95% CI [1.544,1.048]). Post hoc comparison also showed that excluding the ankle position at 0, SWV was higher after dermal suction than before dermal suction (20; r = 0.53, P = 0.006, 95% CI [0.301,0.056], 10; r = 0.43, P = 0.030, 95% CI [0.496,0.028], 10; r = 0.60, P = 0.001, 95% CI [0.941,0.259]). A marginally significant difference was found between the pre- and post-dermal suction SWV values at 0 (r = 0.39, P = 0.054, 95% CI [0.521, 0.004]).
The passive ankle joint stiffness gastrocnemius pre- and post-dermal suction for each ankle joint before and after dermal suction is demonstrated in angle. *P < 0.05, **P < 0.01. Figure 5. The two-way repeated measures ANOVA revealed the significant main effects of the joint angle (F value = 10.091, P < 0.001, partial h2 = 0.305). In contrast, the main effect of time (F value = 2.362, P = 0.138, partial h2 = 0.093) and interaction between the time and the joint angle (F value = 2.207, P = 0.122, partial h2 = 0.088) were not significant. The post hoc comparison demonstrated that joint stiffness at 0 to10 was higher than that at 20 to Figure 4. angle. *P 10 (r = 0.55, P = 0.004, 95% CI [0.206,0.035]) and 10 to 0 (r = 0.46, P = 0.014, 95% CI [0.144,0.014]). There was no significant difference between the joint stiffness at 20 to Shear wave velocity of the medial head of the gastrocnemius pre- and post-dermal suction for each ankle joint < 0.05, **P < 0.01. 10 and 10 to 0 (r = 0.29, P = 0.225, 95% CI [0.100, 0.016]). We carried out a post hoc test to calculate the power (1-b) by setting an a level of 0.05, the effect size for the main effects of time in SWV, and the sample size using G*Power (version 3.1.9.3). As a result, the power was 1.00.
Discussion
In the present study, we compared the passive muscle stiffness of the MG and passive ankle joint stiffness before and after dermal suction to verify the hypothesis that dermal suction decreases passive muscle stiffness and increases passive joint flexibility. Based on the results, two main findings were noted: (a) dermal suction significantly increased passive muscle stiffness; and (b) it had no significant effect on passive joint stiffness.
In contrast to our hypothesis, the current results showed a significant acute increase in the SWV after dermal suction, indicating that dermal suction acutely increases muscle stiffness. A possible explanation for the observed acute increase in muscle stiffness following dermal suction is that the suction may result in an increase in intramuscular water content. Yoshitake et al. [26] investigated the influence of the tissue covering the skeletal muscles on the mechanical properties of the muscles using shear wave elastography. The results demonstrated a 50% significant decrease in the muscle shear modulus after removal of the skin. This report [26] implied that the higher the internal pressure in the muscle, the greater the muscle stiffness. A recent study [27] examined the hemodynamic changes during cupping therapy and found that cupping therapy increased the blood volume and tissue oxygenation at the treatment site. Taking this evidence into consideration, it seems likely that dermal suction increases the blood flow and internal pressure in the muscle, which may increase muscle stiffness.
This phenomenon may manifest as an increase in the muscle volume after dermal suction. Thus, we additionally calculated the muscle thickness of the MG before and after dermal suction. The results showed no significant change in muscle thickness (cm) (20: pre-dermal suction 1.64 [0.21] vs. post-dermal suction 1.68 [0.18], 10: pre-dermal suction 1.71 [0.21] vs. post-dermal suction 1.77 [0.19], 0: pre-dermal suction 1.78 [0.22] vs. post-dermal suction 1.80 [0.20],10: pre-dermal suction 1.83 [0.22] vs. post-dermal suction 1.80 [0.16], all P > 0.05). These findings, however, do not lead to the conclusion that the intramuscular water content did not affect our results. In the current study, muscle thickness was only measured in one slice. The changes in muscle thickness induced by resistance training have been reported to be different within the same muscle [28,29]. If there is an inhomogeneous change in the muscle thickness within the same muscle after the dermal suction, it is possible that the muscle thickness measured in only one slice may not have accurately indicated the acute increase in muscle volume due to dermal suction. Further studies attempting to clarify this point should be undertaken.
The results of the present study on muscle stiffness contradict those of a previous study, which found a decrease in muscle hardness after cupping [15]. Several factors might have affected the different outcomes of the two studies. As above-mentioned, several different ultrasound elastography methods are in use [11]: the previous study assessed muscle hardness using strain elastography [15], whereas in our study, muscle stiffness was assessed using shear wave elastography. Differences in the mechanical properties of the muscles measured might have led to the different results. In addition, the differences in target muscles, cup size, duration of treatment, and degree of vacuum pressure might be associated with the change in mechanical properties of the muscle after dermal suction.
