The autoradiographic technique was used to analyze the degeneration and regeneration of sensory nerves to rat molars and gingiva following cut or crush injury to the right inferior alveolar nerve. At 2 days after nerve injury there was almost complete denervation of the first molar, partial denervation of the second molar, and minimal effect on the innervation to the third molar and gingiva. The degree of sensory deficit and recovery for these same rats had been previously determined. Reinnervation of the first molar was analyzed in terms of axon number and location, intensity of axon labeling, and type of nerve injury. At 6 days, neither the cut injury nor crush injury rats had any reinnervation of their first molars. By 7 days, 3 of 4 rats had axons reinnervating first molars; in those teeth there was approximately one-fourth of the normal number of axons in the pulp, and very few axons in the dentin. These rats still had as large a molar sensory deficit as the 7 day rat and 6 day rats that had no reinnervation. By 3 weeks there were one-half to three-fourths of the normal axon numbers in the pulp, one-fourth to one-half of the normal axon numbers in dentin; and sensitivity was at least half-recovered. By 6 weeks, numbers of axons in the pulp and dentin were either normal or slightly less than normal; axons had grown back into dentin to the same depth as in normal teeth; and complete recovery of sensitivity had occurred. The regenerating axons had greater than normal labeling intensity at 1 week and 3 weeks in all rats. Those with the crush nerve injury had somewhat greater numbers of reinnervating axons at 1 week and 3 weeks than the cut injury rats. A structure-function comparison for the molars showed that return of sensitivity correlated with reinnervation of both pulp and dentin.
Return of sensory nerve function in rat molars following cut or crush injury to the inferior alveolar nerve (IAN) was measured by observing the jaw opening reflex (JOR) response of the digastric muscle to electrical stimulation of individual molars or the gingiva. The IAN was injured from a lateral approach to the mandibular ramus at a site approximately 2 mm proximal to the incisor apex. Following nerve injury, the JOR threshold to stimulation of the first molars increased 6-fold: preoperative threshold mean = 47.4 +/- 21.3 microA (n = 27), postoperative threshold mean = 248.5 +/- 127.1 microA (n = 25). A 4-fold postoperative increase in JOR threshold was found for the second molars, and the thresholds were not significantly affected for third molars or gingiva. These postoperative results indicated that the major pathway of sensory innervation to the first and second molars was affected by the IAN injury, whereas the third molars and gingiva had alternate sources of innervation which remained unaffected by the IAN injury. At 1 week following injury, there was partial return of sensitivity, by 3 weeks there was approximately 50% recovery, and by 6 weeks complete return to normal JOR thresholds was found. The degree of sensory deficit, as reflected in JOR inhibition, and the rate of recovery were not significantly different after cut or crush injury in these experiments; however, there was a tendency for greater sensory loss and for more rapid recovery after crush injury. This study forms the basis for a subsequent autoradiographic analysis of nerve location in rat molars of known sensory deficit, partial recovery, or full sensory recovery.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.