Introduction
As a rule, the highest achievements in sports competitions are associated with extreme physical and emotional stress, which imposes increased demands on health. In most cases, overwork and overtraining are superimposed on each other, giving a symptom complex of an organism’s function disturbances, including the central nervous system (CNS), which can be considered a neurosis (Kholodny et al., 2021; Meftahi et al., 2023). Overfatigue disrupts the coherence of interactions between the cerebral cortex, underlying parts of the nervous system, and internal organs (Ilyin & Alvani, 2016; Jaber Al-Mamoori et al., 2022).
Allogeneic biomaterial, including skeletal muscle tissue, is known as a regeneration stimulator when applied locally (Lebedeva et al. 2019a). However, studies of systemic influence, remote action, and feedback have not previously been conducted. To identify the pharmacological effects of the allogeneic biomaterial on the central nervous system, the behavioral despair test or Porsolt forced swimming test (forced swimming to complete fatigue with a load that reflects the state of depression of the animals) was performed. This complex, severe stress test combines physical and emotional components (Khabibullin et al. 2019). This research aimed to study the experimental animals’ cerebral cortex structure after forced physical activity and allogeneic biomaterial use.
Materials and Methods
The experiment involved mature male Wistar rats weighing 200–240 g (n=20). The rats were kept in plastic cages at 22-24 ºС, fed with pelleted mixed fodder. Water was supplied ad libitum. Before starting the forced swimming test, all experimental rats were allowed to swim for 3 days without a load for 10 minutes once a day.
The model of anaerobic physical activity was chosen as the method of forced swimming of rats until complete fatigue with a load—the Porsolt test, or the despair test (Zhou et al., 2021) in modification (patent for invention No. 261706 dated April 21, 2017). The swimming test was conducted daily for 30 consecutive days, from 9:00 to 11:00 AM. The weight of the animals was measured daily. The weight of the load was selected following the weighing results and was equal to 10% of the body weight.
In the main group (n=10), after all 30 training sessions, a dispersed allogeneic biomaterial (BMA) suspension was injected intramuscularly. One vial (10 mg) was diluted in 5 mL of saline for a 0.2% concentration. A total of 8 intramuscular single injections were made into the muscles of the thoracic limbs, including the shoulder biceps (m. biceps brachii), the superficial muscles of the forearm flexors, the ulnar and radial flexors of the wrist (m. flexor carpi ulnaris, m. flexor carpi radialis), and the pelvic limbs (gastrocnemius (m. triceps surae), and quadriceps femoris (m. quadriceps femoris). Then, 0.5 mL of BMA suspension was injected (4 mL). The dose of BMA was chosen arbitrarily. As BMA dispersed form, the alloplant biomaterial was used with a particle size of 50–80 μm. The alloplant biomaterial was developed at the All-Russian Center for Eye and Plastic Surgery, Ministry of Health of the Russian Federation, Ufa. The biomaterial is manufactured following the technical specifications 42-2-537-87, certified and approved for use in clinical practice by order of the Ministry of Health of the USSR No. 87 901-87 of July 22, 1987. For the present study, BMA was made from the extracellular matrix of rat tendons. In the control group (n=10), the animals were injected with physiological saline in similar zones and at the same volume.
Five and twenty-one days after the injections, a tolerance load test was performed, and swimming time (minutes) was recorded. After that, the animals were killed by insufflation of a chloroform vapor lethal dose (695 mg/kg) (Customs Documents, 2024). Next, decapitation and extraction of the brain were carried out. For histological examination, tissue pieces of the precentral gyrus were fixed in a 10% neutral formalin solution, dehydrated in increasing alcohol concentrations, and embedded in paraffin according to the generally accepted method. Histological sections were prepared on a LEICA RM 2145 microtome (Germany) and stained with hematoxylin and eosin (H&E).
Four-µm thick paraffin sections were stained using a Leica Microsystems Bond™ immunohistotainer (Germany) for immunohistochemical studies. The primary antibodies used were CD 68 diluted at 1:300 (ED1 clone), Gfap at 1:300, and bcl-2 (Santa Cruz Biotechnology, USA). The indirect streptavidin-biotin detection system Leica BOND (Novocastra™, Germany) was used for staining (Ozawa, 2019; Magaki et al., 2019; Sukswai & Khoury, 2019; Moreno et al., 2022; Prichard, 2014).
