|Year : 2016 | Volume
| Issue : 3 | Page : 91-98
The effect of cerebrolysin treatment on skeletal muscle healing in adult albino rat: a histological and immunohistochemical study
Gamal H Mohamed MD , Mohamed H Shaaban
Department of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt
|Date of Submission||19-Apr-2016|
|Date of Acceptance||10-Jul-2016|
|Date of Web Publication||16-Dec-2016|
Gamal H Mohamed
Assisted Professor of Anatomy and Embryology Faculty of Medecine Cairo University, Shoubra, Cairo
Source of Support: None, Conflict of Interest: None
The aim of this study was to evaluate the role of Cerebrolysin in muscle healing in vivo.
Materials and methods
Twenty adult albino rats were used in this study. Both right and left gastrocnemius muscles of the albino rats were cut at 60% of their length from their distal insertion through 75% of their width and 50% of their thickness and then sutured with simple sutures using absorbable catgut sutures. The gastrocnemius muscles of all albino rats were injected directly in the lesion with 100 ng/ml/kg of cerebrolysin at 1, 3, and 5 days after laceration. The sham control muscles were subjected to the same treatment but were injected with the same volume of physiological normal saline. One week after the injury the animals were killed and the gastrocnemius muscles were removed and processed for paraffin sectioning and stained with hematoxylin and eosin, Bcl-2 (B-cell lymphoma 2), and P53 (tumor suppressor gene) immune peroxidase stains.
There was a significant increase in the mean myonuclei/myofiber diameter ratio and the size of the regenerating myofibers as an index of muscle regeneration in the cerebrolysin-injected group compared with the control. It is anticipated that cerebrolysin is a potent stimulator of muscle regeneration in vivo. It has also been found that regenerating myofibers were located both in the deep and the superficial areas of the injured site of muscles only when treated with cerebrolysin, thereby demonstrating greater initial healing when the injured muscle is treated with cerebrolysin. Cerebrolysin retarded apoptosis in neutrophils, macrophages, and other inflammatory cells by activating the anti-apoptotic Bcl-2 (B-cell lymphoma 2) protein leading to accumulation of these inflammatory cells.
This study has shown that injections of cerebrolysin into an injured muscle improved muscle healing in vivo. Also, documents the occurrence of a protective Bcl-2 in inflammatory neutrophils and macrophages, which were expressed in cerebrolysin-treated muscles, leading to enhancement of the effect of these inflammatory cells. We have also found that Inflammatory cells play a role in satellite cell activation and proliferation but, the tumor suppressor gene p53, which is recognized as a central regulator of cell cycle and apoptosis, had no role in muscle regeneration in this in-vivo study.
Keywords: Bcl-2, cerebrolysin, muscle regeneration, muscle trauma, p53
|How to cite this article:|
Mohamed GH, Shaaban MH. The effect of cerebrolysin treatment on skeletal muscle healing in adult albino rat: a histological and immunohistochemical study. Kasr Al Ainy Med J 2016;22:91-8
|How to cite this URL:|
Mohamed GH, Shaaban MH. The effect of cerebrolysin treatment on skeletal muscle healing in adult albino rat: a histological and immunohistochemical study. Kasr Al Ainy Med J [serial online] 2016 [cited 2018 Mar 18];22:91-8. Available from: http://www.kamj.eg.net/text.asp?2016/22/3/91/195888
| Introduction|| |
Skeletal muscle regeneration after injury is both rapid and efficient; in the rodent, muscle patterning and contractile ability are regained within days of myonecrotic injury, with complete recovery of mass and strength within 21 days. ‘This process is dependent on satellite cells, the resident stem cell of skeletal muscle. When stimulated by factors released by damaged muscle, satellite cells rapidly exit the quiescent state and proliferate extensively to build up a supply of adult myoblasts, which will subsequently differentiate and fuse either with each other or with existing myofibers to repair local damage .
Satou et al.  showed that ‘in the normal state, these satellite cells remain in a nonproliferative quiescent state. On the other hand, in response to stimuli such as cerebrolysin injection, remodeling, denervation, or muscle injury, satellite cells become activated and stimulated to enter the cell cycle. They appear as a swelling on the myofibers with cytoplasmic processes extending from one or both poles of the cell’. ‘Satellite cells proliferate and express myogenic markers (now termed myoblasts). Ultimately, during regeneration of damaged skeletal muscle, these cells fuse to existing muscle fibers or fuse together to form new myofibers’ .
