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Transcranial magnetic stimulation in the rat
A R Luft1, A Kaelin-Lang, T K Hauser
1Department of Neurology, Johns Hopkins University, Baltimore, MD 21287, USA. aluft@anatom.uni-tuebingen.de
Experimental Brain Research
|August 14, 2001
Summary
This study establishes a reproducible method for assessing motor excitability in rats using transcranial magnetic stimulation (TMS). The findings demonstrate TMS
Area of Science:
- Neuroscience
- Motor Control
- Animal Models
Background:
- Transcranial magnetic stimulation (TMS) is a valuable tool for quantifying motor system excitability in humans.
- Its application in animal models is limited, with scarce data on rodent TMS characteristics.
- Non-invasive TMS is crucial for evaluating injury and recovery in animal models of neurological conditions.
Purpose of the Study:
- To characterize rodent motor evoked potentials to TMS (MEPTMS).
- To develop a reproducible methodology for assessing motor excitability in rats.
- To compare MEPTMS with responses from electrical stimulation of the cervical spinal cord (MEPCES) and peripheral nerve.
Main Methods:
- MEPTMS and MEPCES were recorded from rats using subcutaneous electrodes over the calf.
- Stimulation was delivered via a figure-of-eight coil for TMS and electrical stimulation for MEPCES.
- Measurements were taken before and after a 2-hour idle period under propofol infusion and stereotactic restraint.
Main Results:
- MEPTMS exhibited onset latencies of 6.7±1.3 ms, decreasing with higher stimulation intensity.
- Two distinct MEPTMS morphologies (MEPTMS, 1 and MEPTMS, 2) were identified, with MEPTMS, 2 more frequent at higher intensities.
- Spinal transection abolished TMS responses, while MEPCES showed shorter latencies (5.29±0.24 ms); neither response changed significantly after 2 hours.
Conclusions:
- This study demonstrates the feasibility and reproducibility of TMS in rats for motor excitability assessment.
- Sigmoid recruitment curves of MEPTMS, 1 suggest input-output properties analogous to the human corticospinal system.
- Latency differences and morphologies indicate supraspinal origins for MEPTMS, potentially reflecting diverse cortical or subcortical pathways.