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. 2026 Jan 15;17(1):39–45. doi: 10.30466/vrf.2025.2062525.4786

Antioxidant, biochemical, hematological indices and handling stress resistance in rainbow trout (Oncorhynchus mykiss) fed with diets supplemented with nano-selenium and vitamin C

Ferdows Momeni 1, Saeid Meshkini 2,*, Ahmad Imani 3
PMCID: PMC13268024  PMID: 42306474

Abstract

Use of various nanoparticles and vitamins to strengthen the immune system of fish to improve growth and biochemical indice, and to mitigate the harmful effects of free radicals through enhanced antioxidant enzyme activity has become the subject of numerous studies. In this study, fish with an average weight of 55.20 ± 7.90 g, after a two-week acclimation period, were randomly distributed into 18 polyethylene 300-L tanks, with 25 fish per tank. The experiment consisted of six treatments with three replicates: Control, vitamin (Vit) C100, nano-selenium (N-Se)0.40, Vit C100 + N-Se0.10, Vit C200 + N-Se0.20, and Vit C400 + N-Se0.40. Blood samples were collected post-treatment for analysis of antioxidant enzyme activities, biochemical and hematological indices as well as post-handling stress. Results indicated significant differences in antioxidant enzyme activities among treatments. The highest catalase activity was observed in Vit C100 and Vit C100 + N-Se0.10 groups. Glutathione peroxidase activity was significantly higher in the control and Vit C200 + N-Se0.20 groups. Malondialdehyde was the highest in Vit C100 + N-Se0.10 group. Superoxide dismutase activity peaked in Vit C200 + N-Se0.20 group. Biochemical indices showed significant differences among treatments except for high-density lipoprotein. Hemoglobin and red blood cell counts were significantly different. The Vit C100 + N-Se0.10 group showed the highest serum cortisol and glucose levels post-handling stress. Overall, dietary N-Se and Vit C supplementation improved antioxidant, biochemical, hematological indices and stress resistance in rainbow trout.

Key Words: Antioxidant enzyme, Biochemical indices, Nanoparticles, Rainbow trout

Introduction

Minerals and vitamins (Vits) are two essential micro-nutrients required for the maintenance of normal physiological functions. Among micronutrients, selenium (Se) and Vit C are both known as potent antioxidants.   1  Antioxidant defense is a complex system comprising enzymatic and non-enzymatic components. The non-enzymatic elements in fish depend on behavior, diet and feeding. Previous studies demonstrated that oxidative stress, antioxidant defenses and hematological parameters in aquatic species were influenced by dietary components.2,3 It has been reported that stress increases the requirement for minerals and vitamins in fish due to enhanced mobilization and excretion of these nutrients.     4  Hence, mineral supplementation is considered a strategy to alleviate stress-related damages.   5  Selenium, as an essential trace element, plays a protective role against oxidative stress by forming selenoproteins such as glutathione peroxidase (GPX).   6  Nano (N)-Se, compared to other forms, offers higher bioavailability and reduced toxicity.   7  Studies have confirmed its positive effects on growth and oxidative stress resistance.8,9 Similarly, Vit C is vital for growth and physiological health, as most bony fish cannot synthesize ascorbic acid and require dietary supplementation.10-12 Vitamin C improves erythropoiesis and tissue oxygenation leading to better stress tolerance and immune responses. Given the potential synergistic effects of these two nutrients, their combined dietary application may benefit aquatic species.   13  However, limited information exists on their modulatory roles in aquaculture.   14  This study investigated the effects of Vit C and N-Se on antioxidant, biochemical, hematological indices and handling stress in rainbow trout.

Materials and Methods

Treatments and experimental diets. Healthy rainbow trout were procured from a commercial farm and acclimated for 2 weeks while fed with a basal diet (Kimiyagaran, Tehran, Iran) consisted of extrude trout grower (EXG1) with the size of 4.00 ± 0.30 mm, proximate composition of basal diet (as percent of dry weight): Protein = 39.81, Fat = 18.39, Fiber = 4.00, Ash = 10.77, moisture = 6.02, phosphorus = 5.00. The fish (55.20 ± 7.90 g) were randomly assigned to six dietary treatments in 300-L tanks (25 fish per tank). Experimental treatments include: Control diet , Diet with 100 mg kg-1 vitamin C (Vit C100), Diet with 0.40 mg kg-1 N-Se(N-Se0.40), Diet with 100 mg kg-1 Vit C + 0.10 mg kg-1 N-Se (Vit C100 + N-Se0.10), Diet with 200 mg kg-1 Vit C + 0.20 mg kg-1 N-Se (Vit C200 + N-Se0.20), Diet with 400 mg kg-1 Vit C + 0.40 mg kg-1 N-Se (Vit C400 + N-Se0.40). The basal diet contained 0.16 mg kg-1 Se and 220 mg kg-1 Vit C. Diets were prepared weekly by spraying N-Se and Vit C on commercial feed followed by gelatin coating. Feeds were stored at 4.00˚C until use. Nano-selenium (10.00 - 45.00 nm; USNano, Houston, USA) and ascorbic acid (Sigma-Aldrich, St. Louis, USA) were used.

