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Synergistic effects of high fat feeding and apolipoprotein E deletion on enterocytic amyloid-beta abundance

机译:高脂喂养和载脂蛋白E缺失对肠淀粉样β-丰度的协同作用

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Background Amyloid-β (Aβ), a key protein found in amyloid plaques of subjects with Alzheimer's disease is expressed in the absorptive epithelial cells of the small intestine. Ingestion of saturated fat significantly enhances enterocytic Aβ abundance whereas fasting abolishes expression. Apolipoprotein (apo) E has been shown to directly modulate Aβ biogenesis in liver and neuronal cells but it's effect in enterocytes is not known. In addition, apo E modulates villi length, which may indirectly modulate Aβ as a consequence of differences in lipid absorption. This study compared Aβ abundance and villi length in wild-type (WT) and apo E knockout (KO) mice maintained on either a low-fat or high-fat diet. Wild-type C57BL/6J and apo E KO mice were randomised for six-months to a diet containing either 4% (w/w) unsaturated fats, or chow comprising 16% saturated fats and 1% cholesterol. Quantitative immunohistochemistry was used to assess Aβ abundance in small intestinal enterocytes. Apo E KO mice given the low-fat diet had similar enterocytic Aβ abundance compared to WT controls. Results The saturated fat diet substantially increased enterocytic Aβ in WT and in apo E KO mice, however the effect was greater in the latter. Villi height was significantly greater in apo E KO mice than for WT controls when given the low-fat diet. However, WT mice had comparable villi length to apo E KO when fed the saturated fat and cholesterol enriched diet. There was no effect of the high-fat diet on villi length in apo E KO mice. Conclusion The findings of this study are consistent with the notion that lipid substrate availability modulates enterocytic Aβ. Apo E may influence enterocytic lipid availability by modulating absorptive capacity.
机译:背景淀粉样蛋白-β(Aβ)是在阿尔茨海默氏病患者的淀粉样斑块中发现的一种关键蛋白,在小肠的吸收性上皮细胞中表达。摄入饱和脂肪可显着增强肠内Aβ的丰度,而禁食则可消除表达。载脂蛋白(apo)E已被证明可直接调节肝和神经元细胞中Aβ的生物发生,但其在肠细胞中的作用尚不清楚。此外,载脂蛋白E调节绒毛长度,由于脂质吸收差异,它可能间接调节Aβ。这项研究比较了维持低脂或高脂饮食的野生型(WT)和载脂蛋白E基因敲除(KO)小鼠的Aβ丰度和绒毛长度。将野生型C57BL / 6J和载脂蛋白E KO小鼠随机分为六个月,饮食包含4%(w / w)不饱和脂肪或包含16%饱和脂肪和1%胆固醇的食物。定量免疫组织化学用于评估小肠肠上皮细胞的Aβ丰度。与野生型对照组相比,低脂饮食的Apo E KO小鼠具有相似的肠内Aβ丰度。结果饱和脂肪饮食能显着增加野生型和apo E KO小鼠的肠内Aβ水平,但后者的作用更大。当给予低脂饮食时,载脂蛋白E KO小鼠的绒毛高度显着高于野生型对照组。然而,当喂饱饱和脂肪和胆固醇的饮食时,野生型小鼠的绒毛长度可与载脂蛋白E KO相媲美。高脂饮食对apo E KO小鼠的绒毛长度没有影响。结论这项研究的发现与脂质底物可利用性调节肠细胞Aβ的观点一致。 Apo E可能通过调节吸收能力来影响肠脂质的利用。

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