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Salt taste responses in the frog glossopharyngeal nerve: different receptor sites for Mg2+ and Na+.

The glossopharyngeal nerve of the frog responds to MgCl2 and NaCl applied to the tongue. To learn whether or not Mg2+ and Na+ react with different receptor sites, a proteolytic enzyme was topically applied to the tongue dorsum. Responses were recorded from the frog glossopharyngeal nerve during stimulation of the tongue with 100 mM MgCl2 and 500 mM NaCl. The magnitude of the MgCl2 response was selectively reduced after application of 0.1% pronase E to the dorsal tongue surface. The selective suppression of the MgCl2 response by the pronase treatment indicates that the receptor site responsible for the MgCl2 response differs from that for the NaCl response. The effect of pronase on the MgCl2 response was due to the proteolytic action. This suggests that the receptor site responsible for the MgCl2 response is composed of a protein or interacts secondarily with a protein affected by pronase treatment. It is suggested that there are multiple receptor sites for cations in salt taste reception of the frog.

Animals↗

[Anatomic and topographical characteristics of the correlations between glossopharyngeal nerve and autonomic nervous system in Canidae and Mustelidae].

Using macro-microanatomical approach, the study of glossopharyngeal nerve was performed on carcasses of fur animals belonging to Canidae and Mustelidae families (mink, sable, sable polar fox, fox). The species peculiarities of interconnections of tympanic nerve with inner carotid nerve and ear branch of vagus nerve were established. The characteristics of the course and connection of the carotid sinus branch of glossopharyngeal nerve with sympathetic branches of cranial cervical ganglion, were defined. The variants of total absence of vagal pharyngeal branch with significant development of similar branch of glossopharyngeal nerve, were noted.

Animals↗

Fiber types of the lingual branch of the trigeminal nerve, chorda tympani, lingual-tonsillar and pharyngeal branches of the glossopharyngeal nerve, and superior laryngeal nerve and their relation to the cardiovascular responses in rats.

The effect of repetitive electrical stimulation at 50 Hz for 20 s of the lingual branch of the trigeminal nerve (LN), chorda tympani (CT), lingual-tonsillar (LT-IXth) and pharyngeal (PH-IXth) branches of the glossopharyngeal nerve, and superior laryngeal nerve (SLN) on the changes in arterial blood pressure (BP) and heart rate (HR) were investigated in anesthetized and paralyzed rats. The compound action potentials in these nerves were simultaneously recorded to know the relationships between the fiber types and the cardiovascular responses. In all nerves except the CT, repetitive electrical stimulation of the nerve elicited a tachycardia and an increase in BP. These cardiovascular responses were mainly related to the component-2 in the compound action potentials in respective nerves. The conduction velocities of the component-2 in the five nerves examined in the present experiment were between 9.5 and 17.0 m/s (mean, n = 4-7). Other components which have faster (component-1) or slower conduction velocities (component-3 and -4) than the component-2 were not likely to elicit the cardiovascular responses. These results suggest that nociceptive and taste fibers of A-delta fibers innervating the oral cavity and pharyngolaryngeal region largely contribute to the cardiovascular responses.

Animals↗

Responses to umami substances in taste bud cells innervated by the chorda tympani and glossopharyngeal nerves.

The chorda tympani (CT) and glossopharyngeal (GL) nerves of several mammalian species respond differently to umami substances (US) such as monosodium glutamate (MSG), disodium 5'-inosinate (IMP) and disodium 5'-guanylate (GMP). In mice and rhesus monkeys, responses to US are greater in the GL than the CT nerve, with the GL nerve containing larger numbers of MSG-sensitive fibers. Gurmarin, a sweet response inhibitor, suppresses the mouse CT responses to the mixture of MSG and IMP to approximately 65% of control levels but not to the metabotropic and ionotropic glutamate agonists 2-amino-4-phophonobutyrate and N-methyl-D-aspartate. Gurmarin does not inhibit any taste responses in the GL. In mice, CT responses to MSG may be masked by their greater sensitivity to sodium ions. Calcium imaging studies demonstrate that some mouse taste cells isolated from the fungiform papilla innervated by the CT respond selectively (as indicated by a rise in intracellular Ca(2+) concentrations) to MSG and/or IMP or GMP. These MSG responses are not suppressed notably by reducing the Ca(2+) concentration of the stimulus solution, suggesting that the observed Ca(2+) release is from intracellular stores. Measurements of second messengers in the mouse fungiform papilla have revealed consistently that MSG elicits increases in both inositol 1,4,5-trisphosphate and adenosine 3', 5'-cyclic monophosphate levels. Together, these results suggest that US may stimulate two different transduction mechanisms in the fungiform papilla. They also suggest that gurmarin-insensitive components of receptors for US, including metabotropic and ionotropic glutamate receptors, may be commonly involved in transduction for umami taste in taste cells on both anterior and posterior parts of the tongue.