Experimental design. The 60-day trial involved feeding fish four times daily at 2.30% body weight. Water temperature (15.50 ± 0.50˚C), pH (8.00 ± 0.50) and dissolved oxygen (7.00 ± 0.50 mg L-1) were monitored weekly. Tanks were cleaned daily and maintained under a 12 : 12 light : dark cycle. Sampling procedure. Feeding was stopped 24 hr before sampling. Three fish per tank were anesthetized using 250 mg L-1 clove oil.   15  Blood samples were collected—half for hematology, and the remainder centrifuged and stored at – 80.00˚C for biochemical assays.   16 

Hematological analysis. Red- and white blood cells (RBCs and WBCs) were counted based on the method of Lewis et al.   17  Hematocrit (HCT) was measured via microhematocrit.   18  Hemoglobin (Hb) was determined spectrophotometrically.   19 

Biochemical parameters. Total protein was measured calorimetrically.   20  Albumin, cholesterol and triglycerides were determined using Pars Azmoon kits (Tehran, Iran).21,22 

Antioxidant enzyme activities. Superoxide dismutase (SOD) enzyme activity was measured using chemical kits from ZellBo GmbH (Lonsee, Germany), according to the method recommended by Bolann and Ulvik,   23  and using a spectrophotometer at a wavelength of 420 nm. Catalase (CAT) enzyme activity was determined by hydrogen per-oxide decomposition at a wavelength of 240 nm according to the method of Góth.   24  Glutathione peroxidase enzyme activity was determined at a wavelength of 340 nm according to the method of Paglia and Valentine.   25  Serum malondialdehyde (MDA) was measured colorimetrically based on its reaction with thiobarbituric acid at a wavelength of 535 nm according to the method reported by Dawn-Linsley et al.   26 

Handling stress. Test Stress was induced by air exposure for 90 sec according to the guidelines provided by Eslamloo and Falahatkar.   27  Blood was sampled 3 hr post-stress for cortisol, glucose, sodium, and chloride assays. Cortisol: enzyme-linked immunosorbent assay.   28  Glucose: enzymatic method, 546 nm.   21  Electrolytes: electrolyte analyzer.   29 

Statistical analysis. Data normality was tested (Kolmogorov-Smirnov and Levene's Test). One-way ANOVA and Tukey’s HSD test were used in SPSS Software (version 20.0; IBM Corp., Armonk, USA). Results are presented as Mean ± SE with significance at p < 0.05. GraphPad software was used for charting.

Results

Hematological parameters. The results of hematological profiles including red and WBC counts and erythrocyte indices in rainbow trout fed with diets supplemented with Vit C and N-Se are shown in Tables 1 and 2. A significant difference (p < 0.05) was observed in RBC count and Hb content with the highest values in the Vit C400 + N-Se0.40 group and the lowest in the N-Se0.40 group. No significant differences (p > 0.05) were found among treatments for HCT, mean corpuscular Hb, mean corpuscular Hb concentration and mean corpuscular volume. The highest WBC count was observed in the Vit C100 + N-Se0.10 group which was significantly different from the control. The highest neutrophil percentage was recorded in Vit C100 and the lowest in Vit C200 + N-Se0.20. Lymphocyte percentages were the highest in Vit C100 + N-Se0.10 and Vit C400 + N-Se0.40, while Vit C100 had the lowest. Monocyte and eosinophil percentages showed no significant differences among treatments (p > 0.05).

Table 1.

Total and differential white blood cell counts.

Treatments WBC (×10³ mL -1 ) Neutrophils (%) Lymphocytes (%) Monocytes (%) Eosinophils (%)
Control 17.46 ± 1.19a 15.00 ± 3.00ab 79.67 ± 2.52ab 5.00 ± 1.00a 0.33 ± 0.58a
Vit C100 18. 40 ± 0.90ab 17.00 ± 1.73b 77.00 ± 2.00a 6.00 ± 1.00a 0.00 ± 0.00a
N-Se0.4 18.23 ± 1.30ab 14.33 ± 2.08ab 79.33 ± 1.53ab 6.00 ± 1.00a 0.33 ± 0.58a
Vit C100 + N-Se0.1 22.26 ± 2.51b 10.33 ± 2.08a 84.00 ± 2.65b 5.67 ± 0.58a 0.00 ± 0.00a
Vit C200 + N-Se0.2 21.16 ± 1.23ab 9.67 ± 3.06a 83.00 ± 2.65b 6.67 ± 1.53a 0.67 ± 1.15a
Vit C400 + N-Se 0.4 21.76 ± 1.19ab 10.00 ± 1.00a 84.00 ± 1.00b 6.00 ± 1.00a 0.00 ± 0.00a

Vit: Vitamin, and N-Se: Nano-selenium

ab Different letters in each column indicate significant differences (p < 0.05).

Table 2.

Red blood cell counts and erythrocyte indices.

