Lentinan Impairs the Early Development of Zebrafish Embryos, Possibly by Disrupting Glucose and Lipid Metabolism

LNT is the major biologically active substance extracted from Lentinus edodes (L. edodes). Although functional and pharmacological studies have demonstrated that LNT has multiple benefits for animals and humans, the safety assessment is far from sufficient. To evaluate the potential safety risk, larval zebrafish were continuously exposed to varying concentrations of LNT for 120 h. The 96 h LC50 of LNT was determined to be 1228 μg/mL, and morphological defects including short body length, reduced eye and swim bladder sizes and yolk sac edema were observed. In addition, LNT exposure significantly reduced the blood flow velocity and locomotor activity of larval zebrafish. The biochemical parameters were also affected, showing reduced glucose, triglyceride and cholesterol levels in zebrafish larvae after being exposed to LNT. Correspondingly, the genes involved in glucose and lipid metabolism were disrupted. In conclusion, the present study demonstrates the adverse potential of high concentrations of LNT on the development of zebrafish larvae in the early life stage.

Because of their functions and taste, β-glucans are widely used as medicine, antimicrobial agents, dietary supplements and nutrition enhancers. For instance, two kinds of β-glucans, LNT and krestin, have been approved as anti-tumor drugs for gastric cancer treatment in Japan [22]. Extensive studies have been conducted to elucidate the mechanism underlying the anti-tumor activity of LNT. Two chief mechanisms have identified: (1) enhancing the immunity against tumors, including cellular and humoral immunities [23,24]; (2) preventing cancer cell proliferation or metastasis through direct induction of cell apoptosis and death [25]. Besides the applications in cancer therapy, LNT has been approved as a safe food ingredient in the European Union and used in various products, such as dietary supplements, processed foods and drinks [26]. The efficacy and effectiveness studies carried out in animals and humans partially support the safety of LNT, however, only limited value was provided. The LD50 values of LNT were determined to Processes 2022, 10, 120 2 of 13 be 250-500 mg/kg and >2500 mg/kg in mice (intravenously) and rats (intraperitoneally, subcutaneously and orally), respectively [27]. In a 6-month study, different doses of LNT (0.01, 0.1, 1, 10 mg/kg/day) were intravenously injected into the tail vein of rats to assess the chronic toxicity of LNT. All treated groups showed different degrees of arteritis, pulmonary hemorrhage and hypospermatogenesis, and the maximum no-effect level was lower than 0.01 mg/kg/day [28]. Based on this result and considering the direct cellular toxicity on cancer cells and the anti-bacterial effect [8,25,28], LNT may exert adverse effects on receivers. Thus, the health risk of LNT should be assessed adequately in different species and the underlying mechanism should be elucidated.
Before being administered to humans, the safety assessments of medicines, food ingredients or chemicals are essential. Currently, most of the toxicity assays are using animals, especially rodents. To improve animal welfare, test methods meeting the 3R principles (replacement, reduction, and refinement) are encouraged [29,30]. Zebrafish are becoming popular as an alternative animal model in safety assessment because of their particular advantages that partially obey the 3R principles. For instance, zebrafish are lower sentient vertebrates compared with rodents, which means the suffering during the experiments would be on a lower degree. The use of zebrafish for early screening could largely reduce the number of rodents in the subsequent research phase. Moreover, the fecundity of zebrafish is high and the embryos can be handled easily in vitro, which significantly increases the efficiency of experiments [31]. Zebrafish larva is a prominent model organism used in developmental biology due to its transparency, which allows easy staging under optical microscopy. A large number of studies have used zebrafish larvae to evaluate the developmental toxicity of chemicals [32][33][34]. More importantly, since the genome of zebrafish has been sequenced [35], the mechanism underlying the toxic phenotype is able to be elucidated at the molecular level.
In the present study, larval zebrafish were used to investigate the impacts of high concentrations of LNT on the developmental process in the early life stage. The hatching rate at 72 and 96 h post fertilization (hpf) and the median lethal concentration (LC50) at 96 hpf were determined. Furthermore, the morphological changes, heartbeat, blood flow velocity and locomotor activity of larval zebrafish that were continuously exposed to varying concentrations of LNT were studied at 120 hpf. In addition, the biochemical indexes reflecting energy metabolism were evaluated. To reveal the underlying mechanism, the genes involved in glucose and lipid metabolism were quantified at the transcriptional level. This study evaluated the potential adverse effects of LNT by using larval zebrafish for the first time. Moreover, these findings provided evidence that high concentrations of LNT would alter the energy metabolism process.

