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Proceeding Paper

Chemical Features and Biological Effects of Astaxanthin Extracted from Haematococcus pluvialis Flotow: Focus on Gastrointestinal System †

1
Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, 40126 Bologna, Italy
2
Department of Biomolecular Sciences, Università degli Studi di Urbino “Carlo Bo”, 61029 Urbino, Italy
3
Department of Pharmacy, University of Naples Federico II, Via Domenico Montesano 49, 80131 Naples, Italy
4
International Research Center for Food Nutrition and Safety, Jiangsu University, Zhenjiang 212013, China
5
Department of Experimental, Diagnostic and Specialty Medicine—DIMES, Alma Mater Studiorum-University of Bologna, 40138 Bologna, Italy
*
Author to whom correspondence should be addressed.
Presented at the 2nd International Electronic Conference on Nutrients, 15–31 March 2022; Available online: https://iecn2022.sciforum.net/.
Biol. Life Sci. Forum 2022, 12(1), 31; https://doi.org/10.3390/IECN2022-12376
Published: 14 March 2022
(This article belongs to the Proceedings of The 2nd International Electronic Conference on Nutrients)

Abstract

:
The main purpose of this review is to analyze published data concerning the antioxidant properties of astaxanthin, a xanthophyll, produced by the microalga Haematococcus pluvialis in response to specific conditions of “environmental stress” and characterized by its typical deep red color. Natural astaxanthin establishes effective protections against oxidative stress, neutralizing free radicals in both the inner and outer layer of cell membranes, especially in mitochondria. The most recent preclinical and clinical studies that have investigated the beneficial properties of this molecule toward the gastrointestinal tract were included.

1. Introduction

Astaxanthin is a xanthophyll of the antioxidant group of carotenoids; widely present in the aquatic kingdom, it is produced by the microalga Haematococcus pluvialis as a natural reaction to specific environmental stress conditions, such as solar irradiation or a prolonged absence of nutrients. It has a typical intense red coloration, characteristic, for example, of krill, shrimps, lobsters, flamingos, crabs and salmon, which are species that feed directly or indirectly on the alga.

2. Astaxanthin: “The Red Gold”

2.1. Main Sources of Astaxanthin

Astaxanthin is a natural carotenoid, with red color, belonging to the class of xanthophylls [1]. The biosynthesis of astaxanthin occurs exclusively in plant organisms, bacteria and fungi, from which it reaches, through the food chain, crustaceans and fish [2]; it is responsible for the pigmentation—which turns from deep red–blue to pale pink—of the internal tissues and tegument of aquatic species (such as salmonids, shrimp, lobsters and krill) and the color of the feathers and skin of some birds, such as flamingos [3,4,5].
The primary source of astaxanthin is the microalga H. pluvialis, a unicellular, biciliate class Chlorophyceae of order Volvocales, whose habitat is found in freshwater lakes, rivers, natural pools or puddles (which dry out regularly) and is widespread in the islands of the Stockholm archipelago (Stockholms skärgård), one of the largest in the Baltic Sea [6,7].
H. pluvialis has greater biosynthetic and accumulation capacities for astaxanthin than other organisms that synthesize it, and that results in 6% of its dry weight [8].

2.2. Chemical Structure of Astaxanthin

Astaxanthin (3,3′-dihydroxy-β-carotene-4,4′-dione) is part of the xanthophylls family—carotenoids-oxygenated derivatives. The basic skeleton is an unsaturated hydrocarbon chain with 40 carbon atoms with thirteen conjugated double bonds that are perfectly symmetrical with respect to positions 15-15′ (Figure 1).
The presence of oxygen atoms in the tetraterpenic molecule makes the “small-big” difference in terms of functional capacity: these atoms provide the molecule with strong antioxidant properties. The chain of conjugated double bonds is also responsible for the antioxidant function because it produces a molecular region where electrons can be donated to reduce the number of ROS (Reactive Oxygen Species), oxidizing more reactive molecules.
The terminal rings contribute strongly to the antioxidant ability of astaxanthin, while the oxygen atoms on both sides of the terpenoid chain provides the molecule with a remarkable polarity, which allows it to fit symmetrically from one side to the other of the plasma membranes, stabilizing and protecting them more effectively than other antioxidants.

