1. Introduction
Adaptogens are pharmacologically active compounds or plant extracts from different plant classes (for example: Araliaceae—Panax ginseng, Eleutherococcus senticosus, Asteraceae—Rhaponticum carthamoides, Crassulaceae—Rhodiola rosea, and Schisandraceae—Schisandra chinensis) [1,2,3]. They have the ability to enhance the body’s stability against physical loads without increasing oxygen consumption. The intake of adaptogens is associated not only with the body’s better ability to adapt to stress and maintain/normalize metabolic functions, but also with better mental and physical performance [1,2,3].
There are two main classes of adaptogens. The first class includes plant adaptogens, while the other includes synthetic adaptogens, which are also called actoprotectors.
Although plant adaptogens have been used by people since ancient times, the term “adaptogen” is relatively young—it was introduced in 1947 by the Soviet scientist Lazarev [1,4]. It defines adaptogens as substances that cause non-specific resistance of the living organisms [1,2,4]. Adaptogens have a positive effect on humans and animals. The use of plant adaptogens has a rich history. They have been used by man for hundreds of years in different parts of the world, while data on the use of the first synthetic adaptogen, bemethyl, date back to the 1970s. Bemethyl was introduced in the 1970s by Professor Vladimir Vinogradov. Since then, numerous synthetic adaptogens have been developed: bromantane, levamisole, aphobazole, chlodantane, trekrezan. Their intake is associated not only with increased physical and mental resistance, but also with vasodilation and decreased blood sugar and lactate [3]. They are widely used in sports medicine, but since 2009, WADA has included bromantane in the prohibited list and since 2018, bemethyl has also been included in the monitoring program of WADA [5,6].
In 1980, the scientists Breckham and Dardimov found that adaptogens increase the body’s resistance not only to physical but also to chemically and biologically harmful agents [1,2,7], which further expands the potential of their use.
Breckham and Dardimov systematized the plants with adaptogenic properties. These are: Panax ginseng, Eleutherococcus senticosus, Rhaponticum carthamoides, Rhodiola rosea, and Schisandra chinensis [7].
Although plant adaptogens have been used for centuries, their effects continue to be studied to this day. They also have promising potential for wider applications in the future.
The biological effects of plant adaptogens are related to the complex of biologically active compounds they contain. Plant adaptogens have very rich phytochemical composition. Some of the most important phytochemicals with adaptogenic properties are: triterpenoid saponins (in Panax ginseng—ginsenosides; in Eleutherococcus senticosus—eleutherosides); phytosterols and ecdysone (in Rhaponticum carthamoides); lignans (in Schisandra chinensis); alkaloids; flavonoids, vitamins, etc. [4,8,9].
The mechanism of action of the plant adaptogens is complex and is not fully understood. Recent studies report that the intake of plant adaptogens like extracts of Eleutherococcus senticosus root, Schisandra chinensis root, Rhodiola rosea root is associated with affecting the hypothalamic—pituitary—adrenal axis [10] and some stress mediators [11]. Moreover, the intake of such extracts affects nitric oxide levels, lactate levels, blood glucose levels, cortisol levels, plasma lipid profile, hepatic enzymes, etc. [8,11,12,13,14].
Current and potential uses of these medicinal plants are associated with mental diseases and behavioural disorders, cognitive function and stress-induced diseases (anxiety, cardiovascular diseases, diabetes) [4,9,15,16,17,18,19,20]. The intake of plant adaptogens is not associated with serious side effects [20,21].
The aim of our study is to evaluate the data about the use of adaptogens in the past and the future perspectives of their use.
2. Materials and Methods
The first step of the screening process included identifying eligible studies. An expanded search for articles without language restrictions was conducted on the following databases: Google Scholar, PubMed, and Web of Science. In the search process, the following search key words were used: “adaptogens”, “actoprotectors”, “plant adaptogens”, “Panax ginseng”, “Eleutherococcus senticosus”, “Schisandra chinensis”, “Rhodiola rosea”, “Rhaponticum carthamoides”, “Leuzea carthamoides”, “ginseng adaptogen properties study”, “Eleutherococcus senticosus adaptogen properties study”, “randomized controlled study Eleutherococcus senticosus”, “Leuzea carthamoides adaptogen properties study”, “Rhaponticum carthamoides adaptogen properties study”, "ecdysterone adaptogen properties study”, “20-hydroxyecdisone adaptogen study”, “ecdysterone from Leuzea adaptogen studies”, “Leuzea carthamoides adaptogen properties in rats”, “performance gain Rhaponticum carthamoides”, “Rhodiola rosea in sport”, “Rhodiola rosea adaptogen properties study”, “Schisandra chinensis in sport”, “Schisandra chinensis randomized study”, “Schisandra chinensis adaptogen properties study”, and “Schisandra chinensis mice study”.
