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Article

Yucasin Alleviates Aluminum Toxicity Associated with Regulating Reactive Oxygen Species Homeostasis in Tomato Seedlings

by
Huabin Liu
1,*,
Chuangyang Bai
1,
Jiahui Cai
1,
Yue Wu
1,2 and
Changwei Zhu
1,*
1
College of Biomedicine and Health, Anhui Science and Technology University, Chuzhou 233100, China
2
College of Life Sciences, Nanjing Forestry University, Nanjing 210037, China
*
Authors to whom correspondence should be addressed.
Toxics 2025, 13(5), 406; https://doi.org/10.3390/toxics13050406
Submission received: 28 March 2025 / Revised: 6 May 2025 / Accepted: 15 May 2025 / Published: 17 May 2025
(This article belongs to the Section Toxicity Reduction and Environmental Remediation)
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Abstract

The phytotoxicity of aluminum (Al) to plants is well known. Auxin accumulation and reactive oxygen species (ROS) burst induced by Al toxicity are the key factors in root growth inhibition. Yucasin, an auxin synthesis inhibitor, effectively ameliorates Al phytotoxicity in tomato seedlings. However, the physiological mechanisms by which yucasin alleviates Al phytotoxicity in tomatoes remain elusive. Here, we examined the regulatory mechanisms of yucasin involved in tomato seedling growth under Al conditions through phenotypic, plant physiology analysis, and cellular experiments. Exogenous indole-3-acetic acid (IAA) application increased Al accumulation in tomato seedling roots, while yucasin decreased Al accumulation. Yucasin application reduced Al-induced ROS accumulation, lipid peroxidation, and cell death, enhanced root viability, and promoted tomato seedling root growth. Further, yucasin enhanced the antioxidant enzyme activities of superoxide dismutase, catalase, and peroxidase in plants under Al conditions. The results suggest that yucasin improves the scavenging capacity of ROS by maintaining the activities of antioxidative enzymes. This study elucidates the physiological mechanism by which yucasin alleviates Al phytotoxicity, highlighting its potential to enhance plant tolerance under acidic Al conditions.

