Csonka Csaba, Baranyai Tamás, Tiszlavicz László, Fébel Hedvig, Szűcs Gergő, Varga Zoltán V, Sárközy Márta, Puskás László G, Antal Otilia, Siska Andrea, Földesi Imre, Ferdinandy Péter, Czakó László, Csont Tamás
Metabolic Diseases and Cell Signaling Research Group, Department of Biochemistry, University of Szeged, Dóm tér 9, Szeged, H-6720, Hungary.
1st Department of Internal Medicine, University of Szeged, Szeged, Hungary.
Lipids Health Dis. 2017 Jul 27;16(1):144. doi: 10.1186/s12944-017-0537-z.
Lipid accumulation in the liver and pancreas is primarily caused by combined hyperlipidemia. However, the effect of isolated hypercholesterolemia without hypertriglyceridemia is not fully described. Therefore, our aim was to investigate whether hypercholesterolemia alone leads to alterations both in hepatic and pancreatic lipid panel and histology in rats.
Male Wistar rats were fed with 2% cholesterol +0.25% cholate-supplemented diet or standard chow for 12 weeks. Blood was collected at weeks 0, 4, 8 and 12 to measure serum cholesterol and triglyceride levels. At week 12, both the pancreas and the liver were isolated for further histological and biochemical analysis. Hepatic and plasma fatty acid composition was assessed by gas chromatography. Expression of mRNA of major enzymes involved in saturated/unsaturated fatty acid synthesis was analyzed by qPCR. In separate experiments serum enzyme activities and insulin levels were measured at week 9.
At week 12, rats fed with 2% cholesterol +0.25% cholate-supplemented diet were characterized by elevated serum cholesterol (4.09 ± 0.20 vs. 2.89 ± 0.22 mmol/L, *p < 0.05) while triglyceride (2.27 ± 0.05 vs. 2.03 ± 0.03 mmol/L) and glucose levels (5.32 ± 0.14 vs. 5.23 ± 0.10 mmol/L) remained unchanged. Isolated hypercholesterolemia increased hepatic lipid accumulation, hepatic cholesterol (5.86 ± 0.22 vs. 1.60 ± 0.15 ng/g tissue, *p < 0.05) and triglyceride contents (19.28 ± 1.42 vs. 6.78 ± 0.71 ng/g tissue, *p < 0.05), and hepatic nitrotyrosine level (4.07 ± 0.52 vs. 2.59 ± 0.31 ng/mg protein, *p < 0.05). The histology and tissue lipid content of the pancreas was not affected. Serum total protein level, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities remained unchanged in response to isolated hypercholesterolemia while serum alkaline phosphatase activity (ALP) significantly increased. Plasma insulin levels did not change in response to isolated hypercholesterolemia suggesting an intact endocrine function of the pancreas. Isolated hypercholesterolemia caused a significantly increased hepatic and serum fatty acid level associated with a marked alteration of fatty acid composition. Hepatic expression of Δ9-desaturase (SCD1) was increased 4.92×, while expression of Δ5-desaturase and Δ6-desaturase were decreased (0.447× and 0.577×, respectively) due to isolated hypercholesterolemia.
Isolated hypercholesterolemia leads to hepatic steatosis and marked alterations in the hepatic lipid profile without affecting the pancreas. Altered fatty acid profile might mediate harmful effects of cholesterol in the liver.
肝脏和胰腺中的脂质蓄积主要由混合性高脂血症引起。然而,单纯高胆固醇血症(无高甘油三酯血症)的影响尚未得到充分描述。因此,我们的目的是研究单纯高胆固醇血症是否会导致大鼠肝脏和胰腺的脂质谱及组织学发生改变。
将雄性Wistar大鼠用含2%胆固醇+0.25%胆酸盐的饲料或标准饲料喂养12周。在第0、4、8和12周采集血液,检测血清胆固醇和甘油三酯水平。在第12周,分离胰腺和肝脏进行进一步的组织学和生化分析。通过气相色谱法评估肝脏和血浆脂肪酸组成。通过qPCR分析参与饱和/不饱和脂肪酸合成的主要酶的mRNA表达。在单独的实验中,在第9周测量血清酶活性和胰岛素水平。
在第12周,用含2%胆固醇+0.25%胆酸盐的饲料喂养的大鼠血清胆固醇升高(4.09±0.20 vs. 2.89±0.22 mmol/L,*p<0.05),而甘油三酯(2.27±0.05 vs. 2.03±0.03 mmol/L)和葡萄糖水平(5.32±0.14 vs. 5.23±0.10 mmol/L)保持不变。单纯高胆固醇血症增加了肝脏脂质蓄积、肝脏胆固醇(5.86±0.22 vs. 1.60±0.15 ng/g组织,*p<0.05)和甘油三酯含量(19.28±1.42 vs. 6.78±0.71 ng/g组织,*p<0.05),以及肝脏硝基酪氨酸水平(4.07±0.52 vs. 2.59±0.31 ng/mg蛋白,*p<0.05)。胰腺的组织学和组织脂质含量未受影响。单纯高胆固醇血症时血清总蛋白水平、丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST)活性保持不变,而血清碱性磷酸酶活性(ALP)显著升高。单纯高胆固醇血症时血浆胰岛素水平未改变,提示胰腺内分泌功能完好。单纯高胆固醇血症导致肝脏和血清脂肪酸水平显著升高,伴有脂肪酸组成的明显改变。由于单纯高胆固醇血症,肝脏Δ9-去饱和酶(SCD1)的表达增加4.92倍,而Δ5-去饱和酶和Δ6-去饱和酶的表达降低(分别为0.447倍和0.577倍)。
单纯高胆固醇血症导致肝脏脂肪变性和肝脏脂质谱的明显改变,而不影响胰腺。脂肪酸谱的改变可能介导胆固醇在肝脏中的有害作用。