1. Introduction
For living organisms, carbohydrates provide energy and organic carbon [
1]. A carbohydrate source is regarded as the most economical energy source for artificial feed. In addition, including carbohydrates in the diet has a protein-sparing effect, lowers ammonia nitrogen excretion, and minimizes water pollution, all of which contribute to the feed industry’s sustainable growth. Fish, however, have a restricted capacity to use dietary carbohydrates. Usually, hyperglycemia shows up after glucose loading or carbohydrate intake [
2]. Carnivorous fish exhibit limited utilization of carbohydrates as a result of their shorter intestine, inadequate secretion of α-amylase, a low count of insulin receptors, and the absence of inhibition in postprandial gluconeogenesis [
3]. However, the metabolic variations among fish remain inadequately characterized, thus necessitating an investigation into the dietary carbohydrates’ mechanism of metabolic regulation in fish.
The liver serves as the primary site for glucose metabolism in fish, encompassing various processes such as glycolysis, gluconeogenesis, the pentose phosphate pathway, glycogen synthesis, and glycogenolysis. The regulation of glucose production and storage is influenced by hormonal and nutritional factors, which are contingent upon the expression and activity levels of crucial enzymes involved in the gluconeogenic and glycolytic pathways. Both the loss of glycemic control in coho salmon (
O. kisutch) given a streptozotocin injection and insulin production by Atlantic hagfish (
Myxine glutinosa) induced by glucose demonstrate the existence of a glucose homeostasis system in fish [
4,
5]. Glycolysis, gluconeogenesis, glycogen synthesis, and glycogenolysis are all involved in the control of homeostasis glucose [
6]. As a result of increased 6-phosphofructo-1-kinase (
FBP), pyruvate kinase (
PK), and glucokinase (
GK) activity, the glycolytic pathway is up-regulated in the liver of many carnivorous fish species during postprandial settings. In earlier studies, carbohydrates had an impact on the gut microbiota and the transcription of genes involved in glucose metabolism. According to a previous study on
Megalobrama amblycephala, neither the number of dietary carbohydrates nor the timing of the samples had an impact on the transcription of phosphoenolpyruvate carboxylase (
PEPCK). However, the transcriptions of
GK,
PK, and glycogen synthase (
GS) were considerably greater in the high-carbohydrates group than in the control group, whereas the transcriptions of
FBP were the opposite [
3]. High carbohydrate levels were found to enhance the prevalence of the hazardous microorganisms Vibrio, Photobacterium, and Mycoplasma in
Trachinotus ovatus studies [
7]. Glycogen synthase (
GS) and glycogen phosphorylase are two important enzymes that control the accumulation of glycogen with regard to glycogen metabolism; increased hepatic glycogen after dietary carbohydrate consumption has been documented in certain fish. According to previous studies, after consuming a high-carbohydrate diet, the hepatic glycogen levels were increased by inducing glycogen synthesis and inhibiting glycogenolysis [
8,
9]. However, the exact mechanism by which a high-carbohydrate diet affects crucial glucose metabolism enzymes and thus results in abnormalities of glucose metabolism in
Lateolabrax maculatus is still not fully understood and warrants further study.
Animals’ bodies require intestinal microflora, which also plays a crucial physiological function in the host’s immunological antagonism and the absorption of nutrients [
8]. The consumed feed served as the major source of gut flora [
10]. Numerous studies have demonstrated a connection between diseases and metabolic disorders and excessive carbohydrate intake [
11]. Studies on the impact of dietary carbohydrate levels on the health of fish guts, however, are few [
11].
