Effects of High Levels of Dietary Linseed Oil on the Growth Performance, Antioxidant Capacity, Hepatic Lipid Metabolism, and Expression of Inflammatory Genes in Large Yellow Croaker (Larimichthys crocea)

A growth experiment was conducted to evaluate the effects of dietary fish oil (FO) replaced by linseed oil (LO) on the growth performance, antioxidant capacity, hepatic lipid metabolism, and expression of inflammatory genes in large yellow croaker (Larimichthys crocea). Fish (initial weight: 15.88 ± 0.14 g) were fed four experimental diets with 0% (the control), 33.3%, 66.7%, and 100% of FO replaced by LO. Each diet was randomly attributed to triplicate seawater floating cages (1.0 × 1.0 × 2.0 m) with 60 fish in each cage. Results showed that the growth performance of fish fed the diet with 100% LO was markedly decreased compared with the control group (P < 0.05), while no remarkable difference was observed in the growth performance of fish fed diets within 66.7% LO (P > 0.05). The percentage of 18:3n-3 was the highest in the liver and muscle of fish fed the diet with 100% LO among the four treatments. When dietary FO was entirely replaced by LO, fish had a markedly higher total cholesterol, total triglyceride, low-density lipoprotein cholesterol content, and alanine transaminase activity in the serum than the control group (P < 0.05). The concentration of malondialdehyde was markedly higher, while the activity of catalase was markedly lower in fish fed the diet with 100% LO than the control group (P < 0.05). When dietary FO was entirely replaced by LO, hepatic lipid content, transcriptional levels of fatp1 and cd36, and CD36 protein expression were significantly higher, while transcriptional level of cpt-1 and CPT-1 protein expression were significantly lower than the control group (P < 0.05). As for the gene expression of cytokines, fish fed the diet with 100% LO had markedly higher transcriptional levels of il-1β, tnfα, and il-6 than the control group (P < 0.05). In conclusion, the substitution of 66.7% FO with LO had no significant effects on the growth performance of fish, while 100% LO decreased the growth performance and increased the inflammation and hepatic lipid content of fish. The increase of hepatic lipid content was probably due to the increased fatty acid uptake and decreased fatty acid oxidation in fish.

Introduction

Linseed oil (LO) is rich in α-linoleic acid (18:3n-3), which is a vital fatty acid (FA) for fish to maintain good growth performance and health status (Menoyo et al., 2007; Wu and Chen, 2012). Furthermore, due to its relatively economical price and high production, LO is considered as a promising lipid source to replace fish oil (FO) in aquafeed (Turchini et al., 2009). Previous investigations have elucidated that LO can be effectively utilized by certain freshwater fishes; dietary FO could be partially replaced by LO in silver barb (Puntius gonionotus) (Nayak et al., 2017) or even entirely replaced by LO in murray cod (Maccullochella peelii peelii) (Turchini et al., 2011), rainbow trout (Oncorhynchus mykiss) (Filiz et al., 2017), and tilapia (Oreochromis niloticus) (Peng et al., 2016) without severely compromising the growth performance and health status. Nevertheless, when dietary FO was excessively replaced by LO, fish growth and health were reduced, and hepatic lipid deposition was increased in certain marine fishes, such as the yellow drum (Nibea albiflora) (Qin et al., 2020), turbot (Scophthalmus maximus) (Wang et al., 2016), and gilthead seabream (Sparus aurata) (Menoyo et al., 2004; Montero et al., 2008).

