生物活性 | |||
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描述 | L-Cycloserine is an irreversible inhibitor of 3-ketodihydrosphingosine synthetase, which is the first enzyme of the sphingolipid pathway, and causes the synthesis of sphingolipids to decrease[3]. L-cycloserine injected subcutaneously in young mice have shown that cerebroside synthesis is inhibited specifically. It is also resulted in significant reduction in brain cerebroside level with low-dose injection for two month; liver and spleen glucocerebroside levels were also significantly reduced[4]. L-Cycloserine inhibited the activity of gamma-aminobutyric acid (GABA)-transaminase (GABA-T) and elevated the level of GABA in whole mouse brain with a peak effect 3-4 hr after injection. L-Cycloserine (10-30 mg/kg, p.o. or i.p.) prevented tonic seizures induced by 3-mercaptopropionic acid (3-MPA) and audiogenic seizures in DBA/2 mice. Similarly, small doses of L-cycloserine reduced the level of cGMP in the cerebellum of rats. Larger doses of L-cycloserine (greater than 30-100 mg/kg) impaired the performance of mice in the rotarod, chimney and horizontal wire tests, and reduced spontaneous locomotor activity of rats[5]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
9.80mL 1.96mL 0.98mL |
48.98mL 9.80mL 4.90mL |
97.95mL 19.59mL 9.80mL |
参考文献 |
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