‘During regeneration after cerebrolysin injection, macrophages are essential in the repair process as they secrete a collection of cytokine factors that regulate the satellite cell pool’ . ‘Importantly, in the presence of an enhanced macrophage response, there is an increase in satellite cell proliferation and differentiation’ . Madison et al.  suggest that regulation of macrophage apoptosis may be pivotal in the outcome of an inflammatory response. The cytokines, which are a unique family of growth factors, might either promote or prevent macrophage apoptosis. This process is effectively reversed by the addition of growth stimuli, suggesting that apoptosis may represent the mechanism for eliminating activated macrophages that are no longer necessary as inflammation wanes.
‘Neurotrophic factors are known to play a crucial role in neural growth and differentiation. Neurotrophic factors are produced by various cell types including vascular smooth muscle cells and fibroblasts following wounding’ . ‘They might play an accessory role in the regulation of immune and inflammatory reactions through stimulation of chemotactic migration of human polymorphonuclear leukocytes both in vitro and in vivo. They also have an additional role in promotion of the proliferation, growth, and differentiation of other blood elements’ . Gharaibeh et al.  observed that ‘neurotrophic factors are a potent stimulator of myoblast proliferation and fusion in vitro. However, their role and effect on muscle healing following trauma need further investigation. Therefore, the present work was carried out to study the effect of cerebrolysin on the early events of muscle regeneration following mechanical injury in vivo’.
| Materials and methods|| |
Twenty adult male albino rats obtained from the Animal House, Faculty of Medicine, Cairo University, were used in this study. Their ages varied from 2 to 3 months (birth date recorded on the cage), and they weighed 200–300 g. They had free access to standard diet and drinking water. The animals were housed in polypropylene cages and maintained under standard laboratory conditions (temperature 25±2°C, 12:12 h; light–dark cycle and 50±5% relative humidity with free access to food and water). They were acclimatized to laboratory conditions before the test (5 min daily for 1 week). All experiments were carried out during the light period (08:00–16:00 h). This study was carried out according to the international ethics standard for animal experiments and was approved by the Kasr Al-Ainy Experimental Ethics Committee.
Cerebrolysin (100 ng/ml) injected directly into the lesion was obtained from Arzneimittel Pharmaceutical Laboratories, Unterbach, Austria, Europe.
The animals were randomly divided into two equal groups (10 rats each):
Group I (controls): In this group two plain control rats were not subjected to any procedure and eight sham control rats were anesthetized with ether inhalation. This method of anesthesia was suitable as the surgical procedure required only a few minutes. Injury to skeletal muscle was induced by subjecting gastrocnemius muscles to a cut injury as described by Menetrey et al. . Under sterile precautions both right and left gastrocnemius muscles of the albino rats were cut at 60% of their length from their distal insertion, through 75% of their width and 50% of their thickness, and then sutured with simple sutures using absorbable catgut sutures (6-0) with rounded nontraumatic needles. The severity of the lesion sustained by the muscle had been previously determined as a grade III injury according to the classification of Buckwalter et al. . A nonabsorbable suture such as prolene was used for skin sutures and served as a mark for injection. All albino rats were injected directly in the lesion of the gastrocnemius muscles with the same volume of physiological normal saline at 1, 3, and 5 days after injury using a microsyringe.
Group II: In this group, as in sham controls, the gastrocnemius muscles of all albino rats were injected directly in the lesion with 100 ng/ml/kg of cerebrolysin at 1, 3, and 5 days after injury using a microsyringe. Animals were killed with an overdose of ether inhalation on the seventh day after the injury, and the gastrocnemius muscles were removed and processed for histological examination.
Histological study: The isolated gastrocnemius muscles of both sides were fixed in 10% neutral formalin and processed for paraffin sectioning. For histological analyses, 4–6 mm cross and longitudinal sections were collected along the entire length of the muscle and at the site of the lesion to evaluate muscle regeneration. The sections were stained with hematoxylin and eosin.
Immunohistochemical study: It was performed using streptavidin–biotin peroxidase complex  using monoantibodies for Bcl-2 (B-cell lymphoma 2: Ab-3 1 : 501; Lab Vision, Fremont, California, USA) and P53 (tumor suppressor gene: Do-7 prediluted IgG, Kappa; Dako AS, Copenhagen, Denmark) and counterstained with hematoxylin. All selected sections were examined and photographed using an Olympus microscope, Olympus Corporation, Shinjuku, Tokyo, Japan.
