The baboon as a good model for studies of human kidney development

被引:42
作者
Gubhaju, L [1 ]
Black, MJ [1 ]
机构
[1] Monash Univ, Dept Anat & Cell Biol, Clayton, Vic 3800, Australia
关键词
D O I
10.1203/01.PDR.0000179397.20862.73
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Because of the improved survival of premature neonates in recent years, it is important to investigate the effects of premature delivery on the kidney, in which nephrogenesis is still ongoing during the third trimester. Hence, an appropriate animal model that is similar to humans is essential. The aim of the current study is to determine the time course of nephrogenesis in the baboon, to establish whether it is a suitable model of human nephrogenesis. At the Southwest Foundation for Biomedical Research (San Antonio, TX), fetal baboons were delivered prematurely by cesarean delivery and at term by natural delivery. Fixed kidneys from 125-, 140-, 175-, and 185-d gestation baboons were assessed morphologically for evidence of a nephrogenic zone. Nephron number, kidney volume, and glomerular and corpuscle volume were also estimated using unbiased stereology. Morphologic assessment confirmed the presence of metanephric mesenchyme and immature glomeruli in the nephrogenic zone of the kidneys from the prematurely delivered fetuses at 125 and 140 d gestation. At 175 d gestation and at term, the nephrons seemed to be mature. Both kidney weight (R-2 = 0.918, p = 0.0002) and kidney volume (R-2 = 0.837, p = 0.001) were very strongly correlated with nephron number. There was also a direct relationship between gestational age (R-2 = 0.589, p = 0.03) and birth weight (R-2 = 0.562, p = 0.03) with nephron number. In conclusion, in this study, nephrogenesis in the baboon is complete before term by 175 d gestation, which is similar to humans. Hence, the baboon is a suitable model for future studies to investigate human kidney development.
引用
收藏
页码:505 / 509
页数:5
相关论文
共 28 条
[1]   Quantitative study of the comma-shaped body, S-shaped body and vascularized glomerulus in the second and third human gestational trimesters [J].
Almeida, JR ;
Mandarim-de-Lacerda, CA .
EARLY HUMAN DEVELOPMENT, 2002, 69 (1-2) :1-13
[2]  
Bendon Robert W, 2004, Semin Neonatol, V9, P281, DOI 10.1016/j.siny.2003.10.003
[3]   Counting in the kidney [J].
Bertram, JF .
KIDNEY INTERNATIONAL, 2001, 59 (02) :792-796
[4]   Effect of angiotensin-converting enzyme inhibition on renal filtration surface area in hypertensive rats [J].
Black, MJ ;
Briscoe, TA ;
Dunstan, HJ ;
Bertram, JF ;
Johnston, CI .
KIDNEY INTERNATIONAL, 2001, 60 (05) :1837-1843
[5]   Molecular regulation of nephron endowment [J].
Clark, AT ;
Bertram, JF .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 276 (04) :F485-F497
[6]   DECREASED ALVEOLARIZATION IN BABOON SURVIVORS WITH BRONCHOPULMONARY DYSPLASIA [J].
COALSON, JJ ;
WINTER, V ;
DELEMOS, RA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (02) :640-646
[7]   Renal aspects of the term and preterm infant: a selective update [J].
Drukker, A ;
Guignard, JP .
CURRENT OPINION IN PEDIATRICS, 2002, 14 (02) :175-182
[8]   Direct fetal glucocorticoid treatment alters postnatal adaptation in premature newborn baboons [J].
Ervin, MG ;
Seidner, SR ;
Leland, MM ;
Ikegami, M ;
Jobe, AH .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 274 (04) :R1169-R1176
[9]   Single dose fetal betamethasone administration stabilizes postnatal glomerular filtration rate and alters endocrine function in premature lambs [J].
Ervin, MG ;
Berry, LM ;
Ikegami, M ;
Jobe, AH ;
Padbury, JF ;
Polk, DH .
PEDIATRIC RESEARCH, 1996, 40 (05) :645-651
[10]   THE EFFICIENCY OF SYSTEMATIC-SAMPLING IN STEREOLOGY AND ITS PREDICTION [J].
GUNDERSEN, HJG ;
JENSEN, EB .
JOURNAL OF MICROSCOPY-OXFORD, 1987, 147 :229-263