Edwards M C, Evans F J, Barrett M L, Gordon D
Inflammation. 1985 Mar;9(1):33-8. doi: 10.1007/BF00915409.
Eight phorbol esters were studied for their ability to stimulate prostaglandin production in human rheumatoid synovial cells over the dose range 0.1 ng to 1.0 micrograms. These derivatives were based upon phorbol, 4-deoxyphorbol, and 12-deoxyphorbol nuclei. This activity was structurally dependent and, although it did not correlate with the actions of the same compounds to induce erythema in vivo, it did correlate with their ability to stimulate human lymphocyte mitogenesis. Stimulation of PGE2 production by a phorbol and a 12-deoxyphorbol analog was inhibited in this system by both indomethacin and dexamethasone.
研究了8种佛波酯在0.1纳克至1.0微克剂量范围内刺激人类风湿性滑膜细胞产生前列腺素的能力。这些衍生物基于佛波醇、4-脱氧佛波醇和12-脱氧佛波醇核。这种活性具有结构依赖性,尽管它与相同化合物在体内诱导红斑的作用不相关,但与它们刺激人淋巴细胞有丝分裂的能力相关。在该系统中,吲哚美辛和地塞米松均抑制了佛波醇和一种12-脱氧佛波醇类似物对PGE2产生的刺激作用。