2022
DOI: 10.1016/j.xpro.2022.101518
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Protocol for assessing ex vivo lipolysis of murine adipose tissue

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Cited by 6 publications
(4 citation statements)
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“…Viceral, epidydymal adipose depots were dissected from 3 month old RIAD mice (n=5) and control mice (n=5) to assess ex vivo lipolysis of visceral adipose tissue, as previously described by Roy et al., 25 with minor adjustments. Briefly, ∼50 mg of adipose depots were incubated in KRBH buffer with or without isoproterenol for 2 hours.…”
Section: Methodsmentioning
confidence: 99%
“…Viceral, epidydymal adipose depots were dissected from 3 month old RIAD mice (n=5) and control mice (n=5) to assess ex vivo lipolysis of visceral adipose tissue, as previously described by Roy et al., 25 with minor adjustments. Briefly, ∼50 mg of adipose depots were incubated in KRBH buffer with or without isoproterenol for 2 hours.…”
Section: Methodsmentioning
confidence: 99%
“…An ex vivo lipolysis assay was performed based on the protocol presented in [ 17 ]. Briefly, 50–100 mg chunks of gWAT tissue were harvested from control and HFD-fed PexRAP-AKO mice and immediately transferred to prewarmed (37 °C) KRBH buffer in 12-well plates.…”
Section: Methodsmentioning
confidence: 99%
“…Lipolytic activity in white adipose tissue was performed as described elsewhere. 87 Briefly, eWAT and iWAT (left side) were isolated in Krebs-Ringer bicarbonate buffer (KRBH) (30 mM HEPES, 120 mM NaCl, 1 mM CaCl 2 , 1 mM MgCl 2 , 10mM NaHCO 3 , 4 mM K 2 HPO 4 ) prewarmed at 37°C. Adipose tissue was divided into 30–50 mg specimens and incubated at 37°C in KRBH buffer supplemented with 2% fatty acid-free BSA (A7030, Sigma) with either vehicle (sterile dH 2 O) or 10 μM isoproterenol (ab146724, Abcam) for 2 h with constant agitation.…”
Section: Methodsmentioning
confidence: 99%