Enhanced Antitumoral Activity of Extracts Derived from Cultured Udotea flabellum (Chlorophyta)

Very few studies have been performed to evaluate the effect of culture conditions on the production or activity of active metabolites in algae. Previous studies suggest that the synthesis of bioactive compounds is strongly influenced by irradiance level. To investigate whether the antiproliferative activity of Udotea flabellum extracts is modified after cultivation, this green alga was cultured under four photon flux densities (PFD) for 30 days. After 10, 20, and 30 days, algae were extracted with dichloromethane: methanol and screened for antiproliferative activity against four human cancer cell lines (laryngeal—Hep-2, cervix—HeLa, cervix squamous—SiHa and nasopharynx—KB) by SRB assay. Lipid and phenol content were evaluated by standardized methods on algae organic extracts. After 10 days of cultivation, organic U. flabellum extracts showed a significant increase in antiproliferative activity on Hela and SiHa cells when compared to noncultured algae extracts. Extracts obtained after 10 and 20 days of culture were active on KB and Hep-2 cells. Total phenol and polyunsaturated fatty acid content in organic extracts changed with cultivation time but not by irradiance treatment. Extracts from U. flabellum obtained after 10 and 20 days of culture have been selected for fractionation and isolation of active compounds

Antiprotozoal Activities of Organic Extracts from French Marine Seaweeds

Marine macrophytes contain a variety of biologically active compounds, some reported to have antiprotozoal activity in vitro. As a part of a screening program to search for new natural antiprotozoals, we screened hydroalcoholic and ethyl acetate extracts of 20 species of seaweeds from three phyla (Rhodophyta, Heterokontophyta and Chlorophyta), sampled along the Normandy (France) coast. We tested them in vitro against the protozoa responsible for three major endemic parasitic diseases: Plasmodium falciparum, Leishmania donovani and Trypanosoma cruzi. The selectivity of the extracts was also evaluated by testing on a mammalian cell line (L6 cells). Ethyl acetate extracts were more active than hydroalcoholic ones. Activity against T. cruzi and L. donovani was non-existent to average, but almost half the extracts showed good activity against P. falciparum. The ethyl acetate extract of Mastocarpus stellatus showed the best antiplasmodial activity as well as the best selectivity index (IC50 = 2.8 μg/mL; SI > 30). Interestingly, a red algae species, which shares phylogenetic origins with P. falciparum, showed the best antiplasmodial activity. This study is the first to report comparative antiprotozoal activity of French marine algae. Some of the species studied here have not previously been biologically evaluated

Effect of Elatol, Isolated from Red Seaweed Laurencia dendroidea, on Leishmania amazonensis

In the present study, we investigated the antileishmanial activity of sesquiterpene elatol, the major constituent of the Brazilian red seaweed Laurencia dendroidea (Hudson) J.V. Lamouroux, against L. amazonensis. Elatol after 72 h of treatment, showed an IC50 of 4.0 μM and 0.45 μM for promastigote and intracellular amastigote forms of L. amazonensis, respectively. By scanning and transmission electron microscopy, parasites treated with elatol revealed notable changes compared with control cells, including: pronounced swelling of the mitochondrion; appearance of concentric membrane structures inside the organelle; destabilization of the plasma membrane; and formation of membrane structures, apparently an extension of the endoplasmic reticulum, which is suggestive of an autophagic process. A cytotoxicity assay showed that the action of the isolated compound is more specific for protozoa, and it is not toxic to macrophages. Our studies indicated that elatol is a potent antiproliferative agent against promastigote and intracellular amastigote forms, and may have important advantages for the development of new anti-leishamanial chemotherapies

Impact of Marine Drugs on Cytoskeleton-Mediated Reproductive Events

Marine organisms represent an important source of novel bioactive compounds, often showing unique modes of action. Such drugs may be useful tools to study complex processes such as reproduction; which is characterized by many crucial steps that start at gamete maturation and activation and virtually end at the first developmental stages. During these processes cytoskeletal elements such as microfilaments and microtubules play a key-role. In this review we describe: (i) the involvement of such structures in both cellular and in vitro processes; (ii) the toxins that target the cytoskeletal elements and dynamics; (iii) the main steps of reproduction and the marine drugs that interfere with these cytoskeleton-mediated processes. We show that marine drugs, acting on microfilaments and microtubules, exert a wide range of impacts on reproductive events including sperm maturation and motility, oocyte maturation, fertilization, and early embryo development

Structural Color in Marine Algae

Structural colouration is widespread in the marine environment. Within the large variety of marine organisms, macroalgae represent a diverse group of more than 24,700 species. Some macroalgae have developed complex optical responses using different nanostructures and material compositions. In this review, we describe the mechanisms that are employed to produce structural colour in algae and provide a discussion on the functional relevance by analysing the geographical distribution and ecology in detail. In contrast to what is observed in the animal kingdom, we hypothesise that structural colour in algae predominantly functions for a non-communicative purpose, most likely protection from radiation damage, e.g. by harmful UV light. We suggest that the presence of structural colour in algae is likely influenced by local factors such as radiation intensity and turbidity of the water.Biotechnology and Biological Sciences Research Council (Grant ID: BBSRC David Phillips, 13 BB/K014617/1), European Research Council (Grant ID: ERC-2014-STG H2020 639088), Department of Chemistry, Cambridge (Philip and Patricia Brown Next Generation Fellowship), National Centre of Competence in Research “Bio-Inspired Materials”, Adolphe Merkle Foundatio

Improved Antitumoral Activity of Extracts Derived from Cultured Penicillus dumetosus

Purpose: Extracts of the green alga, Penicillus dumetosus , have shown antiproliferative activity against several cancer cell lines. The aim of this study was to evaluate if this activity is modified after cultivation. Methods: P. dumetosus was cultured under different light treatments. After 10, 20 and 30 days, alga samples were collected and their organic extracts prepared. Lipid and phenol contents were evaluated by standardized methods. Antiproliferative activity was assayed in four cancer cell lines (Hep-2, HeLa, SiHa, and KB) while cytotoxic activity was evaluated on a normal cell line (MDCK). Results: The 10-day cultivation organic extract exhibited increased antiproliferative activity compared with the control on human carcinoma nasopharynx (KB) and laryngeal (Hep-2) cell lines. The inhibition of cell growth (IC50) of 20-and 30-day extracts decreased compared with the control, except for KB. This activity was related to induction of apoptosis as evidenced by DNA fragmentation. All the extracts showed low cytotoxicity. Total phenol content in the organic extracts did not change during cultivation; however, polyunsaturated fatty acid content was modified under different light treatments. Conclusion: The 10-day cultivation extract from P. dumetosus culture under conditions described in this study showed increased antiproliferative activity compared with the control and induced apoptosis on SiHa, HeLa, Hep-2 and KB cells