PubMed · 14639133
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Omeed Sani, Steven L Shafer. 2003. MAC Attack?. https://doi.org/10.1097/00000542-200312000-00002
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We measured binocular horizontal eye movements in the gerbil following unilateral labyrinthectomy during the acute phase (1-24 h) of vestibular compensation. Regardless of whether the animals compensated in the light or the dark, VOR gain progressively reduced following the lesion, and normal oculomotor symmetry was disrupted. Initially, the VOR was comparable at 1 h post-lesion for both visual conditions. However, by 3 h post-lesion the VOR response for head turns away from the lesion continued to drop in animals compensating in the dark. By 24 h, both groups displayed reduced VOR gains, but animals compensating in the light had improved frequency response characteristics. Optokinetic responses became unstable but were generally elevated compared to pre-lesion levels. Animals with vision had reduced optokinetic gains by 24 h, while the OKR response for animals in the dark remained elevated. Brainstem Fos labeling generally increased from 1 to 3 h, then decreased by 24 h. However, at 1 h, Fos labeling in the inferior olivary dorsal cap and prepositus contralateral to the lesion was significantly increased in animals compensating in the light. In both visual conditions, flocculus and paraflocculus Purkinje cell labeling was also observed, and some of the Fos-labeled cells in the medial vestibular nucleus were commissural. Fos in the dorsal cap and prepositus could be attributed to the presence of visual input. While the visually related prepositus Fos labeling preceded improved VOR performance, the dorsal cap appeared to be involved in resolving visual and motor deficits from spontaneous nystagmus.
BACKGROUND: Isoflurane and xenon are inhalation general anaesthetics with differing clinical profiles and contrasting synaptic actions. Both agents have been shown to depress excitatory synaptic responses. Whether this is via pre-synaptic or post-synaptic mechanisms has not been determined clearly. N-type calcium channels are a putative pre-synaptic target for these agents. We tested whether N-type calcium channels were sensitive to isoflurane and xenon and whether there was any stereoselectivity in the effect of isoflurane. METHODS: We used patch-clamp electrophysiology on isolated HEK293 cells stably expressing N-type calcium channels to investigate the effects of isoflurane and xenon on barium currents mediated by N-type calcium channels. RESULTS: Racemic isoflurane caused a concentration-dependent reduction (11-35%) in the peak current through the N-type channels in the concentration range 0.15-1.22 mM. In the clinically relevant concentration range the inhibition was small. At an isoflurane concentration of 0.31 mM (equivalent to 1 MAC), the peak N-type current was inhibited by 14 (1)%. The optical isomers of isoflurane were found to be equally potent at inhibiting currents through N-type channels. The inert gas anaesthetic xenon was found to have no measureable effect on N-type channels at a concentration of 3.4 mM (approximately 1 MAC). CONCLUSIONS: These results suggest that N-type calcium channels are not the targets mediating general anaesthesia with these two inhalation agents.
The effects of wastewater salinity on both nitrogen removal efficiency and N2O emission rate were investigated in a single nitrification process, a single denitrification process and an anoxic-oxic activated sludge process. In the single nitrification process, by increasing the salt concentration from 1.0 to 2.0 wt%, the N2O conversion ratio in the steady state increased by 2.2 times, from 0.22 to 0.48%. In the single denitrification process, a minimal change in the N2O conversion ratio was observed in the steady state even when the salt concentration was increased from 3.0 to 5.0 wt%. From the results of the anoxic-oxic activated sludge process, it was found that a salt concentration increase from 1.6 to 3.0 wt% significantly increases the N2O conversion ratio from 0.7 to 13%. It is suggested that an increase in salt concentration markedly influences N2O emission both directly and indirectly via the inhibition of N2O reductase activity. The indirect inhibition is due to the high concentration of dissolved oxygen which is transported from the oxic tank to the anoxic tank through the circulated liquid. Thus, the salt concentration should be maintained below 3.0% to suppress N2O emission in an anoxic-oxic activated sludge process.