What is maral root
Maral root is also known as Rhaponticum carthamoides or Russian leuzea is a member of the Asteraceae family, is a perennial, herbaceous species naturally growing in the mountains of South Siberia, Middle Asia, and Mongolia 1. Maral root has been used for centuries in Siberian (eastern parts of Russia) folk medicine as a stimulant, mostly in the case of overstrain and weakness after illness 2. The root and rhizome extracts of Rhaponticum carthamoides possess a wide range of biological activities, including adaptogenic, antioxidant, cardioprotective, immunomodulatory, antihyperlipidemic, antihyperglycemic, and antimicrobial effects 2. These pharmacological properties are attributed to the presence of a variety of secondary metabolites including triterpenoids, polyacetylenes, sesquiterpene lactones, phenolic acids, flavonoids, and ecdysteroids with 20-hydroxyecdysone as the principal component 2.
Figure 1. Rhaponticum carthamoides (Maral root)
Rhaponticum carthamoides extracts from roots and rhizomes of this species are used in various dietary supplements or nutraceutical preparations to increase energy level and eliminate physical weakness or for recovery after surgery 3. Rhaponticum carthamoides is also known to have adaptogenic, immunomodulatory, anticarcinogenic, antioxidant, and antimicrobial activities 4. The antiradical effects of the aerial part of Rhaponticum carthamoides have already been evaluated by the most common radical-scavenging assays based on 2,2-diphenyl-1-picrylhydrazyl (DPPH) 5, 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays 6 and ferric reducing antioxidant power (FRAP) tests 7. The important antioxidant compounds of this plant are polyphenolic compounds such as flavonoids (e.g., quercetin, quercetagetin, luteolin, patuletin, and kaempferol) and phenolic acids (e.g., caffeic, chlorogenic, and ferulic acids and caffeoylquinic acid derivatives) 8.
Table 1. Bioactive compounds from maral root extracts – quantification of polyphenols and 20-hydroxyecdysone
Number | Compound | t R (min) | HR-L | HR-D | SR |
---|---|---|---|---|---|
mg g−1 DW | mg g−1 DW | mg g−1 DW | |||
1 | 3-O-Caffeoylquinic acid | 4.0 | 0.06 (4.80)a | — | 0.70 (0.34)b |
2 | 5-O-Caffeoylquinic acid | 7.4 | 5.12 (2.24)b | 1.96 (2.92)a | 18.26 (0.46)c |
3 | 4-O-Caffeoylquinic acid | 8.1 | 0.12 (5.03)b | 0.06 (2.35)a | 0.42 (0.95)c |
4 | 1,3-Di-O-caffeoylquinic acid | 10.2 | 0.22 (3.90)b | 0.12 (2.68)a | 1.21 (1.88)c |
5 | Quercetagetin hexoside | 10.7 | 0.96 (1.65) | — | — |
6 | Quercetin hexoside | 11.4 | 0.93 (1.71) | — | — |
7 | Quercetin hexoside | 11.9 | 0.52 (0.61) | — | — |
8 | 20-Hydroxyecdysone | 12.0 | — | — | 5.60 (1.36) |
9 | Luteolin hexoside | 12.1 | 0.27 (1.43) | — | — |
10 | Patuletin hexoside | 12.2 | 0.25 (1.24) | — | — |
11 | 3,4-Di-O-caffeoylquinic acid | 13.1 | 0.22 (0.95)b | 0.15 (3.67)a | 0.52 (2.62)c |
12 | 3,5-Di-O-caffeoylquinic acid | 13.4 | 3.08 (3.32)b | 1.92 (2.75)a | 8.47 (0.51)c |
13 | 1,5-Di-O-caffeoylquinic acid | 13.9 | 0.28 (3.28)b | 0.12 (3.01)a | 1.44 (2.75)c |
14 | 4,5-Di-O-caffeoylquinic acid | 14.1 | 1.97 (3.39)c | 1.23 (1.77)b | 1.04 (2.05)a |
15 | 1,4,5-Tri-O-caffeoylquinic acid | 15.3 | 1.38 (4.67)b | 1.08 (2.86)a | — |
16 | Tricaffeoylquinic acid derivative | 15.6 | 5.97 (4.88)c | 4.34 (2.09)b | 0.26 (2.18)a |
17 | Tricaffeoylquinic acid derivative | 16.4 | 0.66 (0.24)b | 0.47 (4.58)a | 2.88 (1.38)c |
Footnotes: Results are mean values of triplicate analyses calculated per DW of the plant material; the values in parentheses are relative standard deviations RSD (%); different superscript letter within the rows indicates significant differences in the mean values at P < 0.01 (one-way ANOVA by Tukey’s test).
