Discovery of a Spontaneous Genetic Mouse Model of Preeclampsia

Article Properties
  • Language
    English
  • Publication Date
    2002/02/01
  • Journal
  • Indian UGC (Journal)
  • Refrences
    22
  • Citations
    125
  • Robin L. Davisson From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Darren S. Hoffmann From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Genelle M. Butz From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Gilbert Aldape From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Gunther Schlager From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • David C. Merrill From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Sanjeev Sethi From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • Robert M. Weiss From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
  • James N. Bates From the Departments of Anatomy and Cell Biology (R.L.D., D.S.H., G.M.B.), Anesthesia (G.A., J.N.B.), Pathology (S.S.), and Internal Medicine and Veterans Affairs (R.M.W.), University of Iowa College of Medicine, Iowa City; the Department of Biological Sciences (G.S.), University of Kansas, Lawrence; and the Department of Obstetrics and Gynecology (D.C.M.), Wake Forest School of Medicine, Wake Forest, NC.
Abstract
Cite
Davisson, Robin L., et al. “Discovery of a Spontaneous Genetic Mouse Model of Preeclampsia”. Hypertension, vol. 39, no. 2, 2002, pp. 337-42, https://doi.org/10.1161/hy02t2.102904.
Davisson, R. L., Hoffmann, D. S., Butz, G. M., Aldape, G., Schlager, G., Merrill, D. C., Sethi, S., Weiss, R. M., & Bates, J. N. (2002). Discovery of a Spontaneous Genetic Mouse Model of Preeclampsia. Hypertension, 39(2), 337-342. https://doi.org/10.1161/hy02t2.102904
Davisson RL, Hoffmann DS, Butz GM, Aldape G, Schlager G, Merrill DC, et al. Discovery of a Spontaneous Genetic Mouse Model of Preeclampsia. Hypertension. 2002;39(2):337-42.
Journal Categories
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the blood and blood-forming organs
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the circulatory (Cardiovascular) system
Medicine
Internal medicine
Specialties of internal medicine
Diseases of the respiratory system
Medicine
Medicine (General)
Description

Can mice help us understand preeclampsia? This breakthrough report details the discovery of a spontaneous genetic mouse model for preeclampsia, a leading cause of maternal and fetal morbidity. BPH/5 mice, with mildly elevated blood pressure, develop a pregnancy-induced hypertensive syndrome closely resembling preeclampsia in humans, opening new avenues for research. Before pregnancy, the BPH/5 strain had elevated baseline MAP compared with the C57BL/6 strain, but both strains had similar total urinary protein levels and renal histology. The MAP began to rise further in the BPH/5 mice during the last trimester. Accompanied by late-gestational proteinuria and progressive glomerulosclerosis, this new spontaneous genetic mouse model could greatly improve our understanding of preeclampsia. This novel model spontaneously develops a syndrome closely resembling preeclampsia. This represents a significant advance in understanding the pathophysiology of this disorder, offering a platform for testing potential therapies and improving outcomes for pregnant women.

Published in Hypertension, a top journal focused on hypertension and related cardiovascular issues, this study on a mouse model of preeclampsia is highly relevant. By exploring the genetic and physiological mechanisms underlying preeclampsia, the paper contributes to the journal's goal of advancing knowledge and improving treatment strategies for hypertensive disorders.

Refrences
Citations
Citations Analysis
The first research to cite this article was titled Vascular adaptations to pregnancy in mice: effects on myogenic tone and was published in 2002. The most recent citation comes from a 2024 study titled Vascular adaptations to pregnancy in mice: effects on myogenic tone . This article reached its peak citation in 2022 , with 12 citations.It has been cited in 77 different journals, 22% of which are open access. Among related journals, the Hypertension cited this research the most, with 6 citations. The chart below illustrates the annual citation trends for this article.
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