The information on this page has been prepared with reference to published scientific literature, not by a medically qualified expert. It is not medical advice. Any decision to use a supplement or herb-based product is your responsibility. Consult a suitably qualified medical professional, especially if you have underlying conditions. Remember, nothing is for everyone, and not everything sold is what it claims to be. Some things work for some people, some of the time.
Rhodiola rosea, commonly known as golden root, rose root, Arctic root, or King's crown, is an adaptogenic herb that has been used in traditional medicine systems across Europe and Asia for centuries. It belongs to the Crassulaceae family and grows primarily in cold, mountainous regions of Europe, Asia, and North America. It's important to note that while several species of Rhodiola exist (including Rhodiola crenulata, Rhodiola quadrifida, and Rhodiola imbricata), the majority of scientific research has focused specifically on Rhodiola rosea, and these species are not interchangeable despite sometimes being marketed similarly.
Image source and license: https://commons.wikimedia.org/wiki/File:Rhodiola_rosea_kz02.jpg.
Modified by Peter Jorgensen.
The therapeutic effects of Rhodiola rosea are attributed primarily to its bioactive compounds, which include rosavins (rosavin, rosin, and rosarin) and salidroside (rhodioloside). Most standardized extracts contain 3% rosavins and 1% salidroside, which reflects the natural ratio of these compounds in the plant. Other beneficial compounds include tyrosol, flavonoids, monoterpenes, triterpenes, and phenolic acids.
Based on peer-reviewed scientific literature, Rhodiola rosea has shown potential benefits for the following conditions:
It's crucial to note that while these benefits have been observed in studies, Rhodiola rosea has not been conclusively proven to "cure" any medical condition, and should be considered as a potential complementary approach rather than a replacement for conventional medical treatment.
Based on clinical studies, the following dosage recommendations have been established:
Most clinical trials have used extracts standardized to contain 3% rosavins and 1% salidroside, which reflects the natural ratio in the plant. Dosing is typically divided, with administration once or twice daily, preferably before meals. Morning dosing is often recommended to avoid potential sleep disturbances.
Rhodiola rosea is generally well-tolerated in studied dosages. However, the following side effects have been reported:
Long-term safety beyond 12 weeks has not been well-established in clinical studies. Most adverse events reported in trials were mild and transient.
There is a notable gap in research regarding doses significantly higher than the typically recommended range of 200-680 mg daily. Few studies have systematically evaluated doses above 1000 mg daily for efficacy or safety. Panossian et al. (2021) noted that while traditional use sometimes involved higher doses, modern clinical trials have not thoroughly investigated potential dose-dependent effects or toxicity at substantially elevated dosages. This represents a significant knowledge gap in the literature. Current evidence does not support benefits from doses exceeding the upper range of clinical studies (approximately 680 mg daily of standardized extract), and potential risks of higher doses remain inadequately characterized.
While numerous dietary supplements containing Rhodiola rosea are available globally, few meet the definition of registered pharmaceutical products. Some notable exceptions include:
Unlike many herbs that have led to significant pharmaceutical development, Rhodiola's active compounds have generally not been synthesized into novel pharmaceutical analogues with widespread clinical application. Most commercial products remain in the supplement category rather than as approved medications with specific therapeutic claims.
Rhodiola rosea shows promise as an adaptogenic herb with potential benefits for stress, fatigue, cognitive function, and mood disorders. However, the evidence base, while growing, still has significant limitations including relatively small sample sizes, varying methodologies, and inconsistent extract standardization across studies. More rigorous, large-scale clinical trials are needed to definitively establish efficacy, optimal dosing protocols, and long-term safety. Individuals interested in using Rhodiola should consult healthcare providers, especially when taking medications or managing chronic health conditions.
Amsterdam, J. D., & Panossian, A. G. (2016). Rhodiola rosea L. as a putative botanical antidepressant. Phytomedicine, 23(7), 770-783.
Anghelescu, I. G., Edwards, D., Seifritz, E., & Kasper, S. (2018). Stress management and the role of Rhodiola rosea: a review. International journal of psychiatry in clinical practice, 22(4), 242-252.
Darbinyan, V., Aslanyan, G., Amroyan, E., Gabrielyan, E., Malmström, C., & Panossian, A. (2007). Clinical trial of Rhodiola rosea L. extract SHR-5 in the treatment of mild to moderate depression. Nordic journal of psychiatry, 61(5), 343-348.
Ishaque, S., Shamseer, L., Bukutu, C., & Vohra, S. (2012). Rhodiola rosea for physical and mental fatigue: a systematic review. BMC complementary and alternative medicine, 12, 1-9.
Olsson, E. M., von Schéele, B., & Panossian, A. G. (2009). A randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract shr-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Planta medica, 75(02), 105-112.
Pu, W. L., Zhang, M. Y., Bai, R. Y., Sun, L. K., Li, W. H., Yu, Y. L., ... & Li, T. X. (2020). Anti-inflammatory effects of Rhodiola rosea L.: A review. Biomedicine & Pharmacotherapy, 121, 109552.
Schutgens, F. W. G., Neogi, P., Van Wijk, E. P. A., Van Wijk, R., Wikman, G., & Wiegant, F. A. C. (2009). The influence of adaptogens on ultraweak biophoton emission: a pilot‐experiment. Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, 23(8), 1103-1108.