Zebrafish Maintenance and Embryo Collection
Wild-type AB strain zebrafish were housed in a light-and temperature-controlled aquaculture facility with a light/dark photoperiod of 14:10 h. The fish were maintained in fish water at 28 • C (0.2% Instant Ocean Salt in deionized water, pH 6.9-7.2, conductivity 480-510 µS/cm and hardness 53.7-71.6 mg/L CaCO 3 ) and were fed with live brine shrimp twice a day. Male and female zebrafish were set up for natural mating. All healthy embryos from different pairs of zebrafish were mixed and washed with E3 medium for further experiments. The experiment was performed following the ethical guideline of Experimental Animal Ethics Committee of Hunter Biotechnology, Inc. (AAALAC 001458).

Embryo Acute Toxicity Test
Fertilized eggs before 16 cell-stage were selected and randomly transferred into the six-well plates with 30 embryos per well, containing 3 mL of E3 medium. The embryos were exposed to series concentrations of LNT (600, 800, 1000, 1200, 1400, 1600, 1800, 2000, and 4000 µg/mL) continuously for 96 h. The media were refreshed every day. During the exposure period, the lethality was recorded according to the OECD guidelines [36], and the dead embryos were removed. The number of dead larvae at each concentration was plotted and a concentration-response curve was fitted. The LC50 value was calculated from independent experiments performed in triplicate. According to the 96 h LC50 value, four LNT concentrations (30, 100, 300, and 900 µg/mL) were set for further evaluation.

Pathological Alteration Analyses
The embryos at 6 hpf were exposed to series concentrations of LNT (30, 100, 300, and 900 µg/mL), and larval zebrafish at 120 hpf were collected. The numbers of hatched embryos at 72 and 96 hpf were recorded. The hatching rate was summarized from three independent assays. For morphological observation, the zebrafish larvae were anesthetized and images were captured using optical microscopy (SZX7, OLYMPUS, Japan). The body length, swim bladder size, eye area, and yolk sac area were analyzed using NIS-ElementsD 3.20 software (Nikon, Japan). The relative values were calculated by the following formula: relative values = individual values/mean value of control group. The zebrafish larvae were not anesthetized and the heartbeats in 20 s were recorded manually. The blood flow velocity was calculated using MicroZebraLab (Viewpoint, Lyon, France). For behavioral analyses, the zebrafish larvae were assigned individually into a 96-well microplate. After being acclimated for 5 min under the lighting conditions, the swimming ability in the light/dark cycle (5 min/5 min) was recorded for 25 min using Zebrabox (ViewPoint, Lyon, France).

Biochemical Indexes Determination
A total of 30 zebrafish larvae at 120 hpf were homogenized with 60 µL of ice-cold PBS using a homogenizer, centrifuged at 5000× g for 10 min at 4 • C, and the supernatant was collected for further analyses. The contents of Glucose (Glu), triglyceride (TG), and total cholesterol (T-CHO) were measured using the commercial kits obtained from Nanjing Jiancheng Institute of Biotechnology (Nanjing, China) according to the manufactures' instructions. Briefly, 2.5 µL of supernatant from each sample was used to measure the glucose content by using the glucose oxidase method (GOD). Similarly, 2.5 µL of supernatant from each sample was used to measure the triglyceride content by using the GPO-PAP method and 2.5 µL of supernatant from each sample was used to measure the total cholesterol content by using the COD-PAP method.

Quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) Analyses
Total RNA was isolated from 30 zebrafish larvae at 120 hpf using RNA-easy Isolation Reagent (Vazyme Biotech, Nanjing, China). Briefly, 30 larvae were homogenized with 300 µL of lysis buffer using a homogenizer, centrifuged at 12,000× g for 15 min, and the supernatant was transferred to a new tube. The same volume of isopropanol was added to precipitate the RNA. After being centrifuged at 12,000× g for 10 min, the pellet was washed with 75% ethanol. The RNA was dissolved with RNase-free ddH 2 O and the purity was checked using Nano Drop 2000 (Thermo Scientific, WALTHAM, MA, USA). A total of 2 µg RNA was reverse transcribed into cDNA by using FastKing RT kit (Tiangen Biotech, Beijing, China). Gene expressions were detected by qRT-PCR using iTaq Universal SYBR Green (Bio-Rad, Hercules, CA, USA) on the CFX Connect Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). The primer sequences were referred to other studies and listed in Table S1 [37][38][39][40][41]. The relative expression levels of the genes were normalized to actb2, and calculated using the 2−∆∆CT method.

Statistical Analysis
All data in this study were presented as mean ± standard error (SE), and analyzed by one-way analysis of variance (ANOVA) followed by the Dunnett's multiple comparisons test using GraphPad Prism 7. Compared with the control group, p < 0.05 was considered significant.

Lethal Effect and Developmental Toxicity of LNT in Larval Zebrafish
To investigate the lethal effect of LNT, fertilized eggs were exposed to series concentrations of LNT for 96 h. By analyzing the fitting curve shown in Figure 1A, the 96 h LC50 value of LNT was determined to be 1228 µg/mL. Green (Bio-Rad, Hercules, CA, USA) on the CFX Connect Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). The primer sequences were referred to other studies and listed in Table S1 [37][38][39][40][41]. The relative expression levels of the genes were normalized to actb2, and calculated using the 2-ΔΔCT method.

Statistical Analysis
All data in this study were presented as mean ± standard error (SE), and analyzed by one-way analysis of variance (ANOVA) followed by the Dunnett's multiple comparisons test using GraphPad Prism 7. Compared with the control group, p < 0.05 was considered significant.

Lethal Effect and Developmental Toxicity of LNT in Larval Zebrafish
To investigate the lethal effect of LNT, fertilized eggs were exposed to series concentrations of LNT for 96 h. By analyzing the fitting curve shown in Figure 1A, the 96 h LC50 value of LNT was determined to be 1228 μg/mL.  (C) representative images of larvae at 120 hpf; (D) body length of larvae at 120 hpf (each group n = 20); (E) heartbeats of larvae at 120 hpf (each group n = 10); (F) blood flow velocity of larvae at 120 hpf (each group n = 10). All data were compared with the control group, *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Based on the LC50 value, LNT at concentrations of 30, 100, 300, and 900 µg/mL (1/36, 1/12, 1/4, and 3/4 LC50, respectively) were set for further evaluations. As shown in Processes 2022, 10, 120 5 of 13 Figure 1B, the hatching rates at 72 h and 96 h were not affected by LNT treatment, even in the 900 µg/mL group. Except for yolk sac edema, no obvious deformity was observed in all LNT treated groups ( Figure 1C). Nevertheless, the body length of zebrafish larvae decreased significantly in a dose-dependent manner ( Figure 1D), suggesting that LNT exposure inhibited the growth of individuals. Interestingly, the blood flow velocity was remarkably reduced in all LNT treated groups, without any effect on the heartbeats in 20 s ( Figure 1E,F).

