Suppr超能文献

痛经与前列腺素:药理学及治疗学考量

Dysmenorrhoea and prostaglandins: pharmacological and therapeutic considerations.

作者信息

Dawood M Y

出版信息

Drugs. 1981 Jul;22(1):42-56. doi: 10.2165/00003495-198122010-00003.

Abstract

Primary dysmenorrhoea is characterised by painful menstrual cramps which appear to have no macroscopically identifiable pelvic pathology. 50% of postpubescent females suffer from dysmenorrhoea, and 10% are incapacitated for 1 to 3 days each month. Many of these patients have an increased synthesis of prostaglandins in their endometrial tissue with increased prostaglandin release in the menstrual fluid. The increased amount of prostaglandins induces incoordinate hyperactivity of the uterine muscle resulting in uterine ischaemia and pain. Recent clinical and laboratory studies have shown that many of the non-steroidal anti-inflammatory drugs such as ibuprofen, naproxen, flufenamic acid, mefenamic acid and indomethacin are capable of relieving primary dysmenorrhoea. These drugs are inhibitors of the prostaglandin synthetase enzymes which are necessary for prostaglandin biosynthesis. Thus, with ibuprofen it has been shown that clinical relief of the dysmenorrhoeic symptoms accompanies the reduction of menstrual fluid prostaglandins. With the oral contraceptive pill there is good relief of primary dysmenorrhoea, significant decrease in menstrual fluid prostaglandins, but no reduction in menstrual fluid volume; this suggests that the reduction in prostaglandins is secondary to the inhibition of endometrial growth and development. In some forms of secondary dysmenorrhoea elevated prostaglandin levels have been implicated. However, the evidence is less conclusive for dysmenorrhoea secondary to endometriosis and uterine myomas than for dysmenorrhoea associated with intrauterine devices. With the intrauterine device, prostaglandin synthetase inhibitors such as flufenamic acid, ibuprofen and naproxen are able not only to relieve dysmenorrhoea but also to reduce menstrual blood loss to normal levels. Thus, the use of appropriately selected prostaglandin synthetase inhibitors can offer effective relief from the miseries of some types of dysmenorrhoea with subsequent restoration of normal daily activities.

摘要

原发性痛经的特征是痛经,且似乎没有肉眼可见的盆腔病理改变。50%的青春期后女性患有痛经,其中10%每月会有1至3天无法正常活动。许多此类患者的子宫内膜组织中前列腺素合成增加,月经液中前列腺素释放也增加。前列腺素数量的增加会导致子宫肌肉不协调的过度活动,进而引起子宫缺血和疼痛。近期的临床和实验室研究表明,许多非甾体抗炎药,如布洛芬、萘普生、氟芬那酸、甲芬那酸和吲哚美辛,都能够缓解原发性痛经。这些药物是前列腺素生物合成所必需的前列腺素合成酶的抑制剂。因此,使用布洛芬已表明,痛经症状的临床缓解伴随着月经液中前列腺素的减少。口服避孕药对原发性痛经有良好的缓解作用,月经液中前列腺素显著减少,但月经液量并未减少;这表明前列腺素的减少是子宫内膜生长发育受到抑制的继发结果。在某些继发性痛经形式中,前列腺素水平升高被认为与之有关。然而,对于子宫内膜异位症和子宫肌瘤继发的痛经,证据不如与宫内节育器相关的痛经那样确凿。对于宫内节育器导致的痛经,氟芬那酸、布洛芬和萘普生等前列腺素合成酶抑制剂不仅能够缓解痛经,还能将月经量减少至正常水平。因此,使用适当选择的前列腺素合成酶抑制剂可以有效缓解某些类型痛经带来的痛苦,随后恢复正常的日常活动。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验