Histological features of masticatory muscles after botulinum toxin A injection into the right masseter muscle of dystrophin deficient (mdx-) mice

• Published in: Annals of anatomy Vol. 229; p. 151464
• Main Authors: Botzenhart, Ute Ulrike, Gredes, Tomasz, Gerlach, Ricarda, Zeidler-Rentzsch, Ines, Gedrange, Tomasz, Keil, Christiane
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.05.2020
• Subjects: Animals; Botulinum Toxins, Type A - administration & dosage; Botulinum Toxins, Type A - pharmacology; BTX-A; Collagen - analysis; Disease Models, Animal; Dystrophin - deficiency; Female; Histological features; Image Processing, Computer-Assisted; Injections, Intramuscular; Male; Masseter Muscle - anatomy & histology; Masseter Muscle - chemistry; Masseter Muscle - drug effects; Masseter Muscle - pathology; Masticatory muscles; mdx mice; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscular Dystrophy, Duchenne - pathology; Time Factors; Histological features; BTX-A; Masticatory muscles; mdx mice
• ISSN: 0940-9602; 1618-0402
• DOI: 10.1016/j.aanat.2020.151464

The most frequently used animal model for human DMD (Duchenne muscular dystrophy) research is the mdx mouse. In both species, characteristic histological changes like inflammation, muscle fiber degeneration and fibrosis are the same, but in contrast to humans, in mdx mice, phases of muscle fiber degeneration are compensated by regeneration processes. Therefore, the interest of this study was to evaluate histological features in masticatory muscles after BTX-A injection into the right masseter muscle of wild type and dystrophic (mdx) mice, illustrating de- and regeneration processes induced by this substance. The right masseter muscle of 100 days old healthy and mdx mice were selectively paralyzed by a single intramuscular BTX-A injection. Masseter as well as temporal muscle of injection and non-injection side were carefully dissected 21 days and 42 days after injection, respectively, and fiber diameter, cell nuclei position, necrosis and collagen content were analyzed histomorphologically in order to evaluate de- and regeneration processes in these muscles. Statistical analysis was performed using SigmaStat Software and Mann Whitney U-test (significance level: p < 0.05). At both investigation periods and in both mouse strains fiber diameter was significantly reduced and collagen content was significantly increased in the right injected masseter muscle whereas fiber diameters in mdx mice were much smaller, and these differences were even more apparent at the second investigation period. Necrosis and central located nuclei could generally be found in all mdx mice muscles investigated with an amount of centronucleation exceeding 60%, and a significant increase of necrosis six weeks after injection. In wild type mice central located nuclei could primarily be found in the treated masseter muscle with a portion of 2.7%, and this portion decreased after six weeks, whereas in mdx mice a decrease could also be seen in the non-injected muscles. In contrast, in wild type mice necrosis was not apparent at any time and in all muscles investigated. From our results it can be concluded that in mdx mice masticatory muscles de- and regeneration processes were extended, triggered by a selective BTX-A injection, or mdx mice at this age, independently of BTX-A treatment, went through another cycle of de- and regeneration as a characteristic of this disease.