1. Mastication was studied in awake rabbits that had previously been prepared for chronic recording of jaw movement and jaw muscle electromyography (EMG) under general anesthesia. Data were stored on tape and replayed for computer-assisted analysis. Most data was taken from the mastication of rabbit chow, but the basic features described in the paper also apply to eating of other foods. The series of movements was divided into cycles, and the phases that compose them, using peaks in the vertical movement, velocity, and acceleration. 2. The whole series of movements from ingestion to swallowing was termed the masticatory sequence. We found, as have others, that the sequence can be divided into three consecutive periods, based on the form of the movements. These were named the preparatory, reduction, and preswallowing series of cycles. 3. The results of earlier studies suggest that the food is transported back to the molar teeth during the preparatory series, ground up during the reduction series, and that the bolus is formed for swallowing during the preswallowing series. 4. The typical cycle of the preparatory series was called type I; it had two phases: opening (O) and fast closing (FC). The jaw-opening muscles were very active during O, but EMG bursts from the closer muscles were small or undefinable during FC. There was not much movement away from the midline in either phase, and the cycles were the shortest in the sequence. 5. The reduction series was predominantly composed of type II cycles. These were of intermediate duration and had three phases [O, a short FC, and a slow closing phase (SC)], during which the pellets were crushed between the molar teeth. The jaw moved toward the working side during FC. At or soon after the start of SC, the closer muscles became very active and continued to contract as the teeth were drawn toward the midline and slightly backwards. 6. The preswallowing series was made up of five-phase cycles that we called type III. These were the longest of the sequence. Jaw opening now occurred in three stages: O1 was the fall from tooth contact to approximately the postural position, O2 was a pause, and O3 was defined as the final movement to maximum opening. The digastric burst occurred during O3. There were again two closing phases, FC and SC, but closer bursts were smaller than in type II, and SC was shorter.(ABSTRACT TRUNCATED AT 400 WORDS)

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Neurons found in the medial bulbar reticular formation were activated by stimulation of the orbital gyrus and responded with antidromic spike potentials to selective stimulation of either the masseter or anterior digastric motoneuron pool in the trigeminal motor nucleus in cats anesthetized with alpha-chloralose. These two kinds of reticular neurons were assumed to be inhibitory neurons projecting to masseter motoneurons (IM neurons) and excitatory neurons projecting to anterior digastric motoneurons (ED neurons), involved in the effects of stimulation of the orbital gyrus on trigeminal motoneurons: inhibition of masseter motoneurons and excitation of anterior digastric motoneurons. Input-output properties of IM and ED neurons were studied intracellularly with the following results: (1) stimulation of the orbital gyrus evoked EPSPs in IM and ED neurons with mono- and polysynaptic latencies; and (2) stimulation of the lingual nerve evoked a spike potential in a few IM and ED neurons after a rather long latency, indicating that the pathways involved in the cortical control of trigeminal motoneurons via IM and ED neurons were basically separate from those responsible for the reflex control by the peripheral inputs. Intracellular injection of horseradish peroxidase revealed that both IM and ED neurons were small or medium in size and the former were smaller than the latter, while none of the large reticular neurons directly projected to the trigeminal motor nucleus. This suggests a possible functional differentiation among bulbar reticular neurons according to cell size.

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