Ericson T, Bratt P
Department of Cariology, University of Umeå, Sweden.
J Oral Pathol. 1987 Sep;16(8):421-4. doi: 10.1111/j.1600-0714.1987.tb02079.x.
The effect of ascorbic acid oxidation and of peroxide on salivary glycoproteins has been studied. No signs of depolymerization of the glycoproteins were observed as a result of treatment of whole saliva or the isolated glycoprotein fraction from human saliva with an ascorbic acid, hydrogen peroxide and cupric ion combination. Sialic acid was analyzed with two methods which gave different chromogens of the acid. The conclusion could be drawn from the results that the effect of ascorbic acid oxidation was a decarboxylation of sialic acid in salivary glycoproteins. This also destroys the bacteria-agglutinating activity of saliva. Full protection of the agglutinin activity is given by salivary peroxidase. It is suggested that one role of peroxidases in saliva is to protect biologically active proteins from the action of oxygen or its radicals.
已经研究了抗坏血酸氧化和过氧化物对唾液糖蛋白的影响。用抗坏血酸、过氧化氢和铜离子组合处理全唾液或从人唾液中分离出的糖蛋白部分,未观察到糖蛋白解聚的迹象。用两种方法分析唾液酸,这两种方法产生不同的酸显色剂。从结果可以得出结论,抗坏血酸氧化的作用是使唾液糖蛋白中的唾液酸脱羧。这也破坏了唾液的细菌凝集活性。唾液过氧化物酶能完全保护凝集素活性。有人提出,过氧化物酶在唾液中的一个作用是保护生物活性蛋白免受氧或其自由基的作用。