For electron microscopic examination, tissue pieces were fixed in 2.5% glutaraldehyde solution prepared in cacodylate buffer (pH 7.2–7.4) with additional fixation in 1% OsO4 solution in the same buffer. The material was dehydrated in alcohols of increasing concentration and poured into Epon-812 according to the generally accepted method. One-µm thick semithin sections were preliminarily prepared and stained with toluidine blue in a 2.5% anhydrous soda solution. In these sections, areas for electron microscopic examination were selected. Semithin and ultrathin sections were prepared on an EM UC 7 ultramicrotome (Leica, Germany). Ultrathin sections were counterstained with a 2% aqueous solution of uranyl acetate and lead citrate, according to Reynolds, and studied under a JEM-1011 transmission microscope (Jeol, Japan) at an accelerating voltage of 80 kV (Condello et al., 2013; Kim et al., 2021; Klang et al., 2013).
Cells were counted in 20 fields of view for each sample. The examination and visualization of samples were carried out using a Leica DMD 108 microscope (Germany) with specialized software for controlling settings and image capture. Kruskal-Wallace rank analysis of variance was used: Median (Me) and quartiles (Q1 - 25%; Q3 - 75%), and the Mann-Whitney test to compare the results of individual observation periods within one series of experiments or between them (Schlattmann et al., 2019). Differences were considered statistically significant at P<0.05. The SPSS software, version 10 was used for all analyses.
Results
In the experimental group after the administration of BMA, after 5 days, the Me level of multiplicity was significantly (Z=2.17, P<0.04) higher than in the control group: Me=1.70 (Q1=1.46, Q3=2.01) and Me=1 (Q1=0.62, Q3=1.14). After 21 days in the experimental and control groups, the level of multiplicity increased (Me=1.88; Q1=1.88, Q3=2.02, and Me=1.47; Q1=1.37, Q3=1.56), but it was not significant (Z=0.96, P>0.37 and Z=1.85, P>0.07, respectively). At the same time, in the experimental group, the higher multiplicity level over the control group remained statistically significant (Z=2.13, P<0.04; Figure 1)
Morphological analysis revealed that in the control group, after 5 days, in the cerebral cortex of the precentral gyrus, all the cell layers characteristic of the cerebral cortex were traced. However, there were many hyperchromic pyknomorphic nerve cells of medium and small sizes with a dense, elongated nucleus and jagged edges, containing a dense osmiophilic nucleoplasm, in which signs of chromatin disorganization and condensation were revealed. The optically dark cytoplasm contained hypertrophied Golgi complexes with dilated canals, signs of secretion stagnation, and condensation of the granular cytoplasmic reticulum. These cells were often detected in direct contact with macroglial cells and astrocytes. The perinuclear cytoplasm in these cells was optically clear due to the accumulation of vacuoles and destruction, followed by the reduction of cytoplasmic organelles. In astrocytes, the body and terminal processes surrounding the capillaries were edematous and showed signs of organelle destruction. Lipofuscin inclusions (aging or “wear-and-tear” pigment) were observed in them. Also, certain sections of the basement membrane thickened many pinocytic vesicles in the cytoplasm of endothelial cells and pericytes, microvesicular bodies, which is not typical for the norm. The capillary lumen was not free; it was filled with cell fragments and various inclusions (Figure 2). Consequently, signs of pericellular and perivascular edema were observed, evidence of a breach of the blood-brain barrier.
The neurocyte profiles were sharply expanded, the organelles were vacuolized, and the mitochondria were enlarged and rounded with partial cristae fragmentation. The synaptic apparatus was poorly developed (Figure 3).
In the inner pyramidal layer, along with a small number of hyperchromic neurocytes, light cells were observed, shadows (“melting neurons”), which arose as a result of their chromatolysis (irreversible necrobiotic changes). Microglial cells were often detected in close contact with necrobiotically altered neurocytes, such as Betz cells.
