Cited by 837Plant Stress Responses and ToleranceRedox biology and oxidative stressGlutathione Transferases and Polymorphisms

The DOI matches its Crossref record; 73 of the 74 references it cites were found in a registry or an index.

Tolerance of pea (Pisum sativum L.) to long‐term salt stress is associated with induction of antioxidant defences

Open access

Hernández, J. A., Jiménez, A., Mullineaux, P., Sevilia, F.·2000·Plant, Cell & Environment

DOI 10.1046/j.1365-3040.2000.00602.x

Open this paper in CoChat — free account Open PDF

Abstract

ABSTRACT Using two cultivars of Pisum sativum L. with different sensitivity to NaCl, the effect of long‐term (15 d) NaCl (70 m M) treatments on the activity and expression of the foliar ascorbate–glutathione cycle enzymes, superoxide dismutase isozymes and their mRNAs was evaluated and related to their ascorbate and glutathione contents. High‐speed supernatant (soluble) fractions, enriched for cytosolic components of the antioxidant system, were used. In this fraction from the NaCl‐tolerant variety (cv Granada), the activities of ascorbate peroxidase (APX), glutathione reductase (GR), monodehydroascorbate reductase (MDHAR), Mn‐superoxide dismutase (Mn‐SOD) and dehydroascorbate reductase (DHAR) increased, while CuZn‐SOD activity remained constant. In the NaCl‐sensitive plants (cv Challis), salinity did not produce significant changes in APX, MDHAR and GR activities. Only DHAR activity was induced in cv Challis, whereas soluble CuZn‐SOD activity decreased by about 35%. Total ascorbate and glutathione contents decreased in both cultivars, but the decline was greater in NaCl‐sensitive plants. This difference between the two cultivars was more pronounced when the transcript levels of some these enzymes were examined. Transcript levels for mitochondrial Mn‐SOD, chloroplastic CuZn‐SOD and phospholipid hydroperoxide glutathione peroxidase (PHGPX), cytosolic GR and APX were strongly induced in the NaCl‐tolerant variety but not in the NaCl‐sensitive variety. These data strongly suggest that induction of antioxidant defences is at least one component of the tolerance mechanism of peas to long‐term salt‐stress.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1046/j.1365-3040.2000.00602.x

Cites

73 of 73 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
Feinberg, A. P., & Vogelstein, B. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90418-9 · Cited by 24,512
ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control
Noctor, G., & Foyer, C. H. (1998) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.49.1.249 · Cited by 5,722
Some genetic consequences of ice ages, and their role in divergence and speciation
Hewitt, G. M. (1996) · Biological Journal of the Linnean Society · doi:10.1111/j.1095-8312.1996.tb01434.x · Cited by 4,110
H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response
Levine, A., Tenhaken, R., Dixon, R. A., & Lamb, C. J. (1994) · Cell · doi:10.1016/0092-8674(94)90544-4 · Cited by 2,773
The presence of glutathione and glutathione reductase in chloroplasts: A proposed role in ascorbic acid metabolism
Foyer, C. H., & Halliwell, B. B. (1976) · Planta · doi:10.1007/bf00386001 · Cited by 2,643
THE FUNCTIONS AND REGULATION OF GLUTATHIONE S-TRANSFERASES IN PLANTS
Marrs, K. A. (1996) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.47.1.127 · Cited by 1,409
Glucose-6-phosphate Dehydrogenase
Löhr, G. W., & Waller, H. D. (1974) · Elsevier eBooks · doi:10.1016/b978-0-12-091302-2.50026-8 · Cited by 1,189
Production and scavenging of active oxygen in photosynthesis
Asada, K. (1987) · Medical Entomology and Zoology · Cited by 1,062
Oxidative stress and the molecular biology of antioxidant defenses.
Scandalios, J. G. (1997) · Cited by 1,027

Show all 74 references

Research works printed but not linked: 2

Asada K., 1987, Photoinhibition, 227
Halliwell B., 1982, Superoxide Dismutase, Vol 1, 89

