A HYBRID CLINICAL-RESEARCH DEPTH ELECTRODE FOR ACUTE AND CHRONIC IN-VIVO MICROELECTRODE RECORDING OF HUMAN BRAIN NEURONS - TECHNICAL NOTE

Citation
Ma. Howard et al., A HYBRID CLINICAL-RESEARCH DEPTH ELECTRODE FOR ACUTE AND CHRONIC IN-VIVO MICROELECTRODE RECORDING OF HUMAN BRAIN NEURONS - TECHNICAL NOTE, Journal of neurosurgery, 84(1), 1996, pp. 129-132
Citations number
15
Categorie Soggetti
Neurosciences,"Clinical Neurology",Surgery
Journal title
ISSN journal
00223085
Volume
84
Issue
1
Year of publication
1996
Pages
129 - 132
Database
ISI
SICI code
0022-3085(1996)84:1<129:AHCDEF>2.0.ZU;2-7
Abstract
For several decades, important scientific information has been gained from in vivo microelectrode recordings of individual human cerebral co rtical neurons in patients with epilepsy. The experimental methods use d, however, are technically complex and require a highly skilled intra operative team. There are also significant experimental time Limitatio ns, as well as constraints on the type of behavioral tests conducted, and the brain regions that may be safely studied. In this report, a ne w method is described for obtaining in vivo microelectrode recordings using a hybrid depth electrode (HDE). High-impedance research recordin g contacts are interspersed between low-impedance clinical electroence phalographic (EEG) contacts along the HDE shaft. The HDE has the same external physical properties as a standard clinical depth electrode (D E). Following preclinical laboratory testing, 15 HDEs were used in the evaluation of six patients with medically refractory epilepsy. High-q uality EEG recordings were obtained in all cases (two acute intraopera tive, four from the chronic epilepsy monitoring unit). Action potentia ls from individual neurons were successfully recorded during all exper imental sessions; however, the chronic preparations were clearly super ior. Chronic HDEs are placed using a standard stereotactic system, and the locations of recording contacts are documented on a postimplantat ion imaging study. The quality of the chronic research recordings was excellent over study periods ranging from 5 to 14 days. The patients r ested comfortably on the ward and were able to cooperate with complex experimental instructions. Basic neuroscientists participated fully in all aspects of the chronic investigations. The use of an HDE in place of a standard clinical DE may now allow detailed physiological invest igations of any brain region targeted for clinical DE implantation.