Sakura S, Fujimoto D
J Biochem. 1981 May;89(5):1541-6. doi: 10.1093/oxfordjournals.jbchem.a133347.
Pyridinoline is a crosslinking amino acid isolated from collagen. Polarographic oxidation and reduction potentials of pyridinoline were measured and compared with those of structurally related compounds, 3-hydroxypyridine, pyridoxine, pyridoxal, and N-methylpyridoxine. Oxidation and reduction potentials of these compounds were found to be near anodic and cathodic limit potentials, respectively, except for pyridoxal. This indicates that a 3-hydroxypyridine ring is very difficult to be reduced or oxidized. The reducibility of pyridinoline with a reducing agent, sodium borohydride, was also studied. It was not reduced by the reagent, however, it was found to be decomposed by light during the treatment. These results indicate that pyridinoline is a so-called "non-reducible" crosslink.
吡啶啉是从胶原蛋白中分离出的一种交联氨基酸。测定了吡啶啉的极谱氧化和还原电位,并与结构相关化合物3-羟基吡啶、吡哆醇、吡哆醛和N-甲基吡哆醇的电位进行了比较。发现除吡哆醛外,这些化合物的氧化和还原电位分别接近阳极和阴极极限电位。这表明3-羟基吡啶环很难被还原或氧化。还研究了吡啶啉与还原剂硼氢化钠的可还原性。该试剂未使其还原,然而,发现在处理过程中它会被光分解。这些结果表明吡啶啉是一种所谓的“不可还原”交联物。