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1.
Protoplasma ; 254(2): 817-837, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27352314

RESUMO

Sargassum cymosum was exposed to cadmium (Cd) to determine any physiological and ultrastructural effects. To accomplish this, S. cymosum samples were cultivated under photosynthetic active radiation (PAR) and Cd (0, 0.1, 0.2, 0.4 and 0.8 mg L-1) during 7 and 14 days in laboratory-controlled conditions (0 mg L-1 Cd at both exposure times as control). Seaweeds had high retention capacity (over 90 %) for both exposure times. Growth rates showed significant increases by 14 days, especially for 0.1 and 0.4 mg L-1 Cd. Photosynthetic parameters were unaffected by Cd treatments. Chlorophyll contents were present in higher concentrations for all Cd treatments compared to respective control. Carotenoid profile showed significant differences in total composition and proportion of fucoxanthin and ß-carotene, and no lutein was detected at 14 days. Phenolic and flavonoid compounds showed major accumulation at 14 days. Transmission electron microscopy (TEM) analyses presented major alterations in Cd-treated samples, when compared with respective control, in particular disorganization of cell wall fibrils. When compared to respective control samples, multivariate analyses showed disparate and complex interactions among metabolites in Cd-exposed seaweeds, giving evidence of physiological defence response. Thus, it can be concluded that Cd is a stressor for S. cymosum, resulting in physiological and structural alterations related to defence mechanisms against oxidative stress and toxicological effects resulting from long-term metal exposure. However, in the present paper, some observed changes also appear to result from acclimation mechanisms under lower concentration of Cd relative to the tolerance of S. cymosum to experimental conditions.


Assuntos
Cádmio/toxicidade , Sargassum/citologia , Sargassum/metabolismo , Alga Marinha/citologia , Alga Marinha/metabolismo , Análise de Variância , Antioxidantes/metabolismo , Cádmio/análise , Carboidratos/análise , Sobrevivência Celular/efeitos dos fármacos , Clorofila/metabolismo , Clorofila A , Cromatografia Líquida de Alta Pressão , Flavonoides/análise , Fluorescência , Análise Multivariada , Fenóis/análise , Fotossíntese/efeitos dos fármacos , Análise de Componente Principal , Sargassum/efeitos dos fármacos , Sargassum/ultraestrutura , Água do Mar/química , Alga Marinha/efeitos dos fármacos , Alga Marinha/ultraestrutura , Solubilidade
2.
Ying Yong Sheng Tai Xue Bao ; 22(8): 2167-72, 2011 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-22097383

RESUMO

This paper studied the dynamics of reproductive allocation (RA) of Sargassum thunbergii during its sexual reproductive season and the related environmental factors at the Taiping Cape of Yellow Sea. The sexual reproduction of S. thunbergii initiated in early June, peaked in mid July when the sea water temperature was about 22 degrees C (the mean proportion of biomass allocated to reproductive organs on July 19 was 76.7%), and ended in late August. The RA had a significant linear correlation with the average length of thallus branches (r = 0.855, P < 0.01). The thalli with a length less than 10 cm showed a lower RA in the whole sexual reproductive season, while the thalli longer than 10 cm had a RA up to averagely 70.0% at the peak maturing stage. UNIANOVA analysis showed that both tidal level and wave strength had significant effects on the RA of S. thunbergii (tidal level: F = 175.62, P < 0.01; wave strength: F = 95.35, P < 0.01), and there was a significant interaction between tidal level and wave strength (F = 9.14, P < 0.05). The sizes of the effects were in the order of tidal level > wave strength > tidal level x wave strength.


Assuntos
Ecossistema , Sargassum/crescimento & desenvolvimento , Sargassum/fisiologia , Biomassa , China , Oceanos e Mares , Reprodução/fisiologia , Sargassum/citologia , Movimentos da Água
3.
Clin Exp Pharmacol Physiol ; 34(3): 142-7, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17250630

RESUMO

1. The aim of the present study was to assess the protective effect of Sargassum polycystum (sulphated polysaccharide) extract against paracetamol-induced DNA strand breaks and modulation of membrane-bound phosphatases, protein thiols and inorganic cations during toxic hepatitis. 2. Seaweed extract (200 mg/kg per day for 21 days) was administered to male Wistar rats against paracetamol challenge. Serum and liver tissues were used to assess levels of ATPase, protein thiols and inorganic cations using atomic absorption spectroscopy. The fragmentation of DNA was assessed by agarose gel electrophoresis. 3. Paracetamol induced intracellular stress, accompanied by changes in the structural and functional characteristics of liver cell membranes, which affected DNA integrity, membrane-bound ATPase and inorganic cations homeostasis. Rats intoxicated with paracetamol (800 mg/kg, i.p.) showed significant impairment in activities of total ATPase, Mg2+-ATPase, Ca+-ATPase and Na+/K+-ATPase, with concomitant changes in the levels of tissue protein thiols and inorganic cations, such as Na+, K+ and Ca2+. These changes were prevented in animals pretreated with S. polycystum extract, which indicates that S. polycystum supplementation could exert some protective effect against paracetamol-induced toxic hepatitis in rats. 4. The protective effect of the seaweed extract may be due to the presence of sulphated compounds that have free radical-scavenging activity.


Assuntos
Acetaminofen/antagonistas & inibidores , Acetaminofen/toxicidade , Antioxidantes , Doença Hepática Induzida por Substâncias e Drogas/patologia , Fragmentação do DNA/efeitos dos fármacos , Monoéster Fosfórico Hidrolases/metabolismo , Polissacarídeos/farmacologia , Sargassum/química , Adenosina Trifosfatases/metabolismo , Animais , Cátions/metabolismo , Doença Hepática Induzida por Substâncias e Drogas/enzimologia , DNA/efeitos dos fármacos , Histocitoquímica , Fígado/enzimologia , Masculino , Membranas/enzimologia , Polissacarídeos/administração & dosagem , Ratos , Ratos Wistar , Sargassum/citologia , Espectrofotometria Atômica , Sulfatos , Compostos de Sulfidrila/metabolismo
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