LNT Induced Pathological Alterations in Larval Zebrafish
To further assess the adverse effects of LNT exposure on the development of larval zebrafish, more detailed characteristics, including eye and swim bladder sizes and yolk sac area, were quantified ( Figure 2A). Inflated swim bladders (Figure 2A, blue dotted lines) were observed in the control group, while the sizes of the swim bladders were dosedependently decreased in the LNT treated groups ( Figure 2B). Notably, almost 50% of the zebrafish larvae completely lost the inflated swim bladders in the 900 µg/mL group. In addition, the eyes ( Figure 2A, red dotted lines) in the 900 µg/mL group were significantly smaller than those in the control group ( Figure 2C). Another obvious deformity observed was yolk sac edema. As shown in Figure 2D, the yolk sac area clearly increased along with the concentrations of LNT. All these morphological changes, including body length, eye and swim bladder sizes and yolk sac area, demonstrate that high concentrations of LNT inhibited the normal development of the larval zebrafish. 20); (E) heartbeats of larvae at 120 hpf (each group n = 10); (F) blood flow velocity of larvae at 120 hpf (each group n = 10). All data were compared with the control group, *, p < 0.05; **, p < 0.01; ***, p < 0.001.
Based on the LC50 value, LNT at concentrations of 30, 100, 300, and 900 μg/mL (1/36, 1/12, 1/4, and 3/4 LC50, respectively) were set for further evaluations. As shown in Figure  1B, the hatching rates at 72 h and 96 h were not affected by LNT treatment, even in the 900 μg/mL group. Except for yolk sac edema, no obvious deformity was observed in all LNT treated groups ( Figure 1C). Nevertheless, the body length of zebrafish larvae decreased significantly in a dose-dependent manner ( Figure 1D), suggesting that LNT exposure inhibited the growth of individuals. Interestingly, the blood flow velocity was remarkably reduced in all LNT treated groups, without any effect on the heartbeats in 20 s ( Figure  1E,F).

LNT Induced Pathological Alterations in Larval Zebrafish
To further assess the adverse effects of LNT exposure on the development of larval zebrafish, more detailed characteristics, including eye and swim bladder sizes and yolk sac area, were quantified (Figure 2A). Inflated swim bladders (Figure 2A, blue dotted lines) were observed in the control group, while the sizes of the swim bladders were dosedependently decreased in the LNT treated groups ( Figure 2B). Notably, almost 50% of the zebrafish larvae completely lost the inflated swim bladders in the 900 μg/mL group. In addition, the eyes (Figure 2A, red dotted lines) in the 900 μg/mL group were significantly smaller than those in the control group ( Figure 2C). Another obvious deformity observed was yolk sac edema. As shown in Figure 2D, the yolk sac area clearly increased along with the concentrations of LNT. All these morphological changes, including body length, eye and swim bladder sizes and yolk sac area, demonstrate that high concentrations of LNT inhibited the normal development of the larval zebrafish. All data were compared with the control group, *, p < 0.05; ***, p < 0.001.

Effects of LNT Exposure on the Locomotor Activity in Larval Zebrafish
The impact of LNT on locomotor activity in larval zebrafish is shown in Figure 3. A light/dark rhythm was observed in the control group and all LNT treated groups ( Figure  3A), suggesting that LNT exposure didn't disrupt the response of zebrafish larvae to light

Effects of LNT Exposure on the Locomotor Activity in Larval Zebrafish
The impact of LNT on locomotor activity in larval zebrafish is shown in Figure 3. A light/dark rhythm was observed in the control group and all LNT treated groups ( Figure 3A), suggesting that LNT exposure didn't disrupt the response of zebrafish larvae to light and dark stimulation. Whereas, the total distance moved during the light and dark phases by the zebrafish larvae in the LNT treated groups decreased remarkably ( Figure 3B,C). and dark stimulation. Whereas, the total distance moved during the light and dark phases by the zebrafish larvae in the LNT treated groups decreased remarkably ( Figure 3B,C).

Effects of LNT Exposure on the Glu, TG and T-CHO Levels in Larval Zebrafish
As shown in Figure 4, the contents of Glu and TG decreased dramatically in 100, 300 and 900 μg/mL groups, and T-CHO levels decreased in all LNT treated groups.

