Astaxanthin

Nutrient group: plant extracts & active ingredients

Sources and physiological effects

Dietary Sources

Natural astaxanthin is considered one of the strongest antioxidants and belongs chemically to the carotenoid group, more precisely to the xanthophylls (1). Industrially, astaxanthin is mainly extracted from the green algae Haematococcus pluvialis. These algae reacts under stress, due to lack of food or water, high salt content in the water, nitrogen deficiency, strong sunlight or extreme temperature, by forming the characteristic red dye astaxanthin. Astaxanthin enters animals and humans via the food chain and is responsible, for example, for the reddish colouring of crustaceans, lobsters and salmon (2). Although its ability to eliminate free radicals is much stronger than that of vitamin C, vitamin E and synthetic astaxanthin, natural astaxanthin is considered a "gentle" antioxidant (3)(4).
 

Physiological functions
Antioxidants
  • Important role as a free radical scavenger. Antioxidants "defuse" free radicals either by acting as electron donors or by splitting the radical molecule
    Support of oxidative balance

Eyes Protection against age-related eye damage and general changes in visual behaviour (e.g. presbyopia or Computer Vision Syndrome (CVS))
Skin
  • Increases skin elasticity and skin moisture
    Protection against UV-induced skin damage
    Protection against lipid peroxidation

Cardiovascular system
  • Potentially supportive in the prevention and therapy of cardiovascular diseases

Exercise
  • Nutritive supplement in performance-oriented recreational sports

Recommended intake

Increased needs People with high sun exposure, diabetes mellitus, presbyopia, smokers and frequent users of computers and digital devices. 

Detailed information

Astaxanthin, the antioxidant powerhouse - general information and metabolism

The "super antioxidant" astaxanthin (C40H52O4) is structurally similar to beta-carotene (C40H56). However, while beta-carotene has only 11 double bonds, astaxanthin has 13 conjugated double bonds. These and the two oxo groups (double bonded oxygen to carbon atom) give astaxanthin its antioxidative effect. Comparative studies have shown that astaxanthin has a much stronger antioxidant effect than other compounds. For example, astaxanthin is 6000 times stronger than vitamin C, 770 times stronger than coenzyme Q10, 100 times stronger than vitamin E, 55 times stronger than synthetic astaxanthin, 5 times stronger than beta-carotene, 3 times stronger than lutein and 2 times stronger than lycopene. In terms of its antioxidant activity, astaxanthin has other advantages. Its chemical structure enables it to intercept different types of free radicals. At the same time, astaxanthin is considered a "gentle" antioxidant because, compared to other antioxidants, the molecule does not itself become a highly reactive compound after the absorption of a free radical (3)(4). Astaxanthin is considered safe and has been certified by the United States Food and Drug Administration (FDA) as GRAS (generally recognized as safe) status (5). After ingestion in the form of supplements or carotenoid-rich food, astaxanthin enters the intestinal cells together with dietary fats through passive diffusion. Similar to other carotenoids, astaxanthin is transported in chylomicrons and via the lymph into the blood. This is also how the transport to the respective target tissue takes place (6). The bioavailability of astaxanthin depends on numerous factors. For example, the combination with dietary fats increases bioavailability 2.4-fold, so simultaneous intake with a meal should be considered (7). In addition, the combination of Astaxanthin with dietary fats in supplements increases its bioavailability 2 to 4-fold (8). Another advantage is obtained by extracting astaxanthin from Haematococcus pluvialis. As this form of astaxanthin is esterified, it is more stable and is better absorbed by the body. Unesterified astaxanthin can oxidise particularly easily (9)(10)(11). Finally, smoking increases the breakdown of astaxanthin and can greatly reduce bioavailability (12).
 

