Apoptosis in the rat spinal cord during postnatal development; The effect of perinatal asphyxia on programmed cell death

被引:17
作者
De Louw, AJA
De Vente, J
Steinbusch, HPJ
Gavilanes, AWD
Steinbusch, HWM
Blanco, CE
Troost, J
Vles, JSH
机构
[1] Acad Hosp Maastricht, Dept Neurol, NL-6202 AZ Maastricht, Netherlands
[2] Univ Maastricht, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[3] Acad Hosp Maastricht, Dept Pediat, NL-6202 AZ Maastricht, Netherlands
关键词
TUNEL; O4; ED1;
D O I
10.1016/S0306-4522(02)00134-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aim of our study was to investigate the effect of perinatal asphyxia on developmental apoptosis in the cervical and lumbar spinal cord in the neonatal rat. Perinatal asphyxia was induced by keeping pups at term in utero in a water bath at 37degreesC for 20 min, followed by resuscitation. Effects of this treatment on developmental apoptosis, were studied on postnatal days 2, 5 and 8 using terminal deoxynucleotidyl transferase (TdT)-dUTP-biotin nick end labelling (TUNEL) and caspase-3 staining. TUNEL positive cells were identified using double immunostaining. On postnatal day 2 an increase of 215% in TUNEL positive cells was detected (P = 0.005) in laminae IV-VII of the lumbar spinal cord of rats which underwent perinatal asphyxia compared to controls. An increase of 55% compared to controls (P = 0.03) was seen in laminae I-III of the lumbar spinal cord at postnatal day 8. TUNEL positive cells could be partly identified as microglia cells (ED I positive) and oligodendrocytes (04 positive). The effect of perinatal asphyxia on programmed cell death in the neonatal rat spinal cord was mainly observed in the intermediate zone and dorsal horn of the lumbar spinal cord, We conclude that perinatal asphyxia has a pronounced effect on the survival of cells in a specific region of the spinal cord and thus may have a profound effect on the development of motor networks. (C) 2002 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 41 条
[31]  
Puskar Z, 1997, J COMP NEUROL, V389, P377, DOI 10.1002/(SICI)1096-9861(19971222)389:3<377::AID-CNE2>3.0.CO
[32]  
2-Y
[33]   Target cells of apoptosis in the adult murine dentate gyrus and O4 immunoreactivity after ionizing radiation [J].
Sasaki, R ;
Matsumoto, A ;
Itoh, K ;
Kawabe, T ;
Ota, Y ;
Yamada, K ;
Maruta, T ;
Soejima, T ;
Sugimura, K .
NEUROSCIENCE LETTERS, 2000, 279 (01) :57-60
[34]  
SLADKY J T, 1986, Pediatric Pathology, V6, P87
[35]   Development of spinal motoneurons in rats after a neonatal hypoxic insult [J].
Takahashi, S ;
Tanaka, H ;
Oki, J .
PEDIATRIC NEUROLOGY, 1999, 21 (04) :715-720
[36]   Medullary reticulospinal tract mediating the generalized motor inhibition in cats: Parallel inhibitory mechanisms acting on motoneurons and on interneuronal transmission in reflex pathways [J].
Takakusaki, K ;
Kohyama, J ;
Matsuyama, K ;
Mori, S .
NEUROSCIENCE, 2001, 103 (02) :511-527
[37]   DIPLEGIC CEREBRAL-PALSY IN SWEDISH TERM AND PRETERM CHILDREN - DIFFERENCES IN REDUCED OPTIMALITY, RELATIONS TO NEUROLOGY AND PATHOGENETIC FACTORS [J].
VEELKEN, N ;
HAGBERG, B ;
HAGBERG, G ;
OLOW, I .
NEUROPEDIATRICS, 1983, 14 (01) :20-28
[38]   Patterns of programmed cell death in populations of developing spinal motoneurons in chicken, mouse, and rat [J].
Yamamoto, Y ;
Henderson, CE .
DEVELOPMENTAL BIOLOGY, 1999, 214 (01) :60-71
[39]  
Yoshida M, 2001, J NEUROSCI RES, V63, P284, DOI 10.1002/1097-4547(20010201)63:3<284::AID-JNR1022>3.0.CO
[40]  
2-6