Graphical Abstract

1. Introduction

Al in the soil predominantly exists in the form of insoluble silicates or aluminum oxides, which cannot be absorbed by plants. Therefore, these forms of Al are less phytotoxic or non-phytotoxic to plants [1,2]. In acidic soils, Al forms facilitate conversion to soluble Al3+ and absorption by plants. Al3+ ions are phytotoxic to most plants [3]. The accumulation of excessive Al destroys the structure of the cell walls, affects cell division, inhibits root growth, and impacts water and nutrient absorption [4,5]. Therefore, Al has become a crucial limiting factor for plant growth and crop productivity in acidic arable land.
The plant root tips are the primary target site for Al3+, and the transition zone (TZ) is the key site where plants perceive Al toxicity signals [6,7]. Al stress triggers signal responses in the TZ, characterized by elevated ROS levels and perturbation of phytohormone profiles [8,9]. Auxin is a key signaling molecule for plants to respond to Al toxicity. Local auxin biosynthesis was enhanced, and auxin transport was disrupted under Al stress, resulting in auxin accumulation within the TZ [6,7,10,11]. This heightened auxin response amplifies the inhibitory effects of Al on root cell growth. Experimental evidence demonstrates that Al stress applied to the elongation zone (EZ) does not affect root growth; however, when Al is applied to the TZ, root growth is significantly inhibited [12]. The disparity in perception and response sites implies a distinct signaling mechanism or crosstalk between cells in the TZ and EZ. Recent evidence supports that auxin functions as a crucial intermediary in establishing the connection between these two zones. Exogenous boron restores auxin distribution in the EZ by re-establishing PIN2-mediated basipetal auxin transport from the TZ to EZ, thereby mitigating Al stress-induced inhibition of root growth [11]. Auxin levels in Arabidopsis are negatively correlated with their ability to tolerate Al. Mutants with excessive auxin synthesis (yucca, sur2, sur1-3) or exogenous application of auxin (NAA) aggravate sensitivity to Al stress [13]. Meanwhile, mutants with reduced auxin synthesis (taa1, yuc8, yuc8/9) or exogenous application of auxin synthesis inhibitors attenuate Arabidopsis sensitivity to Al stress [7,10]. Although multiple auxin biosynthesis pathways have been identified, the indole-3-pyruvate pathway has been established as the primary route for auxin biosynthesis in plants. In this pathway, the aminotransferase TAA and the flavin monooxygenase YUC sequentially catalyze the transformation of tryptophan into IAA [14]. Yucasin, a YUC inhibitor, is commonly used to investigate the regulatory mechanisms of auxin [10,15]. However, the physiological mechanisms by which auxin synthesis inhibitors alleviate Al toxicity in tomatoes remain unclear.
As an early stress response signal, ROS has been known to cope with Al toxicity by activating downstream gene expression or resistance systems in plants [16,17]. Al stress exposure stimulates ROS burst and accumulation in plant roots [18,19]. Excessive ROS oxidatively damage cells and protein structures, disrupt metabolic processes, and cause secondary damage to plants [19,20,21]. One of the main guarantees for protecting cells against oxidative damage is the activation of the antioxidant defense mechanism [22]. The antioxidant system balances plant growth and stress response by scavenging excessive ROS accumulation and maintaining ROS homeostasis. The transcription factor STOP1 is a key resistance factor to Al stress in plants, regulated by way of H2O2 to promote its oxidation and degradation and increase the sensitivity of plants to Al toxicity [23,24,25]. Studying the Al-sensitive mutant rae6 showed that Al toxicity caused H2O2 accumulation in the mitochondria of the rae6 mutant, and the phenotype of Al-sensitive rae6 could be rescued by scavenging H2O2 [24]. Additionally, exogenous application of silicon and boron alleviates Al phytotoxicity by enhancing the antioxidant system and improving the ability to scavenge ROS [11,22,26]. These results implicate H2O2 accumulation as a crucial factor that contributes to plant susceptibility to Al stress.
Precious studies have confirmed that auxin and ROS are jointly involved in plant Al stress responses [27,28,29]. In the auxin transport-related mutant osaux3, auxin levels and ROS accumulation are significantly decreased [30]. Exogenous auxin application has been associated with enhanced ROS accumulation in root tips, and this effect is auxin concentration dependent [31]. In contrast, ROS alters the distribution and levels of auxin by affecting the polar localization of auxin transport carriers on the cell membrane, the oxidation and degradation of auxin, and ultimately controlling auxin-mediated plant growth [32,33,34]. These findings suggest an interaction between ROS and auxin to co-regulate the adaptive response process to plant Al stress. Nevertheless, the mechanisms underlying auxin-mediated plant growth by participating in ROS signaling regulation under Al stress are poorly understood [28,34].
Here, we revealed the regulatory mechanisms of yucasin responsible for tomato aluminum resistance through phenotypic, plant physiology analysis, and cellular experiments. The application of yucasin promotes root growth and significantly alleviates Al toxicity in tomatoes. Together, the findings provide insight into the potential of yucasin application in agricultural production to reduce the effect of Al phytotoxicity.

2. Materials and Methods

2.1. Plant Growth Conditions

The cherry tomato (Solanum lycopersicum L.) ‘Aisheng’ (Jingyan Yinong Seed Sci-Tech Co., Ltd., Beijing, China) was used in this study. After germination on 1/2 MS medium, tomato seeds were vertically cultured in a light incubator for 3 d. The seedlings were transferred to a 1/5 strength Hoagland hydroponic solution and adapted cultivation for one day. The tomato seedlings were held at 24 °C and 75% humidity under a 14/10 h light (10,000 Lux) cycle.