Further records concerned the history of plant adaptogens, botanical and phytochemical characteristics, and application of adaptogens.
In the second step, we followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) presented in Figure 1 [22], guide for a systematic review.
In the third step, the relevant studies were chosen based on exclusion and inclusion criteria. The exclusion criteria were: (i) articles written in a language other than English or Russian; (ii) webinars or blogs; (iii) articles with irrelevant topics, and (iv) lack of data information. Inclusion criteria were: (i) human studies; (ii) animal studies, and (iii) studies investigating the impacts of adaptogens.
During the fourth step, the selected full articles were read and identified.
In total, 56 studies were selected and included in the present review.
3. Results and Discussion
3.1. Panax Ginseng
The first evidence of the use of Panax ginseng (Panax ginseng C.A. Mey.) dates back more than 2000 years [23]. In the past, the stems, leaves, and mainly the roots of ginseng were used. Extracts were prepared and used to maintain homeostasis in the human body, treat fatigue and weakness, increase immune protection, and treat hypertension, diabetes type 2, and erectile dysfunction [2,23,24,25,26]. In Chinese traditional medicine, ginseng extracts have also been used as nootropic agents and as a tonic [24,25,26]. The exact mechanism of adaptogenic action of Panax ginseng is unknown, but it is supposed that it affects the hypothalamic-pituitary-adrenal axis in Figure 2 and the antioxidant effect [24,27,28,29].
Panax ginseng is an example of a medicinal plant, widely used in ancient times, but also with great application today. It is also one of the plants defined as a natural adaptogen.
Panax ginseng has a rich botanical phytochemical composition. Today, more than 200 substances isolated from Korean ginseng are known, ginsenosides predominantly: Ra1, Ra2, Ra3, malonyl-G-Rb1, malonyl-G-Rb2, malonyl-G-Rc, malonyl-GRd, Rs1, Rs2, Rs3, Rg3, Rg5, Rh2, K-R2, Rf, Rf2, 20(R)-G-Rg2, Rg6, 20(R)-G-Rh1, 20(E)-G-F4, Rh4, K-R1, and poly-acetyleneginsenoside-Ro [30].
It is considered that the adaptogenic properties of Panax ginseng extract are due to the ginsenosides [27].
Nowadays, numerous products containing ginseng extracts are available. Most of these products are sold as food supplements but there are also many over-the-counter medicines. Ginseng radix is included in European Pharmacopeia and in the US Pharmacopeia. The principal root has a cylindrical form, sometimes branched, up to about 20 cm long and 2.5 cm in diameter. Its surface is pale yellow/cream in white ginseng, while it is brownish-red in red ginseng. The rootlets, which are many in the lower part of white ginseng, are usually absent in red ginseng. Reduced to a powder, it is light yellow. Ginseng dry extract is produced from the root by a suitable procedure using a hydroalcoholic solvent equivalent in strength to ethanol. The main compounds that can be detected in the extract are: ginsenoside Rg1, ginsenoside Re, ginsenoside Rf, ginsenoside Rb1, ginsenoside Rc, ginsenoside Rd, ginsenoside Rb2 [31].
Although the extract has been used for more than two millenniums, there are a limited number of clinical studies that have investigated the benefits or the side effects of its use. More double-blind randomized studies are needed to be performed.
In Table 1, we have summarized the main benefits of the Panax ginseng extract intake.
The data suggest that an intake of Panax ginseng extracts is associated with ergogenic effects and enhanced muscle strength. The inclusion of Panax ginseng in the diet of athletes would help increase the body’s physical resilience and help the body recover between workouts.
Intake of Panax ginseng extract is associated also with improved plasma lipid profile and blood glucose level. Extracts of Panax ginseng might be included in the diet of patients with cardiovascular diseases, hyperlipidemia, and diabetes. Extracts from the plant not only increase cognitive function and memory functions, but also improve sleep and fatigue.
We did not find multicenter randomized double-blind studies including the intake of Panax ginseng. For better exploration of the benefits and future applications of the Panax ginseng extract, multicenter randomized double-blind studies should be performed. The plant has a great potential to be included in medicines for treatment of different conditions.
The intake of Panax ginseng extract is not associated with serious side effects [21,32,33,34,35,36,37,38,39,40,41]. The safety of the extract is another benefit to be considered.
