Manni A, Chambers M J, Pearson O H
Endocrinology. 1978 Dec;103(6):2168-71. doi: 10.1210/endo-103-6-2168.
Attempts to restore PRL receptors (PRL-R) in liver membranes of hypophysectomized rats with injections of PRL have so far been only partly successful. In the present study, bovine PRL (bPRL) was mixed with polyvinylpyrrolidone (PVP) in order to sustain PRL blood levels with a single injection a day. PRL-R were measured by displacement of the binding of [125I]ovine PRL (lactoperoxidase oxidation) to a 5000 x g particulate fraction of liver by unlabeled ovine PRL. The number of binding sites was calculated by Scatchard analysis and expressed as femtomoles per mg protein. PRL-R were 85 +/- 12 fmol/mg in normal intact female rats. Seven days posthypophysectomy, PRL-R were undetectable. Daily injections of bPRL with PVP for 10 days fully restored PRL-R (117 +/- 32 fmol/mg). No significant change in PRL-R was noted when bPRL was injected with bovine GH (bGH; 120 +/- 23 fmol/mg), bovine LH (bLH; 84 +/- 14 fmol/mg), bGH plus bLH (90 +/- 12 fmol/mg), or estrogens (79 +/- 12 fmol/mg). Daily injections of bGH or bLH, alone or in combination, or estrogens with PVP failed to restore PRL-R. These results demonstrate a direct role of PRL in stimulating the production of its own receptors when a sustained blood level of the hormone is achieved.
迄今为止,通过注射催乳素(PRL)来恢复垂体切除大鼠肝细胞膜中的PRL受体(PRL-R)的尝试仅取得了部分成功。在本研究中,将牛PRL(bPRL)与聚乙烯吡咯烷酮(PVP)混合,以便每天单次注射来维持PRL的血液水平。通过未标记的绵羊PRL取代[125I]绵羊PRL(乳过氧化物酶氧化)与肝脏5000×g微粒部分的结合来测量PRL-R。结合位点的数量通过Scatchard分析计算,并表示为每毫克蛋白质的飞摩尔数。正常完整雌性大鼠的PRL-R为85±12飞摩尔/毫克。垂体切除术后7天,无法检测到PRL-R。每天注射bPRL与PVP,持续10天可使PRL-R完全恢复(117±32飞摩尔/毫克)。当bPRL与牛生长激素(bGH;120±23飞摩尔/毫克)、牛促黄体生成素(bLH;84±14飞摩尔/毫克)、bGH加bLH(90±12飞摩尔/毫克)或雌激素(79±12飞摩尔/毫克)一起注射时,PRL-R没有显著变化。每天单独或联合注射bGH或bLH,或雌激素与PVP均未能恢复PRL-R。这些结果表明,当激素的血液水平持续维持时,PRL在刺激其自身受体产生方面具有直接作用。