2.2. Treatment with AlCl3, IAA and Yucasin

At least 10 plant seedlings per group were pretreated with 0.5 mM CaCl2 for 12 h, transferred to a 1/5 strength Hoagland solution with 50 μM AlCl3, 50 μM AlCl3 plus 5 nM IAA or 5 μM yucasin for 6 d or the indicated times, respectively. The treatment solution (pH 5.0) was refreshed every two days.

2.3. Al Content Determination

The root system was obtained by cutting the treated tomato seedlings with a blade. After drying them, the samples were ground into a powder before being digested with HNO3-H2O2 [35]. Briefly, 5 mL of 65% HNO3 was added to the sample and incubated for 12 h, followed by boiling at 120 °C for 3 h. After cooling, 1 mL of H2O2 was added to make the solution transparent. The aluminum contents were measured using ICP-MS (NexION 2000, PerkinElmer, Waltham, MA, USA).

2.4. ROS Assays

The tomato seedlings were transferred to 1/5 Hoagland containing 50 μM AlCl3, or 50 μM AlCl3 + 5 μM yucasin for 1 day. After treatment, O2− was detected using NBT staining in the roots. Briefly, the roots were rinsed with ddH2O and immersed in 0.25 mg/mL NBT. Roots were observed with a microscope. The NBT staining intensity was measured and analyzed using ImageJ (v1.51). Three biological replicates with 10–15 seedlings per treatment.
For H2O2 detection, 0.1 g of the treated fresh plant seedling was thoroughly ground into a homogenate with a mortar and pestle at 0 °C, and H2O2 was extracted by H2O2 content detection kit (BC3590, Solarbio, Beijing, China) following the instructions provided by the suppliers. The H2O2 content was determined at 415 nm.

2.5. Evaluation of Malondialdehyde (MDA) and Proline Content

To determine the MDA content, 0.5 g of the treated fresh tomato seedlings were homogenized in trichloroacetic acid (5%, v/v) with a mortar and pestle, and the supernatant was collected after centrifugation. The samples were incubated with 2 mL of 0.67% (w/v) TBA at 100 °C for 30 min, chilled, and collected for further analysis. TBA (0.67%) was dissolved in 10% trichloroacetic acid solution. The content of MDA was determined as described previously [36].
The proline content was measured as previously described [37]. The treated tomato seedling tissue was thoroughly ground in aqueous sulfosalicylic acid (3%, w/v), incubated at 100 °C for 10 min, and filtered after cooling. The sample filtrate, glacial acetic acid, and acid-ninhydrin (1:1:1, v/v/v) were reacted at 100 °C, chilled, and toluene was then introduced into the mixture for extraction before detecting the absorbance at 520 nm.

2.6. TTC and Evans Blue Staining

Root viability and cell death were detected by TTC [38] and Evans blue staining [39], respectively, as previously described. The treated tomato seedlings were immersed in 0.4% TTC for 4 h or 0.25% Evans blue in 10 mM PBS (pH 7.4) (P397924-5EA, Aladdin, Shanghai, China) for 5 min, respectively. Roots were observed with a light microscope. The TTC and Evans blue staining intensity was measured and analyzed using ImageJ (v1.51). Three biological replicates with 10–15 seedlings per treatment.

2.7. Enzyme Activity Assays

Approximately 0.5 g of the treated fresh plant seedling samples was collected and ground into a homogenate in phosphate buffer with a mortar and pestle. They were centrifuged, and the supernatant was used for the determination of enzyme activities. Superoxide dismutase and peroxidase activities in tomato seedlings were determined according to Yang et al. [40]. Catalase was determined using a CAT activity assay kit (BC0205, Solarbio, Beijing, China). CAT is the primary enzyme responsible for scavenging H2O2 and is extensively distributed across plant tissues and cells. H2O2 exhibits a characteristic absorption at 240 nm, and the absorbance decreases as it is decomposed by CAT. For the experiment, 0.1 g of the treated fresh tomato seedlings was thoroughly homogenized in a mortar and pestle. The resulting homogenate was transferred to a centrifuge tube, and 1 mL of phosphate buffer was added. After centrifugation at 8000× g for 10 min, the supernatant containing the CAT was collected. The reaction solution consisted of the supernatant and H2O2, and the absorbance was detected at 240 nm using a UV-2600 spectrophotometer (SHIMADZU, Suzhou, China). The enzymatic activity of CAT was subsequently evaluated based on the change in absorbance of the reaction solution.

