The effects of a multi-ingredient supplement on markers of muscle damage and inflammation following downhill running in females
© The Author(s). 2016
Received: 24 May 2016
Accepted: 19 November 2016
Published: 25 November 2016
The effects of a multi-ingredient performance supplement (MIPS) on markers of inflammation and muscle damage, perceived soreness and lower limb performance are unknown in endurance-trained female athletes. The purpose of this study was to determine the impact of MIPS (NO-Shotgun®) pre-loaded 4 weeks prior to a single-bout of downhill running (DHR) on hsC-Reactive Protein (hsCRP), interleukin (IL)-6, creatine kinase (CK), muscle soreness, lower limb circumferences and performance.
Trained female runners (n = 8; 29 ± 5.9 years) (VO2max: ≥ 50 ml-1.kg-1.min-1, midfollicular phase (7-11 days post-menses) were randomly assigned in a double-blind manner into two groups: MIPS (n = 4) ingested one serving of NO Shotgun daily for 28 days prior to DHR and 30 min prior to all post-testing visits; Control (CON) (n = 4) consumed an isocaloric maltodextrin placebo in an identical manner to MIPS. hsCRP, IL-6, CK, perceived soreness, limb circumferences, and performance measures (flexibility, squat jump peak power) were tested on 5 occasions; immediately before (PRE), immediately post-DHR, 24, 48 and 72 h post-DHR.
There were main effects of time for CK (p = 0.05), pain pressure threshold (right tibialis anterior (p = 0.010), right biceps femoris (p = 0.01), and left iliotibial band (ITB) (p = 0.05) across all time points), and maximum squat jump power (p = 0.04). Compared with 24 h post-DHR, maximum squat jump power was significantly lower at 48 h post-DHR (p = 0.05). Lower body perceived soreness was significantly increased at 24 h (p = 0.02) and baseline to 48 h (p = 0.02) post DHR. IL-6 peaked immediately post-DHR (p = 0.03) and hsCRP peaked at 24 h post-DHR (p = 0.06). Calculation of effect sizes indicated a moderate attenuation of hsCRP in MIPS at 72 h post-DHR.
Consumption of MIPS for 4 weeks prior to a single bout of DHR attenuated inflammation three days post, but did not affect perceived soreness and muscle damage markers in endurance trained female runners following a single bout of DHR.
Exhaustive or unaccustomed high-intensity exercise [1, 2] or eccentric contractions [3, 4] are known to inflict muscle damage. This leads to increased muscle soreness, decreased muscle strength, increased concentration of plasma muscle enzymes, and decreased range of motion [1, 2, 4], for several days post exercise, and further promotes an unbalanced ratio of protein breakdown to protein synthesis . A level of muscle discomfort related to the exercise-induced muscle damage (EIMD), otherwise known as delayed onset muscle soreness (DOMS), increases until subsiding five to seven days post-exercise . Downhill running (DHR) is commonly used to induce muscle damage , as it involves greater eccentric contraction of the knee extensors, leading to more tissue damage, compared with level or uphill running [8, 9].
Although similar decrements associated with EIMD have been reported in both males and females, it has been documented that females are susceptible to longer periods of recovery when compared to males; however, reasons for this are unclear . However, contrary to this, estrogen appears to have a protective effect with regards to DOMS , as it has been reported that estrogen results in significant decreases in serum creatine kinase (CK) activities post-exercise or post-injury when compare to men or a placebo [12, 13]. It has therefore been hypothesized that several of the sex-related differences are attributed to the female sex hormone 17β-estradiol [14, 15]; such that estrogen has been reported to possess the ability to enhance skeletal muscle growth, gene expression, metabolism, contraction characteristics, and maintain muscle mass.
