Dunn C D
Blut. 1981 May;42(5):307-14. doi: 10.1007/BF00996847.
Ten prostaglandin derivatives have been investigated for their ability to stimulate heme synthesis in serum-free cultures of fetal mouse liver cells in an attempt to define the structural requirements of the prostaglandin molecule necessary for erythrostimulation. In descending order of potency, only PGE2, PGF2 alpha and PGB1 produced at least 50% stimulation of endogenous heme synthesis. Seven of the ten prostaglandin derivatives tested were inhibitory at high concentrations. The PGE2 effect was pharmacologically distinct from that of Ep and could be antagonized by 15 epi PGF2 alpha. Unit gravity cell sedimentation studies demonstrated that PGE2 stimulated only the larger cells within the erythropoietin responsive cell population.
为了确定前列腺素分子刺激红细胞生成所需的结构要求,研究了十种前列腺素衍生物刺激无血清培养的胎鼠肝细胞中血红素合成的能力。按效力从高到低排序,只有PGE2、PGF2α和PGB1能使内源性血红素合成至少增加50%。所测试的十种前列腺素衍生物中有七种在高浓度时具有抑制作用。PGE2的作用在药理学上与Ep不同,且可被15-表- PGF2α拮抗。单位重力细胞沉降研究表明,PGE2仅刺激促红细胞生成素反应性细胞群体中的较大细胞。