3. Astaxanthin: The “Supernutrient”

Astaxanthin has only recently obtained the status of “supernutrient”, becoming the subject of an increasing number of scientific studies [9,10]. Since our organism is not able to synthesize this precious molecule, the presence of astaxanthin at a systemic level has always been exclusively correlated with food intake and also because astaxanthin is characterized by discrete solubility in aqueous environments and presents good intestinal absorption [11]. The critical aspect related to the intake of astaxanthin from food is represented by the very high quantity of fish and crustaceans needed to reach the useful dosage (it would be necessary to consume from 600 g to 2 kg of salmon per day to obtain the optimal dosage) [12]. As this is practically impossible—also considering the problem of contamination with chemicals and heavy metals—it is essential to use astaxanthin as a food supplement (with a concentration useful for its functional effect). Compared to other carotenoids, such as β-carotene and lycopene, astaxanthin is more bioavailable since it is a lipophilic compound and endowed with polarity and, therefore, with amphipathic peculiarities (Figure 2) [11]. This molecule likely represents one of the few cases of phytochemical that, administered at low dosages (typically between 4 and 20 mg/day), reaches in vivo concentrations similar to those used in in vitro experiments. This fact means that many of the in vitro experiments are really indicative of the potential efficacy of this substance also in vivo.

4. Areas of Action and Use of Astaxanthin

Astaxanthin features make it an extraordinarily versatile nutraceutical that is able to play significant antioxidant and anti-inflammatory activities on skin, brain system, visual and the cardiovascular system. It also seems to act as an anti-aging agent, as is extensively described in the literature. We chose to turn our attention mainly on the antioxidant and anti-inflammatory effect, focusing on the gastrointestinal tract.

4.1. Antioxidant Action

An antioxidant is a molecule able to inhibits oxidation and, thus, to prevent oxidative damages: Free radicals are produced by normal aerobic metabolism, in living organisms, to support vital processes. However, when excessive amounts of oxidative species react with cellular components, such as proteins, lipids and DNA through a chain reaction, they cause excessive oxidation, resulting in damage [13]. These cellular biochemical reactions that occur physiologically and produce free radicals can also be abnormally induced by external factors such as pollution, smoking, UV rays, prolonged stress, too much physical activity or the use of additives [13,14,15]. Oxidative stress can be inhibited by endogenous and exogenous antioxidants: some foods represent great sources, as they are able to boost endogenous antioxidant systems. Carotenoids are endowed with very strong antioxidant ability: by extinguishing singlet oxygen (quenching) and eliminating radicals to end chain reactions, they can be considered excellent scavengers of peroxyl radicals that are able to interrupt the reactions that lead to oxidative damage of lipophilic compartments. The potential benefits of astaxanthin, administered as a dietary supplement, are explicated by several studies that show how its antioxidant activity is almost five times greater than β-carotene, three thousand times more powerful than resveratrol and even six thousand times more effective than vitamin C [16,17,18]. By virtue of the unique characteristics of its chemical structure, astaxanthin is much more stable than other antioxidants: While most other molecules lose their antioxidant status after capturing a free radical (becoming pro-oxidant), astaxanthin retains only the antioxidant capacity and not the pro-oxidant capacity [19,20,21]. Astaxanthin has the ability to establish effective protection against oxidative stress, neutralizing free radicals in both the inner and outer layer of cell membranes: In particular, it exerts antioxidant and anti-inflammatory properties in the mitochondria. Here, it neutralizes free radicals and protects the two membranes from oxidative stress [22].

