Pipkin J L, Anson J F, Hinson W G, Duffy P H, Burns E R, Casciano D A
Department of Health and Human Services, Food and Drug Administration, Jefferson, AR 72079.
Toxicol Lett. 1987 Nov;39(1):15-26. doi: 10.1016/0378-4274(87)90252-9.
Exposure to a 12 h light/12 h dark (L/D) cycle for 1 month, followed by reversal to a 12 h D/12 h L (D/L) cycle stimulated within 18 h the incorporation of [3H]leucine and [32P]orthophosphoric acid into new proteins (130-25 kDa) in the G0 phase of the cell cycle of the non-regenerating and regenerating rat liver as observed in two-dimensional gel autoradiograms. Six additional proteins from the rat submaxillary gland (130-20 kDa) revealed labeling with 32P within 3 h following combined administration of isoproterenol and sodium arsenite. Labeling disappeared within 7 days for all stressed proteins.
将大鼠置于12小时光照/12小时黑暗(L/D)周期下1个月,然后反转至12小时黑暗/12小时光照(D/L)周期,在18小时内刺激未再生和再生大鼠肝脏细胞周期G0期新蛋白质(130 - 25 kDa)中[3H]亮氨酸和[32P]正磷酸的掺入,这在二维凝胶放射自显影片中可见。在联合给予异丙肾上腺素和亚砷酸钠后3小时内,大鼠颌下腺的另外六种蛋白质(130 - 20 kDa)显示出32P标记。所有应激蛋白质的标记在7天内消失。