Skip to main content
Avicenna Journal of Phytomedicine logoLink to Avicenna Journal of Phytomedicine
. 2017 Jan-Feb;7(1):16–26.

Herbs and natural supplements in the prevention and treatment of delayed-onset muscle soreness

Abbas Meamarbashi 1
PMCID: PMC5329173  PMID: 28265543

Abstract

Objective:

Unaccustomed and intense eccentric exercise is a common cause of delayed-onset muscle soreness (DOMS). There are multiple remedies for the treatment of DOMS, but its clinical and laboratory pieces of evidence are scarce. Currently, the treatments proposed for DOMS are numerous and include pharmaceuticals, herbal remedies, stretching, massage, nutritional supplements, and other alternatives. To find a holistic treatment with effective pain relief and minimum side effects, complementary and alternative medicine, including herbal therapies, plays a main role.

Methods:

In this review, the existing published studies investigating the efficacy of herbal and natural supplementation therapies for the prevention or treatment of side effects, symptoms, and signs of DOMS are summarized.

Results:

Previous studies have documented the efficacy of herbal therapies to treat pain, inflammation, as well as laboratory and clinical side effects of DOMS.

Conclusion:

The use of herbs in DOMS seems safer and has lower side effects than pharmacotherapy. However, the potential for side effects and drug interactions should be considered.

Key Words: Herbs, Natural products, Delayed onset muscle soreness

Introduction

Any type of physical activity that causes unaccustomed and high loads on muscles may lead to delayed-onset muscle soreness (DOMS). Amateur and professional athletes are concerned about muscular discomfort and pain phenomena, because they can limit further exercise and training activity (Udani et al., 2009). However, DOMS can appear after any unaccustomed and eccentric activity in normal people. Exercise-induced muscle soreness is classified into acute and delayed muscle soreness. Acute muscle soreness occurs during the exercise and may continue for about 4 to 6 h. Delayed-onset muscle soreness occurs 8 to 24 h after strenuous exercise and peak of this muscle soreness occurs 24 to 48 h after the exercise. Exhaustive eccentric exercise is usually responsible for DOMS. During an eccentric contraction, the muscles must be active when stretched; therefore, repeated eccentric muscle contractions are responsible for inducing delayed-onset muscle soreness. Eccentric muscular contractions in downhill running, hopping, plyometric exercising, squatting, and the lowering phase of lifting weights can produce DOMS (Connolly et al., 2003). The main symptoms in DOMS are muscular stiffness, tenderness, and pain during active movements (Fridén et al., 1981); (Gleeson et al., 1998). There are many symptoms related to the muscle inflammation and damage such as muscle fiber swelling (Fridén et al., 1988), elevated serum activities of muscle specific enzymes such as creatine kinase (CK) and lactate dehydrogenase (LDH) (Cleak and Eston, 1992; Tartibian et al., 2009), as well as reduced muscle strength (Connolly et al., 2003) and knee joint range of movement (Saxton et al., 1995).

Figure 1.

Figure 1

General cytochemical mechanism of DOMS

The mechanisms underlying the cause of DOMS are not fully understood; however, it is generally accepted that DOMS is associated with muscle and/or connective tissue damage and/or subsequent inflammatory responses (Cheung et al., 2003). Following the muscle injury, enzymatic reactions and inflammatory mediators such as thromboxanes, prostaglandins, and leukotrienes from the cyclooxygenase and lipoxygenase pathways correspond to the increase in vascular permeability and pain perception by sensitizing type III and IV afferent nerve fibers to both chemical and mechanical stimuli (Connolly et al., 2003; Kim and Lee, 2014). Swelling results from the movement of immune cells and fluid from the bloodstream into the interstitial spaces with inflammation and can contribute to pain sensation. Increase in vascular permeability causes neutrophils recruitment across endothelium to the site of damage. The muscle microscopic injury is instigated by a mechanical disruption to sarcomeres (Warren et al., 2002), T-tubules, myofibrils, cytoskeletal protein, and sarcoplasmic reticulum (SR) (Armstrong, 1984; Child et al., 1998; Clarkson and Sayers, 1999), which lead to an inflammatory response (Gleeson et al., 1995). Recent studies have reported that bradykinin and nerve growth factors also play a pivotal role for developing DOMS (Murase et al., 2010).

Multiple preventive or treatment methods have been advocated to alleviate DOMS. These methods are pharmacological (e.g. non-steroidal anti-inflammatory medications) (Francis and Hoobler, 1987; Gulick et al., 1996; Hasson et al., 1990; High et al., 1989; Janssen et al., 1983), exercise (Rodenburg et al., 1994; Weber et al., 1994), stretching (Buroker and Schwane, 1989), cryotherapy (Crystal et al., 2013; Denegar and Perrin, 1992; Gulick et al., 1996; Isabell et al., 1992; Yackzan et al., 1984), transcutaneous electrical nerve stimulation (Denegar and Perrin, 1992), ultrasound (Hasson et al., 1990; Tiidus, 1997), hyperbaric oxygen therapy (HBOT) and electromagnetic shielding, whey protein (Buckley et al., 2008), fish oil and isoflavones (Lenn et al., 2002), caffeine (Maridakis et al., 2007), l-carnitine (Giamberardino et al., 1996), antioxidant vitamins (Shafat et al., 2004), and branched-chain amino acid (BCAA)(Ra et al., 2013). However, these results are not consistent in attenuating pain or have a small or non-significant effect (Connolly et al., 2003).

In addition, in the last decades, the application of herbs in the prevention and treatment of DOMS is growing. In recent years, herbal supplements have become increasingly popular in the prevention and treatment of somatic pain and discomfort (Arent et al., 2010; Meamarbashi and Abedini, 2011; Meamarbashi and Rajabi, 2014). Interestingly, this application has the advantage of lacking many of the side effects of the common nonsteroidal anti-inflammatory medicines (NSAIDs), such as gastrointestinal distress and cardiovascular complications (Graumlich, 2001; Mukherjee et al., 2001).