Numerous studies have examined the effects of nutritional supplementation interventions to reduce the effects of EIMD by increasing the net protein balance within skeletal muscle. These studies have included supplementation with whey protein isolate [5, 16], branched-chain amino acids (BCAAs: leucine, isoleucine, and valine) [17, 18], protein hydrolysates , leucine only , creatine ; increasing anti-inflammatory and anti-oxidant activity through tart cherry juice [22, 23], blueberry  and caffeine ingestion , as well as enhancing recovery through the consumption of chocolate milk [26, 27] to name a few. The majority of studies investigating the ergogenic effects of nutritional supplementation on exercise performance and recovery have primarily focused on males [20, 28, 29]. However, there are a few studies that examined female rats and other animals, and female humans [30, 31].
Recent studies have investigated the effects of a multi-ingredient performance supplement (MIPS; NO Shotgun®) following a single bout of DHR in trained males  as well as in resistance trained males . However, there is little known about the effects of this MIPS on the reduction of muscle damage and repair after EIMD from DHR in endurance-trained female athletes. We hypothesized that 4 weeks of pre-loading with a MIPS prior to a single bout of DHR would decrease perceived soreness and circumferences, enhance flexibility, and improve biochemical markers of muscle damage and inflammation (i.e. CK, IL-6 and CRP), and improve squat jump performance when compared to an isocaloric placebo (CON) in endurance-trained female runners for up to 72 h post-DHR.
All procedures were carried out in the Human Performance Laboratory situated at the University of KwaZulu-Natal (UKZN) Discipline of Biokinetics, Exercise and Leisure Sciences following approval from the UKZN Biomedical Research Ethics Committee (Ethics Approval Number: BFC033/13).
Participant Characteristics (N = 8)
MIPS (n = 4)
CON (n = 4)
TOTAL (n = 8)
Body Mass (kg)
Body Fat (%)
All participants reported running more than 30 km per week, for more than three time a week, exercising at either a moderate or high intensity.
This was a randomized, placebo-controlled, double-blind study. After baseline testing, subjects were randomly assigned to either a MIPS group (n = 4) or an isocaloric flavour-matched placebo control (CON) group (n = 4). The MIPS group was required to consume one serving (21 g) of a multi-ingredient sports supplement (NO-Shotgun®, Vital Pharmaceuticals, Inc., Davie, FL) containing ~72 kcals; 18 g protein; 9.7 g protein hydrolysate matrix including BCAAs; 8.06 g muscle volumizing and 3.17 g power/speed/strength and endurance matrix that includes multiple forms of creatine and beta alanine; 376 mg of Redline® Energy matrix including caffeine; once a day for four weeks prior to the DHR. The CON group was required to consume an isocaloric, flavour-matched placebo beverage (maltodextrin, 28 g) once a day for four weeks prior to the DHR. All participants received their supplement in identical commercially labelled containers after baseline testing. Subjects consumed either MIPS or CON 30 min prior to exercise on reported training days, or first thing in the morning on all non-training and recovery days.
A 15 mL venous blood sample was collected and perceived muscle soreness, pain pressure threshold/tissue tenderness, squat jump performance, circumferences, and flexibility were measured, at the 5 different laboratory visits: baseline (28 days before DHR), immediately before DHR, Immediately post DHR, and 24, 48 and 72 h post-DHR. Following the blood draws, muscle soreness and tissue tenderness measurements were taken, participants were required to complete a warm-up walk for a duration of five minutes at 4.8 km.hr-1 on a motorized treadmill, prior to any performance measurements. The DHR was performed on visit 4 (Fig. 1). Prior to completing the DHR, participants consumed their commercial PVM Energy Bar® 3 h before testing, and replicated their 24 h dietary food logs.
Height and body mass were measured using a Sanny stadiometer and a balance scale (Detecto Medic, Detecto Scales Inc., Brooklyn, N.Y., U.S.A.) respectively. All measurements were taken without shoes and any excess clothing and accessories. Body composition was measured non-invasively using the sum of 7 skinfold measurements (triceps, chest, mid-axillary, subscapular, supra-iliac, abdominal, and thigh), all taken by the same technician, that were used to calculate body fat percentage .
