Carpéné, ChristianGarcia-Vicente, SilviaSerrano, MartaMartí, LucBelles, ChloéRoyo Expósito, MiriamGalitzky, JeanZorzano Olarte, AntonioTestar, Xavier2020-05-032020-05-032017-04-151948-9358https://hdl.handle.net/2445/158439This study investigates in murine and human adipocytes the antilipolytic properties of a conjugate of benzylamine and decavanadate (B6V10), already reported to lower hyperglycaemia in diabetic rodents. Data indicated that the conjugate dose-dependently inhibited submaximal activation of lipolysis in all the species studied. Such antilipolytic action deals with the in vivo FFA-lowering properties already described for B6V10 in diabetic rats. B6V10 also activated lipogenesis and glucose transport in fat cells. B6V10 should therefore be useful in preventing the lipotoxicity constituted by the unrestrained lipolytic activity of insulin-resistant adipocytes in obese individuals presenting type 2 diabetes, a state named diabesity.11 p.application/pdfengcc-by-nc (c) Carpéné, Christian et al., 2017http://creativecommons.org/licenses/by-nc/3.0/esTeixit adipósResistència a la insulinaObesitatAdipose tissuesInsulin resistanceObesityInsulin-mimetic compound hexaquis (benzylammonium) decavanadate is antilipolytic in human fat cellsinfo:eu-repo/semantics/article6722682020-05-03info:eu-repo/semantics/openAccess28465791