Geesin J C, Gordon J S, Berg R A
Department of Biochemistry, University of Medicine & Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854.
Arch Biochem Biophys. 1990 May 1;278(2):350-5. doi: 10.1016/0003-9861(90)90270-9.
Ascorbate has been shown to stimulate collagen synthesis in cultured human dermal fibroblasts by increasing transcription of the collagen genes. In the present studies, ascorbate stimulates lipid peroxidation at concentrations similar to those necessary to affect collagen synthesis. Molecules which inhibit lipid peroxidation, such as propyl gallate, cobalt chloride, and alpha-naphthol, also inhibit collagen synthesis, suggesting a correlation between the two phenomena. Retinoic acid and some synthetic retinoids have previously been shown to inhibit collagen synthesis in cultured human dermal fibroblasts. In our studies two different retinoids, at similar concentrations, inhibit both ascorbate-stimulated lipid peroxidation and collagen synthesis. Since high concentrations of retinoids were required, the ability of retinoids to inhibit the oxidant effect of ascorbate, and not their receptor-mediated activity, may be responsible for their effect on collagen synthesis.
已证明抗坏血酸盐可通过增加胶原蛋白基因的转录来刺激培养的人皮肤成纤维细胞中的胶原蛋白合成。在本研究中,抗坏血酸盐在与影响胶原蛋白合成所需浓度相似的情况下刺激脂质过氧化。抑制脂质过氧化的分子,如没食子酸丙酯、氯化钴和α-萘酚,也抑制胶原蛋白合成,表明这两种现象之间存在相关性。视黄酸和一些合成类视黄醇先前已被证明可抑制培养的人皮肤成纤维细胞中的胶原蛋白合成。在我们的研究中,两种不同的类视黄醇在相似浓度下可抑制抗坏血酸盐刺激的脂质过氧化和胶原蛋白合成。由于需要高浓度的类视黄醇,类视黄醇抑制抗坏血酸盐氧化作用的能力,而非其受体介导的活性,可能是其对胶原蛋白合成产生影响的原因。