{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T18:04:12Z","timestamp":1793124252170,"version":"4.5.0"},"reference-count":81,"publisher":"MDPI AG","issue":"14","license":[{"start":{"date-parts":[[2024,7,9]],"date-time":"2024-07-09T00:00:00Z","timestamp":1720483200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Ministry of Education and Science of Russia","award":["122041400162-3"],"award-info":[{"award-number":["122041400162-3"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Plants"],"abstract":"<jats:p>Nitric oxide (NO) is a multifunctional signalling molecule involved in the regulation of plant ontogenesis and adaptation to different adverse environmental factors, in particular to osmotic stress. Understanding NO-induced plant protection is important for the improvement of plant stress tolerance and crop productivity under global climate changes. The root system is crucial for plant survival in a changeable environment. Damages that it experiences under water deficit conditions during the initial developmental periods seriously affect the viability of the plants. This work was devoted to the comparative analysis of the pretreatment of wheat seedlings through the root system with NO donor sodium nitroprusside (SNP) for 24 h on various parameters of redox homeostasis under exposure to osmotic stress (PEG 6000, 12%) over 0.5\u201324 h. The active and exhausted solutions of SNP, termed as (SNP\/+NO) and (SNP\/\u2212NO), respectively, were used in this work at a concentration of 2 \u00d7 10\u22124 M. Using biochemistry and light microscopy methods, it has been revealed that osmotic stress caused oxidative damages and the disruption of membrane cell structures in wheat roots. PEG exposure increased the production of superoxide (O2\u2022\u2212), hydrogen peroxide (H2O2), malondialdehyde (MDA), and the levels of electrolyte leakage (EL) and lipid peroxidation (LPO). Stress treatment enhanced the activities of superoxide dismutase (SOD), ascorbate peroxidase (APX), catalase (CAT), the excretion of proline, and the rate of cell death and inhibited their division. Pretreatment with (SNP\/+NO) decreased PEG-induced root damages by differently regulating the antioxidant enzymes under stress conditions. Thus, (SNP\/+NO) pretreatment led to SOD, APX, and CAT inhibition during the first 4 h of stress and stimulated their activity after 24 h of PEG exposure when compared to SNP-untreated or (SNP\/\u2212NO)-pretreated and stress-subjected plants. Osmotic stress triggered the intense excretion of proline by roots into the external medium. Pretreatment with (SNP\/+NO) in contrast with (SNP\/\u2212NO) additionally increased stress-induced proline excretion. Our results indicate that NO is able to mitigate the destructive effects of osmotic stress on the roots of wheat seedlings. However, the mechanisms of NO protective action may be different at certain periods of stress exposure.<\/jats:p>","DOI":"10.3390\/plants13141895","type":"journal-article","created":{"date-parts":[[2024,7,10]],"date-time":"2024-07-10T09:23:08Z","timestamp":1720603388000},"page":"1895","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Exogenous Sodium Nitroprusside Affects the Redox System of Wheat Roots Differentially Regulating the Activity of Antioxidant Enzymes under Short-Time Osmotic Stress"],"prefix":"10.3390","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6044-8646","authenticated-orcid":false,"given":"Alsu","family":"Lubyanova","sequence":"first","affiliation":[{"name":"Institute of Biochemistry and Genetics-Subdivision of