Hawley C J
Prostaglandins. 1982 Mar;23(3):397-409. doi: 10.1016/0090-6980(82)90085-5.
The effect of prednisolone on prostaglandin (PG) synthesis by rectal biopsies in organ culture was investigated using laminary flow bioassay and radioimmunoassay (RIA) or PGE2. Prednisolone was consistently found to inhibit basal synthesis in cultures whose duration ranged from 2-40 hours. This appeared to be both time and dose dependent. The ability of biopsies homogenised at the end of culture to transform exogenous arachidonic acid into PGE2 under defined conditions was also investigated and operationally designated cyclooxygenase activity. Prior treatment with prednisolone resulted in a reduction in cyclooxygenase activity. This inhibition occurred with a longer latency and to a lesser extent than inhibition of overall basal synthesis. These results suggest that corticosteroids, in addition to their know (indirect) inhibitory action on phospholipase activity, also affect cycloooxygenase activity. The most likely mechanism are either a repression of synthesis of fresh cyclooxygenase enzyme of induction of an endogenous inhibitor of cyclooxygenase activity.
使用层流生物测定法和放射免疫测定法(RIA)检测前列腺素E2,研究了泼尼松龙对器官培养中直肠活检组织前列腺素(PG)合成的影响。在培养时间为2至40小时的培养物中,始终发现泼尼松龙可抑制基础合成。这似乎与时间和剂量均有关。还研究了培养结束时匀浆的活检组织在特定条件下将外源性花生四烯酸转化为前列腺素E2的能力,并将其操作性地定义为环氧化酶活性。泼尼松龙预处理导致环氧化酶活性降低。这种抑制作用的潜伏期较长,且程度小于对总体基础合成的抑制。这些结果表明,皮质类固醇除了对磷脂酶活性有已知的(间接)抑制作用外,还会影响环氧化酶活性。最可能的机制要么是抑制新鲜环氧化酶的合成,要么是诱导环氧化酶活性的内源性抑制剂。