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Review
. 2015 Aug 14;13(8):5128-55.
doi: 10.3390/md13085128.

Carotenoids from Marine Microalgae: A Valuable Natural Source for the Prevention of Chronic Diseases

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Review

Carotenoids from Marine Microalgae: A Valuable Natural Source for the Prevention of Chronic Diseases

Maria Filomena de Jesus Raposo et al. Mar Drugs. .

Abstract

Epidemiological studies have shown a relation between antioxidants and the prevention of several chronic diseases. Microalgae are a potential novel source of bioactive molecules, including a wide range of different carotenoids that can be used as nutraceuticals, food supplements and novel food products. The objective of this review is (i) to update the research that has been carried out on the most known carotenoids produced by marine microalgae, including reporting on their high potentialities to produce other less known important compounds; (ii) to compile the work that has been done in order to establish some relationship between carotenoids and oxidative protection and treatment; (iii) to summarize the association of oxidative stress and the various reactive species including free radicals with several human diseases; and (iv) to provide evidence of the potential of carotenoids from marine microalgae to be used as therapeutics to treat or prevent these oxidative stress-related diseases.

Keywords: RNS; ROS; aging; astaxanthin; carotenoids; chronic diseases; free radicals; fucoxanthin; inflammatory diseases; marine microalga; oxidative stress; β-carotene.

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Figures

Figure 1
Figure 1
Pathways for the carotenogenesis and biosynthesis of astaxanthin, based on Han et al. [27], Dambek et al. [48] and Takaichi [29], and the synthesis of fucoxanthin and diadinoxanthin in diatoms [61], including P. tricornutum, proposed by Dambek and colleagues [48]. The genes and enzymes involved in the process and already identified in some microalgae are evidenced; the underlined ones were reported by Bertrand [61].
Figure 2
Figure 2
Cascade triggered within a cell by O2•− (superoxide radical) generated mainly by NADPH oxidase. Some reactions with lipid hydroperoxides (LOOH) are also included (dashed arrows; M = transition metal) [58,63,64,65].

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