Twenty-one days after the intramuscular injection of physiological saline, signs of trophic disorders in the blood-brain barrier persisted. Destruction of lamellar structures and accumulation of aging pigment were determined in neurons. Apoptotic-altered cells and glial proliferation were noted. All layers of neurons in the cerebral cortex were viewed. The outer granular layer was thinned and sparse—zones of local accumulation of glial cells and scars formed in the surrounding brain tissue. Neurocytes were detected in a state of programmed cell death or apoptosis. The nuclei of these cells were hyperchromic with condensed clumps, and euchromatin was absent. An increased electron density marked the cytoplasm due to ribosomal dispersion. The cisternae of the Golgi complex are vacuolated, sharply dilated, and elongated. Their hypertrophy was observed. Mitochondria are darkly destroyed, and cristae are not determined. The cytoplasm contained numerous phagosomes and residual bodies (Figure 4).
After 5 days, no pathomorphological signs in the form of cell edema and inflammatory cell infiltration were detected in the autopsy material of the cerebral cortex of rats in the experimental group. Identifying all the layers characteristic of the cerebral cortex on histological samples was possible. Pyramidal normochromic neurocytes showed mosaic structural and functional activity in this period. On the one hand, the nucleus was large, outlined by a clear double karyolemma, in which nuclear pores were revealed. Euchromatin uniformly filled the entire karyoplasm. In the cytoplasm, mitochondria of various sizes were found, from rounded to elongated. The lamellar cristae were parallel.
On the other hand, they were swollen and destroyed in places. The mitochondrial matrix is light and moderately edematous. Signs of hyperplasia were determined in the lamellar Golgi complex. Also, both ribosomal rosettes and free ribosomes were observed in the cytosol. The morphological characteristics of these cells’ nuclear elements and cytoplasm are linked to their enhanced functional activity. These neurons formed contact with each other (Figure 5).
Twenty-one days after the intramuscular injection of BMA, the layers of neurocytes of the cerebral cortex were visible. There were no signs of edematous phenomena in the perivascular and pericellular spaces. The neuropil is dense, not sparse. The hemocapillaries had a dense, well-defined basement membrane that formed splits. Pericytes were located in these duplications. The perivascular space was free from pathological changes and inclusions. The end legs of astrocytes adjoined to the basement membrane, tightly covering the hemocapillaries and forming a sleeve. Numerous axon-dendritic and axon-axon synapses were noted in the perivascular field (Figure 6).
Immunohistochemical determination of some functionally significant cells revealed that on the fifth day of observation, the number of GFAP+ cells in the main group was significantly lower than in the control groups (Z=3.7; P<0.0001). On the 21st day, in the experimental and control groups, there was a significant, sometimes double (Z=2.1÷ Z=4.92; P<0.04 ÷ P<0.0001, respectively) decrease in the number of GFAP-cells. However, when using BMA, the level of GFAP cells was remarkably lower than in the control group (Z=3.0, P<0.002). GFAP is manifested in the cytoplasm of astrocytes, which perform a trophic, supporting role, form the glial membrane and the blood-brain barrier, and isolate the receptive surfaces of neurons from extraneous afferent influences but do not conduct nerve impulses (Flanagan et al. 2017; Aziz Anah & Aziz Anah, 2023). A reparative function consists of the proliferation and replacement of dead nerve cells. Therefore, it is a marker of gliosis in the cerebral cortex.
After 5 days, the levels of Bcl-2+ cells in the main group were significantly (Z=3.5 ÷ Z=4.25; P<0.0005÷ P<0.0001, respectively) higher than in the control groups. On the 21st day, the number of Bcl-2+ cells in the main group increased (Z=4.0, P<0.0001). In the control group, the number of Bcl-2+ cells, on the contrary, remarkably decreased (Z=2.18, P<0.03). Bcl-2 suppresses apoptosis in many cellular systems, including lymphohematopoietic and neuronal cells. These cells regulate cell death by controlling mitochondrial membrane permeability (Elgendy et al., 2022).