There are many different factors which influence the incremental trend of herbal supplementation. Most people believe herbs are cheaper and safer with lower side effects and also are easily available. By contrast, some herbs may have antagonistic interactions with some drugs (Abebe, 2002). These products are available to consumers as over-the-counter (OTC) and are mostly used to alleviate pain. Most of the medicine used in pain management can be addictive and produce side effects. On the other hand, herbs are mostly safer if being wisely consumed.

Application of herbs and natural supplements in the prevention and treatment of DOMS

Some herbs and spices are widely used in the human diet. Traditionally, many benefits of herbs are discovered to alleviate pain and reduce inflammation, which are studied or not yet studied in the experimental research. This article reviews some health benefits of natural products that are more related to the prevention and treatment of muscle soreness.

Saffron

Saffron has been traditionally used in ancient medicine to cure various human diseases. It has many nonvolatile active components (Abdullaev, 2002), many of which are carotenoids, including zeaxanthin, lycopene, and various α- and β-carotenes. Recent experimental findings indicate that saffron's major compounds, crocin and crocetin, which are the derivatives of carotenoids, are powerful antioxidants (Asdaq and Inamdar, 2010), with anti-inflammatory (Poma et al., 2012) and antinociceptive (Hosseinzadeh and Shariaty, 2007; Hosseinzadeh and Younesi, 2002) activities. Recently, the oral supplementation of saffron (300 mg/day for 7 days before and 3 days after eccentric exercise) in a human study has shown a significant effect in terms of reducing DOMS symptoms (Meamarbashi and Rajabi, 2014).

Turmeric

In the traditional medicine, turmeric is applied for reducing inflammation and pain. The most important chemical component of turmeric or curcuma Iongarhizomes is curcumin; tt has anti-inflammatory properties. In some experimental studies, curcumin has similar anti-inflammatory effects to some of the common nonsteroidal anti-inflammatory drugs (NSAIDs), like indomethacin, Vioxx, Celebrex, and ibuprofen. The molecular basis of the anti-inflammatory properties of curcumin is linked to its effects on several targets, including transcription factors, growth regulators, and cellular signaling molecules. Previous research has indicated its anti-inflammatory properties that reduce the activation of cyclooxygenase-2 (COX-2) and remove free radicals (Huang et al., 1991). Davis (2007) and others have provided the results of a decreased creatine kinase (CK) and inflammatory cytokine concentrations (Il-6, TNF-alpha, and IL-beta) in rats supplemented with curcumin compared with placebo. Curcumin ingestion has been reported to attenuate the cause of DOMS (Nicol et al., 2015; Tanabe et al., 2015). However, some research has indicated that curcumin has no effects on muscle soreness (Drobnic et al., 2014).

Curcumin is reported to directly influence the activity of various inflammatory regulators; it has been shown to reduce nuclear factor-kappaB (NF-KB) activation and activator protein 1 (AP-1) binding to DNA as well as to decrease the production of the COX-2 enzyme, all of which play a pivotal role in the inflammatory cascade (Chun et al., 2003; Han et al., 2002; Kang et al., 2004; Singh and Aggarwal, 1995). Furthermore, several studies have reported that curcumin can indirectly inhibit these inflammatory regulators through its ability to scavenge free radicals (Biswas et al., 2005; Rahman and Adcock, 2006). The effects of curcumin on the inflammation and recovery of running performance after downhill running in male mice has been reported and found to be effective in terms of reducing cytokines and creatine kinase enzyme (Davis et al., 2007).

Caffeine

Caffeine, also known as 1,3,7 trimethylxanthine, is a member of the family of methylated xanthine. Caffeine has been examined as a hypoalgesic. Reductions in ischemic forearm muscle pain have been found with the dose of 200 mg caffeine (Myers et al., 1997). Caffeine has also shown moderate to large hypoalgesic effects on quadriceps muscle pain during cycling exercise with the pre-exercise doses of 5 and 10 mg/kg, respectively (Motl et al., 2003; O'Connor and Cook, 1999). The most plausible mechanism of action for methylxanthines and its hypoalgesia is the competitive nonselective blockade of adenosine A1 and A2 receptors (Daly et al., 1999; James, 1997). Both caffeine and theophylline have been observed to have analgesic effects, while paraxanthine and theobromine do not have similar effects.

Caffeine implements its pharmacological effect primarily by blocking the adenosine A1, A2A, and A2B receptors, but has less affinity for A3 receptors (Fredholm et al., 1999). These receptors are reported to be located in peripheral afferent nerves (Bryan and Marshall, 1999), the dorsal horn of the spinal cord, as well as higher brain areas associated with pain processing. Caffeine may inhibit phosphodiesterase, promote Ca2+ release, and block GABAA receptors if its consumption dose is one hundred times higher than its normal dietary use (Fredholm et al., 1999).

Ginger

Ginger (Zingiberofficinale) has analgesic and anti-inflammatory properties. There are many scientific pieces of evidence regarding the effectiveness of ginger for the alleviation of muscle soreness. Traditionally, ginger has been widely used for a variety of medicinal purposes, especially in the treatment of pain. One of the features of inflammation is increase in the oxygenation of arachidonic acid which is metabolized by two enzymatic pathways, cyclooxygenase (CO), and 5-lipoxygenase, leading to the production of prostaglandins and leukotrienes, respectively. Among the CO products, PGE2, and among the 5-lipoxygenase products, Leukotriene B4 (LTB4), are considered important mediators of inflammation. Ameliorative effects of ginger could be related to the inhibition of prostaglandin and leukotriene biosynthesis, i.e. it works as a dual inhibitor of eicosanoid biosynthesis (Srivastava and Mustafa, 1992). In a study about the effect of supplementation with ginger on muscle soreness, 74 adults who consumed ginger for 11 days had less muscle soreness after lifting weights. It is necessary to mention that the ingestion of single dose of 2 g ginger does not attenuate eccentric exercise-induced muscle pain, inflammation, or dysfunction 45 min after ingestion. However, ginger may attenuate the day-to-day progression of muscle pain (Black and O'Connor, 2010). Due to the paucity of well-conducted trials, the evidence for the efficacy of ginger for pain alleviation remains to be insufficient (Terry et al., 2011).

