正常和震颤小鼠周围神经系统脂肪酰基含量的发育研究。

A Heape, F Boiron, C Cassagne
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引用次数: 14

摘要

我们对出生后5 ~ 60天正常小鼠和Trembler小鼠坐骨神经脂肪酰基的含量进行了定量分析。在出生后的前9天,Trembler小鼠坐骨神经中棕榈酰、硬脂酰和不饱和18-碳基团的含量正常增加,之后它们的含量明显低于正常窝鼠。脂肪酸合成酶在9 d龄震颤小鼠PNS中正常合成棕榈酸。“髓磷脂特异性”饱和甚长链脂肪酸酰基(VLCFAG)在所有年龄的研究中都缺乏,从第5天的2.5倍增加到第60天的26倍,相比之下,在更普遍的短链中观察到最大的3到4倍的减少。本文的结果表明,突变神经中高度异常的VLCFAG含量不能由脂肪酸合成酶活性异常来解释。然而,对于含有18个碳原子的脂肪酰基链,9天后观察到的缺陷几乎完全可以用棕榈酸水平的降低来解释。与VLCFAG相比,棕榈酸缺乏症的发生相对较晚,并且在年轻突变小鼠中观察到棕榈酸合成酶活性正常,这表明前者是Trembler突变的间接后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A developmental study of fatty acyl group contents in the peripheral nervous system of normal and trembler mice.

We quantitated the content of the fatty acyl groups of sciatic nerves from normal and Trembler mice between the postnatal ages of 5 and 60 d. Palmitoyl, stearoyl, and unsaturated 18-carbon groups increased normally in Trembler nerves during the first 9 d, after which their levels were notably lower than those observed for the normal littermates. In good agreement, the synthesis of palmitic acid by the fatty acid synthetase was normal in the PNS of 9-d-old Trembler mice. "Myelin-specific" saturated very long chain fatty acyl groups (VLCFAG) were deficient at all ages studied, the deficiency increasing from about 2.5-fold at 5 d, to 26-fold at 60 d, compared to the maximal 3- to 4-fold decrease observed for the more ubiquitous shorter chains. The results presented in this paper suggest that the highly abnormal VLCFAG content of the mutant nerves cannot be accounted for by an abnormal fatty acid synthetase activity. For the fatty acyl chains with 18 carbon atoms, however, the deficiency observed after 9 d of age can be almost entirely explained by the diminished levels of palmitic acid. The relatively late occurrence of the palmitic acid deficiency compared with that of the VLCFAG and the normal palmitate synthetase activity observed in young mutant mice indicates that the former is an indirect consequence of the Trembler mutation.

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