the Ufa Federal Research Centre of the Russian Academy of Sciences, Prospect Oktyabrya 71, lit.1e, 450054 Ufa, Russia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chulpan","family":"Allagulova","sequence":"additional","affiliation":[{"name":"Institute of Biochemistry and Genetics-Subdivision of the Ufa Federal Research Centre of the Russian Academy of Sciences, Prospect Oktyabrya 71, lit.1e, 450054 Ufa, Russia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2024,7,9]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1007\/s00299-019-02447-5","article-title":"Root Exudates: From Plant to Rhizosphere and Beyond","volume":"39","year":"2020","journal-title":"Plant Cell Rep."},{"key":"ref_2","doi-asserted-by":"crossref","unstructured":"Soares, C., Rodrigues, F., Sousa, B., Pinto, E., Ferreira, I.M.P.L.V.O., Pereira, R., and Fidalgo, F. (2021). Foliar Application of Sodium Nitroprusside Boosts Solanum lycopersicum L. Tolerance to Glyphosate by Preventing Redox Disorders and Stimulating Herbicide Detoxification Pathways. Plants, 10.","DOI":"10.3390\/plants10091862"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1007\/s11104-018-3691-9","article-title":"Global Metabolomics Analysis Reveals Distinctive Tolerance Mechanisms in Different Plant Organs of Lentil (Lens culinaris) upon Salinity Stress","volume":"429","author":"Skliros","year":"2018","journal-title":"Plant Soil"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/j.plantsci.2012.12.004","article-title":"Water Stress Induces a Differential and Spatially Distributed Nitro-oxidative Stress Response in Roots and Leaves of Lotus japonicas","volume":"201\u2013202","author":"Signorelli","year":"2013","journal-title":"Plant Sci."},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"529","DOI":"10.1016\/j.devcel.2020.10.012","article-title":"Thriving under Stress: How Plants Balance Growth and the Stress Response","volume":"55","author":"Zhang","year":"2020","journal-title":"Dev. Cell"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"1122","DOI":"10.1007\/s42729-020-00198-x","article-title":"Nitric Oxide Stimulates Antioxidant System and Osmotic Adjustment in Soybean Under Drought Stress","volume":"20","author":"Rezayian","year":"2020","journal-title":"J. Soil Sci. Plant Nutr."},{"key":"ref_7","first-page":"6","article-title":"Proline: Physiological Functions and Regulation of Content in Plants Under Stress Conditions","volume":"2","author":"Kolupaev","year":"2014","journal-title":"Visn. Khark. Nats. Agrar. Univ. Ser. Biol."},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1111\/plb.13363","article-title":"Proline, a Multifaceted Signalling Molecule in Plant Responses to Abiotic Stress: Understanding the Physiological Mechanisms","volume":"24","author":"Ghosh","year":"2022","journal-title":"Plant Biol."},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"18","DOI":"10.15407\/ubj86.04.018","article-title":"Reactive Oxygen Species and Stress Signaling in Plants","volume":"86","author":"Kolupaev","year":"2014","journal-title":"Ukr. Biochem. J."},{"key":"ref_10","doi-asserted-by":"crossref","unstructured":"Allagulova, C.R., Lubyanova, A.R., and Avalbaev, A.M. (2023). Multiple Ways of Nitric Oxide Production in Plants and Its Functional Activity under Abiotic Stress Conditions. Int. J. Mol. Sci., 24.","DOI":"10.3390\/ijms241411637"},{"key":"ref_11","doi-asserted-by":"crossref","unstructured":"Gupta, D.K., Palma, J.M., and Corpas, F.J. (2018). Plant Superoxide Dismutases: Function Under Abiotic Stress Conditions. Antioxidants and Antioxidant Enzymes in Higher Plants, Springer International Publishing AG.","DOI":"10.1007\/978-3-319-75088-0"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"374","DOI":"10.1111\/ppl.13021","article-title":"Regulation of Physiological Aspects in Plants by Hydrogen Sulfide and Nitric Oxide Under Challenging Environment","volume":"168","author":"Paul","year":"2020","journal-title":"Physiol. Plant."