3.2. Eleutherococcus Senticosus
Siberian ginseng (Eleutherococcus senticosus ((Rupr. and Maxim.) Maxim.) was first described by Porfiry Kirilov in the 19th century [42]. Its adaptogenic effects were widely studied in Russia between 1960 and 1970 [43]. The first data on the use of plant extracts in athletes were reported from Russia. Today, plant extracts are used not only by athletes around the world, but also by many other consumers who are not actively involved in sports.
The phytochemical composition consists of phenylpropanoid—syringin; lignans—sesamin; saponins—daucosterol; coumarins, terpenoids, flavonoids, organic acids, and vitamins [44,45]. Extracts of Eleutherococcus senticosus root are obtained, stimulating the immune system, influencing adaptation against external factors, improving mental and physical conditions and memory functions, and have a hypoglycaemic effect and are anti-inflammatory [13,45,46]. Eleutherococcus senticosus is thought to exert its adaptogenic effects by influencing the hypothalamic-pituitary-adrenal axis [44].
Most of the extracts of Eleutherococcus senticosus are prepared by the roots. The rhizome of Eleutherococcus senticosus is described in European pharmacopeia. The rhizome has a diameter of 1.5 to 4 cm and an irregular cylindrical shape. The surface is longitudinally wrinkled with grayish-brown to blackish-brown colour [47].
Although Eleutherococcus senticosus were described a few hundred years ago, research into its use continues. In Table 2, we summarized results of studies with Eleutherococcus senticosus.
The data suggest that the intake of Eleutherococcus senticosus supports the physical activity, weight reduction, mental health, and fatigue. Extracts of the plant can be used only for fatigue, but also in the case of disturbed sleep.
The intake of Eleutherococcus senticosus extract may help to increase the cognitive function. Siberian ginseng extract could be included in the diet of patients with hyperlipidemia because it has a beneficial effect on the lipid profile. There is a potential for development of medicinal products containing Eleutherococcus senticosus extract to be taken by patients with various pathologies such as: obesity, overweight, hyperlipidemia, etc. New nootropic drugs containing a standardized plant extract could also be registered.
We did not find multicenter randomized double-blind studies that included the intake of Siberian ginseng. For better exploration of the benefits and future applications of the Eleuterococcus senticosus extract, multicenter randomized double-blind studies should be performed. The plant has a great potential to be included in medicines for treatment of different conditions; moreover, the intake of Eleuterococcus senticosus extract is not associated with serious side effects [46,48,49,50,51,52,53,54,55].
3.3. Rhaponticum Carthmoides
Rhaponticum carthamoides (Rhaponticum carthamoides IIjin.) is a perennial herb which has been used for centuries in Russia, China, and Mongolia [14]. The plant is also known as Leuzea. Extracts of the plant have been used to treat weakness [14,56], lung diseases, kidney diseases, fever, and angina [57].
In 1969, Brekhman and Dardymov classified this plant as an adaptogen [14]. The use of products containing Rhaponticum carthamoides root extract has increased in recent decades. The extract has many beneficial effects on humans like: enhanced physical endurance and performance, anabolic effect, hypocholesterolemic effects, neuroprotective effect, antidiabetic properties, anti-oxidative, and increased immunity [14,57]. The mechanism by which ecdysteroids act is binding with signal transduction pathways, rather than with steroid and estrogen receptors [58].
In the 1970s, the extracts from Leuzea showed beneficial effects in athletes and their use became a routine practice in the training of many athletes. The intake of Leuzea extract increases the body’s adaptation to various factors, which can be defined as stress for the body [14,57] and at the same time has a good level of safety.
The phytochemical composition of Rhaponticum carthamoides is rich of ecdysteroids and phenols. The main ecdysteroid is 20-hydroxyecdysone in Figure 3 [14]. The adaptogenic properties of the extract are related mainly to its presence [14]. Other components of the phytochemical composition are phenols and essential oil [14].
20-hydroxyecdysone has a typical steroidal structure. A recent study, funded by WADA and conducted in 2019, reported 20-hydroxyecdisone as a non-conventional anabolic agent, which can significantly increase the muscle mass. A significant dose-responsive anabolic effect of 20-hydroxyecdysone was reported [59].
In 2020, 20-hydroxyecdysone was included in the WADA monitoring program and it is very likely that the substance will be included in the prohibited list in the next few years [60]. In the past few years, other adaptogens were included in WADA’s prohibited list and monitoring program, because these compounds were considered to improve the performance of the athletes. Bromantane is included in the prohibited list as a non-specified stimulant. Since 2018, bemethyl is monitored by WADA, but it is still not included on the prohibited list [5,6]. The main difference between 20-hydroxyecdysone and these two compounds is that 20-hydroxyecdysone is a natural compound while the other two are synthetic adaptogens. The main reason 20-hydroxyecdysone is monitored by WADA is that the intake of this compound improves the performance of athletes. Nowadays, food supplements containing Leuzea (which contain 20-hydroxyecdysone) are often included in the supplementation of professional athletes.
