IN-UTERO SURGERY RESCUES NEUROLOGICAL FUNCTION AT BIRTH IN SHEEP WITH SPINA-BIFIDA

被引:269
作者
MEULI, M
MEULISIMMEN, C
HUTCHINS, GM
YINGLING, CD
HOFFMAN, KM
HARRISON, MR
ADZICK, NS
机构
[1] DAVIES MED CTR,MICROSURG LAB,SAN FRANCISCO,CA 94114
[2] JOHNS HOPKINS MED INST,DEPT PATHOL,BALTIMORE,MD 21287
[3] UNIV CALIF SAN FRANCISCO,DEPT ANESTHESIA,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,ANIM CARE FACIL,SAN FRANCISCO,CA 94143
关键词
D O I
10.1038/nm0495-342
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We hypothesize that the neurologic deficit associated with open spina bifida is not directly caused by the primary defect but rather is due to chronic mechanical and chemical trauma since the unprotected neural tissue is exposed to the intrauterine environment. We report here that exposure of the normal spinal cord to the amniotic cavity in midgestational sheep fetuses leads to a human-like open spina bifida with paraplegia at birth, indicating that the exposed neural tissue is progressively destroyed during pregnancy. When open spina bifida was repaired in, utero at an intermediate stage, the animals mars had near-normal neurologic function. The spinal cord was deformed but largely preserved. These findings suggest that secondary neural tissue destruction during pregnancy is primarily responsible for the functional loss and that timely in utero repair of open spina bifida might rescue neurologic function.
引用
收藏
页码:342 / 347
页数:6
相关论文
共 29 条
[1]   FETAL SURGICAL THERAPY [J].
ADZICK, NS ;
HARRISON, MR .
LANCET, 1994, 343 (8902) :897-902
[2]   BOTH REGENERATING AND LATE-DEVELOPING PATHWAYS CONTRIBUTE TO TRANSPLANT-INDUCED ANATOMICAL PLASTICITY AFTER SPINAL-CORD LESIONS AT BIRTH [J].
BREGMAN, BS ;
BERNSTEINGORAL, H .
EXPERIMENTAL NEUROLOGY, 1991, 112 (01) :49-63
[3]   ANATOMICAL PLASTICITY AND SPARING OF FUNCTION AFTER SPINAL-CORD DAMAGE IN NEONATAL CATS [J].
BREGMAN, BS ;
GOLDBERGER, ME .
SCIENCE, 1982, 217 (4559) :553-555
[4]  
CAMERON AH, 1956, LANCET, V2, P171
[5]   NEURAL-TUBE DEFECTS - A REVIEW OF HUMAN AND ANIMAL STUDIES ON THE ETIOLOGY OF NEURAL-TUBE DEFECTS [J].
CAMPBELL, LR ;
DAYTON, DH ;
SOHAL, GS .
TERATOLOGY, 1986, 34 (02) :171-187
[6]   THE EMBRYONIC-DEVELOPMENT OF MAMMALIAN NEURAL-TUBE DEFECTS [J].
COPP, AJ ;
BROOK, FA ;
ESTIBEIRO, JP ;
SHUM, ASW ;
COCKROFT, DL .
PROGRESS IN NEUROBIOLOGY, 1990, 35 (05) :363-+
[7]   NEURAL-TUBE DEFECTS [J].
COPP, AJ .
TRENDS IN NEUROSCIENCES, 1993, 16 (10) :381-383
[8]   LOCAL CORD LESION IN NEUROSPINAL DYSRAPHISM (MENINGOMYELOCELE) [J].
EMERY, JL ;
LENDON, RG .
JOURNAL OF PATHOLOGY, 1973, 110 (01) :83-+
[9]   CENTRAL-NERVOUS-SYSTEM ANOMALIES ASSOCIATED WITH MENINGOMYELOCELE, HYDROCEPHALUS, AND THE ARNOLD-CHIARI MALFORMATION - REAPPRAISAL O THEORIES REGARDING THE PATHOGENESIS OF POSTERIOR NEURAL-TUBE CLOSURE DEFECTS [J].
GILBERT, JN ;
JONES, KL ;
RORKE, LB ;
CHERNOFF, GF ;
JAMES, HE .
NEUROSURGERY, 1986, 18 (05) :559-564
[10]  
HARRISON MR, 1980, SURGERY, V88, P174