O2 TENSION IN ADULT AND NEONATAL BRAIN-SLICES UNDER SEVERAL EXPERIMENTAL CONDITIONS

被引:88
作者
CHUN, J [1 ]
AGULIAN, S [1 ]
HADDAD, GG [1 ]
机构
[1] YALE UNIV, SCH MED,DEPT PEDIAT,RESP MED SECT, RESP NEUROBIOL LAB,333 CEDAR ST, FITKIN BLDG, NEW HAVEN, CT 06510 USA
关键词
BRAIN TISSUE OXYGEN; HYPOXIA; HYPOGLOSSAL NUCLEUS; POLAROGRAPHIC OXYGEN MICROELECTRODE;
D O I
10.1016/0006-8993(91)91392-E
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain tissue O2 tension (pO2) was measured in brainstem slices of adult and neonatal rats using carbon fiber polarographic microelectrodes. These studies were performed in order to examine the relation between pO2 and a variety of experimental conditions including temperature, distance from slice surface, brain region, animal age, tissue thickness and ambient O2 levels. Baseline brain tissue pO2 was inversely proportional to temperature and depth from slice surface. White matter had a much higher pO2 than gray matter. Tissue thickness and animal age had major effects on tissue pO2. In slices of 800-mu-m thick at 37-degrees-C, for example, brain tissue pO2 in the adult dropped to 0 mm Hg at a depth of 200-300-mu-m, but remained above 45 mm Hg throughout neonatal (3-10 days) slices, when O2 tension in the perfusate was about 600 mm Hg. In thicker neonatal slices (1500-mu-m), pO2 decreased also to 0 mm Hg in deep areas. An N2 environment produced a rapid reduction in pO2 to 0 mm Hg within 15 s, and O2 levels of 21, 10 and 5% induced graded pO2 minima and graded latencies to reach each pO2 nadir. We conclude that: (1) tissue thickness has a major effect on tissue pO2 level: pO2 can reach zero if the slice is thicker than 600-mu-m in the adult and 1500-mu-m thick in the neonate; (2) pO2 level is higher in neonatal brain tissue at all ambient O2 concentrations than in the adult; and (3) graded hypoxia produces patterned and graded reductions in tissue pO2.
引用
收藏
页码:159 / 164
页数:6
相关论文
共 29 条
[1]  
ACKER H, 1983, ADV EXP MED BIOL, V159, P445
[2]   THE PRESERVATION OF NERVE-CELLS IN RAT NEOSTRIATAL SLICES MAINTAINED INVITRO - A MORPHOLOGICAL-STUDY [J].
BAK, IJ ;
MISGELD, U ;
WEILER, M ;
MORGAN, E .
BRAIN RESEARCH, 1980, 197 (02) :341-353
[3]  
BINGMANN D, 1982, EXP BRAIN RES, V48, P89
[4]  
Brezina M, 1958, POLAROGRAPHY MED BIO, pZuman
[5]   INFLUENCE OF THE OXYGEN-PRESSURE IN THE CULTURE-MEDIUM ON THE OXYGENATION OF DIFFERENT TYPES OF MULTICELLULAR SPHEROIDS [J].
CARLSSON, J ;
ACKER, H .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1985, 11 (03) :535-546
[6]   MEMBRANE AND CELLULAR PROPERTIES IN OSCILLATING NETWORKS - IMPLICATIONS FOR RESPIRATION [J].
DEKIN, MS ;
HADDAD, GG .
JOURNAL OF APPLIED PHYSIOLOGY, 1990, 69 (03) :809-821
[7]  
ENNEMA M, 1989, ADV EXP MED BIOL, V248, P451
[8]  
Erdmann W., 1988, Advances in Experimental Medicine and Biology, V222, P397
[9]   EFFECTS OF HYPOXIA ON RAT HIPPOCAMPAL-NEURONS INVITRO [J].
FUJIWARA, N ;
HIGASHI, H ;
SHIMOJI, K ;
YOSHIMURA, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 384 :131-151
[10]   DIRECTLY MEASURED TISSUE OXYGEN-TENSION AND ARTERIAL OXYGEN-TENSION ASSESS TISSUE PERFUSION [J].
GOTTRUP, F ;
FIRMIN, R ;
RABKIN, J ;
HALLIDAY, BJ ;
HUNT, TK .
CRITICAL CARE MEDICINE, 1987, 15 (11) :1030-1036