Treatments RBC (×10⁶ mL -1 ) Hemoglobin (g dL -1 ) Hematocrit (%) MCV (fL) MCH (pg) MCHC (g dL -1 )
Control 1.79 ± 0.03bc 8.88 ± 0.22bc 52.10 ± 1.25a 290.33 ± 1.15a 49.53 ± 0.25a 17.04 ± 0.05a
Vit C100 1.67 ± 0.03ab 8.27 ± 0.16ab 48.40 ± 1.05a 288.33 ± 0.58a 49.37 ± 0.15a 17.09 ± 0.06a
N-Se0.4 1.62 ± 0.02a 7.99 ± 0.17a 46.63 ± 1.15a 287.00 ± 3.21a 49.30 ± 0.50a 17.13 ± 0.10a
Vit C100 + N-Se0.1 1.72 ± 0.55abc 8.53 ± 0.26abc 50.07 ± 1.50a 289.33 ± 0.58a 49.37 ± 0.15a 17.04 ± 0.03a
Vit C200 + N-Se0.2 1.74 ± 0.08abc 8.55 ± 0.39abc 50.33 ± 2.26a 289.33 ± 1.73a 49.13 ± 0.40a 16.99 ± 0.05a
Vit C400 + N-Se0.4 1.84 ± 0.04c 9.03 ± 0.16c 50.30 ± 4.23a 291.33 ± 2.65a 49.00 ± 0.36a 16.93 ± 0.12a

Vit: Vitamin, N-Se: Nano-selenium, RBC: Red blood cell, MCV: Mean corpuscular volume, MCH: Mean corpuscular hemoglobin, and MCHC: Mean corpuscular hemoglobin concentration.

abc Different letters in each column indicate significant differences (p < 0.05).

Biochemical parameters. According to the statistical analysis of serum biochemical indices (Table 3), all values showed significant differences (p < 0.05) except for high-density lipoprotein (HDL). The highest cholesterol levels were found in N-Se0.4 and Vit C400 + N-Se0.40 groups, while the lowest was in Vit C100 + N-Se0.10. Triglyceride levels were the highest in Vit C100 + N-Se0.10 and the lowest in Vit C100. Although HDL differences were not statistically significant, Vit C100 + N-Se0.10 showed the highest value. Low-density lipoprotein (LDL) levels were significantly affected, the highest in Vit C100 and Vit C400 + N-Se0.40 and the lowest in Vit C100 + N-Se0.10. Total protein was significantly higher in control and Vit C100 + N-Se0.10, the lowest in Vit C400 + N-Se0.40. Albumin was the highest in control and Vit C200 + N-Se0.20, and the lowest in N-Se0.40.

Table 3.

Serum biochemical parameters.

Treatments Cholesterol (mg dL -1 ) Triglycerides (mg dL -1 ) HDL (mg dL -1 ) LDL (mg dL -1 ) TP (g dL -1 ) Albumin (g dL -1 )
Control 195.53 ± 1.20ab 177.13 ± 7.66a 53.33 ±1.12a 105.87 ± 2.17b 4.00 ± 0.15ab 1.05 ± 0.01d
Vit C100 200.03 ± 0.97cd 164.40 ± 9.20a 53.87 ± 1.39a 114.10 ± 1.85c 3.59 ± 0.19cd 0.97 ± 0.02b
N-Se0.4 201.57 ± 1.10d 179.73 ± 2.40a 52.93 ± 1.75a 112.87 ± 1.22c 3.39 ± 0.17d 0.89 ± 0.01a
Vit C100 + NSe0.1 193.37 ± 1.60a 193.37 ± 7.39b 54.47 ± 0.78a 99.43 ± 1.81a 3.65 ± 0.27a 0.99 ± 0.01bc
Vit C200 + NSe0.2 197.73 ± 1.40bc 182.30 ± 11.01a 51.33 ± 0.96a 109.07 ± 3.36bc 3.62 ± 0.13bc 1.01 ± 0.01c
Vit C400 + NSe0.4 201.33 ± 0.96d 166.10 ± 12.21a 54.23 ± 0.72a 113.97 ± 1.47c 3.36 ± 0.04d 0.98 ± 0.10bc

Vit: Vitamin, N-Se: Nano-selenium, HDL: High-density lipoprotein, LDL: Low-density lipoprotein, and TP: Total protein.

a-d Different letters in each column indicate significant differences (p < 0.05).

Antioxidant enzyme activities. Table 4 presents antioxidant enzyme activities and MDA levels. Catalase activity was significantly influenced, with the highest in Vit C100 + N-Se0.10 and the lowest in N-Se0.4 (p < 0.05). Glutathione peroxidase activity was peaked in the control and Vit C200 + N-Se0.20 groups, while was the lowest in N-Se0.40. The SOD activity was the highest in Vit C200 + N-Se0.20 and the lowest in Vit C400 + N-Se0.40. MDA levels were the highest in Vit C100 + N-Se0.10 and the lowest in Vit C400 + N-Se0.40.

Table 4.

Antioxidant enzyme activity.