Lipid metabolism consists of lipid uptake, FA oxidation, lipid synthesis, and triglyceride-rich lipoprotein secretion (Musso et al., 2009). After the digestion and hydrolysis of dietary lipid, the circulating lipoproteins and non-esterified FAs are absorbed into hepatocytes through lipoprotein receptors, fatty acid transport protein 1 (fatp1) and cluster of differentiation 36 (cd36) (Stahl, 2004; Musso et al., 2009). After absorption, cytoplasmic FAs can be oxidized by carnitine palmitoyltransferase 1 (cpt-1) in mitochondria, and acyl CoA oxidase (aco) in peroxisomes, respectively (Ruyter et al., 1997; Mcgarry and Brown, 2010; Li et al., 2018). Furthermore, the acetyl CoA, produced by FA oxidation or other metabolic reactions, is an intermediate of the de novo lipogenesis. Fatty acid synthase (fas) and sterol-regulatory element-binding protein 1 (srebp1) represent a key lipogenic enzyme and a key transcription factor in lipid synthesis, respectively (Eberlé et al., 2004; Menendez and Lupu, 2007). However, when lipids are excessively synthesized in the cytoplasm, lipids can be excreted from the hepatocytes in the form of triglyceride-rich lipoproteins that are mediated by microsomal triacylglycerol transfer protein (mtp) and apolipoprotein B100 (apoB100) (Olofsson and BorÈN, 2005; Hussain et al., 2012). Thus, lipid metabolism is a useful approach to evaluate the utilization of vegetable oils in fish (Yan et al., 2015).

An imbalance in lipid accumulation (lipoprotein and FA uptake as well as lipid synthesis) and lipid consumption (FA oxidation and very-low-density lipoprotein secretion) can induce abnormal lipid deposition, which is always accompanied by inflammation in fish (Tan et al., 2017). Interleukin-1β (il-1β), interferon γ (ifnγ), cyclooxygenase-2 (cox-2), tumor necrosis factor α (tnfα), and interleukin-6 (il-6) are significant pro-inflammatory and chemotactic cytokines in fish (Pohlenz and Gatlin, 2014; Zou and Secombes, 2016). Meanwhile, interleukin-4 (il-4), interleukin-10 (il-10), and transforming growth factor β (tgfβ) are deemed to be anti-inflammatory cytokines, and arginase-1 (arg-1) is deemed to be an anti-inflammatory enzyme. Those anti-inflammatory factors can be regulated by FAs to limit the over-activation of immune regulatory pathways (Kühn et al., 1993; Berg et al., 1995). Furthermore, the aforementioned lipid metabolism-related proteins and inflammatory factors can partly reflect the physiological state of fish (Montero et al., 2008; Xu et al., 2015). Nevertheless, few studies have systematically evaluated the lipid metabolism and the inflammation of fish that were fed diets with different LO levels.

Large yellow croaker (Larimichthys crocea) is a widely cultivated marine fish in China (Xiao et al., 2015; Chen et al., 2018; Huang et al., 2020). The appropriate use of LO in aquafeed can yield considerable benefits in terms of fish health, growth, and the economy (Wabike et al., 2020). Although a previous study has shown that passive effects were found in large yellow croaker when FO was entirely replaced by LO (Mu et al., 2020), the specific growth performance, lipid metabolism and inflammation in this fish fed diets with different LO levels still needs to be assessed to determine an appropriate substitution level of FO in the diet. Thus, the aim of this study was to evaluate the effects of dietary LO on the growth performance, antioxidant capacity, hepatic lipid metabolism, and inflammation in this fish for the further utilization of LO in aquafeed.

Materials and Methods

Diet Formulation

Four isonitrogenous (approximately 42% protein) and isolipidic (approximately 12% lipid) experimental diets were formulated to contain graded levels (0%, 33.3%, 66.7%, and 100%) of FO replaced by LO, and the FO group was regarded as the control (Table 1). Raw materials were pulverized into a fine powder and thoroughly mixed with water and oils to make diets (2.0 × 5.0 mm). Specific procedures of making diets and storing them were applied according to Ai et al. (2006). Four experimental diets were similar in quality and sinking properties, and FA composition of oils and diets was determined in this study (Table 2).

TABLE 1

Table 1. Formulation and chemical proximate analysis of the experimental diets (% dry weight).

TABLE 2

Table 2. Fatty acid composition of linseed oil and the experimental diets (% total fatty acids)ⁱ.