The spotted sea bass (
L. maculatus), a carnivorous fish that belongs to the family Moronidae (Perciformes), has distinctive conspicuous black spots on the side of its body [
12]. Since the creation of the genus
Lateolabrax, it has been regarded as a congeneric species alongside
Lateolabrax japonicus. The
L. maculatus has a larger geographic range than
L. japonicus, extending from the Bohai Sea to the Indo-Chinese peninsula [
13]. Due to its broad adaptability, quick growth, and high market demand, the cultivation of
L. maculatus is becoming more widespread. According to the 2022 China Fisheries Statistical Yearbook, 199,106 tons of this fish are produced in China [
14]. In light of this, the authors of this study examined the effects of increased carbohydrate intake on growth performance, plasma biochemical indices, intestinal and liver enzyme activities, liver glucose metabolism gene expression, and intestinal microflora in
L. maculatus.
4. Discussion
As one of the three main sources of energy, carbohydrates are also one of the least expensive. Carbohydrates are added to the feed and utilized effectively, lowering feed costs and reducing the need for protein [
21]. High-carbohydrate diets have been linked to low disease resistance, slow growth, and high mortality in fish, according to earlier research [
22]. In the current study, the CF in the HCD group was noticeably higher than that in the NCD group, which was comparable to hybrid snakehead [
23]. The growth balance was evaluated using the CF [
24]. Therefore, it is hypothesized that the rise in CF shows that increased carbohydrate levels might promote lipid deposition. The SR, WGR, SGR, and VSI in the HCD group dropped, indicating that a 30% cornstarch level could negatively affect the growth of
L. maculatus and cause some nutritional stress, similar to what occurs in
Micropterus salmoides [
25]. These findings suggested that the inability of fish to efficiently utilize carbohydrates may be related to their congenital diabetes [
26]. Specifically in the liver or abdominal cavity, carbohydrates are transformed into glycogen through glycogen synthesis or lipid through lipid synthesis [
27]. High carbohydrate intake improved liver glycogen, HSI, CI, and VAI in the current study. Similar results were seen for HSI and hepatic glycogen in other fish species, including
Nile tilapia and
M. amblycephala [
3,
28]. The steady rise in HSI, glycogen, or lipid is thought to be the outcome of either glycogen deposition or lipid deposition in
L. maculatus.
An essential biomarker for assessing the body’s health is the blood indicator [
27]. Many fish species (mostly carnivorous fish) exhibit chronic postprandial hyperglycemia after being fed digestible carbohydrates, which stimulates INS secretion [
27]. In the present study, high carbohydrate intake caused higher INS. Reducing sugars (like glucose, for example) and free amino groups on proteins, lipids, and nucleic acids intensify their non-enzymatic glycosylation process, which results in the formation of irreversible Maillard products AGEs [
29]. In mice, AGEs disrupted the metabolism of glucolipids and enhanced the inflammatory reaction [
30]. GSP is a glycated protein with ketamine bonds created by a non-enzymatic glycation process between blood glucose and the amino group at the N-terminus of albumin and other protein molecules [
31]. High-carbohydrate stimulation on
M. amblycephala results in an increase in GLU, AGEs, and GSP, which is similar to the findings of the present study [
32]. The glycolysis cycle produces PA, which can be changed into lactic acid [
33]. High carbohydrate intake in the current study increased plasma PA. The balance of lipid metabolism depends on the transport of TC by HDL and LDL to organs such as the liver [
34]. As a result, an increase in TC levels will likewise cause an increase in HDL and LDL levels. In the present study, elevated levels of TC, TG, HDL, and LDL levels in the HCD group suggested that high carbohydrate intake increased the production of lipids. This result is in line with the previous investigation into
M. amblycephala [
3]. The liver contains the enzymes AST and ALT, which are only released into the bloodstream in the event that the cell membranes and mitochondria of the liver are damaged [
35]. In this study, high carbohydrate intake led to a rise in AST and ALT values. These findings suggested that