Table 3 presents studies related to the use and effects of Rhaponticum carthamoides.
We expanded our search with animal studies; found results are presented in Table 4.
The data suggest that intake of Rhaponticum carthamoides extracts is associated with anabolic effects—increased body mass weight and enhanced muscle strength. Other important benefits are improved mental endurance and improved plasma lipid profiles. Improvement of cardiac and cognitive functions has also been reported.
Because of improvement in cardiac functions, the Rhaponticum carthamoides extract might be especially useful for patients with cardiovascular diseases.
Despite the benefits of the extract use, the studies on humans are limited in number and not sufficient for a more complete and comprehensive assessment.
The anabolic effects were also reported in animal studies. The data from animal studies suggests that application of Rhaponticum carthamoides is also associated with a neuroprotective effect.
The intake of Rhaponticum carthamoides is not associated with serious side effects [19,59,60,61,62,63,64,65,66,67,68,69,70,71,72].
The data obtained from human and animal studies about synergetic anabolic effect of Rhaponticum carthamoides and Rhodiola rosea are contradictory. Further studies are needed to confirm the synergetic effect of these adaptogenic plants.
For better exploration of the benefits and future applications of the Rhaponticum carthamoides extract, more in vivo studies and multicenter randomized double-blind studies should be performed.
3.4. Rhodiola rosea
In traditional medicine, its (Rhodiola rosea L.) applications are described as an adaptive agent that increases physical endurance, affects fatigue, depression, and disorders of the nervous system. It has been used in the past in Asia to treat flu and colds, and there is reported use in tuberculosis. In the Scandinavian part of Europe, plant extracts have been used to increase physical endurance [73].
Six groups of compounds predominate in the phytochemical composition of the plant: phenylpropanoids, phenylethanol derivatives, flavonoids, phenolic acids, and mono- and triterpene [74].
The main phenylethanol derivatives are salidroside (rhodioloside), para-tyrosol, and phenylpropanoid-rosavin. These are also responsible for the adaptogenic and ergogenic effects of Rhodiola rosea [8,73,75].
The adaptogenic effect of Rhodiola rosea is associated with activation of the cerebral cortex by increasing norepinephrine and serotonin levels. In addition, it affects the hypothalamic-pituitary-adrenal axis, reducing the levels of corticotropin-releasing hormones, corticotropin, cortisol, and epinephrine [29,73,76].
Studies of Rhodiola rosea began with Dioscorides and continues nowadays. In Table 5, we summarized beneficial effects of Rhodiola rosea based on studies.
The data suggest that the intake of the extract of Rhodiola rosea is associated with antioxidant and adaptogen properties. Rhodiola rosea extract might be used not only for overcoming the fatigue but might be included in the diet of people with heart diseases, because of the beneficial effect on heart rate and muscle contractions. The use of plant extracts is recommended for sleep disorders and anxiety. The hepatoprotective effect of the plant determines the use of its extract in liver diseases. Improving physical strength during exercise and recovery after training are the reasons why Rhodiola rosea extracts are also taken by athletes as a supplement to their diet.
The intake of Rhodiola rosea is not associated with serious side effects [77,78,79,80,81,82,83,84,85,86].
For better exploration of the benefits and future applications of the Rhodiola rosea extract, more multicenter randomized double-blind studies should be performed. The plant has a great potential to be included in medicines for treatment of different conditions.
3.5. Schisandra chinensis
Schisandra chinensis (Schisandra chinensis (Turcz.) Bail) is first described in the book Shen Nong Ben Cao Jing, around 200 AD, as a remedy for cough and asthma [87]. In the past, Schisandra chinensis fruits and seeds were used to improve night vision, reduce hunger, thirst, and exhaustion. In 1960 in Russia, the adaptogenic properties of the plant were proven [88]. The fruits of Schisandra chinensis are used today [87,88,89,90].
According European Pharmacopoeia, Schisandra berry is more or less spherical, up to 8 mm in diameter. It could be red/reddish-brown/blackish, it could be covered in a whitish frost. It has a strongly shriveled pericarp. The seeds are only 1 or 2, yellowish-brown and lustrous. The seed-coat is thin [91].
For production of the extract, the fruit should be reduced to a powder. The colour of powder should be reddish-brown.
The Schisandra fruit has a complex phytochemical composition in which the lignans are the major characteristic constituents. Five classes of different lignans are found in the fruits of Schisandra: dibenzocyclooctadiene lignans (type A), spirobenzofuranoid dibenzocyclooctadiene lignans (type B), 4-aryltetralin lignans (type C), 2,3-dimethyl-1,4-diarylbutane lignans (type D), and 2,5-diaryltetrahydrofuran lignans (type E) [88].