Proximate Composition and FA Composition Determination

The crude protein, lipid, ash, and moisture of experimental diets and fish were determined according to the Association of Official Analytical Chemists (AOAC, 1995). Fish tissue was lyophilized to determine the moisture content, and the freeze-dried tissue was used to analyze the lipid content according to Folch et al. (1957). The gross energy content of experimental diets was analyzed by combustion in an oxygen bomb calorimeter PARR6400 (Parr Instrument Company, United States). Moreover, the FA composition of muscle and liver samples was analyzed according to Metcalfe et al. (1966) with a few modifications (Zuo et al., 2012). Specific procedures for determining FA composition were conducted according to Li X. S. et al. (2019) and Feng et al. (2017). The extracted FA methyl esters were detected by a gas chromatograph HP6890 (Agilent, Santa Clara, CA, United States).

Experimental Procedures

L. crocea of the same batch were supplied by a local farm in Ningde, Fujian, China. Fish were cultured in floating cages (2 × 4 × 2.5 m) and adapted to the FO diet for 14 days. After the adaptation period, juveniles (initial weight: 15.88 ± 0.14 g) were randomly apportioned to 12 floating cages (1 × 1 × 2 m) with 60 juveniles in each cage. Each experimental diet was randomly allocated to three experimental cages. Juveniles were well fed twice daily (5:30 a.m. and 5:00 p.m.) to apparent visual satiation (when fish were not actively eating) for 10 weeks. This study was approved by the Institutional Animal Care and Use Committee of the Ocean University of China. The protocols for animal care and handling were strictly conducted according to Standard Operation Procedures (approval number: 20001001) of the Institutional Animal Care and Use Committee of the Ocean University of China.

Sample Collection

At the end of the experiment, juveniles fasted for an entire day and were anesthetized with eugenol (Sigma-Aldrich, United States, 1:10,000) before sample collection (Mai et al., 2006). Subsequently, final fish numbers and total fish weight per cage were determined to calculate survival rate and growth performance. Four fish per cage were randomly collected for proximate composition analysis. The weight of the liver and visceral mass and the length of seven fish per cage were recorded to analyze morphological parameters. After then, the liver and muscle samples of the aforementioned seven fish were sampled to determine the proximate composition, FA composition, enzyme activity, and transcriptional level of genes. Blood was collected and placed at 4°C overnight to collect the serum after centrifugation (4°C, 4,000 × g for 10 min), and the serum was kept at −80°C until analysis.

Biochemical Analysis

Total triglyceride (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), activities of serum aspartate aminotransferase (AST), and alanine transaminase (ALT) were determined by an automatic chemistry analyzer (BS200, Mindray, China) using diagnostic reagent kits (Mindray Bio Medical Co., Ltd., China). The concentration of malondialdehyde (MDA), total antioxidant capacity (T-AOC), and activities of catalase (CAT) and superoxide dismutase (SOD) in the liver were detected using commercial reagent kits provided by Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

Real-Time Quantitative Polymerase Chain Reaction (RT-qPCR)

Three fish livers from the same cage were mixed into a tube, and the mixed samples were pulverized into powder in liquid nitrogen. RNA was isolated from 18 fish samples per group using TRIzol reagent (Takara, Japan) according to the manufacturer’s instructions. The DNA contaminant in isolated RNA was removed, and cDNA was synthesized with 1,000 ng of the isolated RNA using the PrimeScript^TM RT reagent Kit (Takara, Japan). The primer sequences were designed based on the nucleotide sequences of L. crocea (Table 3), where β-actin and glyceraldehyde 3-phosphate dehydrogenase (gapdh) were considered as house-keeping genes (Zheng et al., 2016). The volume of reaction system and the RT-qPCR program were performed according to Zuo et al. (2012) and Li X. S. et al. (2019). Transcriptional level of genes was analyzed using the 2^{–Δ Δ Ct} method (Livak and Schmittgen, 2001).

TABLE 3

Table 3. Sequences of the PCR primers used in this study.