2.8. Statistical Analysis

Data were analyzed by one-way ANOVA using PASW statistics 18. Duncan’s multi-comparison test was employed to assess statistical differences between various treatments at the p < 0.05 level.

3. Results

3.1. Yucasin Enhances Tomato Seedling Tolerance to Al Stress by Maintaining Root Viability

Auxin has been recognized as a regulator of plant responses to Al stress [41]. To investigate the functions of auxin in plant Al toxicity, the seedlings were co-treated with IAA or auxin synthesis inhibitor yucasin in the presence of AlCl3. IAA enhanced Al-induced root growth inhibition, while yucasin promoted tomato root elongation (Figure 1A, Figures S1 and S2). This indicates that yucasin plays positive regulatory roles in tomato seedling root growth under Al toxicity.
Maintaining the cell activity of root tips is the main driver promoting plant root elongation. To analyze the roles of yucasin on the root activity in tomatoes under Al toxicity, cell viability and cell death were assessed by histochemical staining. As shown in Figure 1, the TTC staining intensity was significantly reduced, while the Evans blue staining intensity was significantly enhanced in tomato seedling roots exposed to Al stress (Figure 1B–E). This indicates that Al stress induced cell death and reduced cell viability. Consistent with the root growth phenotype, the effects of Al toxicity were reversed by applying yucasin. Compared to tomato seedlings exposed to Al stress, adding yucasin increased root activity and reduced cell death (Figure 1B–E). These results suggested that yucasin contributes to the Al detoxification and tolerance of tomato seedlings by enhancing root activity and reducing cell death.

3.2. Yucasin Reduces Al Accumulation in Tomato Seedling Roots

Al3+ is absorbed by the roots and accumulates in the cell wall and cytoplasm, thereby disrupting cellular physiological processes and inhibiting cell division, which ultimately suppresses plant growth. To analyze whether auxins affect the uptake of Al3+ in tomato, we used ICP-MS to analyze the aluminum ion levels in tomato seedling roots treated with exogenous auxin IAA and yucasin. Treatment with IAA led to an enhanced accumulation of Al3+ in tomato seedling roots (Figure 2). Conversely, applying yucasin decreases such aluminum ion accumulation (Figure 2). These findings suggest that IAA facilitates the absorption of Al3+ by tomato roots, whereas yucasin impedes the root absorption of aluminum ions.

3.3. Yucasin Reduces ROS Accumulation and Oxidative Damage Under Al Toxicity

ROS include H2O2 and O2−, important signals for plants to respond to abiotic stresses. The appropriate level of ROS signal mediates plant response to stress by activating downstream resistance genes. Meanwhile, excessive ROS accumulation causes oxidative stress to plants, exacerbating the damage of stress to plants. To investigate whether yucasin mitigates Al toxicity in tomato seedlings by modulating ROS production, we analyzed the H2O2 content in tomato seedlings and monitored the level and distribution of O2− in tomato root tips using NBT staining. As shown in Figure 3, Al treatment triggers ROS production in tomato seedlings. ROS bursts mainly occurred in the meristematic and transitional zones of the tomato roots. In contrast, exogenous yucasin application significantly reduced ROS accumulation (Figure 3). The results suggest that plant root tips are the primary target sites for Al3+, while yucasin mitigates Al phytotoxicity by regulating Al-induced ROS accumulation in seedlings.
MDA is a byproduct of lipid peroxidation in cell membranes under oxidative stress conditions. Its content is an indicator of the extent of plasma membrane oxidative damage. To evaluate oxidative damage induced by Al stress, the MDA levels in tomato seedlings were analyzed. Consistent with the ROS accumulation, the MDA content in tomatoes significantly increased under Al stress (Figure 4). When yucasin was applied, the accumulation of MDA content caused by Al stress was significantly reduced (Figure 4). These results suggested that yucasin alleviates Al toxicity by reducing ROS accumulation and peroxidation damage. Proline is an important regulatory substance in plants’ response to stress. It has the functions of stabilizing the membrane structure and regulating cell osmotic potential. Tomato seedlings exposed to Al stress showed an increase in proline content (Figure 5). Yucasin application reduced Al-induced proline accumulation (Figure 5).