Cinnamon

Cinnamon or Cinnamomum zeylanicum has antioxidant and anti-inflammatory effects and its action is induced through decreasing the generation of reactive oxygen species (ROS) due to its phenolic and flavonoids contents in addition to modifying gene expression by inhibiting NF-kB activation (Azab et al., 2011). The obtained data suggest that cinnamon aqueous extract acts as a candidate radioprotector (Azab et al., 2011). Cinnamon has been used to treat dyspepsia, gastritis, blood circulation disturbance, and inflammatory diseases in many countries since the ancient age (Yu et al., 2007). The significant antiallergic, antiulcerogenic, antipyretic, anaesthetic, and analgesic activities have been verified by some researchers (Kurokawa et al., 1998).

The anti-inflammatory mechanisms of Cinnamomum can be related to modulating macrophage-mediated inflammatory functions such as the over-production of cytokines, nitric oxide, and PGE2, adhesion molecule activation, as well as oxidative responses (Lee et al., 2006).

Dietary ginger and cinnamon for reducing muscle soreness have been investigated in forty-nine female taekwondo players during the six week supplementation with 3 g dietary ginger and cinnamon, which showed significant changes in the muscle soreness, but not interleukin-6, in the cinnamon and ginger groups (Shokri Mashhadi et al., 2013). Oral consumption of 420 mg cinnamon per day, seven days before concentric exercise and three days after training, was effective for DOMS (Meamarbashi and Abbasian, 2013). This effect may be related to the effect of cinnamon on cell membrane integrity (Meamarbashi and Rajabi, 2013).

Black tea

Theaflavin and its derivatives are antioxidant polyphenols in tea leaves which are produced during the enzymatic oxidation (fermentation) of black tea. Consumption of theaflavin-enriched black tea extract could improve the recovery and reduce oxidative stress and DOMS responses to acute anaerobic intervals (Arent et al., 2010).

Pomegranate juice

Pomegranate (Punicagranatum) contains anthocyanins, phytoestrogenic flavonoids and ellagic acid (Mousavinejad et al., 2009). Seventeen resistance trained men who were studied in a crossover design and supplemented with pomegranate juice showed a significant reduction in the elbow flexor muscles, but not knee extensor muscles (Trombold et al., 2011).

Chamomile

Chamomile (Matricariarecutita, Chamamelum mobile) is used for its sedative and antispasmodic, antiseptic, and anti-inflammatory effects. Chamomile contains important flavonoids, including apigenin, luteolin, and quercetin. Some alkylated flavonoids, such as chrysoplenin, chrysoplenol, and jaceidin, have been identified in it as well. In traditional medicine, chamomile is known to be a muscle relaxant; therefore, it may be helpful in reducing muscle soreness.

Watermelon juice

Watermelon (Citrulluslanatus) is a fruit rich of l-Citrulline (Tarazona-DÃaz et al., 2013). Its scientific name is 2-amino-5-(carbamoylamino) pentanoic acid. Citrulline is a precursor for arginine, which is involved in the formation of nitric oxide and creatine, and is a key constituent of the urea cycle, which detoxifies ammonia. Watermelon contains high concentration of lycopene, a carotenoid that may have beneficial effects on the risk of cancer and cardiovascular disease. Watermelon is also rich of vitamins A and C. Research on rats suggests that citrulline may reduce muscle fatigue (Goubel et al., 1997). It is believed that it can be used to reduce muscle soreness (Tarazona-DÃaz et al., 2013).

Cherry juice

In a research, the effectiveness of a fresh tart cherry juice for reducing the effects of eccentrically induced muscle damage was evaluated (Connolly et al., 2006). Tart cherries contain flavonoids and anthocynanins that have high antioxidant and anti-inflammatory properties that inhibiting the effects of cyclo-oxygenase (produce biological mediators) that cause inflammation and pain (Wang et al., 1999).

Garlic

Garlic is used for the treatment of fatigue; however, its mechanism remains unclear (Morihara et al., 2007). The anti-fatigue function of garlic may be closely related to its many favorable biological and pharmacological effects. In animal studies, garlic has been shown to promote exercise endurance. In human studies, it has been confirmed that garlic produces symptomatic improvement in the persons with physical fatigue, systemic fatigue due to cold, or lassitude of indefinite cause, suggesting that garlic can resolve fatigue through a variety of actions. Currently, the available data strongly suggest that garlic may be a promising anti-fatigue agent and that further studies are required for elucidating its application are warranted (Morihara et al., 2007).

Allicin, a compound that results from crushing garlic, has been supplemented to reduce muscle damage resulting from eccentric exercise. Su et al. suggested that the anti-inflammatory and antioxidative capacities of allicin would decrease the inflammatory response and muscle damage after eccentric exercise (Su et al., 2008). Depending on its ingested form, garlic can have immune-enhancing or anti-oxidative capacities that typically result from many different biologically active compounds (Amagase et al., 2001). Effectiveness of garlic in muscle soreness can be related to its antioxidative properties.

Herb-drug interactions

Herbal medicines are becoming increasingly popular. Even though in most countries, herbal medicines are being sold without prescription, medical guidance is necessary because of the adverse effects of these products and the potential for drug interactions. Some of the adverse effects and drug interactions reported for herbal products could be caused by impurities (e.g. allergens, pollen, and spores) (Hussain, 2011).

