Department of Animal Husbandry, University of Zagreb, Faculty of Veterinary Medicine, 10000, Zagreb, Croatia.
Department of Anatomy, Histology and Embryology, University of Split, School of Medicine, 21000, Split, Croatia.
Mol Nutr Food Res. 2018 May;62(9):e1701007. doi: 10.1002/mnfr.201701007. Epub 2018 Apr 20.
We investigated the interaction between streptozotocin (STZ)-induced diabetes and dietary n6/n3 ratio, and its influence on lipogenesis.
The animals were treated with STZ and fed with different dietary n6/n3 ratios: 1, 7, and 60, or supplemented with DHA/EPA. Gene expression was assessed by RT-PCR and protein expression by western blotting and immunohistochemistry. Fatty acid profile was determined by GC-MS. Pancreas and liver histology were assessed by hematoxylin and eosin (H&E) staining. STZ-induced characteristic changes in all STZ treated groups, including: increased blood glucose, decreased body mass, increased lipid peroxidation and CD36 expression, decreased 16:1n7 and 18:1n7, increases in 20:3n6, decreases in phospholipid (PL) content of 20:4n6, as well as decreases in the expression of SREBP1c, Δ-9-desaturase (Δ9D), and Δ-5-desaturase (Δ5D). Additionally, other changes occurred that were dependent on the n6/n3 ratio. Among the diabetic groups, the lower n6/n3 ratio caused higher lipid peroxidation and CD36 expression, a greater decrease in 20:4n6 and decreased Δ6-desaturase (Δ6D) expression, while the higher n6/n3 ratio caused increased partitioning of 20:4n6 into hepatic neutral lipids (NL), a decrease in 20:5n3 content, and increased β-oxidation.
Presented data suggest that the n6/n3 ratio could significantly influence lipogenesis, lipid peroxidation, and β-oxidation in STZ-induced diabetes, which could have clinical significance.
我们研究了链脲佐菌素(STZ)诱导的糖尿病与膳食 n6/n3 比例之间的相互作用,及其对脂肪生成的影响。
动物用 STZ 处理,并喂食不同的膳食 n6/n3 比例:1、7 和 60,或补充 DHA/EPA。通过 RT-PCR 评估基因表达,通过 Western blot 和免疫组织化学评估蛋白表达。通过 GC-MS 测定脂肪酸谱。通过苏木精和伊红(H&E)染色评估胰腺和肝脏组织学。STZ 诱导的所有 STZ 处理组均出现特征性变化,包括:血糖升高、体重减轻、脂质过氧化和 CD36 表达增加、16:1n7 和 18:1n7 减少、20:3n6 增加、20:4n6 的磷脂(PL)含量减少,以及 SREBP1c、Δ-9 去饱和酶(Δ9D)和 Δ-5 去饱和酶(Δ5D)的表达减少。此外,还发生了其他依赖于 n6/n3 比例的变化。在糖尿病组中,较低的 n6/n3 比例导致更高的脂质过氧化和 CD36 表达,20:4n6 减少更大,Δ6 去饱和酶(Δ6D)表达减少,而较高的 n6/n3 比例导致 20:4n6 更多地分配到肝脏中性脂质(NL)中,20:5n3 含量减少,β-氧化增加。
目前的数据表明,n6/n3 比例可显著影响 STZ 诱导的糖尿病中的脂肪生成、脂质过氧化和β-氧化,这可能具有临床意义。