Exogenous Sodium Nitroprusside Affects the Redox System of Wheat Roots Differentially Regulating the Activity of Antioxidant Enzymes under Short-Time Osmotic Stress

Plants Pub Date : 2024-07-09 DOI:10.3390/plants13141895
Alsu Lubyanova, Chulpan Allagulova
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Abstract

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 0.5–24 h. The active and exhausted solutions of SNP, termed as (SNP/+NO) and (SNP/−NO), respectively, were used in this work at a concentration of 2 × 10−4 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•−), 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/−NO)-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/−NO) 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.
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外源硝普钠对小麦根系氧化还原系统的影响差异调节短时渗透胁迫下抗氧化酶的活性
一氧化氮(NO)是一种多功能信号分子,参与调控植物的生长发育和对不同不利环境因素的适应,尤其是对渗透胁迫的适应。了解一氧化氮诱导的植物保护对于提高全球气候变化下的植物抗逆性和作物生产力非常重要。根系是植物在多变环境中生存的关键。根系在发育初期缺水条件下受到的损害会严重影响植物的生存能力。本研究致力于比较分析在 0.5-24 小时的渗透胁迫(PEG 6000,12%)条件下,氮氧化物供体硝普钠(SNP)通过根系对小麦幼苗进行 24 小时的预处理对氧化还原平衡的各种参数的影响。本研究使用的 SNP 活性溶液和衰竭溶液的浓度分别为(SNP/+NO)和(SNP/-NO)2 × 10-4 M。PEG 暴露增加了超氧化物(O2--)、过氧化氢(H2O2)、丙二醛(MDA)的产生,以及电解质渗漏(EL)和脂质过氧化(LPO)的水平。应激处理可提高超氧化物歧化酶(SOD)、抗坏血酸过氧化物酶(APX)、过氧化氢酶(CAT)的活性、脯氨酸的排泄量以及细胞的死亡率,并抑制细胞分裂。在胁迫条件下,(SNP/+NO)通过对抗氧化酶的不同调节,减少了 PEG 诱导的根损伤。因此,与 SNP 未处理或(SNP/-NO)预处理和胁迫受试植物相比,(SNP/+NO)预处理导致 SOD、APX 和 CAT 在胁迫的前 4 小时内受到抑制,而在 PEG 暴露 24 小时后则刺激了它们的活性。渗透胁迫引发根系将大量脯氨酸排泄到外部培养基中。与(SNP/-NO)相比,(SNP/+NO)的预处理可额外增加胁迫诱导的脯氨酸排泄。我们的研究结果表明,NO 能够减轻渗透胁迫对小麦幼苗根系的破坏作用。然而,在某些胁迫时期,NO 的保护作用机制可能有所不同。
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