Sorted by citations

Items 201–300 of 837

Coordinate induction of antioxidant defense and glyoxalase system by exogenous proline and glycinebetaine is correlated with salt tolerance in mung bean
Hossain, M. A., Hasanuzzaman, M., & Fujita, M. (2011) · Frontiers of Agriculture in China · doi:10.1007/s11703-010-1070-2 · Cited by 91
Seed biopriming with drought tolerant isolates of Trichoderma harzianum promote growth and drought tolerance in Triticum aestivum
Shukla, N., Awasthi, R. P., Rawat, L., & Kumar, J. (2014) · Annals of Applied Biology · doi:10.1111/aab.12160 · Cited by 90
The antioxidative response system in Glycine max (L.) Merr. exposed to Deltamethrin, a synthetic pyrethroid insecticide
Bashir, F., Mahmooduzzafar, M., Siddiqi, T. O., & Iqbal, M. M. (2006) · Environmental Pollution · doi:10.1016/j.envpol.2006.08.013 · Cited by 88
Changes of Proline Content, Activity, and Active Isoforms of Antioxidative Enzymes in Two Alfalfa Cultivars Under Salt Stress
Wang, X., & Han, J. (2009) · Agricultural Sciences in China · doi:10.1016/s1671-2927(08)60229-1 · Cited by 88
2,4-D attenuates salinity-induced toxicity by mediating anatomical changes, antioxidant capacity and cation transporters in the roots of rice cultivars
Islam, F., Farooq, M. A., Gill, R. A., Wang, J., Yang, C., Ali, B., Wang, G., & Zhou, W. (2017) · Scientific Reports · doi:10.1038/s41598-017-09708-x · Cited by 86
Physiological and molecular mechanisms of salinity tolerance in grafted cucumber
Elsheery, N. I., Helaly, M. N., Omar, S. A., John, S. V. S., Zabochnicka-Świątek, M., Kalaji, H. M., & Rastogi, A. (2019) · South African Journal of Botany · doi:10.1016/j.sajb.2019.12.014 · Cited by 87
Glutathione Peroxidases in Plants: Innumerable Role in Abiotic Stress Tolerance and Plant Development
Madhu, M., Sharma, A., Kaur, A., Tyagi, S., & Upadhyay, S. K. (2022) · Journal of Plant Growth Regulation · doi:10.1007/s00344-022-10601-9 · Cited by 94
Combined effects of salinity and drought on physiological and biochemical characteristics of pistachio rootstocks
Goharrizi, K. J., Baghizadeh, A., Kalantar, M., & Fatehi, F. (2019) · Scientia Horticulturae · doi:10.1016/j.scienta.2019.108970 · Cited by 87
Flower bud opening and senescence in roses (Rosa hybrida L.)
Kumar, N., Srivastava, G. C., & Dixit, K. (2008) · Plant Growth Regulation · doi:10.1007/s10725-008-9263-x · Cited by 87
Antioxidative Defense Potential to Salinity in the Euhalophyte Salicornia brachiata
Parida, A. K., & Jha, B. (2009) · Journal of Plant Growth Regulation · doi:10.1007/s00344-009-9129-0 · Cited by 85
Optimization of Nutrition in Soilless Systems: A Review
Gorbe, E., & Calatayud, Á. (2010) · Advances in botanical research · doi:10.1016/s0065-2296(10)53006-4 · Cited by 85
Transcriptome changes in foxtail millet genotypes at high salinity: Identification and characterization of a PHGPX gene specifically up-regulated by NaCl in a salt-tolerant line
Sreenivasulu, N., Miranda, M., Prakash, H. S., Wobus, U., & Weschke, W. (2004) · Journal of Plant Physiology · doi:10.1078/0176-1617-01112 · Cited by 84
Antioxidant enzyme activities and hormonal status in response to Cd stress in the wetland halophyte Kosteletzkya virginica under saline conditions
Han, R., Lefèvre, I. S., Albacete, A. A., Pérez‐Alfocea, F., Barba‐Espín, G., Díaz‐Vivancos, P., Quinet, M., Ruan, C., Hernández, J. A., Cantero‐Navarro, E., et al. (2012) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2012.01667.x · Cited by 84
Self-citation
Alleviation of the effects of saline-alkaline stress on maize seedlings by regulation of active oxygen metabolism by Trichoderma asperellum
Fu, J., Liu, Z., Li, Z., Wang, Y., & Yang, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179617 · Cited by 83
Behavior of Four Olive Cultivars During Salt Stress
Regni, L., Pino, A. M. D., Mousavi, S., Palmerini, C. A., Baldoni, L., Mariotti, R., Mairech, H., Gardi, T., D’Amato, R., & Proietti, P. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00867 · Cited by 83
Oxidative stress in herbicide-treated broad bean and maize plants
Hassan, N. M., & Alla, M. M. N. (2005) · Acta Physiologiae Plantarum · doi:10.1007/s11738-005-0047-x · Cited by 82
In vitro selection of salt tolerant cell lines in Solanum tuberosum L.
Queirós, F., Fidalgo, F., Santos, I., & Salema, R. (2007) · Biologia Plantarum · doi:10.1007/s10535-007-0149-y · Cited by 82
The apoplastic antioxidant system and altered cell wall dynamics influence mesophyll conductance and the rate of photosynthesis