On the fifth day, the number of CD-68+ cells in the main group was significantly (P<0.004) higher than in the control group. On the 21st day in the main group, the number of CD-68+ cells increased remarkably (Z=5, P<0.0001). In the control group, on the contrary, there were no significant changes (Z=1.1 ÷ Z=0.1, P>0.24 ÷ 0.93) and, as a result, remarkable excess (Z=5.49 ÷ Z= 5.83, P<0.0001) of the main group data over the control group became even more contrasting. CD-68 is a phagocytic macrophage marker. They are microsialin, an enzyme of secondary lysosomes. CD-68 in the cerebral cortex was found in microglial cells (Stankov et al., 2015).
The number of shadow cells in the main group decreased significantly with time (Z=3.1, P<0.002). It turned out to be a multiple and significantly lower than in the control group at all times of observation (Z=5.56 ÷ Z=5.68, P<0.0001) (Table 1).
Discussion
BMA is a cell-free extracellular matrix of allogeneic origin and contains collagen, glycosaminoglycans, and proteoglycans (Lebedeva et al., 2019). Its pharmacological action stimulates tissue regeneration when applied locally, which activates angiogenesis, causes chemoattraction of mesenchymal stem cells, and stimulates their differentiation, followed by induction into tissue-specific tissues. Also, it is an inhibitor of fibrosis during the healing of various tissues (Lebedeva et al., 2021; Lebedeva et al., 2018). BMA exerts its range of influences through the system of mononuclear phagocytes, M1 macrophages, which migrate in response to biomaterial implantation and phagocytize it, acquiring a special phenotype. BMA is an immunostimulator of the cellular link of immunity (Lebedeva et al., 2019b). The remote effect of BMA biodegradation products has not been studied to date. It can be assumed that in response to the introduction of BMA into the muscle tissue of the upper and lower extremities, which were subjected to intense physical activity, they showed an actoprotective effect, which is confirmed by an increase in the level of the tolerant load multiplicity compared to the control group (Baryshev et al., 2022; Kuznetsov et al., 2022; Ponamarev et al., 2022). Normoxic muscle tissues can also contribute to the immune-adaptive defense of various tissues, including the nervous. CD-68 macrophages in nervous tissue have a similar effect by suppressing tissue gliosis. Recovery, stabilization, or stimulation of angiogenesis takes place, and this is observed in the main group. Due to this effect, neurohumoral homeostasis is maintained; it has a neuroprotective effect and leads to a decrease in chromatolysis in neurocytes, which is confirmed by an increase in the number of Bcl-2+ cells in the main group and, consequently, a decrease in the number of GFAP+ and shadow cells.
Conclusion
Forced anaerobic physical activity contributed to the development of pathomorphological changes in the nervous tissue of the cerebral cortex in the precentral gyrus. Signs of cell edema, neuropil, perivascular pool, and synaptic apparatus inactivation in the control group were determined. Pyknosis and chromatolysis of neurocytes ended with focal gliosis. Moreover, these signs persisted for 21 days. The number of GFAP+ cells and shadow cells increased. Also, the number of Bcl-2+ cells was reduced compared to the main group.
Five days after the injection of BMA under prolonged forced swimming with a load, no signs of edema of the nervous tissue were detected. The layers of neurocytes of the cerebral cortex retained a distinct architectonics. Synaptic activity was noted. Structural features of neurocytes also indicated their functional viability: restoration of energy balance, activation of biosynthetic processes and secretory activity, as well as their cooperation. The content of CD68+ macrophages increased.
Therefore, based on the results, the allogeneic biomaterial has a systemic effect on the animal organism. It has actoprotective, neuroprotective, and immunomodulatory effects when locally injected into muscles.
Ethical Considerations
Compliance with ethical guidelines
This work was approved by Bashkir State Medical University Ufa, Russia (No.: 056-00124-21-00; Dated: 12/23/2020).
Funding
This study was funded by the Strategic Academic Leadership Program of the Bashkir State Medical University, Ufa, Russia (Code: PRIORITET-2030).
Authors' contributions
All authors contributed equally to the conception and design of the study, data collection and analysis, interception of the results and drafting of the manuscript. Each author approved the final version of the mnuscript for submission.
Conflict of interest
The authors declared no conflict of interest.
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