The adaptogenic properties of Schisandra chinensis are due to the lignin complex, mainly dibenzocycloocstadiene lignans, the main schisandrin [92,93]. Schizandrin was isolated and identified for the first time by N.K. Kochetkov in 1961 [88,92,93].
One of methods for identification of the plant, described in the European Pharmacopeia, involves a TLC technique with identification of γ-Schisandrin in Figure 4.
Several studies reported that some lignans (gomisin A, gomisin G, schizandrin, and schisanhenol) possess antitumor bioactivities [94,95,96,97,98].
The Schisandra fruit, particularly the seeds, contains many volatile compounds as well: α-ylangene, α-cedrene, β-chamigrene, and β-himachalene [99,100].
From Schisandra chinensis fruit are also isolated polysaccharides, glycosides (dihydrophaseic acid-3-O--d-glucopyranoside, benzyl alcohol-O--d-glucopyranosyl (1→6)--d-glucopyranoside and benzyl alcohol-O--d-glucopyranosyl (1→2)--d-glucopyranoside), organic acids (vitamin C, malic acid, citric acid, and tartaric acid), and vitamin E. [12,87,101,102]. In small quantities, the fruit of Schisandra chinensis contained flavonoids such as rutine [103]. Preschsanartanin, schintrilactones A–B, schindilactones A–C, and wuweizidilactones A–F are the new isolated triterpenoids from Schisandra chinensis fruit [88].
All of phytochemicals determined beneficial effects such as: cytotoxic, antioxidant, neuroprotective, hepatoprotective, increased physical strength, stress-protective, anti-inflammatory [12,88,104]. The adaptogenic effect of Schisandra chinensis is associated with the antioxidant effect and the influence on the hypothalamic-pituitary-adrenal axis by lowering the level of corticotropin-releasing hormone [29,76].
Research on the effects of Schisandra chinensis continues.
In Table 6, we present summarized data about beneficial effects of Schisandra chinensis.
Discovered trials are insufficient to summarize the use of Schisandra chinensis. We expanded our search with animal studies, the results found are presented in Table 7.
The data from animal and human studies suggest that the application of extract of Schisandra chinensis is associated with adaptogenic, antioxidant properties, tonic, and stress-protective effect.
The intake of plant extract can improve memory and concentration. The plant extract has serious potential to be included in medicinal products for use in the treatment of patients with hypercholesterolemia or patients with cardiovascular disease. Of course, the application of the extract would have a number of benefits in healthy patients due to its pronounced antioxidant properties.
The positive effect of the plant on blood sugar and liver enzymes suggests the inclusion of Rhodiola rosea extracts in the treatment of patients with diabetes and liver disease. In recent decades, Schisandra chinensis extract has been taken by athletes to increase physical activity and the body’s adaptation to stress.
The studies on humans are limited in number, so a full assessment of the effects is difficult to make.
The intake of Schisandra chinensis is not associated with serious side effects [105,106,107,108,109,110,111,112,113,114,115,116].
For a better exploration of the benefits and future applications of the Schisandra chinensis extract, more in vivo studies and multicenter randomized double-blind studies should be performed.
4. Conclusions
The natural adaptogens have the ability to increase the body’s resistance to stress changes caused by different types of stressors. Unlike the synthetic adaptogens, the natural are extracts with an extremely rich phytochemical composition. Their adaptogenic properties are not due to one molecule, but to the combination of different substances. The use of natural adaptogens by humans has a rich history—they have been used in recovery from illness, physical weakness, impaired mental function, and other conditions. For about 50 years, plant adaptogens have been used by professional athletes due to their high potential to increase the body’s resilience and improve physical endurance. Nowadays, some of the most used plant adaptogens are Panax ginseng, Eleutherococcus senticosus, and Rhaponticum carthamoides. Since 2020, ecdysterone, which is rich in Leuzea extract, has been included in WADA’s monitoring program, with prospects for inclusion in the prohibited list. Studies examining the benefits of using extracts of Rhodiola rosea, Eleutherococcus senticosus, Panax ginseng, Schisandra chinensis and Rhaponticum carthamoides are a limited in number. However, there are potentials for the inclusion of the extracts of these plants in medicinal products aimed at treating chronic fatigue, cognitive impairment, as well as boosting immune defenses. Double-blind randomized multicenter studies would be extremely valuable in evaluating the use of the extracts in patients with cardiovascular disease, in patients with compromised immunity, and in patients with chronic fatigue.