Animals↗

Effects of bilateral hypoglossal and glossopharyngeal nerve blocks on epiglottic and soft palate position in exercising horses.

OBJECTIVE: To determine the effect of bilateral hypoglossal and and glossopharyngeal nerve block on epiglottic and soft palate position and tracheal and pharyngeal pressures in exercising horses. ANIMALS: 5 Standardbreds. PROCEDURE: Tracheal and pharyngeal pressures were measured in 5 Standardbreds exercising at the speed at which the horses achieved 50, 75, and 100% of maximal heart rate after bilateral hypoglossal and glossopharyngeal nerve block and without nerve block. Nerve block was achieved by injection of 1 to 2 ml of 2% mepivicaine hydrochloride between the glossopharyngeal and hypoglossal nerves, as they coursed through the medial compartment of the diverticulum of the auditory tube (guttural pouch), using videoendoscopic guidance and an injection apparatus. RESULTS: Compared with control values, peak inspiratory tracheal pressure was significantly (P = 0.02) more negative, and peak pharyngeal inspiratory pressure was less negative (P = 0.004) after bilateral hypoglossal and glossopharyngeal nerve block. Respiratory frequency was significantly (P = 0.024) lower after nerve block, compared with control values. The epiglottis was unstable and retroflexed through the rima glottis during inspiration after bilateral hypoglossal and glossopharyngeal nerve block. Despite loss of contact between the epiglottis and the caudal free margin of the soft palate, dorsal displacement of the soft palate did not occur. CONCLUSIONS AND CLINICAL RELEVANCE: Loss of contact of the epiglottis with the soft palate did not affect soft palate position, suggesting that when the soft palate is normal, the epiglottis does not function as a support, holding the soft palate in a ventral position. Therefore, epiglottic dysfunction is not solely responsible for intermittent dorsal displacement of the soft palate in horses, and neuromuscular dysfunction involving the hyoepiglotticus muscle, geniohyoideus muscle, or the hypoglossal nerve may cause epiglottic retroflexion in horses.

Animals↗

Effect of antidromic stimulation of the glossopharyngeal nerve on afferent discharges occurring with and without sensory stimulation of the frog tongue.

Repetitive stimulation of the bullfrog glossopharyngeal nerve at a rate of 100 Hz for 10 s and at a supra-maximal intensity resulted in little depression of the glossopharyngeal nerve responses to application of quinine and mechanical taps to the tongue, in a 30-40% decrease in the responses to salt, acid, water and warmed saline and in a 80% decrease in the number of spontaneous discharges from the tongue. Such a selective depression existed throughout changes in the frequency and the duration of the antidromic stimuli. The phenomena were attributed to antidromic impulses in high-threshold glossopharyngeal nerve afferents.

Animals↗

[Syncopal neuralgia of the glossopharyngeal nerve caused by tumoral invasiveness. Therapeutic management. Apropos of 2 cases].

Cases of glossopharyngeal neuralgia are relatively rare, and are occasionally secondary to an upper cervical carcinomatous invasion. The combination with syncopal episodes suggests the creation of a reflex pathway between the glossopharyngeal nerve and the vagus nerve by connections between the bulbar nuclei. The fact that the syncopal episode is systematically preceded by a neuralgic crisis enables its differentiation from other active vasomotor phenomena. Treatment is based essentially on pain-killers and occasionally, in the event of escape, by a neurosurgical resection of the root of the glossopharyngeal nerve and of the upper part of the vagus nerve. In the light of two recent cases, the authors recall the therapeutic management and the physiopathological mechanism of this particular form of neuralgia.

