Biomedical subjects

D M Caspary

Publications and source records attributed to D M Caspary.

58 records · Page 4Linked to original sources

PubMedDate not supplied

Response properties in young and old Fischer-344 rat lateral superior olive neurons: a quantitative approach.

Significant age-related functional deficits may result from a selective loss of inhibitory processing in the lateral superior olivary (LSO) nucleus. To test this hypothesis, methods were developed for quantitative comparisons of the excitation evoked by ipsilateral acoustic stimuli and the inhibition evoked by contralateral acoustic stimuli in neurons recorded from this binaural structure. Data were obtained from 103 LSO neurons from 22 young adult (3-6 month) and 70 LSO neurons from 14 old (20-23 month) Fischer-344 (F-344) rats. Age-related increases in the thresholds of auditory brainstem responses as well as in the inhibitory and excitatory responses of LSO neurons were observed. Spike-discharge rates were analyzed using multiple regression analysis for interaural intensity data and by calculating correlation coefficients between excitatory and inhibitory isointensity curves. Most LSO principal cells exhibited ipsilateral excitation and contralateral inhibition of similar strength for similar stimuli. Inhibitory and excitatory response areas of these neurons were similar based on visual inspection and correlation coefficients. No statistically significant age-related changes were observed for (a) rate-level functions generated by ipsilateral or contralateral stimuli; (b) maximal discharge rate; (c) conduction latencies; or (d) measures of binaural function. However, a small percentage of LSO neurons both in young and old rats displayed "unmatched" inhibitory and excitatory response areas. Quantitative methods developed in this study are used to examine age-related changes in binaural function in the inferior colliculus of F-344 rats and in the LSO of the Sprague-Dawley rat. Although no asymmetrical aging changes were observed for the F-344 rat LSO, there appear to be significant differences between the aging auditory system in the F-344 and Sprague-Dawley rats. Age-related changes have been previously described for the F-344 in other brainstem auditory structures.

Acoustic Stimulation↗

PubMedDate not supplied

Age-related decrease in GABAB receptor binding in the Fischer 344 rat inferior colliculus.

Quantitative receptor autoradiography was used to assess GABAB receptor binding in three primary subdivisions of the inferior colliculus (IC): dorsal cortex (DCIC), external cortex (ECIC), and the central nucleus (CIC) of 3-, 18-20-, and 26-month-old Fischer 344 rats. GABAB binding sites were localized using [3H]GABA in the presence of a saturating concentration of isoguvacine, a selective GABAA receptor agonist, to displace [3H]GABA bound to GABAA receptor sites. In the three IC subdivisions examined, GABAB receptor binding was significantly reduced in 26-month-old rats when compared to 3-month-old rats (DCIC, -44%; ECIC, -36%; CIC, -32%; p < 0.05). For comparison, GABAB binding was determined in the portion of cerebellum located in the recess of the IC. In the molecular layer of this region, there was no statistically significant differences in receptor binding between 3, 18-20-, and 26-month-old rats. In addition, there was not a significant age-related change in the cross-sectional area of the IC. These findings provide additional evidence to support the existence of selective age-related changes in GABA neurotransmitter function in the rat IC.

Aging↗

PubMedDate not supplied

Central auditory aging: GABA changes in the inferior colliculus.

Age-related hearing loss (presbycusis) is a complex state that reflects pathologic changes along the entire auditory neuraxis. Loss of speech understanding, decreased ability to localize sounds, and a decreased ability to detect and extract signals in noise are characteristic problems encountered by the elderly. Central (neural) presbycusis frequently results in a dramatic loss in speech understanding without a parallel change in pure-tone thresholds. In spite of evidence that suggests these deficits cannot be fully explained by peripheral changes alone, few studies have examined the neurochemical basis of central auditory dysfunction in aging. Age-related alterations in neural circuits involved in the processing of acoustic information could reflect changes in the synthesis, degradation, uptake, release, and receptor sensitivity of neurotransmitters, perhaps secondary to cell loss and/or progressive deafferentation. A series of studies designed to test this hypothesis has examined aging in the central auditory system of the F344 rate. Age-related changes associated with GABA neurotransmitter function in an important auditory midbrain structure, the inferior colliculus, have been investigated. These studies found: (1) decreased numbers of GABA immunoreactive neurons; (2) decreased basal levels (concentrations) of GABA; (3) decreased GABA release; (4) decreased glutamic acid decarboxylase activity; (5) decreased GABAB receptor binding; (6) decreased numbers of presynaptic terminals; and (7) subtle GABAA receptor binding changes. Collectively, these age-related changes suggest altered GABA neurotransmitter function in the IC. Identification of specific neurotransmitter changes in structures important in speech processing could eventually lead to the development of pharmacotherapy for selective types of age-related hearing loss.

Aging↗

PubMedDate not supplied

Response characteristics of cochlear nucleus neurons to vowel sounds.

Most studies in auditory neurophysiology have utilized tonal stimuli to determine the coding properties of neurons in the cochlear nuclei. In this investigation of the kangaroo rat, cochlear nuclei, neuronal responses to vowel sounds, as well as tones, were studied. The vowel sounds, each about 40 msec in duration were: see article. Five were linked together to form a 200 msec stimulus and various combinations of five vowel sounds provided us with 18 different stimuli. The results show that neurons in the cochlear nuclei are remarkably sensitive and selective to vowel sounds. Furthermore, the responses of these neurons to pure tones do not provide a complete basis to predict the types of responses to the vowel sounds. More significant is the finding that the neural discharge rate and pattern of discharge to a particular vowel may depend on where the vowel appears in the stimulus and what other vowel precedes it. This vowel positional effect is not the same for every neuron. We have called this phenomenon a neural "set".

Acoustic Stimulation↗