3.4. Yucasin Maintains Antioxidant Enzyme Activities in Tomato Seedlings

Maintaining the dynamic balance of ROS by scavenging excessively accumulated ROS is an important regulatory mechanism to protect plants from oxidation stress. It was shown that AlCl3 treatments resulted in an elevation of ROS levels in tomato seedlings, with a notable O2– accumulation observed in root tips (Figure 3A–C). Plants cope with oxidative stress by regulating the activities of ROS-scavenging enzymes, which include SOD, POD, and CAT. As depicted in Figure 6, the activities of SOD, POD, and CAT in tomato seedlings exhibited a trend of initially increasing and subsequently decreasing during Al toxicity (Figure 6A–C). Two days after Al treatment, the activities of these enzymes significantly increased (Figure 6A–C). With the prolongation of AlCl3 treatment (4 or 6 d), the enzyme activities significantly decreased (Figure 6A–C). This indicated that plants cope with excessive ROS production by increasing the antioxidant enzyme activity within the early stage of Al conditions. However, with the prolongation of Al treatment, the antioxidant enzyme activity in plants is significantly inhibited (Figure 6A–C). After 6 d of Al treatment, the SOD, CAT, and POD activity significantly decreased (Figure 6A–C). Applying yucasin for 6 d to the Al-treated tomato seedlings increased the SOD, CAT, and POD activity by 62.5%, 12%, and 35.4%, respectively, compared to the Al treatments (Figure 6A–C).