Analgesics, Opioid↗

Altered regional vasodilator responses to glossopharyngeal nerve stimulation in spontaneously hypertensive rats.

The hindlimb and renal vasodilator responses produced by electrical stimulation of the glossopharyngeal nerve were examined in adult (six to eight months) male spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) normotensive rats to ascertain whether central neurogenically activated vasodilator capacity of these regional vascular beds is altered in SHR. Changes in systemic blood pressure and regional blood flow were simultaneously measured, and vascular resistance was calculated. Glossopharyngeal nerve stimulation (3.0 volts, 0.3 ms) at the frequency of 10 Hz resulted in a significantly greater vasodilation (% decrease in resistance) in SHR than in WKY control for both the hindlimb (SHR - 13.0 +/- 1.5% versus WKY - 3.4 +/- 1.6%, P less than 0.01) and renal (SHR - 7.6 +/- 0.6% versus WKY - 1.3 +/- 0.4%, P less than 0.01) vascular beds. The linear portion of the frequency-response curves of hindlimb or renal vasodilation of SHR was shifted parallel to the left of the WKY curve. Stimulus frequencies required to produce a 20% reduction in hindlimb resistance and a 10% reduction in renal resistance were lower in SHR (hindlimb 17.0 +/- 1.8 Hz; renal 19.9 +/- 1.4 Hz) than in WKY control (hindlimb 24.6 +/- 1.1 Hz; renal 39.3 +/- 4.8 Hz; P less than 0.01). The maximal vasodilator response to glossopharyngeal nerve stimulation in the hindlimb vascular bed was similar in SHR and WKY control, but in the renal vascular bed SHR showed a greater maximal response compared to WKY normotensives (SHR - 16.3 +/- 0.9% versus WKY - 12.7 +/- 1.6%, P less than 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[The influence of stimulation of the glossopharyngeal nerve on the gastric inhibitory and excitatory motor reflexes (author's transl)].

The influence of electrical stimulation of central cut end of the glossopharyngeal nerve on the vagal inhibitory and excitatory reflexes of gastric movements were investigated. Frogs and bullfrogs were employed in all experiments under urethan anaesthesia and also immobilized with 1% solution of d-tubocurarine chloride. Bilateral splanchnic nerves were previously severd, and so the stomach was innervated through the vagus nerves only. 1. The vago-vagal inhibitory reflex of gastric movements was depressed or abolished during the maintenance of stimulation of the glossopharyngeal nerve. But, the vago-vagal excitatory reflex of gastric movements was augmented in the one example and in the other example it was depressed during the glossopharyngeal stimulation. 2. The labyrintho-vagal excitatory reflex of gastric movements was excited during the maintenance of stimulation of the glossopharyngeal nerve.

Afferent Pathways↗

Competitive inhibition of the nickel-induced response to choline by calcium ions in single water fibers of the frog glossopharyngeal nerve.

NiCl2 induces a response to choline Cl and enhances the response to CaCl2 in water-sensitive fibers (water fibers) of the frog glossopharyngeal nerve. The Ni(2+)-induced choline+ response was inhibited by Ca2+ ions and, conversely, the enhanced Ca2+ response by Ni2+ ions was inhibited by choline+ ions. Hence, there exists a mutual antagonism between Ca2+ and choline+ ions. In the present study, the inhibition of the Ni(2+)-induced choline+ response by Ca2+ ions was investigated quantitatively. The assumption was made that receptors for choline (XCh) exist and that binding of a choline+ ion to XCh brings about a neural response. It was further assumed that the magnitude of the neural response is proportional to the amount of choline-XCh complex minus some constant (the threshold concentration of the choline-XCh complex). The results from analysis of double-reciprocal plot were consistent with the hypothesis that Ca2+ ions compete with choline+ ions for XCh. The dissociation constants for the choline-XCh complex and the CaXCh complex were obtained to be 0.6 M and 7.4 x 10(-5) M, respectively. This result indicates that the affinities of XCh for choline+ and Ca2+ ions are very different. Furthermore, Mg2+ ions did not affect the Ni(2+)-induced choline+ response, an indication that the affinity of XCh is not charge-specific, but is chemically specific. The identification of a competitive inhibitor of the choline+ response provides evidence for existence of a choline-specific receptor at the surface of taste cells that are innervated by the water fibers of the frog glossopharyngeal nerve. Differences between the features of the response to choline Cl in the chorda tympani nerve of the rat and those in the frog glossopharyngeal nerve are discussed.

