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1.
Biosci. j. (Online) ; 36(6): 2078-2091, 01-11-2020. tab, graf, ilus
Article in English | LILACS | ID: biblio-1148246

ABSTRACT

The first experiment was conducted to evaluate the impact of seed priming on germination behavior and seedling establishment in Vicia faba and Vicia sativa, for that, seeds priming was done using SA (100 µM) and KH2PO4. In order to determine the optimal concentration of KH2PO4 for improving germination, different concentrations were used: 25 µM, 50 µM, and 100 µM. The best germination behavior and seedling establishment were obtained with 25 and 50 µM KH2PO4, respectively for Vicia faba and Vicia sativa. Moreover, data showed that 100 µM of SA improved seed germination as well as the seedling establishment for both species. The second experiment was carried out to investigate the influence of seed priming for improving phosphorous (P) deficiency tolerance. To do, seedling obtained from primed and nonprimed seeds were grown in a hydroponic culture system with three different treatments: control (C, medium containing sufficient P concentration: 360 µM KH2PO4), direct phosphorus-deficient (DD, medium containing only 10 µM KH2PO4), and induced P deficiency by bicarbonate (ID, medium containing sufficient P concentration: 360 µM KH2PO4 + 0.5 g L-1 CaCO3 + 10 mM NaHCO3). Furthermore, the role of exogenous SA applied to P deficiency tolerance enhancement was explored. Seed priming or the exogenous application of SA significantly reduced the severity effect of P deficiency. In fact, the pretreated plants were observed more tolerant to P deficiency as reflected from the significant increase in plant biomass, P uptake, and an efficient antioxidant system. Overall, this paper highlights the beneficial effect of seeds priming or the exogenous application of SA in the improvement of plant tolerance to phosphorus deficiency.


A deficiência de fósforo (P) é um fator ambiental adverso comum que limita a produção agrícola em todo o mundo. Este estudo é uma avaliação do efeito benéfico da técnica de priming de sementes para tolerância à deficiência de P em Vicia faba e Vicia sativa. Para avaliar o impacto do condicionamento das sementes no comportamento germinativo de Vicia faba e Vicia sativa, suas sementes foram imersas em diferentes concentrações de KH2PO4 (25 µM, 50 µM e 100 µM) e em 100 µM de ácido salicílico (SA) por 24 h. Os resultados obtidos definiram KH2PO4 50 µM (para Vicia sativa) e KH2PO4 25 µM (para Vicia faba) como as concentrações ótimas que garantem uma melhor germinação das sementes. Além disso, os dados mostraram que a SA melhora a germinação de sementes e o estabelecimento de mudas. Posteriormente, para investigar a contribuição dessa técnica no aumento da tolerância à deficiência de P, sementes preparadas e não preparadas foram cultivadas em solução hidropônica com três tratamentos diferentes: controle (C, meio contendo concentração suficiente de P: KH2PO4 360 µM), deficiente em fósforo direto (DD, meio contendo apenas 10 µM de KH2PO4) e deficiência induzida de P por bicarbonato (ID, meio contendo concentração suficiente de P: 360 µM de KH2PO4 + 0,5 g l-1 de CaCO3 + 10 mM de NaHCO3). Além disso, o papel da SA exógeno aplicada no aumento da tolerância à deficiência de P foi explorado. A preparação das sementes ou a aplicação exógena de SA reduziu significativamente o efeito da severidade da deficiência de P. De fato, as plantas pré-tratadas foram observadas mais tolerantes à deficiência de P, refletidas no aumento significativo da biomassa da planta, na absorção de P e em um eficiente sistema antioxidante. No geral, este artigo destaca o efeito benéfico da priming de sementes ou a aplicação exógena de SA na melhoria da tolerância das plantas à deficiência de fósforo.


Subject(s)
Vicia faba , Vicia sativa , Salicylic Acid
2.
Biochim Biophys Acta ; 1832(10): 1591-604, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23643711

ABSTRACT

The mitochondrial redox state plays a central role in the link between mitochondrial overloading and insulin resistance. However, the mechanism by which the ROS induce insulin resistance in skeletal muscle cells is not completely understood. We examined the association between mitochondrial function and H2O2 production in insulin resistant cells. Our hypothesis is that the low mitochondrial oxygen consumption leads to elevated ROS production by a mechanism associated with reduced PGC1α transcription and low content of phosphorylated CREB. The cells were transfected with either the encoded sequence for catalase overexpression or the specific siRNA for catalase inhibition. After transfection, myotubes were incubated with palmitic acid (500µM) and the insulin response, as well as mitochondrial function and fatty acid metabolism, was determined. The low mitochondrial oxygen consumption led to elevated ROS production by a mechanism associated with ß-oxidation of fatty acids. Rotenone was observed to reduce the ratio of ROS production. The elevated H2O2 production markedly decreased the PGC1α transcription, an effect that was accompanied by a reduced phosphorylation of Akt and CREB. The catalase transfection prevented the reduction in the phosphorylated level of Akt and upregulated the levels of phosphorylated CREB. The mitochondrial function was elevated and H2O2 production reduced, thus increasing the insulin sensitivity. The catalase overexpression improved mitochondrial respiration protecting the cells from fatty acid-induced, insulin resistance. This effect indicates that control of hydrogen peroxide production regulates the mitochondrial respiration preventing the insulin resistance in skeletal muscle cells by a mechanism associated with CREB phosphorylation and ß-oxidation of fatty acids.


Subject(s)
Catalase/metabolism , Hydrogen Peroxide/metabolism , Insulin Resistance , Mitochondria, Muscle/physiology , Animals , Antioxidants/metabolism , Cells, Cultured , Male , Mitochondria, Muscle/enzymology , Muscle, Skeletal/cytology , Muscle, Skeletal/enzymology , Muscle, Skeletal/metabolism , Oxygen Consumption , Palmitic Acid/pharmacology , Phosphorylation , Proto-Oncogene Proteins c-akt/metabolism , Rats , Rats, Wistar
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