4. Discussion

Plants coping with environmental stress is a complex growth decision that is influenced and regulated by many factors, among which auxin plays a central role. The mechanisms by which auxin inhibits or promotes plant growth under acid-aluminium stress vary considerably among plant species. Auxin biosynthesis mutants yuc9, taa1-1, and yucQ of Arabidopsis exhibit Al tolerance [7,10], while auxin synthesis excess mutants (yucca, sur2, sur1-3) show sensitivity to Al stress [13]. Consistent with the results, we found that treatment with exogenous auxin IAA increased the sensitivity of tomatoes to Al stress, whereas yucasin significantly reduced the sensitivity (Figure 1 and Figure S1). These results indicate that plant Al tolerance is inversely proportional to auxin levels. However, there are contrary experimental findings that Al stress inhibits maize root growth, accompanied by a significant decrease in auxin content [42]. Exogenous application of auxin analog NAA can alleviate Al-induced maize root growth inhibition [42]. Al, which is phytotoxic to most plants, becomes a beneficial element in Camellia sinensis growth [43]. Al stimulates plant growth and is an essential element for maintaining root development in Camellia sinensis [44]. Al-induced UDP glycosyltransferase CsUGT84J2 promotes root growth in Camellia sinensis by enhancing the accumulation of auxin [45]. These findings suggest the existence of distinct regulatory mechanisms in various plant species under Al conditions.
Certain plants exhibit resilience in aluminum-rich environments, with some even experiencing growth enhancement under low Al concentrations [44,45]. This phenomenon is attributed to the evolutionary development of regulatory mechanisms in Al-tolerant plants to combat Al stress. The mechanisms include the secretion of organic acids to chelate Al3+, elevation of pectin methylation in cell walls, and sequestration of Al3+ within vacuoles to mitigate Al toxicity [46,47,48]. Pectin, a key constituent of plant cell walls, possesses a high affinity for Al3+ [49]. The accumulation of Al damages cell wall integrity, disrupts cell division, and suppresses cellular growth. Here, we showed that applying IAA promoted the uptake of Al3+ by the tomato seedling roots. Meanwhile, yucasin inhibited the acquisition of aluminum ions by roots (Figure 2). Therefore, reducing the absorption of Al3+ by roots and alleviating the pressure induced by Al stress may be crucial factors for yucasin in mitigating Al toxicity.
ROS production and signaling serve as crucial regulatory mechanisms that enable plants to cope with environmental challenges and establish defense responses [33]. However, excessive ROS production can impose oxidative stress on plant cells, trigger oxidative damage, and lead to cell death. We found that aluminum stress triggered ROS overproduction in tomato seedlings (Figure 3). The accumulated ROS inflicted oxidative damage on plant cells. This was manifested by an elevation in MDA levels and a decline in cell viability (Figure 1B and Figure 4). When yucasin was applied, the Al-induced ROS accumulation and MDA content decreased (Figure 3 and Figure 4). Consistently, 4-phenoxyphenylboronic acid (PPBo), another inhibitor of auxin biosynthesis, reduces H2O2 accumulation caused by mild cadmium stress and alleviates the phytotoxicity on rice and barley [50,51]. These results suggest that yucasin and PPBo exhibit comparable functions in reducing ROS accumulation and ameliorating metal stress in plants. However, PPBo does not affect the absorption of cadmium ions by the roots, while yucasin reduces Al accumulation in the tomato seedlings, which may be attributed to distinct mechanisms of action or differences in treatment conditions and experimental materials.
Although it has been established that both auxin and ROS are involved in the Al stress response, their roles in mitigating Al toxicity in plants, especially the regulatory interplay between auxin and ROS, remain poorly understood [28]. Exogenous auxin triggers the production and accumulation of ROS, leading to tomato root growth inhibition [31]. Applying yucasin significantly reduced Al-induced ROS accumulation and promoted root elongation (Figure 3). The results indicate that auxin regulates root growth by affecting ROS levels. However, there is a ROS-auxin-mediated signaling pathway in rice that promotes root elongation in the stress-free area to avoid adverse stress [33]. These results suggest that there is a complex interaction between auxin and ROS involved in plant stress response.
Adverse stresses induce a burst of ROS and disrupt the ROS scavenging system, consequently exacerbating plant stress damage [52]. The ROS level within plant cells is strictly regulated by the antioxidant detoxification systems to protect the plant from the oxidative stresses caused by excessive ROS accumulation. Studies have demonstrated that the application of chemicals, such as silicon and boron, significantly improves plant tolerance to Al stress by enhancing ROS-scavenging ability [11,22]. This, in turn, substantially expands our understanding of the use of exogenous substances for mitigating Al phytotoxicity. Consistently, it was found that yucasin application markedly reduced the contents of H2O2, O2−, and MDA and enhanced antioxidant enzymes activities under AlCl3 treatments (Figure 6). The maintenance or enhancement of the antioxidant enzyme system is regarded as a key strategy for ROS scavenging and an essential regulatory mechanism for mitigating plant stress [53,54]. The results suggest that yucasin enhances ROS-scavenging ability by increasing antioxidant enzyme activities and mitigating oxidative stresses induced by Al toxicity. This provides novel evidence for further elucidation of the aluminum detoxification mechanism of yucasin. However, further investigation is needed to determine whether the reduction in ROS under Al conditions is attributable to the exogenous application of yucasin or a decrease in auxin levels.

5. Conclusions

In this study, tomato seedlings were employed to investigate the regulatory mechanism underlying plants’ response and tolerance to Al conditions. A burst of ROS is a prominent feature of tomato seedlings responding to Al toxicity. With the prolongation of Al treatment, root vitality decreases, and root growth is inhibited. The application experiment of yucasin on tomato seedlings demonstrated that yucasin positively regulates plant aluminum tolerance by maintaining antioxidant enzyme activities to enhance ROS scavenging ability. Moreover, yucasin also reduced Al accumulation in tomato seedlings, further alleviating Al-induced stresses. The present study elucidates the physiological mechanisms by which yucasin mitigates Al toxicity in tomatoes, providing a potential strategy for utilizing yucasin in acid soils to improve plant tolerance to Al stress.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/toxics13050406/s1, Figure S1: Effects of IAA, yucasin and Al stress on the seedling growth of tomatoes. Figure S2: Yucasin promotes root elongation under Al stress.