L. maculatus’s liver health had been negatively impacted by a high-carbohydrate diet.
The organism’s ability to absorb and use nutrients can be seen in the activity of intestinal digestive enzymes. Chymotrypsin is a proteolytic enzyme released by the pancreas and can reflect how an organism uses proteins [
36,
37]. In the present study, the chymotrypsin activity of the HCD group was significantly higher than that in the NCD group, and this finding demonstrated that raising the level of carbohydrates promoted
L. maculatus to use protein. Similar findings were presented in a previous study on
C. carpio songpu, which discovered that the protease activity in the low-starch group was significantly lower than that of the high-starch group [
36]. The study of
Phoxinus lagowskii Dybowski showed that both omnivorous fish and herbivorous fish have a promoting effect on protease activity after the ingestion of high-carbohydrate feed [
38]. In the study of
S. meridionalis, carbohydrates slightly changed the activity of the protease activity. According to research on
S. meridionalis, the variations in amylase activity at different carbohydrate levels were not statistically significant [
39]. In contrast, the results of the present study indicated that amylase activity was significantly higher in the HCD group than in the NCD group, which is comparable with those found in
Acanthopagrus schlegelii,
Pseudosciaena crocea, and carp [
40,
41,
42]. According to these findings, high dietary carbohydrate promotes glucose metabolism. One of the intestinal digestive enzymes, lipase, is involved in lipid synthesis [
43]. In the current study, lipase activity was significantly higher in the HCD group than in the NCD group. Given that the findings were consistent with the elevated TC and TG levels in the plasma and the lipid accumulation in the liver in our investigation, we assume that a high-carbohydrate diet may promote lipid synthesis in
L. maculatus. A similar result was obtained on
Phoxinus lagowskii Dybowski [
38]. However, studies on
A. schlegelii and
S. meridionalis have demonstrated that intestinal lipase activity is not significantly affected by dietary carbohydrate levels [
42,
44]. There is disagreement on how dietary carbohydrates affect lipase, and there are no reliable results. This topic might be further studied in the future.
SOD and CAT are crucial enzymes in the body’s first line of defense against the production of free radicals and other reactive chemicals in cells. Free radicals cause a number of diseases as they accumulate in the body [
45]. MDA, the end product of polyunsaturated fatty acid (PUFA) degradation, is a marker of lipid peroxidation [
46]. The body’s antioxidant system can be evaluated for functionality using T-AOC [
47]. In this study, SOD, CAT, and T-AOC activities were significantly lower in the HCD group compared to the NCD group, although the MDA level was the opposite. It was hypothesized that high levels of carbohydrates would limit the body’s ability to produce antioxidants and result in a significant amount of the harmful chemical MDA. This result is similar to the research on
M. amblycephala [
16].
The first key enzyme in glycolytic and metabolic pathways is hexokinase (HK) [
48]. In the present study, the activity of
HK in the HCD group was significantly higher, indicating that high dietary carbohydrate intake may promote the glycolysis response. A similar result was also obtained in a previous study on
Pelteobagrus vachelli [
49]. However, previous studies on common carp and
Dicentrarchus labrax revealed that the presence of carbohydrates has no impact on the activity of
HK [
50,
51]. This could be due to the fact that hexokinase, which is virtually saturated, cannot react to slight fluctuations in blood glucose levels [
52]. As a rate-limiting enzyme,
PEPCK is a phosphoenolpyruvate carboxykinase that participates in the reaction of gluconeogenesis [
53]. Similar to the findings for rainbow trout [
54], the activity of
PEPCK in this study was unaffected by dietary carbohydrate intake. However, some studies suggest that as carbohydrate levels rise,
PEPCK activity declines [
55]. When evaluating glucose metabolism, it is essential to consider not just diet composition but also feeding habits, life stage, and size, among other factors [
27].
In fish species, the intestine is the primary site for digestion and absorption site [
56]. The villi height and muscular layer thickness are indicators of the intestine’s capacity for absorption and digestion [
57]. In the present study, the intestinal villi’s height was reduced, increasing the villi’s spacing in the high-carbohydrate group. This indicated that excessive carbohydrate levels changed the morphology of the gut and therefore reduced its capacity for digestion and absorption. The decrease in SR, WGR, and SGR in the HCD group correlated with the shortening of the intestinal villi, which decreases the contact area of food with the intestinal villi and weakens intestinal digestion. Similar results were also discovered in previous studies on
M. amblycephala [
58] and gilthead sea bream [
59]. The liver, a crucial organ for the metabolism of glucose in fish species, deposits glycogen and lipids when dietary carbohydrate intake is excessive [
60]. According to previous studies, high dietary carbohydrate intake led to pathologic symptoms including lipid droplet vacuolation with displaced nuclei and cytoplasm loss [
61,
62,
63]. Similar to the present study, the liver cells in the HCD group showed many vacuoles. In line with this, oil red O staining revealed a significant rise in lipid droplets in the HCD group. These findings suggested that liver injury in
L. maculatus may occur from high carbohydrate-induced liver lipid accumulation.
In almost all types of organisms, the metabolic pathway and anaerobic energy source known as glycolysis has evolved [
64].