Astaxanthin and oxidative balance

Oxidative balance describes the relationship between the production of reactive oxygen species (ROS) and the activity of antioxidant protective systems. If this system is in balance, oxidative damage can be minimized and body cells optimally protected. Often, chronic stress, environmental pollution or even exercise can lead to an imbalance: oxidative stress is increased, which can ultimately result in cell damage, various diseases or premature aging. Astaxanthin is able to restore this balance. A classic target group for astaxanthin are smokers. The high levels of ROS in cigarette smoke cause increased oxidative damage to lipid, protein and DNA structures. In addition, smokers experience both reduced activity of antioxidative enzymes and generally lower concentrations of antioxidants. An intervention using astaxanthin demonstrated a significant reduction of biomarkers for oxidative stress after only three weeks. At the same time, the concentrations in antioxidative protective systems increased (12). Astaxanthin is similarly effective in overweight or obese persons.  In one study, treatement with Astaxanthin resulted in reduction of Malondialdehyde by 35 % and isoprostanes by 65 %; both are important biomarkers for oxidative stress. The positive effects on superoxide dismutases - a class of enzymes that metabolize reactive superoxide anions to hydrogen peroxide - were even stronger. Here the activity could be increased almost 3-fold. The total antioxidative capacity (TAS) also increased by more than 120 % (13).
 

Anti-aging and healthy aging with astaxanthin

The human ageing process is associated with mitochondrial damage, increased oxidative stress and less active cell protection systems. This is considered to be one of the main causes for the development of various diseases in old age. Characteristic age-related symptoms are damage to the skin, increased oxidation of blood lipids and retinal damage. Astaxanthin can successfully counteract these aging processes.

Preservation of the skin
As a barrier, the human skin is permanently exposed to various environmental influences: UV radiation, environmental toxins and various mechanical and chemical influences. It is therefore obvious that the skin is particularly stressed by reactive oxygen species. The barrier function of the skin is additionally reduced by the progressive aging process, as the skin, which steadily becomes thinner by nature, is particularly sensitive to UV radiation. The direct consequences are increased pigmentation, reduced elasticity and premature aging of the skin. However, the antioxidant astaxanthin can also be used for this indication. It is not only able to counteract hyperpigmentation and wrinkling but also increases the skin elasticity and moisture. It can also reduce UV-induced skin damage. All in all, astaxanthin supports the preservation of the appearance of youthful skin - even in old age. Two studies from Japan are particularly worth mentioning in which the astaxanthin intervention reduced wrinkles around the eye area and the size of age spots in the cheek area, improved skin texture and increased skin hydration and elasticity (14). A study published in June 2018 on the UV protection of astaxanthin investigated whether supplementation with 4 mg astaxanthin/day increases the skin's minimum erythema dose (MED). The minimum erythema dose (also called erythema threshold dose) is a measure of the tolerance of human skin to solar radiation and indicates the amount of UV radiation the skin tolerates before the first signs of redness appear. After completion of astaxanthin intake, MED was significantly increased; this effect did not occur in the placebo group. At the same time, the UV-irradiated skin areas of the astaxanthin group showed less moisture loss. The subjective perception of improvement in rough skin and overall skin texture was also significantly more positive in the intervention group (15).

Protection from lipid peroxidation
Astaxanthin-mediated protection from lipid peroxidation was investigated in a study examining the effects of astaxanthin supplementation on the lipid profile and antioxidant parameters (TBARS, TAS and 8-isoprostane) of postmenopausal women. TBARS (thiobarbituric acid reactive substances) are biomarkers for the extent of lipid peroxidation; TAS (total antioxidant status) and 8-isoprostane are markers for oxidative stress. Astaxanthin has been shown to increase HDL cholesterol and decrease triglyceride levels. At the same time it reduced the extent of lipid peroxidation by lowering TBARS. TAS levels also increased, reflecting an improvement in the functioning of antioxidant protective systems. However, there was no effect on 8-isoprostane, LDL and total cholesterol (16).