},{"key":"ref_13","unstructured":"Mukherjee, S., and Balu\u0161ka, F. (2021). Role of Nitric Oxide as a Double Edged Sword in Root Growth and Development. Rhizobiology: Molecular Physiology of Plant Roots. Signaling and Communication in Plants, Springer International Publishing AG."},{"key":"ref_14","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1007\/978-1-0716-3044-0_5","article-title":"Functions of NO and H2S Signal Molecules Against Plant Abiotic Stress","volume":"Volume 2642","year":"2023","journal-title":"Plant Abiotic Stress Signaling. Methods in Molecular Biology"},{"key":"ref_15","doi-asserted-by":"crossref","unstructured":"Allagulova, C., Avalbaev, A., Lubyanova, A., Plotnikov, A., Yuldashev, R., and Lastochkina, O. (2023). Nitric Oxide (NO) Improves Wheat Growth under Dehydration Conditions by Regulating Phytohormone Levels and Induction of the Expression of the TADHN Dehydrin Gene. Plants, 12.","DOI":"10.3390\/plants12234051"},{"key":"ref_16","doi-asserted-by":"crossref","first-page":"604","DOI":"10.1016\/j.plantsci.2011.04.005","article-title":"Nitric Oxide Imbalance Provokes a Nitrosative Response in Plants Under Abiotic Stress","volume":"181","author":"Corpas","year":"2011","journal-title":"Plant Sci."},{"key":"ref_17","doi-asserted-by":"crossref","first-page":"1604","DOI":"10.1104\/pp.114.255216","article-title":"S-Nitrosylation Positively Regulates Ascorbate Peroxidase Activity During Plant Stress Responses","volume":"167","author":"Yang","year":"2015","journal-title":"Plant Physiol."},{"key":"ref_18","doi-asserted-by":"crossref","unstructured":"Laxa, M., Liebthal, M., Telman, W., Chibani, K., and Dietz, K.J. (2019). The Role of the Plant Antioxidant System in Drought Tolerance. Antioxidants, 8.","DOI":"10.3390\/antiox8040094"},{"key":"ref_19","doi-asserted-by":"crossref","first-page":"2913","DOI":"10.1093\/jxb\/erv073","article-title":"Nitric Oxide is a Ubiquitous Signal for Maintaining Redox Balance in Plant Cells: Regulation of Ascorbate Peroxidase as a Case Study","volume":"66","author":"Foresi","year":"2015","journal-title":"J. Exp. Bot."},{"key":"ref_20","doi-asserted-by":"crossref","unstructured":"Palma, J.M., Mateos, R.M., L\u00f3pez-Jaramillo, J., Rodr\u00edguez-Ruiz, M., Gonz\u00e1lez-Gordo, S., Lechuga-Sancho, A.M., and Corpas, F.J. (2020). Plant Catalases as NO and H2S Targets. Redox Biol., 34.","DOI":"10.1016\/j.redox.2020.101525"},{"key":"ref_21","doi-asserted-by":"crossref","first-page":"477","DOI":"10.3390\/stresses2040033","article-title":"Involvement of Nitric Oxide in Methyl Jasmonate-Mediated Regulation of Water Metabolism in Wheat Plants under Drought Stress","volume":"2","author":"Lubyanova","year":"2022","journal-title":"Stresses"},{"key":"ref_22","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1104\/pp.103.038554","article-title":"Nitric Oxide Mediates the Indole Acetic Acid Induction Activation of a Mitogen-Activated Protein Kinase Cascade Involved in Adventitious Root Development","volume":"135","author":"Pagnussat","year":"2004","journal-title":"Plant Physiol."