Adaptogens exert a stress-protective effect by modulation of expression of molecular chaperones
Abstract
Adaptogens are medicinal plants that augment resistance to stress, and increase concentration, performance and endurance during fatigue. Experiments were carried out with BALB/c mice taking ADAPT-232 forte, a fixed combination of three genuine (native) extracts of Eleutherococcus senticocus, Schisandra chinensis and Rhodiola rosea, characterised for the content of active markers eleutherosides, schisandrins, salidroside, tyrosol and rosavin and in doses of about 30, 90 and 180 mg/kg for seven consecutive days followed by forced swimming test to exhaustion. ADAPT-232 forte strongly augments endurance of mice, increasing the time taken to exhaustion (TTE) in a dose-dependent manner from 3.0+/-0.5 to 21.1+/-1.7 min, approximately seven fold. Serum Hsp72 was measured by EIA both in normal and stressful conditions before and after swimming test. Repeated administration of adaptogen dose dependently increases basal level of Hsp72 in serum of mice from 0.8-1.5 to 5.5-6.3 pg/ml. This effect is even stronger than the effect of stress, including both physical (swimming) and emotional impacts: 3.2+/-1.2 pg/ml. Cumulative effect of stress and adaptogen was clearly observed in groups of animals treated with adaptogen after swimming to exhaustion, when serum Hsp72 increased to 15.1+/-1 pg/ml and remained at almost the same level during the 7 days. It can be concluded that adaptogens induce increase of serum Hsp72, regarded as a defense response to stress, and increase tolerance to stress (in our model combination of physical and emotional stresses). It can be suggested that increased tolerance to stress induced by adaptogen is associated with its stimulation of expression of Hsp70 and particularly with Hsp72 production and release into systemic circulation, which is known as a mediator of stress response involved in reparation of proteins during physical load. Our studies suggest that this could be one of the mechanisms of action of plant adaptogens.
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Intake of plant adaptogens such as Eleutherococcus senticosus root, Schisandra chinensis root, and Rhodiola rosea root extracts is associated with affecting the hypothalamic-pituitary-adrenal axis and some stress mediators.
“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].”
From Plant Adaptogens—History and Future Perspectives (2021) · cites this paper as [10]
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- Authors
- Panossian, A., Wikman, G., Kaur, P., & Asea, A.
- Affiliations
- Svenska Örtmedicinska Institute (SE)
- Texas A&M Health Science Center (US)
- Corresponding author
- Panossian, Alexander
- Venue
- Phytomedicine
- Publisher
- Elsevier BV
- Published
- 2009-06
- Volume
- 16
- Issue
- 6-7
- Pages
- 617-622
- ISSN
- 0944-7113 (ISSN-L)
- OpenAlex
- W2091170955
- Cited by
- 111
- References
- 33
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 7 · 2023: 5 · 2022: 6 · 2021: 1 · 2020: 9 · 2019: 6 · 2018: 6 · 2017: 5 · 2016: 10 · 2015: 5 · 2014: 6 · 2013: 9 · 2012: 8
- FWCI
- 3.08
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytomedicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Medicinal Plants and Bioactive Compounds
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Keywords
- adaptogens, stress tolerance, heat shock proteins, HSP72, HSP70, molecular chaperones, Schisandra chinensis, Rhodiola rosea, forced swim test, time to exhaustion, fatigue, emotional stress
- MeSH terms
- Animals, Enzyme-Linked Immunosorbent Assay, Female, Mice, Inbred BALB C, Physical Endurance, Plant Extracts, Plants, Medicinal, Molecular Chaperones, HSP70 Heat-Shock Proteins, Mice
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