Western Blot

Total protein of hepatic samples was extracted by RIPA reagent (Beyotime Biotechnology, China) according to the methods described by Xu et al. (2016). Protein concentration was quantified by a BCA Protein Assay Kit (Solarbio, China). The specific procedures of western blot were conducted according to Li X. S. et al. (2019). The GAPDH was used as the reference (Cui et al., 2020). Antibody against MTP (ab186446) was purchased from Abcam (England). Antibody against CPT-1 (#15184-1-AP) was purchased from Proteintech (United States). Antibody against CD36 was made by Genscript (China) via immunizing two adult New Zealand rabbits with antigen polypeptide (sequence: KGPYTYRTRYLPKEC) dissolved with complete Freund’s adjuvant. The validation of CD36 antibody was confirmed according to the methods described by Uhlen et al. (2016). Antibody against GAPDH (#TA-08) was purchased from Golden Bridge Biotechnology (China), and HRP-conjugated secondary antibody (#A0208) was purchased from Beyotime Biotechnology (China).

Calculations and Statistical Methods

The following parameters were calculated:

$Survivalrate\left(SR\%\right)=\frac{N_F}{N_I}\times 100$

$Specificgrowthrate(SGR,\%/d)={\displaystyle \frac{\left(Ln{W}_F-Ln{W}_I\right)}{t}}\times 100$

$Feedintake(FI,\%/d)=\frac{F_C}{\left(\frac{W_F+W_I}{2}\right)\times t}\times 100$

$Feedefficiencyratio\left(FER\right)=\frac{W_G}{F_C}$

$Hepatosomaticindex\left(HSI\%\right)=\frac{W_L}{W_F}\times 100$

$Viscerosomaticindex\left(VSI\%\right)=\frac{W_V}{W_F}\times 100$

$Conditionfactor\left(CF\%\right)=\frac{W_F}{L_F^3}\times 100$

where N_I and N_F represent the initial and final fish number, respectively; W_I and W_F represent the initial and final fish body weight, respectively; t represents the duration of experimental days; F_C represents the dry feed consumption in g; W_G represents the wet weight gain in g; W_L represents the hepatic wet weight; W_V represents the visceral wet weight; and L_F represents the fish body length.

Statistical analyses were processed by one-way analysis of variance (ANOVA) and then carried out Tukey’s test using SPSS 21.0 (IBM, United States) (He et al., 2019; Li S. L. et al., 2019). The column charts were made using GraphPad Prism 5 (GraphPad Software, Inc., La Jolla, CA, United States). The significance of statistics was judged by P < 0.05, and the results were represented as means ± S.E.M (standard error of the mean).

Results

Survival, Growth, and Morphological Parameters

Dietary LO levels had no remarkable difference in the SR of fish among the four treatments (P > 0.05). Compared with the control group, fish fed the diet with 100% LO showed markedly lower SGR and FER (P < 0.05). However, no remarkable differences were observed in the SGR and FER of fish fed diets within 66.7% LO (P > 0.05). Furthermore, there were no remarkable differences in the FI, VSI, HSI, or CF of fish among the four treatments (P > 0.05) (Table 4).

TABLE 4

Table 4. Growth, survival, and morphological parameters of large yellow croaker fed diets with different levels of linseed oil (Means ± S.E.M)^a.

Body Composition Analysis

When dietary FO was entirely replaced by LO, fish had markedly higher hepatic lipid content than the control group (P < 0.05). However, there were no remarkable differences in the lipid or moisture contents of the muscle as well as the moisture, lipid, protein, or ash contents of the whole body among the four treatments (P > 0.05) (Table 5).

TABLE 5

Table 5. Body composition analysis of large yellow croaker fed diets with different levels of linseed oil (Means ± S.E.M)^a.

