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Biomedical subjects

W F Wonderlin

Publications and source records attributed to W F Wonderlin.

21 records · Page 2Linked to original sources

Visual system dysfunction following acute trimethyltin exposure in rats.

Trimethyltin (TMT) has been shown to produce damage in the limbic system and several other brain areas. To date, damage to sensory systems has not been reported. The present study investigated the integrity of the visual system following acute exposure to TMT. Rats were chronically implanted with electrodes for recording the evoked response from either the visual cortex or optic tract following photic stimulation. Following recovery, the animals were exposed to either 0 (saline), 4, 5, 6, or 7 mg/kg trimethyltin chloride (TMT). Evoked potentials were averaged the peak-to-peak amplitudes and latencies were determined. The results indicated that exposure to TMT produced alterations in the visual evoked response. The pattern of changes suggested two effects, an alteration in retinal processing and an alteration in arousal. The manifestation of these changes was an increase in early peak latencies recorded from the visual cortex and the optic tract, a decreased amplitude recorded from the visual cortex and optic tract early peaks (all suggestive of retinal changes) and a decreased P3N3 amplitude and N3 latency recorded from the visual cortex (suggestive of increased arousal). The results demonstrate that TMT does produce alterations in sensory systems as well as in the limbic system.

Analysis of Variance↗

Increased seizure susceptibility following trimethyltin administration in rats.

Acute treatment with trimethyltin (TMT) produces a multitude of behavioral effects including spontaneous convulsions in some animals. The present study used several different experimental seizure models to investigate seizure susceptibility in TMT-treated rats. Rats surgically implanted with electrodes in the amygdala and treated with TMT kindled more rapidly than saline-treated controls. Similarly, rats implanted with electrodes in the dorsal hippocampus kindled more rapidly than controls. Although TMT did not alter the properties of hippocampal afterdischarges, the threshold for production of after discharges was increased in both hippocampal and amygdaloid kindled rats, probably due to cell loss. TMT also increased the sensitivity of rats to pentylenetetrazol, thus suggesting that the increased seizure susceptibility was not limited to the limbic system.

Animals↗

The trimethyltin syndrome in rats.

Trimethyltin (TMT) chloride, administered to adult male Long-Evans hooded rats, produced a unique and distinctive behavioral syndrome consisting of spontaneous seizures, tail mutilation, vocalization and hyperreactivity. The LD50 for TMT was weight dependent; in large rats (e.g., 450 g), 7 mg/kg TMT produced significant weight loss and lethality, whereas in small rats (e.g., 250 g), 7 mg/kg produced neither weight loss nor lethality. TMT produced mild hypothermia and tremors. Results are discussed in comparison with kainic acid-induced morphological alterations and septal lesion-induced behavioral alterations. Histopathological evaluations of hippocampal tissue revealed cell loss that was largely confined to regio inferior pyramidal cells. TMT offers potential as a tool for investigations of limbic system structure and function.

Animals↗