Strömberg P, Akerlund M, Forsling M L, Granström E, Kindahl H
Acta Obstet Gynecol Scand. 1984;63(6):533-8. doi: 10.3109/00016348409156715.
Both vasopressin and PGF2 alpha are effective uterine stimulants in the non-pregnant human uterus, especially around the onset of menstruation. In order to clarify the relationship of these hormones to menstrual pain, plasma concentrations of vasopressin and two prostaglandin metabolites (15-keto-13,14-dihydro-PGF2 alpha and 11-ketotetranor PGF metabolites) were measured in serial blood samples taken premenstrually and during menstruation. Five women with premenstrual pain gave 7-9 blood samples at intervals of 30 minutes on the day preceding the onset of menstruation. From 5 women with severe primary dysmenorrhea a corresponding series of blood samples were taken during the first day of menstruation. Two groups of 5 women with no symptoms served as controls, either premenstrually or during menstruation. In the women with premenstrual pain the vasopressin concentrations were significantly higher than in the corresponding control group. Even higher and markedly fluctuating vasopressin levels were found in the women with dysmenorrhea who, in general, had more intense pain than the women with premenstrual symptoms. In the group with dysmenorrhea there was also a significant rise in plasma concentration of the PG metabolites. No such increase was seen in the group with premenstrual pain. It is concluded that the pathophysiology of premenstrual pain could imply increased vasopressin secretion. The more severe pain in primary dysmenorrhea seems to be the result of a combined effect of vasopressin and PGF2 alpha.
血管加压素和前列腺素F2α在非妊娠人体子宫中都是有效的子宫刺激物,尤其是在月经开始前后。为了阐明这些激素与痛经的关系,在月经前和月经期间采集的系列血样中测量了血管加压素和两种前列腺素代谢物(15-酮-13,14-二氢前列腺素F2α和11-酮四去甲前列腺素代谢物)的血浆浓度。5名有经前疼痛的女性在月经开始前一天每隔30分钟采集7-9份血样。从5名患有严重原发性痛经的女性中,在月经第一天采集了相应系列的血样。两组各5名无症状女性分别在经前或经期作为对照。有经前疼痛的女性中血管加压素浓度明显高于相应的对照组。痛经女性中发现血管加压素水平更高且明显波动,总体而言,她们的疼痛比有经前症状的女性更强烈。在痛经组中,PG代谢物的血浆浓度也显著升高。经前疼痛组未观察到这种增加。结论是经前疼痛的病理生理学可能意味着血管加压素分泌增加。原发性痛经中更严重的疼痛似乎是血管加压素和前列腺素F2α联合作用的结果。