FA Composition in the Liver and Muscle

The percentage of 18:3n-3 (α-linolenic acid, ALA) was the highest in the liver and muscle of fish fed the diet with 100% LO among the four treatments (Tables 6, 7). However, when dietary FO was entirely replaced by LO, the hepatic percentage of ALA was lower than the hepatic percentage of 18:1n-9 (oleic acid, OA) in fish (Table 6). Moreover, percentages of OA and 18:2n-6 (linoleic acid, LNA) were significantly increased, while percentages of 14:0, 16:0, 16:1n-7, 20:4n-6 (arachidonic acid, ARA), 20:5n-3 (eicosapentaenoic acid, EPA), and 22:6n-3 (docosahexenoic acid, DHA) were significantly decreased in the liver and muscle of fish fed the diet with 100% LO compared with the control group (P < 0.05) (Tables 6, 7).

TABLE 6

Table 6. Fatty acid composition (% total fatty acids) in the liver of large yellow croaker fed diets with different levels of linseed oil (Means ± S.E.M)^f.

TABLE 7

Table 7. Fatty acid composition (% total fatty acids) in the muscle of large yellow croaker fed diets with different levels of linseed oil (Means ± S.E.M)^f.

Serum Biochemical Parameters

The activity of ALT and contents of TC, TG, and LDL-C were markedly higher in fish fed the diet with 100% LO than the control group (P < 0.05). However, compared with the control group, the activity of serum ALT and contents of TC, TG, and LDL-C showed no remarkable difference in fish fed diets within 66.7% LO (P > 0.05). No remarkable differences were observed in the content of HDL-C or the activity of AST of fish among the four treatments (P > 0.05) (Table 8).

TABLE 8

Table 8. Serum biochemical indexes and enzyme activities of large yellow croaker fed diets with different levels of linseed oil (Means ± S.E.M.)^g.

Antioxidant Capacity

When dietary FO was entirely replaced by LO, fish had the lower activity of CAT and the higher concentration of MDA in the liver than the control group (P < 0.05) (Figures 1A,D). However, no remarkable differences were observed in the activity of CAT and the concentration of MDA in fish fed diets within 66.7% LO (P > 0.05). Furthermore, there were no remarkable differences observed in activities of SOD or T-AOC of fish among the four treatments (P > 0.05) (Figures 1B,C).

FIGURE 1

Figure 1. Concentration of (A) malondialdehyde (MDA) and activities of (B) superoxide dismutase (SOD), (C) total antioxidant capacity (T-AOC), and (D) catalase (CAT) in the liver of large yellow croaker. 0%: control diet with 0% fish oil replaced by linseed oil; 33.3%: diet with 33.3% fish oil replaced by linseed oil; 66.7%: diet with 66.7% fish oil replaced by linseed oil; 100%: diet with fish oil totally replaced by linseed oil; Data are presented as means ± S.E.M. Columns sharing the same superscript letter or absence of superscripts are not significantly different determined by Tukey’s test (P > 0.05). S.E.M., standard error of means.

Expression of Lipid Metabolism-Related Genes

When dietary FO was entirely replaced by LO, fish had higher transcriptional levels of fatp1 and cd36 and a lower transcriptional level of cpt-1 than the control group (P < 0.05). There were no remarkable differences in transcriptional levels of srebp1, fas, aco, mtp, or apoB100 of fish among the four treatments (P > 0.05) (Figure 2).

FIGURE 2

Figure 2. Expression of genes related to lipid metabolism in the liver of large yellow croaker. (A) srebp1, sterol-regulatory element-binding protein 1; fas, fatty acid synthase; cpt-1, carnitine palmitoyltransferase 1; aco, acyl-CoA oxidase; (B) mtp, microsomal triglyceride transfer protein; apoB100, apolipoprotein B100; fatp1, fatty acid transport protein 1; cd36, cluster of differentiation 36; 0%: control diet with 0% fish oil replaced by linseed oil; 33.3%: diet with 33.3% fish oil replaced by linseed oil; 66.7%: diet with 66.7% fish oil replaced by linseed oil; 100%: diet with fish oil totally replaced by linseed oil; Data are presented as means ± S.E.M. Columns sharing the same superscript letter or absence of superscripts are not significantly different determined by Tukey’s test (P > 0.05). S.E.M., standard error of means.