Author Contributions

H.L. and C.Z. conceived the study. C.B., J.C., H.L. and Y.W. carried out the experiments. H.L. and J.C. analyzed the experimental data. H.L. and C.Z. wrote the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The work was supported by Undergraduate Innovation Training Project (S202410879190) and Natural Science Foundation of Education Department of Anhui Province (2022AH051624).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is available in the article.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Yucasin promotes root growth under Al conditions by increasing root viability and reducing cell death. (A) Phenotypes of tomato seedlings after 6 d under 50 μM AlCl3 (Al), 5 nM IAA (IAA), 50 μM AlCl3 + 5 nM IAA (Al + IAA), 5 μM yucasin (yucasin), 50 μM AlCl3 + 5 μM yucasin (Al + yucasin) treatment as indicated. (B,D) TTC (B) staining for root activity and Evans blue (D) staining for cell death in the tomato seedlings exposed or not to 50 μM AlCl3 or 50 μM AlCl3 + 5 μM yucasin for 48 h. (C,E) indicated quantification analyses of staining intensities in the roots of tomato seedlings in (B,D), respectively. Error bars indicate SD (n = 10–15 per treatment on each replicate). Bars = 1 cm (A) and 200 μm (B,D). Different letters indicate significant differences.
Figure 1. Yucasin promotes root growth under Al conditions by increasing root viability and reducing cell death. (A) Phenotypes of tomato seedlings after 6 d under 50 μM AlCl3 (Al), 5 nM IAA (IAA), 50 μM AlCl3 + 5 nM IAA (Al + IAA), 5 μM yucasin (yucasin), 50 μM AlCl3 + 5 μM yucasin (Al + yucasin) treatment as indicated. (B,D) TTC (B) staining for root activity and Evans blue (D) staining for cell death in the tomato seedlings exposed or not to 50 μM AlCl3 or 50 μM AlCl3 + 5 μM yucasin for 48 h. (C,E) indicated quantification analyses of staining intensities in the roots of tomato seedlings in (B,D), respectively. Error bars indicate SD (n = 10–15 per treatment on each replicate). Bars = 1 cm (A) and 200 μm (B,D). Different letters indicate significant differences.
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Figure 2. Effects of IAA and yucasin on Al concentration in tomato seedling roots under Al stress. Quantification analysis of Al3+ content in the tomato seedlings exposed or not to 50 μM AlCl3 (Al), 50 μM AlCl3 + 10 nM IAA (Al + IAA), 50 μM AlCl3 + 1 μM yucasin (Al + yucasin) treatment as indicated for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
Figure 2. Effects of IAA and yucasin on Al concentration in tomato seedling roots under Al stress. Quantification analysis of Al3+ content in the tomato seedlings exposed or not to 50 μM AlCl3 (Al), 50 μM AlCl3 + 10 nM IAA (Al + IAA), 50 μM AlCl3 + 1 μM yucasin (Al + yucasin) treatment as indicated for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
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Figure 3. Yucasin reduces Al-induced ROS accumulation in seedlings. (A) NBT staining for O2– in roots of tomato seedling exposed or not to AlCl3, AlCl3 (Al) plus yucasin (Al + yucasin) for 24 h. (B) Quantification analysis of staining intensities (A) in the roots of tomato seedlings in (B). Bars = 200 μm. Values represent the means ± SD ((A,B): n = 10–15 per treatment on each replicate). (C) Quantification of the yucasin effect on H2O2 level in the tomatoes under control (CK), Al, and Al + yucasin conditions. Error bars indicate SD (n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
Figure 3. Yucasin reduces Al-induced ROS accumulation in seedlings. (A) NBT staining for O2– in roots of tomato seedling exposed or not to AlCl3, AlCl3 (Al) plus yucasin (Al + yucasin) for 24 h. (B) Quantification analysis of staining intensities (A) in the roots of tomato seedlings in (B). Bars = 200 μm. Values represent the means ± SD ((A,B): n = 10–15 per treatment on each replicate). (C) Quantification of the yucasin effect on H2O2 level in the tomatoes under control (CK), Al, and Al + yucasin conditions. Error bars indicate SD (n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
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Figure 4. Yucasin alleviates Al-induced oxidative stress in tomato seedlings. Quantification of MDA content in the tomato seedlings exposed or not to AlCl3, yucasin, and AlCl3 + yucasin for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
Figure 4. Yucasin alleviates Al-induced oxidative stress in tomato seedlings. Quantification of MDA content in the tomato seedlings exposed or not to AlCl3, yucasin, and AlCl3 + yucasin for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan test).
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Figure 5. Effect of yucasin on proline level in Al-treated tomato seedlings. Quantification analysis of proline content in the tomato seedlings exposed or not to AlCl3, yucasin, and AlCl3 + yucasin for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan’s test).
Figure 5. Effect of yucasin on proline level in Al-treated tomato seedlings. Quantification analysis of proline content in the tomato seedlings exposed or not to AlCl3, yucasin, and AlCl3 + yucasin for 6 d (mean ± SD, n = 3). Letters above the columns indicate statistically different (ANOVA followed by Duncan’s test).
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Figure 6. Effects of yucasin on antioxidant enzyme activities. (A–C) Quantification analysis of the activities of SOD (A), CAT (B), and POD (C) in the tomato seedlings exposed or not (CK) to AlCl3 (Al), yucasin (yucasin), and AlCl3 + yucasin (Al + yucasin) for 2, 4, and 6 d (mean ± SD, n = 3). Different letters within an indicated time point represent significant differences among the control (CK), Al, yucasin, and Al + yucasin treatments (ANOVA followed by Duncan’s test).
Figure 6. Effects of yucasin on antioxidant enzyme activities. (A–C) Quantification analysis of the activities of SOD (A), CAT (B), and POD (C) in the tomato seedlings exposed or not (CK) to AlCl3 (Al), yucasin (yucasin), and AlCl3 + yucasin (Al + yucasin) for 2, 4, and 6 d (mean ± SD, n = 3). Different letters within an indicated time point represent significant differences among the control (CK), Al, yucasin, and Al + yucasin treatments (ANOVA followed by Duncan’s test).
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MDPI and ACS Style

