Miki T, Harris S, Wilce P, Takeuchi Y, Bedi K S
Department of Anatomy, Faculty of Medicine, Kagawa Medical University, Japan.
J Anat. 1999 Apr;194 ( Pt 3)(Pt 3):423-31. doi: 10.1046/j.1469-7580.1999.19430423.x.
We have previously shown that exposing rats to a high dose of ethanol on postnatal d 5 can affect Purkinje cell numbers in the cerebellum whilst similar exposure on d 10 had no such effect. The question arose whether a longer period of ethanol exposure after d 10 could produce loss of Purkinje cells. We have examined this question by exposing young rats to a relatively high dose (approximately 420-430 mg/dl) of ethanol for 6 d periods between the ages of either 4 and 9 d or 10 and 15 d of age. Exposure was carried out by placing the rats in an ethanol vapour chamber for 3 h per day during the exposure period. Groups of ethanol-treated (ET), separation controls (SC) and mother-reared controls (MRC) were anaesthetised and killed when aged 30 d by perfusion with buffered 2.5% glutaraldehyde. Stereological methods were used to determine the numbers of Purkinje cells in the cerebellum of each rat. MRC, SC and rats treated with ethanol between 10-15 d of age each had, on average, about 254-258 thousand cerebellar Purkinje cells; the differences between these various groups were not statistically significant. However, the rats treated with ethanol vapour between 4-9 d of age had an average of only about 128000+/-20000 Purkinje cells per cerebellum. This value was significantly different from both the MRC and group-matched SC animals. It is concluded that the period between 4 and 9 d of age is an extremely vulnerable period during which the rat cerebellar Purkinje cells are particularly susceptible to the effects of a high dose of ethanol. However, a similar level and duration of ethanol exposure commencing after 10 d of age has no significant effect on Purkinje cell numbers.
我们之前已经表明,在出生后第5天将大鼠暴露于高剂量乙醇会影响小脑浦肯野细胞的数量,而在第10天进行类似暴露则没有这种影响。于是出现了一个问题,即出生后第10天之后较长时间的乙醇暴露是否会导致浦肯野细胞丢失。我们通过在4至9日龄或10至15日龄之间将幼鼠暴露于相对高剂量(约420 - 430mg/dl)的乙醇中6天来研究这个问题。在暴露期间,每天将大鼠置于乙醇蒸汽室中3小时进行暴露。当30日龄时,对乙醇处理组(ET)、隔离对照组(SC)和母养对照组(MRC)进行麻醉并通过灌注2.5%戊二醛缓冲液处死。使用体视学方法确定每只大鼠小脑中浦肯野细胞的数量。MRC、SC以及在10至15日龄之间用乙醇处理的大鼠,平均每只小脑约有254000 - 258000个浦肯野细胞;这些不同组之间的差异无统计学意义。然而,在4至9日龄之间用乙醇蒸汽处理的大鼠,每只小脑平均只有约128000±20000个浦肯野细胞。这个值与MRC和组匹配的SC动物均有显著差异。结论是,4至9日龄期间是一个极其脆弱的时期,在此期间大鼠小脑浦肯野细胞对高剂量乙醇的影响特别敏感。然而,10日龄后开始的类似水平和持续时间的乙醇暴露对浦肯野细胞数量没有显著影响。