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Failure of Parturition in Mice Lacking the Prostaglandin F Receptor
Abstract
Mice lacking the gene encoding the receptor for prostaglandin F 2α (FP) developed normally but were unable to deliver normal fetuses at term. Although these FP-deficient mice showed no abnormality in the estrous cycle, ovulation, fertilization, or implantation, they did not respond to exogenous oxytocin because of the lack of induction of oxytocin receptor (a proposed triggering event in parturition), and they did not show the normal decline of serum progesterone concentrations that precedes parturition. Ovariectomy at day 19 of pregnancy restored induction of the oxytocin receptor and permitted successful delivery in the FP-deficient mice. These results indicate that parturition is initiated when prostaglandin F 2α interacts with FP in ovarian luteal cells of the pregnant mice to induce luteolysis.
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“Multiple factors initiate parturition, including fetal cortisol, maternal drop in progesterone, oxytocin, prostaglandin F2α and other endocrine factors56–59.”
From Conditional loss of ERK1 and ERK2 results in abnormal placentation and delayed parturition in the mouse (2019) · cites this paper as [58]
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Items 201–300 of 608
Roizen, J. D., Asada, M., Tong, M., Tai, H., & Muglia, L. J. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0178 · Cited by 48
“The observation of the early initiation of labor in the context of sustained circulating progesterone in the 15HPGD hypomorphic mice is notable in light of the delayed labor observed in the FP receptor knockout mice (13).”
BackgroundInfluentialCoordinate Regulation of Prostaglandin Metabolism for Induction of Parturition in Mice
Winchester, S. K., Imamura, T., Gross, G. A., Muglia, L. M., Vogt, S. K., Wright, J., Watanabe, K., Tai, H., & Muglia, L. J. (2002) · Endocrinology · doi:10.1210/endo.143.7.8926 · Cited by 48
“The temporal association of the increase in uterine PGF2 and the decline in serum progesterone, together with previous gene ablation and pharmacological studies (2, 3, 7, 13), define the regulated induction of uterine PGF2 production as a key event for the timing of labor in the mouse.”
Biochemical and endocrinological preparation for parturition
Terzidou, V. (2007) · Best Practice & Research Clinical Obstetrics & Gynaecology · doi:10.1016/j.bpobgyn.2007.05.001 · Cited by 48
Prostaglandin E2 increases cyp19 expression in rat granulosa cells: Implication of GATA-4
Cai, Z., Kwintkiewicz, J., Young, M. E., & Stocco, C. O. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2006.09.012 · Cited by 48
“In mice, the absence of PGF2α receptors causes a failure in parturition due to the lack of luteal regression (Sugimoto et al., 1997).”
BackgroundMurata, T., Narita, K., HONDA, K., Matsukawa, S., & Higuchi, T. (2003) · Endocrine Journal · doi:10.1507/endocrj.50.579 · Cited by 48
“also been reported in pregnant rats [26] and prostaglandin F 2 -deficient pregnant mice [36].”
BackgroundSelf-citationPutative Role of Prostaglandin Receptor in Intracerebral Hemorrhage
Mohan, S., Ahmad, A. S., Glushakov, A. V., Chambers, C., & Doré, S. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00145 · Cited by 47
“However, PGF2α is known to play a significant role in the initiation of parturition, renal function, control of cerebral blood flow, and intraocular pressure principally by an increase in uveoscleral outflow of aqueous humor, autoregulation in newborn piglets, contraction of arteries, and myocardial dysfunction (Chemt…”
BackgroundThe Comparative Physiology of Parturition in Mammals
Young, I. R. (2001) · KARGER eBooks · doi:10.1159/000061036 · Cited by 49
What knockout mice can tell us about parturition
Kimura, T. (1999) · Reviews of Reproduction · doi:10.1530/revreprod/4.2.73 · Cited by 47
PG F2α Receptor: A Promising Therapeutic Target for Cardiovascular Disease
Zhang, J., Gong, Y., & Yu, Y. (2010) · Frontiers in Pharmacology · doi:10.3389/fphar.2010.00116 · Cited by 46
“…is disrupted in mice lacking either cytosolic phospholipase A 2 (cPLA 2 ; Bonventre et al., 1997), that mobilizes arachidonic acid release for COX metabolism, COX-2, the more regulated form of that enzyme (Dinchuk et al., 1995; Morham et al., 1995) or the FP receptor (Sugimoto et al., 1997).”