Protection against age-related eye damage and changes in visual behaviour
Presbyopia, also known as the ageing eye condition, is not a disease, but describes the progressive age-related loss of the eye's ability to adapt to near vision. A sharp vision in the near range without suitable correction is then no longer possible. If this loss of function is left untreated, asthenopic complaints - such as stiff neck and shoulders, eye pain and headaches - occur, which significantly impair the quality of life. A 2009 study investigated whether and how astaxanthin affects the side effects of incipient presbyopia. The results were unequivocal: the convergence miosis improved significantly in the majority of subjects. This describes the unilateral or bilateral pupil constriction following a visual stimulus. Symptoms such as overstrained eyes, blurred vision or shoulder and neck tension also improved (17). There is also initial evidence of the benefit of astaxanthin in Computer Vision Syndrome (CVS). CVS, also known as digital eye strain, is the combination of eye and vision problems caused by regular use of computers and other digital devices such as smartphones. Typical symptoms range from headaches and sleep disturbances to exhaustion, reddened eyes, dizziness or blurred vision. Astaxanthin is able to counteract the effects of the everyday digital life. For example, the carotenoid reduced the refocusing time of the eye by 46 % and improved accommodation - the ability of the eye to actively adapt visual acuity to different distances - by 27 % (18)(19).
 

Potential cardioprotective effects of astaxanthin

Cardiovascular disease, and in particular coronary heart disease (CHD), accounts for almost half of all deaths in the European Union and is the leading cause of mortality. Chronic inflammatory processes and increased oxidative stress are significantly involved in the pathophysiology of cardiovascular disease and atherosclerosis. Nonetheless, the study results on antioxidant micronutrients for primary and secondary prevention of atherosclerosis are the subject of controversy. Since drugs - such as statins, calcium antagonists or diuretics - are associated with a wide variety of side effects, they suffer from low compliance among patients. This makes the development of new prevention and therapy methods all the more important: The cardioprotective effects of astaxanthin, with its unique chemical properties, have been studied for some time. The following sections discuss individual aspects and reflect the current consensus in the literature (20).

Protection against LDL oxidation
The oxidative modification of LDL or the change in size and density of LDL particles is seen as the underlying cause for the initiation of the atherosclerotic process. Whether astaxanthin can protect LDL particles from oxidation is not yet clearly established. In some animal studies, the antioxidant astaxanthin reduced LDL by 30%, other studies did not show significant results. In human studies conducted between 2000 and 2011, the results tend to suggest that astaxanthin protects against lipid and LDL peroxidation (20).

Reduction of blood pressure
It is estimated that by 2025 more than 1.56 billion people will be affected by high blood pressure. This makes it all the more important to adopt effective measures to counteract existing hypertension. The hypotensive effects of astaxanthin in animal models are clear and show significant reductions in systolic (up to 28 mmHg) and diastolic (up to 23 mmHg) blood pressure. Results from human studies are still too few to make a reliable statement (20).

Reduction of blood glucose and diabetes
The most recent meta-analysis of the antidiabetic effects of astaxanthin indicates that the carotenoid has at least a minor blood glucose-lowering effect. Potential mechanisms discussed are improvement of insulin sensitivity, reduction of oxidative stress and inflammation, and support of endothelial function (20)(21). Further evidence for the cardioprotective potential of astaxanthin is provided by an RCT published in 2018: An eight week intervention with 8 mg astaxanthin/day was performed in diabetics. Particularly noteworthy were the significant astaxanthin-induced reduction in total fat mass and the reduction in triglyceride levels. At the same time, blood pressure and VLDL levels decreased compared to a placebo. Positive effects on fructosamine and adiponectin levels were also observed. Fructosamine provides a longer-term picture of blood glucose levels and is also known as "blood sugar memory". Adiponectin is a peptide hormone which is produced in fat cells. It regulates both the feeling of hunger and food intake and modulates the effect of insulin. Overweight people often have reduced adiponectin levels, which weakens insulin efficiency (22). 
 

Effects of astaxanthin on athletic performance and regeneration

Intensive training and competition periods are accompanied by an increased production of oxidative and nitrosative stress molecules (ROS and NOS). These can damage proteins, lipids and other body structures. The complex interaction of antioxidative systems normally ensures that this damage is limited or prevented. However, if the training workload is too high for a longer period of time, a disbalance occurs and the production of reactive oxygen species predominates. This imbalance can also be aggravated by psychological factors (e.g. stress in work and private life), which is particularly relevant for amateur athletes. In order to counteract these negative effects, the targeted use of antioxidant nutrients has been established in both high performance and amateur athletes.

