Screening for Cerebroprotective Agents Using an In Vivo Model of Cerebral Reversible Depolarization in Awake Rats

The need to screen cerebroprotective compounds wifl'out anesthetic interference prompted the development of a model using hypoxic rats. in this model two outcome measures were used: (1) the time to reach isoelectric electroencephalogram (iEEG), caused by nitrogen gas inhalation in the test cham...

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Bibliographic Details
Main Authors: Bodo, Michael, Perjes, Gabriella, Kalman, Eszter, Bacskai, Emma, Berko, Klara, Sarkadi, Adam, Nagy, Istvan, Keim, Kevin L, Matyski, Frank M, McCarron, Katalin, Csomor, Richard, Zagvazdin, Yuri
Format: Report
Language:English
Subjects:
Anatomy and Physiology
ANESTHETICS
AWAKE RATS
BASE LINES
BLOOD CHEMISTRY
BLOOD CIRCULATION
BLOOD GASES
CENTRAL NERVOUS SYSTEM
CEREBRAL BLOOD FLOW
CEREBROPROTECTIVE AGENTS
CEREBRUM
DEPOLARIZATION
ELECTROENCEPHALOGRAPHY
HYPOXIA
IN VIVO ANALYSIS
INHALATION
ISOELECTRIC ELECTROENCEPHALOGRAM
Medicine and Medical Research
NITROGEN
Optics
PHARACEUTICAL SCREENING
RATS
REPRINTS
REVERSIBLE
REVERSIBLE DEPOLARIZATION
TEST FACILITIES
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Summary:The need to screen cerebroprotective compounds wifl'out anesthetic interference prompted the development of a model using hypoxic rats. in this model two outcome measures were used: (1) the time to reach isoelectric electroencephalogram (iEEG), caused by nitrogen gas inhalation in the test chamber, and (2) the time for behavioral recovery measuring the latency of restoration of the head-withdrawal reflex upon vibrissae stimulation. We report here data of blood chemistry cerebral tissue oxygen measurements, a definition of a proposed scoring system, and the pharmacological results of RGH-2202. The findings with RGH-2202 are used here to show the utility of the screening method. Evetits duritig hypoxia: Arterial and venous pO1, pCO1, and pH, and brain tissue PO2 significantly declined. Significant correlations were established among the PO2 of cerebral tissue, blood, and the test chamber. RGH-2202 significantly and dose-dependently shortened the iEEG time; the compound's Effective Dose30 was 227.8 mg kg(exp -1). Events during recovery: Immediately after the iEEG, when the atmosphere in the chamber was replaced with room air, the arterial, venous and brain tissue P02 increased above the control level and subsequently recovered to baseline levels. Behavioral recovery occurred before blood chemistry was otherwise normalized. RGH-2202 significantly and dose-dependently shortened the recovery time; the Effective Dose30 was 8.71 mg kg(exp -1). The available data define and support the physiological basis of this practicable rat-screening model. Published in Pharmacological Research, v44 n5, p419-429, 2001.