Scientific Name: Lepidium meyenii (synonym: Lepidium peruvianum) Family Brassicaceae/Cruciferae ther Common Names Ayak Chichira, Ayuk Willku, Ginseng Andin, Ginseng Péruvien, Maca Maca, Maca Péruvien, Maino, Maka, Peruvian Ginseng, Peruvian Mac |
Maca is a root vegetable that grows in the Andes mountains, especially in Peru, at an elevation of 3700-4500 meters (40231, 60705, 104516). The root occurs in three colors (red, yellow, and black) and has been eaten baked, roasted, or in soup for over 3000 years (9926, 40231, 104516). Traditionally, it has been used for improving the fertility of humans and livestock (9925, 9926).
Likely Safe when maca is consumed in food amounts (9926).
Possibly Safe when used orally and appropriately, short term. Maca appears to be safe in doses up to 3 grams daily for 4 months (9928, 10218, 18289, 90278, 108603).
PREGNANCY AND LACTATION: Insufficient reliable information available; avoid using.
Orally, no adverse effects have been reported with the medicinal use of maca. However, a thorough evaluation of safety outcomes has not been conducted.
It is unclear if oral maca is beneficial for age-related testosterone deficiency.
Although there has been interest in using oral maca for amenorrhea, there is insufficient reliable information about the clinical effects of maca for this purpose.
Although there has been interest in using oral maca for anemia of chronic disease, there is insufficient reliable information about the clinical effects of maca for this purpose.
It is unclear if oral maca is beneficial in patients with sexual dysfunction due to antidepressants.
It is unclear if oral maca is beneficial for athletic performance.
Although there has been interest in using oral maca for CFS, there is insufficient reliable information about the clinical effects of maca for this purpose.
Although there has been interest in using oral maca for depression, there is insufficient reliable information about the clinical effects of maca for this purpose.
Although there has been interest in using oral maca for fatigue, there is insufficient reliable information about the clinical effects of maca for this purpose.
Although there has been interest in using oral maca for leukemia, there is insufficient reliable information about the clinical effects of maca for this purpose.
It is unclear if oral maca is beneficial for male infertility.
Although there has been interest in using oral maca for memory, there is insufficient reliable information about the clinical effects of maca for this purpose.
Although there has been interest in using oral maca for osteoporosis, there is insufficient reliable information about the clinical effects of maca for this purpose.
It is unclear if oral maca is beneficial for postmenopausal conditions.
It is unclear if oral maca improves male sexual desire; it has not been evaluated for female sexual desire.
Although there has been interest in using oral maca for tuberculosis, there is insufficient reliable information about the clinical effects of maca for this purpose.
More evidence is needed to rate maca for these uses.
Maca has been used in doses of 1.5-3.5 grams daily, usually in divided doses, for 6-16 weeks. See Effectiveness section for condition-specific information.
Two classes of polyunsaturated fatty acids, macaenes and macamides, are used as marker compounds for maca (9926). Analysis of commercially available maca products shows that the percentage of total macaenes and macamides in preparations varies from 0.15% to 0.84% (9926).
In one clinical trial, the maca sample contained the macamides N-benzyl-palmitamide 42.2 mg/gram, N-benzyl-stearamide 10.6 mg/gram, N-benzyl-oleamide 16.4 mg/gram, N-(methoxy-benzyl)-oleamide 2.4 mg/gram, N-benzyl-linoleamide 49.8 mg/gram, N-(methoxy-benzyl)-linoleamide 7.3 mg/gram, N-benzyl-linoleniamide 53.5 mg/gram, N-(methoxy-benzyl)-linoleniamide 4.1 mg/gram, and N-(methoxy)-benzylpalmitamide 4.4 mg/gram (90278).
There is insufficient reliable information available about the presentation or treatment of overdose with maca. There is insufficient available evidence about the pharmacokinetics of maca.
The applicable part of maca is the root. Dried maca root contains 55% to 60% carbohydrates; 10% to 12% protein; 8% to 9% fiber; and 2% to 3% lipids, including linolenic, palmitic, and oleic acids. It also contains sterols such as campesterol, stigmasterol, and beta-sitosterol, and significant amounts of minerals including iron, calcium, copper, and zinc, as well as amino acids and B, C, and E vitamins (9929, 40231, 90606, 104516).
Two classes of polyunsaturated fatty acids, macaenes and macamides, are used as marker compounds for maca (9926). Analysis of commercially available maca products shows that the percentage of total macaenes and macamides in preparations varies from 0.15% to 0.84% (9926).