Effects of LNT Exposure on the Genes Involved in Glucose, Lipid and Cholesterol Metabolism in Larval Zebrafish
To elucidate the mechanism underlying the decrease in glucose, triglyceride, and cholesterol induced by LNT, the mRNA levels of the genes involved in the metabolism of these substances were quantified using qRT-PCR. The results from Figure 5A showed that the expression of Hexokinase (HK1) increased significantly after being treated with 300

Effects of LNT Exposure on the Glu, TG and T-CHO Levels in Larval Zebrafish
As shown in Figure 4, the contents of Glu and TG decreased dramatically in 100, 300 and 900 µg/mL groups, and T-CHO levels decreased in all LNT treated groups. and dark stimulation. Whereas, the total distance moved during the light and dark phases by the zebrafish larvae in the LNT treated groups decreased remarkably ( Figure 3B,C).

Effects of LNT Exposure on the Glu, TG and T-CHO Levels in Larval Zebrafish
As shown in Figure 4, the contents of Glu and TG decreased dramatically in 100, 300 and 900 μg/mL groups, and T-CHO levels decreased in all LNT treated groups.

Effects of LNT Exposure on the Genes Involved in Glucose, Lipid and Cholesterol Metabolism in Larval Zebrafish
To elucidate the mechanism underlying the decrease in glucose, triglyceride, and cholesterol induced by LNT, the mRNA levels of the genes involved in the metabolism of these substances were quantified using qRT-PCR. The results from Figure 5A showed that the expression of Hexokinase (HK1) increased significantly after being treated with 300

Effects of LNT Exposure on the Genes Involved in Glucose, Lipid and Cholesterol Metabolism in Larval Zebrafish
To elucidate the mechanism underlying the decrease in glucose, triglyceride, and cholesterol induced by LNT, the mRNA levels of the genes involved in the metabolism of these substances were quantified using qRT-PCR. The results from Figure 5A showed that the expression of Hexokinase (HK1) increased significantly after being treated with 300 and 900 µg/mL of LNT. On the contrary, the mRNA levels of pyruvate kinase (PK) in the 30, 300, and 900 µg/mL groups were lower than that in the control group. Additionally, the transcription level of cytosolic phosphoenolpyruvate carboxy kinase (PEPCK-C) decreased significantly in the 900 µg/mL group. These results suggest that LNT exposure affected the genes related to glucose metabolism. and 900 μg/mL of LNT. On the contrary, the mRNA levels of pyruvate kinase (PK) in the 30, 300, and 900 μg/mL groups were lower than that in the control group. Additionally, the transcription level of cytosolic phosphoenolpyruvate carboxy kinase (PEPCK-C) decreased significantly in the 900 μg/mL group. These results suggest that LNT exposure affected the genes related to glucose metabolism.  In addition, the transcription levels of the genes involved in the lipid metabolism process were also disrupted by LNT exposition. The mRNA levels of peroxisome proliferatoractivated receptor-α (PPAR-α), sterol regulatory element binding protein 1α (SREBP1α), fatty acid synthase (FAS), acyl-oxidase (ACO), and apolipoprotein A-IV (Apo) were downregulated after being treated with 900 µg/mL of LNT ( Figure 5B). The mRNA levels of Processes 2022, 10, 120 8 of 13 fatty acid binding protein 6 (FABP6) decreased in both the 300 and 900 µg/mL groups. Nevertheless, the transcription of carnitine palmitoyl transferase 1 (CPT1) was induced by 300 and 900 µg/mL of LNT ( Figure 5B).

