Centre of Excellence for Nutrition, North-West University, Private Bag X6001, 2520 Potchefstroom, South Africa.
Lipids Health Dis. 2014 Jun 13;13:97. doi: 10.1186/1476-511X-13-97.
We recently showed that a combined deficiency of iron (ID) and n-3 fatty acids (n-3 FAD) in rats disrupts brain monoamine metabolism and produces greater memory deficits than ID or n-3 FAD alone. Providing these double-deficient rats with either iron (Fe) or preformed docosahexaenoic acid (DHA)/eicosapentaenoic acid (EPA) alone affected brain monoamine pathways differently from combined repletion and even exacerbated cognitive deficits associated with double-deficiency. Iron is a co-factor of the enzymes responsible for the conversion of alpha-linolenic acid (ALA) to EPA and DHA, thus, the provision of ALA with Fe might be more effective in restoring brain EPA and DHA and improving cognition in double-deficient rats than ALA alone.
In this study we examined whether providing double-deficient rats with ALA and Fe, alone or in combination, can correct deficits in monoamine metabolism and cognition associated with double-deficiency. Using a 2 × 2 design, male rats with concurrent ID and n-3 FAD were fed an Fe + ALA, Fe + n-3 FAD, ID + ALA, or ID + n-3 FAD diet for 5 weeks (postnatal day 56-91). Biochemical measures, and spatial working and reference memory (using the Morris water maze) were compared to age-matched controls.
In the hippocampus, we found a significant Fe × ALA interaction on DHA: Compared to the group receiving ALA alone, DHA was significantly higher in the Fe + ALA group. In the brain, we found significant antagonistic Fe × ALA interactions on serotonin concentrations. Provision of ALA alone impaired working memory compared with age-matched controls, while in the reference memory task ALA provided with Fe significantly improved performance.
These results indicate that providing either iron or ALA alone to double-deficient rats affects serotonin pathways and cognitive performance differently from combined provision. This may be partly explained by the enhancing effect of Fe on the conversion of ALA to EPA and DHA.
我们最近发现,大鼠同时缺乏铁(ID)和 n-3 脂肪酸(n-3 FAD)会破坏大脑单胺代谢,并且比单独缺乏 ID 或 n-3 FAD 产生更大的记忆缺陷。为这些双重缺乏的大鼠单独提供铁(Fe)或预先形成的二十二碳六烯酸(DHA)/二十碳五烯酸(EPA)会以不同于联合补充的方式影响大脑单胺途径,甚至加剧与双重缺乏相关的认知缺陷。铁是负责将α-亚麻酸(ALA)转化为 EPA 和 DHA 的酶的辅助因子,因此,与单独提供 ALA 相比,向 Fe 中提供 ALA 可能更有效地恢复大脑 EPA 和 DHA,并改善双重缺乏的大鼠的认知能力。
在这项研究中,我们研究了向双重缺乏的大鼠单独或联合提供 ALA 和 Fe 是否可以纠正与双重缺乏相关的单胺代谢和认知缺陷。使用 2×2 设计,同时存在 ID 和 n-3 FAD 的雄性大鼠在出生后第 56-91 天期间接受 Fe+ALA、Fe+n-3 FAD、ID+ALA 或 ID+n-3 FAD 饮食。将生化指标、空间工作和参考记忆(使用 Morris 水迷宫)与年龄匹配的对照组进行比较。
在海马体中,我们发现 Fe 和 ALA 之间存在显著的相互作用,即 DHA:与单独接受 ALA 的组相比,Fe+ALA 组中的 DHA 显著更高。在大脑中,我们发现血清素浓度存在显著的拮抗 Fe 和 ALA 相互作用。单独提供 ALA 会损害工作记忆,使其与年龄匹配的对照组相比明显降低,而在参考记忆任务中,Fe 与 ALA 联合提供可显著改善表现。
这些结果表明,向双重缺乏的大鼠单独提供铁或 ALA 会以不同于联合提供的方式影响血清素途径和认知表现。这可能部分解释为 Fe 对 ALA 向 EPA 和 DHA 的转化的增强作用。