Sakai T, Yanagihara S, Ushio K
Br J Ind Med. 1981 Aug;38(3):268-74. doi: 10.1136/oem.38.3.268.
Erythrocyte factors are concerned in the inhibition of delta-aminolaevulinic acid dehydratase (ALA-D) by lead at 20 to 100 nM concentrations. The activity of the factors in detected in Hb fractions from Sephadex G-200 gel filtration of erythrocyte supernatant. After gel filtration of erythrocyte supernatant from a lead worker, 50% of lead is found in ALA-D fractions, although the fractions recover from ALA-D inhibition. The recovered activity is reinhibited if the enzyme fraction is preincubated with Hb fraction obtained from the same chromatography. Similarly obtained enzyme from a normal subject is also inhibited when it is preincubated with normal Hb fraction and lead acetate at 20 to 100 nM concentrations. The extent of the inhibition depends on the concentrations of Hb fraction and lead acetate preincubated. Reinhibition of lead worker enzyme with normal Hb fraction may be deleted not only by heating but also by zinc or DTT as well. Hb fraction heated at 60 degrees C for 5 min is also able to induce the lead-inhibition of the activity in ALA-D fraction. Half life of the factors is 26 min at 60 degrees C and 3 min at 80 degrees C.
红细胞因子与铅在20至100纳摩尔浓度下对δ-氨基乙酰丙酸脱水酶(ALA-D)的抑制作用有关。这些因子的活性可在红细胞上清液经Sephadex G - 200凝胶过滤后的血红蛋白组分中检测到。对一名铅作业工人的红细胞上清液进行凝胶过滤后,50%的铅存在于ALA-D组分中,尽管这些组分可从ALA-D抑制中恢复。如果将酶组分与从同一色谱法获得的血红蛋白组分预孵育,恢复的活性会再次受到抑制。同样,从正常受试者获得的酶在与正常血红蛋白组分和20至100纳摩尔浓度的醋酸铅预孵育时也会受到抑制。抑制程度取决于预孵育的血红蛋白组分和醋酸铅的浓度。用正常血红蛋白组分对铅作业工人的酶进行再次抑制不仅可通过加热消除,也可通过锌或二硫苏糖醇(DTT)消除。在60℃加热5分钟的血红蛋白组分也能够诱导ALA-D组分中活性的铅抑制。这些因子在60℃时的半衰期为26分钟,在80℃时为3分钟。