Expression of MTP, CPT-1 and CD36 Proteins

When dietary FO was entirely replaced by LO, fish had the higher expression of CD36 protein and lower expression of CPT-1 protein than the control group (P < 0.05). There was no remarkable difference in the expression of CPT-1 and CD36 proteins in fish fed diets within 66.7% LO (P > 0.05). No remarkable difference was observed in the expression of MTP protein of fish among the four treatments (P > 0.05) (Figure 3).

FIGURE 3

Figure 3. Expression of MTP, CD36, and CPT-1 proteins in the liver of large yellow croaker. MTP, microsomal triglyceride transfer protein; CPT-1, carnitine palmitoyltransferase 1; CD36, cluster of differentiation 36; GAPDH: glyceraldehyde-3-phosphate dehydrogenase. Data are expressed as A.U. of the western blot and are depicted as a ratio of MTP to GAPDH, CPT-1 to GAPDH, and CD36 to GAPDH. 0%: control diet with 0% fish oil replaced by linseed oil; 33.3%: diet with 33.3% fish oil replaced by linseed oil; 66.7%: diet with 66.7% fish oil replaced by linseed oil; 100%: diet with fish oil totally replaced by linseed oil; Data are presented as means ± S.E.M. Columns sharing the same superscript letter or absence of superscripts are not significantly different determined by Tukey’s test (P > 0.05). S.E.M., standard error of means.

Expression of Pro-inflammatory and Anti-inflammatory Genes

When dietary FO was entirely replaced by LO, fish had higher transcriptional levels of pro-inflammatory genes (il-6, il-1β, and tnfα) and lower transcriptional levels of anti-inflammatory genes (arg1 and tgfα) than the control group (P < 0.05). Compared with the control group, transcriptional levels of il-6, il-1β, tnfα, arg1, and tgfβ showed no remarkable difference in fish fed diets within 66.7% LO (P > 0.05). No remarkable differences were found at the transcriptional levels of ifnγ, cox-2, il-10, or il-4 of fish among the four treatments (P > 0.05) (Figures 4A,B).

FIGURE 4

Figure 4. Expression of genes related to inflammation in the liver of large yellow croaker. (A) arg-1, arginase-1; il-10, interleukin-10; tgfβ, transforming growth factor β; il-4, interleukin-4; (B) il-6, interleukin-6; il-1β, interleukin-1β; cox-2, cyclooxygenase-2; ifnγ, interferon γ; tnfα, tumor necrosis factor α; 0%: control diet with 0% fish oil replaced by linseed oil; 33.3%: diet with 33.3% fish oil replaced by linseed oil; 66.7%: diet with 66.7% fish oil replaced by linseed oil; 100%: diet with fish oil totally replaced by linseed oil; Data are presented as means ± S.E.M. Columns sharing the same superscript letter or absence of superscripts are not significantly different determined by Tukey’s test (P > 0.05). S.E.M., standard error of means.

Discussion

In this study, the growth performance was compromised in L. crocea fed the diet with 100% LO, which was consistent with results found in turbot (Wang et al., 2016) and gilthead seabream (Montero et al., 2008). The decreased growth performance of L. crocea was probably due to the increase of ALA/LNA ratio and the decrease of n-3 LC-PUFA content with the increasing inclusion of LO. Evidence in the literature has shown that an appropriate ratio of ALA/LNA in diets can increase the growth performance of yellow catfish (Pelteobagrus fulvidraco) (Tan et al., 2009) and Atlantic salmon (Salmo salar). However, a high ratio of ALA/LNA in diets showed passive effects on the growth performance of tilapia (Li et al., 2016) and grass carp (Ctenopharyngodon idellus) (Zeng et al., 2016). In this study, the ratio of ALA/LNA was increased by 12.38 times in the 100% LO diet compared with that in the FO diet. In addition, n-3 LC-PUFA was deemed to be essential for marine fish, Zuo et al. (2012) have reported that the requirement of n-3 LC-PUFA for L. crocea is about 0.60–0.98% to maintain good growth performance and non-specific immunity. In this study, the content of n-3 LC-PUFA was approximately 0.34% in the 100% LO diet, which did not meet the requirement of n-3 LC-PUFA for L. crocea.