Prostaglandins and Prostanoid Receptors in Human Pregnancy and Parturition
Slater, D. M., Zervou, S., & Thornton, S. (2002) · Journal of the Society for Gynecologic Investigation · doi:10.1016/s1071-5576(02)00151-x · Cited by 46
Effect of Latanoprost on Intraocular Pressure in Mice Lacking the Prostaglandin FP Receptor
Crowston, J. G., Lindsey, J. D., Aihara, M., & Weinreb, R. N. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.04-0338 · Cited by 46
“Both the homozygous and heterozygous knockout mice develop normally and have no gross abnormalities in behavior, macro- and microscopic anatomy, or biochemical or hematologic indices.(17) Hence, the purpose of this study was to determine whether latanoprost lowers IOP in mice that do not express the PG FP receptor.”
BackgroundMethodInfluentialChien, E. K., & MacGregor, C. (2003) · American Journal of Obstetrics and Gynecology · doi:10.1067/s0002-9378(03)00764-6 · Cited by 46
Prostaglandin E Inhibits Indomethacin-Induced Gastric Lesions through EP-1 Receptors
Suzuki, K., Araki, H., Mizoguchi, H., Furukawa, O., & Takeuchi, K. (2001) · Digestion · doi:10.1159/000051876 · Cited by 46
Word, R. A., Landrum, C. P., Timmons, B. C., Young, S. G., & Mahendroo, M. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.042663 · Cited by 46
“Animals with null mutations in the genes encoding phospholipase A2 (Pla2g4a) [4], the prostaglandin F2a receptor (Ptgfr) [5], cyclooxygenase (COX)-1 (Ptgs1) [6], or 20a-hydroxysteroid dehydrogenase (Akr1c18) [7] fail to undergo normal parturition at term because of failed luteolysis.”
BackgroundMouse Placental Prostaglandins Are Associated with Uterine Activation and the Timing of Birth1
Cook, J. L., Shallow, M. C., Zaragoza, D. B., Anderson, K. I., & Olson, D. M. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.008789 · Cited by 46
“This increase in PGHS-1 leads to enhanced circulating levels of PGF2a, the luteolytic agent [3, 4].”
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Self-citationYuhki, K., Ueno, A., Naraba, H., Kojima, F., Ushikubi, F., Narumiya, S., & Oh‐ishi, S. (2004) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.104.071548 · Cited by 45
Self-citationThe Genetics of Birth Timing: Insights into a Fundamental Component of Human Development
Chaudhari, B. P., Plunkett, J., Ratajczak, C., Shen, T., DeFranco, E., & Muglia, L. (2008) · Clinical Genetics · doi:10.1111/j.1399-0004.2008.01124.x · Cited by 44
“Perhaps most importantly, mice, but not humans, experience a decline in serum progesterone levels as term approaches (48, 49).”
BackgroundProstaglandins in pathogenesis and treatment of multiple sclerosis
Mirshafiey, A., & Jadidi‐Niaragh, F. (2010) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923971003667627 · Cited by 44
“protein leading to the activation of PLC, generation of IP3 followed by an increase in intracellular Ca.((110)) In practice, no FP receptor expression has been observed in immune cell populations and thus it does not seem that PGF2α plays a role in inflammatory processes.”
BackgroundSharif, N. A., & Klimko, P. G. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14335 · Cited by 44
Takeuchi, K., Araki, H., Umeda, M., Komoike, Y., & Suzuki, K. (2001) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)29646-4 · Cited by 44
Zeng, Z., Velarde, M. C., Simmen, F. A., & Simmen, R. C. M. (2008) · Biology of Reproduction · doi:10.1095/biolreprod.107.065821 · Cited by 45
“Consistent with the reported rapid decline in serum P levels near term [29], circulating levels of P dramatically decreased in pregnant WT mice (Fig.”
