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Fibroblast growth factor (FGF)-21 is a novel regulator of insulin-independent glucose transport in 3T3-L1 adipocytes and has glucose and triglyceride lowering effects in rodent models of diabetes. In this study, we found that FGF-21 can significantly attenuate ischemia-reperfusion (I/R) induced damage in H9c2 cells (rat heart). However, it is unclear which signal transduction pathway is involved in the cardioprotective effect of FGF-21. Thus, this study was designed to investigate the potential mechanism induced by FGF-21. The results showed that FGF-21 treatment prevented the oxidative stress and apoptosis associated with I/R damage by reducing the levels of superoxide anions, inhibiting glycogen synthase kinase (GSK) 3β by activating Akt phosphorylation, and recovering the levels of ATP synthase pyruvate kinase isozymes M1 and protein kinase C, thereby improving energy supply. In summary, we conclude that FGF-21 protects H9c2 cells against I/R injury mainly through the Akt-GSK-3β-caspase-3 dependent pathway, preventing oxidative stress, and recovery of the energy supply. Key words: FGF-21, myocardial ischemia-reperfusion, H9c2, proteomics, Akt, ROS, apoptosis, signaling pathway. Le facteur de croissance des fibroblastes (FGF)-21 est nouveau regulateur du transport de glucose independant de l'insuline dans les adipocytes 3T3-L1 qui diminue le glucose et les triglycerides dans des modeles de diabete chez le rongeur. Dans cette etude, nous avons trouve que le FGF-21 pouvait attenuer significativement le dommage induit par l'ischemiereperfusion (I/R) chez les cellules H9c2. Cependant, la voie de transduction impliquee dans l'effet cardioprotecteur du FGF-21 n'est pas clairement definie. Ainsi, cette etude a ete concue pour examiner le mecanisme d'action potentiel du FGF-21. Les resultats ont montre que le traitement au FGF-21 prevenait le stress oxydant et l'apoptose associes au dommage d'I/R en reduisant les anions superoxydes, inhibait la glycogene synthase kinase (GSK)-3β en activant la phosphorylation d'Akt, et restaurait l'ATP synthase, les isozymes M1 de la pyruvate kinase et la proteine kinase C afin d'ameliorer l'apport en energie. En resume, nous concluons que le FGF-21 protege les cellules H9c2 du dommage d'I/R principalement par l'intermediaire de la voie dependante d'Akt-GSK-3β-caspase-3, du stress anti-oxydant et de la restauration de l'apport energetique. [Traduit par la Redaction] Mots-cles: FGF-21, ischemie-reperfusion myocardique, H92c, proteomique, Akt, ERO, apoptose, voie de signalisation., Introduction It has been reported that ischemia-reperfusion (I/R) injury is commonly associated with oxidative stress, and that reactive oxygen species (ROS) are the major mediators contributing to acute myocardial injury [...]

A Schiff base compound derived from naphthalene has been synthesized and characterized as an Al3+-selective fluorescent probe. The chemosensor ( L) exhibits high selectively for Al3+ in aqueous solution, even in the presence of biologically relevant cations such as Na+, K+, Ca2+, Mg2+, Pb2+ and several transition metal ions. There was no observed interference from anions like Br−, Cl−, HSO3−, SO32−, S2O32−, NO2−, CO32− and AC−. The lowest detection limit for the chemosensor L was found to be 1.89 × 10−8 M with a linear response towards Al3+ over a concentration range of 5 × 10−6 to 4 × 10−5 M. Furthermore, the proposed chemosensor has been used for imaging of Al3+ in two different types of cells with satisfying results, which further demonstrates its value for practical application in biological systems. [ABSTRACT FROM AUTHOR]

In this study, we aimed to demonstrate the antidiabetic potential of (E)-N-(4-(3-(5-bromo-4-hydroxy-2-methoxyphenyl)acryloyl) phenyl)-4- tert -butylbenzamide (SN158) through peroxisome proliferator-activated receptor (PPAR)-α/γ dual activation. SN158 interacted with both PPARα and PPARγ, and increased their transcriptional activities. Simultaneously, SN158 treatment led to an increase in adipogenic differentiation of 3T3-L1 preadipocytes and fatty acid oxidation in hepatocytes. In addition, glucose uptake in myotubes was significantly increased by SN158 treatment. Finally, SN158 significantly lowered the plasma levels of glucose, triglycerides, and free fatty acids in ob/ob mice without severe weight gain and hepatomegaly. These results suggest that SN158 can be useful as a potential therapeutic agent against type 2 diabetes and related metabolic disorders by alleviating glucose and lipid abnormalities. [ABSTRACT FROM AUTHOR]

As a non-covalent fluorescence probe, in this study, salicylaldehyde azine (SA) was introduced as a sensitive fluorescence-based dye for detecting proteins both in 1-D and 2-D polyacrylamide electrophoresis gels. Down to 0.2 ng of single protein band could be detected within 1 h, which similars to that of glutaraldehyde (GA)-silver stain, but approximately four times higher than that of SYPRO Ruby fluorescent stain. Furthermore, comparative analysis of the MS compatibility of SA stain with SYPRO Ruby stain indicated that SA stain is compatible with the downstream of protein identification by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Additionally, the probable mechanism of the SA stain was investigated by molecular docking. The results demonstrated that the interaction between SA and protein was mainly contributed by hydrogen bonding and hydrophobic forces., (2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A fast and matrix-assisted laser desorption/ionization mass spectrometry compatible protein staining method in one- and two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis is described. It is based on the counterion dye staining method that employs oppositely charged two dyes, zincon and ethyl violet, to form an ion-pair complex. The protocol, including fixing, staining, and quick washing steps, can be completed in 1-1.5 h, depending upon gel thickness. It has the sensitivity comparable to the colloidal Coomassie Brilliant Blue G stain using phosphoric acid as a component of staining solution (4-8 ng). The counterion dye stain does not induce protein modifications that complicate interpretation of peptide mapping data from mass spectrometry. Considering the speed, sensitivity, and compatibility with mass spectrometry, the counterion dye stain may be more practical than any other dye-based protein stains for routine proteomic researches.