Liu, H.; Bai, C.; Cai, J.; Wu, Y.; Zhu, C. Yucasin Alleviates Aluminum Toxicity Associated with Regulating Reactive Oxygen Species Homeostasis in Tomato Seedlings. Toxics 2025, 13, 406. https://doi.org/10.3390/toxics13050406

AMA Style

Liu H, Bai C, Cai J, Wu Y, Zhu C. Yucasin Alleviates Aluminum Toxicity Associated with Regulating Reactive Oxygen Species Homeostasis in Tomato Seedlings. Toxics. 2025; 13(5):406. https://doi.org/10.3390/toxics13050406

Chicago/Turabian Style

Liu, Huabin, Chuangyang Bai, Jiahui Cai, Yue Wu, and Changwei Zhu. 2025. "Yucasin Alleviates Aluminum Toxicity Associated with Regulating Reactive Oxygen Species Homeostasis in Tomato Seedlings" Toxics 13, no. 5: 406. https://doi.org/10.3390/toxics13050406

APA Style

Liu, H., Bai, C., Cai, J., Wu, Y., & Zhu, C. (2025). Yucasin Alleviates Aluminum Toxicity Associated with Regulating Reactive Oxygen Species Homeostasis in Tomato Seedlings. Toxics, 13(5), 406. https://doi.org/10.3390/toxics13050406

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