Patterns of cell death in the perinatal mouse forebrain
Mosley, M., Shah, C. R., Morse, K. A., Miloro, S. A., Holmes, M. M., Ahern, T. H., & Forger, N. G. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24041 · Cited by 44
“[Color figure can be viewed at wileyonlinelibrary.com] 58 The Journal of Comparative Neurology | Research in Systems Neuroscience hormonal or genetic manipulations (Sugimoto et al., 1997; Langenbach et al., 1997; Gross et al., 1998; Jeff et al., 2000; Hashimoto et al., 2010).”
Ishida, M., Choi, J., Hirabayashi, K., Matsuwaki, T., Suzuki, M., Yamanouchi, K., Horai, R., Sudo, K., Iwakura, Y., & Nishihara, M. (2007) · Journal of Reproduction and Development · doi:10.1262/jrd.18125 · Cited by 43
“In fact, the estrous cycle of FP–/– mice is normal [9] despite the luteal expression of PGF2α receptor in estrous cycle of wild-type mice [11].”
BackgroundKunikata, T., Araki, H., TAKEEDA, M., Kato, S., & Takeuchi, K. (2001) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(01)00021-3 · Cited by 43
The hormonal control of parturition
Hamburg‐Shields, E., & Mesiano, S. A. (2024) · Physiological Reviews · doi:10.1152/physrev.00019.2023 · Cited by 46
The regulation of oxytocin and oxytocin receptor in human placenta according to gestational age
Kim, S.-C., Lee, J., Kang, S. S., Yang, H., Kim, S. S., & An, B. (2017) · Journal of Molecular Endocrinology · doi:10.1530/jme-16-0223 · Cited by 42
Decidual cell FKBP51–progesterone receptor binding mediates maternal stress–induced preterm birth
Guzeloglu‐Kayisli, O., Semerci, N., Guo, X., Larsen, K. A., Özmen, A., Arlıer, S., Mutluay, D., Nwabuobi, C. K., Sipe, B. H., Buhimschi, I. A., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010282118 · Cited by 44
“Luteal regression precedes labor in mice accompanied by a reduction in serum P4 levels (39).”
Expression of the prostaglandin F receptor (FP) gene along the mouse genitourinary tract
Saito, O., Guan, Y., Qi, Z., Davis, L. S., Kömhoff, M., Sugimoto, Y., Narumiya, S., BREYER, R. M., & Breyer, M. D. (2003) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00441.2002 · Cited by 44
“The present studies used both in situ hybridization and a -gal reporter knocked into the endogenous FP locus (47) to map the distribution of the FP receptor.”
BackgroundMethodInfluentialSelf-citationThe Regulation of Uterine Function During Parturition: an Update and Recent Advances
Ilicic, M., Zakár, T., & Paúl, J. (2020) · Reproductive Sciences · doi:10.1007/s43032-019-00001-y · Cited by 41
Progesterone Withdrawal Promotes Remodeling Processes in the Nonpregnant Mouse Cervix1
Yellon, S. M., Burns, A. E., See, J. L., Lechuga, T. J., & Kirby, M. A. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.108.074997 · Cited by 41
“In Ptgfr / mice, the optical density of cervical sections increases with the same time course as that in controls that gave birth [14, 34, 43].”
BackgroundWood, C. E., & Walker, C. (2015) · Comprehensive physiology · doi:10.1002/cphy.c150005 · Cited by 48
“mouse, deletion of the receptor for prostanglandin F2-alpha (FP) impairs parturition, an effect that is likely caused by a failure of maternal luteolysis (311).”
Core Binding Factor β Expression in Ovarian Granulosa Cells Is Essential for Female Fertility
Lee-Thacker, S., Choi, Y., Taniuchi, I., Takarada, T., Yoneda, Y., Ko, C. J., & Jo, M. (2018) · Endocrinology · doi:10.1210/en.2018-00011 · Cited by 38
Identification of uterine pacemaker regions at the myometrial–placental interface in the rat
Lutton, J. E., Lammers, W. J. E. P., James, S. G., van den Berg, H. A., & Blanks, A. M. (2018) · The Journal of Physiology · doi:10.1113/jp275688 · Cited by 40
“Central to the onset of labour is the systemic withdrawal of progesterone caused by prostanoid-induced collapse of the corpus luteum (Bonventre et al. 1997; Sugimoto et al. 1997; Gross et al. 1998).”
