Irene Fernández

Utility of biliary microscopy for the prediction of the chemical composition of gallstones and the outcome of dissolution therapy with ursodeoxycholic acid

To learn whether microcrystalline solids in bile could predict gallstone composition, the findings determined by polarizing microscopy of gallbladder bile were related to stone type at cholecystectomy in 53 patients. Cholesterol crystals were present in 36 of 39 cholesterol stone bile and absent in 12 of 14 bile from non-cholesterol stones. Fifteen cholesterol stones (eight radiopaque) contained calcium carbonate, and characteristic vaterite microspheroliths were observed in 53% of their bile. In another study, crystals in basal duodenal bile were related to the outcome of gallstone dissolution treatment with ursodeoxycholic acid, 10 mg/kg X day. In 39 patients treated for 1 yr, efficacy (complete gallstone dissolution) was 41% overall and 52% in patients with stones less than or equal to 10 mm in diameter. In connection with the findings of biliary microscopy, efficacy was 93% in 14 patients with cholesterol crystals in bile, and 27% in 11 patients with microspheroliths in bile. Cholecystectomies in 9 patients with dissolution failure revealed 4 cases of non-cholesterol stones and 5 cases (including 3 with on-therapy calcification) of calcium carbonate-rich cholesterol stones with a surface/interior mineral ratio greater than 3. The results confirm that cholesterol crystals in bile are a sensitive measure of cholesterol gallstones. They also show that vaterite microspheroliths in bile indicate the presence of calcium carbonate in gallstones. Both findings suggest that biliary crystals reflect gallstone composition, and it is demonstrated that this information is useful in predicting the success or failure of cholelitholysis with ursodeoxycholic acid. Finally, the data show that radiologically undetectable stone calcification reduces the probability of dissolution, and that the calcified structures appearing in some stones during treatment are composed of calcium carbonate.

Novel charged [14]azolophanes: associative behaviour revealed by electrospray ionization

Electrospray ionization mass spectrometry has been used to investigate simple multicharged [1(4)]heterophanes containing heterocyclic betaine subunits as building blocks. The formation of stable noncovalent polymolecular self-assembled structures in the gas phase is reported.

Putative one-pot prebiotic polypeptides with ribonucleolytic activity.

KIA7, a peptide with a highly restricted set of amino acids (Lys, Ile, Ala, Gly and Tyr), adopts a specifically folded structure. Some amino acids, including Lys, Ile, Ala, Gly and His, form under the same putative prebiotic conditions, whereas different conditions are needed for producing Tyr, Phe and Trp. Herein, we report the 3D structure and conformational stability of the peptide KIA7H, which is composed of only Lys, Ile, Ala, Gly and His. When the imidazole group is neutral, this 20-mer peptide adopts a four-helix bundle with a specifically packed hydrophobic core. Therefore, one-pot prebiotic proteins with well-defined structures might have arisen early in chemical evolution. The Trp variant, KIA7W, was also studied. It adopts a 3D structure similar to that of KIA7H and its previously studied Tyr and Phe variants, but is remarkably more stable. When tested for ribonucleolytic activity, KIA7H, KIA7W and even short, unstructured peptides rich in His and Lys, in combination with Mg(++), Mn(++) or Ni(++) (but not Cu(++), Zn(++) or EDTA) specifically cleave the single-stranded region in an RNA stem-loop. This suggests that prebiotic peptide-divalent cation complexes with ribonucleolytic activity might have co-inhabited the RNA world.

Drosophila dSAP18 is a nuclear protein that associates with chromosomes and the nuclear matrix, and interacts with pinin, a protein factor involved in RNA splicing

SAP18 is a highly conserved protein that was proposed to be involved in multiple cellular processes from autophagy to gene regulation and mRNA processing. In this paper we show that, in Drosophila, dSAP18 is a predominantly nuclear protein that associates to both chromosomes and the nuclear matrix. dSAP18 becomes nuclear early during development, at the onset of cellularization, and remains so all through embryo development. dSAP18 is also nuclear in salivary glands, ovaries and cultured S2 cells. Here we also show that dSAP18 forms a complex with the Drosophila homolog of pinin (dPnn), a protein factor involved in mRNA splicing. dSAP18-dPnn interaction was confirmed in vivo, through co-immunoprecipitation experiments, as well as in vitro, through GST pull-down assays. These results are discussed in the context of the possible functions played by SAP18.

Selection of Betaine Building Blocks for the Construction of Quadrupolar Heterophane Frameworks

The synthesis of a set of [(azolio)methyl]azolate betaines 3−6 designed by combination of a variety of heterocyclic fragments based on pyrazole, 1,2,4-triazole, and benzimidazole is reported. The dipolar nature of the betaines is discussed on the basis of 1H and 13C NMR spectroscopic data and dipole moment values, which range between 13.4 and 16.5 D. By exploitation of the sensitivity of electrospray ionization mass spectrometry in both the positive and negative modes, several informative peaks and stable noncovalent polymolecular self-assembled structures in the gas phase were observed. From these results, the [(imidazolio)methyl]-1,2,4-triazolate betaine subunits 1 were chosen as the most suitable building blocks for the construction of quadrupolar [1n]heterophanes. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

Role of dichloromethane in the photocyclization—oxidation of vinylheterocyclic systems

Abstract The photochemical behaviour of 3-cyanovinyl-2-aryl(heteroaryl)indoles has been studied in dichloromethane under non-oxidative conditions. The photocyclization—oxidation reaction observed affording carbazoles proceeds, by contrast with the reversible conrotatory ring closure of stilbenes or vinylbiphenyls, through the formation of a substrate—dichloromethane radical ion pair obtained by photoinduced electron transfer from the vinyl compounds to dichloromethane. The phototransformation observed is not an exclusive property of vinylindoles, being chemically productive for the synthesis of heteroaromatic polycyclic systems.