Author Contributions
Conceptualization, V.T., K.I. and S.I.; data curation, V.T. and S.I.; writing—original draft preparation, V.T., K.I., C.D., V.N., D.K.-B. and S.I.; writing—review and editing, K.I., C.D., V.N., D.K.-B. and S.I.; visualization, V.T., K.I., V.N., D.K.-B. and S.I.; supervision, K.I. and C.D. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figures and Tables
Enlarge this image.Figure 1. PRISMA 2020 flow diagram for new systematic reviews which included searches of databases and registers only.
Panax ginseng studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Evaluation of the effects on subjective mood and memory of a single and sub-chronic Panax ginseng dose. | Thirty adults, aged 22.87 ± 4.01 years, |
Improved calmness, mood, |
[21] |
| Examine the effects of Panax ginseng on the lipid profile. | Eight men, aged 21.1 ± 2.1 years, |
Decreased levels of serum total |
[32] |
| Examine the effects on |
Twelve men, aged 20–24 years, |
Increased endurance time, blood |
[33] |
| Evaluation of benefits on |
Fifty-two women, aged 18–50 years, |
Reduced fatigue. |
[34] |
| Examine the effects of Panax ginseng on work performance. | Nineteen women, 21–35 years of age, |
No change in maximal work |
[35] |
| Evaluation of the efficacy of a combination of Panax ginseng and vitamins on physical and mental stress. | One-hundred and fourteen women and men, aged 30–60 years, participated in the study. There were 59 participants who received 200 mg daily of ginseng dried extract and vitamins; 55 were in the placebo group. |
Increased quality of life, |
[36] |
| Evaluation of the efficacy of Panax ginseng extract on physical and mental |
Fifteen men, aged 19.07 ± 0.62 years, |
Increased lactate levels. No change in VO2 and heart rate. Decreased cortisone levels and no change in testosterone levels. | [37] |
| The influence of Panax ginseng on cortisol, growth hormone, and lactate. | Ten women, aged 23.4 ± 0.69 years, |
Increased cortisol. No change in |
[38] |
| Evaluation of the effects of Panax ginseng on sleep. | Fifteen men, aged 19–25 years, participated in the study. There were eight participants who received |
Increased deep sleep. |
[39] |
| Evaluation of anti-fatigue |
Eighty-eight men and women 20–60 years of age participated in the study. There were |
Reduced the severity of fatigue. |
[40] |
| Assessment of an ergogenic effect on Malaysian population of Panax ginseng in humid and hot conditions. | Nine men, 25.4 ± 6.9 years of age, participated in the study. In the first trial, they had an intake of 200 mg of Panax ginseng one hour before an exercise test and in the second trial, they had an intake placebo. | Decreased lactate, plasma glucose, plasma insulin. |
[41] |
Eleutherococcus senticosus studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Examine the effects of Eleutherococcus senticosus extract on |
Six men, aged 21–22 years, participated in the study. They were in the control group, placebo group, and the group that received 2 mL |
Increased maximal oxygen uptake, oxygen pulse, total work, and |
[46] |
| Examine the effects of |
Twenty men and women, aged 37 ± 8 years, participated in the study. There were 10 participants who received 3.4 mL Eleutherococcus senticosus |
No changes in heart rate, VO2, lactate. | [48] |
| Assessment of the effects of Eleutherococcus senticosus on |
Nine men, aged 19 ± 2.1 years, participated in the study. The participants received 800 mg daily of Eleutherococcus senticosus or placebo. |
Decreased blood glucose levels. |
[49] |
| Assessment of the impact of Eleutherococcus senticosus |
Twenty volunteers, aged over 65 years, |
Improved mental health and social functioning, but prolonged use |
[50] |
| Assessment of the influence of Eleutherococcus senticosus |
Forty-six men and women, aged 23–73 years, participated in the study. There were 31 participants who |
Decreased total cholesterol, LDL, |
[51] |
| Examine the effects of a dietary supplement containing |
Eighty-seven volunteers, aged 27–63 years, participated in the study. There were 44 participants who |
Decreased fatigue score and |
[52] |
| Evaluate the effects of |
One-hundred and thirty women and men, aged 30–50 years, participated in the study. There were 49 participants who received 120 mg/day of dry Eleutherococcus senticosus extract, |
Improvement in fatigue, exhaustion, sleep, and restlessness. | [52] |
| Examine physiological reactions from the intake of Eleutherococcus senticosus on cyclists. | Nine men, aged 28 ± 2 years, participated in the study. The participants received 1200 mg per day of Eleutherococcus senticosus extract for |
No difference in respiratory |
[53] |
| Evaluate the effects of |
In the second series of study, |
Decreased body weight. Increased physical endurance and |