},{"key":"ref_23","doi-asserted-by":"crossref","first-page":"900","DOI":"10.1007\/s00425-003-1172-7","article-title":"Nitric Oxide Plays a Central Role in Determining Lateral Root Development in Tomato","volume":"218","author":"Graziano","year":"2004","journal-title":"Planta"},{"key":"ref_24","doi-asserted-by":"crossref","first-page":"240","DOI":"10.3390\/plants4020240","article-title":"Functions of Nitric Oxide (NO) in Roots during Development and under Adverse Stress Conditions","volume":"4","author":"Corpas","year":"2015","journal-title":"Plants"},{"key":"ref_25","unstructured":"Singh, V.P., Singh, S., and Sandalio, L.M. (2022). Nitric Oxide (NO) and Lateral Root Development in Plants Under Stress. Nitric Oxide in Plant Biology: An Ancient Molecule with Emerging Roles, Academic Press."},{"key":"ref_26","doi-asserted-by":"crossref","first-page":"665","DOI":"10.1134\/S1021443717040094","article-title":"Cytokinins Contribute to Realization of Nitric Oxide Growth-Stimulating and Protective Effects on Wheat Plants","volume":"64","author":"Maslennikova","year":"2017","journal-title":"Russ. J. Plant Physiol."},{"key":"ref_27","doi-asserted-by":"crossref","unstructured":"Gro\u00df, F., Durner, J., and Gaupels, F. (2013). Nitric Oxide, Antioxidants and Prooxidants in Plant Defence Responses. Front. Plant Sci., 4.","DOI":"10.3389\/fpls.2013.00419"},{"key":"ref_28","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1016\/j.plaphy.2020.07.005","article-title":"Nitric Oxide Regulates Water Status and Associated Enzymatic Pathways to Inhibit Nutrients Imbalance in Maize (Zea mays L.) Under Drought Stress","volume":"155","author":"Majeed","year":"2020","journal-title":"Plant Physiol. Biochem."},{"key":"ref_29","doi-asserted-by":"crossref","first-page":"651","DOI":"10.1016\/j.plaphy.2022.11.041","article-title":"Nitric Oxide and Hydrogen Sulfide Work Together to Improve Tolerance to Salinity Stress in Wheat Plants by Upraising the AsA-GSH Cycle","volume":"194","author":"Kaya","year":"2023","journal-title":"Plant Physiol. Biochem."},{"key":"ref_30","doi-asserted-by":"crossref","unstructured":"Mhamdi, A., and Van Breusegem, F. (2018). Reactive Oxygen Species in Plant Development. Development, 145.","DOI":"10.1242\/dev.164376"},{"key":"ref_31","doi-asserted-by":"crossref","unstructured":"Ruan, J., Zhou, Y., Zhou, M., Yan, J., Khurshid, M., Weng, W., Cheng, J., and Zhang, K. (2019). Jasmonic Acid Signaling Pathway in Plants. Int. J. Mol. Sci., 20.","DOI":"10.3390\/ijms20102479"},{"key":"ref_32","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1038\/s41580-022-00499-2","article-title":"Reactive Oxygen Species Signalling in Plant Stress Responses","volume":"23","author":"Mittler","year":"2022","journal-title":"Nat. Rev. Mol. Cell Biol."},{"key":"ref_33","doi-asserted-by":"crossref","first-page":"318","DOI":"10.1111\/ppl.13004","article-title":"Nitric Oxide-Mediated Regulation of Oxidative Stress in Plants Under Metal Stress: A Review","volume":"168","author":"Sharma","year":"2020","journal-title":"Physiol. Plant."},{"key":"ref_34","doi-asserted-by":"crossref","unstructured":"Iqbal, N., Sehar, Z., Fatma, M., Umar, S., Sofo, A., and Khan, N.A. (2022). Nitric Oxide and Abscisic Acid Mediate Heat Stress Tolerance through Regulation of Osmolytes and Antioxidants to Protect Photosynthesis and Growth in Wheat Plants. Antioxidants, 11.","DOI":"10.3390\/antiox11020372"},{"key":"ref_35","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1016\/j.plaphy.2019.01.007","article-title":"Cadmium Tolerance is Associated with the Root-Driven Coordination of Cadmium Sequestration, Iron Regulation, and ROS Scavenging in Rice","volume":"136","author":"Bari","year":"2019","journal-title":"Plant Physiol. Biochem."