The penetration of a syringe needle or electrode into the brain, causing localized physical changes such as a high compression front with displacement of whole cells and other cells suffering from various degrees of temporary distortion, would be expected to produce disturbances in metabolism. Subsequent intracranial injection of small quantities of fluid may produce changes in pH, electrolyte concentration, ionic strength, temperature, and the disequilibrium of colloidal suspensions. Less clearly defined effects on metabolism due to inflammatory processes and trauma would also be likely to occur. This paper reports the effects of intracranial penetration of a microneedle and subsequent injection of 5 p,l. physiological saline on the metabolic activities of enzymes controlling important metabolic pathways in the brain. Two areas were investigated-namely, the cerebral cortex and the corpus callosum. Following injection, the animals were allowed to recover and observations on enzymes of glucose, thiamine and phosphate metabolism, amine oxidation, and acetylcholinesterase within nerve cells and glia during the period of 31 days post-operation were made by histochemical techniques.
MATERIALS AND METHODSAdult male Lister rats weighing between 250 and 300 g were anaesthetized with ether, the hair shaved off the scalp, and the animal secured in a stereotaxic apparatus. Under aseptic conditions a sagittal incision was made, the skull exposed and scraped clean. The dura mater was exposed by drilling a burr-hole at Area 4 of the motor cortex (Krieg, 1946) and a sterilized specially drawn fine glass microneedle (less than 200 t in diameter) was introduced to the predetermined depth. Using a Hamilton 100p1. syringe, 5 pl. isotonic saline solution were injected over a period of 10 min by a motor-driven micrometer. The syringe needle was withdrawn, 300,000 u. Penidural given intraperitoneally, and the skin incision 'Present address: