Literature DB >> 12596225

Kidney development and the fetal programming of adult disease.

Karen M Moritz1, Miodrag Dodic, E Marelyn Wintour.   

Abstract

Recent evidence, from both epidemiological and animal experimental studies, suggest that the very first environment, the intrauterine, is extremely important in determining the future health of the individual. Genetic and 'lifestyle' factors impinge on, and can exacerbate, a 'programming' effect of an adverse fetal environment. In this review, we present compelling evidence to suggest that one of the major organs affected by an unfavourable prenatal environment is the kidney. Many of the factors that can affect fetal renal development (i.e. exposure to excess glucocorticoids, insufficient vitamin A, protein/calorie malnutrition (in rats) and alterations in the intrarenal renin angiotensinogen system), also produce hypertension in the adult animal. When nephron number is compromised during kidney development, maladaptive functional changes occur and can lead, eventually, to hypertension and/or renal disease. Surprisingly, it is during the very earliest stages of kidney development that the vulnerability to these effects occurs. Copyright 2003 Wiley Periodicals, Inc.

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Year:  2003        PMID: 12596225     DOI: 10.1002/bies.10240

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  33 in total

1.  Sex-specific impact of prenatal stress on growth and reproductive parameters of guinea pigs.

Authors:  Hanna Schöpper; Teresa Klaus; Rupert Palme; Thomas Ruf; Susanne Huber
Journal:  J Comp Physiol B       Date:  2012-06-20       Impact factor: 2.200

Review 2.  Intrauterine growth restriction: fetal programming of hypertension and kidney disease.

Authors:  Norma B Ojeda; Daniela Grigore; Barbara T Alexander
Journal:  Adv Chronic Kidney Dis       Date:  2008-04       Impact factor: 3.620

3.  Role of fetal programming in the development of hypertension.

Authors:  Norma B Ojeda; Daniela Grigore; Barbara T Alexander
Journal:  Future Cardiol       Date:  2008-03

4.  Renal impairment induced by prenatal exposure to angiotensin II in male rat offspring.

Authors:  Pavel Svitok; Monika Okuliarova; Ivan Varga; Michal Zeman
Journal:  Exp Biol Med (Maywood)       Date:  2019-05-14

5.  Systems biology analysis reveals role of MDM2 in diabetic nephropathy.

Authors:  Rintaro Saito; Anaïs Rocanin-Arjo; Young-Hyun You; Manjula Darshi; Benjamin Van Espen; Satoshi Miyamoto; Jessica Pham; Minya Pu; Simone Romoli; Loki Natarajan; Wenjun Ju; Matthias Kretzler; Robert Nelson; Keiichiro Ono; Dana Thomasova; Shrikant R Mulay; Trey Ideker; Vivette D'Agati; Ergin Beyret; Juan Carlos Izpisua Belmonte; Hans Joachim Anders; Kumar Sharma
Journal:  JCI Insight       Date:  2016-10-20

6.  Fetal development and renal function in adult rats prenatally subjected to sodium overload.

Authors:  Henriqueta D Cardoso; Edjair V Cabral; Leucio D Vieira-Filho; Adalberto Vieyra; Ana D O Paixão
Journal:  Pediatr Nephrol       Date:  2009-07-15       Impact factor: 3.714

7.  Developmental effect of antenatal exposure to betamethasone on renal angiotensin II activity in the young adult sheep.

Authors:  Stephen A Contag; Jianli Bi; Mark C Chappell; James C Rose
Journal:  Am J Physiol Renal Physiol       Date:  2010-01-13

Review 8.  Developmental origins of cardiovascular disease: Impact of early life stress in humans and rodents.

Authors:  M O Murphy; D M Cohn; A S Loria
Journal:  Neurosci Biobehav Rev       Date:  2016-07-20       Impact factor: 8.989

Review 9.  Urine concentration and avian aquaporin water channels.

Authors:  Hiroko Nishimura
Journal:  Pflugers Arch       Date:  2008-02-16       Impact factor: 3.657

10.  Maternal nutrient restriction during early fetal kidney development attenuates the renal innate inflammatory response in obese young adult offspring.

Authors:  Don Sharkey; David S Gardner; Michael E Symonds; Helen Budge
Journal:  Am J Physiol Renal Physiol       Date:  2009-09-16
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