[54] |
Rhaponticum carthamoides studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Evaluation of the effects of an increased dose of Rhaponticum carthamoides during the training |
Twenty women, aged 25–40 years, |
Decreased body weight. Increased physical endurance and performance. Improvement of cardiac and cognitive function. | [19] |
| Examine the effect of ecdysterone-containing products on sport physical exercises. | Forty-six men, aged 25.6 ± 3.7 years, |
Ecdysterone increased body weight, muscle mass. Increased power and strength of performance. Without negative effects on creatinine, glutamate–oxaloacetate transaminase, gamma-glutamyl transferase, and glutamate–pyruvate transaminase. Did not affect steroid profile. | [59] |
| Evaluation of the |
Twenty-six women aged 18–22 years |
Increased VO2 lactate, |
[61] |
| Evaluation of the |
No information—number of participants. The age of the participants ranged between 27–58 years. Participants received 2–3 g Rhaponticum carthamoides tea, infusion, tincture, |
Increased resistance to disease, physical, and mental endurance. | [62] |
| Assessment of effects |
Forty-five men, aged 20.5 ± 3 years, |
No change in training adaptation and in anabolic and catabolic effect |
[63] |
| Evaluation of the effects of the combination of Rhaponticum carthamoides and Rhodiola rosea on |
Twenty-seven men, aged 22.3 ± 4.1 years, participated in the study. The participants received a 350 mg tablet which contains 70:30 Rhaponticum carthamoides extract and |
No change in muscle strength |
[64] |
Rhaponticum carthamoides animal studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Evaluating Rhaponticum carthamoides effects—growth, |
For study, 60 rats were used, divided into |
Increased growth and |
[65] |
| Evaluating Rhaponticum carthamoides effects on lipid profile on rats with cerebral ischemia. | For the study, 18 rats were used and |
Decreased lysophospholipids in erythrocyte membrane. Increased total lipids and phospholipids. | [66] |
| Examine ecdysterone |
For the study, 35 rats were used, aged |
Removed glutamatergic excitotoxicity. Neuroprotective effect. | [67] |
| Examine the anti-obesity effect of 20-hydroxyecdysone. | For the study, 60 rats were used, aged |
Decreased LDL. Increased muscle mass. No changes in |
[68] |
| Examine anabolic effects of |
For the study, 1000 quails were used. They were divided into six groups—the control group, four groups that had received a standard diet |
Increased body mass and growth. | [69] |
| Examine anabolic effects of |
For the study, 200 quails were used; 160 were in the control group. There were 10 that received 20 mg/kg, |
Increased growth. Anabolic effect. | [70] |
| Examine the improving memory effect of |
For the study, 80 rats were used, divided into two groups: 10 were in the control group, 70 in the experimental group. |
Induced superoxide dismutase (SOD), catalase, glutathione peroxidase (GSH-Px), and glutathione |
[71] |
| Examine the effects of Rhapoticum carthamoides, Rhodiola rosea, and their combination on resistance exercise and mechanical power. | For the study, 56 rats were used. Rats were divided into seven groups, eight rats in each group: control group, a group that received only Rhodiola rosea extract, a group that received only Rhaponticum carthamoides extract, and four groups that received a combination of Rhaponticum carthamoides and Rhodiola rosea extracts in different quantitative ratios. | Rhaponticum carthamoides extract |
[72] |
Rhodiola rosea studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Studying the effects of short-term supplementation with |
Eleven women, aged 19.4 ± 0.8 years, |
Increased anaerobic capacity, |
[77] |
| Examine hormonal and oxidative stress of Rhodiola rosea supplementation and the effects on mental and physical performance. | Twenty-six men participated in the study. |
Improved reaction and response time. Increased antioxidant capacity. Without changes in hormone profile and endurance exercise capacity. | [78] |
| Examine the levels of inflammatory C-reactive protein and creatinine kinase in blood after intake of Rhodiola rosea. | Thirty-six volunteers aged 21–24 years |
Increased levels of C-reactive |
[79] |
| Examine the effects and safety of Rhodiola rosea extract for |
There were 101 women and men, aged 30–60 years, who |
Improved mood, stress symptoms, and quality of life. | [80] |
| Examine the effects of a single dose of standardized Rhodiola rosea extract. | There were 121 men aged 19–21 years participated in the study; 41 participants received 370 mg dry |
Improvement in the |
[81] |
| Examine the effects of |
Eighty-nine women and men, aged 18–70 years, participated in the study. Thirty-one participants received 340 mg/day extract of Rhodiola rosea, |
