, 2011) Several data are not fully consistent with a strict caus

, 2011). Several data are not fully consistent with a strict causal linkage between

formation of ET pore and cellular effects, especially for the early cellular manifestations of ET. Indeed, ET can cause ATP depletion and oncosis in renal collecting duct mpkCCDcl4 cells despite ET heptamerization is prevented by pre-treating cells with mβCD (Chassin et al., 2007). Thus the cytotoxic effects of ET in mpkCCDcl4 cells appears dual and comprised of a pore-forming cholesterol-dependent phase that occurs in DRMs, and an ATP depletion induced Epacadostat oncosis that is almost completely resistant to the removal of cholesterol. Pre-treatment of cerebellar granule cells with mβCD prior to ET application inside the recording pipette does not abolish appearance of ET-induced transmembrane currents, but delays them and reduce their amplitude (Lonchamp et al., 2010). Are these current due to activation of endogenous membrane conductance? Altogether, the emerging picture is that some of the early cellular effects of ET may not be caused by http://www.selleckchem.com/products/gsk-j4-hcl.html formation of ET pore. This is in line with recent proposal that certain pore-forming toxins act on

host cells by another way than forming pores, as recently reported for a staphylococcal toxin (Jover et al., 2013). Several of the manifestations associated with C. perfringens type B and D enterotoxaemia (seizure, opisthotonus, convulsion… see Table 1) indicate hyperexcitability of the central nervous system, possibly resulting from an imbalance between excitatory (i.e. glutamate) and inhibitory (i.e. GABA) transmission. Thus, numerous studies have investigated whether release of transmitters is increased following ET administration, and may explain some of the observed ET-induced manifestations. The intraperitoneal administration of antagonists of the ionotropic glutamate receptors (as MK801 to block NMDA subtype glutamate receptors, or CNQX to antagonize AMPA receptors) prior intravenous

injection of ET in rat decreases the number of pyramidal dark cells in the hippocampus (Miyamoto et al., 1998) pinpointing these damage are due to dramatic increase in ambient glutamate concentration in neural tissue (i.e. dark cells manifest glutamate-induced excitotoxicity). Accordingly, direct evidence for induction of increased glutamatergic transmission has been obtained using micro dialysis in the hippocampus Dichloromethane dehalogenase in rat and mice submitted to ET (Miyamoto et al., 2000, 1998). Moreover, depletion in zinc ions – which has been shown contained into glutamate-containing synaptic vesicles – in the mossy layers of the hippocampal CA3 region has suggested that the excess of glutamate was due to its vesicular release by the nerve terminals (Miyamoto et al., 1998). Importantly, these effects were demonstrated not due to brain ischemia. In cultured cerebellum slices, the frequency of excitatory (glutamatergic) spontaneous responses in Purkinje cells is strongly increased (Lonchamp et al., 2010).

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