Clemente‐Moreno, M. J., Gago, J., Díaz‐Vivancos, P., Bernal‐Vicente, A., Miedes, E., Bresta, P., Λιακόπουλος, Γ., Fernie, A. R., Hernández, J. A., & Flexas, J. (2019) · The Plant Journal · doi:10.1111/tpj.14437 · Cited by 81
Self-citation
Differential variations in total flavonoid content and antioxidant enzymes activities in pea under different salt and drought stresses
Farooq, M., Ahmad, R., Shahzad, M., Sajjad, Y., Hassan, A., Shah, M. M., Naz, S., & Khan, S. A. (2021) · Scientia Horticulturae · doi:10.1016/j.scienta.2021.110258 · Cited by 81
Long‐term plum pox virus infection produces an oxidative stress in a susceptible apricot,Prunus armeniaca, cultivar but not in a resistant cultivar
Hernández, J. A., Díaz‐Vivancos, P., Rubio, M., Olmos, E., Ros‐Barceló, A., & Martínez-Gómez, P. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00581.x · Cited by 81
Self-citation
Coupled expression of Cu/Zn-superoxide dismutase and catalase in cassava improves tolerance against cold and drought stresses
Jia, X., Duan, X., Yang, J., BEECHING, J. R., & Zhang, P. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.24525 · Cited by 81
Nitrate retention and physiological adjustment of maize to soil amendment with superabsorbent polymers
Eneji, A. E., Islam, R., An, P., & Amalu, U. C. (2013) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2013.02.027 · Cited by 80
Elucidation of physiological and biochemical mechanisms of an endemic halophyte Centaurea tuzgoluensis under salt stress
Yıldıztugay, E., Sekmen, A. H., Türkan, İ., & Küçüködük, M. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.01.021 · Cited by 80
The Glutathione Peroxidase Gene Family in Gossypium hirsutum: Genome-Wide Identification, Classification, Gene Expression and Functional Analysis
Chen, M., Li, K., Li, H., Song, C., & Miao, Y. (2017) · Scientific Reports · doi:10.1038/srep44743 · Cited by 79
Exogenous melatonin improves salt stress adaptation of cotton seedlings by regulating active oxygen metabolism
Jiang, D., Lu, B., Liu, L., Duan, W., Chen, L., Li, J. H., Zhang, K., Sun, H., Zhang, Y., Dong, H., et al. (2020) · PeerJ · doi:10.7717/peerj.10486 · Cited by 79
Salicylic acid negatively affects the response to salt stress in pea plants
Barba‐Espín, G., Clemente‐Moreno, M. J., Álvarez, S., García‐Legaz, M. F., Hernández, J. A., & Díaz‐Vivancos, P. (2011) · Plant Biology · doi:10.1111/j.1438-8677.2011.00461.x · Cited by 79
Self-citation
Molecular mechanisms of stress resistance of the photosynthetic apparatus
Kreslavski, V. D., Carpentier, R., Klimov, V. V., Murata, N., & Allakhverdiev, S. I. (2007) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747807030014 · Cited by 79
The alteration of mRNA expression of SOD and GPX genes, and proteins in tomato ( Lycopersicon esculentum Mill) under stress of NaCl and/or ZnO nanoparticles
Alharby, H. F., Metwali, E. M. R., Fuller, M. P., & Aldhebiani, A. Y. (2016) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2016.04.012 · Cited by 79
Mechanism of Nanosilicon-Mediated Alleviation of Salinity Stress in Faba Bean (Vicia faba L.) Plants
Qados, A. M. S. A. (2015) · Journal of Experimental Agriculture International · doi:10.9734/ajea/2015/15110 · Cited by 78
Designing, spectroscopic characterization, biological screening and antioxidant activity of mononuclear transition metal complexes of bidentate Schiff base hydrazones
Yadav, M., Sharma, S. D., & Devi, J. (2021) · Journal of Chemical Sciences · doi:10.1007/s12039-020-01854-6 · Cited by 78
Jasmonic Acid Impairs Arabidopsis Seedling Salt Stress Tolerance Through MYC2-Mediated Repression of CAT2 Expression
Song, R., Li, T., & Liu, W. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.730228 · Cited by 78
NaCl treatment markedly enhances H2O2‐scavenging system in leaves of halophyte Suaeda salsa
Pang, C., Su‐Jun, Z., Zhi‐Zhong, G., & Bao‐Shan, W. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00585.x · Cited by 78
NaCl amendment improves vinblastine and vincristine synthesis in Catharanthus roseus: a case of stress signalling as evidenced by antioxidant enzymes activities
Fatima, S., Mujib, A., & Tonk, D. (2015) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-015-0715-5 · Cited by 77
Fine and coarse regulation of reactive oxygen species in the salt tolerant mutants of barnyard grass and their wild-type parents under salt stress
Abogadallah, G. M., Serag, M. M., & Quick, W. P. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01297.x · Cited by 77
