Effect of Cucumis sativus on Dysfunctional 3T3-L1 Adipocytes

被引:0
作者
Méndez-Martínez Marisol
Trejo-Moreno Celeste
Maldonado-Mejía Laura
Esquivel-Guadarrama Fernando
Pedraza-Chaverri José
Zamilpa Alejandro
Medina-Campos Omar
Alarcón-Aguilar Francisco
Almanza-Pérez Julio César
Contreras-Nuñez Erika
Santana-Calderón Angélica
Fragoso Gladis
Jiménez-Ferrer Enrique
Rosas Gabriela
机构
[1] Universidad Autónoma del Estado de Morelos,Instituto de Investigación en Ciencias Básicas y Aplicadas
[2] Cuernavaca,Facultad de Medicina
[3] Universidad Autónoma del Estado de Morelos,Laboratorio de Farmacología
[4] Cuernavaca,Departamento de Biología
[5] Centro de Investigación Biomédica del Sur,Departamento de Ciencias de la Salud
[6] Instituto Mexicano del Seguro Social,Centro de Investigación en Dinámica Celular (IICBA)
[7] Xochitepec,Departamento de Inmunología
[8] Facultad de Química,undefined
[9] Universidad Nacional Autónoma de México,undefined
[10] Coyoacán,undefined
[11] Universidad Autónoma Metropolitana de Iztapalapa,undefined
[12] Universidad Autónoma del Estado de Morelos,undefined
[13] Cuernavaca,undefined
[14] Instituto de Investigaciones Biomédicas,undefined
[15] Universidad Nacional Autónoma de México,undefined
来源
Scientific Reports | / 9卷
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摘要
Obesity is caused by lipid accumulation in adipose tissues inducing adipocyte dysfunction, characterized by insulin resistance, increased lipolysis, oxidative stress, and inflammation, leading to increased levels of adipokines. Herein the capacity of the subfractions (SFs) SF1, SF2, and SF3 from the Cucumis sativus aqueous fraction and their combinations (M) to control adipocyte dysfunction in vitro, in 3T3-L1 adipocytes was studied. Adipocytes, previously treated with dexamethasone or IL-1 to induce dysfunction, were incubated with different concentrations of the subfractions for 24 h. 2-deoxyglucose consumption and glycerol release were evaluated, and a surface model was constructed to determine the most effective SF concentrations to improve both parameters. Effective SF combinations were assessed in their capacity to control metabolic, pro-oxidative, and pro-inflammatory conditions. SF1, SF2 (40 μg/ml each) and SF3 (20 μg/ml) improved 2-deoxyglucose consumption by 87%, 57%, and 87%, respectively. SF1 and SF2 (5 μg/ml each) and SF3 (40 μg/mL) increased glycerol secretion by 10.6%, 18.9%, and 11.8%, respectively. Among five combinations tested, only M4 (SF1 40 μg/ml:SF2 60 μg/ml:SF3 30 μg/ml) and M5 (SF1 40 μg/ml:SF2 60 μg/mL:SF3 10 μg/ml) controlled effectively the metabolic, pro-oxidative, and proinflammatory conditions studied. Glycine, asparagine, and arginine were the main components in these SFs.
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