},{"key":"ref_36","doi-asserted-by":"crossref","first-page":"4","DOI":"10.1093\/plphys\/kiab022","article-title":"A Systemic Whole-Plant Change in Redox Levels Accompanies the Rapid Systemic Response to Wounding","volume":"186","author":"Fichman","year":"2021","journal-title":"Plant Physiol."},{"key":"ref_37","doi-asserted-by":"crossref","first-page":"28","DOI":"10.15407\/frg2019.01.028","article-title":"Antioxidant System and Plant Resistance to Water Deficit","volume":"51","author":"Kolupaev","year":"2019","journal-title":"Fiziol. Rast. Genet."},{"key":"ref_38","doi-asserted-by":"crossref","unstructured":"Cao, X., Zhu, C., Zhong, C., Zhang, J., Wu, L., Jin, Q., and Ma, Q. (2019). Nitric Oxide Synthase-Mediated Early Nitric Oxide Burst Alleviates Water Stress-Induced Oxidative Damage in Ammonium-Supplied Rice Roots. BMC Plant Biol., 19.","DOI":"10.1186\/s12870-019-1721-2"},{"key":"ref_39","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1007\/s12374-009-9013-2","article-title":"Protective Effect of Nitric Oxide Against Oxidative Damage in Arabidopsis Leaves Under Ultraviolet-B Irradiation","volume":"52","author":"Zhang","year":"2009","journal-title":"J. Plant Biol."},{"key":"ref_40","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1016\/j.niox.2019.03.008","article-title":"Deciphering The Nitric Oxide, Cyanide and Iron-Mediated Actions of Sodium Nitroprusside in Cotyledons of Salt Stressed Sunflower Seedlings","volume":"88","author":"Keisham","year":"2019","journal-title":"Nitric Oxide"},{"key":"ref_41","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/j.niox.2019.09.006","article-title":"A Forty Year Journey: The Generation and Roles of NO in Plants","volume":"93","author":"Kolbert","year":"2019","journal-title":"Nitric Oxide"},{"key":"ref_42","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1023\/A:1005837012203","article-title":"NO\u2022\u2013Releasing Substances That Induce Growth Elongation in Maize Root Segments","volume":"21","author":"Gouvea","year":"1997","journal-title":"Plant Growth Regul."},{"key":"ref_43","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1093\/jxb\/erj045","article-title":"Nitric Oxide Modulates the Expression of Cell Cycle Regulatory Genes During Lateral Root Formation in Ttomato","volume":"57","author":"Graziano","year":"2006","journal-title":"J. Exp. Bot."},{"key":"ref_44","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1016\/j.plaphy.2018.06.012","article-title":"Nitric Oxide Mitigates the Effect of Water Deficit in Crambe abyssinica","volume":"129","author":"Batista","year":"2018","journal-title":"Plant Physiol. Biochem."},{"key":"ref_45","doi-asserted-by":"crossref","first-page":"989","DOI":"10.1093\/jxb\/eru458","article-title":"Differential Inhibition of Arabidopsis Superoxide Dismutases by Peroxynitrite-Mediated Tyrosine Nitration","volume":"66","author":"Holzmeister","year":"2015","journal-title":"J. Exp. Bot."},{"key":"ref_46","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1080\/07388551.2021.1874280","article-title":"Drought Stress-Induced Physiological Mechanisms, Signaling Pathways and Molecular Response of Chloroplasts in Common Vegetable Crops","volume":"41","author":"Razi","year":"2021","journal-title":"Crit. Rev. Biotechnol."},{"key":"ref_47","doi-asserted-by":"crossref","first-page":"1033","DOI":"10.1111\/pce.13475","article-title":"CLE9 Peptide-Induced Stomatal Closure is Mediated by Abscisic Acid, Hydrogen Peroxide, and Nitric Oxide in Arabidopsis thaliana","volume":"42","author":"Zhang","year":"2019","journal-title":"Plant Cell Environ."