Deslauriers N, Gaudreau P, Brazeau P
Neuroendocrinology Laboratory, Notre-Dame Hospital Research Center, Montreal, Que, Canada.
Regul Pept. 1988 Mar;20(3):261-71. doi: 10.1016/0167-0115(88)90082-1.
We studied the effect of rat growth hormone-releasing factor-(1-43) acid, rGRF(1-43)OH, on the long-term secretion of rat growth hormone (rGH) in dispersed primary cultured cells of rat anterior pituitaries over a period of 7 days or longer. Results of the perifusion assay show that freshly dispersed cells secrete more rGH than 4-day-old redispersed cells (P less than 0.05), that a stabilization period ranging from 4 to 24 h allows a greater production of rGH per day than longer periods (P less than 0.05) and that the working concentrations of rGRF-(1-43)OH and prostaglandin E2 (PGE2) that insured the best responsiveness and longer viability are 50 pM and 10-1000 nM, respectively. Under these conditions, the cells continued secreting rGH after 42 days of perifusion, and 315 milligrams of rGH was produced over that period.
我们研究了大鼠生长激素释放因子(1-43)酸[rGRF(1-43)OH]对大鼠垂体前叶分散原代培养细胞中大鼠生长激素(rGH)长达7天或更长时间的长期分泌的影响。灌流测定结果表明,新鲜分散的细胞比4日龄再分散的细胞分泌更多的rGH(P<0.05),4至24小时的稳定期比更长时间每天产生更多的rGH(P<0.05),并且确保最佳反应性和更长活力的rGRF-(1-43)OH和前列腺素E2(PGE2)的工作浓度分别为50 pM和10 - 1000 nM。在这些条件下,细胞在灌流42天后继续分泌rGH,在此期间产生了315毫克rGH。