0000000000204843
AUTHOR
Daina Gustina
<title>Optically induced switching of dicyclohexylamino substituted azobenzene derivatives in thin ordered films</title>
During the last years, there has been an increasing interest in the photoinduced switching effects. Among the objects of concern azobenzene derivatives, isomerizing under UV and visible light, occupy a prominent position. To understand the photoresponse of these materials in the condensed phase, their spectroscopic and electrical properties are studied. It is shown that the photoresponse depends on the orientation of the molecules and their packing. A number of novel azobenzene derivatives containing a N,N-dicyclohexyl sulfonamide moiety is synthesized. The derivatives differ in the length of alkyl chains between the azobenzene moiety and SH or COOH groups. The morphology and the photoinduc…
Suppression of intestinal microbiota-dependent production of pro-atherogenic trimethylamine N-oxide by shifting L-carnitine microbial degradation.
Abstract Aims Trimethylamine-N-oxide (TMAO) is produced in host liver from trimethylamine (TMA). TMAO and TMA share common dietary quaternary amine precursors, carnitine and choline, which are metabolized by the intestinal microbiota. TMAO recently has been linked to the pathogenesis of atherosclerosis and severity of cardiovascular diseases. We examined the effects of anti-atherosclerotic compound meldonium, an aza-analogue of carnitine bioprecursor gamma-butyrobetaine (GBB), on the availability of TMA and TMAO. Main methods Wistar rats received L-carnitine, GBB or choline alone or in combination with meldonium. Plasma, urine and rat small intestine perfusate samples were assayed for L-car…