摘要
目的:比较唾液酸单体间的生物活性和揭示唾液酸与吗丙嗪间的关系。方法:以兔红细胞膜上钙调蛋白作为手段。结果:N乙酰神经氨酸(5AcNeu,>200μmol/L)和N葡萄糖代神经氨酸(NeuGc,>50μmol/L)能在体外显著抑制兔红细胞膜钙调蛋白(CaM)活性(P<0.05)。抑制率与所用浓度基本呈对数线性。NeuGc的抑制强度约为5AcNeu的2~4倍。此外5AcNeu(200μmol/L)能使低浓度的吗丙嗪(25~100μmol/L)增加对CaM的抑制率,因为在这一浓度范围内,吗丙嗪不能显示抗兔红细胞CaM的活性。结论:本工作进一步证明唾液酸单体具抗细胞钙调蛋白作用。吗丙嗪可能通过唾液酸产生药理活性。
Objective: To compare the biological activity of sialic acid in single forms and mechanism of the correlation between sialic acid and probimane. Methods: Calmodulin activity on rabbit red cell membrane were used. Results: Nacetylneuraminic acid (5 AcNeu,>200 mol/L)and Nglycolylneuraminic acid (NeuGc,>50 mol/L)could significantly inhibit the calmodulin activity on rabbit red cells in vitro(P<0.05).There is a logarithmic linear relation between neuraminic acid concentrations and inhibitory rates.The values of inhibitory rates of NeuGc was approximately 24 times higher than that of 5AcNeu.2 5AcNeu(200 mol/L)could enhance the inhibition of probimane (at low concentrations 25100 mol/L)for calmodulin.]Conclusion: Sialic acid in single form can inhibit calmodulin activity in certain concentration.There is relationship between sialic acid and probimane in calmodulin system.
出处
《河南医学研究》
CAS
1999年第2期105-106,共2页
Henan Medical Research
基金
上海高等教育科学技术发展基金
关键词
唾液酸
乙酰神经氨酸
葡萄糖代
神经氨酸
sialic acid
Nacetylneuraminic acid
Nglycolylneuraminic acid
calmodulin
calcium antagonist
probimane