Improved in overall depression, insomnia, somatization, and |
[82] |
| Evaluating the changes of |
There were 48 men and women, aged 25–60 years, who participated in the study. Twenty-four participants |
Increased myoglobin, creatine phosphokinase, aspartate |
[83] |
| Examine the effects of Rhodiola rosea supplementation on |
Twenty-two men aged 20.4 ± 1.2 participated in the study. Eleven of them had an intake of |
Decreased levels of superoxide |
[84] |
| Examine the effects of chronic intake of Rhodiola rosea on |
Fourteen men, aged 25 ± 5 years, participated in the study. All of the participants received a |
Decreased free fatty acids levels, blood lactate, and creatinine kinase levels. No change in VO2max. | [85] |
| The efficacy of Rhodiola rosea in generalized anxiety disorder. | Ten men and women, aged 34–55 years, |
Decreased scores in Hamilton |
[86] |
Schisandra chinensis studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Examine the effects of |
Forty-five volunteers aged 61.9 ± 8.4 years |
Decreased lactate levels. |
[105] |
| Examine the effects of |
Thirty-six women aged 40–70 years participated in the study. Eighteen participants received Schisandra chinensis extract 748 mg twice a day for 6 weeks; 18 were in the placebo group. |
Decreased hot flushes, sweating, and heart rate. | [106] |
| Examine the effects of |
Twenty-eight women participated in the study. Thirteen participants received 6.7 g/day dried |
Decreased blood glucose, |
[107] |
Schisandra chinensis animal studies.
| Study Objectives | Study Design | Main Results | References |
|---|---|---|---|
| Examine the anti-athletics |
For the study, eight mice were used, divided into five groups—the control group, low-dose group—treated with 15 mg/kg Schisandra chinensis aqueous extract; the medium-dose group—treated with |
Prevented an increase of lactate levels and blood urea nitrogen. Increased blood |
[108] |
| Examine Schisandra chinensis |
For the study, 45 rats were used, aged 6 weeks old. |
Decreased blood glucose levels, cortisol, and interleukins |
[109] |
| Examine Schisandra chinensis |
For the study, there were 60 rats used, aged 4 weeks, and 20 mice, aged 6 weeks. They were divided into |
Decreased TG and LDL levels. Increased HDL. | [110] |
| Examine the effect of Schisandra chinensis on mice with hyperlipidemia. | For the study, 48 mice were used. There were 24 mice in the control group and 24 received 100 mg/kg/day Schisandra chinensis lignans for 4 weeks. | Decreased TC, TG, LDL. |
[111] |
| Examine Schisandrine B effects on hepatic glutathione |
For the study, mice were used, with no information for number of mice. They were divided into five groups. Control group and the rest had received Schisandrine B 1 to 4 mmol/kg for 3 days; after that, they were threatened with CCl4 0.1 mL/kg. | Decreased glucose-6-phosphate dehydrogenase, gama-glutamilcysteine synthetase, and Se-glutathione peroxidase. Increased hepatic gluthatione S-transferase and glutathione reductase. | [112] |
| Examine the preventive effect of Schisandrine B on scopolamine-induced dementia in mice. | For the study, 30 mice were used, aged 12–14 weeks. They were divided into groups—the control group, three groups that had received |
Prevented scopolamine-induced oxidative stress. Prevented the decrease of acetylcholine levels. | [113] |
| Evaluated muscle-protective |
For the study, 48 mice were used, aged 10 months. They were divided into six groups with eight mice in each group. The first group received distilled water. |
Decreased creatine, creatine |
[114] |
| Examine the immunostimulatory effect of polysaccharides from Schisandra chinensis. | For the study, 50 mice were used, divided into five groups. Three of the groups were administered with 50, 100, or 200 mg/kg/day Schisandra chinensis polysaccharides IIa; the other two groups were the control and model groups. Period of study—10 days. | Increased the phagocytic |
[115] |
| Examine the anti-diabetic effect of polysaccharides from |
For the study, 60 mice were used, divided into six groups: control group, control group with diabetes, alloxan-induced diabetic mice treated with sodium chloride solution, and three groups treated with 162, 324, or 648 mg/kg Schisandra chinensis polysaccharides, and a placebo group. |
Decreased blood glucose levels. Improved lipid metabolism. | [116] |
© 2021 by the authors.
Details
; Nalbantova, Vanya 1 ; Karcheva-Bahchevanska, Diana 1 ; Ivanova, Stanislava 1 1 Department of Pharmacognosy and Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University-Plovdiv, 4002 Plovdiv, Bulgaria;
2 Université Clermont Auvergne, Clermont Auvergne INP, CNRS, Institut Pascal, 63000 Clermont-Ferrand, France;