Treatments SOD (U mL -1 ) CAT (U mL -1 ) GPX (U mL -1 ) MDA (nmol mL -1 )
Control 72.17 ± 2.97ab 48.73 ± 1.08d 203.00 ± 7.79b 125.00 ± 3.46b
Vit C100 69.53 ± 1.42a 42.27 ± 0.87ab 198.67 ± 3.51ab 111.00 ± 2.94a
N-Se0.4 73.37 ± 0.75ab 38.67 ± 2.75a 186.33 ± 3.06a 125.33 ± 3.06b
Vit C100 + NSe0.1 76.77 ± 1.34bc 48.50 ± 1.80cd 191.67 ± 5.03ab 128.00 ± 1.00b
Vit C200 + NSe0.2 79.33 ± 1.85c 42.60 ± 1.01ab 200.33 ± 2.08b 124.33 ± 2.08b
Vit C400 + NSe0.4 69.20 ± 1.32a 44.43 ± 0.75bc 189.67 ± 1.32ab 107.33 ± 2.52a

Vit: Vitamin, N-Se: Nano-selenium, MDA: Malondialdehyde, GPX: Glutathione peroxidase, CAT: Catalase, and SOD: Superoxide dismutase.

a-d Different letters in each column indicate significant differences (p < 0.05).

Handling stress test. Table 5 summarizes the effects of N-Se and Vit C on resistance to handling stress. Before stress, the highest serum cortisol level was observed in Vit C100 + N-Se0.10, and the lowest in control. After stress, N-Se0.40 group had the highest cortisol level, and Vit C200 + N-Se0.20 the lowest (p < 0.05). Glucose levels before stress followed a similar pattern. Post-stress glucose was the highest in N-Se0.4 and the lowest in Vit C100. No significant differences were found in sodium levels before stress, but after stress, control had the highest and Vit C200 + N-Se0.20 had the lowest. Chloride levels were the highest in control and the lowest in Vit C200 + N-Se0.20 before stress. Post-stress, they were the highest in N-Se0.40 and the lowest in Vit C100 + N-Se0.10.

Table 5.

Comparing stress indices before and after manipulation (stress).

Treatments Cortisol (ng mL -1 ) Glucose (mg dL -1 ) Sodium (mmol L -1 ) Chloride (mmol L -1 )
Before After Before After Before After Before After
Control 50.97 ± 5.50a 114.24 ± 11.32ab 75.97 ± 2.80a 109.13 ± 3.01ab 145.17 ± 2.32a 149.25 ± 0.07b 134.93± 6.18 b 110.37± 6.61bc
Vit C100 55.27 ± 3.90a 119.43 ± 9.34ab 79.73 ± 2.71ab 102.27 ± 3.07a 146.43 ± 1.07a 147.40 ± 1.27ab 130.43 ± 15.40ab 101.73 ± 2.10ab
N-Se0.4 51.27 ± 5.86a 145.37 ± 7.80c 80.50 ± 5.86ab 165.00 ± 18.62d 144.93 ± 1.50a 146.20 ± 1.179a 112.70 ± 7.41ab 119.97 ± 2. 86c
Vit C100 + NSe0.1 68.13 ± 4.75b 135.17 ± 9.75b 97.13 ± 3.61c 124.23 ± 6.30abc 146.87 ± 1.07a 148.37 ± 0.61ab 119.47 ± 5.16ab 97.27 ± 1. 89a
Vit C200 + NSe0.2 58.23 ± 4.61ab 108.67 ± 8.84a 88.93 ± 7.03bc 130.43 ± 12.45bc 143.20 ± 1.35a 145.87 ± 0.45a 109.10 ± 5.26a 103.1 ± 2. 42ab
Vit C400 + NSe0.4 59.97 ± 2.01ab 112.93 ± 2.32ab 90.73 ± 1.94bc 147.63 ± 6.52cd 145.97 ± 0.68a 147.60 ± 1.10ab 111.47 ± 3.25a 100.77 ± 1. 99ab

Vit: Vitamin, N-Se: Nano-selenium

a-d Different letters in each column indicate significant differences (p < 0.05).

Discussion

It is well known that hematological indices such as Hb and HCT values, red and WBC counts in fish are associated with their health and immune response.   30  Similar to other animals, elevated hematological indices in fish are vital for immune function and disease resistance.   2  In this study, the RBC count and Hb levels were increased in the Vit C400 + N-Se0.4 group. However, HCT, mean corpuscular Hb, mean corpuscular Hb concentration and mean corpuscular volume were not significantly different among treatments (p > 0.05). Vitamin C might protect phagocytic cells and surrounding tissues from oxidative damage.   31 

Others suggested that Vit C extends RBC life span and supports cellular respiration.   32  In the present study, the combination of N-Se and Vit C enhanced erythropoiesis and Hb concentration. Similar improvements have been reported in sea bass fed N-Se.   33  Nano-selenium antioxidant role helps maintain RBC membrane integrity, reducing hemolysis and increasing oxygen availability.8,34

In the present study, HCT, mean corpuscular Hb, mean corpuscular Hb concentration and mean corpuscular volume were not affected by Vit C and N-Se. Dietary N-Se increased the values of hematological indices, which increased oxygen availability in tissue cells, and subsequently regulated the rate of nutrient metabolism.   6  Increased Se increased the protection of RBC membranes against the harmful effects of oxygen free radicals and reduced hemolysis and degeneration.   35  Similarly, others noted that dietary N-Se improved RBC Hb, packed cell volume parameters in common carp.   9  Yellow tail fish fed with 2.00 mg of Se showed increased RBCs and HCT activity.   36  In a study conducted on tilapia by others, it was reported that Hb was increased in tilapia fed with N-Se and Se powder, while fish fed with 0.80 mg kg-1 diet of N-Se recorded the highest RBC, HCT, WBC.   35  Such differences may be explained by differences in the type and content of supplements, experimental period, feed composition or the combined synergistic effects of supplements with their different individual effects.   37 