Quantitative study: Sections containing the largest area of damage were selected for analysis. An image of the core of the damaged area, defined as the region that was least regenerated, was taken. For analysis of control muscles, sections were selected from the same anatomical region as those from injured muscles. The diameter of the regenerating myofibers in both group II and sham control muscles was measured from photomicrographs. Centronucleated cells were considered as regenerating myofibers. All the centrally nucleated myofibers within this field were counted and their diameters were measured and compared with those of the sham control muscle. Nuclei at the periphery of the myofibers (satellite cells nuclei and myonuclei) were counted and the mean number and ratio of their diameter compared with myofiber diameter. Nucleocytoplasmic ratio was calculated and measured in group II and sham control muscles .
Statistical analysis: The diameters of the regenerating muscle fibers and the nucleocytoplasmic ratio were compared in all groups using a paired Student t-test. The satellite/myonuclear number was compared in all groups using the Mann–Whitney test. All values are expressed as means±SD. Significant difference was considered at P value less than 0.05.
| Results|| |
Histological examination of group I
In plain controls the muscle was seen covered in a layer of connective tissue known as the epimysium. The muscle was arranged in bundles of fibers, known as fasciculi, which were seen surrounded by another connective tissue, called the perimysium. Endomysium, which insulates each muscle fiber, was also seen. Muscle fibers or myofibers appeared as multinucleated syncytium with a striated appearance resulting from the regular pattern of sarcomeres within the cells ([Figure 1]). Sham control muscles showed signs of degeneration and acute inflammation. There was invasion of the site of laceration by inflammatory cells seen perimysial and endomysial. Some degenerated muscle fibers appeared pale, and others with interstitial edema ([Figure 2]). In longitudinal sections, degenerated muscle fibers appeared pale and contracted and were invaded by phagocytic inflammatory cells ([Figure 3]). New regenerating myofibers identified by their centrally located nuclei and basophilic sarcoplasm were found deep to the site of laceration, whereas the superficial part was infiltrated by inflammatory cells ([Figure 4]).
|Figure 1 Photomicrograph of a longitudinal section of a plain control muscle showing muscle fibers or myofibers appearing as multinucleated (arrows) syncytium with striated appearance (s), resulting from the regular pattern of sarcomeres within the cells. Endomysium, which insulates each muscle fiber, was also seen (*) (hematoxylin & eosin, ×400).|
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|Figure 2 Photomicrograph of a transverse section of a sham control muscle 1 week after injury at the site of the lesion showing degenerated muscle fibers (arrows) and infiltration of the area by inflammatory cells (arrowheads) (hematoxylin & eosin, ×100).|
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|Figure 3 Photomicrograph of a longitudinal section of a sham control muscle 1 week after injury at the site of the lesion showing pale contracted muscle fibers invaded by inflammatory cells (arrows) (hematoxylin & eosin, ×400).|
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|Figure 4 Photomicrograph of a transverse section of a sham control muscle 1 week after injury at the site of the lesion showing a few regenerated myofibers (arrowheads) in the deep part of the section (d). The superficial part of the section (s) infiltrated by inflammatory cells (hematoxylin & eosin, ×100).|
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Immunohistochemical examination of group I
In the sham control sections stained with immunoperoxidase with anti-Bcl-2 monoclonal antibodies, there was an invasion of the injury site by inflammatory cells, mainly granulocytes, which were negatively expressing Bcl-2 ([Figure 5]). Fibroblasts, fibrocytes, and lymphocytes were seen among the regenerating myofibers and were positively stained with Bcl-2 ([Figure 6]). The sham control sections stained with immunoperoxidase with anti-p53 monoclonal antibody showed that p53 protein was not expressed in the nuclei of the satellite cells (peripheral nuclei) in the quiescent ([Figure 7]), active, or differentiated stages ([Figure 8]).
|Figure 5 Photomicrograph of a longitudinal section of the sham control muscle 1 week after injury at the site of the lesion showing degenerated muscle fibers (arrows) and infiltration of the area by negatively stained (blue) inflammatory cells, mainly granulocytes (arrowheads) (Bcl-2 immunoperoxidase stain, ×100).|
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|Figure 6 Photomicrograph of a transverse section of a sham control muscle 1 week after injury at the site of the lesion showing positively stained (brown) fibrocytes (arrows) and inflammatory cells, both lymphocytes (arrowhead) and macrophages (short arrows) (Bcl-2 immunoperoxidase stain, ×400).|
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|Figure 7 Photomicrograph of a transverse section of a sham control muscle 1 week after injury away from the site of the lesion showing negatively stained nuclei (blue) of the quiescent satellite (peripheral) cells (arrows) (P53 immunoperoxidase stain, ×400).|
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|Figure 8 Photomicrograph of a transverse section of sham control muscle 1 week after injury at the site of the lesion showing negatively stained nuclei (blue) of the satellite cells and myonuclei (arrows) in the regenerated myofibers (P53 immunoperoxidase stain, ×400).|
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Histological examination of group II
Muscles showed signs of degeneration and acute inflammation. There was invasion of the site of laceration by inflammatory cells seen perimysial and endomysial with degenerated muscle fibers appearing pale ([Figure 9]). In longitudinal sections, degenerated muscle fibers appeared pale and contracted and were invaded by phagocytic inflammatory cells ([Figure 10]). The muscles showed many regenerating myofibers uniformly distributed both in the superficial and the deep parts of the laceration ([Figure 11]).
