Tooth extraction and subsequent dental implant placement in Sprague-Dawley rats induce differential changes in anterior digastric myofibre size and myosin heavy chain isoform expression.

Abstract

OBJECTIVE\nto determine if tooth loss and dental implant placement in rats induce changes in the morphological and histochemical features of the Anterior Digastric muscle.\n\n\nDESIGN\nAdult male Sprague-Dawley rats had their right maxillary molar teeth extracted. Extraction-1 and Extraction-2 groups were sacrificed, respectively, 4 or 8 weeks later, and an Implant group had an implant placement 2 weeks after the molar extraction, and rats were sacrificed 3 weeks later (n\u2009=\u20094/group). Naive rats (n\u2009=\u20093) had no treatment. Morphometric and immunohistochemical techniques quantified Anterior Digastric muscle myofibres cross-sectional area (CSA) and myosin heavy chain (MyHC) isoform proportions. Significant ANOVAs were followed by post-hoc tests; p\u2009<\u20090.05 and 0.1 were considered to reflect levels of statistical significance.\n\n\nRESULTS\nIn naïve rats, the peripheral regions of the Anterior Digastric muscle was dominated by MyHC-IIx/b isoform and there were no MyHC-I isoforms; the central regions dominated by MyHC-IIx/b and MyHC-IIa isoforms. Compared with naive rats, tooth extraction produced, 8 (but not 4) weeks later, a decreased proportion of fast-contracting fatigue-resistant MyHC-IIa isoform (p\u2009=\u20090.08), and increased proportion of fast and intermediate fatigue-resistance MyHC-IIa/x/b isoform (p\u2009=\u20090.03). Dental implant placement following tooth extraction attenuated the extraction effects but produced a decreased proportion of fast-contracting fatiguable MyHC-llx/b isoform (p\u2009=\u20090.03) in the peripheral region, and increased inter-animal variability in myofibre-CSAs.\n\n\nCONCLUSIONS\nGiven the crucial role that the Anterior Digastric muscle plays in many vital oral functions (e.g., chewing, swallowing), these changes may contribute to the changes in oral sensorimotor functions that occur in humans following such treatments.