The current results showed a significant increase in SWV, but not in passive joint stiffness (Figures 4 and 5). Joint flexibility is influenced not only by the muscle but also by all the structures located around the joint including the tendon, skin, subcutaneous tissue, joint capsule, and cartilage [10]. Hence, it is possible that no significant changes were detected in passive joint stiffness because of the altered mechanical properties of the other tissues. Indeed, a previous animal study reported a significant decrease in skin stiffness after cupping therapy [30].
Moreover, the current finding regarding joint stiffness might be related to the intensity of dermal suction. Using the finite element method, a study revealed that stresses in the soft tissue increased with an increase in applied vacuum pressure during cupping therapy [2]. Hence, the application of suction at various intensities could result in a change in joint stiffness after dermal suction. As this point has not been considered in previous studies on cupping therapy and joint flexibility, the influence of the intensity of dermal suction on joint flexibility must be investigated.
Cupping and other dermal suction methods are widely used to reduce muscle stiffness or hardness [15] and to increase joint flexibility [5–9]. The results of this study showed a significant increase in muscle stiffness after applying dermal suction (Figure 4). A recent study revealed that higher passive muscle stiffness measured using shear wave elastography was significantly related to the superior sprint performance [31]. Furthermore, it has also been reported that stiffer muscles are advantageous with respect to the rapid force production (i.e., rate of torque development) [32]. From this viewpoint, an increase in muscle stiffness due to dermal suction may enhance sports performance. Conversely, we obtained no significant change in the joint stiffness among the participants in this study (Figure 5). Previous studies evaluating the effects of cupping therapy on the joint flexibility used joint ROM as an index of joint flexibility [5–9]. However, the joint ROM is influenced by the mechanical properties of tendons, muscles, ligaments, and joint capsules as well as psychological factors such as pain threshold, the subject’s desire to demonstrate progress in flexibility, and stretch tolerance [33,34]. Joint stiffness used in this study was an alternative approach that can eliminate the effect of psychological factors [33]. Physical therapists or conditioning professionals using dermal suction in their practice should understand the limited acute effects of dermal suction on joint stiffness.
The present study had some limitations. First, the intensity and duration of treatment by dermal suction were limited. We believe that multiple combinations of intensity and duration of treatment can provide useful data on dermal suction. Second, this study was not designed to quantify time-course changes (e.g., 10 min or 30 min after dermal suction). Therefore, it should be noted that this study only investigated the immediate effects of dermal suction. Third, we did not investigate the water intake of the subjects. We noted that intramuscular water content may be related to the increase in muscle stiffness after dermal suction in this study. Further experiments with controlled water intake conditions should be undertaken. Fourth, while the increase in muscle stiffness could be related to the increase in intramuscular water content, the actual mechanism underlying increased muscle stiffness is unclear. Further research including various methodologies such as biochemical or physiological analyses are needed to obtain detailed information on the effects of dermal suction on the mechanical properties of muscle.
Conclusions
The findings presented here provide information about the effects of dermal suction on the mechanical properties of muscle and joint. Our results suggest that dermal suction increases passive muscle stiffness and has a limited impact on passive joint stiffness. These results might indicate that dermal suction is useful when physical therapists or conditioning professionals are trying to increase muscle stiffness in their clinical practice. However, how muscles or joints are affected by dermal suction remains unclear. Well-constructed scientific research detailing the mechanism of action of dermal suction would help increase our understanding of this treatment.
Author Contributions: Conceptualization, S.E., T.S., Y.A. and T.O.; Methodology, S.E., T.S., Y.A. and T.O.; Formal analysis, S.E., Y.A. and K.Y.; Investigation, S.E. and Y.A.; Resources, T.S. and T.O.; Data curation, S.E. and Y.A.; Writing—original draft preparation, S.E. and M.N.; Writing—review and editing, Y.A., K.Y. and T.O.; Visualization, S.E., T.S., Y.A., M.N. and T.O.; Supervision, T.O.; Project administration, S.E.; Funding acquisition, T.S. All authors have read and agreed to the published version of the manuscript.
Funding: This research was funded by MJ Company. K.K., Fourleaf. K.K., and the Manufacturing, Commercial, and Service Productivity Enhancement Grants [grant number 3033120243].
Institutional Review Board Statement: The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the ethics committee of Niijimagakuen Junior College (Approval number: 2019-2; date of approval: 9 March 2020).
Informed Consent Statement: We obtained written informed consent from each participant.
Data Availability Statement: The data of this study are available from the corresponding author, upon reasonable requests.
Acknowledgments: The authors thank Ichisuke Kuwagaki, Kenta Osaki, Rui Yokoyama, Satsuki Uemura, Soma Saito, Tomo Tanigaki, and Yuki Higashi for their assistance with the experiments. The authors also thank all subjects who participated in this study.
Conflicts of Interest: This study was funded by MJ Company. K.K. and Fourleaf. K.K. Tomonari Shibutani is the President of the MJ Company. K.K. and Fourleaf. K.K.