Serum biochemical indices are critical indicators of physiological responses.38,39 Serum protein functions in cell metabolism, enzyme activity and hormone secretion.   35  In our study, total serum protein was the highest in control and Vit C100 + N-Se0.1 and the lowest in Vit C400 + N-Se0.4. Higher protein content reflects enhanced physiological health due to antioxidant supplementation. HDL levels were the highest in Vit C100 + N-Se0.1, while LDL and MDA were the lowest in this group indicating reduced oxidative damage. Improved lipid profiles in carp fed with N-Se was also observed. The HDL apo-lipoprotein AI plays a key antioxidant role, reducing lipid peroxidation.   8 

In our study, HDL concentration was the highest in Vit C100 + N-Se0.1 treatment and the lowest in Vit C200 + N-Se0.2 treatment. Also, LDL concentration was the highest in Vit C100 treatment and the lowest in Vit C100 + N-Se0.1 treatment. In agreement with the results of this study, others showed that Se could significantly reduce serum total cholesterol in Wistar rats.   40  It has also been reported that organic Se can significantly reduce LDL and increase HDL.   41  Consistently, in a study conducted by others, supplementation with 2.00 mg kg−1 diet of N-Se was observed to reduce serum total cholesterol and LDL concentration and to significantly increase HDL levels.   8  Consistently, others reported an increase in total protein globulin and albumin content in catfish fed with 5.00 mg kg-1 diet of organic Se.   42  In the present study, the increase in serum HDL was accompanied by a decrease in LDL and MDA. These results might indicate that rainbow trout were protected when fed with a diet containing N-Se and Vit C.

Selenium has a large number of biological functions in animals including fish. The most important and well-known function is its antioxidant effect. As a form of selenoprotein, it is part of the active site in glutathione peroxidase(GSH-PX).   43  During the normal metabolism of organisms, the production and removal of reactive oxygen species maintain a dynamic balance. Antioxidant enzymes such as CAT, SOD, GPX can eliminate excessive ROS and reduce the damage caused by lipid oxidation.   32  The activities of CAT, GPX and SOD as important antioxidant enzymes can be considered as oxidative biomarkers, in addition to indicating the antioxidant capacity of aquatic organisms.   14  However, MDA is a toxic substance produced by the breakdown of lipid peroxides that can cause damage to the body and reflects the extent of cellular damage and lipid peroxidation in animal cells.   44  Antioxidants can protect organisms against free radicals and ROS and reduce the progression of many chronic diseases as well as lipid peroxidation. The antioxidant defense system is a multi-component mechanism with enzymatic and non-enzymatic elements. The non-enzymatic antioxidant elements in fish depend on factors such as feeding behavior and feed. While dietary micronutrients are widely used in animal feed and contribute to the antioxidant defense system, negative perceptions and consumer caution limit their use.   43  In the present study, N-Se and Vit C supplementation successfully showed the highest SOD activity in Vit C200 + N-Se0.2 and Vit C100 + N-Se0.1 treatments, the highest GPX activity in C and Vit C200 + N-Se0.2 treatments and the highest CAT activity in C and Vit C100 + N-Se0.1 treatments. Also, the MDA level at the end of feeding showed the highest activity in Vit C100 + N-Se0.1 treatment and the lowest serum MDA activity in Vit C400 + N-Se0.4 treatment, indicating the role of Se and Vit C in protecting rainbow trout against lipid oxidation. In a study conducted by others, an increase in the antioxidant enzyme activities of CAT, SOD and GPX and a decrease in MDA levels were reported in European bass fed with N-Se.   33  Others also reported that MDA levels were reduced in rainbow trout fish fed with N-Se.8 In a study conducted by others, GPX, GSH-PX and SOD activities were increased in fish fed with Se supplementation while MDA concentration was decreased.   43  Consistently, in a study conducted by others, improved antioxidant enzyme activities and lower MDA were observed in fish fed with 0.4 and 0.8 mg N-Se compared to Se powder and control groups.   35  Further-more, others reported that common carp fed with N-Se had the highest hepatic CAT, SOD and GPX activities and liver MDA content was significantly lower in fish fed diets containing N-Se and selenocysteine compared to the control group.   9  Others reported the highest muscle CAT, SOD and GPX activities and the lowest MDA content in the combined 1.00 mg N-Se and 500 mg kg-1 Vit E group compared to the control treatment.   45  In another study conducted by others, N-Se and Vit C supplementation successfully increased the activities of CAT, SOD, GPX and reduced MDA at the end of feeding.   14  In the present study the increase in antioxidant parameters in fish following the consumption of N-Se and Vit C might be due to the role of Se in the formation of selenocysteine, which is located in the active center of the enzyme (GPX). Vitamin C is also among the vitamins that can protect cells against oxidative stress. Based on the above results, it seems that Vit C and N-Se are excellent stimulants in rainbow trout farming.8,9,46,47 

High-density aquaculture practices increase fish exposure to physical stressors like sorting, transportation and vaccination leading to immunosuppression and physiological disruption. Cortisol and glucose are critical indicators of stress in fish.   48  In this study, pre-stress cortisol was the highest in Vit C100 + N-Se0.1 and the lowest in control. Post-stress, cortisol and glucose were significantly elevated in the N-Se0.4 group while the lowest levels were in Vit C200 + N-Se0.2 and Vit C100, respectively. These results suggested that antioxidant supplementation with N-Se and Vit C mitigated stress response by stabilizing cortisol and glucose levels and preserving osmotic balance.