Besides the growth performance, the physiological state of fish has also become a research hotspot for nutritionists to evaluate lipid sources. Serum biochemical indices were useful terms to evaluate the physiological state of fish (Shi Y. et al., 2019). In this study, contents of serum TC, TG, and LDL-C were increased in fish when dietary FO was entirely replaced by LO. Similarly, the hyperlipidemic effect caused by dietary LO was also observed in black seabream (Acanthopagrus schlegelii) (Jin et al., 2017), and Manchurian trout (Brachymystax lenok) (Yu et al., 2019). Additionally, OA and LNA could increase serum lipid content, while n-3 LC-PUFA could reduce serum lipid content (Vegusdal et al., 2005; Hu et al., 2011; Shearer et al., 2012). In this study, an increase in the percentages of OA and LNA and a decrease in the percentage of n-3 LC-PUFA were found in diets with increasing LO levels. Therefore, the hyperlipemia of fish could be due to the imbalance of FAs in the 100% LO diet. However, different results were also observed that dietary LO decreased contents of serum TC and TG in yellow drum (Qin et al., 2020), hybrid sturgeon (Acipenser baeri Brandt♀ × A. schrenckii Brandt♂) (Liu et al., 2018), and largemouth bass (Micropterus salmoides) (Shi C. M. et al., 2019). Those different results might be related to the culture condition, feed ingredients or species differences in experiments. However, the specific reason remains to be further explored in the future. Since the liver is the central organ for lipid metabolism, liver damage is usually accompanied by increased ALT and AST activity in the serum (Giannini et al., 1999). When dietary FO was entirely replaced by LO, L. crocea had the higher activity of ALT in the serum than the control group. Similar results were found in turbot (Wang et al., 2016), and black seabream (Jin et al., 2017). In this study, the increased activity of ALT in the serum indicated that a high level of LO might cause some damage in the liver of fish.

Antioxidant capacity was also an important term in evaluating the physiological state of fish. CAT was a type II detoxifying enzyme that played a vital role in scavenging toxic intermediates (Samanta et al., 2014), while MDA was commonly used as an index to evaluate lipid peroxidation, which could indirectly reflect the degree of cell impairment (Mendes et al., 2009). The current study reported that L. crocea fed the diet with 100% LO had lower CAT activity and a higher concentration of MDA than the control group. Similar effects were found in Japanese seabass (Lateolabrax japonicus) (Tan et al., 2017) and hybrid grouper (Epinephelus fuscoguttatus ♀ × E. lanceolatus ♂) (An et al., 2020). ALA has been confirmed to increase mitochondrial DNA methylation in the liver, which can induce oxidative stress in fish (Liao et al., 2015). Meanwhile, EPA and DHA have been confirmed to relieve oxidative stress-related mitochondrial dysfunction and can improve activities of type II detoxifying enzymes (Oppedisano et al., 2020). According to these studies, the decrease of antioxidant capacity in L. crocea could be due to the increased content of ALA and the decreased contents of EPA and DHA in the 100% LO diet.

