Site of Cortical Utricular Representation with Special Reference to the Somatosensory Barrel Field in the Gerbil

In mammals, the osseous semicircular canals of the vestibular labyrinths are usually embedded in the pyramis of the temporal bone. Thus, the osseous semicircular canals are a cavity system that can only be visualized by injection molding. Exceptionally, the walls of the osseous semicircular canals of the Mongolian gerbil are not embedded, but exposed in the hollow space in the temporal bone. Under urethane anesthesia, a window was made in the periotic capsule of the gerbil to reach this hollow space (semicircular canal triangle), and a pair of wire electrodes were inserted through an opening made in the horizontal semicircular canal toward the utricular nerve endings. Repetitive electric stimuli at 80 Hz were applied, and the direction of eye movements was noted. Subsequently, the stimulation frequency was reduced to 0.3 Hz, and evoked potentials were recorded from the neocortex. Positive surface potentials and negative deep potentials were recorded in the somatosensory area and, more specifically, in the vibrissa “barrel field,” as judged by later histochemical staining of the cortical specimens. This unique anatomic feature of the gerbil labyrinth offers an opportunity whereby the vestibular organ can be reached without any heavy surgical insult, and the presence of fine-grain vibrissa barrels in this species (seven rows instead of five rows in most rodents) will help elucidate functional interactions between vestibular and somatosensory sensations.

Utriculoocular reflex arc of the cat

1. Intracellular recordings of synaptic potentials in extraocular motoneurons were studied to determine the connectivities between the utricular nerve and the extraocular motoneurons in cats. 2. Stimulating electrodes were placed within the left utricular nerve, while other branches of the vestibular nerve were removed. Subsequently, the N1 field potentials evoked by utricular nerve stimulation were recorded in the vestibular nuclei. The potential typically grew until reaching a plateau (submaximal stimulation). Stimulus spread to the other nerve branches appeared as an additional increase in N1 amplitude after the plateau discontinued (supramaximal stimulation). 3. Intracellular recordings were made from 200 identified motoneurons in the bilateral III, IV, and VI cranial nuclei. 4. Stimulation of the utricular nerve at submaximal intensity evoked a longer latency depolarizing and hyperpolarizing potentials in contra- and ipsilateral medial rectus motoneurons, respectively. Complex potentials with longer latencies also were recorded in ipsilateral inferior oblique and contralateral trochlear motoneurons after stimulation of the utricular nerve at a submaximal intensity. Monosynaptic and disynaptic connections between the utricular nerve and ipsilateral abducens motoneurons and interneurons were recorded as described previously. 5. The results of the present study confirm our initial findings that a disynaptic pathway from the utricular nerve to contralateral trochlear motoneurons is absent or very poorly developed, whereas polysynaptic circuits from the utricular nerve to inferior oblique and trochlear motoneurons may play a role in eye rotation during head tilt.

Connections between utricular nerve and dorsal neck motoneurons of the decerebrate cat

1. We studied connections between the utricular (UT) nerve and dorsal neck motoneurons in decerebrate cats. Electrodes were fixed in place on the UT nerve under visual observation; the other branches of the vestibular nerve were transected. 2. The N1 field potential evoked by UT nerve stimulation was recorded in the vestibular nuclei at the start of each experiment. The potential typically grew until it reached a plateau. Stimulus spread (if any) to the central ends of other nerve branches was revealed by an additional increase in N1 amplitude after the plateau was reached. 3. We recorded intracellularly from 55 motoneurons in C1-C3. Some were identified as having axons in the dorsal rami, which innervate dorsal neck muscles. Others projected in nerves that were not available for stimulation. 4. UT nerve stimulation evoked synaptic potentials in essentially all motoneurons studied. The predominant pattern consisted of disynaptic excitatory postsynaptic potentials in ipsilateral motoneurons and inhibitory postsynaptic potentials that were at least trisynaptic in contralateral motoneurons. 5. The results demonstrate the presence of short-latency connections between the utricular nerve and dorsal neck motoneurons. The functional role of this pathway remains to be investigated.

The vestibular nerve of the chinchilla. III. Peripheral innervation patterns in the utricular macula

1. Nerve fibers supplying the utricular macula of the chinchilla were labeled by extracellular injection of horseradish peroxidase into the vestibular nerve. The peripheral terminations of individual fibers were reconstructed and related to the regions of the end organ they innervated and to the sizes of their parent axons. 2. The macula is divided into medial and lateral parts by the striola, a narrow zone that runs for almost the entire length of the sensory epithelium. The striola can be distinguished from the extrastriolar regions to either side of it by the wider spacing of its hair cells. Calyx endings in the striola have especially thick walls, and, unlike similar endings in the extrastriola, many of them innervate more than one hair cell. The striola occupies 10% of the sensory epithelium; the lateral extrastriola, 50%; and the medial extrastriola, 40%. 3. The utricular nerve penetrates the bony labyrinth anterior to the end organ. Axons reaching the anterior part of the sensory epithelium run directly through the connective tissue stroma. Those supplying more posterior regions first enter a fiber layer located at the bottom of the stroma. Approximately one-third of the axons bifurcate below the epithelium, usually within 5-20 microns of the basement membrane. Bifurcations are more common in fibers destined for the extrastriola than for the striola. 4. Both calyx and bouton endings were labeled. Calyces can be simple or complex. Simple calyces innervate individual hair cells, whereas complex calyces supply 2-4 adjacent hair cells. Complex endings are more heavily concentrated in the striola than in the extrastriola. Simple calyces and boutons are found in all parts of the epithelium. Calyces emerge from the parent axon or one of its thick branches. Boutons, whether en passant or terminal, are located on thin collaterals. 5. Fibers can be classified into calyx, bouton, or dimorphic categories. The first type only has calyx endings; the second, only bouton endings; and the third, both kinds of endings. Calyx units make up 6% of the labeled fibers, bouton units less than 2%, and dimorphic units greater than 92%. The three fiber types differ in the macular zones they supply and in the diameters of their parent axons. Calyx units were restricted to the striola. The few bouton units were found in the extrastriola.(ABSTRACT TRUNCATED AT 400 WORDS)