Hawkey C J, Karmeli F, Rachmilewitz D
Gut. 1983 Oct;24(10):881-5. doi: 10.1136/gut.24.10.881.
Synthesis of prostanoids in Crohn's disease was investigated using rectal biopsy specimens maintained in organ culture. As with ulcerative colitis increased synthesis of prostaglandin (PG)E2 was observed when the mucosa was inflamed, compared with uninflamed mucosa in Crohn's disease, and with control biopsy specimens. In contrast with ulcerative colitis differences from control specimens were observed even in the absence of inflammation. There was a raised synthesis of thromboxane (Tx)B2 (stable breakdown product of TxA2); concentrations of 6-keto PGF1 alpha (stable breakdown product of prostacyclin) were unchanged and hence the ratio of 6-keto PGF1 alpha/TxB2 was reduced. These changes might lead to an altered cytoprotective capacity or reduced suppressor cell activity, such as has previously been reported in intestinal lymphocytes in Crohn's disease.
利用器官培养中保存的直肠活检标本,对克罗恩病中类前列腺素的合成进行了研究。与溃疡性结肠炎一样,当黏膜发炎时,与克罗恩病未发炎的黏膜以及对照活检标本相比,观察到前列腺素(PG)E2的合成增加。与溃疡性结肠炎不同,即使在没有炎症的情况下,也观察到与对照标本存在差异。血栓素(Tx)B2(TxA2的稳定分解产物)的合成增加;6-酮-前列腺素F1α(前列环素的稳定分解产物)的浓度未发生变化,因此6-酮-前列腺素F1α/TxB2的比值降低。这些变化可能导致细胞保护能力改变或抑制细胞活性降低,如先前在克罗恩病的肠道淋巴细胞中所报道的那样。