Castor C W
J Lab Clin Med. 1975 Mar;85(3):392-404.
Prostaglandins added to synovial cultures stimulated hyaluronic acid (HA) synthesis and glycolysis. The order of potency of the prostaglandins was: PGE1 greater than PGE2 greater than PGF2alpha greater than PGF1alpha, PGE1 and PGE2, 1.0 mug per milliliter, stimulated synovial cells, whereas F-series prostaglandins required 5 mug per milliliter for stimulation. Connective tissue-activating peptide (CTAP) activation of synovial cells was markedly potentiated by all four prostaglandins, and by PGE1 in concentrations as low as 0.01 mug per milliliter. Exogenous prostaglandins caused a prompt and marked increment in synovial cell cyclic-AMP, while CTAP caused a delayed peak of cyclic-AMP of lesser magnitude. Treatment of synovial cultures with cortisol (1.0 mug per milliliter), cycloheximide (10 mug per milliliter), or indomethacin (15.0 mug per milliliter) failed to block stimulation by PGE1, 7-OXA-13-Prostynoic acid, a prostaglandin antagonist, substantially inhibited the action of PGE1 and suppressed the effect of CTAP on synovial cells. It is possible that both exogenous and endogenous (synovial prostaglandins are involved in the connective tissue activation sequence.
添加到滑膜培养物中的前列腺素可刺激透明质酸(HA)合成和糖酵解。前列腺素的效力顺序为:PGE1>PGE2>PGF2α>PGF1α,每毫升1.0微克的PGE1和PGE2可刺激滑膜细胞,而F系列前列腺素刺激滑膜细胞则需要每毫升5微克。所有四种前列腺素以及低至每毫升0.01微克的PGE1均可显著增强滑膜细胞的结缔组织激活肽(CTAP)激活作用。外源性前列腺素可使滑膜细胞环磷酸腺苷(cAMP)迅速且显著增加,而CTAP则导致cAMP出现幅度较小的延迟峰值。用皮质醇(每毫升1.0微克)、环己酰亚胺(每毫升10微克)或吲哚美辛(每毫升15.0微克)处理滑膜培养物,未能阻断PGE1的刺激作用,前列腺素拮抗剂7 - OXA - 13 - 前列腺烯酸可显著抑制PGE1的作用,并抑制CTAP对滑膜细胞的影响。外源性和内源性(滑膜前列腺素)可能都参与了结缔组织激活过程。