Posch K C, Enright W J, Napoli J L
Department of Biochemistry, School of Medicine, State University of New York, Buffalo 14214.
Arch Biochem Biophys. 1989 Oct;274(1):171-8. doi: 10.1016/0003-9861(89)90428-1.
Cytosolic alcohol dehydrogenase in the deermouse is coded by a single genetic locus and a strain of the deermouse which is alcohol dehydrogenase negative exists. These two strains of the deermouse were used to extend insight into the role of cytosolic alcohol dehydrogenases in the conversion of retinol into retinoic acid. Retinoic acid synthesis from physiological concentrations of retinol (7.5 microM) with cytosol from the alcohol dehydrogenase negative deermouse was 13% (liver), 14% (kidney), 60% (testes), 78% (lung), and 100% (small intestinal mucosa) of that observed with cytosol from the positive deermouse. The rates in the negative strain ranged from 0.3 to 0.7 nmol/h/mg protein: sufficient to fulfill cellular needs for retinoic acid. Ten millimolar 4-methylpyrazole inhibited retinoic acid synthesis 92, 94, 26, and 30% in kidney, liver, lung, and testes of the positive deermouse, respectively, but only 50, 30, 0, and 0% in the same tissues from the negative deermouse. Ethanol (300 mM) did not inhibit retinoic acid synthesis in kidney cytosol from the negative strain. Therefore multiple cytosolic dehydrogenases, including alcohol dehydrogenases, contribute to retinol metabolism in vitro. The only enzyme(s) likely to be physiologically significant to retinoic acid synthesis in vivo, however, is the class of dehydrogenase, distinct from ethanol dehydrogenase, that is common to both the positive and the negative deermouse. This conclusion is supported by the data described above, the kinetics of retinoic acid synthesis and retinal reduction in kidney cytosol from the negative deermouse, and the very existence of the alcohol dehydrogenase negative deermouse. This work also shows that microsomes inhibit the cytosolic conversion of retinol into retinoic acid and that the synthesis of retinal, a retinoid that has no known function outside of the eye, does not reflect the ability or capacity of a sample to synthesize retinoic acid.
鹿鼠体内的胞质醇脱氢酶由单个基因位点编码,并且存在醇脱氢酶阴性的鹿鼠品系。利用这两种鹿鼠品系来更深入了解胞质醇脱氢酶在视黄醇转化为视黄酸过程中的作用。以生理浓度的视黄醇(7.5微摩尔)为原料,用醇脱氢酶阴性鹿鼠的胞质溶胶合成视黄酸的量,分别为阳性鹿鼠胞质溶胶合成量的13%(肝脏)、14%(肾脏)、60%(睾丸)、78%(肺)和100%(小肠黏膜)。阴性品系的合成速率为0.3至0.7纳摩尔/小时/毫克蛋白质:足以满足细胞对视黄酸的需求。10毫摩尔的4 - 甲基吡唑分别抑制阳性鹿鼠肾脏、肝脏、肺和睾丸中视黄酸合成的92%、94%、26%和30%,但在阴性鹿鼠相同组织中仅抑制50%、30%、0%和0%。乙醇(300毫摩尔)不抑制阴性品系肾脏胞质溶胶中的视黄酸合成。因此,包括醇脱氢酶在内的多种胞质脱氢酶在体外对视黄醇代谢有贡献。然而,在体内对视黄酸合成可能具有生理意义的唯一酶类,是与乙醇脱氢酶不同的脱氢酶类别,它在阳性和阴性鹿鼠中都存在。上述数据、阴性鹿鼠肾脏胞质溶胶中视黄酸合成和视黄醛还原的动力学以及醇脱氢酶阴性鹿鼠的存在都支持了这一结论。这项研究还表明微粒体抑制视黄醇向视黄酸的胞质转化,并且视黄醛(一种在眼外无已知功能的类视黄醇)的合成并不能反映样品合成视黄酸的能力或容量。