Histone acetylation influences the transcriptional activation of POX in Beta vulgaris L. and Beta maritima L. under salt stress
Yolcu, S., Özdemir, F., Güler, A., & Bor, M. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2015.12.019 · Cited by 77
Morpho-Physio-Biochemical and Molecular Responses of Maize Hybrids to Salinity and Waterlogging during Stress and Recovery Phase
Mahmood, U., Hussain, S., Hussain, S., Ali, B., Ashraf, U., Zamir, S., Al‐Robai, S. A., Alzahrani, F. O., Hano, C., & El-Esawi, M. A. (2021) · Plants · doi:10.3390/plants10071345 · Cited by 78
Response of antioxidative enzymes to plum pox virus in two apricot cultivars
Hernández, J. A., Talavera, J. M., Martínez-Gómez, P., Dicenta, F., & Sevilla, F. (2001) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2001.1110308.x · Cited by 76
Self-citation
Involvement of AsA/DHA and GSH/GSSG Ratios in Gene and Protein Expression and in the Activation of Defence Mechanisms Under Abiotic Stress Conditions
Fotopoulos, V., Ziogas, V., Τάνου, Γ., & Molassiotis, A. N. (2010) · Springer eBooks · doi:10.1007/978-90-481-9404-9_10 · Cited by 74
Seawater irrigation: antioxidant defence responses in leaves and roots of a sunflower (Helianthus annuus L.) ecotype
Baccio, D. D., Navari‐Izzo, F., & Izzo, R. (2004) · Journal of Plant Physiology · doi:10.1016/j.jplph.2003.07.001 · Cited by 75
Salt Stress Injury Induces Oxidative Alterations and Antioxidative Defence in the Roots of Lemna minor
Panda, S. K., & Upadhyay, R. K. (2004) · Biologia Plantarum · doi:10.1023/b:biop.0000033452.11971.fc · Cited by 74
Production of porcine cloned transgenic embryos expressing green fluorescent protein by somatic cell nuclear transfer
Zhang, Y., Pan, D., Sun, X., Sun, G., Wang, X., Liu, X., Li, Y., Dai, Y., & Li, N. (2006) · Science in China Series C Life Sciences · doi:10.1007/s11427-005-0071-5 · Cited by 73
Effects of ALA on Photosynthesis, Antioxidant Enzyme Activity, and Gene Expression, and Regulation of Proline Accumulation in Tomato Seedlings Under NaCl Stress
Zhang, Z., Miao, M., & Wang, C.-L. (2015) · Journal of Plant Growth Regulation · doi:10.1007/s00344-015-9499-4 · Cited by 72
Investigating the Role of Respiration in Plant Salinity Tolerance by Analyzing Mitochondrial Proteomes from Wheat and a Salinity-Tolerant Amphiploid (Wheat × Lophopyrum elongatum)
Jacoby, R. P., Millar, A. H., & Taylor, N. L. (2013) · Journal of Proteome Research · doi:10.1021/pr400504a · Cited by 71
Silicon nanoparticles (SiNPs) restore photosynthesis and essential oil content by upgrading enzymatic antioxidant metabolism in lemongrass (Cymbopogon flexuosus) under salt stress
Mukarram, M., Khan, M. M. A., Kurjak, D., Lux, A., & Corpas, F. J. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1116769 · Cited by 73
The suppression of salinity‐associated oxygen radicals production, in pepper (Capsicum annuum) fruit, by manganese, zinc and calcium in relation to its sensitivity to blossom‐end rot
Aktaş, H., Karni, L., Chang, D., Turhan, E., Bar‐Tal, A., & Aloni, B. (2004) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2004.00435.x · Cited by 71
Effect of Putrescine and Paclobutrazol on Growth, Physiochemical Parameters, and Nutrient Acquisition of Salt-sensitive Citrus Rootstock Karna khatta (Citrus karna Raf.) under NaCl Stress
Sharma, D. K., Dubey, A. K., Srivastav, M., Singh, A. K., Sairam, R. K., Pandey, R., Dahuja, A., & Kaur, C. (2011) · Journal of Plant Growth Regulation · doi:10.1007/s00344-011-9192-1 · Cited by 71
Expression of antioxidant enzymes and heat shock proteins in relation to combined stress of cadmium and heat in Vigna mungo seedlings
Kochhar, S., & Kochhar, V. K. (2004) · Plant Science · doi:10.1016/j.plantsci.2004.11.013 · Cited by 70
Alleviation of Water Deficit Stress Effects by Foliar Application of Ascorbic Acid on Zea mays L.
Dolatabadian, A., Sanavy, S. A. M. M., & Sharifi, M. (2009) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2009.00382.x · Cited by 70
Redox control of oxidative stress responses in the C3–CAM intermediate plant Mesembryanthemum crystallinum
Ślesak, I., Miszalski, Z., Karpińska, B., Niewiadomska, E., Ratajczak, R., & Karpiński, S. M. (2002) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(02)01409-2 · Cited by 70
Ectopic overexpression of cytosolic ascorbate peroxidase gene (Apx1) improves salinity stress tolerance in Brassica juncea by strengthening antioxidative defense mechanism
