The results of this research were consistent with the results of the Ameral et al. study (
20). Ameral et al. used 20 four-week-old rats, and, to induce metabolic syndrome, rats received fructose as a drink in combination with water (100 g/L for 18 weeks). Then the subjects were divided into control groups, metabolic syndrome, metabolic syndrome + exercise (walking), and metabolic syndrome + exercise (running) groups. Both training groups (walking and running) started training from the ninth week (5 days a week, 60 minutes each day for 9 weeks). It was observed that animals that received high-dose fructose had significantly higher levels of glucose, triglycerides, and insulin resistance. It seems that the entry of high fructose into the liver, which is the main organ for metabolizing fructose, caused a change in the metabolic pathways and, as a result, increased lipogenesis in the liver, production, and accumulation of triglycerides in the liver, and insulin resistance. All these have caused metabolic syndrome in the rats of the present study (
21).
Insulin resistance caused by high fructose consumption is usually associated with an increase in triglyceride concentration and a decrease in HDL concentration (
20). Research results show that a high intake of refined carbohydrates may increase the risk of developing insulin resistance. Long-term consumption of fructose in the diet can increase the activity of liver lipogenic enzymes, and the synthesis of lipids increases the levels of VLDL and triglycerides (
22).
Also, the results of our research were consistent with the results of Herawati et al., 2020, who investigated the effect of a diet with a high glycemic index (GI). Herawati et al. divided rats into two control groups with a standard diet and a high blood glucose index (HighGL) group. The results of their research showed that the body weight showed a significant change before and after receiving a diet with a high glycemic index, and blood glucose levels increased significantly (
23).
In fact, fructose is converted into fructose 1-phosphate in the liver and causes the separation of glucokinase from its regulatory protein, and, as a result, it leaves the nucleus.
This action may be an opposing factor that sometimes increases with high dietary fructose consumption and excessive use of carbohydrates and fat synthesis in the liver (
24).
Also, the results of this research showed that the induction of metabolic syndrome led to a significant increase in the plasma levels of PTX3, VACM-1, and CRP. In fact, inflammation is the connection point between obesity and metabolic syndrome (
25). Chronic inflammation is associated with metabolic syndrome and obesity. During inflammation, oxidative stress increases while the metabolic balance is not maintained accordingly, and consequently, the disease progresses (
26). Recent studies show that inflammation plays an essential role in various stages of atherosclerosis, such as the beginning and progression and formation of atheroma, instability and rupture of platelets, and vessel stenosis after angioplasty. Adhesion of leukocytes, neutrophils, and monocytes to the endothelium and then the migration of leukocytes through the endothelium into vessel walls is one of the main characteristic stages of the inflammation process. The results of these studies show the relationship between inflammation and cardiovascular diseases (
27).
Proteins with alternating concentrations in the plasma and blood serum of humans and animals due to inflammation, necrosis, and bacterial and viral infections are called acute phase proteins or APPs.
The role of these proteins is to reduce the inflammatory effects in the tissues, remove inflammatory agents, remove and destroy damaged tissue parts, and finally restore the tissue. Therefore, it can be concluded that metabolic syndrome in rats leads to inflammation. To fight this inflammation, the body will start to make and secrete acute-phase proteins in the liver using the innate immune system (
28). The results of the present study demonstrated eight weeks of high-intensity interval training significantly reduced the plasma levels of PTX3, VACM-1, and CRP in male Wistar rats. One of the mechanisms involved in this is the reduction in the production of cytokines secreted from fat tissue (
29). Losing weight and increasing physical activity can affect the immune system by reducing pro-inflammatory cytokines such as TGFB, TNFR, TNF-α, IL-8, and IL-6. Reducing fat tissue will not only reduce the volume of adipocytes and fat precursor cells but also reduces the number of remaining endothelial cells and macrophages. These cells produce pro-inflammatory mediators such as CRP, serum amyloid protein (SAA), and some cytokines. Weight loss and exercise can increase the gene expression of anti-inflammatory mediators such as IL-10 and IL-1 receptor antagonists in cells. As a result, since the liver is involved in fat accumulation and metabolism, it participates in reducing the production of fibrinogen and pro-inflammatory mediators (
29).
Regular daily exercise has anti-inflammatory and protective effects against cardiovascular diseases and leads to a decrease in serum CRP (
30). The possible mechanism of the decrease in CRP levels after exercise may be due to the decrease in the concentration of interleukins after repeated exercise. One of the cytokines is IL-6, which is secreted by adipose tissue and stimulates liver cells to produce CRP (
7). PTX3 is secreted in inflammation and various types of cells, including skeletal muscle, monocytes, macrophages, endothelial cells, and smooth muscle cells, as well as in atherosclerotic wounds (
31).
The main stimulus for the production of PTX3 in the human body is TNF-α. TNF-α plasma levels decrease due to long-term exercise; therefore, decreasing the levels of TNF-α will decrease the levels of PTX3. On the other hand, regular and long-term sports activity limits myeloperoxidase produced by neutrophilsm. Myeloperoxidase is secreted from myeloid cells in neutrophils, and its excessive production causes atheroma formation, rupture of atherosclerotic plaques, and acute coronary events. Therefore, the limitation of myeloperoxidase as a result of long-term sports activity reduces the production of PTX3 by neutrophils. In addition, regular exercise reduces the capacity of monocytes to release PTX3 (
32).
In relation to reducing the levels of vascular adhesion molecules due to interval training, it should be said that interval training decreased the production of TNF-α by increasing the activity of the sympathetic system and increasing anti-inflammatory cytokines. Due to the fact that the secretion of adhesion molecules is stimulated due to the increase in the secretion of inflammatory cytokines, the reduction of pro-inflammatory factors reduces the release of chemical mediators and the reduction of pro-inflammatory transcription factors, such as nuclear factor kappa (NF-Kβ), which can be effective in modulating vascular inflammation, and, subsequently, the concentration of adhesive molecules will decrease (
33). Another mechanism includes the release of catecholamines in the blood circulation after exercise, in a manner that, with the increase of epinephrine, usually the serum levels of adherent cells decrease (
34). In addition, the beneficial effects of exercise on endothelial function include the increase of plasma HDL-c levels, which can lead to the release of prostacyclin-2 (PGL-2) from muscle cells and prevent plaque accumulation and reduce vascular adhesion molecules in the body (
35).
5.1. Conclusions
Induction of fructose diet-induced metabolic syndrome in male Wistar rats, and this metabolic syndrome significantly increased the plasma levels of PTX3, VACM-1, and CRP. However, eight weeks of interval training significantly reduced the plasma levels of PTX3, VACM-1, and CRP in rats with metabolic syndrome.