Nicotinamide desamidase in the culture medium of neuroblastoma cells]

Important amounts of nicotinic acid appear in the growth medium of neuroblastoma cell cultures. It is shown that an enzyme released by the cells into the growth medium deamidates the nicotinamide supplied by the growth medium to nicotinic acid.     

The effect of Nicotinamide Adenine Dinucleotide on lipolysis in adipose tissue in vitro

Zusammenfassung Es wird gezeigt, dass Nikotinamid Adenin Dinukleotid (NAD) eine starke Hemmung auf die Lipolyse der Fettgewebe in vitro ausübt. Untersuchung der antilipolytischen Wirkung verschiedener Bestandteile des NAD ergab, dass für die Hemmungswirkung die Gegenwart des Adenosins, nicht aber die der Nikotinsäure notwendig ist.     

Silymarin,an inhibitor of lipoxygenase

Summary Silybin (I), silydianin (II) and, silychristin (III), the main constituents, of silymarin, non-competitively inhibit the lipoxygenase from soybeans (EC 1.13.11.12) in vitro.F. Fiebrich, Thesis, University of Vienna 1977.H. Koch, Dt. ApothZtg118, 1844 (1978); reported in part at the Colloquium Pharmaceuticum in Münster, 21 st November 1978.     

PPD-induced blastogenesis is auto-regulated by suppressor cells generated in vitro

Summary Suppressor cell induction can be demonstrated during antigen specific blastogenesis by using the same methods which have shown induction of suppressor cells by Con A. Since suppressor cells are rapidly generated during antigen specific blastogenesis, they must regulate the final level of blastogenesis induced during the seven day in vitro incubation.Supported by Unites States Public Health Service grants AM-13377 and CA-19266.     

Silymarin, an inhibitor of lipoxygenase.

Silybin (I), silydianin (II) and silychristin (III), the constituents of silymarin, non-competitively inhibit the lipoxygenase from soybeans (EC 1.13.11.12) in vitro.     

Silymarin,an inhibitor of prostaglandin synthetase

Summary Silybin (I), silydianin (II) and silychristin (III), the main constituents of silymarin, inhibit the formation of prostaglandins in vitro. The inhibition is log-linearly dependent on the concentration of the effectors.F. Fiebrich, Thesis, University of Vienna 1977.H. Koch, Dt. ApothZtg118, 1844 (1978); reported in part at the Colloquium Pharmaceuticum in Münster, 21st November 1978.     

PPD-induced blastogenesis is auto-regulated by suppressor cells generated in vitro.

Suppressor cell induction can be demonstrated during antigen specific blastogenesis by using the same methods which have shown induction of suppressor cells by Con A. Since suppressor cells are rapidly generated during antigen specific blastogenesis, they must regulate the final level of blastogenesis induced during the seven day in vitro incubation.     

Green tea epigallocatechin-3-gallate is an inhibitor of mammalian histidine decarboxylase

(–)-Epigallocatechin-3-gallate, an antiproliferative and antiangiogenic component of green tea, has been reported to inhibit dopa decarboxylase. In this report, we show that this compound also inhibits histidine decarboxylase, the enzymic activity responsible for histamine biosynthesis. This inhibition was proved by a double approach, activity measurements and UV-Vis spectra of enzyme-bound pyridoxal-5-phosphate. At 0.1mM (–)-epigallocatechin-3-gallate, histidine decarboxylase activity was inhibited by more than 60% and the typical spectrum of the internal aldimine form shifted to a stable major maximum at 345nm, suggesting that the compound causes a stable change in the structure of the holoenzyme. Since histamine release is one of the primary events in many inflammatory responses, a new potential application of (–)-epigallocatechin-3-gallate in prevention or treatment of inflammatory processes is suggested by these data.Received 8 April 2003; received after revision 20 May 2003; accepted 3 June 2003     

Silymarin, an inhibitor of prostaglandin synthetase.

Silybin (I), silydianin (II) and silychristin (III), the main constituents of silymarin, inhibit the formation of prostaglandins in vitro. The inhibition is log-linearly dependent on the concentration of the effectors.     

The cell cycle of an established line ofDrosophila melanogaster cells in vitro

Riassunto La durata media delle fasi del ciclo cellulare (G₁, S e G₂) e del tempo di generazione totale (G _T ) in una linea stabilizzata di cellule diDrosophila melanogaster risulta essere rispettivamente di 1.8, 10.0, 7.2 e 18.8 ore.     

Sodium azide,an efficient inhibitor of protein diazotization

Résumé L'azide de sodium est un inhibiteur très efficace de la réaction de diazotation. Il réagit avec l'ion de diazonium à des molarités approximativement égales.     

Faf1 is expressed during neurodevelopment and is involved in Apaf1-dependent caspase-3 activation in proneural cells

Fas-associated factor 1 (Faf1) has been described as a Fas-binding pro-apoptotic protein and as a component of the death-inducing signaling complex (DISC) in Fas-mediated apoptosis. Faf1 is able to potentiate Fas-induced apoptosis in several cell lines, although its specific functions are still not clear. Here we show that Faf1 is highly expressed in several areas of the developing telencephalon. Its expression pattern appears to be dynamic at different embryonic stages and to be progressively confined within limited territories. To decipher the specific role of Faf1 in developing brain, we used cDNA over-expression and mRNA down-regulation experiments to modulate Faf1 expression in telencephalic neural precursor cells, and we showed that in neural cell death Faf1 acts as a Fas-independent apoptotic enhancer. Moreover, we found that Faf1 protein level is down-regulated during apoptosis in a caspase- and Apaf1-dependent manner.     

Synergism of a natural insect growth inhibitor is mediated by bioactivation

Summary Toxic plant allelochemicals are widespread in nature, but their mechanisms of action are largely unexplored. We report an example of bioactivation of a natural product, -asarone, that is mediated via insect mixed-function oxidases (MFO's), enzymes usually involved in detoxication processes. Bioactivity of -asarone is synergised by menthol, a MFO inducer, and antagonized by the MFO inhibitor piperonyl butoxide. Formation of a bioactive epoxide was confirmed by the identification of asarone epoxide and asarone diol in the insect excreta. These experiments represent the first demonstration of synergism between two natural products (-asarone and menthol) where the mechanism involves induction of enzymes usually involved in detoxication.     

Ketoconazole,an inhibitor of calcium transport in skeletal muscle sarcoplasmic reticulum

Summary Ketoconazole, an antimycotic agent, inhibits calcium binding and accumulation, and induces calcium release in sarcoplasmic reticulum. The Mg²⁺-ATPase and the (Ca²⁺+Mg²⁺)-ATPase activities are stimulated at low but inhibited at high concentrations of ketoconazole.The author wishes to thank Dr K. S. Cheah for discussion and Mr C. C. Ketteridge for preparing the sarcoplasmic reticulum and carrying out the ATPase assays.