Sex differences in the developmental origins of hypertension and cardiorenal disease

被引:120
作者
Gilbert, Jeffrey S. [1 ,2 ]
Nijland, Mark J. [3 ,4 ]
机构
[1] Univ Minnesota, Med Sch Duluth, Dept Physiol & Pharmacol, Duluth, MN 55812 USA
[2] Duluth Med Res Inst, Duluth, MN USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Ctr Pregnancy & Newborn Res, San Antonio, TX 78229 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Obstet & Gynecol, San Antonio, TX 78229 USA
基金
美国国家卫生研究院;
关键词
placenta; estrogen; maternal nutrient restriction; hypertension;
D O I
10.1152/ajpregu.90724.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Gilbert JS, Nijland MJ. Sex differences in the developmental origins of hypertension and cardiorenal disease. Am J Physiol Regul Integr Comp Physiol 295: R1941-R1952, 2008. First published October 29, 2008; doi:10.1152/ajpregu.90724.2008. -The "developmental origins of health and disease" (DOHAD) hypothesis derives from clinical observations, indicating long-term health consequences for persons of low birth weight. There is growing evidence, primarily from animal studies, that supports the idea that processes put in motion during development that contribute to DOHAD do not necessarily reflect as significantly compromised growth and altered birth weight. Throughout the body of work investigating the DOHAD hypothesis, several themes have emerged; the importance of the placenta, the presence of critical periods of vulnerability, the involvement of the kidney in programmed hypertension, the presence of sex differences in the progression and development of adult diseases. Despite compelling findings in recent studies, much remains unclear regarding the impact of biological sex in the progression of human diseases, in general, and in the mechanisms underlying developmentally programmed responses, in particular. Although the contribution of biological sex to DOHAD is increasingly recognized, it also appears that it may exert distinctly different influences during fetal and adult life. The mechanisms by which biological sex contributes to these processes remains nebulous at present; nevertheless, several intriguing mechanistic candidates have been proposed ranging from differences in the amounts of sex hormones (e. g., estrogens, androgens) to recently described sexual dimorphism in the transcriptome of a variety of mammalian tissues. Recognizing the influences of biological sex or sex hormones on DOHAD uniquely situates research in this area to provide significant insights into the development and progression of many diseases, recent examples of which are the subject of this review.
引用
收藏
页码:R1941 / R1952
页数:12
相关论文
共 144 条
[1]   Sexual dimorphism of rat liver gene expression: Regulatory role of growth hormone revealed by deoxyribonucleic acid microarray analysis [J].
Ahluwalia, A ;
Clodfelter, KH ;
Waxman, DJ .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (03) :747-760
[2]   Promoter methylation is associated with the age-dependent loss of N-cadherin in the rat kidney [J].
Akintola, Adebayo D. ;
Crislip, Zachary L. ;
Catania, Jeffrey M. ;
Chen, Gang ;
Zimmer, Warren E. ;
Burghardt, Robert C. ;
Parrish, Alan R. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2008, 294 (01) :F170-F176
[3]   Placental insufficiency leads to development of hypertension in growth-restricted offspring [J].
Alexander, BT .
HYPERTENSION, 2003, 41 (03) :457-462
[4]   Developmental programming of aortic and renal structure in offspring of rats fed fat-rich diets in pregnancy [J].
Armitage, JA ;
Lakasing, L ;
Taylor, PD ;
Balachandran, AA ;
Jensen, RI ;
Dekou, V ;
Ashton, N ;
Nyengaard, JR ;
Poston, L .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 565 (01) :171-184
[5]   MORPHOLOGICAL DEVELOPMENT AND SEX OF BOVINE INVITRO-FERTILIZED EMBRYOS [J].
AVERY, B ;
JORGENSEN, CB ;
MADISON, V ;
GREVE, T .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1992, 32 (03) :265-270
[6]  
Barker D J, 1997, Rev Reprod, V2, P105, DOI 10.1530/ror.0.0020105
[7]  
BARKER DJP, 1993, BRIT HEART J, V69, P195
[8]   Uteroplacental insufficiency alters nephrogenesis and downregulates cyclooxygenase-2 expression in a model of IUGR with adult-onset hypertension [J].
Baserga, Mariana ;
Hale, Merica A. ;
Wang, Zheng Ming ;
Yu, Xing ;
Callaway, Christopher W. ;
McKnight, Robert A. ;
Lane, Robert H. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2007, 292 (05) :R1943-R1955
[9]   Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood [J].
Battista, MC ;
Oligny, LL ;
St-Louis, J ;
Brouchu, M .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 283 (01) :E124-E131
[10]   Genetic predisposition to hypertension sensitizes borderline hypertensive rats to the hypertensive effects of prenatal glucocorticoid exposure [J].
Bechtold, Andrea G. ;
Vernon, Kathy ;
Hines, Tina ;
Scheuer, Deborah A. .
JOURNAL OF PHYSIOLOGY-LONDON, 2008, 586 (02) :673-684