Effect of Hypoxia-Ischemia on Striatal Monoamine Metabolism in Neonatal Rat Brains.
- Author:
Youn Hee JEE
1
;
Hyung Gun KIM
;
Woo Sung PARK
;
Young Pyo CHANG
Author Information
1. Department of Pediatrics, Collage of Medicine, Dankook University, Cheonan, Korea. ychang@dku.edu
- Publication Type:Original Article
- Keywords:
Hypoxia-Ischemia;
Striatum;
Monoamine;
Newborn
- MeSH:
3,4-Dihydroxyphenylacetic Acid;
Animals;
Anoxia;
Brain*;
Carotid Artery, Common;
Cerebrospinal Fluid;
Dopamine;
Humans;
Hydroxyindoleacetic Acid;
Infant, Newborn;
Metabolism*;
Microdialysis;
Rats*
- From:Journal of the Korean Pediatric Society
2003;46(8):789-794
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: We intended to evaluate the effect of hypoxia-ischemia on extracellular striatal monoamine metabolism in neonatal rat brains by in vivo microdialysis. METHODS: The right common carotid arteries of five or six-day old rats were surgically ligated, and the probes for microdialysis were inserted into the right striatum with stereotaxic instrument. After stabilization for two hours, artificial cerebrospinal fluid was infused via the probe for microdialysis and samples were collected during hypoxia-ischemia and recovery periods at 20 minute intervals. The concentrations of DA(dopamine), DOPAC(3,4-di-hydroxyphenyl acetic acid), HVA(homovanillic acid), NE(norepinephrine), and 5-HIAA(5-hydroxy indoleacetic acid) were measured by HPLC(high performance liquid chromatography) and the changes were analysed. RESULTS: The striatal levels of dopamine metabolites such as DOPAC and HVA, were significantly decreased during hypoxia-ischemia, and increased to their basal level during reoxygenation(P<0.05). Dopamine mostly increased during hypoxia but statistically not significant(P>0.05). DOPAC showed the most remarkable decrease(23.0+/-4.2%, P<0.05), during hypoxia-ischemia and increase to the basal levels during reoxygenation(120.8+/-54.9%, P<0.05), and HVA showed the same pattern of changes as those of DOPAC during hypoxia-ischemia(35.3+/-7.6% of basal level, P<0.05) and reoxygenation (105.8+/-32.3%). However, the level of NE did not show significant changes during hypoxia-ischemia and reoxygenation. The levels of 5-HIAA decreased(74.9+/-3.1%) and increased(118.1+/-7.8%) during hypoxia-ischemia and reoxygenation, respectively(P<0.005). CONCLUSION: Hypoxia-ischemia had a significant influence on the metabolism of striatal monoamine in neonatal rat brains. These findings suggest that monoamine, especially dopamine, and its metabolites could have a significant role in the pathogenesis of hypoxic-ischemic injury of neonatal rat brains.