Discussion
Natural medicines and functional foods derived from natural products, such as plants and fungi, are of huge value to humans. Compared to synthetic compounds, natural products are supposed to be lower toxic to the receivers [42]. In addition, one natural product contains diverse bioactive components, which may enhance the efficacy due to the synergistic effect [43]. In recent decades, comprehensive studies on natural products have been conducted in many countries, examining various aspects including preparation, bioavailability, and bioactivity. Glucans are products that are used as both medicines and functional foods. However, compared with the research evaluating their function and efficacy, adequate safety assessments are far from sufficient. Therefore, the present study was conducted to evaluate the toxicity and the underlying mechanism of high concentrations of LNT on larval zebrafish. Our results demonstrated that LNT exposure inhibited the development of larval zebrafish and caused morphological and locomotor defects. The glucose, triglyceride, and cholesterol levels were significantly decreased in the LNT treated groups. Further qRT-PCR assays revealed that transcriptions of the genes involved in glucose, lipid, and cholesterol metabolism were disrupted by LNT.
After being established as a model organism, zebrafish embryos have been widely used in scientific research, especially in toxicology [44]. The Organization for Economic Co-operation and Development (OECD) adopted the Fish Embryo Acute Toxicity (FET) Test as a method for the testing of chemicals in 2013 [36], which greatly promoted the use of zebrafish embryos for safety assessment. Recently, Wan-Mohtar et al. investigated the toxicity of the polysaccharides extracted from European Ganoderma applanatum mushrooms, and reported that the LC 50 of exopolysaccharide (EPS) and endopolysaccharide (ENS) were 1410 and 870 µg/mL respectively [45]. Here, the half-lethal concentration of LNT at 96 h was demonstrated to be 1228 µg/mL ( Figure 1A), suggesting that the toxicities of glucans differ by species and even by portions. From another view, these results also reinforced that the FET test is a reliable and sensitive method to assess the safety of natural product extracts.
The hatching rate was not significantly affected by LNT at concentrations of 30, 100, 300, and even 900 µg/mL. Interestingly, several other studies also suggested that the glucans appear to have little effect on the hatching rate of embryos at concentrations lower than 1000 µg/mL [45,46]. However, different degrees of morphological defects were observed in the larval zebrafish, manifesting as short body length, slow blood flow velocity, small eyes and swim bladder, and yolk sac edema, which could be summarized as developmental retardation [47]. It is well known that energy is essential for living organisms to carry out activities such as growth, development, movement, and reproduction [48]. We hypothesized that the energy balance might be disrupted by LNT in the zebrafish embryos. Indeed, the levels of glucose, triglyceride, and cholesterol were significantly lower in the LNT treated groups. The LNT induced growth retardation but did not affect the hatching rate, suggesting that the zebrafish embryos are more resistant to LNT than the larvae, which may attribute to the protective effect of the chorion [49].
Locomotor activity plays a crucial role in the survival of animals, because it has been closely related to migration and predator avoidance [50,51]. It is well known that locomotor activity is influenced by several factors, such as the nervous system, feeding, and growth [50]. Altered locomotor activity has been used as an indicator for investigating Processes 2022, 10, 120 9 of 13 neurotoxicity, developmental toxicity and some diseases [52]. Here, we observed that LNT exposure remarkably inhibited the locomotor activity in larval zebrafish (Figure 3). Combined with the abnormal morphological changes, all these results suggest that LNT adversely affected the growth of larval zebrafish in the early stage. In addition, because movement is an energy cost behavior, the decrease in glucose, lipid, and cholesterol induced by LNT also could directly affect the locomotor activity of zebrafish larvae.