|Figure 9 Photomicrograph of a transverse section of group II muscle 1 week after injury at the site of the lesion showing degenerated muscle fibers with interstitial edema infiltration of the area by inflammatory cells both seen perimysial (arrows) and endomysial (arrowheads) (hematoxylin & eosin, ×100).|
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|Figure 10 Photomicrograph of a longitudinal section of group II muscle 1 week after injury at the site of the lesion showing pale necrotic (M) and lacerated (L) muscle fibers invaded by inflammatory cells (arrows) (hematoxylin & eosin, ×400).|
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|Figure 11 Photomicrograph of a transverse section of group II muscle 1 week after injury at the site of the lesion showing regenerated myofibers (arrowheads) in the deep (d) and superficial (s) parts of the section (hematoxylin & eosin, ×100).|
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Immunohistochemical examination of group II
Bcl-2 protein was strongly positive (dark brown) in the cytoplasm of inflammatory cells. The positive cells were mainly lymphocytes and macrophages; macrophages showed typical kidney-shaped nuclei ([Figure 12] and [Figure 13]). Sections stained with immunoperoxidase with anti-p53 monoclonal antibody showed that p53 protein was not expressed in the nuclei of the satellite cells (peripheral nuclei) either in the quiescent ([Figure 7]), active, or differentiated stages ([Figure 8]).
|Figure 12 Photomicrograph of a transverse section of group II muscle 1 week after injury at the site of the lesion showing positively stained (dark brown) cytoplasm in the inflammatory cell (arrowheads) (Bcl-2 immunoperoxidase stain, ×400).|
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|Figure 13 Photomicrograph of a transverse section of group II muscle 1 week after injury at the site of the lesion showing positively stained cytoplasm of the inflammatory cells, lymphocytes (short arrow), and macrophages with kidney-shaped nuclei (arrowheads) (Bcl-2 immunoperoxidase stain, ×1000).|
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Quantitative histological examination
[Table 1] summarizes the mean diameter±SD of the regenerating myofibers, the mean number±SD of the satellite myonuclear cells, and the mean ratio of the myonuclear/myofiber diameter±SD in both group I and group II. The mean diameter of the regenerating myofibers was 28.1±7.6 in the sham control and 41.3±12.3 in group II. The mean ratio of the myonuclear/myofiber diameter was 0.07±0.02 in the sham control and 0.001±0.03 in group II. The mean number of satellite myonuclei cells was 35.7±8.4 in the sham control and 45.1±15.6 in group II. The mean diameter of the regenerating myofibers and the mean ratio of the myonuclear/myofiber diameter were significantly higher in group II compared with the sham control, whereas the mean number of satellite myonuclei cells in group II was not significantly different from that of the sham control.
|Table 1 The mean diameter of regenerated myofibers and the mean number of satellite/myonuclear cells and the mean myonuclear/cytoplasmic ratio|
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| Discussion|| |
The development of the use of growth factors, which will give quicker and more complete recovery, may significantly affect the downtime after injury. Muscle regeneration following injury depends primarily upon satellite cells and upon other cellular processes involving nonmuscle cells. One of the earliest of these is the inflammatory response, which facilitates myogenesis through phagocytosis of cellular debris and the release of growth factors.
In the present study it was found that when muscle fibers are damaged by cut injury, several overlapping cellular processes, including inflammation and myogenesis, take place. These initial data confirm those of Seale et al. . Skeletal muscle regeneration, initiated by muscle injury, involves the degeneration of damaged myofibers, formation of a hematoma necrosis of muscle tissue, and an inflammatory cell response. Fukushima et al.  reported that ‘neutrophils and macrophages accumulate at the injury zone as early as 30 min after injury. Neutrophils prepare the site for further events in muscle regeneration by releasing compounds that break down both foreign and cellular materials, thus decreasing the likelihood of the wound becoming a route for systemic infection’. They then undergo apoptosis (programmed cell death). ‘Macrophages migrate to the damaged area through the blood stream and from the muscle and surrounding tissue by direct chemotaxis under the effect of soluble signals from tissue destruction’ . Macrophages are thought to be responsible for phagocytosis of the bulk of the macromolecules resulting from damaged myofibers, extracellular matrix, and apoptotic neutrophils. They can also localize the immune responses in the injury zone by producing a large variety of soluble factors . Gharaibeh et al.  ‘showed that release factors such as platelet-derived growth factor and an undefined satellite cell-specific factor stimulate satellite cell proliferation in the injury zone’.