Saxena, S. C., Salvi, P., Kamble, N. U., Joshi, P. K., Majee, M., & Arora, S. (2020) · Acta Physiologiae Plantarum · doi:10.1007/s11738-020-3032-5 · Cited by 69
Enhanced salt-induced antioxidative responses involve a contribution of polyamine biosynthesis in grapevine plants
Ikbal, F. E.-Z., Hernández, J. A., Barba‐Espín, G., Koussa, T., Aziz, A., Faize, M., & Díaz‐Vivancos, P. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.02.006 · Cited by 68
Self-citation
Understanding salt tolerance mechanism using transcriptome profiling and de novo assembly of wild tomato Solanum chilense
Kashyap, S. P., Prasanna, H. C., Kumari, N., Mishra, P., & Singh, B. (2020) · Scientific Reports · doi:10.1038/s41598-020-72474-w · Cited by 71
Effects of exogenous hydrogen sulfide on the redox states of ascorbate and glutathione in maize leaves under salt stress
Shan, C., Liu, H., Zhao, L., & Wang, X. (2013) · Biologia Plantarum · doi:10.1007/s10535-013-0366-5 · Cited by 67
Effect of salt stress on antioxidant system and the metabolism of the reactive oxygen species in Dunaliella salina and Dunaliella tertiolecta
Tammam, A. A., Fakhry, E. M., & El-Sheekh, M. M. (2011) · AFRICAN JOURNAL OF BIOTECHNOLOGY · Cited by 67
Clones of FeSOD, MDHAR, DHAR Genes from White Clover and Gene Expression Analysis of ROS-Scavenging Enzymes during Abiotic Stress and Hormone Treatments
Zhang, Y., Li, Z., Peng, Y., Wang, X., Peng, D., Li, Y., He, X., Zhang, X., Ma, X., Huang, L., et al. (2015) · Molecules · doi:10.3390/molecules201119741 · Cited by 67
Response of maize genotypes to salinity stress in relation to osmolytes and metal-ions contents, oxidative stress and antioxidant enzymes activity
Kholová, J., Sairam, R. K., Meena, R. C., & Srivastava, G. C. (2009) · Biologia Plantarum · doi:10.1007/s10535-009-0047-6 · Cited by 66
Exogenous salicylic acid alleviates cold damage by regulating antioxidative system in two barley (Hordeum vulgareL.) cultivars
Mutlu, S., Atıcı, Ö., Nalbantoğlu, B., & Mete, E. (2016) · Frontiers in Life Science · doi:10.1080/21553769.2015.1115430 · Cited by 66
Influence of Abiotic and Biotic Elicitors on Organogenesis, Biomass Accumulation, and Production of Key Secondary Metabolites in Asteraceae Plants
Petrova, M., Miladinova-Georgieva, K., & Geneva, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084197 · Cited by 65
Effects of water‐saving superabsorbent polymer on antioxidant enzyme activities and lipid peroxidation in oat (Avena sativa L.) under drought stress
Islam, M. R., Xue, X., Sishuai, M., Ren, C., Eneji, A. E., & Hu, Y. (2010) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.4234 · Cited by 65
Thiourea orchestrates regulation of redox state and antioxidant responses to reduce the NaCl-induced oxidative damage in Indian mustard (Brassica juncea (L.) Czern.)
Srivastava, A. K., Srivastava, S., Suprasanna, P., & D’Souza, S. F. (2011) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2011.02.016 · Cited by 64
Growth, Oxidative Damage and Antioxidant Responses in Greengram (Vigna radiata L.) under Short‐term Salinity Stress and its Recovery
Panda, S. K., & Khan, M. H. (2009) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2009.00371.x · Cited by 64
Differential Responses of the Activities of Antioxidant Enzymes to Thermal Stresses between Two Invasive Eupatorium Species in China
Lu, P., Sang, W., & Ma, K. (2008) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00583.x · Cited by 64
Photoinhibition and Photoprotection under Nutrient Deficiencies, Drought and Salinity
Morales, F., Abadía, A., & AbadÞa, J. (2006) · Advances in photosynthesis and respiration · doi:10.1007/1-4020-3579-9_6 · Cited by 64
RETRACTED: Overexpression ofVP, a vacuolar H+-pyrophosphatase gene in wheat (Triticum aestivumL.), improves tobacco plant growth under Pi and N deprivation, high salinity, and drought
Li, X., Guo, C., Gu, J., Duan, W., Zhao, M., Ma, C., Du, X., Lü, W., & Xiao, K. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert442 · Cited by 63
Retracted
Influence of foliar application of polyamines on growth, gas-exchange characteristics, and chlorophyll fluorescence in Bakraii citrus under saline conditions
Khoshbakht, D., Asghari, M., & Haghighi, M. (2017) · Photosynthetica · doi:10.1007/s11099-017-0723-2 · Cited by 63
Combined effects of elevated CO2 and Cd-contaminated soil on the growth, gas exchange, antioxidant defense, and Cd accumulation of poplars and willows
Guo, B., Dai, S., Wang, R., Guo, J., Ding, Y., & Xu, Y. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.02.002 · Cited by 62
