2017
DOI: 10.1016/j.bbrc.2017.07.132
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8-Hydroxy-2-deoxyguanosine ameliorates high-fat diet-induced insulin resistance and adipocyte dysfunction in mice

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Cited by 19 publications
(12 citation statements)
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“…Differentiating cells were subjected to 4 days of total exposure to each of the test compounds (100 μmol/L concentration). Each compound was added at concentrations of 20, 50, and 100 μmol/L to determine morphological cell differentiation following staining with Oil Red O (ORO) stain containing 10 % (v/v) formalin . After staining, the cells were washed with distilled water and representative pictures were taken under the microscope.…”
Section: Methodsmentioning
confidence: 99%
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“…Differentiating cells were subjected to 4 days of total exposure to each of the test compounds (100 μmol/L concentration). Each compound was added at concentrations of 20, 50, and 100 μmol/L to determine morphological cell differentiation following staining with Oil Red O (ORO) stain containing 10 % (v/v) formalin . After staining, the cells were washed with distilled water and representative pictures were taken under the microscope.…”
Section: Methodsmentioning
confidence: 99%
“…For cell culture and differentiation, the 3T3-L1 murine cell lines were purchased from the American Type Culture Collection (Rockville, MD, USA) and were cultured as described previously. [24] The cells were treated with catechins and GA on day 0 and day 2 to investigate their adipogenesis. Differentiating cells were subjected to 4 days of total exposure to each of the test compounds (100 μmol/L concentration).…”
Section: Cell Culture and Differentiationmentioning
confidence: 99%
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“…In an oxidative stress, the reaction of the hydroxyl radical with the DNA nucleoside deoxyguanosine results in the formation of endogenous 8‐hydroxydeoxyguanosine (8‐OHdG) . However, recent several reports have been suggested that exogenous 8‐OHdG could reduce ROS production and proinflammatory mediators through the inhibition of Rac1 and NOX activation in inflammation‐based diseases …”
Section: Introductionmentioning
confidence: 99%
“…Cells were cultured in Dulbecco's modified Eagle's medium (DMEM; Hyclone, Logan, UT) supplemented with 10% fetal bovine serum (FBS; Hyclone) and 1% penicillin/streptomycin and incubated at 37 °C in 5% CO 2 . 3T3-L1 cells were differentiated in a standard protocol where differentiation media 1, 2, and 3 were used 23 . Briefly, two days after the 3T3-L1 preadipocytes reached 100% confluency (day 0), cells were treated with differentiation media 1 where 5 µg/mL insulin (Sigma, St. Louis, MO), 0.25 mM dexamethasone (Sigma), and 0.5 mM 1-methyl-3-isobutylxanthine (Sigma) was added to 10% FBS DMEM media.…”
Section: Methodsmentioning
confidence: 99%