GK is a special type of hexokinase that, strictly speaking, operates on liver glucose as the initial and limiting step in the storage of excess glucose. It occurs in several species [
7,
9]. In the current study, the expression of
GK genes was up-regulated by high carbohydrates. Similar to this, previous studies revealed that the expression of the
GK gene is induced by carbohydrate levels and positively linked with the rise in carbohydrate levels in
C. carpio,
T. ovatus, and
O. mykiss [
52,
65,
66]. According to the results of the current study, high carbohydrate levels had no effect on the expression of
PFK genes, which is in line with the previous findings of
O. mykiss [
67]. However, in
Sparus aurata,
PFK gene expression increased as carbohydrate levels rose [
68].
The liver can replenish and restore glycogen by gluconeogenesis, which can keep plasma glucose steady [
69].
G6pase is mostly found in fish livers, where it is highly active but is inactive in the hearts and muscles of fish [
70]. In previous studies, the expression of the
G6pase gene was affected by high dietary carbohydrate intake in
Erythroculter ilishaeformis [
71]. High dietary carbohydrate intake did not, however, have an impact on the expression of the
G6pase gene in the current study. Similarly, the earlier study found that feeding rainbow trout different starches had no impact on the expression of the
G6pase gene in the liver [
66]. The rate-limiting enzyme,
FBP, is involved in the second step of the gluconeogenesis reaction. According to some earlier studies, dietary carbohydrates cannot regulate the activity or gene expression of
PEPCK and
FBP [
56,
72]. In the present study, high carbohydrate intake had no effect on
FBP gene expression. Similarly, previous studies on
O. mykiss and
M. salmoides found that the
FBP gene in the liver was unaffected by dietary carbohydrates [
56,
73]. In the current study, the expression of the
PEPCK gene was significantly reduced in the HCD group, which is consistent with the results of
Cyprinus carpio [
67]. GSK3-β is an essential gene in glycogen synthesis, and
GP is a key gene for glycogenolysis [
74]. Glucose is stored in liver cells as glycogen, which can be then broken down and converted to glucose and released into the blood [
75]. In the present study, high-carbohydrate diets promoted hepatic glycogen synthesis and inhibited hepatic glycogenolysis in
L. maculatus. Similar results were observed in recent work in
Ctenopharyngodon idella, where gene expression related to glycogen synthesis was significantly increased in the high-carbohydrate group [
9]. In prior work on
Leiocassis longirostris,
GP gene expression in the high-carbohydrate group was likewise significantly reduced [
9].
Animals’ digestive tracts contain intestinal microbiota that are stable and can regulate the metabolisms of glycolipids [
76]. Numerous factors, including fish species, physiological status, feed, and aquatic habitat, have an impact on the intestinal microbiota of fish [
77]. In the present study, it was discovered that
L. maculatus’s intestinal microbial composition was considerably changed by high carbohydrate levels. Similarly, changes in the intestinal microbiota of
T. ovatus were caused by dietary starch levels [
7]. In line with the findings of cobia [
78], the number of phyla Bacteroides gradually rose as the level of carbohydrates increased in our study. Proteobacteria are common in water, soil, flora, and fauna and are members of the Gram-negative phylum. They are pathogens of the digestive system [
79,
80]. In the current study, Proteobacteria grew more in the HCD group. This suggests that
L. maculatus’s susceptibility to diseases was heightened by its high-carbohydrate diet. Similarly, dietary carbohydrates dramatically increased the relative abundance of the Proteobacteria phylum in previous studies on the pearl gentian grouper and
T. ovatus [
7,
81]. Gram-negative bacteria,
Photobacterium damselae, cause septicemic diseases in aquaculture, including sea bass (
Dicentrarchus labrax) and sea bream (
Sparus aurata) [
10]. In the current study,
Photobacterium levels rose in the HCD group, indicating that
L. maculatus is more prone to developing photomycosis when subjected to high dietary carbohydrates.