Dietary supplementation is a key strategy in improving aquafeed quality. This study demonstrated that N-Se and Vit C significantly enhanced physiological parameters in rainbow trout, including hematological, antioxidant, biochemical and stress resistance indices. However, at higher doses (Vit C200 + N-Se0.2 and Vit C400 + N-Se0.4), these benefits declined. Therefore, optimal combinations such as Vit C100 + N-Se0.1 might be effective additives for improving health and productivity in rainbow trout farming.

Acknowledgments

The current work has been funded by Urmia University, Urmia, Iran. The authors would like to thank Sorayya Mahmoudi and Asgar Aliyari for their technical assistance.

Conflict of interest

The authors declare no competing interests.

References

  • 1.Khan KU, Zuberi A, Nazir S, et al. Synergistic effects of dietary nano selenium and vitamin C on growth, feeding, and physiological parameters of mahseer fish (Tor putitora) Aquac Rep. 2017;5:70–75. [Google Scholar]
  • 2.Aramli MS, Sarvi Moghanlou K, Imani A. Effect of dietary antioxidant supplements (selenium forms, alpha-tocopherol, and coenzyme Q10) on growth performance, immunity, and physiological responses in rainbow trout (Oncorhynchus mykiss) using orthogonal array design. Fish Shellfish Immunol. 2023;134:108615. doi: 10.1016/j.fsi.2023.108615. [DOI] [PubMed] [Google Scholar]
  • 3.Asadi T, Meshkini S, Ahmadifard N. Dietary effects of procyanidin and Bio-Aqua® on hematological and immune indices of rainbow trout (Oncorhynchus mykiss) Vet Res Forum. 2023;14(7):359–365. doi: 10.30466/vrf.2023.1972329.3678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Harsij M, Gholipour Kanani H, Adineh H. Effects of antioxidant supplementation (nano‑selenium, vitamin C and E) on growth performance, blood biochemistry, immune status and body composition of rainbow trout (Oncorhynchus mykiss) under sub-lethal ammonia exposure. Aquaculture. 2020;521:734942. [Google Scholar]
  • 5.Naderi M, Keyvanshokooh S, Salati AP, et al. Effects of dietary vitamin E and selenium nanoparticles supplementation on acute stress responses in rainbow trout (Oncorhynchus mykiss) previously subjected to chronic stress. Aquaculture. 2017;473:215–222. [Google Scholar]
  • 6.Dawood MAO, Koshio S, Zaineldin AI, et al. Dietary supplementation of selenium nanoparticles modulated systemic and mucosal immune status and stress resistance of red sea bream (Pagrus major) Fish Physiol Biochem. 2019;45(1):219–230. doi: 10.1007/s10695-018-0556-3. [DOI] [PubMed] [Google Scholar]
  • 7.Wang H, Zhang J, Yu H. Elemental selenium at nano size possesses lower toxicity without compromising the fundamental effect on selenoenzymes: comparison with selenomethionine in mice. Free Radic Biol Med. 2007;42(10):1524–1533. doi: 10.1016/j.freeradbiomed.2007.02.013. [DOI] [PubMed] [Google Scholar]
  • 8.Ashouri S, Keyvanshokooh S, Salati AP, et al. Effects of different levels of dietary selenium nanoparticles on growth performance, muscle composition, blood biochemical profiles and antioxidant status of common carp (Cyprinus carpio) Aquaculture. 2015;446:25–29. [Google Scholar]
  • 9.Saffari S, Keyvanshokooh S, Zakeri M, et al. Effects of different dietary selenium sources (sodium selenite, selenomethionine and nanoselenium) on growth performance, muscle composition, blood enzymes and antioxidant status of common carp (Cyprinus carpio) Aquac Nutr. 2016;23(3):611–617. [Google Scholar]
  • 10.Al-Amoudi MM, El-Nakkadi AMN, El-Nouman BM. Evaluation of optimum dietary requirement of vitamin C for the growth of Oreochromis spilurus fingerlings in water from the Red Sea. Aquaculture. 1992;105(2):165–173. [Google Scholar]
  • 11.Dabrowski K. Past, present, and future of ascorbic acid research in aquatic organisms. Ascorbic acid in aquatic organisms. 1st ed. Boca Raton, USA: CRC Press. 2000:270–293. [Google Scholar]
  • 12.Lin YH, Shiau SY. Dietary selenium requirements of juvenile grouper, Epinephelus malabaricus. Aquaculture. 2005;250(1-2):356–363. [Google Scholar]
  • 13.Khan KU, Zuberi A, Ullah I, et al. Effects of graded level of dietary l-ascorbyl-2-polyphosphate on growth performance and some hematological indices of juvenile Mahseer (Tor putitora) Int J Agric Biol. 2015;17(4):821–827. [Google Scholar]
