Department of Biochemistry and Biomolecular, Faculty of Medicine, University of Brawijaya, Malang 65145, Indonesia.
Medical Study Program, Faculty of Medicine, State Islamic University of Maulana Malik Ibrahim (UIN Maulana Malik Ibrahim), Malang 65144, Indonesia.
Nutrients. 2024 May 10;16(10):1441. doi: 10.3390/nu16101441.
Metabolic syndrome is a global health problem. The use of functional foods as dietary components has been increasing. One food of interest is forest onion extract (FOE). This study aimed to investigate the effect of FOE on lipid and glucose metabolism in silico and in vitro using the 3T3-L1 mouse cell line. This was a comprehensive study that used a multi-modal computational network pharmacology analysis and molecular docking in silico and 3T3-L1 mouse cells in vitro. The phytochemical components of FOE were analyzed using untargeted ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS). Next, an in silico analysis was performed to determine FOE's bioactive compounds, and a toxicity analysis, protein target identification, network pharmacology, and molecular docking were carried out. FOE's effect on pancreatic lipase, α-glucosidase, and α-amylase inhibition was determined. Finally, we determined its effect on lipid accumulation and MAPK8, PPARG, HMGCR, CPT-1, and GLP1 expression in the preadipocyte 3T3-L1 mouse cell line. We showed that the potential metabolites targeted glucose and lipid metabolism in silico and that FOE inhibited pancreatic lipase levels, α-glucosidase, and α-amylase in vitro. Furthermore, FOE significantly ( < 0.05) inhibits targeted protein expressions of MAPK8, PPARG, HMGCR, CPT-1, and GLP-1 in vitro in 3T3-L1 mouse cells in a dose-dependent manner. FOE contains several metabolites that reduce pancreatic lipase levels, α-glucosidase, α-amylase, and targeted proteins associated with lipid and glucose metabolism in vitro.
代谢综合征是一个全球性的健康问题。作为膳食成分的功能性食品的使用正在增加。一种受到关注的食品是野蒜提取物(FOE)。本研究旨在使用 3T3-L1 小鼠细胞系,通过计算机模拟和体外实验来研究 FOE 对脂质和葡萄糖代谢的影响。这是一项综合研究,使用多模式计算网络药理学分析和计算机模拟中的分子对接以及 3T3-L1 小鼠细胞的体外实验。使用非靶向超高效液相色谱-串联质谱法(UPLC-MS)分析 FOE 的植物化学成分。接下来,进行计算机模拟分析以确定 FOE 的生物活性化合物,并进行毒性分析、蛋白质靶标鉴定、网络药理学和分子对接。测定 FOE 对胰腺脂肪酶、α-葡萄糖苷酶和α-淀粉酶抑制的影响。最后,我们测定了其对前脂肪细胞 3T3-L1 小鼠细胞系中脂质积累以及 MAPK8、PPARG、HMGCR、CPT-1 和 GLP1 表达的影响。我们表明,潜在的代谢产物在计算机模拟中靶向葡萄糖和脂质代谢,FOE 抑制了胰腺脂肪酶水平、α-葡萄糖苷酶和α-淀粉酶的体外活性。此外,FOE 显著(<0.05)抑制 MAPK8、PPARG、HMGCR、CPT-1 和 GLP-1 等靶向蛋白在 3T3-L1 小鼠细胞中的表达,呈剂量依赖性。FOE 含有几种代谢产物,可降低体外胰腺脂肪酶水平、α-葡萄糖苷酶、α-淀粉酶和与脂质及葡萄糖代谢相关的靶向蛋白。