Honda H, Fukawa K, Sawabe T
Prostaglandins. 1980 Feb;19(2):259-69. doi: 10.1016/0090-6980(80)90024-6.
The influence of adjuvant arthritis in rats on main urinary metabolites (MUM) of prostaglandin (PG) F and E type was studied. 1) In our model rats, urinary excretion of PGE-MUM increased on day 11 prior to the appearance of secondary lesions, but that of PGF-MUM did not change significantly during the observed period (21 days). The excretion of PGE-MUM was not proportional to the increase in both hind paws volume. 2) Indomethacin, which diminished primary lesions but did not suppress secondary lesions, reduced the increase in urinary excretion of PGE-MUM. 3) Prednisolone and azathiopurine, which suppressed both primary and secondary lesions, increased the excretion of PGE-MUM over adjuvant control values on days 4 and 8. The facts described above suggest that the increase of endogenous PGE during days 4 to 8 may be important in the suppression of secondary lesions in adjuvant arthritis in rats.
研究了佐剂性关节炎大鼠对前列腺素(PG)F型和E型主要尿代谢产物(MUM)的影响。1)在我们的模型大鼠中,在继发性病变出现前的第11天,PGE-MUM的尿排泄量增加,但在观察期(21天)内PGF-MUM的尿排泄量没有显著变化。PGE-MUM的排泄量与双后爪体积的增加不成比例。2)消炎痛可减轻原发性病变但不抑制继发性病变,它减少了PGE-MUM尿排泄量的增加。3)泼尼松龙和硫唑嘌呤可抑制原发性和继发性病变,在第4天和第8天,它们使PGE-MUM的排泄量高于佐剂对照值。上述事实表明,在第4至8天内源性PGE的增加可能对抑制大鼠佐剂性关节炎的继发性病变很重要。