  • 14.Dawood MAO, Zommara M, Eweedah NM, et al. The potential role of nano-selenium and vitamin C on the performances of Nile tilapia (Oreochromis niloticus) Environ Sci Pollut Res Int. 2020;27(9):9843–9852. doi: 10.1007/s11356-020-07651-5. [DOI] [PubMed] [Google Scholar]
  • 15.Yarahmadi P, Kolangi Miandare HK, Fayaz S, et al. Increased stocking density causes changes in expression of selected stress- and immune-related genes, humoral innate immune parameters and stress responses of rainbow trout (Oncorhynchus mykiss) Fish Shellfish Immunol . 2016;48:43–53. doi: 10.1016/j.fsi.2015.11.007. [DOI] [PubMed] [Google Scholar]
  • 16.Siwicki AK, Anderson DP, Rumsey GL. Dietary intake of immunostimulants by rainbow trout affects non-specific immunity and protection against furunculosis. Vet Immunol Immunopathol. 1994;41(1-2):125–139. doi: 10.1016/0165-2427(94)90062-0. [DOI] [PubMed] [Google Scholar]
  • 17.Lewis S, Bain B, Bates I. Dacie and Lewis Practical Hematology. 10th ed. Philadelphia, USA: Churchill Livingstone ; 2006. p. 722. [Google Scholar]
  • 18.Řehulka J. Influence of astaxanthin on growth rate, condition, and some blood indices of rainbow trout, Oncorhynchus mykiss. Aquaculture. 2000;190(1-2):27–47. [Google Scholar]
  • 19.Blaxhall P, Daisley KW. Routine haematological methods for use with fish blood. J Fish Biol. 1973;5(6):771–781. [Google Scholar]
  • 20.Koller A. Kaplan LA. In: Total serum protein, Kaplan LA., editors. Clinical Chemistry: theory, analysis, and correlation. St. Louis, USA: Mosby ; 1984. pp. 1316– 1324. [Google Scholar]
  • 21.Thomas L. Clinical laboratory diagnostics: use and assessment of clinical laboratory results. Frankfurt, Germany: TH-books Verlagsgesellschaft ; 1998. p. 1527. [Google Scholar]
  • 22.Rifai N, Bachorik PS, Albers JJ. Tietz textbook of clinical chemistry. 3rd ed. Florida, USA: WB Saunders; 1999. Lipids, lipoproteins and apolipoproteins; pp. 809–861. [Google Scholar]
  • 23.Bolann B, Ulvik RJ. Improvement of a direct spectrophotometric assay for routine determination of superoxide dismutase activity. Clin Chem. 1991;37(11):1993–1999. [PubMed] [Google Scholar]
  • 24.Góth L. A simple method for determination of serum catalase activity and revision of reference range. Clin Chim Acta. 1991;196(2-3):143–151. doi: 10.1016/0009-8981(91)90067-m. [DOI] [PubMed] [Google Scholar]
  • 25.Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Clin Lab Med. 1967;70(1):158–169. [PubMed] [Google Scholar]
  • 26.Dawn-Linsley M, Ekinci FJ, Ortiz D, et al. Monitoring thiobarbituric acid-reactive substances (TBARs) as an assay for oxidative damage in neuronal cultures and central nervous system. J Neurosci Methods. 2005;141(2):219–222. doi: 10.1016/j.jneumeth.2004.06.010. [DOI] [PubMed] [Google Scholar]
  • 27.Eslamloo K, Falahatkar B. Variations of some physiological and immunological parameters in Siberian sturgeon (Acipenser baerii, Brandt, 1869) subjected to an acute stressor. J Appl Anim Welf Sci. 2014;17(1):29–42. doi: 10.1080/10888705.2014.856243. [DOI] [PubMed] [Google Scholar]
  • 28.Burtis CA, Ashwood ER, Tietz NW. Tietz textbook of clinical chemistry. 3rd ed. Philadelphia, USA: WB Saunders; 1999. pp. 29–150. [Google Scholar]
  • 29.Tietz NW. Clinical guide to laboratory tests. 3rd ed. Philadelphia, USA: WB Saunders; 1995. Clinical guide to laboratory tests (ELISA) pp. 1096–1096. [Google Scholar]
  • 30.Zhou QC, Mai KS, Tan BP, et al. Partial replacement of fishmeal by soybean meal in diets for juvenile cobia (Rachycentron canadum) Aquac Nutr. 2005;11(3):175–182. [Google Scholar]
  • 31.National Research Council. Achieving nutrient and sediment reduction goals in the Chesapeake Bay: an evaluation of program strategies and implementation. Washington DC, USA: National Academies Press; 2011. [Google Scholar]
  • 32.Liang XP, Li Y, Hou YM, et al. Effect of dietary vitamin C on the growth performance, antioxidant ability and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco Richardson) Aquac Res. 2015;48(1):149–160. [Google Scholar]