Blood (15 mL) was collected via venipuncture of the antecubital vein at pre, immediately post-, 24, 48 and 72 h post-DHR. Following blood collection, serum was allowed to clot before centrifuging at 3500 RPM at 4 °C for 15 min (Sorvall ST16R Multispeed Centrifuge; Thermo Electron Corporation, Needham Heights, Massachusetts). Aliquots of 300 μL each were then transferred into microtubes and immediately frozen at -80 °C for later batch analysis. Blood samples were sent to a commercial pathology laboratory for analysis of serum markers of muscle damage and inflammation (CK, IL-6, hsCRP). CK and hsCRP were analyzed using Roche/Hitachi cobas c 311, cobas c 501/502 analyzers (Roche Diagnostics GmbH). IL-6 was analyzed using the Access IL-6 assay (Beckman Coulter, Inc.).
Circumferences of the lower limbs were measured to determine the volume changes in the thigh as an indirect marker of edema. A standard centimetre marked tape measure was utilized to measure changes in muscle girth. The participants were measured at the followings areas: 10 and 15 cm above the superior pole of the patellae, on the quadriceps muscle, as well as along the midline of the calf muscle 15 cm from the joint margin of the knee, and hamstring circumference was measured at the midline from the ischial tuberosity to the lateral epicondyle of the tibia. Perceived muscle soreness of the lower body was measured using a Visual Analogue Scale (VAS) . Participants were requested to rate the level of soreness experienced in the anterior thigh of their left leg by drawing an “X” across a continuum line extending from 0 cm (no soreness) to 10 cm (extreme soreness). To quantify the pressure pain threshold or tissue tenderness of the lower limbs and gluteal muscles, an algometer (Wegner Force Ten ™, Wegner Instruments, Greenwich, CT) was used with an application of at 1 kg.cm-2.sec-1 of pressure . The footplate of the algometer was positioned perpendicular to the muscle belly.
Hamstring flexibility was measured using a sit-and-reach box using standard testing procedures . Each participant performed three trials of the sit-and-reach test, of which the best value was used for analysis .
Dynamic explosive force production of the leg extensors was assessed during a squat jump test recorded using the MyoTest PRO2 (MyoTest performance measurement system)  to determine the height, velocity, and power of the jump. Participants were instructed to assume a squat position, with their knees shoulder width apart, to a knee angle of 90° and explosively jump as high as possible. Participants completed three jumps with a 30 s break between each jump, such that the mean was recorded for analysis.
Downhill running protocol
Participants were tested during the mid-follicular phase (7-11 days post-menses) of the menstrual cycle. None of the participants reported using any form of oral contraceptive. Prior to the DHR on visit 4, participants completed a warm-up run at 8 km.hr-1 for five minutes on a level gradient. Participants were required to perform a jump squat before the warm-up. Once the warm-up was completed, the treadmill gradient was lowered to -10%. The participants continued running for a total duration of 60 min at a previously-determined velocity that generated 75% of their VO2max on a level grade (determined during visit 3; using the ACSM metabolic equation ). Heart rate (HR) and rating of perceived exertion (RPE, Borg CR10 scale)  were monitored continuously and recorded every five minutes during the DHR protocol. Following 30 min of DHR, participants were required to perform a squat jump, if a 40% force decrement was evident compared to the jump-squat measures for prior to the DHR , the participant did not have to continue running, however if no decrement was evident, the participant continued running for the full 60 min.
Normal distribution of the variables was checked by the Shapiro-Wilk Test. In addition, visual inspection of the data distribution was performed. The test indicated that creatine kinase (CK) was not normally distributed (p < 0.01) and therefore a natural logarithm (Ln) was applied. After Ln-transformation, CK was normally distributed. Once CK was transformed, the generalized linear model (GLM) was used on all the data for each parameter tested to identify any significant changes within each subjects set of data, between subjects and over time using a factorial repeated measures ANOVA (2x5). Where appropriate pair wise multiple comparisons were performed using the Bonferroni post-hoc test. p ≤ 0.05 was considered statistically significant. Cohen’s d effect sizes (ES) and 95% confidence intervals (CI) were also calculated for all out come measures. Magnitudes of the standardized effects were interpreted using thresholds of <0.2, 0.2-0.6, 0.6-1.2, 1.2-2.0, 2.0-4.0. These values correspond to trivial, small, moderate, large and very large ES, respectively. However, effects were only claimed as clear if the confidence interval did not cross both the positive and negative thresholds. Statistical analyses were performed using the IBM SPSS Statistics for Windows, Version 22.0. (Armonk, NY: IBM Corp).
