Full metadata record
DC FieldValueLanguage
dc.contributor.authorChang, Chi-Chenen_US
dc.contributor.authorHsieh, Yao-Yuanen_US
dc.contributor.authorHsu, Kung-Haoen_US
dc.contributor.authorLin, Chih-Shengen_US
dc.date.accessioned2014-12-08T15:11:57Z-
dc.date.available2014-12-08T15:11:57Z-
dc.date.issued2011-03-01en_US
dc.identifier.issn1028-4559en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tjog.2009.08.003en_US
dc.identifier.urihttp://hdl.handle.net/11536/9164-
dc.description.abstractCondensation: Both Gonal-F and Puregon, especially in their high-dosage administration, might inhibit the endometrial cell proliferation in the initial 48-hour culture. After 72-hour culture, Gonal-F persisted the inhibition of the endometrial growth, whereas Puregon reversed its effect to enhance endometrial growth. Objectives: Endometrial proliferation or regeneration during menstrual cycle is regulated by sexual hormones. However, the effect of gonadotropins on the endometrial cell growth remains obscure. Herein, we aimed to investigate the effects of recombinant follicle-stimulating hormones (r-FSHs) (Gonal-F and Puregon) on the proliferation of human endometrial cells in vitro. Materials and Methods: Human endometrial cells (RL95-2 cells) were obtained commercially and cultured in the serum-containing media in the presence of r-FSHs (Gonal-F and Puregon at concentrations of 0 mIU/mL, 200 mIU/mL, 400 mIU/mL, and 600 mIU/mL) up to 72 hours. According to the gonadotropin concentrations, all cultured endometrial cells were divided into four groups: (1) 0 mIU/mL (control); (2) 200 mIU/mL; (3) 400 mIU/mL; and (4) 600 mIU/mL. After 72-hour culture, endometrial cell proliferations were assessed overnight by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The influences of different r-FSH agents and dosages on endometrial cell proliferation in each group were evaluated and compared. Results: In the four Gonal-F groups, the cell absorption (control and 200 mIU/mL, 400 mIU/mL, and 600 mIU/mL Gonal-F) after 24/48/72-hour cultures were as follows: (1) 0.57/0.7/0.82; (2) 0.56/0.66/0.78; (3) 0.55/0.64/0.77: and (4) 0.51/0.61/0.78. After 48 hours, higher dosage of Gonal-F appeared to significantly inhibit the endometrial cell proliferation. After 72-hour culture, all three dosages of Gonal-F appeared to inhibit the endometrial cell proliferation similarly. In Puregon groups, the cell absorptions were as follows: (1) 0.62/0.53/0.62; (2) 0.61/0.5/0.66; (3) 0.61/0.49/0.66; and (4) 0.64/0.49/0.66. Puregon administration displayed initial inhibition and subsequent stimulation effects on the endometrial cells. Conclusions: Both Gonal-F and Puregon, especially in their high-dosage administration, appeared to inhibit the endometrial cell proliferation in the initial 48-hour culture. After 72-hour culture, Gonal-F persisted the inhibition of the endometrium, whereas Puregon reversed its effect by enhancing the endometrial growth. The differences might be because of the different formulations or molecular structures existing between alpha and beta follitropins. Copyright (C) 2011, Taiwan Association of Obstetrics & Gynecology. Published by Elsevier Taiwan LLC. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectEndometriumen_US
dc.subjectGonadotropinen_US
dc.subjectGonal-Fen_US
dc.subjectIVFen_US
dc.subjectPuregonen_US
dc.titleEffects of gonadotropins (Gonal-F and Puregon) on human endometrial cell proliferation in vitroen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tjog.2009.08.003en_US
dc.identifier.journalTAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGYen_US
dc.citation.volume50en_US
dc.citation.issue1en_US
dc.citation.spage42en_US
dc.citation.epage47en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000290188000010-
dc.citation.woscount1-
Appears in Collections:Articles


Files in This Item:

  1. 000290188000010.pdf

If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.