In this study there was a significant increase in the mean myonuclei/myofiber diameter ratio and the size of the regenerating myofibers as an index of muscle regeneration in the cerebrolysin-injected group compared with the control. It is anticipated that cerebrolysin is a potent stimulator of muscle regeneration in vivo. It has also been found that regenerating myofibers were located both in the deep and the superficial areas of the injured site of muscles only when treated with cerebrolysin, thereby demonstrating greater initial healing when the injured muscle is treated with cerebrolysin. This agreed with the results of Hodgetts et al.  and Chazaud et al. , who showed ‘a direct effect of cerebrolysin upon satellite cells or indirectly through upregulation of macrophages, which clean the site of injury by initiating phagocytosis of tissue debris’. Siegel et al.  postulated that ‘during the preparation for the healing process macrophages produce factors that influencing satellite cell proliferation and differentiation through stimulation of its migration and delay its apoptosis by activation of death inhibiting proteins’. Skeletal muscle repair includes activation of satellite cells . ‘When a muscle is damaged, these cells are activated within 18 h of the injury’ . ‘Quiescent satellite cells are activated by various growth factors or myogenic regulatory factors, ‘wound hormones’, which are released from the damaged myofibers and the extracellular matrix surrounding them. This is done through interaction with growth factor receptors on the surface of these cells. Once these satellite cells have undergone differentiation they can fuse to existing muscle cells’ . Musaro et al.  showed that ‘satellite cells fusion allows donating needed myonuclei to the wounded or developing muscle cell. It also appears that these cells are able to migrate, and may move from healthy areas of the muscle to the injured area in response to chemical stimuli and they fuse together to form myoblasts, which in turn fuse to form myotubes’. ‘One of the hallmarks of regenerating myofibers is the centrally located position of the myonuclei. Finally, the regenerated muscle matures and contracts with reorganization of the scar tissue. Upon maturing, muscle fiber nuclei are located along the cell periphery’ .
Inflammation, on the other hand, results in an early and maintained elevation in the levels of cerebrolysin in injured tissue . Li and Huard  postulated that ‘Neutralization of the action of the increased cerebrolysin with specific anti-cerebrolysin antibodies decreases inflammatory hypersensitivity, indicating that this neurotrophin is very important in the production of inflammatory pain’. The systematic and local application of exogenous cerebrolysin has been shown to produce a rapid and prolonged behavioral hyperalgesia in both animals and humans . Such behavior was observed in rats injected with cerebrolysin in this study as they frequently bit their sutures after the injection.
In this study it was found that cerebrolysin retarded apoptosis in neutrophils, macrophages, and other inflammatory cells by activating the anti-apoptotic Bcl-2 (B-cell lymphoma 2) protein leading to accumulation of these inflammatory cells. This was in agreement with the results of Zammit and Beauchamp . Cerebrolysin, on the other hand, has been shown to regulate the life span of both granulocytes and macrophages in vitro .
Tiangco et al.  strongly supported the role of p53 (tumor suppressor gene) in myogenesis in vitro, as expression of p53 increases during differentiation and fusion of skeletal muscle cells. In contrast, myotube formation in vitro is impaired in myogenic cells expressing a dominant-negative p53 protein and in primary myoblasts derived from p53 muscle . This role was not manifested in this in-vivo study. This finding is supported by Foster et al. , who indicated that p53 is not required for the regulation of myoblast proliferation and differentiation and myotube formation in vivo during myogenesis of adult skeletal muscle. This could be explained by the possibility that genes responsible for myoblast differentiation could be upregulated in a way independent of p53 in vivo.
| Conclusion|| |
This study has shown that injections of cerebrolysin into an injured muscle improved muscle healing in vivo. The current study also shows the occurrence of a protective Bcl-2 in inflammatory neutrophils and macrophages, which were expressed in cerebrolysin-treated muscles. It is also concluded that inflammatory cells play a role in satellite cell activation and proliferation. We have also found that the tumor suppressor gene p53, which is recognized as a central regulator of cell cycle had no role in muscle regeneration in this study.
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Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13]