Herbal supplements are often used in combination with the conventional drugs. Non-steroidal anti-inflammatory drugs (NSAIDs), particularly aspirin, have the potential to interact with herbal supplements with antiplatelet activity (ginkgo, garlic, ginger, bilberry, dong quai, feverfew, ginseng, turmeric, meadowsweet, and willow), with those containing coumarin (chamomile, motherworth, horse chestnut, fenugreek, and red clover), and with tamarind, enhancing the risk of bleeding (Abebe, 2002). The concomitant use of opioid analgesics with the sedative herbal supplements, chamomile, valerian, and kava may lead to increased central nervous system (CNS) depression (Abebe, 2002). Ginseng may also inhibit the analgesic effect of opioids. It is suggested that health-care professionals should be more aware of the potential adverse interactions between herbal supplements and analgesic drugs and take appropriate precautionary measures to avoid their possible occurrences.

Discussion

In the light of the available documents in relation to the effectiveness of natural products on DOMS, most researchers seem to favor the application of herbs in the prevention and treatment of DOMS. Currently, no intervention strategies exist for preventing DOMS, except evidence of preventive effect of 10 day supplementation with 300 mg saffron (Meamarbashi and Rajabi, 2014). Therefore, the most potent alternative is to treat the sign and symptoms when complaints occur. Due to the unknown pathology of DOMS, the unique alleviating method is not present. Hence, the effectiveness of therapeutic procedures is mostly dependent on the reduction degree of symptoms and signs and the duration of its effectiveness in combination with minimum possible side effects.

People are increasingly seeking herbal remedies to relief pain, inflammation, and muscle soreness. Herbs are often believed to be “natural” and, therefore, safe; however, many mild to lethal side effects including toxic, allergic, interaction with drugs and other herbs have been reported (Bent and Ko, 2004). Herb-drug interaction often involves drug-metabolizing enzymes and drug transporter systems besides pharmacodynamic interaction (Hussain, 2011). In fact, the pharmacokinetic and pharmacodynamic characteristics of many herbs and commercial and natural dietary supplements are not completely recognized and potential interactions are not often foreseeable. Therefore, consumers should be aware of herbal side effects when frequently consuming herbs.

Conflict of interest

There is no conflict of interest.