Maca also contains glucosinolates, including glucotropaeolin (9927, 9929, 60714). The major components of the steam-distilled essential oil of maca are phenyl acetonitrile (85.9%), benzaldehyde (3.1%), and 3-methoxyphenylacetonitrile (2.1%) (60707). Other constituents of maca include (5-oxo-(6E,8E)-octadecadienoic acid), lepidiline A and B, (1R,3S)-1-methyltetrahydro-beta-carboline-3-carboxylic acid, and macaridine (9927, 60704, 60708).
Animal research in mice shows that pretreatment with maca extract before strenuous exercise may reduce post-exercise levels of serum lactate dehydrogenase, lactic acid, and blood urea nitrogen when compared with a control group. These effects were similar to those seen with caffeine (108602).
In animal research, maca extract improved several markers associated with stress including ulcers, elevated corticosterone levels, and adrenal weights (60730).
Maca contains glucosinolates, which might have cancer-protecting properties (9927, 9929).
In animal models of depression, maca and maca-derived extracellular vesicles (Maca-EVs) improve depressive behaviors (60724, 116973). Maca-EVs improve neurotransmitter levels, including serotonin, possibly by modulating the gut-brain axis (116973).
In vitro research in muscle cell models designed to simulate exercise-induced oxidative damage shows that maca extract may attenuate oxidative effects by preventing the inhibition of dehydrogenase activity and preserving mitochondrial function in skeletal muscle. Research in mice shows that pretreatment with maca extract before strenuous exercise may reduce oxidative stress-induced muscle damage by decreasing levels of reactive oxygen species in both blood and muscle (108602).
Maca contains glucosinolates, which might have central nervous system effects (9927, 9929). The carboline, (1R,3S)-1-methyltetrahydro-beta-carboline-3-carboxylic acid, found in maca has been reported to exert many activities on the central nervous system (9927).
In animal research, maca reduced time required to find water, suggesting beneficial effects on memory (60724).
In animal research, maca extracts increased swimming activity and improved recovery from muscle fatigue based on production of lactic and malonic acids (60732). Other animal research in mice shows that administration of maca extract daily for 4 weeks improves grip strength and exercise endurance more than a control group and similarly to caffeine. Maca also appears to attenuate exercise-induced muscle fatigue and stress by increasing muscle concentrations of coenzyme nicotinamide adenine dinucleotide (NAD+) and NAD(H) and reducing markers of inflammation and oxidative stress (108602).
In female animals, maca extract increased litter size (60718). However, in other animal research it did not increase implantation of embryos (60709).
In an animal model of metabolic syndrome, maca root extract protects against liver damage as shown by improved liver function tests and histopathological analysis (116975).
In animal research, diets supplemented with maca resulted in increased leukocyte counts (60733). Similarly, a small study in mice with immunocompromise due to cyclophosphamide suggests that maca polysaccharides improve immune cell counts, including white blood cells, CD4+ T cells, interleukin-2, and interferon-gamma when compared with control (112013). However, in human research, maca did not affect levels of cytokines involved in immunity (90606).
In an animal model of metabolic syndrome, maca root extract mitigates hyperglycemia, hyperlipidemia, and weight gain(116975).
In animal research, maca extract prevented bone loss associated with estrogen deficiency (60722).
Maca and extracts containing macaene and macamide seem to increase sexual activity and correct erectile dysfunction in animal models. The mechanism for this activity is unknown (10218, 60700, 60702, 60706). Also in animal models, maca increases spermatogenesis and epididymal sperm count (60710, 60711, 60715, 60723), as well as the weight of the testis and epididymis (60703). However, when different types of maca are compared in rats, only the black variety appears to improve spermatogenesis (60719).
Most research suggests that maca is not beneficial for male infertility. Maca does not appear to significantly affect serum concentrations of reproductive hormones including testosterone, estradiol, and 17-hydroxyprogesterone in healthy males (10219, 112012). In males with various combinations of oligospermia, asthenospermia, teratospermia, and azoospermia, taking yellow maca 2.8 grams daily for 16 weeks also does not appear to significantly affect serum concentrations of luteinizing hormone, follicle-stimulating hormone, prolactin, estradiol, or testosterone (108603). However, animal research in rats with monosodium glutamate (MSG)-induced subfertility suggests that maca may partially improve sperm motility(116976).
Reproductive effects of maca in females may differ. Estrogenic effects of maca have been shown in laboratory research in human breast cancer cell lines (18290). Also, in animal research, maca resulted in increased progesterone, but not estrogen, levels in females (60709) and increased testosterone levels in males (60709).
Adaptogens, Testosterone Enhancers
Literature Review Current Through: 5/18/2026, Last Updated: 7/5/2026
The contents of this resource are not intended to be a substitute for professional medical advice, diagnosis, or treatment. Clinical input is needed from a qualified healthcare provider before taking any supplement or starting any therapy. Do not delay or disregard seeking medical advice or treatment based on any information displayed in this resource.
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