BackgroundProstaglandins as the Agents That Modulate the Course of Brain Disorders
Famitafreshi, H., & Karimian, M. (2020) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s240800 · Cited by 44
The IOP-lowering effects and mechanism of action of tafluprost in prostanoid receptor-deficient mice
Ota, T., Aihara, M., Saeki, T., Narumiya, S., & Araie, M. (2006) · British Journal of Ophthalmology · doi:10.1136/bjo.2006.105585 · Cited by 40
“FP receptor-deficient mice (FPKO) were also generated by gene knockout methods using homologous recombination,[9] the murine genotype was determined by PCR,[2] and FP-receptor homozygous knockout mice were used.”
MethodSelf-citationHampl, A., Pachernı́k, J., & Dvořák, P. (2000) · Biology of Reproduction · doi:10.1095/biolreprod62.5.1393 · Cited by 40
“In mice, plasma concentration of progesterone, the major product of luteal cells, declines between Days 17 and 19 of pregnancy ([19, 20] and citations therein) because of functional and structural luteolysis.”
Oxytocin modulates the onset of murine parturition by competing ovarian and uterine effects
Imamura, T., Luedke, C. E., Vogt, S. K., & Muglia, L. J. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.3.r1061 · Cited by 40
“On the other hand, mice with defects in either prostaglandin synthesis or action, which manifest as delayed or absent labor, initiate labor when a fall in progesterone and induction of uterine OTR occur (9, 14).”
BackgroundFemale Reproduction in Mice Lacking the Prostaglandin F Receptor
Sugimoto, Y., Segi, E., Tsuboi, K., Ichikawa, A., & Narumiya, S. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4871-3_39 · Cited by 40
Self-citationHoare, S., Copland, J. A., Wood, T. G., Jeng, Y., Izban, M. G., & Soloff, M. S. (1999) · Endocrinology · doi:10.1210/endo.140.5.6710 · Cited by 40
“initiation of labor (1) milk ejection from the mammary gland”
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Prostaglandins and Uterine Activity
Patel, F. A., & Challis, J. R. G. (2001) · KARGER eBooks · doi:10.1159/000061040 · Cited by 39
PGF2α FP Receptor Contributes to Brain Damage Following Transient Focal Brain Ischemia
Saleem, S., Ahmad, A. S., Maruyama, T., Narumiya, S., & Doré, S. (2009) · Neurotoxicity Research · doi:10.1007/s12640-009-9007-3 · Cited by 39
“FP-/C57BL/6 breeding mice were first obtained from Dr. Narumiya (Sugimoto et al. 1997) and then maintained and genotyped at our animal facility at Johns Hopkins University.”
MethodInfluentialSelf-citationProstaglandins in labor - a translational approach
Abdul, H. K. (2008) · Frontiers in bioscience · doi:10.2741/3117 · Cited by 39
Carámbula, S. F., Pru, J. K., Lynch, M. P., Matikainen, T., Gonçalves, P. B. D., Flavell, R. A., Tilly, J. L., & Rueda, B. R. (2003) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-1-15 · Cited by 38
Cyclooxygenase Metabolites in the Kidney
Harris, R. C., & Zhang, M. (2011) · Comprehensive physiology · doi:10.1002/cphy.c100077 · Cited by 38
Charpigny, G., Reinaud, P., Créminon, C., & Tamby, J. P. (1999) · Reproduction · doi:10.1530/jrf.0.1170315 · Cited by 37
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“Interestingly, in FP knockout mice, spontaneous labor did not commence even 1 wk after term due to failure of PGF2a-induced corpus luteum regression [23].”