4.2. Anti-Inflammatory and Gastrointestinal Protective Action

An efficient digestive system plays a key role in physical and mental wellbeing: Several studies have shown that the administration of astaxanthin promotes the health of the gastrointestinal system for its ability relative to lower inflammatory markers and can decrease clinical symptoms in patients. The gastrointestinal system can undergo acute and chronic inflammatory diseases, including those related to Helicobacter pylori infection that can lead to more severe diseases such as chronic type B gastritis, peptic ulcer and gastric carcinoma: Data suggest that the administration of astaxanthin decreases inflammation and provides protections toward gastric mucosa [23,24,25]. It was observed that the treatment with astaxanthin in patients with functional dyspepsia increased the expression of IFN-γ, IL-10, IL-2 and IL-8; decreased gastric inflammation; and up-regulated CD4 and down-regulated CD8 [26]. Thus, it is evident that astaxanthin significantly reduces oxidative stress, inflammation and cell proliferation in the colon through the inhibition of inflammatory markers, such as IL-1β, IL-6, TNF-α, IL-36α and IL-36γ, and the inhibition of NF-κB, AP-1 and MAPK [27,28]. Furthermore, the use of astaxanthin seems to be associated with a protective action of mitochondria, which are significantly damaged (resulting in increased ROS) by H. pylori infection [29]. A clinical study evaluating antioxidant activities in patients with functional dyspepsia showed that, in the group that was given the highest amount of astaxanthin (40 mg/die), reflux was reduced, especially in patients with H. pylori [30]. The treatment of human macrophages with krill oil—rich in PUFAs and astaxanthin—resulted in a reduction in LPS-induced IL-1β and TNF-α expression in vitro in a concentration-dependent manner. Astaxanthin also decreased the amount of Rickettsiales and several Lactobacillus species and, at the same time, appeared to increase the presence of Firmicutes and Lactobacillaceae in the bowel [31,32,33]. In two recent studies, astaxanthin has been shown to provide important protection toward intestinal mucosa by decreasing oxidative stress, stimulating calyciform cells and increasing IgA secretion. In addition, it decreased the loss of beneficial bacteria such as Lactobacillus and Bifidobacteria and affected Clostridium coccoides and Enterobacteriaceae: as a result, key metabolites of the gut microbiota, including acetic acid, propionic acid, butyric acid and other short-chain fatty acids, were indirectly increased, thereby improving gut function and immunity [33,34]. Further studies confirm that astaxanthin positively modulates the composition of the gut microbiota by optimizing the ratio Bacteroides/Firmicutes while improving the abundance of Akkermansia and Verrucomicrobia species, which protect the gut from pathogens [35,36,37]. In addition, it is noteworthy that, in a recent study in 2021, astaxanthin treatments were shown to effectively reduce intestinal damage, even in necrotizing enterocolitis [38].

5. Conclusions

In conclusion, the feature of natural astaxanthin make it a nutraceutical with a broad spectrum of potential clinical applications, particularly due to its powerful antioxidant and anti-inflammatory activities, even at low doses, and due to its excellent bioavailability. In the gastrointestinal tract, this molecule may be used as nutraceutical approach, even in combination with other nutraceuticals, to help restore physiological balance and inhibiting degenerative events associated with infections, inflammation and various syndromes related to genetic, environmental, psychological and aging factors. Scientific research is introducing new perspectives to the uses of this antioxidant, and it is evaluating a possible use concerning the protection and improvement of the intestinal microbiota, improving the general state of health and the possible onset of dangerous pathologies.

