Simultaneous Determination of Local Cerebral Glucose Utilization and Blood Flow by Carbon-14 Double-Label Autoradiography: Method of Procedure and Validation Studies in the Rat

• Published in: Journal of cerebral blood flow and metabolism 1986-06, Vol.6 (3), p.273-285
• Main Authors: Ginsberg, Myron D., Smith, David W., Wachtel, Mitchell S., Gonzalez-Carvajal, Mayra, Busto, Raul
• Format: Article
• Language: English
• Subjects: Animals; Antipyrine - analogs & derivatives; Autoradiography; Biological and medical sciences; Blood Flow Velocity; Brain - metabolism; Carbon Radioisotopes; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges; Cerebrovascular Circulation; Deoxy Sugars - metabolism; Deoxyglucose - metabolism; Fundamental and applied biological sciences. Psychology; Kinetics; Male; Rats; Rats, Inbred Strains; Regression Analysis; Vertebrates: nervous system and sense organs
• ISSN: 0271-678X; 1559-7016
• DOI: 10.1038/jcbfm.1986.49

Validation studies were undertaken to establish a computer-assisted double-label autoradiographic strategy employing [14C]2-deoxyglucose ([14C]2DG) and [14C]iodoantipyrine ([14C]IAP) to measure local CMRglu (LCMRglu) and CBF (LCBF). An organic solvent was used to extract the majority of IAP between first and second film exposures. In contrast to previously published data, all solvents tested produced partial losses of 2DG from tissue, and all allowed 2–6% of IAP to persist even after 5-day washes. Technical-grade chloroform permitted equal retention of unmetabolized and metabolized 2DG. A linear model was established, which was insensitive to the changes in tissue self-absorption that were shown to occur with chloroform extraction. Propagated error in computing tissue [14C]2DG and [14C]IAP was reduced by maximizing IAP extraction (by longer solvent wash times) and by administering 2.5 times as much IAP as 2DG. Fractional 2DG retention was measured in single-label 2DG sections placed on the films, and fractional IAP retention was evaluated by an optimization procedure. With this strategy, double-label values for LCMRglu and LCBF in anesthetized rats agreed with values obtained in matched single-label series to within 5%. The coefficients of variation for the double- and single-label LCMRglu data were virtually identical, whereas the coefficient of variation for double-label LCBF was 1.8 times that of single-label LCBF. The double-label strategy permitted pixel-by-pixel measurement and video display of the LCMRglu/LCBF ratio; the mean value among structures was 0.472 μmol/ml. With proper attention to methodological detail, this double-label strategy shows great promise for routine laboratory application.