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首页> 外文期刊>Experimental and therapeutic medicine >N-methyl-N-nitrosourea-induced cerebellar hypoplasia in rats: Effect of arachidonic acid supplementation during the gestational, lactational and post-weaning periods
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N-methyl-N-nitrosourea-induced cerebellar hypoplasia in rats: Effect of arachidonic acid supplementation during the gestational, lactational and post-weaning periods

机译:N-甲基-N-亚硝基脲诱导的大鼠小脑发育不全:在妊娠,哺乳期和断奶后阶段补充花生四烯酸的作用

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Arachidonic acid (AA) is a fatty acid that is important for visual and brain development and is commonly added as a functional food ingredient to commercial infant formulas worldwide. However, few studies have examined whether AA supplementation during neonatal life has an effect on neuronal abnormalities. In the present study, the effect of dietary AA supplementation in dams during gestation and lactation was investigated by examining N-methyl-N-nitrosourea (MNU)-induced cerebellar hypoplasia in young Lewis rats. Dams were fed a 2.0% AA diet or a basal diet (<0.01% AA). At birth (postnatal day 0), male and female pups received a single intraperitoneal injection of 35 mg/kg MNU or vehicle. Brain weights were measured and a morphological analysis of macroscopic and histological specimens was conducted after 7, 14, 21, 28 and 60 days. Irrespective of whether the rats had been fed an AA diet, the brain weights of the MNU-treated rats, particularly the weights of the cerebellum, were decreased compared with those of the MNU-untreated rats from the 14th day following the MNU injection. Macroscopic reductions in the cerebellar length and/or width and histologically observed reductions in cerebellar vertex height and/or cortex width were also detected in the MNU-treated rats, irrespective of whether the rats had been fed with AA. Histopathologically, the MNU-treated rats (irrespective of AA supplementation) exhibited disorganization of the cerebellar cortex and disarrangement of the cortical layers (loss and/or disturbance of the molecular, Purkinje and granular cell layers). There were no significant differences in any parameters among the MNU-treated rats, irrespective of whether the rats had been fed an AA diet. In conclusion, an AA-rich diet for dams during gestation and lactation did not modify MNU-induced cerebellar hypoplasia in their offspring.
机译:花生四烯酸(AA)是一种脂肪酸,对于视觉和大脑发育很重要,通常作为功能性食品成分添加到全球商业婴儿配方食品中。但是,很少有研究检查新生儿生命期间补充AA对神经元异常是否有影响。在本研究中,通过检查年轻的Lewis大鼠中N-甲基-N-亚硝基脲(MNU)引起的小脑发育不全,研究了在妊娠和哺乳期补充膳食AA的效果。给大坝喂食2.0%AA饮食或基础饮食(<0.01%AA)。出生时(出生后第0天),雄性和雌性幼犬腹膜内注射35 mg / kg MNU或溶媒。在7、14、21、28和60天后,测量脑重量并进行宏观和组织学标本的形态分析。无论是否给大鼠饲喂AA饮食,从MNU注射后第14天起,与未接受MNU治疗的大鼠相比,经MNU治疗的大鼠的脑部重量,特别是小脑的重量均降低。在MNU处理的大鼠中,无论是否用AA喂养,都可以观察到小脑长度和/或宽度的宏观减少,以及组织学观察到的小脑顶点高度和/或皮质宽度的减少。组织病理学上,经MNU处理的大鼠(无论是否补充AA)均表现出小脑皮质混乱和皮质层紊乱(分子,浦肯野和颗粒细胞层丢失和/或紊乱)。在MNU治疗的大鼠中,无论是否给大鼠饲喂AA饮食,任何参数都没有显着差异。总之,妊娠期和哺乳期富含AA的大坝饮食不会改变MNU诱导的后代小脑发育不全。

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