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围产期缺氧缺血性脑损伤的实验模型

Experimental models of perinatal hypoxic-ischemic brain damage.

作者信息

Vannucci R C

机构信息

Division of Pediatric Neurology, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey 17033.

出版信息

APMIS Suppl. 1993;40:89-95.

PMID:8311995
Abstract

Animal research has provided important information on the pathogenesis of and neuropathologic responses to perinatal cerebral hypoxia-ischemia. In experimental animals, structural brain damage from hypoxia-ischemia has been produced in immature rats, rabbits, guinea pigs, sheep and monkeys (18, 20, 24, 25, 38). Of the several available animal models, the fetal and newborn rhesus monkey and immature rat have been studied most extensively because of their similarities to humans in respect to the physiology of reproduction and their neuroanatomy at or shortly following birth. Given the frequency of occurrence of human perinatal hypoxic-ischemic brain damage and the multiple, often severe neurologic handicaps which ensue in infants and children, it is not surprising that the above described animal models have been developed. These models have provided the basis for investigations to clarify not only physiologic and biochemical mechanisms of tissue injury but also the efficacy of specific management strategies. Hopefully, such animal research will continue to provide important information regarding how best to prevent or minimize the devastating consequences of perinatal cerebral hypoxia-ischemia.

摘要

动物研究为围产期脑缺氧缺血的发病机制和神经病理反应提供了重要信息。在实验动物中,缺氧缺血导致的脑结构损伤已在未成熟大鼠、兔子、豚鼠、绵羊和猴子身上产生(参考文献18、20、24、25、38)。在几种可用的动物模型中,胎猴和新生恒河猴以及未成熟大鼠由于在生殖生理和出生时或出生后不久的神经解剖结构方面与人类相似,因此得到了最广泛的研究。鉴于人类围产期缺氧缺血性脑损伤的发生率以及随之而来的婴儿和儿童中出现的多种且往往严重的神经障碍,上述动物模型的开发也就不足为奇了。这些模型为研究提供了基础,不仅有助于阐明组织损伤的生理和生化机制,还能明确特定治疗策略的疗效。有望此类动物研究将继续提供重要信息,以指导如何最好地预防或尽量减少围产期脑缺氧缺血的灾难性后果。

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