Yuri Gabriela, Cifuentes Mariana, Cisternas Pedro, Paredes Adrián, Ormazabal Paulina
Institute of Health Sciences, Universidad de O'Higgins, Av. Libertador Bernardo O'Higgins 611, Rancagua 2820000, Chile.
Laboratory of Obesity and Metabolism in Geriatrics and Adults (OMEGA), Institute of Nutrition and Food Technology (INTA), Universidad de Chile, Av. El Líbano 5524, Macul, Santiago 7830490, Chile.
Pharmaceuticals (Basel). 2024 Apr 29;17(5):566. doi: 10.3390/ph17050566.
Aging and obesity are associated with insulin resistance (IR) and low-grade inflammation. Molecularly, IR is characterized by a reduction in glucose uptake and insulin signaling (IRS-1/Akt/AS160 pathway), while inflammation may result from upregulated NF-κB pathway after low Tyr-IκBα phosphorylation. Upregulated phosphatase activity of PTP1B is associated with impaired insulin signaling and increased inflammation. Plasma levels of palmitic acid (PA) are elevated in obesity, triggering inflammation and disruption of insulin signaling. Traditional medicine in Northern Chile uses oral infusions of Phil. (Verbenaceae) to treat inflammatory conditions. Significant amounts of flavonoids are found in the hydroethanolic extract of Lampaya (HEL), which may account for its biological activity. The aim of this work was to study the effect of HEL and PA on insulin signaling and glucose uptake as well as inflammatory marker expression in human adipocytes.
We studied HEL effects on PA-induced impairment on insulin signaling, glucose uptake and inflammatory marker content in human SW872 adipocytes. HEL cytotoxicity was assessed in adipocytes at different concentrations (0.01 to 10 g/mL). Adipocytes were incubated or not with PA (0.4 mM, 24 h) with or without HEL (2 h pre-incubation), and then stimulated with insulin (10 min, 100 mM) or a vehicle. Phospho-IRS-1, phospho-Akt, phospho-AS160, phospho-NF-κB and phospho-IκBα, as well as protein levels of PTP1B, were assessed using Western blotting, and glucose uptake was evaluated using the 2-NBDG analogue.
At the assessed HEL concentrations, no cytotoxic effects were observed. PA decreased insulin-stimulated phospho-Akt and glucose uptake, while co-treatment with HEL increased such markers. PA decreased phospho-IRS-1 and phospho-Tyr-IκBα. On the other hand, incubation with HEL+PA decreased phospho-AS160 and phospho-NF-κB compared with cells treated with PA alone.
Our results suggest a beneficial effect of HEL by improving PA-induced impairment on molecular markers of insulin signaling, glucose uptake and inflammation in adipocytes. Further studies are necessary to elucidate whether lampaya may constitute a preventive strategy for people whose circulating PA levels contribute to IR and inflammation during aging and obesity.
衰老和肥胖与胰岛素抵抗(IR)及低度炎症相关。在分子层面,IR的特征是葡萄糖摄取和胰岛素信号传导(IRS-1/Akt/AS160途径)减少,而炎症可能源于低酪氨酸-IκBα磷酸化后NF-κB途径上调。蛋白酪氨酸磷酸酶1B(PTP1B)的磷酸酶活性上调与胰岛素信号受损及炎症增加有关。肥胖人群血浆中棕榈酸(PA)水平升高,会引发炎症并破坏胰岛素信号传导。智利北部的传统医学使用灯帕草(马鞭草科)的口服浸剂治疗炎症性疾病。灯帕草水乙醇提取物(HEL)中含有大量黄酮类化合物,这可能是其具有生物活性的原因。本研究旨在探讨HEL和PA对人脂肪细胞胰岛素信号传导、葡萄糖摄取以及炎症标志物表达的影响。
我们研究了HEL对PA诱导的人SW872脂肪细胞胰岛素信号传导、葡萄糖摄取及炎症标志物含量损伤的影响。在不同浓度(0.01至10 g/mL)下评估HEL对脂肪细胞的细胞毒性。脂肪细胞分别在有或无HEL(预孵育2小时)的情况下与PA(0.4 mM,24小时)一起孵育,然后用胰岛素(10分钟,100 mM)或溶剂刺激。使用蛋白质免疫印迹法评估磷酸化IRS-1、磷酸化Akt、磷酸化AS160、磷酸化NF-κB和磷酸化IκBα以及PTP1B的蛋白水平,并使用2-NBDG类似物评估葡萄糖摄取。
在所评估的HEL浓度下,未观察到细胞毒性作用。PA降低了胰岛素刺激的磷酸化Akt和葡萄糖摄取,而与HEL共同处理则增加了这些标志物。PA降低了磷酸化IRS-1和磷酸化酪氨酸-IκBα。另一方面,与单独用PA处理的细胞相比,用HEL + PA孵育降低了磷酸化AS160和磷酸化NF-κB。
我们的结果表明,HEL通过改善PA诱导的脂肪细胞胰岛素信号传导、葡萄糖摄取和炎症分子标志物损伤具有有益作用。有必要进一步研究灯帕草是否可为循环PA水平导致衰老和肥胖期间IR及炎症的人群构成一种预防策略。