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Biomedical subjects

D Swick

Publications and source records attributed to D Swick.

4 recordsLinked to original sources
PubMed1992

Visual P3-like potentials in squirrel monkey: effects of a noradrenergic agonist.

Event-related potentials (ERPs) were recorded from squirrel monkeys (Saimiri sciureus) in a 90-10 visual "oddball" paradigm. A small, blue rectangle was presented every 2 s on 90% of the trials (background), whereas a yellow rectangle occurred on 10% on the trials (oddball). Electrical activity time-locked to these stimulus events was recorded from epidural electrodes before and following systemic administration of the alpha-2 noradrenergic agonist clonidine (0.1 mg/kg intramuscularly, IM). Baseline data in response to oddball stimuli showed a large, P3-like potential exhibiting a fronto-central maximum along midline electrodes and a parietal maximum along lateral electrodes. A frontally dominant, long-latency, negative slow wave (SN) consistently followed this P3-like potential. Amplitudes for P3 were larger following 10% than 50% probable oddball events. These results suggest that monkeys exhibit large, probability-sensitive P3-like potentials similar to the visual potentials reported in humans. Administration of clonidine had no effect on the amplitude, area, or latency of the monkey P3 component. This contrasts with our previous findings that the same dose of clonidine significantly decreases auditory P3s in these monkeys. Such differences may reflect distinct functional roles for norepinephrine in the processing of low-probability acoustic versus visual signals and argues against the hypothesis that norepinephrine is a common neurotransmitter substrate for auditory and visual P3-like potentials.

Animals↗
PubMed1989

Audiogenic stress response: behavioral characteristics and underlying monoamine mechanisms.

Behavioral characterization of the audiogenic stress response in rats revealed an intensity related multiphasic pattern including an initial, transient activation followed by prolonged periods of response suppression during the remainder of the noise exposure and excitation after noise offset. These observations emphasize the need to consider the temporal proximity between exposure to a stressor and either behavioral characterization and/or determinations of neurochemical changes relevant to the stress response. In a second series of studies, the effect of the NE alpha 2 agonist clonidine and the NE alpha 2 antagonist yohimbine were evaluated on the different components of the audiogenic stress response. The effects of intracerebroventricular xylamine-induced depletion of NE were also examined. The results seem to indicate that CNS noradrenergic systems may not be specifically implicated in regulating the responsiveness to noise stimulation but instead may subserve a more general role in adjusting baseline levels of motoric output in response to environmental conditions.

Adrenergic Fibers↗
PubMed1989

Brain-stem auditory evoked potentials in squirrel monkey (Saimiri sciureus).

To more fully characterize brain-stem auditory evoked potentials (BAEPs) in non-human primates, BAEPs were recorded from chronically implanted epidural electrodes in 10 squirrel monkeys (Saimiri sciureus). The effects of stimulus intensity, repetition rate, and anesthesia (ketamine 20 mg/kg i.m.) on peak latencies and inter-peak intervals were evaluated. Monkey wave forms consisted of approximately 7 peaks (I-VII), each exhibiting similar latencies across sessions, with later peaks exhibiting greater variability. In some subjects, additional peaks (IIa, IIIa) and slow potentials were recorded. The slow potentials provided a substratum for peaks IV through VII. As with human, monkey peaks exhibited systematic changes in latency with changes in stimulus intensity or repetition rate. These shifts included significant decreases in latency with increasing intensity for peaks I-IV and increases in latency with increases in repetition rate for peaks III, V, and VI. Inter-peak intervals were similar to those observed in human. Furthermore, ketamine anesthesia significantly delayed the latencies of most peaks (except I, V, and VII). Some differences between monkey and human BAEPs were evident in the relative amplitude of specific peaks. For example, peak V is typically most prominent in human, while this was true for peak III in monkey. The similarities between unanesthetized monkey and human inter-peak intervals suggest that the times required for impulses to reach particular brain-stem areas are conserved across primate species that vary in brain size. This supports the hypothesis that comparably numbered BAEP peaks in monkey and human index homologous processes. The data also suggest that the differences between animal and human BAEPs commonly reported may result from the use of anesthetics. In summary, unanesthetized monkey BAEPs resemble human BAEPs in morphology, number of peaks, polarity, latency variability, inter-peak intervals, slow potentials superimposed on the high-frequency peaks, and variations in morphology, amplitude, and resolution of peaks as a function of recording site. Thus, unanesthetized monkey BAEPs may be an excellent model for investigating the neural substrates of human BAEP or for determining species differences in acoustic processing among primates.

Anesthesia↗