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The frog spinal cord: a model to study methanethiol-central nervous system interaction.
A De Santis1, C Loguercio, G Nardi
1Neurobiology and Biochemistry laboratories, Stazione Zoologica di Napoli, Italy.
Summary
Methanethiol (MT) and N-ethyl-maleimide (NEM) alter frog spinal cord electrical activity. DL-dithiothreitol (DTT) enhances spontaneous patterns, suggesting sulphydryl groups regulate neural activity.
Area of Science:
- Neuroscience
- Neurophysiology
- Biochemistry
Background:
- Spinal cord electrical activity is crucial for nervous system function.
- The role of specific chemical groups, like sulphydryl (SH) groups, in neural signaling is not fully understood.
- Investigating the impact of chemical agents on spinal cord activity can elucidate underlying mechanisms.
Purpose of the Study:
- To investigate the effects of methanethiol (MT), DL-dithiothreitol (DTT), and N-ethyl-maleimide (NEM) on the electrical activity of the frog spinal cord.
- To explore the potential involvement of sulphydryl groups in spontaneous electrical activity.
- To determine if MT interacts with interneurons and affects membrane SH groups.
Main Methods:
- Electrophysiological recordings of frog spinal cord activity.
- Application of methanethiol (MT), DL-dithiothreitol (DTT), and N-ethyl-maleimide (NEM) to the spinal cord.
- Observation of effects on spontaneous and evoked electrical responses.
Main Results:
- Methanethiol (MT) depressed spontaneous dorsal and ventral root potentials but did not affect evoked responses.
- N-ethyl-maleimide (NEM), a SH modifying agent, caused irreversible depression of electrical cord activities.
- DL-dithiothreitol (DTT), a SH reducing agent, significantly increased spontaneous electrical cord patterns.
Conclusions:
- Interneuronal membrane sulphydryl groups in the dorsal horn are likely involved in generating spontaneous electrical cord activities.
- Methanethiol (MT) appears to interact with these interneurons, potentially through the oxidation of membrane SH groups.
- These findings highlight the importance of SH group dynamics in regulating spinal cord excitability.