Downhill run protocol
Average heart rate (HR) and ratings of perceived exertion (RPE) during the DHR protocol
Response to EIMD protocol
No significant time or time x treatment effects were evident for all lower limb circumferences (Quadriceps, Hamstrings, Calf and Gluteus Maximus). With no significant difference between left and right quadriceps (p = 0.59), hamstrings (p = 0.52), and calves (p = 0.94) over time for combined data. Effect sizes as demonstrated by Cohen’s d <0.2 were trivial for both groups (data not shown).
Perceived muscle soreness
Effect sizes and interpretation for VAS, Peak Power, CK, IL-6 and CRP. Pre versus immediately post (IP), 24, 48 and 72 h post DHR
Pre vs IP
1.8 (0.5, 3.0)
1.5 (0.2, 2.8)
Pre vs 24 h
2.9 (1.2, 4.5)
4.0 (3.0, 5.0)
Pre vs 48 h
2.3 (1.1, 3.4)
3.9 (2.8, 5.0)
Pre vs 72 h
1.3 (0.1, 2.6)
1.9 (0.6, 3.2)
Pre vs IP
0.2 (-3.3, 3.6)
0.2 (-5.1, 5.5)
Pre vs 24 h
0.3 (-2.9, 3.5)
0.3 (-4.1, 4.6)
Pre vs 48 h
1.2 (-1.9, 4.2)
0.8 (-3.6, 5.3)
Pre vs 72 h
0.9 (-2.5, 4.2)
0.4 (-5.2, 5.9)
Pre vs IP
1.3 (-1.4, 1.2)
0.5 (0.2, 0.9)
Pre vs 24 h
1.4 (1.1, 1.7)
1.9 (1.6, 2.2)
Pre vs 48 h
1.0 (0.8, 1.2)
1.1 (0.8, 1.4)
Pre vs 72 h
1.0 (0.9, 1.1)
0.4 (0.1, 0.7)
Pre vs IP
2.5 (2.1, 2.9)
1.1 (0.7, 1.6)
Pre vs 24 h
1.6 (1.4, 1.9)
0.2 (0.2, 0.6)
Pre vs 48 h
0.3 (0.3, 0.9)
0.4 (0.4, 1.3)
Pre vs 72 h
0.4 (0.2, 1.1)
0.5 (0.8, 1.7)
Pre vs IP
-0.1 (-0.3, 0.1)
-0.1 (-0.3, 0.2)
Pre vs 24 h
0.1 (-0.1, 0.3)
0.2 (-0.2, 0.7)
Pre vs 48 h
-0.5 (-0.3, 0.6)
1.9 (1.5, 2.3)
Pre vs 72 h
-0.9 (-1.0, -0.7)
0.8 (0.2, 1.4)
The pressure pain threshold or tissue tenderness was quantified using a force algometer. Significant time effects were only noted for the right tibialis anterior (p = 0.01), right biceps femoris (p = 0.01), and the left iliotibial band (ITB) (p = 0.05) for combined data for both groups across all time points (Fig. 4). Combined data of tissue tenderness showed that majority of the areas experienced increased tenderness (decreased algometer force), from baseline; however, the right hip flexor values remained above baseline across all time points; and the left hip flexor values increased at 24 h, decreasing at 48 h but remaining above baseline, and then decreasing further beyond baseline, at 72 h following the DHR protocol. Effect sizes as demonstrated by Cohen’s d <0.2 were trivial for both groups (data not shown).