References

  1. Abdullaev FI. Cancer chemopreventive and tumoricidal properties of saffron (Crocus sativus L) Exp Biol Med. 2002;227:20–25. doi: 10.1177/153537020222700104. [DOI] [PubMed] [Google Scholar]
  2. Abebe W. Herbal medication: potential for adverse interactions with analgesic drugs. J Clin Pharm Ther. 2002;27:391–401. doi: 10.1046/j.1365-2710.2002.00444.x. [DOI] [PubMed] [Google Scholar]
  3. Amagase H, Petesch BL, Matsuura H, Kasuga S, Itakura Y. Intake of Garlic and Its Bioactive Components. J Nutr. 2001;131:955S–962S. doi: 10.1093/jn/131.3.955S. [DOI] [PubMed] [Google Scholar]
  4. Arent S, Senso M, Golem D, McKeever K. The effects of theaflavin-enriched black tea extract on muscle soreness, oxidative stress, inflammation, and endocrine responses to acute anaerobic interval training: a randomized, double-blind, crossover study. J Int Soc Sports Nutr. 2010;7:11. doi: 10.1186/1550-2783-7-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Armstrong RB. Mechanisms of exercise-induced delayed onset muscular soreness: a brief review. Med Sci Sports Exerc. 1984;16:529–538. [PubMed] [Google Scholar]
  6. Asdaq SMB, Inamdar MN. Potential of Crocus sativus (saffron) and its Constituent, Crocin, as Hypolipidemic and Antioxidant in Rats. Appl Biochem Biotechnol. 2010;162:358–372. doi: 10.1007/s12010-009-8740-7. [DOI] [PubMed] [Google Scholar]
  7. Azab KS, Mostafa AHA, Ali EMM, Abdel-Aziz MAS. Cinnamon extract ameliorates ionizing radiation-induced cellular injury in rats. Ecotoxicol Environ Saf. 2011;74:2324–2329. doi: 10.1016/j.ecoenv.2011.06.016. [DOI] [PubMed] [Google Scholar]
  8. Bent S, Ko R. Commonly used herbal medicines in the United States: a review. Am J Med. 2004;116:478–485. doi: 10.1016/j.amjmed.2003.10.036. [DOI] [PubMed] [Google Scholar]
  9. Biswas SK, McClure D, Jimenez LA, Megson IL, Rahman I. Curcumin induces glutathione biosynthesis and inhibits NF-kappa B activation and interleukin-8 release in alveolar epithelial cells: Mechanism of free radical scavenging activity. Antioxidants & Redox Signaling. 2005;7:32–41. doi: 10.1089/ars.2005.7.32. [DOI] [PubMed] [Google Scholar]
  10. Black CD, O'Connor PJ. Acute effects of dietary ginger on muscle pain induced by eccentric exercise. Phytother Res. 2010;24:1620–1626. doi: 10.1002/ptr.3148. [DOI] [PubMed] [Google Scholar]
  11. Bryan PT, Marshall JM. Cellular mechanisms by which adenosine induces vasodilatation in rat skeletal muscle: significance for systemic hypoxia. J Physiol (Lond) 1999;514:163–175. doi: 10.1111/j.1469-7793.1999.163af.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Buckley JD, Thomson RL, Coates AM, Howe PR, DeNichilo MO, Rowney MK. Supplementation with a whey protein hydrolysate enhances recovery of muscle force-generating capacity following eccentric exercise. J Sci Med Sport. 2008;13:178–181. doi: 10.1016/j.jsams.2008.06.007. [DOI] [PubMed] [Google Scholar]
  13. Buroker KC, Schwane JA. Does post-exercise static stretching alleviate delayed muscle soreness? Phys Sportsmed. 1989;17:65–83. doi: 10.1080/00913847.1989.11709806. [DOI] [PubMed] [Google Scholar]
  14. Cheung K, Hume PA, Maxwell L. Delayed onset muscle soreness: treatment strategies and performance factors. Sports Med. 2003;33:145–164. doi: 10.2165/00007256-200333020-00005. [DOI] [PubMed] [Google Scholar]
  15. Child RB, Saxton JM, Donnelly AE. Comparison of eccentric knee extensor muscle actions at two muscle lengths on indices of damage and anglespecific force production in humans. J Sports Sci. 1998;16:301–308. doi: 10.1080/02640419808559358. [DOI] [PubMed] [Google Scholar]
  16. Chun K-S, Keum Y-S, Han SS, Song Y-S, Kim S-H, Surh Y-J. Curcumin inhibits phorbol ester-induced expression of cyclooxygenase-2 in mouse skin through suppression of extracellular signal-regulated kinase activity and NF-κB activation. Carcinogenesis. 2003;24:1515–1524. doi: 10.1093/carcin/bgg107. [DOI] [PubMed] [Google Scholar]
  17. Clarkson PM, Sayers SP. Etiology of exercise-induced muscle damage. Appl Physiol Nutr Metab. 1999;24:234–248. doi: 10.1139/h99-020. [DOI] [PubMed] [Google Scholar]
  18. Cleak MJ, Eston RG. Delayed onset muscle soreness: mechanisms and management. J Sports Sci. 1992;10:325–341. doi: 10.1080/02640419208729932. [DOI] [PubMed] [Google Scholar]
  19. Connolly DA, Lauzon C, Agnew J, Dunn M, Reed B. The effects of vitamin C supplementation on symptoms of delayed onset muscle soreness. J Sports Med Phys Fitness. 2006;46:462–4677. [PubMed] [Google Scholar]
  20. Connolly DAJ, Sayers SE, McHugh MP. Treatment and prevention of delayed onset muscle soreness. J Strength Cond Res. 2003;17:197–208. doi: 10.1519/1533-4287(2003)017<0197:tapodo>2.0.co;2. [DOI] [PubMed] [Google Scholar]
  21. Connolly DAJ, Sayers SE, McHugh MP. Treatment and prevention of delayed onset muscle soreness. J Strength Cond Res. 2003;17:197–208. doi: 10.1519/1533-4287(2003)017<0197:tapodo>2.0.co;2. [DOI] [PubMed] [Google Scholar]
  22. Crystal N, Townson D, Cook S, LaRoche D. Effect of cryotherapy on muscle recovery and inflammation following a bout of damaging exercise. Eur J Appl Physiol. 2013;113:1–10. doi: 10.1007/s00421-013-2693-9. [DOI] [PubMed] [Google Scholar]
  23. da Silva LA, Tromm CB, Bom KF, Mariano I, Pozzi B, da Rosa GL, Tuon T, da Luz G, Vuolo F, Petronilho F, Cassiano W, De Souza CT, Pinho RA. Effects of taurine supplementation following eccentric exercise in young adults. Appl Physiol Nutr Metab. 2014;39:101–104. doi: 10.1139/apnm-2012-0229. [DOI] [PubMed] [Google Scholar]