Author Contributions

Conceptualization, L.B.M. and R.B.; methodology, L.B.M. and G.B.; validation, R.B., M.M. and M.D.; writing—original draft preparation, L.B.M. and R.B.; writing—review and editing, L.B.M., R.B., M.M., M.D. and I.C.; visualization, R.B., M.M., I.C. and G.B.; supervision, R.B., M.M. and M.D.; funding acquisition, L.B.M. and R.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study did not require ethical approval.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Tan, B.L.; Norhaizan, M.E. Carotenoids: How Effective Are They to Prevent Age-Related Diseases? Molecules 2019, 24, 1801. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Yuan, J.-P.; Peng, J.; Yin, K.; Wang, J.-H. Potential Health-Promoting Effects of Astaxanthin: A High-Value Carotenoid Mostly from Microalgae. Mol. Nutr. Food Res. 2011, 55, 150–165. [Google Scholar] [CrossRef] [PubMed]
  3. Farruggia, C.; Yang, Y.; Kim, B.; Pham, T.; Bae, M.; Park, Y.-K.; Lee, J.-Y. Astaxanthin Plays Anti-Inflammatory and Antioxidant Effects by Inhibiting NFkB Nuclear Translocation and NOX2 Expression in Macrophages. FASEB J. 2015, 29, 603–608. [Google Scholar]
  4. Candore, G.; Scapagnini, G.; Caruso, C. Aging and Anti-Aging Strategies. In Textbook of Aging Skin; Farage, M.A., Miller, K.W., Maibach, H.I., Eds.; Springer: Berlin/Heidelberg, Germany, 2010; pp. 1055–1061. ISBN 978-3-540-89656-2. [Google Scholar]
  5. Komatsu, T.; Sasaki, S.; Manabe, Y.; Hirata, T.; Sugawara, T. Preventive Effect of Dietary Astaxanthin on UVA-Induced Skin Photoaging in Hairless Mice. PLoS ONE 2017, 12, e0171178. [Google Scholar] [CrossRef] [Green Version]
  6. Collins, A.M.; Jones, H.D.T.; Han, D.; Hu, Q.; Beechem, T.E.; Timlin, J.A. Carotenoid Distribution in Living Cells of Haematococcus Pluvialis (Chlorophyceae). PLoS ONE 2011, 6, e24302. [Google Scholar] [CrossRef] [Green Version]
  7. Shah, M.; Liang, Y.; Cheng, J.J.; Daroch, M. Astaxanthin-Producing Green Microalga Haematococcus Pluvialis: From Single Cell to High Value Commercial Products. Front. Plant Sci. 2016, 7, 531. [Google Scholar] [CrossRef] [Green Version]
  8. Baralic, I.; Djordjevic, B.; Dikic, N.; Kotur-Stevuljevic, J.; Spasic, S.; Jelic-Ivanovic, Z.; Radivojevic, N.; Andjelkovic, M.; Pejic, S. Effect of Astaxanthin Supplementation on Paraoxonase 1 Activities and Oxidative Stress Status in Young Soccer Players. Phytother. Res. 2013, 27, 1536–1542. [Google Scholar] [CrossRef]
  9. Capelli, B.; Bagchi, D.; Cysewski, G.R. Synthetic Astaxanthin Is Significantly Inferior to Algal-Based Astaxanthin as an Antioxidant and May Not Be Suitable as a Human Nutraceutical Supplement. Nutrafoods 2013, 12, 145–152. [Google Scholar] [CrossRef]
  10. Natural Astaxanthin Hawaii’s Supernutrient by William Sears MD: VERY GOOD Paperback (2015)|Discover Books. Available online: https://www.abebooks.com/9780979235344/Natural-Astaxanthin-Hawaiis-Supernutrient-William-0979235340/plp (accessed on 1 March 2022).
  11. Yang, Y.; Kim, B.; Lee, J.Y. Astaxanthin Structure, Metabolism, and Health Benefits. J. Hum. Nutr. Food Sci. 2013, 1, 1–1003. [Google Scholar]
  12. Seabra, L.M.J.; Pedrosa, L.F.C. Astaxanthin: Structural and Functional Aspects. Rev. Nutr. 2010, 23, 1041–1050. [Google Scholar] [CrossRef] [Green Version]
  13. Higuera-Ciapara, I.; Félix-Valenzuela, L.; Goycoolea, F.M. Astaxanthin: A Review of Its Chemistry and Applications. Crit. Rev. Food Sci. Nutr. 2006, 46, 185–196. [Google Scholar] [CrossRef]
  14. Hussein, G.; Sankawa, U.; Goto, H.; Matsumoto, K.; Watanabe, H. Astaxanthin, a Carotenoid with Potential in Human Health and Nutrition. J. Nat. Prod. 2006, 69, 443–449. [Google Scholar] [CrossRef]
  15. Okada, Y.; Ishikura, M.; Maoka, T. Bioavailability of Astaxanthin in Haematococcus Algal Extract: The Effects of Timing of Diet and Smoking Habits. Biosci. Biotechnol. Biochem. 2009, 73, 1928–1932. [Google Scholar] [CrossRef] [Green Version]
