Barbiturates protect retinal cells from hypoxia in cell culture.

A culture system was used to screen for drugs that can protect mammalian retinal cells from damage induced by hypoxia. Using a special incubator, cultures could be made hypoxic for defined periods. Phase contrast photomicroscopy facilitated comparison of retinal cells before hypoxia and 1 to 2 days after hypoxia. Using 2- to 3-week-old cultures, certain glutamate antagonists, anesthetics, calcium blockers, and thiopental sodium were screened for their effect in protecting cells from hypoxia. The most remarkable effect was noted with thiopental. Quantitative measurements showed a significant increase in the percent of cells surviving after exposure to hypoxia in the presence of 100 mumol/L of thiopental sodium compared with control hypoxic cultures--82% vs 59% at 48 hours. A dose-response curve demonstrated maximal effect at 50 mumol/L of thiopental sodium, with toxic effects noted at 200 mumol/L of thiopental sodium. Our results show that thiopental reduces hypoxia-induced damage to retinal cells in culture.

[1]  M. Marmor,et al.  Dextromethorphan protects retina against ischemic injury in vivo. , 1989, Archives of ophthalmology.

[2]  M. Lusky,et al.  Involvement of excitatory neurotransmitters in the damage produced in chick embryo retinas by anoxia and extracellular high potassium. , 1988, Experimental eye research.

[3]  J. Grotta Current medical and surgical therapy for cerebrovascular disease. , 1987, The New England journal of medicine.

[4]  C. Cartheuser Verapamil enhances brain function tolerance against severe hypoxia without enhancing cerebral blood flow in the rat. , 1987, Pharmacology.

[5]  D. Choi,et al.  Effect of anticonvulsant drugs on glutamate neurotoxicity in cortical cell culture , 1987, Neurology.

[6]  A. Kriegstein,et al.  Glutamate neurotoxicity in cortical cell culture , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  C. Zucker,et al.  Neurotoxic action of kainic acid in the isolated toad and goldfish retina: II. Mechanism of action , 1986, The Journal of comparative neurology.

[8]  B. Engelsen Neurotransmitter glutamate: its clinical importance , 1986, Acta neurologica Scandinavica.

[9]  J. Olney,et al.  Glutamate and the pathophysiology of hypoxic–ischemic brain damage , 1986, Annals of neurology.

[10]  S. Schiff,et al.  High Dose Barbiturate Therapy in Neurosurgery and Intensive Care , 1984, Neurosurgery.

[11]  T. Asano,et al.  Cerebral Protective Effect and Radical Scavenging Action , 1981, Journal of neurochemistry.

[12]  S. Rehncrona,et al.  Inhibitory effects of different barbiturates on lipid peroxidation in brain tissue in vitro: comparison with the effects of promethazine and chlorpromazine. , 1980, Anesthesiology.

[13]  J. Michenfelder,et al.  Cerebral Protection by Thiopental during Hypoxia , 1973, Anesthesiology.

[14]  J. Sheffield,et al.  Electron microscopic analysis of aggregation of embryonic cells: the structure and differentiation of aggregates of neural retina cells. , 1970, Developmental biology.