HR-L: hairy roots cultured in the WPM liquid medium, in the presence of light.
HR-D: hairy roots cultured in the WPM liquid medium, in darkness.
SR: roots of 3-year-old soil-grown plants.
[Source 9]Ecdysterones (also known as ectysterone, 20 Beta-Hydroxyecdysterone, turkesterone, ponasterone, ecdysone, or ecdystene) are naturally derived phytoecdysteroids (i.e., insect hormones) 10. They are typically extracted from the herbs Rhaponticum carthamoides, Leuza rhaptonticum sp., or Cyanotis vaga. They can also be found in high concentrations in the herb Suma (also known as Brazilian Ginseng or Pfaffia). Research from Russia and Czechoslovakia conducted over the last 30 years indicates that ecdysterones may possess some potentially beneficial physiological effects in insects and animals 11. However, since most of the data on ecdysterones have been published in obscure journals, results are difficult to interpret. Wilborn and coworkers 12 gave resistance trained males 200 mg of 20-hydroxyecdysone per day during 8-weeks of resistance training. It was reported that the 20-hydroxyecdysone supplementation had no effect on fat free mass or anabolic/catabolic hormone status 12. Due to the findings of this well controlled study in humans, ecdysterone supplementation at a dosage of 200 mg per day appears to be ineffective in terms of improving lean muscle mass 10. While future studies may find some ergogenic value of ecdysterones, it is the view of the International Society of Sports Nutrition that it is too early to tell whether phytoecdysteroids serve as a safe and effective nutritional supplement for athletes.
The principal bioactive constituents of the whole Rhaponticum carthamoides plant are ecdysteroids, flavonoids, and phenolic acids. The aerial parts also contain sesquiterpene lactones of the guaianolide type, while the roots contain thiophene-based polyines 13. There have been two recent studies about antioxidant properties of Rhaponticum carthamoides. The first study dealt with the antioxidant screening of 12 medical plants and concludes that the extract of Rhaponticum carthamoides possesses high radical scavenging activity 14. The second study identifies 7 natural compounds of Rhaponticum carthamoides by means of on-line LC-DAD-SPE-NMR system. Nevertheless, incomplete evaluation of the radical scavenging or antioxidant activity of Rhaponticum carthamoides extracts or pure compounds has occured 15. The results of DPPH and FRAP tests evaluated 6-hydroxykaempferol-7-O-(6″-O-acetyl-β-D-glucopyranoside) as the most antioxidant active compound. The antioxidant activity of maral roots is currently under investigation.
