We studied energy metabolism after experimental subarachnoid hemorrhage in rats. Four different cerebral areas were tested: frontal cortex, occipital cortex, hippocampus, and brainstem. V m of the following enzymatic activities was evaluated: in the homogenate: hexokinase, phosphofructokinase, and lactate dehydrogenase for the glycolytic pathway, and glucose-6-phosphate dehydrogenase for the hexose monophosphate shunt; in the purified nonsynaptic mitochondria: NAD + -isocitrate dehydrogenase, citrate synthase, and succinate dehydrogenase for the Krebs cycle, and cytochrome oxidase for the electron transfer chain. We also evaluated some parameters related to the respiration of nonsynaptic mitochondria (State 3, State 4, uncoupled state, respiratory control ratio, and ADP: O ratio). Subarachnoid hemorrhage did not significantly affect V m of the enzymatic activities related to anaerobic and aerobic metabolism; however, mitochondrial respiration was affected, particularly in the presence of NADH-producing substrates (glutamate + malate). (Stroke 1988; 19:378-384) I n humans, subarachnoid hemorrhage (SAH) from ruptured intracranial aneurysms may produce dramatic events, namely severe central nervous system dysfunction 1 "3 and complications such as cerebral vasospasm, rebleeding, and hydrocephalus responsible for extensive neurologic deterioration and/or irreversible neurologic deficits. SAH may cause a sequential cellular impairment and even irreversible neuronal damage similar to that occurring in ischemia. Many experimental animal models have been proposed to study the pathogenesis, prevention, and therapy of some complications (such as cerebral vasospasm) without paying marked attention to the neuronal impairment and brain metabolic derangement caused by SAH.Recently, a suitable rat SAH model was used to define the cerebral blood flow alterations 7 -8 and/or cerebral vasospasm pathogenesis.8 " 10 Using the described SAH rat model, our study was aimed at depicting the regional modification of cerebral energy metabolism.
Materials and Methods
Animals and Surgical ProcedureWe used male Sprague-Dawley rats (Charles River strain) weighing 325-350 g.Anesthesia was induced with 3% halothane in a 70:30 N 2 O:O 2 mixture and maintained with 0.75% From the Institute of Pharmacology, Faculty of Science (F.M., G.B.) and Department of Surgery, Section of Neurosurgery (P.G., R.R.B., V.S., P.P.), University of Pavia, Pavia, Italy.Address for reprints: Dr. Fulvio Marzatico, Istituto di Farmacologia, Facolta' di Scienze MM.FF.NN., Piazza Botta 11, 27100 Pavia, Italy.Received April 4, 1987; accepted August 18, 1987. halothane in the same gas mixture. A scalp incision was made in the dorsal midline. A burr hole was placed at the interparietal/occipital suture in the midline using a refrigerated twist-drill. A small PE-10 polyethylene catheter (0.62 mm o.d.) was inserted into the cisterna magna. Suitable placement of the catheter was assessed by testing the cerebrospinal fluid flowing through the catheter and by observing wit...