A genome-wide identification and expression analysis was performed to examine the response of the amino acid permease (AAP) gene family to drought stress in tomato (Solanum lycopersicum L.). Ten AAP genes were identified across seven of the twelve chromosomes and classified into four subfamilies (I–IV) based on phylogenetic relationships. Expansion of the SlAAP family appears to have been driven mainly by segmental and tandem duplication events. Members within the same subfamily displayed high similarity in exon–intron organization and conserved motif architecture. Promoter analysis revealed the presence of multiple cis-acting elements associated with stress and defence regulation. Under drought stress, all putative genes exhibited significant transcriptional induction, with SlAAP8, SlAAP9 and SlAAP10 showing the strongest upregulation, suggesting their potential involvement in drought adaptation. Drought treatment also led to a marked decline in nitrate (NO3−) and total nitrogen (N) contents, while simultaneously increasing the accumulation of total amino acids, ammonium (NH4+), and proline in both leaf and root tissues of tomato. The expression profiles of the ten putative SlAAP genes showed strong positive correlations with total amino acid levels in both organs, suggesting their involvement in amino acid redistribution under stress. Collectively, these results underscore the functional complexity of the SlAAP gene family and provide a robust foundation for future investigations into their molecular roles and potential applications in enhancing drought tolerance in tomato and other crop species.

Accumulating evidence suggests that exposure to pollution from environmental cadmium (Cd) contributes to diabetic kidney disease as indicated by albuminuria and a progressive decrease in the estimated glomerular filtration rate (eGFR). This study examined the effects of Cd exposure on eGFR and the excretion rates of albumin (Ealb) and β2-microglobulin (Eβ2M) in 65 diabetics and 72 controls. Excretion of Cd (ECd) was a measure of exposure, while excretion of N-acetylglucosaminidase (ENAG) reflected the extent of kidney tubular cell injury. In participants with an elevated excretion of Eβ2M, the prevalence odds ratios (POR) for a reduced eGFR rose 6.4-fold, whereas the POR for albuminuria rose 4.3-fold, 4.1-fold, and 2.8-fold in those with a reduced eGFR, diabetes, and hypertension, respectively. Using covariance analysis, which adjusted for the interactions, 43% of the variation in Ealb among diabetics could be explained by female gender (η2 = 0.176), ENAG (η2 = 0.162), hypertension (η2 = 0.146), smoking (η2 = 0.107), and body mass index (η2 = 0.097), while the direct contribution of ECd to Ealb variability was minimal (η2 = 0.005). Results from a mediating-effect analysis imply that Cd could contribute to albuminuria and a falling eGFR through inducing tubular cell injury, leading to reduced reabsorption of albumin and β2M.

In this study, we aimed to evaluate physiological and agronomic traits in 120 sugarcane genotypes under early drought stress conditions in a field trial across various soil types. The experiment used a split-plot arrangement, with a randomized complete block design and two replications. Two different water regimes were assigned to the main plot: (1) non-water stress (CT) and (2) drought (DT) at the early growth stage, during which sugarcane was subjected to drought stress by withholding water for 4 months. The subplot consisted of 120 sugarcane genotypes. The stalk height, stalk diameter, number of stalks, photosynthetic traits including SPAD chlorophyll meter reading (SCMR) and maximum quantum efficiency of photosystem II photochemistry (Fv/Fm), and normalized difference vegetation index (NDVI) were measured at 3, 6, and 9 months after planting (MAP). Yield and yield component parameters were measured at 12 MAP. Drought treatments lead to significant changes in various physiological traits in the sugarcane. Clustering analysis classified 36 sugarcane varieties grown in sandy loam soil and 15 genotypes in loam soil into two main clusters. In sandy loam soils, Biotec4 and CO1287 exhibited outstanding performance in drought conditions, delivering high cane yields. Meanwhile, in loam soil, MPT13-118, MPT07-1, Q47, F174, MPT14-1-902, and UT1 exhibited the best drought tolerance. Under drought conditions, cluster 1 showed higher values for SCMR, NDVI, height growth rate (HGR), cane yield, and drought tolerance index compared to cluster 2. These findings suggest that breeders can utilize these genotypes to enhance drought resistance, and the identified physiological traits can assist in selecting stronger candidates for drought tolerance.

Sunflower (Helianthus annuus L.) is an essential oilseed crop known for its adaptability to harsh environments including drought. However, salinity stress, affecting over 20% of global agricultural land, poses a serious threat to its productivity. This study evaluated the response of 17 sunflower genotypes under salinity stress (200 mM NaCl) and optimum (0 mM NaCl) conditions in the laboratory. The experiment was arranged in a completely randomized design with three replications and was validated through a second experimental run. Measured parameters included germination percentage and speed, root and shoot length, biomass, and water content. Stress tolerance indices (STIs) for germination, seedling length, and biomass were calculated. Combined ANOVA showed that genotype and environment interactions significantly (p < 0.001) affected all measured traits. Salinity stress significantly reduced germination, seedling growth, and biomass across genotypes, with some experiencing complete germination inhibition. Genotypes 9, 14, 16, and 17 consistently maintained higher germination, seedling length, and biomass under stress, with high STIs, indicating tolerance to salinity stress during the early growth stages. These results identified genotypes 9, 14, 16, and 17 as promising candidates for breeding programs aimed at enhancing salinity tolerance, offering sustainable solutions for the utilization of saline soils and for enhancing food security. Future research should focus on the field-based validation of these genotypic responses.

The climbing perch, Anabas testudineus, is one of the most widely distributed freshwater amphibious fishes in South and Southeast Asia, exhibiting terrestrial movements. Our experimental study aimed to investigate endocrinological and biochemical changes in the blood of climbing perch associated with their terrestrial movements. To achieve this, the fish were divided into two groups: one group was exposed to aquatic conditions for twenty minutes, while the other group was subjected to terrestrial conditions for the same duration through rapid water level decrease. In terrestrial conditions, the fish predominantly exhibit movements on land, whereas in aquatic environments, they primarily remain immobile or swim. Elevated levels of stress-induced cortisol and glucose after short-term exposure indicate a high-stress response involving both neuroendocrine and metabolic mechanisms. Changes in the activity of aspartate aminotransferase and increased concentrations of triglycerides in the blood serum suggest energy mobilization through aerobic metabolic pathways. Extreme environmental changes did not affect thyroid axis function, including deiodination, thereby maintaining essential physiological activities under new conditions. Additionally, the anaerobic metabolic pathway appears to be minimally utilized at the onset of terrestrial movement, as no significant changes in lactate dehydrogenase concentrations were observed. Overall, the terrestrial movements of the climbing perch are likely predominantly forced and associated with high stress.

Cellular stressors have been demonstrated to exert a substantial influence on the functionality of organelles, thereby impacting cellular homeostasis and contributing to the development of disease pathogenesis. This review aims to examine the impact of diverse stressors, including environmental, chemical, biological, and physical factors, on critical organelles such as the cell membrane, mitochondria, endoplasmic reticulum, Golgi apparatus, lysosomes, and membrane-less organelles. The intricate molecular mechanisms underlying cellular stress responses, encompassing oxidative stress, protein misfolding, and metabolic reprogramming, have the capacity to elicit adaptive responses or culminate in pathological conditions. The interplay between these stressors and organelle dysfunction has been implicated in a myriad of diseases, including neurodegenerative disorders, cancer, metabolic disorders, and immune-related pathologies. A comprehensive understanding of the mechanisms by which organelles respond to stress can offer valuable insights into the development of therapeutic strategies aimed at mitigating cellular damage.

Climate change significantly impacts agriculture by increasing the frequency and intensity of environmental stresses, which can severely reduce agricultural yields. Adopting sustainable practices is crucial to mitigating these risks and enhancing crop resilience. Applying natural compounds and microorganisms as biostimulants has gained popularity as an eco-friendly approach to alleviating abiotic stress in agricultural plants. This study reviews the current research on applying biostimulants in horticulturally significant crops to boost their resistance to abiotic stressors such as salinity, drought, and high temperatures. It explores the mechanisms through which these stimulants offer protection, focusing on the roles of key bioactive substances in regulating physiological and molecular processes for stress adaptation. The study addresses biostimulant formulation, regulation, and application challenges. Future research directions are suggested to harness biostimulants’ potential fully, aiming to develop climate-resilient horticultural systems that follow sustainability principles. This comprehensive review underscores the use of biostimulants as a sustainable strategy to increase crop yields in the face of climate change, reducing reliance on synthetic agrochemicals.

