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Changes in recruitment of motor cortex excitation and inhibition in patients with drug-induced tardive syndromes.

مؤلف البحث
Khedr EM1, Al Fawal B2, Abdelwarith AM2, Saber M2, Tony AAH2, El-Bassiony A3, Rothwell JC4.
مجلة البحث
Neurophysiol Clin. doi: 10.1016/j.neucli.2018.10.001. Epub 2018 Oct 23.
المشارك في البحث
الناشر
Elsevier
تصنيف البحث
1
عدد البحث
2019 Feb;49(1):33-40.
موقع البحث
pubmed central
سنة البحث
2019
صفحات البحث
2019 Feb;49(1):33-40.
ملخص البحث

Abstract
OBJECTIVES:
It has recently been suggested that drug-induced tardive syndromes (TS) might be due to maladaptive plasticity, which increases motor excitability in cerebral cortex and basal ganglia. In order to test this hypothesis, we performed the first measurements of cortical excitability in TS.

METHODS:
Motor cortex excitability was examined using transcranial magnetic stimulation (TMS) in 22 TS patients and compared with that in 20 age and sex-matched healthy individuals. Resting and active motor threshold (RMT, AMT) and input-output curves (I/O curves) assessed corticospinal excitability. The duration of the contralateral silent period (cSP) at a range of stimulation intensities and ipsilateral silent period (iSP) were used as measures of inhibition.

RESULTS:
There were no significant differences in RMT and AMT between patients and controls, although the input-output curves were significantly steeper in patients. The cSP (at different stimulus intensities) and iSP were both longer in the patients compared to the control group. However, most of this difference could be accounted for by increased recruitment of motor evoked potentials (MEPs) in patients.

CONCLUSION:
TS is characterized by hyperexcitability of corticospinal output that might contribute to the lack of selectivity in muscle recruitment and contribute to excess involuntary movement. The findings are opposite to those in naturally-occurring hyperkinesia such as Sydenham's and Huntington's chorea, suggesting a fundamental difference in the pathophysiology.