Effect of Super Absorbent Application on Antioxidant Enzyme Activities in Canola ( Brassica napus L.) Cultivars under Water Stress Conditions
Shirani-R (2009) · American Journal of Agricultural and Biological Sciences · doi:10.3844/ajabssp.2009.215.223 · Cited by 61
Alterations in antioxidant enzyme activities and proline content in pea leaves under long-term drought stress
Karataş, İ., Öztürk, L., Demir, Y., Ünlükara, A., Kurunç, A., & Düzdemır, O. (2012) · Toxicology and Industrial Health · doi:10.1177/0748233712462471 · Cited by 61
Adaptations to High Salt in a Halophilic Protist: Differential Expression and Gene Acquisitions through Duplications and Gene Transfers
Harding, T., Roger, A. J., & Simpson, A. G. B. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00944 · Cited by 63
Targeting the Redox Regulatory Mechanisms for Abiotic Stress Tolerance in Crops
Kundu, P., Gill, R., Ahlawat, S., Anjum, N. A., Sharma, K. K., Ansari, A. A., Hasanuzzaman, M., Ramakrishna, A., Chauhan, N. S., Tuteja, N., et al. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813066-7.00010-3 · Cited by 62
Transcriptome profiling of Puccinellia tenuiflora during seed germination under a long-term saline-alkali stress
Ye, X., Wang, H., Cao, X., Jin, X., Cui, F., Bu, Y., Liu, H., Wu, W., Takano, T., & Liu, S. (2019) · BMC Genomics · doi:10.1186/s12864-019-5860-5 · Cited by 61
Assessment of Growth, Physiological and Biochemical Parameters and Activities of Antioxidative Enzymes in Salinity Tolerant and Sensitive Basmati Rice Varieties
Singh, M. P., Singh, D. K., & Rai, M. (2007) · Journal of Agronomy and Crop Science · doi:10.1111/j.1439-037x.2007.00267.x · Cited by 60
Biochemical responses of Hyacinth bean (Lablab purpureus) to salinity stress
D'Souza, M. R., & Devaraj, V. R. (2009) · Acta Physiologiae Plantarum · doi:10.1007/s11738-009-0412-2 · Cited by 60
Some Biochemical Markers for Evaluation of Flax Cultivars Under Salt Stress Conditions
EL-BELTAGI, H. S., SALAMA, Z. A. E.-R., & Hariri, D. M. E. (2008) · Journal of Natural Fibers · doi:10.1080/15440470802252487 · Cited by 60
Salt-Induced Stress Effects on Biomass, Photosynthetic Rate, and Reactive Oxygen Species-Scavenging Enzyme Accumulation in Common Bean
Gama, P. B. S., Tanaka, K., Eneji, A. E., Eltayeb, A. E., & Siddig, K. E. (2009) · Journal of Plant Nutrition · doi:10.1080/01904160902787925 · Cited by 60
Males exhibit competitive advantages over females ofPopulus deltoidesunder salinity stress
Li, Y., Duan, B., Chen, J., Korpelainen, H., Niinemets, Ü., & Li, C. (2016) · Tree Physiology · doi:10.1093/treephys/tpw070 · Cited by 60
Long‐term effects of mild salt stress on growth, ion accumulation and superoxide dismutase expression of Arabidopsis rosette leaves
Attia, H., Arnaud, N., Karray‐Bouraoui, N., & Lachaâl, M. (2007) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2007.01009.x · Cited by 60
Microbe-Mediated Thermotolerance in Plants and Pertinent Mechanisms- A Meta-Analysis and Review
Dastogeer, K. M. G., Zahan, M. I., Rhaman, M. S., Sarker, M. S. A., & Chakraborty, A. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.833566 · Cited by 60
Effect of salt stress on tomato fruit antioxidant systems depends on fruit development stage
Murshed, R., Lopez, F., & Sallanon, H. (2013) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-013-0209-z · Cited by 59
Salt tolerance traits increase the invasive success of Acacia longifolia in Portuguese coastal dunes
Morais, M. C., Panuccio, M. R., Muscolo, A., & Freitas, H. M. D. O. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.03.013 · Cited by 59
Evaluating relative contribution of osmotolerance and tissue tolerance mechanisms toward salinity stress tolerance in three Brassica species
Chakraborty, K., Bose, J., Shabala, L., Eyles, A., & Shabala, S. N. (2016) · Physiologia Plantarum · doi:10.1111/ppl.12447 · Cited by 59
ROS and Oxidative Stress: Origin and Implication
Bhattacharjee, S. (2019) · Springer eBooks · doi:10.1007/978-81-322-3941-3_1 · Cited by 63
Silicon Nanoparticles and Methyl Jasmonate Improve Physiological Response and Increase Expression of Stress-related Genes in Strawberry cv. Paros Under Salinity Stress
Moradi, P., Vafaee, Y., Mozafari, A. A., & Tahir, N. A.-R. (2022) · Silicon · doi:10.1007/s12633-022-01791-8 · Cited by 58
Biochemical and Molecular Basis of Varietal Difference in Plant Salt Tolerance
Roychoudhury, A., & Chakraborty, M. (2013) · Annual Research & Review in Biology · Cited by 58
