Abstract | OBJECTIVE: METHODS: RESULTS: Both 0.1 g/L Glu-BSA and Gal-BSA could slightly decrease GSH level, while 1 g/L of them significantly decreased GSH level by 35% and 43% respectively. The MDA levels of both 1 g/L AGEs treated groups (306 +/- 13 and 346 +/- 22) were higher than that of the normal group (189 +/- 18), which could be inhibited by free radical scavenger NAC. The SOD activities of both 1 g/L AGEs treated groups (67.0 +/- 5.2 and 74.0 +/- 11.0) were lower than that of the normal group (85.2 +/- 8.0). Both 0.1 g/L AGEs could slightly increase the activity of MAO-B, while 1 g/L of them could increase MAO-B activity by 1.5 and 1.7 folds respectively. Both AGEs stimulation could produce NO level by 1.7 and 2 folds respectively. CONCLUSION: Enhanced levels of astrocytic oxidation stress and decrease of antioxidation abilities may contribute to, at least partially, the detrimental effects of AGEs in neuronal disorders and aging brain.
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Authors | Jian-Ming Jiang, Zhen Wang, Dian-Dong Li |
Journal | Biomedical and environmental sciences : BES
(Biomed Environ Sci)
Vol. 17
Issue 1
Pg. 79-86
(Mar 2004)
ISSN: 0895-3988 [Print] China |
PMID | 15202867
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Glycation End Products, Advanced
- advanced glycation end products-bovine serum albumin
- Serum Albumin, Bovine
- Nitric Oxide
- Malondialdehyde
- Superoxide Dismutase
- Monoamine Oxidase
- Glutathione
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Topics |
- Animals
- Astrocytes
(drug effects, enzymology, metabolism)
- Cattle
- Cells, Cultured
- Cerebral Cortex
(cytology)
- Glutathione
(metabolism)
- Glycation End Products, Advanced
(pharmacology)
- Malondialdehyde
(metabolism)
- Monoamine Oxidase
(metabolism)
- Nitric Oxide
(metabolism)
- Oxidative Stress
(drug effects)
- Rats
- Rats, Wistar
- Serum Albumin, Bovine
(pharmacology)
- Superoxide Dismutase
(metabolism)
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