In this study, the total substitution of dietary FO with LO increased the hepatic lipid content of L. crocea. Similarly, dietary LO increased the abnormal lipid deposition in rainbow trout (Turchini and Francis, 2009), Japanese seabass (Xu et al., 2015), tilapia (Li et al., 2016), and yellow drum (Qin et al., 2020). The increase of abnormal lipid deposition was probably due to the increased percentage of ALA in the 100% LO diet, which could alter lipid metabolism. Previous studies have shown that FATP1 and CD36 are vital FA transport proteins in the liver (Stahl, 2004; Musso et al., 2009). In this study, when dietary FO was entirely replaced by LO, L. crocea had higher transcriptional levels of fatp1 and cd36 and a higher expression of the CD36 protein than the control group. A previous study have showed that the uptake of PUFA was dependent on membrane proteins in Atlantic salmon hepatocytes, where the uptake process was on this ranking list: EPA > ALA = DHA > LNA > OA (Zhou et al., 2010). Although the percentage of n-3 LC-PUFA in the 100% LO diet was lower than that in the FO diet, the percentage of ALA in the 100% LO diet was much higher than the percentage of n-3 LC-PUFA in the FO diet. The increased transcriptional levels of fatp1 and cd36 and expression of the CD36 protein were probably due to the high amount of the ALA in the 100% LO diet. Furthermore, CPT-1 is considered a significant enzyme in the FA oxidation pathway (Mcgarry and Brown, 2010). In this study, when dietary FO was entirely replaced by LO, fish had lower cpt-1 mRNA expression than the control group. Moreover, dietary perilla oil (rich in ALA) was reported to increase the methylation of mitochondrial DNA in L. crocea which could cause the depression in FA oxidation (Liao et al., 2015). The decrease of cpt-1 mRNA expression could be due to the excessive ALA in the 100% LO diet that might increase the mitochondrial DNA methylation. Therefore, the increase of lipid deposition in L. crocea fed the diet with 100% LO could be attributed to the up-regulation in FA uptake and the down-regulation in FA oxidation.

As abnormal lipid deposition was associated with chronic inflammation in fish (Tan et al., 2017), we investigated whether the inflammation was related to the negative physiological status of L. crocea. When dietary FO was entirely replaced by LO, fish had higher transcriptional levels of pro-inflammatory genes (il-6, il-1β, and tnfα) but lower transcriptional levels of anti-inflammatory genes (arg1 and tgfβ) than the control group. Similarly, total substitution dietary FO with LO induced inflammation in yellow drum (Qin et al., 2020), and gilthead seabream (Montero et al., 2010). The inflammation caused by a high level of dietary LO was most likely attributed to the imbalance of dietary FAs. Although the 100% LO diet contained enough ALA, L. crocea had a limited capacity to synthesize EPA and DHA (essential FAs for marine fish) from C18 PUFA (Tocher, 2010; Li et al., 2017). The limited capacity and low n3 LC-PUFA content in the 100% LO diet would result in an unsatisfied amount of essential FA for L. crocea to maintain positive inflammatory responses.

Conclusion

In conclusion, no more than 66.7% of FO can be substituted with LO without significantly decreasing the growth performance of large yellow croaker. However, high levels of dietary LO caused growth reduction, abnormal lipid deposition, and inflammation in the liver of fish. In addition, the increase of hepatic lipid deposition caused by 100% LO was probably attributed to the increase of fatty acid uptake and the decrease of fatty acid oxidation in fish.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary file, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The animal study was reviewed and approved by the Standard Operation Procedures (approval number: 20001001) of the Institutional Animal Care and Use Committee of the Ocean University of China.

Author Contributions

KM, QA, and XL designed the research. XL, QC, and KC conducted the research. XL, QL, and JL analyzed the data. XL wrote the manuscript. XL, YZ, and AK provided language help. All authors reviewed and approved the final manuscript.

Funding

This study was funded by the National Science Fund for Distinguished Young Scholars of China (Grant No. 31525024), the China Agriculture Research System (Grant No. CARS47-11), Aoshan Talents Program Supported by Qingdao National Laboratory for Marine Science and Technology (Grant No. 2015ASTP), Key Program of National Natural Science Foundation of China (Grant No. 31830103), Ten-thousand Talents Program (Grant No. 2018-29), and Scientific and Technological Innovation of Blue Granary (Grant No. 2018YFD0900402).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We thank Chuanwei Yao, Wenxing Huang, Shengnan Gao and Wenxuan Xu for their assistance in revising the article and JL, QC, and Tingting Hao for providing the antibodies.

References

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