  • 33.Abd El-Kader MF, Fath El-Bab AF, Abd-Elghany MF, et al. Selenium nanoparticles act potentially on the growth performance, hemato-biochemical indices, antioxidative, and immune-related genes of European seabass (Dicentrarchus labrax) Biol Trace Elem Res. 2021;199(8):3126–3134. doi: 10.1007/s12011-020-02431-1. [DOI] [PubMed] [Google Scholar]
  • 34.Khan KU, Zuberi A, Nazir S, et al. Effects of dietary selenium nanoparticles on physiological and biochemical aspects of juvenile Tor putitora. Turk Zool Derg. 2016;40(5):704–712. [Google Scholar]
  • 35.Ibrahim MS, El-Gendy GM, Ahmed AI, et al. Nanoselenium versus bulk selenium as a dietary supplement: effects on growth, feed efficiency, intestinal histology, haemato-biochemical and oxidative stress biomarkers in Nile tilapia (Oreochromis niloticus Linnaeus, 1758) fingerlings. Aquac Res. 2021;52(11):5642–5655. [Google Scholar]
  • 36.Le KT, Fotedar R. Immune responses to Vibrio anguillarum in yellowtail kingfish, Seriola lalandi, fed selenium supplementation. J World Aquac Soc. 2014;45(2):138–148. [Google Scholar]
  • 37.Dawood MAO, Zommara M, Eweedah NM, et al. Synergistic effects of selenium nanoparticles and vitamin E on growth, immune-related gene expression, and regulation of antioxidant status of Nile tilapia (Oreochromis niloticus) Biol Trace Elem Res. 2020;195(2):624–635. doi: 10.1007/s12011-019-01857-6. [DOI] [PubMed] [Google Scholar]
  • 38.Hassaan MS, Mohammady EY, Soaudy MR, et al. Exo-genous xylanase improves growth, protein digestibility and digestive enzymes activities in Nile tilapia, Oreochromis niloticus, fed different ratios of fish meal to sunflower meal. Aquac Nutr. 2019;25(2):841–853. [Google Scholar]
  • 39.Hassaan MS, Mohammady EY, Adnan AM, et al. Effect of dietary protease at different levels of malic acid on growth, digestive enzymes and haemato-immuno-logical responses of Nile tilapia, fed fish meal free diets. Aquaculture. 2020;522:735124. [Google Scholar]
  • 40.Bunglavan S, Garg AK, Dass RS, et al. Effect of supplementation of different levels of selenium as nanoparticles/sodium selenite on blood biochemical profile and humoral immunity in male Wistar rats. Vet World. 2014;7(12):1075–1081. [Google Scholar]
  • 41.Hao X, Ling Q, Hong F. Effects of dietary selenium on the pathological changes and oxidative stress in loach (Paramisgurnus dabryanus) Fish Physiol Biochem. 2014;40(5):1313–1323. doi: 10.1007/s10695-014-9926-7. [DOI] [PubMed] [Google Scholar]
  • 42.Abdel-Tawwab M, Mousa MAA, Abbass FE. Growth performance and physiological response of African catfish, Clarias gariepinus (B ) fed organic selenium prior to the exposure to environmental copper toxicity. Aquaculture. 2007;272(1-4):335–345. [Google Scholar]
  • 43.Hunt AO, Berkoz M, Ozkan F, et al. Effects of organic selenium on growth, muscle composition, and antioxidant system in rainbow trout. Isr J Aquac. 2011;562(1):1–10. [Google Scholar]
  • 44.Yao J, Wang JY, Liu L, et al. Anti-oxidant effects of resveratrol on mice with DSS-induced ulcerative colitis. Arch Med Res. 2010;41(4):288–294. doi: 10.1016/j.arcmed.2010.05.002. [DOI] [PubMed] [Google Scholar]
  • 45.Naderi M, Keyvanshokooh S, Ghaedi A, et al. Interactive effects of dietary nano selenium and vitamin E on growth, hematology, innate immune responses, antioxidant status, and muscle composition of rainbow trout under high rearing density. Aquac Nutr. 2019;25(5):1156–1168. [Google Scholar]
  • 46.Affonso EG, Silva Eda C, Tavares-Dias M, et al. Effect of high levels of dietary vitamin C on the blood responses of matrinxã (Brycon amazonicus) Comp Biochem Physiol A Mol Integr Physiol. 2007;147(2):383–388. doi: 10.1016/j.cbpa.2007.01.004. [DOI] [PubMed] [Google Scholar]
  • 47.Abdel-Daim MM, Abushouk AI, Donia T, et al. The nephroprotective effects of allicin and ascorbic acid against cisplatin-induced toxicity in rats. Environ Sci Pollut Res Int. 2019;26(13):13502–13509. doi: 10.1007/s11356-019-04780-4. [DOI] [PubMed] [Google Scholar]
  • 48.Merrifield D, Bradley G, Baker RTM, et al. Probiotic applications for rainbow trout (Oncorhynchus mykiss Walbaum) II effects on growth performance feed utilization intestinal microbiota and related health criteria postantibiotic treatment. Aquac Nutr. 2010;16(5):496–503. [Google Scholar]

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