},{"key":"ref_48","doi-asserted-by":"crossref","unstructured":"Iqbal, N., Umar, S., Khan, N.A., and Corpas, F.J. (2021). Nitric Oxide and Hydrogen Sulfide Coordinately Reduce Glucose Sensitivity and Decrease Oxidative Stress via Ascorbate-Glutathione Cycle in Heat-Stressed Wheat (Triticum aestivum L.) Plants. Antioxidants, 10.","DOI":"10.3390\/antiox10010108"},{"key":"ref_49","doi-asserted-by":"crossref","unstructured":"Ozfidan-Konakci, C., Yildiztugay, E., Elbasan, F., Kucukoduk, M., and Turkan, I. (2020). Hydrogen Sulfide (H2S) and Nitric Oxide (NO) Alleviate Cobalt Toxicity in Wheat (Triticum aestivum L.) by Modulating Photosynthesis, Chloroplastic Redox and Antioxidant Capacity. J. Hazard. Mater., 388.","DOI":"10.1016\/j.jhazmat.2020.122061"},{"key":"ref_50","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1179\/135100006X116718","article-title":"NO\u2022 Chemistry: A Diversity of Targets in the Cell","volume":"11","author":"Reiter","year":"2006","journal-title":"Redox Rep."},{"key":"ref_51","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1016\/j.niox.2017.01.001","article-title":"Nitric Oxide-Induced Synthesis of Hydrogen Sulfide Alleviates Osmotic Stress in Wheat Seedlings Through Sustaining Antioxidant Enzymes, Osmolyte Accumulation and Cysteine Homeostasis","volume":"68","author":"Khan","year":"2017","journal-title":"Nitric Oxide"},{"key":"ref_52","doi-asserted-by":"crossref","unstructured":"Ghaffari, H., Tadayon, M.R., Bahador, M., and Razmjoo, J. (2021). Investigation of the Proline Role in Controlling Traits Related to Sugar and Root Yield of Sugar Beet Under Water Deficit Conditions. Agric. Water Manag., 243.","DOI":"10.1016\/j.agwat.2020.106448"},{"key":"ref_53","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1016\/j.plantsci.2015.07.012","article-title":"NO to Drought-Multifunctional Role of Nitric Oxide in Plant Drought: Do We Have All the Answers?","volume":"239","author":"Santisree","year":"2015","journal-title":"Plant Sci."},{"key":"ref_54","doi-asserted-by":"crossref","unstructured":"Merillon, J.M., and Ramawat, K.G. (2019). Nitric Oxide as a Signal in Inducing Secondary Metabolites During Plant Stress. Co-Evolution of Secondary Metabolites. Reference Series in Phytochemistry, Springer Nature.","DOI":"10.1007\/978-3-319-76887-8"},{"key":"ref_55","doi-asserted-by":"crossref","unstructured":"Cai, W., Liu, W., Wang, W.S., Fu, Z.W., Han, T.T., and Lu, Y.T. (2015). Overexpression of Rat Neurons Nitric Oxide Synthase in Rice Enhances Drought and Salt Tolerance. PLoS ONE, 10.","DOI":"10.1371\/journal.pone.0131599"},{"key":"ref_56","doi-asserted-by":"crossref","unstructured":"Bhaskarla, V., Zinta, G., Ford, R., Jain, M., Varshney, R.K., and Mantri, N. (2020). Comparative Root Transcriptomics Provide Insights into Drought Adaptation Strategies in Chickpea (Cicer arietinum L.). Int. J. Mol. Sci., 21.","DOI":"10.3390\/ijms21051781"},{"key":"ref_57","first-page":"81","article-title":"Mitotic Cycle and its Regulation","volume":"18","author":"Vysotskaya","year":"2014","journal-title":"Vavilov J. Genet. Breed."},{"key":"ref_58","doi-asserted-by":"crossref","first-page":"1434","DOI":"10.1104\/pp.113.216416","article-title":"Redox Modulation of Plant Developmental Regulators from the Class I TCP Transcription Factor Family","volume":"162","author":"Viola","year":"2013","journal-title":"Plant Physiol."