- Skała E, Kicel A, Olszewska MA, Kiss AK, Wysokińska H. Establishment of Hairy Root Cultures of Rhaponticum carthamoides (Willd.) Iljin for the Production of Biomass and Caffeic Acid Derivatives. BioMed Research International. 2015;2015:181098. doi:10.1155/2015/181098. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354965/[↩]
- Chemistry and pharmacology of Rhaponticum carthamoides: a review. Kokoska L, Janovska D. Phytochemistry. 2009 May; 70(7):842-55. https://www.ncbi.nlm.nih.gov/pubmed/19457517/[↩][↩][↩]
- Skała E, Sitarek P, Różalski M, et al. Antioxidant and DNA Repair Stimulating Effect of Extracts from Transformed and Normal Roots of Rhaponticum carthamoides against Induced Oxidative Stress and DNA Damage in CHO Cells. Oxidative Medicine and Cellular Longevity. 2016;2016:5753139. doi:10.1155/2016/5753139. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789442/[↩]
- Kokoska L., Janovska D. Chemistry and pharmacology of Rhaponticum carthamoides: a review. Phytochemistry. 2009;70(7):842–855. doi: 10.1016/j.phytochem.2009.04.008 https://www.ncbi.nlm.nih.gov/pubmed/19457517[↩]
- Miliauskas G., van Beek T. A., de Waard P., Venskutonis R. P., Sudhölter E. J. R. Identification of radical scavenging compounds in Rhaponticum carthamoides by means of LC-DAD-SPE-NMR. Journal of Natural Products. 2005;68(2):168–172. doi: 10.1021/np0496901 https://www.ncbi.nlm.nih.gov/pubmed/15730237[↩]
- Miliauskas G., Venskutonis P. R., van Beek T. A. Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chemistry. 2004;85(2):231–237. doi: 10.1016/j.foodchem.2003.05.007[↩]
- Biskup E., Szynklarz B., Golebiowski M., Borsuk K., Stepnowski P., Lojkowska E. Composition and biological activity of Rhaponticum carthamoides extracts obtained from plants collected in Poland and Russia. Journal of Medicinal Plants Research. 2013;7(11):687–695.[↩]
- Skała E., Kicel A., Olszewska M. A., Kiss A. K., Wysokinska H. Establishment of hairy root cultures of Rhaponticum carthamoides (Willd.) Iljin for the production of biomass and caffeic acid derivatives. BioMed Research International. 2015;2015:11. doi: 10.1155/2015/181098.181098 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354965/[↩]
- Skała E, Kicel A, Olszewska MA, Kiss AK, Wysokińska H. Establishment of Hairy Root Cultures of Rhaponticum carthamoides (Willd.) Iljin for the Production of Biomass and Caffeic Acid Derivatives. BioMed Research International. 2015;2015:181098. doi:10.1155/2015/181098 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354965/[↩]
- Kreider RB, Wilborn CD, Taylor L, et al. ISSN exercise & sport nutrition review: research & recommendations. Journal of the International Society of Sports Nutrition. 2010;7:7. doi:10.1186/1550-2783-7-7. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853497/[↩][↩]
- Toth N, Szabo A, Kacsala P, Heger J, Zador E. 20-Hydroxyecdysone increases fiber size in a muscle-specific fashion in rat. Phytomedicine. 2008;15(9):691–8. doi: 10.1016/j.phymed.2008.04.015[↩]
- Wilborn C, Taylor L, Campbell B, Kerksick C, Rasmussen C, Greenwood M, Kreider R. Effects of methoxyisoflavone, ecdysterone, and sulfo-polysaccharide supplementation on training adaptations in resistance-trained males. Journal of the International Society of Sports Nutrition. 2006;3(2) doi: 10.1186/1550-2783-3-2-19 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2129166/[↩][↩]
- Opletal L, Sovova M, Dittrich M, Solich P, Dvorak J, Kratky F, Cerovsky J, Hofbauer J. Phytotherapeutic aspects of diseases of the circulatory system. 6. Leuzea carthamoides (WILLD.) DC: the status of research and possible use of the taxon. Ceska Slov Farm 1997; 46: 247–255[↩]
- Miliauskas G, Venskutonis PR, van Beek TA. Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chem 2004; 85: 231–237[↩]
- Miliauskas G, van Beek TA, de Waard P, Venskutonis RP, Sudhoolter EJR. Identification of radical scavenging compounds in Rhaponticum carthamoides by means of LC-DAD-SPE-NMR. J Nat Prod 2005; 68: 168–172[↩]