Effects of MK-801 on cerebral regional oxygen consumption in focal cerebral ischemia in rats.
Effects of MK-801 on cerebral regional oxygen consumption in focal cerebral ischemia in rats.
复制标题
MK-801 对局灶性脑缺血大鼠脑局部耗氧量的影响。
DOI:
10.1161/01.res.69.2.414
复制
发表时间:
1991
影响因子:
20.1
通讯作者:
Weiss,HR
中科院分区:
文献类型:
--
作者:
Chi,OZ;Anwar,M;Sinha,AK;Weiss,HR
This investigation tested in rats whether MK-801, an N-methyl-D-aspartate receptor antagonist, would improve the balance of oxygen supply and consumption in the focal ischemic area of the brain induced by occlusion of the middle cerebral artery. Fifteen minutes after middle cerebral artery occlusion, 5 mg/kg MK-801 was administered intravenously to the MK-801 group (n = 12), and normal saline was given to the control group (n = 12). One hour after the occlusion in each group, regional cerebral blood flow was determined in six rats using [14C]iodoantipyrine, and regional arterial and venous oxygen saturations were determined using a microspectrophotometric technique in the other six rats. In both groups of animals, the cerebral blood flow of the ischemic cortex was significantly lower than that of the contralateral cortex (36 +/- 16 [SD] and 67 +/- 14 ml/min/100 g for the control group; 33 +/- 10 and 58 +/- 11 ml/min/100 g for the MK-801 group, respectively). Oxygen extraction was significantly higher in the ischemic cortex (8.8 +/- 2.1 ml O2/100 ml blood) than in the contralateral cortex (5.6 +/- 0.3) for the control group. However, for the MK-801 group, there was no significant difference between the ischemic cortex (6.1 +/- 1.0) and the contralateral cortex (5.7 +/- 1.1). Oxygen extraction in the ischemic cortex of the MK-801 group was significantly lower than that of the control group. Calculated ischemic regional oxygen consumption was similar to the nonischemic values in the control group, whereas the ischemic value was reduced to 61% of the value of the contralateral cortex in the MK-801 group.(ABSTRACT TRUNCATED AT 250 WORDS)
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影响因子:
8.3
作者:
R. Slater;M. Reivich;H. Goldberg;R. Banka;J. Greenberg
通讯作者:
J. Greenberg
影响因子:
20.1
作者:
M. Anwar;E. Buchweitz;H. Weiss
通讯作者:
H. Weiss
影响因子:
4.7
作者:
D. Cox;R. Osborne;J. Watkins
通讯作者:
J. Watkins
影响因子:
2.1
作者:
L. Nilsson;B. K. Siesjô
通讯作者:
B. K. Siesjô
影响因子:
6.3
作者:
HAGBERG, H;LEHMANN, A;HAMBERGER, A
通讯作者:
HAMBERGER, A