BackgroundIncreased Innervation and Ripening of the Prepartum Murine Cervix
Kirby, L. S., Kirby, M. A., Warren, J. W., Tran, L. T., & Yellon, S. M. (2005) · Journal of the Society for Gynecologic Investigation · doi:10.1016/j.jsgi.2005.08.006 · Cited by 36
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“However, other reproductive processes (follicular growth, ovulation, embryonic growth) appear to be normal in FP-receptor knock-out mice, indicating an essential role of PGF2a only in the process of luteolysis [7].”
BackgroundRegulation of Parturition Update: Endocrine and Paracrine Effectors of Term and Preterm Labor
Kniss, D. A., & Iams, J. D. (1998) · Clinics in Perinatology · doi:10.1016/s0095-5108(18)30085-x · Cited by 36
Xu, C., Long, A. J., Fang, X., Wood, S. L., Slater, D. M., Ni, X., & Olson, D. M. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-2829 · Cited by 35
“normally but were unable to be delivered on time at term due to the diminished OTR expression, suggesting that PGF2 stimulates OTR expression (29).”
BackgroundRegulations of Tumor Microenvironment by Prostaglandins
Nie, J. Z., Wang, M.-T., & Nie, D. (2023) · Cancers · doi:10.3390/cancers15123090 · Cited by 39
“PGF2α-FP plays important roles in many physiological and pathological situations, such as ovulation, parturition [71], renal function, myocardial dysfunction, and pain [72].”
BackgroundHenkes, L. E., Sullivan, B. T., Lynch, M. P., Kolesnick, R. N., Arsenault, D. A., Puder, M., Davis, J. S., & Rueda, B. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712260105 · Cited by 35
“This role for PGF is further supported by studies of the PGF receptor KO mice, which fail to undergo luteal regression at the end of pregnancy and, as a result, fail to undergo parturition (19).”
BackgroundMolecular biology of histidine decarboxylase and prostaglandin receptors
Ichikawa, A., Sugimoto, Y., & Tanaka, S. (2010) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.86.848 · Cited by 35
Self-citationDenda, K., Nakao-Wakabayashi, K., Okamoto, N., Kitamura, N., Ryu, J.-Y., Tagawa, Y., Ichisaka, T., Yamanaka, S., & Komada, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.258160 · Cited by 35
Stocco, C. O., Chedrese, J., & Deis, R. P. (2001) · Biology of Reproduction · doi:10.1095/biolreprod65.4.1114 · Cited by 35
“Noteworthy, in rodents, a fall in progesterone secretion is absolutely essential for the induction of parturition [1, 2].”
BackgroundArai, K. (2003) · Gut · doi:10.1136/gut.52.9.1242 · Cited by 35
Tsuboi, K., Iwane, A., Nakazawa, S., Sugimoto, Y., & Ichikawa, A. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.013870 · Cited by 35
Self-citationThe prostaglandin receptor EP4 suppresses colitis, mucosal damage and CD4 cell activation in the gut
Kabashima, K., Saji, T., Murata, T., Nagamachi, M., Matsuoka, T., Segi‐Nishida, E., Tsuboi, K., Sugimoto, Y., Kobayashi, T., Miyachi, Y., et al. (2002) · Journal of Clinical Investigation · doi:10.1172/jci200214459 · Cited by 35
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Hébert, R., Carmosino, M., Saito, O., Yang, G., Jackson, C. A., Qi, Z., BREYER, R. M., Natarajan, C., Hata, A. N., Zhang, Y., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m505852200 · Cited by 34
Molecular mechanisms of trophoblast survival: From implantation to birth
Jurisicova, A., Detmar, J., & Caniggia, I. (2005) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20053 · Cited by 34
Developing a theoretical evolutionary framework to solve the mystery of parturition initiation
Rokas, A., Mesiano, S. A., Tamam, O., LaBella, A. L., Zhang, G., & Muglia, L. J. (2020) · eLife · doi:10.7554/elife.58343 · Cited by 33
Prostaglandin F2α-Induced Functional Regression of the Corpus Luteum and Apoptosis in Rodents
Wang, Z., Tamura, K., Yoshie, M., Tamura, H., Imakawa, K., & Kogo, H. (2003) · Journal of Pharmacological Sciences · doi:10.1254/jphs.92.19 · Cited by 33
Analysis of uterine contractions: a dynamical approach
Nagarajan, R., Eswaran, H., Wilson, J. D., Murphy, P., Lowery, C. L., & Preissl, H. T. (2003) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/713606508 · Cited by 33
Beck, H., Thaler, T., Meibom, D., Meininghaus, M., Jörißen, H., Dietz, L., Terjung, C., Bairlein, M., von Bühler, C.-J., Anlauf, S., et al. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c00834 · Cited by 33
Non-inflammatory Physiology of “Inflammatory” Mediators – Unalamation, a New Paradigm
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Guo, C., Wang, W., Liu, C., Myatt, L., & Sun, K. (2014) · Endocrinology · doi:10.1210/en.2013-1848 · Cited by 33
The Comparative Physiology of Parturition in Mammals: Hormones and Parturition in Mammals
Young, I. R., Renfree, M. B., Mesiano, S. A., Shaw, G., Jenkin, G., & Smith, R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-374928-4.10006-9 · Cited by 33
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“Prostaglandins (PGs) are believed to play pivotal roles in a number of reproductive processes such as ovulation (see Gelety & Chaudhuri 1992 for a review), luteolysis (see Poyser 1995 for a review) and parturition (Sugimoto et al. 1997, Uozumi et al. 1997).”