  24. Daly JW, Shi D, Nikodijevic O, Jacobson KA. The role of adenosine receptors in the central action of caffeine. In: aUG Gupta B., editor. Caffeine and behavior-current views and research trends. Boca Raton: CRC; 1999. pp. 1–16. Boca Raton, FL, CRC Press. [Google Scholar]
  25. Davis JM, Murphy EA, Carmichael MD, Zielinski MR, Groschwitz CM, Brown AS, Gangemi JD, Ghaffar A, Mayer EP. Curcumin effects on inflammation and performance recovery following eccentric exercise-induced muscle damage. Am J Physiol Regul Integr Comp Physiol. 2007;292:R2168–73. doi: 10.1152/ajpregu.00858.2006. [DOI] [PubMed] [Google Scholar]
  26. Denegar CR, Perrin DH. Effect of transcutaneous electrical nerve stimulation, cold, and a combination treatment on pain, decreased range of motion, and strength loss associated with delayed onset muscle soreness. J Athl Train. 1992;27:200–206. [PMC free article] [PubMed] [Google Scholar]
  27. Drobnic F, Riera J, Appendino G, Togni S, Franceschi F, Valle X, Pons A, Tur J. Reduction of delayed onset muscle soreness by a novel curcumin delivery system (Meriva®): a randomised, placebo-controlled trial. J Int Soc Sports Nutr. 2014;11 doi: 10.1186/1550-2783-11-31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Francis KT, Hoobler T. Effects of aspirin on delayed muscle soreness. J Sports Med Phys Fitness. 1987;27:333–337. [PubMed] [Google Scholar]
  29. Fredholm BB, Bättig K, Holmén J, Nehlig A, Zvartau EE. Actions of caffeine in the brain with special reference to factors that contribute to its widespread use. Pharmacol Rev. 1999;51:83–133. [PubMed] [Google Scholar]
  30. Fridén J, Sfakianos PN, Hargens AR, Akeson WH. Residual muscular swelling after repetitive eccentric contractions. J Orthop Res. 1988;6:493–498. doi: 10.1002/jor.1100060404. [DOI] [PubMed] [Google Scholar]
  31. Fridén J, SjÖstrÖm M, Ekblom B. A morphological study of delayed muscle soreness. Experientia. 1981;37:506–507. doi: 10.1007/BF01986165. [DOI] [PubMed] [Google Scholar]
  32. Giamberardino MA, Dragani L, Valente R. Effects of prolonged L-carnitine administration on delayed muscle pain and CK release after eccentric effort. Int J Sports Med. 1996;17:320–4. doi: 10.1055/s-2007-972854. [DOI] [PubMed] [Google Scholar]
  33. Gleeson M, Blannin AK, Walsh NP, Field CNE, Pritchard JC. Effect of exercise-induced muscle damage on the blood lactate response to incremental exercise in humans. Eur J Appl Physiol. 1998;77:292–295. doi: 10.1007/s004210050336. [DOI] [PubMed] [Google Scholar]
  34. Gleeson M, Blannin AK, Zhu B, Brooks S, Cave R. Cardiorespiratory, hormonal and haematological responses to submaximal cycling performed 2 days after eccentric or concentric exercise bouts. J Sports Sci. 1995;13:471–479. doi: 10.1080/02640419508732264. [DOI] [PubMed] [Google Scholar]
  35. Goubel F, Vanhoutte C, Allaf O, Verleye M, Gillardin J. Citrulline malate limits increase in muscle fatigue induced by bacterial endotoxins. Can J Physiol Pharmacol. 1997;75:205–207. [PubMed] [Google Scholar]
  36. Graumlich JF. Preventing gastrointestinal complications of NSAIDs. Risk factors, recent advances, and latest strategies. Postgrad Med. 2001;109:117–120. doi: 10.3810/pgm.2001.05.931. [DOI] [PubMed] [Google Scholar]
  37. Gulick DT, Kimura IF, Sitler M, Paolone A, Kelly Iv JD. Various treatment techniques on signs and symptoms of delayed onset muscle soreness. J Athl Train. 1996;31:145–152. [PMC free article] [PubMed] [Google Scholar]
  38. Han SS, Keum YS, Seo HJ, Surh YJ. Curcumin suppresses activation of NF-kappa B and AP-1 induced by phorbol ester in cultured human promyelocytic leukemia cells. J Biochem Mol Biol. 2002;35:337–342. doi: 10.5483/bmbrep.2002.35.3.337. [DOI] [PubMed] [Google Scholar]
  39. Hasson S, Mundorf R, Barnes W, Williams J, Fujii M. Effect of pulsed ultrasound versus placebo on muscle soreness perception and muscular performance. Scand J Rehabil Med. 1990;22:199–205. [PubMed] [Google Scholar]
  40. High DM, Howley ET, Franks BD. The effects of static stretching and warm-up on prevention of delayed-onset muscle soreness. Res Q Exerc Sport. 1989;60:357–361. doi: 10.1080/02701367.1989.10607463. [DOI] [PubMed] [Google Scholar]
  41. Hosseinzadeh H, Shariaty VM. Anti-nociceptive effect of safranal, a constituent of Crocus sativus (saffron), in mice. Pharmacologyonline. 2007;2:498–503. [Google Scholar]
  42. Hosseinzadeh H, Younesi HM. Antinociceptive and anti-inflammatory effects of Crocus sativus L. stigma and petal extracts in mice. BMC Pharmacol. 2002;2:7–15. doi: 10.1186/1471-2210-2-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Huang M-T, Lysz T, Ferraro T, Abidi TF, Laskin JD, Conney AH. Inhibitory effects of curcumin on in vitro lipoxygenase and cyclooxygenase activities in mouse epidermis. Cancer Res. 1991;51:813–819. [PubMed] [Google Scholar]
  44. Hussain S. Patient Counseling about Herbal-Drug Interactions. Afr J Tradit Complement Altern Med. 2011;8:152–163. doi: 10.4314/ajtcam.v8i5S.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Isabell WK, Durrant E, Myrer W, Anderson S. The effects of ice massage, ice massage with exercise, and exercise on the prevention and treatment of delayed onset muscle soreness. J Athl Train. 1992;27:208–217. [PMC free article] [PubMed] [Google Scholar]
