Sigel M B, Thorpe N A, Kobrin M S, Lewis U J, Vanderlaan W P
Endocrinology. 1981 Apr;108(4):1600-3. doi: 10.1210/endo-108-4-1600.
The dose-dependent displacement characteristics of a biologically active 20,000 molecular weight human pituitary growth hormone variant (20K) and of human growth hormone (hGH) were compared using hGH liver plasma membrane receptors both from 20-30 day pregnant rabbits and from normal female rats and also using mammary gland plasma membrane receptors from 5-6 day lactating rabbits. Different preparations of 20K were found to be only 3-20% as potent as hGH when compared at the dose necessary to cause 50% displacement of (125I)iodo-hGH from liver receptor and was 22-53% as effective as hGH in the mammary receptor assay system. These findings suggest that 20K and hGH may have separate receptors or that the binding characteristics of the two hormones may be quite different.
使用来自20至30天孕兔和正常雌性大鼠的hGH肝细胞膜受体,以及来自5至6天泌乳兔的乳腺细胞膜受体,比较了具有生物活性的20,000分子量人垂体生长激素变体(20K)和人生长激素(hGH)的剂量依赖性置换特性。当比较引起(125I)碘-hGH从肝受体50%置换所需剂量时,发现不同制剂的20K效力仅为hGH的3%至20%,在乳腺受体测定系统中,其效力为hGH的22%至53%。这些发现表明,20K和hGH可能具有不同的受体,或者这两种激素的结合特性可能有很大差异。