BackgroundArachidonic Acid Metabolites and the Kidney
Harris, R. C., Breyer, M. D., & BREYER, R. M. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-6193-9.10013-2 · Cited by 32
Targeting the Prostaglandin F2α Receptor for Preventing Preterm Labor with Azapeptide Tocolytics
Bourguet, C. B., Goupil, E., Tassy, D., Hou, X., Thouin, E., Polyak, F., Hébert, T. E., Claing, A., Laporte, S. A., Chemtob, S., et al. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm200608k · Cited by 31
Takeuchi, K., Ogawa, Y., Kagawa, S., & Ukawa, H. (2002) · Alimentary Pharmacology & Therapeutics · doi:10.1046/j.1365-2036.16.s2.21.x · Cited by 31
O’Brien, C. M., Herington, J. L., Brown, N., Pence, I. J., Paria, B. C., Slaughter, J. C., Reese, J., & Mahadevan-Jansen, A. M. (2017) · Scientific Reports · doi:10.1038/s41598-017-07047-5 · Cited by 30
Cirillo, R., Tos, E. G., Page, P., Missotten, M., Quattropani, A., Scheer, A., Schwarz, M. K., & Chollet, A. (2007) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2007.02.010 · Cited by 30
Stocco, C. O. (2004) · Endocrinology · doi:10.1210/en.2004-0625 · Cited by 30
“PGF2 receptor knockout mice with a mixed genetic background of 129/Ola and C57BL/6 strains were used (4).”
BackgroundMethodReproductive Biology of the Laboratory Mouse
RPRITCHETT, K., & Taft, R. A. (2007) · Elsevier eBooks · doi:10.1016/b978-012369454-6/50057-1 · Cited by 29
Farhat, A., Philibert, P., Sultan, C., Poulat, F., & Boizet‐Bonhoure, B. (2011) · Journal of Ovarian Research · doi:10.1186/1757-2215-4-3 · Cited by 29
“progesterone levels and stimulating luteolysis, a crucial stage in inducing labor and pup delivery during parturition in human and mice [11,12].”
BackgroundFoyouzi, N., Cai, Z., Sugimoto, Y., & Stocco, C. O. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.104.037598 · Cited by 29
“PGF2a receptor knockout mice with a mixed genetic background of 129/Ola and C57BL/6 strains were used [2].”
BackgroundMethodInfluentialSelf-citationPohl, O., Chollet, A., Kim, S. H., Riaposova, L., Spézia, F., Gervais, F., Guillaume, P., Lluel, P., Méen, M., Lemaux, F., et al. (2018) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.118.247668 · Cited by 29
“activation and contractile activity in rodents (Sugimoto et al., 1997).”
