PubMed · 4387821
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
W Horn. 1967. [Spasmolytics. 5].. https://pubmed.ncbi.nlm.nih.gov/4387821/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
Laser scanning confocal microscopy in combination with the fluorescent calcium indicators Fluo-3 and Fura-Red was employed to estimate the intracellular concentration of free calcium ions in individual olfactory receptor neurons and to monitor temporal and spatial changes in the Ca(2+)-level upon stimulation. The chemosensory cells responded to odorants with a significant increase in the calcium concentration, preferentially in the dendritic knob. Applying various stimulation paradigma, it was found that in a population of isolated cells, subsets of receptor neurons display distinct patterns of responsiveness.
The aerobic biodegradability of aniline, used as reference chemical, has been performed in synthetic seawater with attached biomass in a continuously fed reactor (biofilm chemostat reactor, BCR). Marine bacteria inocula came from local marine fish aquarium filters to limit the geographic and seasonal variations in quality. A pretreatment of these inocula combining 5-microns filtration and centrifugation was used to concentrate bacteria and remove organic carbon contamination of the test. The performances of the BCR were tested in comparison with simple shake flask tests. Among the different variables tested, the ratio S0/X0 (initial concentration of xenobiotic to initial density of the inoculum), the presence of dissolved oxygen, and the hydraulic residence time appear to be the key parameters controlling the length of the biodegradation process. On the other hand, the addition of a cosubstrate (easily biodegradable compound) does not provide advantages. Thus, marine biofilm chemostat reactors with a high density of attached bacteria (around 10(7) cells cm-2) and fed with synthetic seawater plus nitrogen provide good tools for screening biodegradability of chemicals in the marine environment.
Using confocal laser scanning microscopy and time-lapse reconstruction, we monitored [Ca2+]i in living mouse oocytes loaded with the calcium-sensitive fluorescent dyes fluo-3/AM or NuCa Green (specific for nuclear calcium) at the time of meiosis reinitiation. Our data confirm that spontaneous Ca2+ oscillations occurred in most of the immature fully grown mouse oocytes at least during the first half hour after release of the follicle and these oscillating oocytes underwent GVB in a large proportion after 1 h of culture. These spontaneous oscillations were disrupted when GVB was inhibited by dbcAMP and suppressed in the absence of external calcium. They were dependent on intracellular InsP3-sensitive Ca2+ stores since they were inhibited by heparin, an InsP3-receptor antagonist, or thapsigargin, which depletes InsP3-sensitive Ca2+ stores. A relation appeared between the germinal vesicle chromatin appearance and the oocyte's ability to exhibit calcium oscillations. NuCa Green-loaded oocytes exhibited clear fluorescence oscillations in the nuclear region which lead us to discuss the implication of the nuclear calcium in the meiotic process. Moreover, the observation of a clear polarization of the Ca2+ waves in 30% of the oocytes permits us to hypothesize the existence of a predetermined localization for the initial point of the calcium wave.