All animal-related procedures were approved by the Laboratory Animal Care and Use Committee of Keimyung University School of Medicine and conducted in accordance with the recommendations of the Committee (KM-2019-17). The studies are in compliance with the ARRIVE Guidelines for Reporting Animal Research.
Animal model
A total of thirty adult male Sprague-Dawley (SD) rats (Orient Bio, Inc., Seongnam, Korea) weighing 230 to 260 g were used in this study. All experimental procedures conducted in the study were approved by The University Animal Care Committee for Animal Research of Keimyung University. The animals were anesthetized via intraperitoneal injection of a mixture of zolazepam/tiletamine (30 mg/kg, Zoletil®; Virbac, Carros, France) and xylazine (10 mg/kg, Rompun®; Bayer, Leverkusen, Germany). A small linear incision was made in the right axillary skin. The triceps muscle was exposed via blunt dissection and cut horizontally along the midline using a no. 15 blade. Then, the muscle was repaired with three different suture techniques: simple interrupted sutures (simple group, n=10), overlapping sutures (overlapping group, n=10), and splitting-interdigitating sutures (splitting group, n=10; Fig. 1).
Grip strength test
Forelimb grip strength was measured bilaterally using the grasping test as described by Bertelli and Mira.29 The animal was held by its tail, allowed to grip a rigid bar, and then slowly pulled upward until it released its grip. A customized aluminum grip bar was mounted to a force transducer connected to a digital display and recording unit (digital force gauge HF-3000®; Shenzhen Aermanda Technology, Guangdong, China). The test was repeated twice, and the average grip force per weight (N/100 g) was used for the statistical analysis. The person carrying out the testing was blinded to the measurements (Fig. 2). The 5 SD rats per group that were not sacrificed for biopsy at week 1 were subjected to the grip strength, which was performed before surgery to obtain baseline measurements and at postoperative weeks 1, 2, 4, and 8.
Spatial gait symmetry test
A gait test was performed to analyze range of motion by comparing the strides of the forepaw on the operated side with those of the forepaw on the nonoperated side. First, the right forepaw was painted with a thin layer of water-soluble pink dye, and the left forepaw was painted blue. Each rat was placed at the open end of a passageway that was 60 cm in length and covered with a sheet of clear plastic and allowed to proceed to the opposite end in the absence of any external stimuli. As the rat voluntarily proceeded through the passageway, its steps were recorded on an underlying sheet of paper. Spatial symmetry was calculated as the ratio of the step length (distance from the left forepaw to the right forepaw) to the stride length (distance from the left forepaw to next left forepaw) (Fig. 3). A spatial symmetry of approximately 0.5, which suggested that the right foot strikes (operated side) were spatially centered between two left foot strikes (nonoperated side), indicated a spatially symmetrical gait. A spatially nonsymmetrical gait indicates that the rat may have problems stretching the right forelimb or shifting its weight from the right forelimb to the left forelimb. The 5 SD rats per group that were not sacrificed for biopsy at week 1 were subjected to the spatial gait symmetry test at postoperative weeks 1, 2, 4, and 8.
Histological analysis
After 5 SD rats per group were sacrificed in a carbon oxide chamber at postoperative weeks 1 and 8, the triceps muscles were isolated for histological and immunohistochemical examination.
The specimens were fixed in formalin, embedded in paraffin, and sectioned into 5-μm-thick slices. Standard hematoxylin and eosin (H&E) staining was performed to evaluate the inflammatory cell response and general morphological features. The tissue samples were observed using a light microscope. All slides were reviewed by pathologists blinded to the study conditions.
Western blot analysis
Rabbit polyclonal antibodies against IL-1 (Santa Cruz Biotechnology, TX, USA) and TNF-α (Abcam, Cambridge, UK) were used as primary antibodies; the expression of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a housekeeping gene, was also measured with a specific antibody. Immunoreactive bands were detected by image scanning using a Fusion FX system (Vilber, Collégien, France).
Immunohistochemistry
Formalin-fixed, paraffin-embedded, 5-μm-thick tissue sections were subjected to automated immunohistochemistry with a Ventana BenchMark XT immunostainer (Ventana Medical Systems, AZ, USA). The sections were incubated with a mouse anti-TNF-α antibody (Abcam, Cambridge, UK) diluted 1:10000 and a mouse anti-IL-1β antibody (Santa Cruz Biotechnology, TX, USA) diluted 1:5000 for 32 min and then visualized with an Optiview DAB IHC Detection Kit (Ventana Medical Systems, AZ, USA ) following amplification of the signal. The specimens were counterstained with a Ventana kit (hematoxylin for 4 min and Bluing Reagent for 4 min).
To detect regenerating muscle fibers, fluorescence immunohistochemistry was performed with anti-laminin (Novus Biologicals, CO, USA) and anti-MyoD antibodies (Santa Cruz Biotechnology, TX, USA). Each specimen was also stained with DAPI to visualize the nuclei of mitotic cells. Immunohistochemistry was carried out using typical methods.
Statistical analysis
Spatial gait symmetry and grip strength were statistically analyzed using two-way ANOVA with GraphPad Prism 8TM (GraphPad Software, Inc., CA, USA). Differences with a value of p < 0.05 were considered statistically significant.