BackgroundThe plasma levels of the endocannabinoid, anandamide, increase with the induction of labour
Nallendran, V., Pmw, L., Marczylo, T. H., Bankart, M. J., Taylor, A. H., Taylor, D., & Konje, J. (2010) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2010.02555.x · Cited by 28
Taniguchi, K., Matsuoka, A., Kizuka, F., Lee, L., Tamura, I., Maekawa, R., Asada, H., Taketani, T., Tamura, H., & Sugino, N. (2010) · Reproduction · doi:10.1530/rep-10-0240 · Cited by 27
“In fact, in PGF2a receptor-deficient mice, serum progesterone concentrations do not decline, and parturition does not occur (Sugimoto et al. 1997).”
BackgroundCross Talk between PKC and CREB in the Induction of COX-2 by PGF2α in Human Amnion Fibroblasts
Guo, C., Kasaraneni, N., Sun, K., & Myatt, L. (2012) · Endocrinology · doi:10.1210/en.2012-1441 · Cited by 28
Maintenance or regression of the corpus luteum during multiple decisive periods of bovinepregnancy
Wiltbank, M. C., Median, R., Ochoa, J. C., Báez-Sandoval, G. M., Giordano, J. O., Ferreira, J. C. P., & Sartori, R. (2016) · Animal Reproduction · doi:10.21451/1984-3143-ar865 · Cited by 28
“Inhibition of PGF production by treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) will delay or prevent luteolysis near parturition (Jenkin, 1992; Sugimoto et al., 1998; Jenkin and Young, 2004).”
BackgroundRegulation of cyclo-oxygenase-2
Stack, E., & DuBois, R. N. (2001) · Best Practice & Research Clinical Gastroenterology · doi:10.1053/bega.2001.0235 · Cited by 28
Hasumoto, K., Sugimoto, Y., Gotoh, M., Segi‐Nishida, E., Yamasaki, A., Yamaguchi, M., Honda, H., Hirai, H., Negishi, M., Kakizuka, A., et al. (1997) · Genes to Cells · doi:10.1046/j.1365-2443.1997.1420340.x · Cited by 28
“…signals per cells in the stomach, where þ þ corresponds to the level of mouse FP. nd, not determined. disruption of the FP gene by replacement with the lacZ gene clearly demonstrated that b-galactosidase can be expressed in the corpora lutea without any toxic effects (Sugimoto et al. 1997).”
BackgroundSelf-citationSander, V. A., Piehl, L. L., Facorro, G. B., de Celis, E. R., & Motta, A. B. (2008) · Reproduction Fertility and Development · doi:10.1071/rd08051 · Cited by 27
Kelley, L. P., & Kinsella, B. T. (2004) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705695 · Cited by 27
Algovik, M., Nilsson, E. M. E., Cnattingius, S., Lichtenstein, P., Nordenskjöld, A., & Westgren, M. (2004) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1111/j.0001-6349.2004.00544.x · Cited by 27
“Mice models lacking the genes for prostaglandin F2a receptor (5) and testosterone 5-a-reductase type 1 (6), respectively, exhibit an absence of parturition.”
BackgroundExpression of Apoptosis in Placentae from Mice Lacking the Prostaglandin F Receptor
Mu, J., Kanzaki, T., Tomimatsu, T., Fukuda, H., Wasada, K., Fujii, E., Endoh, M., Kozuki, M., Murata, Y., Sugimoto, Y., et al. (2002) · Placenta · doi:10.1053/plac.2001.0759 · Cited by 26
Self-citationMu, J., Kanzaki, T., Si, X., Tomimatsu, T., Fukuda, H., Shioji, M., Murata, Y., Sugimoto, Y., & Ichikawa, A. (2003) · Biology of Reproduction · doi:10.1095/biolreprod.102.008029 · Cited by 26
“Therefore, this PGF2a receptor-deficient mouse provides a good animal model for studying intrauterine fetal death in postterm pregnancy [10, 19].”
BackgroundMethodResultInfluentialSelf-citationDuffy, D. M., & VandeVoort, C. A. (2011) · Fertility and Sterility · doi:10.1016/j.fertnstert.2010.12.048 · Cited by 26
“Oocytes of mice lacking expression of the PGF2α (FP) receptor ovulate and fertilize normally, but overall fertility is compromised by defects during implantation (33).”