Rhizoremediation prospects of Polyaromatic hydrocarbon degrading rhizobacteria, that facilitate glutathione and glutathione-S-transferase mediated stress response, and enhance growth of rice plants in pyrene contaminated soil
Singha, L. P., Sinha, N., & Pandey, P. (2018) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2018.08.069 · Cited by 58
Exogenous Methyl Jasmonate Improves Cold Tolerance with Parallel Induction of Two Cold-Regulated (COR) Genes Expression in Triticum aestivum L.
Repkina, N., Игнатенко, А. А., Холопцева, Е. С., Miszalski, Z., Kaszycki, P., & Таланова, В. В. (2021) · Plants · doi:10.3390/plants10071421 · Cited by 57
The long-term resistance mechanisms, critical irrigation threshold and relief capacity shown by Eugenia myrtifolia plants in response to saline reclaimed water
Acosta‐Motos, J. R., Hernández, J. A., Álvarez, S., Barba‐Espín, G., & Sánchez-Blanco, M. J. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2016.12.003 · Cited by 57
Self-citation
Kinetics of the Anti‐oxidant Response to Salinity in the Halophyte Cakile maritima
Amor, N. B., Jiménez, A., Megdiche-Ksouri, W., Lundqvist, M., Sevilla, F., & Abdelly, C. (2007) · Journal of Integrative Plant Biology · doi:10.1111/j.1672-9072.2007.00491.x · Cited by 57
Self-citation
Moderate salinity enhances the antioxidative response in the halophyte Hordeum maritimum L. under potassium deficiency
Hafsi, C., Romero‐Puertas, M. C., Gupta, D. K., del Río, L. A., Sandalio, L. M., & Abdelly, C. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.04.008 · Cited by 54
Identification and characterization of a novel chloroplast/mitochondria co-localized glutathione reductase 3 involved in salt stress response in rice
Wu, T., Lin, W.-R., Kao, Y., Hsu, Y., Yeh, C.-H., Hong, C., & Kao, C. H. (2013) · Plant Molecular Biology · doi:10.1007/s11103-013-0095-3 · Cited by 56
Interplay between GST and nitric oxide in the early response of soybean (Glycine max L.) plants to salinity stress
Dinler, B. S., Antoniou, C., & Fotopoulos, V. (2014) · Journal of Plant Physiology · doi:10.1016/j.jplph.2014.07.026 · Cited by 56
Responses of transgenic Arabidopsis plants and recombinant yeast cells expressing a novel durum wheat manganese superoxide dismutase TdMnSOD to various abiotic stresses
Feki, K., Farhat, A., Kamoun, Y., Saibi, W., Gargouri, A. F., & Brini, F. (2016) · Journal of Plant Physiology · doi:10.1016/j.jplph.2016.03.019 · Cited by 56
Lipoic acid and redox status in barley plants subjected to salinity and elevated CO2
Pérez‐López, U., Robredo, A., Lacuesta, M., Sgherri, C. L. M., Mena‐Petite, A., Navari‐Izzo, F., & Muñoz‐Rueda, A. (2010) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2010.01361.x · Cited by 55
Superoxide Dismutase (SOD) and Abiotic Stress Tolerance in Plants
Szőllősi, R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-799963-0.00003-4 · Cited by 57
Algal extracts improve antioxidant defense abilities and salt tolerance of wheat plant irrigated with sea water
El‐Baky, H. H. A., Hussein, M. M., & El-Baroty, G. S. (2008) · African Journal of Biochemistry Research · doi:10.5897/ajbr.9000014 · Cited by 55
Ectopic expression of Mn-SOD in Lycopersicon esculentum leads to enhanced tolerance to salt and oxidative stress
Wang, Y., Wisniewski, M., Richard Meilan, C., Uratsu, S. L., Minggang Cui, A., Dandekar, A. M., & Fuchigami, L. H. (2007) · Journal of Applied Horticulture · doi:10.37855/jah.2007.v09i01.01 · Cited by 54
Exogenous Salicylic Acid and Trehalose Ameliorate Short Term Drought Stress in Wheat Cultivars by Up-regulating Membrane Characteristics and Antioxidant Defense System
Aldesuquy, H. S. (2015) · Journal of Horticulture · doi:10.4172/2376-0354.1000139 · Cited by 54
EFFECTS OF SALINITY STRESS ON PHYSIOLOGICAL PERFORMANCE OF VARIOUS WHEAT AND BARLEY CULTIVARS
Izadi, M. H., Rabbani, J., Emam, Y., Pessarakli, M., & Tahmasebi, A. (2014) · Journal of Plant Nutrition · doi:10.1080/01904167.2013.867980 · Cited by 53
Impact of salinity stress on cotton and opportunities for improvement through conventional and biotechnological approaches
Chaudhary, M. T., Majeed, S., Rana, I. A., Ali, Z., Jia, Y., Du, X., Hinze, L. L., & Azhar, M. T. (2024) · BMC Plant Biology · doi:10.1186/s12870-023-04558-4 · Cited by 53
Exogenous proline alleviates oxidative stress and increase vase life in rose (Rosa hybrida L. ‘Grand Gala’)
Kumar, N., Pal, M., Singh, A., Sairam, R. K., & Srivastava, G. C. (2010) · Scientia Horticulturae · doi:10.1016/j.scienta.2010.09.009 · Cited by 53