},{"key":"ref_59","doi-asserted-by":"crossref","unstructured":"Viola, I.L., Alem, A.L., Jure, R.M., and Gonzalez, D.H. (2023). Physiological Roles and Mechanisms of Action of Class I TCP Transcription Factors. Int. J. Mol. Sci., 24.","DOI":"10.3390\/ijms24065437"},{"key":"ref_60","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1007\/s11104-021-05010-y","article-title":"Root Anatomy and Soil Resource Capture","volume":"466","author":"Lynch","year":"2021","journal-title":"Plant Soil"},{"key":"ref_61","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1016\/0003-2697(87)90489-1","article-title":"Assaying for Superoxide Dismutase Activity: Some Large Consequences of Minor Changes in Conditions","volume":"161","author":"Beyer","year":"1987","journal-title":"Anal. Biochem."},{"key":"ref_62","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1016\/S0076-6879(84)05016-3","article-title":"Catalase in vitro","volume":"105","author":"Aebi","year":"1984","journal-title":"Methods Enzymol."},{"key":"ref_63","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1016\/S0168-9452(03)00022-0","article-title":"Lead Toxicity Induces Lipid Peroxidation and Alters the Activities of Antioxidant Enzymes in Growing Rice Plants","volume":"164","author":"Verma","year":"2003","journal-title":"Plant Sci."},{"key":"ref_64","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1016\/0003-2697(76)90527-3","article-title":"A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding","volume":"72","author":"Bradford","year":"1976","journal-title":"Anal. Biochem."},{"key":"ref_65","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1007\/BF01289421","article-title":"Role of Extracellular Peroxidase in the Superoxide Production by Wheat Root Cells","volume":"217","author":"Minibayeva","year":"2001","journal-title":"Protoplasma"},{"key":"ref_66","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1111\/j.1469-8137.1994.tb02957.x","article-title":"Role of Superoxide, Lipid Peroxidation and Superoxide Dismutase in Membrane Perturbation During Loss of Viability in Seeds of Shorea robusta Gaertn. f","volume":"126","author":"Chaitanya","year":"1994","journal-title":"New Phytol."},{"key":"ref_67","first-page":"286","article-title":"Chitooligosacharide-Induced Activation of o-Phenylenediamine Oxidation by Wheat Seedlings in the Presence of Oxalic Acid","volume":"66","author":"Khairullin","year":"2001","journal-title":"Biochemistry"},{"key":"ref_68","doi-asserted-by":"crossref","first-page":"1379","DOI":"10.1104\/pp.122.4.1379","article-title":"Extracellular H2O2 Induced by Oligogalacturonides is not Involved in the Inhibition of the Auxin-Regulated rolB Gene Expression in Tobacco Leaf Explants","volume":"122","author":"Bellincampi","year":"2000","journal-title":"Plant Physiol."},{"key":"ref_69","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1016\/0003-9861(68)90654-1","article-title":"Photoperoxidation in Isolated Chloroplasts: Kinetics and Stoichiometry of Fatty Acid Peroxidation","volume":"125","author":"Heath","year":"1968","journal-title":"Arch. Biochem. Biophys."},{"key":"ref_70","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1007\/BF00018060","article-title":"Rapid Determination of Free Proline for Water Stress Studies","volume":"39","author":"Bates","year":"1973","journal-title":"Plant Soil"},{"key":"ref_71","doi-asserted-by":"crossref","first-page":"1971","DOI":"10.1007\/s00299-017-2214-0","article-title":"Citrus Plants Exude Proline and Phytohormones Under Abiotic Stress Conditions","volume":"36","year":"2017","journal-title":"Plant Cell Rep."