Metabolic situation of the athlete
In order for fat to be used as an energy source, the fatty acids must first enter the mitochondria. This is done with the help of the carnitine acyltransferase system. Carnitine acyltransferase I is particularly relevant in this respect. This enzyme transfers the acyl group to L-carnitine. During sporting activities, the enzyme is affected by the increased occurrence of oxidative stress. The direct consequence: the energy supply from fat is reduced. Whether astaxanthin can prevent this process has been tested in various animal models. One was able to show that astaxanthin reduces the oxidative modification of carnitine acyltransferase I by 41%. At the same time, the glycogen stores in the intervention group were significantly higher, indicating a glycogen-saving effect of the carotenoid. This effect was also demonstrated in further animal studies. However, proof in humans is still pending.

Efficiency
As astaxanthin is said to have a glycogen-saving effect, an ergogenic effect is also likely, which has been demonstrated in several animal studies. These showed that astaxanthin can, for example, increase the time spent swimming and the time until exhaustion. The (few) human studies on the performance-enhancing effect of astaxanthin are contradictory: In a study with racing cyclists over a distance of 20 km, for example, astaxanthin intervention led to a time saving of 121 seconds; the placebo group only improved by 18 seconds. A further study with a very similar design could not reproduce these results; no significant effects were observed. Here, too, further studies are required.

Regeneration
Intensive training sessions lead to muscle damage, oxidative stress and inflammation. In animal experiments Astaxanthin has been shown to improve biomarker values indicating physical exhaustion. Unfortunately, the number of available studies in humans to assess this potential relationship is far from representative (23).

Deficiency symptoms

Impact on Symptoms
Eyes
  • Prevention of age-related eye damage
    Support of general changes in visual behaviour

Skin
  • Increased lipid peroxidation
    Increased skin damage due to UV radiation

Immune system
  • Increased risk of cardiovascular disease
    Increased oxidative stress and thus potential cell damage, various diseases or premature aging

Vascular system
  • Increased LDL oxidation

Indications

Effects Indications Dose
Physiologic effects at a low intake To support oxidative balance 4 mg/d

To maintain a youthful skin appearance (reduction of wrinkles, increase of skin elasticity and skin moisture protection against UV-induced skin damage)

4 mg/d
Protection against lipid peroxidation 4 mg/d

Protection against age-related eye damage and general changes in visual behaviour (e.g. presbyopia or Computer Vision Syndrome (CVS))

4 mg/d

Potentially supportive in the prevention and therapy of cardiovascular diseases

4 mg/d

As a nutritional supplement in performance-oriented recreational sports

4 mg/d

Administration

General mode of Administration
 
When
 

Astaxanthin should be taken with a meal.

Side effects

According to current knowledge, no side effects are to be expected at a dosage of 4 mg/d.

Contraindications

If pregnant or breastfeeding, consult a doctor.

