2018
DOI: 10.1007/s10646-018-1984-7
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Spermidine application alleviates salinity damage to antioxidant enzyme activity and gene expression in alfalfa

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Cited by 26 publications
(16 citation statements)
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“…ETH treatment significantly decreased the content of MDA, while STS treatment elevated MDA level in NaCl-stressed alfalfa. After NaCl stress, the content of H 2 O 2 increases in salt-sensitive varieties Juneng 418Q and Sibeide, which was same with the result for alfalfa cultivar Magnum Salt (Lou et al, 2018). H 2 O 2 content decreases after ETH or ACC treatment, which alleviates the degree of oxidative damage of cell membrane system and improves the salt tolerance of alfalfa to a certain extent.…”
Section: Discussionsupporting
confidence: 79%
“…ETH treatment significantly decreased the content of MDA, while STS treatment elevated MDA level in NaCl-stressed alfalfa. After NaCl stress, the content of H 2 O 2 increases in salt-sensitive varieties Juneng 418Q and Sibeide, which was same with the result for alfalfa cultivar Magnum Salt (Lou et al, 2018). H 2 O 2 content decreases after ETH or ACC treatment, which alleviates the degree of oxidative damage of cell membrane system and improves the salt tolerance of alfalfa to a certain extent.…”
Section: Discussionsupporting
confidence: 79%
“…Radhakrishnan et al [ 150 ] reported that the addition of spermidine significantly ameliorated the devastating effects of osmotic stress by regulating the level of plant hormones and antioxidants. In a most recent study in alfalfa, the exogenous application of sperimidine positively alleviates SS-induced damage [ 151 ]. Nahar et al [ 152 ] reported that exogenous application of polyamines maintained nutrient homeostasis and reduced cellular Na content as well as regulated endogeneous polyamine concentrations in mungbean under salinity stress.…”
Section: Management Strategies To Improve Salt Tolerance In Legumementioning
confidence: 99%
“…The pigment concentration was calculated based on the method of Porra et al 19 Briey, the absorbance of the extracted supernatant was measured spectrophotometrically at 652 nm (A 652 ) and 665 nm (A 665 ). Intracellular chlorophyll a and b concentrations were calculated using the following eqn (4) Chlorophyll uorescence parameters of the microalgal cells were tested by pulse modulation uorometer (FMS-2, Hansatech, Britain). The dark adaptation time in this experiment was 10 minutes.…”
Section: Analysis Of Chlorophyll Content In Microalgal Cellsmentioning
confidence: 99%