L-NNA-sensitive regional cerebral blood flow augmentation during hypercapnia in type III NOS mutant mice

被引:44
作者
Ma, JY
Meng, W
Ayata, C
Huang, PL
Fishman, MC
Moskowitz, MA
机构
[1] MASSACHUSETTS GEN HOSP, STROKE & NEUROVASC REGULAT LAB, DEPT NEUROSURG & NEUROL, CARDIOVASC RES CTR, CHARLESTOWN, MA 02129 USA
[2] MASSACHUSETTS GEN HOSP, DEPT MED, CHARLESTOWN, MA 02129 USA
[3] HARVARD UNIV, SCH MED, CHARLESTOWN, MA 02129 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1996年 / 271卷 / 04期
关键词
nitric oxide; knockout mice;
D O I
10.1152/ajpheart.1996.271.4.H1717
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effect of N-G-nitro-L-arginine (L-NNA) on regional cerebral blood flow (rCBF) response to hypercapnia (5% CO2 inhalation) was studied in urethan-anesthetized wild-type (SV-129) and type III nitric oxide (NO) synthase (NOS)-deficient mice, using laser-Doppler flowmetry and the closed cranial window technique. Resting rCBF during normocapnia decreased by similar to 25% after L-NNA superfusion in wild-type mice only (n = 18), suggesting a role for type III NOS in baseline blood flow. Hypercapnia augmented rCBP similar to 50% in both wild-type and type III NOS mutant mice. L-NNA superfusion (1 mM) inhibited this increase by similar to 60% in both strains. Hence, synthesis of NO by the constitutively expressed type I NOS contributes to blood flow augmentation during hypercapnia.
引用
收藏
页码:H1717 / H1719
页数:3
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