  46. James JE. Book Understanding caffeine: A biobehavioral analysis. Thousand Oaks, CA: Sage Publications, Inc; 1997. Understanding caffeine: A biobehavioral analysis; 227 pp. [Google Scholar]
  47. Janssen E, Kuipers H, Verstappen F, Costill D. Influence of an anti-inflammatory drug on muscle soreness. Med Sci Sports Exerc. 1983;15:165. [Google Scholar]
  48. Kang G, Kong PJ, Yuh YJ, Lim SY, Yim SV, Chun WJ, Kim SS. Curcumin suppresses lipopolysaccharide-induced cyclooxygenase-2 expression by inhibiting activator protein 1 and nuclear factor kappa B bindings in BV2 microglial cells. J Pharmacol Sci. 2004;94:325–328. doi: 10.1254/jphs.94.325. [DOI] [PubMed] [Google Scholar]
  49. Kim J, Lee J. A review of nutritional intervention on delayed onset muscle soreness. Part I. J Exerc Rehabil. 2014;10:349–356. doi: 10.12965/jer.140179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Kurokawa M, Kumeda CA, Yamamura J, Kamiyama T, Shiraki K. Antipyretic activity of cinnamyl derivatives and related compounds in influenza virus-infected mice. Eur J Pharmacol. 1998;348:45–51. doi: 10.1016/s0014-2999(98)00121-6. [DOI] [PubMed] [Google Scholar]
  51. Lee HJ, Hyun E-A, Yoon WJ, Kim BH, Rhee MH, Kang HK, Cho JY, Yoo ES. In vitro anti-inflammatory and anti-oxidative effects of Cinnamomum camphora extracts. J Ethnopharmacol. 2006;103:208–216. doi: 10.1016/j.jep.2005.08.009. [DOI] [PubMed] [Google Scholar]
  52. Lenn JON, Uhl T, Mattacola C, Boissonneault G, Yates J, Ibrahim W, Bruckner G. The effects of fish oil and isoflavones on delayed onset muscle soreness. Med Sci Sports Exerc. 2002;34:1605–1613. doi: 10.1097/00005768-200210000-00012. [DOI] [PubMed] [Google Scholar]
  53. Maridakis V, O’Connor PJ, Dudley GA, McCully KK. Caffeine Attenuates Delayed-Onset Muscle Pain and Force Loss Following Eccentric Exercise. J Pain. 2007;8:237–243. doi: 10.1016/j.jpain.2006.08.006. [DOI] [PubMed] [Google Scholar]
  54. Meamarbashi A, Abbasian M. The effects of Cinnamon and Indomethacin in prevention of Delayed Onset Muscle Soreness (DOMS). Proceedings of International Conference on Medical & Health Sciences; 22-24 May 2013; Kota Bharu, Malaysia: [Google Scholar]
  55. Meamarbashi A, Abedini F. Preventive effects of purslane extract on delayed onset muscle soreness induced by one session bench-stepping exercise. Isokinet Exerc Sci. 2011;19:199–206. [Google Scholar]
  56. Meamarbashi A, Rajabi A. Erythrocyte Osmotic Fragility Test Revealed Protective Effects of Supplementation with Saffron and Cinnamon on the Red Blood Cell Membrane. Asian J Exp Biol Sci. 2013;4:322–326. [Google Scholar]
  57. Meamarbashi A, Rajabi A. Preventive Effects of 10-Day Supplementation With Saffron and Indomethacin on the Delayed-Onset Muscle Soreness. Clin J Sport Med. 2014;25:105–112. doi: 10.1097/JSM.0000000000000113. [DOI] [PubMed] [Google Scholar]
  58. Morihara N, Nishihama T, Ushijima M, Ide N, Takeda H, Hayama M. Garlic as an anti-fatigue agent. Mol Nutr Food Res. 2007;51:1329–1334. doi: 10.1002/mnfr.200700062. [DOI] [PubMed] [Google Scholar]
  59. Motl RW, O’Connor PJ, Dishman RK. Effect of caffeine on perceptions of leg muscle pain during moderate intensity cycling exercise. J Pain. 2003;4:316–321. doi: 10.1016/s1526-5900(03)00635-7. [DOI] [PubMed] [Google Scholar]
  60. Mousavinejad G, Emam-Djomeh Z, Rezaei K, Khodaparast MHH. Identification and quantification of phenolic compounds and their effects on antioxidant activity in pomegranate juices of eight Iranian cultivars. Food Chem. 2009;115:1274–1278. [Google Scholar]
  61. Mukherjee D, Nissen SE, Topol EJ. Risk of cardiovascular events associated with selective COX-2 inhibitors. J Am Med Assoc. 2001;286:954–959. doi: 10.1001/jama.286.8.954. [DOI] [PubMed] [Google Scholar]
  62. Murase S, Terazawa E, Queme F, Ota H, Matsuda T, Hirate K, Kozak Y, Katanosaka K, Taguchi T, Urai H, Mizumura K. Bradykinin and Nerve Growth Factor Play Pivotal Roles in Muscular Mechanical Hyperalgesia after Exercise (Delayed-Onset Muscle Soreness) J Neurosci. 2010;30:3752–3761. doi: 10.1523/JNEUROSCI.3803-09.2010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Myers DE, Shaikh Z, Zullo TG. Hypoalgesic effect of caffeine in experimental ischemic muscle contraction pain. Headache. 1997;37:654–658. doi: 10.1046/j.1526-4610.1997.3710654.x. [DOI] [PubMed] [Google Scholar]
  64. Nicol L, Rowlands D, Fazakerly R, Kellett J. Curcumin supplementation likely attenuates delayed onset muscle soreness (DOMS) Eur J Appl Physiol. 2015;115:1769–1777. doi: 10.1007/s00421-015-3152-6. [DOI] [PubMed] [Google Scholar]
  65. O'Connor PJ, Cook DB. Exercise and Pain: The Neurobiology, Measurement, and Laboratory Study of Pain in Relation to Exercise in Humans. Exerc Sport Sci Rev. 1999;27:119–166. [PubMed] [Google Scholar]
  66. Poma A, Fontecchio G, Carlucci G, Chichiricco G. Anti-inflammatory properties of drugs from saffron crocus. Antiinflamm Antiallergy Agents Med Chem. 2012;11:37–51. doi: 10.2174/187152312803476282. [DOI] [PubMed] [Google Scholar]
  67. Ra S-G, Akazawa N, Choi Y, Matsubara T, Oikawa S, Kumagai H, Tanahashi K, Ohmori H, Maeda S. Taurine Supplementation Reduces Eccentric Exercise-Induced Delayed Onset Muscle Soreness in Young Men. Taurine 9. Springer International Publishing; 2015. pp. 765–772. [DOI] [PubMed] [Google Scholar]
