Electrophysiological and behavioral studies of taste discrimination in the axolotl (Ambystoma mexicanum).

Electrophysiological and behavioral experiments were performed to determine whether the taste system of the aquatic salamander, axolotl, discriminates taste stimuli. Taste responses were recorded extracellularly from the glossopharyngeal nerve bundle. The behavioral responses of axolotls towards various concentrations of NaCl, KCl, citric acid, quinine-hydrochloride, and sucrose were quantified by measuring the ratio of rejection towards gel pellets, each containing either unitary stimuli or binary mixtures of these chemicals. Rejection ratios [rejection/(rejection+swallowing)] towards the unitary stimuli except sucrose increased with concentration, but were not a single function of the magnitude of neural response induced by the stimuli. Degree of rejection was different depending on the quality of taste stimuli, suggesting that information processing of taste quality occurs in axolotls. The potential of NaCl to induce positive feeding behavior (swallowing) was suggested by a reduction in the rejection ratio of quinine-tainted pellets when they were mixed with 100 mM NaCl. Differential behavioral responses to quinine and NaCl show that axolotls have the ability to discriminate the taste quality of these stimuli.

Morphology and distribution of the glossopharyngeal nerve afferent and efferent neurons in the Mexican salamander, axolotl: a cobaltic-lysine study.

Cobaltic-lysine complex was used to label the afferent and efferent components of the glossopharyngeal nerve in the ganglion and brainstem of the Mexican salamander, axolotl (Ambystoma mexicanum). The distribution of afferent cell bodies in the combined glossopharyngeal-vagus ganglion (the IX-X ganglion) was reconstructed from serial sections, and the sizes of the cell bodies were measured. The central projection of afferents and the location of efferent cell bodies were determined by the tracer. The afferent cell bodies in the ganglion were medium-sized (ca. 25 microns). Cell bodies with a single process were seen. The ganglion was not clearly divided into superior and inferior ganglia, as is observed in mammals and frogs, but comprised a single ganglion. Labelled cells were diffusely distributed in the rostral part of the IX-X ganglion. A few labelled cells also were seen in the caudal part, where the vagus nerve fibers and cell bodies were mainly distributed. Double labellings of the glossopharyngeal and vagus nerves with HRP and cobaltic-lysine demonstrated that the ganglion cells of each nerve are not clearly separated in the IX-X ganglion. In the brainstem, the majority of afferent fibers formed thick ascending and descending limbs in the solitary fasciculus. The remaining afferent fibers formed a thin bundle in the spinal tract of the trigeminal nerve, which had a short ascending limb and a long descending limb. These two bundles had terminal areas in the ipsilateral brainstem: in the dorsal gray matter for the solitary fasciculus and in the lateral funiculus for the spinal tract of the trigeminal nerve, respectively. The cell bodies of the efferent neurons possessed developed dendritic arborizations in the ventrolateral white matter, and formed a longitudinal cell column in the ventrolateral margin of the gray matter. Thus, the glossopharyngeal nerve system in the axolotl assumes a primordial form in its ganglions, but its topographical organization in the brainstem is basically similar to that in anurans.

Viremia and neutralizing antibody response in infants with exanthem subitum.

Mononuclear cell-associated viremia caused by human herpesvirus type 6 was detected in 39 (66%) of 59 blood samples from 38 children with exanthem subitum between day 0 and day 7 of the disease. The rate of virus isolation from mononuclear cells was 100% (26/26) on days 0 to 2 (just before appearance of skin rash), 82% (9/11) on day 3, 20% (2/10) on day 4, 7% (2/12) on days 5 to 7, and 0% (0/37) on day 8 and thereafter. The cell-free virus was detected in blood in 10 (21%) of 47 blood samples during the same period. The antibody activity to the virus, evaluated by a newly developed neutralization assay, was first detected on day 3 of the disease with a positive rate of 18% (2/11). It became 60% (6/10) on day 4, 75% (9/12) on days 5 to 7, and 100% on day 8 and thereafter. Thus the disappearance of the virus from blood was associated with the induction of specific immunity to the virus.

Intraindividual changes in theophylline clearance during constant aminophylline infusion in children with acute asthma.

Intraindividual changes in theophylline clearance were examined in 13 children with acute exacerbation of asthma receiving a 72-hour constant intravenous infusion of aminophylline. The mean (+/- SD) first, second, and third clearances measured at 24, 48, and 72 hours after the infusion increased from 58.1 +/- 13.8 to 69.7 +/- 28.0 to 84.1 +/- 36.3 ml/hr/kg, respectively (P less than 0.02 from the first and P less than 0.05 from the second). Our results suggest that substantial intraindividual changes in theophylline clearance can occur over a rather short time during intravenously administered aminophylline therapy for acute asthma in children. We recommend that plasma theophylline concentrations be monitored frequently and that aminophylline infusion rate be adjusted on the basis of the measured theophylline concentration data during an acute episode of asthma in the pediatric patient.