Effect of the marine brown alga Canistrocarpus cervicornis on promastigote forms of Leishmania (L.) amazonensis

Planta Medica ◽  
2009 ◽  
Vol 75 (09) ◽  
Author(s):  
AO Santos ◽  
EA Britta ◽  
T Ueda-Nakamura ◽  
BP Dias Filho ◽  
EM Bianco ◽  
...  
Author(s):  
Laura De Andrade Moura ◽  
Eládio Florez Sanchez ◽  
Éverson Miguel Bianco ◽  
Renato Crespo Pereira ◽  
Valéria Laneuville Teixeira ◽  
...  

2011 ◽  
Vol 21 (2) ◽  
pp. 234-238 ◽  
Author(s):  
Thaisa Francielle S. Domingos ◽  
Magui Aparecida Vallim ◽  
Carla Carvalho ◽  
Eladio Flores Sanchez ◽  
Valéria Laneuville Teixeira ◽  
...  

2011 ◽  
Vol 1 (1) ◽  
pp. 61-66 ◽  
Author(s):  
Laura De Andrade Moura ◽  
Eládio Florez Sanchez ◽  
Éverson Miguel Bianco ◽  
Renato Crespo Pereira ◽  
Valéria Laneuville Teixeira ◽  
...  

2017 ◽  
Vol 41 (2) ◽  
pp. 296-304
Author(s):  
Fredy A. Ortiz-Ramírez ◽  
Magui Aparecida Vallim ◽  
Diana Negrão Cavalcanti ◽  
Valéria Laneuville Teixeira

Marine organisms are rich sources of natural products that, among other activities, help to maintain the species equilibrium. Samples of the marine brown alga Canistrocarpus cervicornis (Kützing) De Paula & De Clerck were collected in Búzios, Rio de Janeiro, Brazil, in June 2006. The extract was obtained in CH2Cl2 and subjected to fractionation by chromatographic methods in order to isolate and purify the compound (4R, 7R, 14S)-4α, 7α-diacethoxy-14-hydroxydolastane-1(15), 8-dien. Then, the effects of the extract and the dolastane diterpene on zygotes and gametes of the sea urchin Lytechinus variegatus were evaluated. The exposure of male and female gametes to the C. cervicornis extract promoted, respectively, a reduction of 10-30% in fertilization and a 20 to 70% decrease in the number of eggs. Furthermore, the exposure of zygotes to the extract inhibited their development up to 86.7 ± 1.6% (at a concentration of 250 µg mL-1), as well as generating abnormalities in 39-50% of zygotes. The results of the dolastane diterpene showed no evidence of inhibition in the zygotes’ development, thought it was proved to induce anomalies. At higher concentrations (25 and 50 µg mL-1), it was possible to observe cell lyses.


2011 ◽  
Vol 31 (2) ◽  
pp. 235-240 ◽  
Author(s):  
Laura de Andrade Moura ◽  
Éverson Miguel Bianco ◽  
Renato Crespo Pereira ◽  
Valéria Laneuville Teixeira ◽  
André Lopes Fuly

2009 ◽  
Vol 70 (2) ◽  
pp. 250-255 ◽  
Author(s):  
Priyanka Reddy ◽  
Sylvia Urban
Keyword(s):  

Pathogens ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 550
Author(s):  
Aya C. Taki ◽  
Robert Brkljača ◽  
Tao Wang ◽  
Anson V. Koehler ◽  
Guangxu Ma ◽  
...  

Eight secondary metabolites (1 to 8) were isolated from a marine sponge, a marine alga and three terrestrial plants collected in Australia and subsequently chemically characterised. Here, these natural product-derived compounds were screened for in vitro-anthelmintic activity against the larvae and adult stages of Haemonchus contortus (barber’s pole worm)—a highly pathogenic parasitic nematode of ruminants. Using an optimised, whole-organism screening system, compounds were tested on exsheathed third-stage larvae (xL3s) and fourth-stage larvae (L4s). Anthelmintic activity was initially evaluated on these stages based on the inhibition of motility, development and/or changes in morphology (phenotype). We identified two compounds, 6-undecylsalicylic acid (3) and 6-tridecylsalicylic acid (4) isolated from the marine brown alga, Caulocystis cephalornithos, with inhibitory effects on xL3 and L4 motility and larval development, and the induction of a “skinny-straight” phenotype. Subsequent testing showed that these two compounds had an acute nematocidal effect (within 1–12 h) on adult males and females of H. contortus. Ultrastructural analysis of adult worms treated with compound 4 revealed significant damage to subcuticular musculature and associated tissues and cellular organelles including mitochondria. In conclusion, the present study has discovered two algal compounds possessing acute anthelmintic effects and with potential for hit-to-lead progression. Future work should focus on undertaking a structure-activity relationship study and on elucidating the mode(s) of action of optimised compounds.


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