No significant time x treatment (p = 0.81) or time effect (p = 0.43) was noted for hamstring flexibility for combined data. Effect sizes as demonstrated by Cohen’s d <0.2 were trivial for both groups (data not shown)..
Serum markers of muscle damage and inflammation
The main findings of this study were that consumption of MIPS for 4 weeks prior to a single bout of DHR did not attenuate the changes of ratings of perceived soreness, muscle damage and performance (flexibility, squat jump peak power), greater than an isocaloric placebo (CON) in well-trained female endurance runners for up to 72 h post-DHR. However, based on ES, CRP, a marker of inflammation, was moderately attenuated at 72 h in MIPS compared with CON that exhibited a moderate increase.
Delayed onset muscle soreness
Delayed onset muscle soreness (DOMS) generally develops 24 – 48 h following exercise, peaks at 24 – 72 h, and typically subsides five to seven days post-exercise [6, 32, 44]. Two days following DHR, tissue tenderness, measured by pressure transducers, has shown to be greatest in the gluteus maximus, rectus femoris, vastus medialis, vastus lateralis, tibialis anterior, gastrocnemius, and the biceps femoris . Our findings confirmed that the greatest amount of perceived muscle soreness (VAS and pressure algometer measurements) was reported during 24 and 48 h following the DHR, with no difference between treatment groups. Additionally, Ormsbee et al.  indicated greater perceived muscle soreness following a single-bout of DHR in the rectus femoris, vastus medialis, vastus lateralis, biceps femoris and gluteus maximus of the right leg compared to prior to completing a DHR. The findings of our study are in agreement with these findings. Furthermore, the findings of this study are in accordance with findings from other DHR-induced muscle damage studies [8, 32], as well as a study on female athletes following a repeat sprint protocol, in which VAS was reported to peak at 48 h post .
Several studies have attempted to reduce DOMS and stimulate protein synthesis following strenuous exercise through supplementation with whey protein isolate . Acute ingestion of protein (100 g protein containing 40 g EAAs) immediately following a single 30 min bout of DHR did not attenuate DOMS during 72 h of recovery ; however, BCAA supplementation (2.5 g BCAAs ingested immediately prior to and during exercise) has shown to significantly decrease DOMS from 24 to 72 h post-endurance exercise . Matsumoto et al.  further support this finding of reduced DOMS with BCAA supplementation (0.8% total BCAA: 5 g valine, 10 g leucine, 5 g isoleucine; 0.2% arginine; and 3.5% CHO). Moreover, Green et al.  demonstrated that ingestion of a supplement containing carbohydrates (CHO) and protein one hour (1.2 g CHO.kg BW-1 with 0.3 g Protein.kg BW-1), and two hours (0.6 g CHO.kg BW-1 with 0.15 g Protein.kg BW-1) following 30 min of DHR at -12% gradient in females did not reduce the amount of DOMS experienced, when compared to ingestion of CHO only. Additionally, Green et al.  did note that muscle soreness peaked at 48 h post-DHR, and decreased, but remained elevated above baseline, at 72 h for both groups. In the present study, no significant difference was reported in perceived muscle soreness between groups, which is in agreement with others using protein [47, 50], BCAAs [17, 51], leucine only , or creatine [21, 52]. Irregularities in studies identifying the effects of supplementation on EIMD could be due to varying individual dosages of each individual supplement in previous studies compared to the MIPS used in this study.
Jump performance and flexibility
Decrements in strength performance measures, including jump performance, following eccentric exercise have been well documented [20, 53]. According to Eston et al. , an acute loss of strength following DHR is the most noticeable effect of the eccentric nature of the run. Following a dance muscle damaging protocol in female dancers, Brown et al.  indicated that counter-movement jump (CMJ) measurements returned to near baseline levels by 24 h post damaging exercise, while Keane et al.  showed return to near baseline of CMJ at 72 h following a repeat sprint protocol. Supplementation with NO-Shotgun® was not effective in attenuating the strength decrements observed following the DHR. The average squat jump power, peak squat jump power, squat jump velocity, and jump height and force all indicated peak decrements 48 h post-DHR. This is in accordance with previous research, indicating that the strength decrements following DHR will require longer recovery time compared to other forms of muscle damaging protocols , as well as being in accordance with findings elicited in a study supplementing with NO-Shotgun® following DHR in male participants . The delayed recovery in strength/power output following DHR in females was also noted by Green et al. . Furthermore, the lack of effect of supplementation on recovery in strength has been observed in studies supplementing with protein  and creatine , while others have observed a positive effect of supplementation on strength decline following EIMD [5, 22, 55].