  68. Ra S-G, Miyazaki T, Ishikura K, Nagayama H, Komine S, Nakata Y, Maeda S, Matsuzaki Y, Ohmori H. Combined effect of branched-chain amino acids and taurine supplementation on delayed onset muscle soreness and muscle damage in high-intensity eccentric exercise. J Int Soc Sports Nutr. 2013;10:1–11. doi: 10.1186/1550-2783-10-51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Rahman I, Adcock IM. Oxidative stress and redox regulation of lung inflammation in COPD. Eur Respir J. 2006;28:219–242. doi: 10.1183/09031936.06.00053805. [DOI] [PubMed] [Google Scholar]
  70. Rodenburg JB, Steenbeek D, Schiereck P, Bar PR. Warm-up, stretching and massage diminish harmful effects of eccentric exercise. Int J Sports Med. 1994;15:414–419. doi: 10.1055/s-2007-1021080. [DOI] [PubMed] [Google Scholar]
  71. Saxton JM, Clarkson PM, James R, Miles M, Westerfer M, Clark S. Neuromuscular dysfunction following eccentric exercise. Med Sci Sports Exerc. 1995;27:1185–1193. [PubMed] [Google Scholar]
  72. Shafat A, Butler P, Jensen RL, Donnelly AE. Effects of dietary supplementation with vitamins C and E on muscle function during and after eccentric contractions in humans. Eur J Appl Physiol. 2004;93:196–202. doi: 10.1007/s00421-004-1198-y. [DOI] [PubMed] [Google Scholar]
  73. Shokri Mashhadi N, Ghiasvand R, Askari G, Feizi A, Hariri M, Darvishi L, Barani A, Taghiyar M, Shiranian A, Hajishafiee M. Influence of Ginger and Cinnamon Intake on Inflammation and Muscle Soreness Endued by Exercise in Iranian Female Athletes. Int J Prev Med. 2013;4:S11–15. [PMC free article] [PubMed] [Google Scholar]
  74. Singh S, Aggarwal BB. Activation of Transcription Factor NF-kappa B is Suppressed by Curcumin (Diferuloylmethane) J Biol Chem. 1995;270:24995–25000. doi: 10.1074/jbc.270.42.24995. [DOI] [PubMed] [Google Scholar]
  75. Srivastava KC, Mustafa T. Ginger (Zingiber officinale) in rheumatism and musculoskeletal disorders. Med Hypotheses. 1992;39:342–348. doi: 10.1016/0306-9877(92)90059-l. [DOI] [PubMed] [Google Scholar]
  76. Su Q-S, Tian Y, Zhang J-G, Zhang H. Effects of allicin supplementation on plasma markers of exercise-induced muscle damage, IL-6 and antioxidant capacity. Eur J Appl Physiol. 2008;103:275–283. doi: 10.1007/s00421-008-0699-5. [DOI] [PubMed] [Google Scholar]
  77. Tanabe Y, Maeda S, Akazawa N, Zempo-Miyaki A, Choi Y, Ra S, Imaizumi A, Otsuka Y, Nosaka K. Attenuation of indirect markers of eccentric exercise-induced muscle damage by curcumin. Eur J Appl Physiol. 2015;115:1949–1957. doi: 10.1007/s00421-015-3170-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  78. Tarazona-DÃaz MP, Alacid F, Carrasco M, MartÃnez I, Aguayo E. Watermelon Juice: Potential Functional Drink for Sore Muscle Relief in Athletes. J Agric Food Chem. 2013;61:7522–7528. doi: 10.1021/jf400964r. [DOI] [PubMed] [Google Scholar]
  79. Tartibian B, Maleki BH, Abbasi A. The effects of ingestion of omega-3 fatty acids on perceived pain and external symptoms of delayed onset muscle soreness in untrained men. Clin J Sport Med. 2009;19:115–119. doi: 10.1097/JSM.0b013e31819b51b3. [DOI] [PubMed] [Google Scholar]
  80. Terry R, Posadzki P, Watson LK, Ernst E. The use of ginger (Zingiber officinale) for the treatment of pain: a systematic review of clinical trials. Pain Med. 2011;12:1808–1818. doi: 10.1111/j.1526-4637.2011.01261.x. [DOI] [PubMed] [Google Scholar]
  81. Tiidus PM. Manual massage and recovery of muscle function following exercise: a literature review. J Orthop Sports Phys Ther. 1997;25:107–112. doi: 10.2519/jospt.1997.25.2.107. [DOI] [PubMed] [Google Scholar]
  82. Trombold JR, Reinfeld AS, Casler JR, Coyle EF. The effect of pomegranate juice supplementation on strength and soreness after eccentric exercise. J Strength Cond Res. 2011;25:1782–1788. doi: 10.1519/JSC.0b013e318220d992. [DOI] [PubMed] [Google Scholar]
  83. Udani J, Singh B, Singh V, Sandoval E. BounceBackTM capsules for reduction of DOMS after eccentric exercise: a randomized, double-blind, placebo-controlled, crossover pilot study. J Int Soc Sports Nutr. 2009;6:14. doi: 10.1186/1550-2783-6-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  84. Wang H, Nair MG, Strasburg GM, Chang Y-C, Booren AM, Gray JI, DeWitt DL. Antioxidant and Antiinflammatory Activities of Anthocyanins and Their Aglycon, Cyanidin, from Tart Cherries. J Nat Prod. 1999;62:294–296. doi: 10.1021/np980501m. [DOI] [PubMed] [Google Scholar]
  85. Warren GL, Ingalls CP, Lowe DA, Armstrong RB. What mechanisms contribute to the strength loss that occurs during and in the recovery from skeletal muscle injury? J Orthop Sports Phys Ther. 2002;32:58–64. doi: 10.2519/jospt.2002.32.2.58. [DOI] [PubMed] [Google Scholar]
  86. Weber MD, Servedio FJ, Woodall WR. The effects of three modalities on delayed onset muscle soreness. J Orthop Sports Phys Ther. 1994;20:236–242. doi: 10.2519/jospt.1994.20.5.236. [DOI] [PubMed] [Google Scholar]
  87. Yackzan L, Adams C, Francis KT. The effects of ice massage on delayed muscle soreness. Am J Sports Med. 1984;12:159–165. doi: 10.1177/036354658401200214. [DOI] [PubMed] [Google Scholar]
  88. Yu H-S, Lee S-Y, Jang C-G. Involvement of 5-HT1A and GABAA receptors in the anxiolytic-like effects of Cinnamomum cassia in mice. Pharmacol Biochem Behav. 2007;87:164–170. doi: 10.1016/j.pbb.2007.04.013. [DOI] [PubMed] [Google Scholar]

Articles from Avicenna Journal of Phytomedicine are provided here courtesy of Mashhad University of Medical Sciences

RESOURCES