Without any doubt, the nutrients, such as glucose and lipids, are the foundation of development for all organisms [53]. Hence, the contents of these substances were measured in the larval zebrafish at 5 dpf. In accordance with our hypothesis, the glucose, triglyceride, and cholesterol levels were dramatically downregulated by LNT (Figure 4). Indeed, it was reported that β-glucans from different sources reduced the blood glucose level in both healthy and diabetic individuals [54][55][56]. In a mouse model, the β-glucan from barley was demonstrated to have the potential to reduce blood glucose and serum lipid [56]. Further investigation revealed that the genes involved in lipid metabolism were significantly altered after the β-glucan treatment [57]. Similarly, several key genes related to glucose and lipid metabolism were found to be regulated by LNT in the present study. HK, the initial enzyme in the glycolysis pathway [58], was induced by LNT. On the contrary, PEPCK-C, the key enzyme in glucose synthesis [59], was suppressed at the transcription level by LNT. These results indicated that the consumption of glucose was increased, while the production of glucose was decreased. As a consequence, the glucose content reduced significantly in the larval zebrafish. Interestingly, PK, the enzyme involved in the last step of glycolysis [60], was inhibited at the transcription level by LNT, which may lead to a deficiency in energy. In addition, LNT suppressed the expression of genes involved in lipid synthesis, such as SREBP1α and FAS, and enhanced the expression of genes related to catabolism of lipids, like CPT1. Similar results were observed in a previous study [57], showing that barley β-glucan induced the expression of CPT1 and reduced the expression of SREBP1α.
The cholesterol-lowering effect of β-glucan has been demonstrated in humans and animal models previously and different mechanisms were elucidated [61][62][63]. For instance, by-products of β-glucan digestion were reported to affect the synthesis of cholesterol [64]. Moreover, metabolism and circulation of bile acid were also influenced by β-glucan, which may be responsible for the lowering of cholesterol [63]. Our results showed that HMGCRa and HMGCRb, two key genes involved in cholesterol synthesis, were not altered by LNT. Whereas, the mRNA level of CYP7A1 was significantly inhibited by LNT, indicating that LNT regulated the cholesterol through the bile acid system, instead of direct regulation of cholesterol synthesis. However, the detailed mechanism remains unclear.
LNT has been tested in several clinical trials. For instance, LNT significantly prolonged the survival of gastric cancer patients treated with fluoropyrimidine-based chemotherapy. The ratio of granulocytes/lymphocytes was enhanced by LNT in the patients receiving LNT compared to the individuals with chemotherapy alone, supporting the immunomodulatory effect of LNT [65]. A meta-analysis also suggested that LNT prolonged the survival of advanced gastric cancer patients treated with standard chemotherapy [66]. The beneficial effects of β-glucans from mushrooms on the cardio-metabolic system have been reported in in vitro and animal experiments, with different mechanisms which were not completely understood [67,68]. However, the data from humans supporting the beneficial effect of LNT on lipid and cholesterol metabolism is scarce. A clinical trial showed that an eight-week intervention with β-glucans obtained from Shiitake mushrooms did not alter the lipidor cholesterol-related parameters in hypercholesterolemic subjects receiving β-glucans or placebo [69]. Nevertheless, our results showed that LNT significantly affected the metabolism of glucose, triglyceride, and cholesterol at both biochemical and transcriptional levels. Although the exact reasons involved in the different results observed in humans and zebrafish are still to be elucidated, several potential factors may have contributed to the uncertain and inconsistent findings: (1) the type of subjects included in the studies (healthy, hypercholesterolemic, and diabetic subjects); (2) the different mushroom species used as the source of β-glucans; (3) different digestion processes in humans and zebrafish.

Conclusions
LNT exposure had toxic effects on the zebrafish embryos. The 96 h LC50 value was estimated to be 1228 µg/mL in the present study. LNT at the concentrations of 30, 100, 300, and 900 µg/mL did not alter the hatching rate of embryos at 72 and 96 hpf. However, the development of the embryos was impaired, which was evidenced by shortened body length, slowed blood flow velocity, small eyes and swim bladder, and yolk sac edema. In addition, the locomotor activity was also inhibited by LNT. Detection of the biochemical indexes and the gene transcriptions revealed that LNT significantly disrupted the glucose, lipid, and cholesterol metabolism, which might contribute to the LNT-induced energy deficiency. All these results suggested that high concentrations of LNT induced developmental toxicity in the zebrafish embryos, which can possibly be attributed to the disruption of energy metabolism induced by LNT.
Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/pr10010120/s1, Table S1: The primer sequence pairs used in the qRT-PCR. Table S2: Effects of LNT on the GLU, TG and T-CHO in zebrafish larvae.