As previously indicated, EIMD is characterized by both strength and range of motion decrements. Proske, Morgan  noted that eccentric exercise leads to an increase in passive tension in the muscle, and indicated that muscular stiffness increased immediately post- and remained elevated up to four days post-exercise. A sit-and-reach test was used to assess the flexibility of the hamstrings following the DHR protocol. Our findings suggest that there was no significant change in hamstring flexibility following the DHR in both the MIPS and CON groups, this is in agreement with findings found by Ormsbee et al. . Furthermore, it appears that although pain was experienced in the hamstrings, the flexibility of the hamstrings was not significantly compromised due to the DHR-protocol, as DHR results in greater damage to the knee extensor muscles in comparison to level running [8, 9]. Supplementation with NO-Shotgun® did not elicit significant improvements in hamstring flexibility in comparison to an isocaloric placebo.
Biochemical markers of muscle damage and inflammation
Our findings of elevated markers of muscle damage (CK and IL-6) following eccentric exercise support previous findings [32, 57]. Although variability in the response of muscle damage indicators (e.g. CK, IL-6) to eccentric exercise still persists , the simultaneous elevations in subsequent pain experienced (DOMS ratings) by participants suggests that the two (CK and IL-6 with DOMS) are linked, as demonstrated by Byrne et al. . Our findings certainly support this relationship, as both increases in mean perceived muscle soreness (VAS) (Fig. 2) and reductions in pressure pain threshold exhibited similar trends as was found with the serum CKLog levels (Fig. 4). VAS and serum CKLog both showed peak increases at 24 h post-DHR, whilst the pressure pain threshold reached peak decrement at the same time point. Ormsbee et al.  indicated a significant time effect for CK following a single-bout of DHR in male athletes after supplementation with NO-Shotgun®. Our findings are consistent with these. Additionally, mean serum IL-6 levels increased post DHR, peaking immediately post and remaining elevated up to 72 h post (Fig. 5), however these findings were not significant. The findings of this study agree with others examining the effects of eccentrically-induced CK response to supplementation with whey protein [5, 53], BCAAs [17, 49], leucine [20, 51], creatine , but not others showing a reduction in CK as a result of creatine  or BCAA supplementation .
The mean response of hsCRP to the DHR showed a slight increase, with a significant decrease occurring between 24 (15.73% of baseline) and 48 h post-DHR (-5.44% of baseline), following which hsCRP levels increased beyond baseline (37.10% of baseline) (Fig. 6). Interestingly, although not significantly so, hsCRP continued to decrease below baseline in the MIPS group, experiencing a peak decline at 72 h post-DHR (-38.89% of baseline, moderate ES), while the CON group remained above baseline at all time points following the DHR with a moderate effect size at 72 h post-DHR). Similar findings were noted by Tara et al.  following supplementation with whey protein (89.3 g protein, 1.1 g fat, and 3.6 g CHO per 100 g), in which the group supplementing with whey protein experienced greater decreases in CRP compared to those supplementing with soy protein (83.3 g protein, 4.2 g fat, <2.1 g CHO, 175 mg isoflavones per 100 g). Previous studies have noted attenuation of CRP levels in response to regular exercise [60, 61], while increases in CRP have been noted in response to acute exercise protocols. Increases in CRP immediately post- and 24 h post-marathon have been evident in endurance trained males and females, with CRP levels returning to baseline two to six days post-marathon . Several studies have suggested that the increase in CRP values is stimulated by the increase in the pro-inflammatory cytokine IL-6, which stimulates hepatic CRP stimulation [63, 64]. However, Michigan et al.  have indicated that the type of exercise and training may result in varied effects on CRP. Our findings do not support the notion that an increase in IL-6 increases the hsCRP response to EIMD. As is evident in Figs. 5 and 6, IL-6 peaked immediately post-DHR and hsCRP peaked 72 h post-DHR. Although it would appear that the MIPS did attenuate hsCRP response to the DHR, however, not significantly so, in comparison to an isocaloric placebo. These findings should be examined further in future research.