Animals↗

Role of glossopharyngeal nerve on the control of pigeon cervical esophagus motility.

The effects of i) glossopharyngeal section on the occurrence of the primary peristalsis and ii) electrical efferent stimulation of glossopharyngeal nerve on the EMG activity were studied in the pigeon cervical esophagus. The results pointed out that glossopharyngeal nerve is an indispensable requirement for the primary peristalsis occurrence and that motor sequence is centrally programmed.

Animals↗

Taste-responsive neurons of the glossopharyngeal nerve of the rat.

1. Taste sensibilities of neurons in mammalian glossopharyngeal nerves have been inadequately studied, although they innervate the majority of taste buds and may provide unique taste information. 2. Extracellular responses of glossopharyngeal neural units to taste stimuli infused into foliate or vallate papillae were recorded in anesthetized rats. A 0.3-ml/min infusion of stimuli into papillae resulted in short-latency, 5-s nerve-impulse rates that approached 10 times the response rates observed using less invasive means of stimulation. 3. Sucrose, Na saccharin, NaCl, NH4Cl, KCl, HCl, citric acid, acetic acid, MgSO4, and quinine.HCl were effective stimuli for glossopharyngeal neurons at concentrations that have behavioral significance. 4. Response spectra for individual neural units with either foliate or vallate receptive fields fell into three clusters. Forty-six percent were A units that responded most strongly to acids and chloride salts, NH4Cl being the most effective; neither quinine nor sucrose was effective. Twenty-three percent were S units that responded to sugars and saccharin; quinine, salts, and acids were not effective. Thirty-one percent were Q units that responded to quinine; neither NaCl, HCl, nor sucrose was effective stimulus for these fragile units. 5. Glossopharyngeal A neural units were more sensitive to 1 mM HCl than were electrolyte-sensitive H units of the chorda tympani, although both respond generally to salts and acids. Units relatively specific for sodium salts (N units), which are common in the chorda tympani nerve, were not found in the glossopharyngeal nerve, which explains losses in sodium-specific behavior after cutting only the chorda tympani nerve. 6. Q units were the only glossopharyngeal neural units that responded significantly to quinine, and units with similar response spectra do not occur in the chorda tympani nerve. Q units probably mediate aversive reflexes to quinine that are eliminated by cutting only the glossopharyngeal nerve. Glossopharyngeal S neural units were more sensitive to sucrose and are more common than their counterparts in the chorda tympani, although it is not known how they might compare with sugar-sensitive units in the greater superficial petrosal nerve. 7. These data strongly suggest that posterior taste bud fields innervated by the glossopharyngeal nerve are specialized for functions different from those of anterior taste bud fields innervated by the facial nerve.

Animals↗

[Lingual taste buds following application of colchicine to the glossopharyngeal nerve in the rat].

Dissection of the glossopharyngeal nerve and application to it of colchicine that blocks axoplasmic drug transport were performed to study the effect of the nerves on the taste buds of foliate lingual papillae. It was observed that colchicine application to the nerve gave rise to destruction of the taste buds. The process of destruction proceeded more slowly as compared to that induced by nerve dissection. Colchicine application led to changes in the protein spectrum of the epithelium of foliate papillae. The absence of changes in the protein spectrum of the epithelium of foliate papillae and the presence of nerve fibers in the epithelium of the taste buds on exposure to colchicine provide evidence against its direct toxic effect on the taste buds, giving rise to their destruction. The changes seen in the taste buds result from the blocked transport of factors that participate in neurotropic control of the taste buds.

Animals↗

The sweet taste in the calf. II. Glossopharyngeal nerve responses to taste stimulation of the tongue.