  16. Ranga Rao, A.; Raghunath Reddy, R.L.; Baskaran, V.; Sarada, R.; Ravishankar, G.A. Characterization of Microalgal Carotenoids by Mass Spectrometry and Their Bioavailability and Antioxidant Properties Elucidated in Rat Model. J. Agric. Food Chem. 2010, 58, 8553–8559. [Google Scholar] [CrossRef]
  17. Nishida, Y.; Yamashita, E.; Miki, W. Quenching Activities of Common Hydrophilic and Lipophilic Antioxidants against Singlet Oxygen Using Chemiluminescence Detection System. Carotenoid Sci. 2007, 11, 16–20. [Google Scholar] [CrossRef]
  18. Paterson, E.; Gordon, M.H.; Niwat, C.; George, T.W.; Parr, L.; Waroonphan, S.; Lovegrove, J.A. Supplementation with Fruit and Vegetable Soups and Beverages Increases Plasma Carotenoid Concentrations but Does Not Alter Markers of Oxidative Stress or Cardiovascular Risk Factors. J. Nutr. 2006, 136, 2849–2855. [Google Scholar] [CrossRef] [Green Version]
  19. Kidd, P. Astaxanthin, Cell Membrane Nutrient with Diverse Clinical Benefits and Anti-Aging Potential. Altern. Med. Rev. 2011, 16, 355–364. [Google Scholar]
  20. Camera, E.; Mastrofrancesco, A.; Fabbri, C.; Daubrawa, F.; Picardo, M.; Sies, H.; Stahl, W. Astaxanthin, Canthaxanthin and Beta-Carotene Differently Affect UVA-Induced Oxidative Damage and Expression of Oxidative Stress-Responsive Enzymes. Exp. Dermatol. 2009, 18, 222–231. [Google Scholar] [CrossRef]
  21. Beutner, S.; Bloedorn, B.; Frixel, S.; Hernández Blanco, I.; Hoffmann, T.; Martin, H.-D.; Mayer, B.; Noack, P.; Ruck, C.; Schmidt, M.; et al. 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. 2001, 81, 559–568. [Google Scholar] [CrossRef]
  22. Choi, Y.-E.; Yun, Y.-S.; Park, J.M.; Yang, J.-W. Determination of the Time Transferring Cells for Astaxanthin Production Considering Two-Stage Process of Haematococcus Pluvialis Cultivation. Bioresour. Technol. 2011, 102, 11249–11253. [Google Scholar] [CrossRef]
  23. Han, H.; Lim, J.W.; Kim, H. Astaxanthin Inhibits Helicobacter Pylori-Induced Inflammatory and Oncogenic Responses in Gastric Mucosal Tissues of Mice. J. Cancer Prev. 2020, 25, 244–251. [Google Scholar] [CrossRef]
  24. Chang, M.X.; Xiong, F. Astaxanthin and Its Effects in Inflammatory Responses and Inflammation-Associated Diseases: Recent Advances and Future Directions. Molecules 2020, 25, 5342. [Google Scholar] [CrossRef]
  25. Wang, X.; Willén, R.; Wadström, T. Astaxanthin-Rich Algal Meal and Vitamin C Inhibit Helicobacter Pylori Infection in BALB/cA Mice. Antimicrob. Agents Chemother. 2000, 44, 2452–2457. [Google Scholar] [CrossRef] [Green Version]
  26. Andersen, L.P.; Holck, S.; Kupcinskas, L.; Kiudelis, G.; Jonaitis, L.; Janciauskas, D.; Permin, H.; Wadström, T. Gastric Inflammatory Markers and Interleukins in Patients with Functional Dyspepsia Treated with Astaxanthin. FEMS Immunol. Med. Microbiol. 2007, 50, 244–248. [Google Scholar] [CrossRef] [Green Version]
  27. Sakai, S.; Nishida, A.; Ohno, M.; Inatomi, O.; Bamba, S.; Sugimoto, M.; Kawahara, M.; Andoh, A. Astaxanthin, a Xanthophyll Carotenoid, Prevents Development of Dextran Sulphate Sodium-Induced Murine Colitis. J. Clin. Biochem. Nutr. 2019, 64, 66–72. [Google Scholar] [CrossRef] [Green Version]
  28. Kochi, T.; Shimizu, M.; Sumi, T.; Kubota, M.; Shirakami, Y.; Tanaka, T.; Moriwaki, H. Inhibitory Effects of Astaxanthin on Azoxymethane-Induced Colonic Preneoplastic Lesions in C57/BL/KsJ-Db/Db Mice. BMC Gastroenterol. 2014, 14, 212. [Google Scholar] [CrossRef] [Green Version]
  29. Kim, S.H.; Lim, J.W.; Kim, H. Astaxanthin Inhibits Mitochondrial Dysfunction and Interleukin-8 Expression in Helicobacter Pylori-Infected Gastric Epithelial Cells. Nutrients 2018, 10, 1320. [Google Scholar] [CrossRef] [Green Version]
  30. Kupcinskas, L.; Lafolie, P.; Lignell, A.; Kiudelis, G.; Jonaitis, L.; Adamonis, K.; Andersen, L.P.; Wadström, T. Efficacy of the Natural Antioxidant Astaxanthin in the Treatment of Functional Dyspepsia in Patients with or without Helicobacter Pylori Infection: A Prospective, Randomized, Double Blind, and Placebo-Controlled Study. Phytomedicine 2008, 15, 391–399. [Google Scholar] [CrossRef]