Low statistical power because of the modest sample size in the present study (n = 8) played a role in limiting the significance of the statistical comparisons conducted. A post hoc power analysis revealed that on the basis of the mean, between-groups comparison effect sizes observed in the present study (d = 1.1), an n of approximately 9 participants in each group was needed to obtain statistical power at the recommended .80 level. The strict inclusion criteria as well as performance of the DHR during the correct phase of the menstrual cycle and supplementation with a “muscle boosting” supplement, made recruitment for participants difficult. Although hormone levels were not tested to establish the phase of the menstrual cycle, verbal verification was obtained from the participants, and all participants were tested as close to the mid-follicular phase (7-11 days after menses) of the menstrual cycle as possible. This may have influenced the results obtained, as not all participants would have had similar levels of estrogen. Additionally, due to the small sample size, it was difficult to control for the use of contraceptives (oral, transdermal patch, vaginal ring), which would have impacted on the hormone levels and, as such, the time of testing; however during the testing period, participants did not report using any form of contraceptives. Furthermore, the indirect markers of muscle damage used in the present study may have been restricted with regards to their sensitivity to identify specific responses to the DHR and the effects of MIPS. It has been suggested that voluntary eccentric muscle actions do not result in muscle damage and inflammation, but rather provide evidence for myofibrillar remodelling and adaptation. Therefore, the use of an unbiased method to determine the degree of muscle adaptation is an important methodological concern to consider for future research [65, 66]. Although the sample size was small, it provided useful information for the planning of future larger studies.
The results of this study are in accordance with others reporting increases in perceived muscle soreness, CK and IL-6, and decreases in pressure pain thresholds, squat jump performance, and hamstring flexibility following strenuous DHR exercise. The use of a propriety blend MIPS did not have an effect on markers of muscle damage, perceived soreness or performance compared to an isocaloric placebo, however, it may have attenuated the inflammatory response at 72 h post-DHR. Although numerous studies have documented results in attenuation of markers of muscle damage, perceived soreness, and improved performance with supplementation, other studies using protein, BCAAs, creatine and leucine have reported similar findings to ours. A key difference between our study and those supplementing with MIPS is that this study used endurance-trained female athletes compared to that of trained or recreationally active males in similar studies. However, the responses experienced in this study are similar to those using male participants, possibly indicating that the perceived muscle soreness, muscle damage markers and recovery following a single-bout of DHR do not vary between well trained males and females in terms of the responses to muscle damaging exercise.
We would like to thank all participants who volunteered their time and contributing to this project. We would like to thank AMPATH for their assistance with the data collection.
The study was funded by the University of KwaZulu-Natal (UKZN) Research Office that provided research productivity funding to AJM. The UKZN Research Office had no role in the design of the study, collection of data, analysis, interpretation or writing of the manuscript.
Availability of data and material
Please contact author for data requests.
The study was designed by JLK, AJM and MJO. Funding was obtained by JLK and AJM; data were collected and analyzed by JLK and AJM; data interpretation and manuscript preparation were undertaken by JLK, AJM, and MJO. All authors approved the final version of the paper.
This study was supported by product donation from Vital Pharmaceuticals, Inc. (Davie, FL) to MJO and AJM. The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Ethics approval for the study was received from the University of KwaZulu-Natal Biomedical Research Ethics Committee (Ethics Approval Number: BFC033/13). All participants provided written consent before participating in the study.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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