Coulter C L, Young I R, Browne C A, McMillen I C
Department of Physiology, Monash University, Clayton, Victoria, Australia.
J Endocrinol. 1992 Sep;134(3):369-75. doi: 10.1677/joe.0.1340369.
We have investigated the possible role of the fetal pituitary and ACTH in the control of the synthesis and post-translational processing of the enkephalin precursor, proenkephalin A (proEnk A), in the fetal sheep adrenal gland in late gestation. Fetal hypophysectomy (n = 8) or sham operations (n = 4) were performed between 109 and 118 days of gestation. At 138-139 days, either ACTH(1-24) (10.5 micrograms/0.24 ml saline per h, n = 4) was infused intravenously for 72 h into hypophysectomized fetal sheep or 0.9% (w/v) NaCl alone (0.24 ml/h, n = 4) was infused for 72 h into hypophysectomized fetal sheep and sham-operated animals. At the end of the infusion the pregnant ewe was killed and left or right adrenal glands (n = 12) were collected from the fetal sheep that were intact and given saline (Intact + sal; n = 4), hypophysectomized and given saline (Hx + sal; n = 4) and hypophysectomized and given ACTH (Hx + ACTH; n = 4). Each adrenal was homogenized in acid (acetic acid (1 mol/l)/HCl (20 mmol/l)/2-mercaptoethanol (0.2%)). After centrifugation, the supernatant was loaded onto a Sephadex G-75 column (2.0 x 50 cm), eluted at 80 ml/24 h and fractions were collected (5 ml, n = 42). An aliquot of each fraction (2 ml) was dried down prior to enzymatic digestion (trypsin/carboxypeptidase B) and oxidation with H2O2, and assay for methionine-O-enkephalin (immunoreactive Met-O-Enk).(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了胎儿垂体和促肾上腺皮质激素(ACTH)在妊娠晚期胎羊肾上腺中对脑啡肽前体——前脑啡肽A(proEnk A)的合成及翻译后加工过程的控制中可能发挥的作用。在妊娠109至118天之间进行了胎儿垂体切除术(n = 8)或假手术(n = 4)。在138 - 139天时,将促肾上腺皮质激素(1 - 24)(每小时10.5微克/0.24毫升生理盐水,n = 4)静脉输注到垂体切除的胎羊体内72小时,或者将0.9%(w/v)氯化钠(0.24毫升/小时,n = 4)单独输注到垂体切除的胎羊和假手术动物体内72小时。输注结束时,处死妊娠母羊,从完整且接受生理盐水的胎羊(完整 + 生理盐水;n = 4)、垂体切除且接受生理盐水的胎羊(垂体切除 + 生理盐水;n = 4)以及垂体切除且接受促肾上腺皮质激素的胎羊(垂体切除 + 促肾上腺皮质激素;n = 4)中收集左或右肾上腺(n = 12)。每个肾上腺在酸(乙酸(1摩尔/升)/盐酸(20毫摩尔/升)/2 - 巯基乙醇(0.2%))中匀浆。离心后,将上清液加载到葡聚糖凝胶G - 75柱(2.0×50厘米)上,以80毫升/24小时的流速洗脱,并收集馏分(5毫升,n = 42)。每个馏分取一份等分试样(2毫升),在进行酶消化(胰蛋白酶/羧肽酶B)和用过氧化氢氧化之前进行干燥,然后测定甲硫氨酸 - O - 脑啡肽(免疫反应性甲硫氨酸 - O - 脑啡肽)。(摘要截取自250字)