In the case of studied soybean peptides, these inhibited mRNA iNOS expression levels and TNF and NO production, while also reduced the pro-inflammatory enzymatic activity of COX-2 in LPS-induced macrophages [8]. Glut-4, and PI3K, improving glucose uptake, while decreasing pro-inflammatory mediators as iNOs, TNF, IL-1, INF, IL-6, IL-12, IL-17, and IL-27; (4) Conclusion: These results suggest a promising use of NLL -conglutin protein in functional foods, which could also be implemented in alternative diagnosis and therapeutic molecular tools helping to prevent and treat inflammatory-related diseases. 2S albumin and lectin-like protein, which were associated with genes expression modulation of inflammatory molecules [12]. In this work, we have studied the anti-inflammatory properties of narrow-leafed lupin (NLL) -conglutin protein from mature seeds using in vitro human PANC-1 pancreatic cell-line in both, an induced inflammation model using bacteria lipopolysaccharide (LPS), and an induced insulin resistance Palovarotene (IR) cell model, with the aim of assessing the capability of NLL -conglutin to improve the oxidative stress homeostasis of cells, the inflammatory induced state and the IR improvement at molecular level by decreasing several pro-inflammatory mediators genes expression and proteins levels, as well as up-regulating of insulin signaling pathway gene expression. 2. Material and Methods 2.1. Isolation and Purification of -Conglutin from NLL Mature Seeds The isolation and purification of -conglutin proteins from NLL was accomplished following the Czubiski et al. [13] method. Briefly, NLL seed proteins were extracted using Tris buffer pH 7.5 [20 mmol L?1], having 0.5 mol L?1 NaCl/gr defatted seeds. After sample centrifugation at 20,000 and two times PBS washing, PANC-1 cells were collected. Afterward, cells counting and viability assessment were achieved by using a Countess II FL Automated Cell Counter (Thermo Fisher) at both, the initial and final step of each experiment. Viability of cells was higher than 95%. Cell cultures were stablished at 80% of confluence and treated with LPS (1 g/mL) for 24 h. PANC-1 cells were challenged with purified -conglutin protein for 24 h alone or in combination adding LPS. Aliquots of -conglutin protein stored at ?20 C in PBS were thawed just before use and dissolved in culture media to target concentrations and to be added to the cultures. After treatment, cells were harvested for further analyses. 2.5. MTT Assay for Cell Viability Cell viability was evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) following the manufacturers instructions (Roche). Briefly, 96-well microtitre plates were inoculated at a density of 1 1 103 PANC-1 cells per well in 300 L of growth media. Plates were incubated overnight under 5% CO2 in humidified air to allow the cells to adhere to the wells. After incubation, cells were treated for 24 h Palovarotene with either LPS or -conglutin protein, and washed three times with PBS in order to prevent any interfering issue because of the phenolic compounds when making the MTT assay. A volume of 200 L of free red-phenol DMEM containing 1 mg mL?1 of MTT was added to the cells, and these were incubated for 3 h. Metabolically active viable cells are able to convert MTT into formazan crystals (purple color), and the former compound was solubilized with 200 L of DMSO to absorb at 570 nm (test) and 690 nm using a iMark microplate reader (Bio-Rad, USA). 2.6. Insulin Resistance PANC-1 Cell Model and Glucose Uptake Culture PANC-1 control cells were seeded in DMEM PRKM12 supplemented with 10% (v/v) FBS, using 96-well microtiter plates under standard conditions (5% CO2 and 37 C in humidified air), and a density of 2 104 cells per mL in 200 mL. Optimal dose of insulin and treatment time as requisite to establish insulin-resistant IR_PANC-1 (IR-C) cells. Cells display reduced glucose uptake, and this is one of the main feature of the insulin resistance impaired glucose uptake since decreasing cells responses to glucose uptake to Palovarotene increasing levels of insulin. Thus, the cell culture was separated into two groups having six independent replicates per each group: (1) Cultured cells in 200 L complete medium (control cells, group C); (2) Treated cells with insulin (10?5 to 10?9 nmol L?1) when the cells became adherent (group IR-C). These PANC-1 cells were then cultured for 24, 48, and 72 h and the concentration of glucose in the media was measured using the glucose oxidase method (Abcam, UK). The concentration required to stablish IR-C PANC-1 cells was 10?7 nmol L?1 and cultured for.