  31. Liu, F.; Smith, A.D.; Solano-Aguilar, G.; Wang, T.T.Y.; Pham, Q.; Beshah, E.; Tang, Q.; Urban, J.F.; Xue, C.; Li, R.W. Mechanistic Insights into the Attenuation of Intestinal Inflammation and Modulation of the Gut Microbiome by Krill Oil Using in Vitro and in Vivo Models. Microbiome 2020, 8, 83. [Google Scholar] [CrossRef]
  32. Wu, L.; Lyu, Y.; Srinivasagan, R.; Wu, J.; Ojo, B.; Tang, M.; El-Rassi, G.D.; Metzinger, K.; Smith, B.J.; Lucas, E.A.; et al. Astaxanthin-Shifted Gut Microbiota Is Associated with Inflammation and Metabolic Homeostasis in Mice. J. Nutr. 2020, 150, 2687–2698. [Google Scholar] [CrossRef]
  33. Zhang, X.; Zhao, X.; Tie, S.; Li, J.; Su, W.; Tan, M. A Smart Cauliflower-like Carrier for Astaxanthin Delivery to Relieve Colon Inflammation. J. Control Release 2022, 342, 372–387. [Google Scholar] [CrossRef] [PubMed]
  34. Cao, Y.; Yang, L.; Qiao, X.; Xue, C.; Xu, J. Dietary Astaxanthin: An Excellent Carotenoid with Multiple Health Benefits. Crit. Rev. Food Sci. Nutr. 2021, 1–27. [Google Scholar] [CrossRef] [PubMed]
  35. Wang, J.; Liu, S.; Wang, H.; Xiao, S.; Li, C.; Li, Y.; Liu, B. Xanthophyllomyces Dendrorhous-Derived Astaxanthin Regulates Lipid Metabolism and Gut Microbiota in Obese Mice Induced by A High-Fat Diet. Mar. Drugs 2019, 17, 337. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Liu, H.; Liu, M.; Fu, X.; Zhang, Z.; Zhu, L.; Zheng, X.; Liu, J. Astaxanthin Prevents Alcoholic Fatty Liver Disease by Modulating Mouse Gut Microbiota. Nutrients 2018, 10, 1298. [Google Scholar] [CrossRef] [Green Version]
  37. Wang, M.; Ma, H.; Guan, S.; Luo, T.; Zhao, C.; Cai, G.; Zheng, Y.; Jia, X.; Di, J.; Li, R.; et al. Astaxanthin from Haematococcus Pluvialis Alleviates Obesity by Modulating Lipid Metabolism and Gut Microbiota in Mice Fed a High-Fat Diet. Food Funct. 2021, 12, 9719–9738. [Google Scholar] [CrossRef]
  38. Akduman, H.; Tayman, C.; Korkmaz, V.; Akduman, F.; Fettah, N.D.; Gürsoy, B.K.; Turkmenoglu, T.T.; Çağlayan, M. Astaxanthin Reduces the Severity of Intestinal Damage in a Neonatal Rat Model of Necrotizing Enterocolitis. Am. J. Perinatol. 2021. [Google Scholar] [CrossRef]
Figure 1. Natural astaxanthin chemical structure.
Figure 1. Natural astaxanthin chemical structure.
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Figure 2. Location of astaxanthin and other antioxidants in the cell membrane.
Figure 2. Location of astaxanthin and other antioxidants in the cell membrane.
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Budriesi, R.; Micucci, M.; Daglia, M.; Corazza, I.; Biotti, G.; Mattioli, L.B. Chemical Features and Biological Effects of Astaxanthin Extracted from Haematococcus pluvialis Flotow: Focus on Gastrointestinal System. Biol. Life Sci. Forum 2022, 12, 31. https://doi.org/10.3390/IECN2022-12376

AMA Style

Budriesi R, Micucci M, Daglia M, Corazza I, Biotti G, Mattioli LB. Chemical Features and Biological Effects of Astaxanthin Extracted from Haematococcus pluvialis Flotow: Focus on Gastrointestinal System. Biology and Life Sciences Forum. 2022; 12(1):31. https://doi.org/10.3390/IECN2022-12376

Chicago/Turabian Style

Budriesi, Roberta, Matteo Micucci, Maria Daglia, Ivan Corazza, Giulia Biotti, and Laura Beatrice Mattioli. 2022. "Chemical Features and Biological Effects of Astaxanthin Extracted from Haematococcus pluvialis Flotow: Focus on Gastrointestinal System" Biology and Life Sciences Forum 12, no. 1: 31. https://doi.org/10.3390/IECN2022-12376

APA Style

Budriesi, R., Micucci, M., Daglia, M., Corazza, I., Biotti, G., & Mattioli, L. B. (2022). Chemical Features and Biological Effects of Astaxanthin Extracted from Haematococcus pluvialis Flotow: Focus on Gastrointestinal System. Biology and Life Sciences Forum, 12(1), 31. https://doi.org/10.3390/IECN2022-12376

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