The aim of the present study was to explore heavy metal tolerance and accumulation potential in Anthyllis vulneraria subsp. maritima plants from coastal sand dunes in controlled conditions. Plants were established from seeds collected in coastal sand dunes and cultivated in substrates in greenhouse conditions. A gradual treatment with CdCl2, PbOAc, CuSO4, MnSO4, and ZnSO4 was performed until three final concentrations for each metal were reached. The number of leaves, their biomass, and biomass of roots were negatively affected by increasing concentrations of lead (Pb) and manganese (Mn) in substrate, but no negative effect was evident for cadmium (Cd), copper (Cu), and zinc (Zn). Visible effects of metal toxicity were evident for Pb-treated plants (appearance of thinner leaves, yellowing of older leaves), as well as for Mn-treated plants (reduced leaf size, curled leaves, red leaf venation). There was a significant decrease in water content in old leaves at high Pb and increasing Mn concentration, indicating accelerated leaf senescence. Increase in polyphenol oxidase activity in leaves was evident in all the plants treated with heavy metals. In contrast, an increase in peroxidase activity was evident only for plants treated with 50 and 100 mg L−1 Cd, 500 mg L−1 Pb, 200–1000 mg L−1 Mn, and 500 mg L−1 Zn. Metal accumulation potential for Cd and Cu was the highest in the roots, but for Pb, Mn, and Zn, more metal accumulated in old leaves. It can be concluded that A. vulneraria subsp. maritima plants are tolerant to high Cd, Cu, and Zn, but moderately susceptible to Pb and Mn. However, oxidative enzyme activity cannot be unequivocally used as a specific indicator of metal tolerance. In respect to phytoremediation potential, the plants have very good accumulation capacity for Pb, Mn, and Zn.

Diabetes mellitus (DM) induces the production of reactive oxygen species, which may lead to cell injury and death. This study aimed to assess the effects of rosmarinic acid (RA) on testicular damage, oxidative stress, and apoptosis in streptozotocin (STZ)-induced diabetic albino mice. DM in four- to six-week-old BALB/c male albino mice was induced via 50 mg/kg STZ, IP for 5 days. Twelve mice were randomly assigned into each of following groups: a control group, a diabetic (DM) group, RA5 mg/kg and RA15 mg/kg groups, and DM + RA5 mg/kg and DM + RA15 mg/kg groups. RA doses were intraperitoneally injected six times a week for seven weeks. Diabetes increased blood sugar and HbA1c levels and decreased all assessed sperm parameters. Testicular tissues of the diabetic mice showed increased lipid peroxidation, decreased reduced glutathione levels and catalase and superoxide dismutase activities, and increased apoptosis associated with histological abnormalities. Both RA doses had no effects on final body weight, blood sugar, and HbA1c in the diabetic mice. It is concluded that the administration of the potent antioxidant RA to diabetic mice improved the redox status in testicular tissues, protected them from diabetes-induced oxidative damage, and improved the quality of spermatozoa, mostly in a dose-dependent manner, which suggests a potential application value of RA in treating DM-related testicular injury and perhaps other complications.

Fetal growth restriction (FGR) and low birth weight increase the risk of non-communicable diseases such as type 2 diabetes and heart failure in adulthood. Placental insufficiency is widely considered a major contributor to FGR. Two crucial placental proteins involved in nutrient and stress sensing—O-linked N-acetylglucosamine transferase (OGT) and mechanistic target of rapamycin (mTOR) kinase—play roles in post-translational protein modification and protein translation, influencing cellular growth and metabolism in response to maternal stress, hypoxia, and nutritional status in the placenta. In our study, we examined the gene and protein profiles of OGT and mTOR in FGR and control placentae, comparing those appropriate for gestational age (AGA), while also considering potential confounding effects of fetal sex and delivery mode. Our findings revealed no significant differences in gene expression, protein levels, or activity of OGT, OGA, mTOR, or their associated markers between female AGA and FGR cesarean placentae, nor between female AGA and male AGA cesarean placentae. Additionally, the mode of delivery in female AGA placentae did not affect the levels or activity of these proteins. Overall, our study did not observe significant differences in nutrient sensor protein expression after stratifying by FGR, sex, and delivery mode. Nevertheless, these unbiased results provide a more comprehensive understanding of the complexities of placental gene expression involving OGT and mTOR.