Authors: Hernández, J. A., Jiménez, A., Mullineaux, P., & Sevilia, F.
Affiliations: Consejo Superior de Investigaciones Científicas (ES)
John Innes Centre (GB)
ORCID: Hernández, J. A.
Jiménez, A.
Mullineaux, P.
Venue: Plant, Cell & Environment
Publisher: Wiley
Published: 2000-08
Volume: 23
Issue: 8
Pages: 853-862
ISSN: 0140-7791 (ISSN-L)
1365-3040
DOI: 10.1046/j.1365-3040.2000.00602.x
OpenAlex: W2125614572
Cited by: 837
References: 74
Citations by year: 2026: 15 · 2025: 23 · 2024: 22 · 2023: 32 · 2022: 33 · 2021: 45 · 2020: 43 · 2019: 39 · 2018: 36 · 2017: 46 · 2016: 34 · 2015: 44 · 2014: 50 · 2013: 54 · 2012: 44
FWCI: 12.90
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 511 d)
Locations: Plant Cell & Environment (publishedVersion)
Funders: Royal Society
Universidad de Murcia
Directorate for Biological Sciences
Biotechnology and Biological Sciences Research Council
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
Keywords: pea, Pisum sativum, salt stress, NaCl tolerance, antioxidant defense, ascorbate-glutathione cycle, superoxide dismutase, ascorbate peroxidase, glutathione reductase, monodehydroascorbate reductase, dehydroascorbate reductase, cultivar differences

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Tolerance of pea (Pisum sativum L.) to long‐term salt stress is associated with induction of antioxidant defences

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks