Structure of two biologically active sesquiterpenoid amino-quinones from the marine spongeDysidea avara

Summary The structures of 2 minor constituents of the marine spongeDysidea avara, which induce developmental aberrations in sea-urchin eggs, are described. The structures were confirmed also by a simple synthesis from avarol (1).Acknowledgments. The authors wish to thank Mr A. Crispino for his skillfull laboratory technical assistance. Thanks are also due to Mr C. Di Pinto (NMR) and Mr A. Milone (MS).     

Pleraplysillin-2, a further furanosesquiterpenoid from the spongePleraplysilla spinifera

Cellular and Molecular Life Sciences - Si riporta l'isolamento dalla spugnaPleraplysilla spinifera di un ulteriore furanosesquiterpenoide pleraplysillina-2 per il quale si dimostra la struttura 3.     

Injection of adult neurospheres induces recovery in a chronic model of multiple sclerosis

Widespread demyelination and axonal loss are the pathological hallmarks of multiple sclerosis. The multifocal nature of this chronic inflammatory disease of the central nervous system complicates cellular therapy and puts emphasis on both the donor cell origin and the route of cell transplantation. We established syngenic adult neural stem cell cultures and injected them into an animal model of multiple sclerosis--experimental autoimmune encephalomyelitis (EAE) in the mouse--either intravenously or intracerebroventricularly. In both cases, significant numbers of donor cells entered into demyelinating areas of the central nervous system and differentiated into mature brain cells. Within these areas, oligodendrocyte progenitors markedly increased, with many of them being of donor origin and actively remyelinating axons. Furthermore, a significant reduction of astrogliosis and a marked decrease in the extent of demyelination and axonal loss were observed in transplanted animals. The functional impairment caused by EAE was almost abolished in transplanted mice, both clinically and neurophysiologically. Thus, adult neural precursor cells promote multifocal remyelination and functional recovery after intravenous or intrathecal injection in a chronic model of multiple sclerosis.     

Distribution of radioactivity after administration of3H-5-hydroxytryptamine by three different routes to the musselMytilus edulis

Summary Intracardiac injection gives proportionately higher and earlier peak concentration in tissues that specifically accumulates it, i.m. injection gives slower but longer lasting accumulations, and topical application to a ganglia essentially localizes the drug in that structure.We wish to thank Drs Hiripi and Nemcsok for the demonstration of the intracardiac technique. We also wish to thank Drs Haley and Ledeen for the use of the scintillation counter.     

Naloxone selectively blocks dopamine response of Br-type neuron inHelix pomatia L.

Summary The present study demonstrates that the potent opiate antagonist, naloxone can selectively block the DA induced inhibition of the bursting activity pattern of the RPal or Br-type neuron. The dopamine inhibitory affect can also be blocked by haloperidol, a established dopamine receptor blocker.This work partially supported by a grant from the National Academy of Sciences and the Hungarian Academy of Sciences awarded to G.B.S. We also gratefully acknowledge thoughtful comments from Dr J. Salanki.     

Chemistry of mediterranean gorgonians. II. Pregna 4,20-dien-11α-ol-3-one acetate,a novel steroid from the gorgonianEunicella cavolini

Summary The compound titled1 has been isolated from the gorgonianE. cavolini and synthesized from 11-acetoxy-progesterone (3).This work has been carried out in the frame of the Progetto Finalizzato per l'Oceanografia e i Fondi marini, C.N.R., Roma. Acknowledgments. We are grateful to the Zoological Station (Naples) for the collection of Gorgonians. Thanks are also due to Mr G. Scognamiglio, for technical assistance and to Mr C. Di Pinto, for NMR-experiments.     

CFD simulation of fluidization quality in the three-dimensional fluidized bed

Multiphase computational fluid dynamics (CFD) has become an alternative method to experimental investigation on predicting the fluid dynamics in gas-solid fluidized beds. The model of Brandani and Zhang, which contains additional terms in both the gas- and solid-phase momentum equations, is employed to explore homogenous fluidization of Geldart type A particles and bubbling fluidization of Geldart type B particles in three-dimensional gas-fluidized beds. In this model, only a correlation for drag force is necessary to close the governing equations. Two kinds of solids, i.e., fine alumina powder (d_p=60 μm and ρ_p=1500 kg/m³) and sand (d_p=610 μm and ρ_p=2500 kg/m³), are numerically simulated in a rectangular duct of 0.2 m (long) ×0.2 m (wide) ×0.5 m (high). The results show good agreement with the classic theory of Geldart.     

Enteric glial cells are susceptible to <Emphasis Type="Italic">Clostridium difficile</Emphasis> toxin B

Clostridium difficile causes nosocomial/antibiotic-associated diarrhoea and pseudomembranous colitis. The major virulence factors are toxin A and toxin B (TcdB), which inactivate GTPases by monoglucosylation, leading to cytopathic (cytoskeleton alteration, cell rounding) and cytotoxic effects (cell-cycle arrest, apoptosis). C. difficile toxins breaching the intestinal epithelial barrier can act on underlying cells, enterocytes, colonocytes, and enteric neurons, as described in vitro and in vivo, but until now no data have been available on enteric glial cell (EGC) susceptibility. EGCs are crucial for regulating the enteric nervous system, gut homeostasis, the immune and inflammatory responses, and digestive and extradigestive diseases. Therefore, we evaluated the effects of C. difficile TcdB in EGCs. Rat-transformed EGCs were treated with TcdB at 0.1–10 ng/ml for 1.5–48 h, and several parameters were analysed. TcdB induces the following in EGCs: (1) early cell rounding with Rac1 glucosylation; (2) early G2/M cell-cycle arrest by cyclin B1/Cdc2 complex inactivation caused by p27 upregulation, the downregulation of cyclin B1 and Cdc2 phosphorylated at Thr161 and Tyr15; and (3) apoptosis by a caspase-dependent but mitochondria-independent pathway. Most importantly, the stimulation of EGCs with TNF-α plus IFN-γ before, concomitantly or after TcdB treatment strongly increased TcdB-induced apoptosis. Furthermore, EGCs that survived the cytotoxic effect of TcdB did not recover completely and showed not only persistent Rac1 glucosylation, cell-cycle arrest and low apoptosis but also increased production of glial cell-derived neurotrophic factor, suggesting self-rescuing mechanisms. In conclusion, the high susceptibility of EGCs to TcdB in vitro, the increased sensitivity to inflammatory cytokines related to apoptosis and the persistence of altered functions in surviving cells suggest an important in vivo role of EGCs in the pathogenesis of C. difficile infection.