Recordings were obtained from the glossopharyngeal nerve in 1-5-week-old calves during stimulation of the circumvallate tongue area with NaCl, quinine hydrochloride, citric acid, and the sweet compounds: acesulfam-K, aspartame, fructose, galactose, glucose, glycine, lactose, maltose, monellin, Na-saccharin, sucrose, thaumatin, and xylitol. All compounds except aspartame, monellin and thaumatin gave a nerve response. Glycine, followed by Na-saccharin, elicited the largest responses. Sucrose gave the largest response among the disaccharides, while there was no significant difference between the monosaccharides. Expressed as percent of the NaCl responses, the responses to glycine, sucrose, xylitol, fructose, galactose, glucose, lactose and maltose were considerably larger in the glossopharyngeal nerve than in the chorda tympani nerve. This can be taken as an indication that the posterior region of the tongue serves as the major receptive area for sweet in cattle.

Animals↗

Reflex response of the hypoglossal nerve induced by chemical stimulation of the tongue and electrical stimulation of the glossopharyngeal nerve in the frog.

While applying solutions of 5 mM QHCl, 2 M NaCl and HCl at pH 3.0 to three different ipsilateral portions, root, middle and tip of the tongue surface of the frog, reflex discharges were recorded from three main branches of the hypoglossal nerve. Reflex discharges in the hypoglossal branch were elicited mainly when the caudal two-thirds of the tongue was stimulated with the chemicals, whereas those in the genioglossal branch occurred predominantly when the rostral two-thirds of the tongue was stimulated. The intrinsic branch responded reflexly to stimulation of any portion of the tongue. The hypoglossal branch was also highly sensitive to mechanical stimulation of the tip of the tongue. Action potentials reflexly elicited by electrical stimulation of medial and lateral branches of the glossopharyngeal nerve were recorded from the following two of the three efferent branches simultaneously. Then it was revealed that the activity of the hypoglossal branch was induced by sensory inputs from low threshold fibers in the medial branch, whereas that of the genioglossal branch was mainly by the lateral branch. Latencies between the electrical stimulation of the afferent branches and the potential in the hypoglossal branch produced by stimulation of the medial branch had the shortest latency. This reflex are may functionally play a role in retracting the tongue quickly after capturing a prey at the tip of the frog tongue.

Action Potentials↗

The anatomy of the inferior petrosal sinus, glossopharyngeal nerve, vagus nerve, and accessory nerve in the jugular foramen.

PURPOSE: To define the variations of the courses of the cranial nerves and the inferior petrosal sinuses as they enter and traverse the jugular foramen. METHODS: Thirty-nine cadaveric specimens containing the jugular foramen were scanned with 1-mm contiguous axial and coronal CT sections. Each specimen was dissected to evaluate the position of the cranial nerves and inferior petrosal sinus as they entered the jugular foramen. RESULTS: The glossopharyngeal nerve entered the most superior, anterior, and medial aspect of the jugular foramen and descended in the anterior portion of the jugular foramen, often within a groove. The vagus and accessory nerves could not be separated by CT. They entered the jugular foramen most often anterior or anterior and inferior to the jugular spine of the temporal bone and descended in a position ranging from medial to anterior to the jugular vein. The inferior petrosal sinus most often coursed inferior to the horizontal portion of the glossopharyngeal nerve and entered the jugular system in the jugular foramen, at the exocranial opening or below the skull base. A pars nervosa and pars venosa could be identified only at the endocranial opening, where the jugular spine separated the pars nervosa containing the inferior petrosal sinus and three cranial nerves from the pars venosa containing the jugular vein. CONCLUSION: Our evaluation demonstrated anatomic variation in the area of the jugular foramen.

Accessory Nerve↗

Different receptor sites for Ca2+ and Na+ in single water fibers of the frog glossopharyngeal nerve.

Unitary discharges were recorded from single water-sensitive fibers (water fibers) of the frog glossopharyngeal nerve during stimulation of the tongue with chemical stimuli. Low CaCl2 (1 mM CaCl2) and relatively high NaCl (500 mM NaCl) are effective stimuli which excite water fibers. To learn whether or not Ca2+ and Na+ react with different receptor sites, a proteolytic enzyme was topically applied to the tongue dorsum. After treatment of the tongue with 0.05% pronase E, the magnitude of the NaCl response remained unchanged, but the magnitude of the CaCl2 response markedly decreased. The selective elimination by the pronase E treatment indicates that there exist different receptor sites for Ca2+ and Na+ in single water fibers of the frog glossopharyngeal nerve. The effect of pronase E treatment was due to the proteolytic action. The results suggest that the Ca2+ receptor site may be composed of a protein.

Animals↗