O'Moráin C, Smethurst P, Doré C J, Levi A J
Gut. 1984 Oct;25(10):1078-84. doi: 10.1136/gut.25.10.1078.
Sulphasalazine treatment for inflammatory bowel disease in man causes oligospermia, reduced sperm motility and an increased proportion of abnormal forms. On withdrawal of sulphasalazine these effects are found to be reversible and 15 pregnancies occurred at a median of 2.5 months after stopping sulphasalazine therapy. Seminal plasma concentrations of acid phosphatase fructose and PGE2 as well as the hormone profiles of patients on sulphasalazine for three months were found to be within normal limits. Sulphasalazine fed to male Sprague Dawley rats caused a dose dependent and reversible infertility with a significant reduction in litter size. Rats fed the metabolite sulphapyridine also had a reduced litter size when mated, while those fed the metabolite 5'aminosalicylic acid and a polymer of 5'aminosalicylic acid did not. It seems likely that the sulphapyridine moiety of sulphasalazine is responsible for the infertility seen, the effect being mediated at a late stage in sperm maturation.
柳氮磺胺吡啶用于治疗人类炎性肠病时会导致少精子症、精子活力降低以及异常形态比例增加。停用柳氮磺胺吡啶后,这些影响是可逆的,在停止柳氮磺胺吡啶治疗后的中位时间2.5个月时出现了15例妊娠。发现服用柳氮磺胺吡啶三个月的患者精液中酸性磷酸酶、果糖和前列腺素E2的浓度以及激素水平均在正常范围内。给雄性斯普拉格-道利大鼠喂食柳氮磺胺吡啶会导致剂量依赖性和可逆性不育,产仔数显著减少。喂食代谢产物磺胺吡啶的大鼠交配时产仔数也减少,而喂食代谢产物5-氨基水杨酸和5-氨基水杨酸聚合物的大鼠则没有。柳氮磺胺吡啶的磺胺吡啶部分似乎是导致所观察到的不育的原因,其作用是在精子成熟的后期介导的。