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家兔中类似瑞氏综合征的脑病特征的发展。

Development of encephalopathic features similar to Reye syndrome in rabbits.

作者信息

Kang E S, Olson G, Jabbour J T, Solomon S S, Heimberg M, Sabesin S, Griffith J F

出版信息

Proc Natl Acad Sci U S A. 1984 Oct;81(19):6169-73. doi: 10.1073/pnas.81.19.6169.

Abstract

The progression of neurological abnormalities through four or five clinically distinguishable levels of deepening coma and the development of a fatty liver are the hallmarks of Reye syndrome. A number of animal models have been described that result in fatty liver formation with minimal, static, or catastrophic neurological changes. In this study, we attempted to produce neurological features in rabbits that reflected a rostral-caudal progression of abnormalities that could be categorized into clinically distinguishable levels reminiscent of Reye syndrome. This was accomplished by the intracisternal administration of 0.5-25 mg of 11,14-icosadienoic acid (20:2 omega 6) suspended in a mixture of rabbit serum and isotonic saline solution. A reproducible, dose-titratable spectrum of at least four levels of deepening coma could be produced at will. Increases in serum glutamate-oxaloacetate transaminase and creatine kinase and changes in serum glucose resulted 1-2 hr after the neurological abnormalities were evoked. Other unsaturated fatty acids produced similar responses. Those tested included 18:1 omega 9, 18:2 omega 6, 18:3 omega 3, 20:3 omega 6, 20:4 omega 6, and 22:4 omega 6 fatty acids. Saturated fatty acids, including 6:0, 8:0, 16:0, 18:0, and 20:0, failed to elicit these effects. The abnormalities were sustained for 30-120 min after a single dose. Full recovery was observed in some animals that had not reached the fourth level of our grading system for coma. Pretreatment of the rabbits with aspirin modulated the neurological abnormalities. Twenty micrograms of bee venom melittin, which activates endogenous phospholipase A2, administered intracisternally into rabbits also produced signs of level 3 (our grading system) coma for several hours. These findings suggest a possible role for polyunsaturated fatty acids in the development of Reye syndrome and offer a means of producing the neurological components of that syndrome in a laboratory animal.

摘要

神经功能异常经四到五个临床上可区分的深度昏迷阶段进展以及脂肪肝的形成是瑞氏综合征的标志。已经描述了许多动物模型,这些模型会导致脂肪肝形成,同时伴有轻微、静止或灾难性的神经变化。在本研究中,我们试图在兔子身上产生神经学特征,这些特征反映出异常从头部到尾部的进展,且可分为临床上可区分的阶段,让人联想到瑞氏综合征。这是通过脑池内注射悬浮于兔血清和等渗盐溶液混合物中的0.5 - 25毫克11,14 - 二十碳二烯酸(20:2 ω6)来实现的。可以随意产生至少四个深度昏迷阶段的可重复、剂量可滴定的谱。在诱发神经功能异常后1 - 2小时,血清谷氨酸草酰乙酸转氨酶和肌酸激酶升高以及血清葡萄糖发生变化。其他不饱和脂肪酸也产生了类似反应。所测试的包括18:1 ω9、18:2 ω6、18:3 ω3、20:3 ω6、20:4 ω6和22:4 ω6脂肪酸。饱和脂肪酸,包括6:0、8:0、16:0、18:0和20:0,未能引发这些效应。单次给药后,异常持续30 - 120分钟。在一些尚未达到我们昏迷分级系统第四级的动物中观察到完全恢复。用阿司匹林预处理兔子可调节神经功能异常。向兔子脑池内注射20微克激活内源性磷脂酶A2的蜂毒溶血磷脂也会产生数小时的3级(我们的分级系统)昏迷体征。这些发现表明多不饱和脂肪酸在瑞氏综合征发展中可能起作用,并提供了一种在实验动物中产生该综合征神经学成分的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ab7/391881/4650f6cfe027/pnas00620-0266-a.jpg

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