},{"key":"ref_72","doi-asserted-by":"crossref","first-page":"682","DOI":"10.1016\/j.plantsci.2009.09.007","article-title":"Involvement of Nitric Oxide in Water Stress-Induced Responses of Cucumber Roots","volume":"177","year":"2009","journal-title":"Plant Sci."},{"key":"ref_73","first-page":"295","article-title":"Histochemical Detection of Lipid Peroxidation in the Liver of Bromobenzene-Poisoned Mice","volume":"129","author":"Pompella","year":"1987","journal-title":"Am. J. Pathol."},{"key":"ref_74","doi-asserted-by":"crossref","unstructured":"Gill, M.B., Zeng, F., Shabala, L., Zhang, G., Yu, M., Demidchik, V., Shabala, S., and Zhou, M. (2019). Identification of QTL Related to ROS Formation Under Hypoxia and Their Association With Waterlogging and Salt tolerance in Barley. Int. J. Mol. Sci., 20.","DOI":"10.3390\/ijms20030699"},{"key":"ref_75","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1007\/s10725-007-9248-1","article-title":"WGA Reduces the Level of Oxidative Stress in Wheat Seedlings Under Salinity","volume":"54","author":"Bezrukova","year":"2008","journal-title":"Plant Growth Regul."},{"key":"ref_76","doi-asserted-by":"crossref","unstructured":"Farnese, F.S., Menezes-Silva, P.E., Gusman, G.S., and Oliveira, J.A. (2016). When Bad Guys Become Good Ones: The Key Role of Reactive Oxygen Species and Nitric Oxide in the Plant Responses to Abiotic Stress. Front. Plant Sci., 7.","DOI":"10.3389\/fpls.2016.00471"},{"key":"ref_77","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1016\/j.niox.2017.12.005","article-title":"Nitric Oxide-Mediated Integrative Alterations in Plant Metabolism to Confer Abiotic Stress Tolerance, NO Crosstalk with Phytohormones and NO-Mediated Post Translational Modifications in Modulating Diverse Plant Stress","volume":"73","author":"Sami","year":"2018","journal-title":"Nitric Oxide"},{"key":"ref_78","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1134\/S1021443722030037","article-title":"Current Concepts of the Mechanisms of Nitric Oxide Formation in Plants","volume":"69","author":"Allagulova","year":"2022","journal-title":"Russ. J. Plant Physiol."},{"key":"ref_79","doi-asserted-by":"crossref","first-page":"462","DOI":"10.1111\/pce.12707","article-title":"Nitric Oxide Function in Plant Abiotic Stress","volume":"40","author":"Fancy","year":"2017","journal-title":"Plant Cell Environ."},{"key":"ref_80","doi-asserted-by":"crossref","unstructured":"Ahluwalia, O., Singh, P.C., and Bhatia, R. (2021). A Review on Drought Stress in Plants: Implications, Mitigation and the Role of Plant Growth Promoting Rhizobacteria. Resour. Environ. Sustain., 5.","DOI":"10.1016\/j.resenv.2021.100032"},{"key":"ref_81","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1111\/jac.12620","article-title":"Atmospheric and Soil Water Deficit Induced Changes in Chemical and Hydraulic Signals in Wheat (Triticum aestivum L.)","volume":"209","author":"Tatar","year":"2023","journal-title":"J. Agron. Crop. Sci."}],"container-title":["Plants"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.mdpi.com\/2223-7747\/13\/14\/1895\/pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,10]],"date-time":"2025-10-10T15:12:28Z","timestamp":1760109148000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.mdpi.com\/2223-7747\/13\/14\/1895"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,7,9]]},"references-count":81,"journal-issue":{"issue":"14","published-online":{"date-parts":[[2024,7]]}},"alternative-id":["plants13141895"],"URL":"https:\/\/doi.org\/10.3390\/plants13141895","relation":{},"ISSN":["2223-7747"],"issn-type":[{"value":"2223-7747","type":"electronic"}],"subject":[],"published":{"date-parts":[[2024,7,9]]}}}