Nitric Oxide Production Inhibition and Anti-Mycobacterial Activity of Extracts and Halogenated Sesquiterpenes from the Brazilian Red Alga Laurencia Dendroidea J. Agardh

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Abstract
Pharmacognosy Magazine,2015,11,44s3,s611-s618.
Published:December 2015
Type:Original Article
Authors:
Author(s) affiliations:

Thatiana Lopes Biá Ventura1,2, Fernanda Lacerda da Silva Machado3,4, Marlon Heggdorne de Araujo1,2, Lísia Mônica de Souza Gestinari4, Carlos Roland Kaiser3, Francisco de Assis Esteves4, Elena B. Lasunskaia1, Angélica Ribeiro Soares3,4, Michelle Frazão Muzitano2

1 Laboratory of Biology of Recognition, Center of Bioscience and Biotechnology, Darcy Ribeiro University of Northern Fluminense, Campos dos Goytacazes-RJ,

2 Laboratory of Bioactive Products, School of Pharmacy , Federal University of Rio de Janeiro, Macaé/ IMMT-RJ,

3 Department of Organic Chemistry, Institute of Chemistry, Federal University of Rio de Janeiro, Rio de Janeiro,

4 Group of Natural Products from Aquatic Organisms, Center for Ecology and Socio-Environmental Development, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil

Abstract:

Background: Red algae of the genus Laurencia J. V. Lamouroux are a rich source of secondary metabolites with important pharmacological activities such as anti‑tumoral, anti‑inflammatory, anti‑fungal, anti‑viral, anti‑leishmanial, anti‑helminthic, anti‑malarial, anti‑trypanosomal, anti‑microbial as well as anti‑bacterial against Mycobacterium tuberculosis. Objective: In the present study, we evaluated the inhibition of nitric oxide  (NO) and tumor necrosis factor‑α production and the anti‑mycobacterial activity of crude extracts from the red Alga Laurencia dendroidea  (from the South‑Eastern coast of Brazil). Halogenated sesquiterpenes elatol  (1), obtusol  (2) and cartilagineol (3), previously isolated from this Alga by our group, were also studied. Materials and Methods: The lipopolysaccharide‑activated macrophage cells  (RAW 264.7) were used as inflammation model. Cytotoxic effect was determined using a commercial lactate dehydrogenase (LDH) kit and 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyltetrazolium bromide assay. The growing Mycobacterium inhibition was verified against Mycobacterium bovis Bacillus Calmette–Guérin and M. tuberculosis H37Rv strains. Results: The crude extract from Alga collected at Angra dos Reis, RJ, Brazil, was the most active inhibitor of both mycobacterial growth  (half maximal inhibitory concentration [IC50] 8.7 ± 1.4 µg/mL) and NO production by activated macrophages (IC50 5.3 ± 1.3 µg/mL). The assays with isolated compounds revealed the anti‑mycobacterial activity of obtusol  (2), whereas  (‑)‑elatol (1) inhibited the release of inflammatory mediators, especially NO. To our knowledge, this is the first report describing an anti‑mycobacterial effect of L. dendroidea extract and demonstrating the association of this activity with obtusol  (2). Conclusion: The described effects of active compounds from L. dendroidea are promising for the control of inflammation in infectious diseases and specifically, against mycobacterial infections associated with exacerbated inflammation.

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