Interactions

Drug interactions
None

No relevant drug interactions are known to date

Nutrient interactions
None

No relevant nutrient interactions are known to date

Description and related substances

Description

Fat-soluble carotenoid

References

Referenzen

1. Fakhri, S. et al. 2018. Astaxanthin: A Mechanistic Review on Its Biological Activities and Health Benefits. Pharmacol Res. 136:1-20.
2. Ambati, R. R. et al. 2014. Astaxanthin: sources, extraction, stability, biological activities and its commercial applications – a review. Mar Drugs. 12(1):128–52.
3. Nishida, Y. et al. 2007. Quenching Activities of Common Hydrophilic and Lipophilic Antioxidants against Singlet Oxygen Using Chemiluminescence Detection System. Carotenoid Sci. 11:16–20.
4. Beutner, S. et al. 2001. Quantitative assessment of antioxidant properties of natural colorants and phytochemicals: carotenoids, flavonoids, phenols and indigoids. The role of β-carotene in antioxidant functions. J Sci Food Agric. 81(6):559–68.
5. Fuji Chemical Industry Co., Ltd. 2009. Notification of GRAS Determination for Haematococcus pluvialis extract characterized by component astaxanthin esters (of common edible fatty acids)
6. Bjerkeng, B. et al. 2000. Astaxanthin and its metabolites idoxanthin and crustaxanthin in esh, skin, and gonads of sexually immature and maturing Arctic charr (Salvelinus alpinus (L.)). Comp Biochem Physiol B. Biochem Mol Biol. 125(3):395–404.
7. Okada, Y. et al. 2009. Bioavailability of astaxanthin in Haematococcus algal extract: the eects of timing of diet and smoking habits. Biosci Biotechnol Biochem. 73(9):1928–32.
8. FDA. 2000. Technical Report (Aquaresearch Inc.) Haematococcus Pluvialis and Astaxanthin Safety For Human Consumption
9. Zhou, Q. et al. 2015. The effect of various antioxidants on the degradation of O/W microemulsions containing esterifed astaxanthins from Haematococcus pluvialis. J Oleo Sci. 64(5):515–25.
10. de Bruijn, W. J. et al. 2016. Fatty acids attached to all-trans-astaxanthin alter its cis-trans equilibrium, and consequently its stability, upon lightaccelerated autoxidation. Food Chem. 194:1108–15.
11. Decker, E. A. et al. 2000. Antioxidants in Muscle Foods: Nutritional Strategies to Improve Quality. John Wiley & Sons, Inc.
12. Kim, J. H. et al. 2011. Protective effects of Haematococcus astaxanthin on oxidative stress in healthy smokers. J Med Food. 14(11):1469–75.
13. Choi, H. D. et al. 2011. Effects of astaxanthin on oxidative stress in overweight and obese adults. Phytother Res. 25(12):1813–8.
14. Tominaga, K. et al. 2012. Cosmetic benefts of astaxanthin on human subjects. Acta Biochim Pol. 59(1):43–7.
15. Ito, N. et al. 2018. The Protective Role of Astaxanthin for UV-Induced Skin Deterioration in Healthy People – A Randomized, Double-Blind, Placebo-Controlled Trial. Nutrients. pii: E817.
16. Kim, Y. K., Chyun, J.-H. 2004. The effects of astaxanthin supplements on lipid peroxidation and antioxidant status in postmenopausal women. Nutr Sci. 7(1):41–6.
17. Kajita, M. et al. 2009. The Effects of a Dietary Supplement Containing Astaxanthin on the Accommodation Function of the Eye in Middle-aged and Older People. Med Consult N Remed. 46(3):89–93.
18. Nagaki, Y. et al. 2002. Effects of astaxanthin on accommodation, critical flicker fusion, and pattern visual evoked potential in visual display terminal workers. J Trad Med. 19:170–3.
19. Nitta, T. et al. 2005. Effects of astaxanthin on accommodation and asthenopia – dose finding study in healthy volunteers. J Clin Ther Med. 21(5):543–56.
20. Visioli, F. Artaria, C. 2017. Astaxanthin in cardiovascular health and disease: mechanisms of action, therapeutic merits, and knowledge gaps. Food Funct. 8(1):39–63.
21. Ursoniu, S. et al. 2015. Lipid profile and glucose changes after supplementation with astaxanthin: a systematic review and meta-analysis of randomized controlled trials. Arch Med Sci. 11(2):253–66.
22. Mashhadi, N. S. et al. 2018. Astaxanthin improves glucose metabolism and reduces blood pressure in patients with type 2 diabetes mellitus. Asia Pac. J Clin Nutr. 27(2):341–6.
23. Brown, D. R. et al. 2018. Astaxanthin in Exercise Metabolism, Performance and Recovery: A Review. Front Nutr. 4:76.

Referenzen Interaktion
Stargrove, M. B. et al. Herb, nutrient and Drug Interactions: clinical implications and therapeutic strategies, 1. Auflage. St. Louis, Missouri: Elsevier Health Sciences, 2008.
Gröber, U. Mikronährstoffe: Metabolic Tuning – Prävention – Therapie, 3.
Auflage. Stuttgart: WVG Wissenschaftliche Verlagsgesellschaft Stuttgart, 2011.
Gröber, U. Arzneimittel und Mikronährstoffe: Medikationsorientierte Supplementierung. 3. aktualisierte und erweiterte Auflage. Stuttgart: WVG Wissenschaftliche Verlagsgesellschaft Stuttgart, 2014.

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