| 引用本文:唐悦恒，赵莉，邹欣，徐丽君，陆付耳，董慧.交泰丸组分配伍改善小鼠胰岛素瘤B细胞脂质沉积的机制研究[J].世界中医药,2021,(19):. |
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| 交泰丸组分配伍改善小鼠胰岛素瘤B细胞脂质沉积的机制研究 |
| Mechanism of Combination of Active Compounds of Jiaotai Pill on Improving Lipid Accumulation in Insulinoma B Cells of Mice |
| 投稿时间：2021-08-10 |
| DOI：10.3969/j.issn.1673-7202.2021.19.002 |
| 中文关键词: 交泰丸 小檗碱 肉桂酸 NIT-1胰岛B细胞 脂肪 |
| English Keywords:Jiaotai pills Berberine Cinnamic Acid NIT-1 pancreatic B cells Lipid |
| 基金项目:国家重点研发计划“中医药现代化研究”重点专项（2018YFC1704202） |
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| 中文摘要: |
| 目的：研究交泰丸中主要活性成分小檗碱（BBR）、肉桂酸（CA）及其配伍（BBR/CA）对软脂酸（PA）诱导的NIT-1胰岛B细胞内脂质沉积的影响。方法：将细胞在PA的培养基中培养24 h，建立高脂诱导的细胞内脂肪沉积模型。分为模型组、BBR组、CA组、BBR/CA组、二甲双胍（Met）组，分别给予相应药物干预，另设对照组。油红O染色法评估细胞内脂肪沉积情况；酶法检测细胞内三酰甘油（TG）含量；使用Western Blotting和实时荧光定量PCR（RT-PCR）法检测细胞腺苷酸活化蛋白激酶（AMPK）及其下游脂肪生成和脂肪酸氧化基因的表达水平，包括脂肪酸合成酶（FAS）、乙酰辅酶A羧化酶（ACC）、磷酸化乙酰辅酶A羧化酶（p-ACC）、肉碱酰转移酶-1（CPT-1）、固醇调节元件结合蛋白（SREBP-1c）。结果：PA诱导使NIT-1胰岛B细胞中脂肪沉积明显增加，TG含量显著升高，AMPK蛋白及其下游靶标（如p-ACC、CPT-1等）表达显著降低。同时，AMPK下游脂肪生成基因包括SREBP-1c mRNA、FAS和ACC蛋白表达显著增加。BBR单药和BBR/CA配伍处理优于CA单药，可显著逆转NIT-1胰岛B细胞中上述基因表达水平的变化。结论：在体外，交泰丸活性组分配伍可减少高脂诱导的NIT-1胰岛B细胞内脂肪沉积，其机制可能与减少脂肪合成和增加脂肪氧化有关。 |
| English Summary: |
| To investigate the effects of berberine(BBR) and cinnamic acid(CA),the main active compounds of Jiaotai pills,and the combination of berberine and cinnamic acid(BBR/CA) on palmitic acid(PA)-induced lipid accumulation in NIT-1 pancreatic B cells.Methods:Cells were incubated in culture medium containing PA for 24 hours to establish a model of lipid accumulation induced by high fat.Then treatments with BBR,CA,the combination of BBR and CA(BBR/CA) and Metformin(Met) were performed respectively,and a control group was set up.Intracellular lipid accumulation was assessed by Oil Red O staining and TG content was measured by enzymatic assay.The expression of adenosine monophosphate-activated protein kinase(AMPK) protein and its downstream lipogenic and fatty acid oxidation genes,including fatty acid synthase(FAS),acetyl-CoA carboxylase(ACC),phosphorylation acetyl-CoA carboxylase(p-ACC),carnitine acyl transferase 1(CPT-1) and sterol regulatory element binding protein 1c(SREBP-1c) were determined by Western blot or real time polymerase chain reaction(RT-PCR).Results:PA induced an obvious lipid accumulation and a significant increase in intracellular TG content in NIT-1 pancreatic B cells.PA also induced a remarkable decrease in AMPK protein expression and its downstream targets such as p-ACC and CPT-1.Meanwhile,AMPK downstream lipogenic genes,including SREBP-1c mRNA,FAS and ACC protein expressions,were increased significantly.Treatments with BBR and BBR/CA,superior to CA,significantly reversed the above genes changes in NIT-1 pancreatic B cells.Conclusion:It can be concluded that in vitro,the active compounds of Jiaotai pills inhibits PA-induced lipid accumulation by decreasing lipogenesis and increasing lipid oxidation in NIT-1 pancreatic B cells. |
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