BackgroundElmes, M. J., Green, L., Poore, K. R., Newman, J., Burrage, D., Abayasekara, D. R. E., Cheng, Z., Hanson, M. A., & Wathes, D. C. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.071969 · Cited by 26
Gaytán, F., Tarradas, E., Bellido, C., Morales, C., & Sánchez‐Criado, J. E. (2002) · Biology of Reproduction · doi:10.1095/biolreprod67.4.1140 · Cited by 26
“In addition, mice lacking the PGF2a receptor do not show ovulatory defects [33].”
BackgroundMuratani, T., Nishizawa, M., Matsumura, S., Mabuchi, T., Abe, K., Shimamoto, K., Minami, T., & Ito, S. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01840.x · Cited by 26
“The reproductive roles of PGF2a and FP, such as ovulation, luteolysis and parturition, have been emphasized (Sakamoto et al. 1995; Sugatani et al. 1996; Unezaki et al. 1996; Sugimoto et al. 1997).”
BackgroundProstaglandins and reproduction—what do knockouts really tell us?
Challis, J. R. G. (1997) · Nature Medicine · doi:10.1038/nm1297-1326 · Cited by 26
Anti-inflammatory effects of gallic acid in human gestational tissues in vitro
Nguyen‐Ngo, C., Salomón, C., Lai, A., Willcox, J. C., & Lappas, M. (2020) · Reproduction · doi:10.1530/rep-20-0249 · Cited by 25
Transcriptional control of parturition: insights from gene regulation studies in the myometrium
Khader, N., Shchuka, V. M., Shynlova, O. P., & Mitchell, J. A. (2021) · Molecular Human Reproduction · doi:10.1093/molehr/gaab024 · Cited by 26
“The actions of progesterone on the myometrium during gestation and the necessary removal of its inhibitory effects near term are similar across species, although some mechanistic differences exist (Csapo, 1956; Sugimoto et al., 1997; Piekorz et al., 2005).”
BackgroundSpecific PGF2α receptor (FP) antagonism and human uterine contractility in vitro
Friel, A. M., O’Reilly, M., Sexton, D. J., & Morrison, J. J. (2005) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2005.00658.x · Cited by 25
“8 In addition, disruption of the PGF2a receptor gene, in knockout mice studies, results in failure of the animals to go into labour.(13) Finally, it has recently been reported that THG113.”
Background
Metadata
- Authors
- Sugimoto, Y., Yamasaki, A., Segi, E., Tsuboi, K., Aze, Y., Nishimura, T., Oida, H., Yoshida, N., Tanaka, T., Katsuyama, M., Hasumoto, K.-Y., Murata, T., Hirata, M., Ushikubi, F., Negishi, M., Ichikawa, A., & Narumiya, S.
- Affiliations
- Kyoto University (JP)
- Y. Sugimoto, A. Yamasaki, E. Segi, K. Tsuboi, M. Katsuyama, K. Hasumoto, M. Negishi, A. Ichikawa, Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Kyoto 606, Japan.
- Corresponding author
- Ichikawa, Atsushi
- ORCID
- Venue
- Science
- Published
- 1997-08
- Volume
- 277
- Issue
- 5326
- Pages
- 681-683
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2142980049
- Cited by
- 608
- References
- 16
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 11 · 2023: 10 · 2022: 12 · 2021: 12 · 2020: 24 · 2019: 19 · 2018: 18 · 2017: 12 · 2016: 17 · 2015: 17 · 2014: 21 · 2013: 15 · 2012: 11
- FWCI
- 85.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Reproductive Physiology in Livestock
- Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- childbirth, prostaglandin F2alpha, FP receptor, oxytocin receptor, luteolysis, progesterone, ovariectomy, luteal cells, pregnancy, knockout mice, estrous cycle
- MeSH terms
- Animals, Corpus Luteum, Female, Heterozygote, Homozygote, Labor, Obstetric, Male, Mice, Inbred C57BL, Ovariectomy, Oxytocin, Pregnancy, Progesterone, Receptors, Prostaglandin, Uterine Contraction, Uterus, Dinoprost, Receptors, Oxytocin, Gene Targeting, Mice
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