Activities of the respiratory enzymes succinate dehydrogenase (SDH) and nicotinamide adenyldinucleotide dehydrogenase (NADH-DH) were measured in neuronally isolated netcortical strips and in homotopic regions of the contralateral hemisphere 2, 21, 60, and 90 days after surgery as well as in the cerebral cortex of intact animals. The density of glial cells in the neocortex was evaluated in the same period. Changes in the activities of SDH and NADH-DH in isolated neocortical strips correlated with the dynamics of morphological changes. The data indicate that chronically isolated strips of the neocortex can be an adequate and useful model for electrophysiological, pharmacological, genetic, and other studies.
Key Words: neocortex; neuronally isolated strip; SDH; NADH-DH; gliaCortical zones disconnected from the adjacent regions and subcortical structures with preservation of pial circulation exhibit structural and functional changes which can be observed for several months. Thus, degeneration of afferent terminals is seen 2-3 days after the isolation procedure [3], an increased density of spines and synapses, an increased number of axon collaterals [8], and intensified dendrite sprouting [7] can be observed at the end of the first month. These structural changes result in considerable shifts in the functional state of isolated cortical strip (ICS) [8]. The most informative indices of the tissue conditions are the activities of the main redox enzymes succinate dehydrogenase (SDH) and NADH dehydrogenase (NADH-DH) and their balance [4][5][6]. In this work we investigated the dynamics of structural changes and energy metabolism in surviving ICS from the rat brain and in homotopic cortical zone of the contralateral hemisphere (HCZ).Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Moscow
MATERIALS AND METHODSExperiments were carried out on 60 male Wistar rats weighing 180-200 g. A fragment of the sensorimotor cortex of the left hemisphere was isolated under ketamine (Kalipsol) anesthesia (70 mg/kg) by means of a special laboratory-made instrument. The neocortical activity of the principal energy metabolism enzymes SDH and NADH-DH was determined in 24 experimental and 6 intact rats by a quantitative hystochemical technique using cytospectrophotometry [2]. Enzyme activity in ICS and HCZ was measured 2, 21, 60 and 90 days after surgery. Control indices were measured in the analogous cortical zones of intact animals. Enzyme activity was expressed in arbitrary units (mmol formazan produced by 1 mol protein nitrogen for 1 min at 37~The density of glial cells was determined in ICS and HCZ of the experimental rats (n=24) and in the neocortex of intact rats (n=6). Brain tissue blocks were fixed in 10% formaldehyde in phosphate buffer (pH= 7.2-7.4). Frontal serial sections of 20 ~t thickness were 0007-4888/99/0002-0129522,00 9 Publishers