3 resultados para P6 Acupressure

em ArchiMeD - Elektronische Publikationen der Universität Mainz - Alemanha


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The goal of this thesis was an experimental test of an effective theory of strong interactions at low energy, called Chiral Perturbation Theory (ChPT). Weak decays of kaon mesons provide such a test. In particular, K± → π±γγ decays are interesting because there is no tree-level O(p2) contribution in ChPT, and the leading contributions start at O(p4). At this order, these decays include one undetermined coupling constant, ĉ. Both the branching ratio and the spectrum shape of K± → π±γγ decays are sensitive to this parameter. O(p6) contributions to K± → π±γγ ChPT predict a 30-40% increase in the branching ratio. From the measurement of the branching ratio and spectrum shape of K± → π±γγ decays, it is possible to determine a model dependent value of ĉ and also to examine whether the O(p6) corrections are necessary and enough to explain the rate.About 40% of the data collected in the year 2003 by the NA48/2 experiment have been analyzed and 908 K± → π±γγ candidates with about 8% background contamination have been selected in the region with z = mγγ2/mK2 ≥ 0.2. Using 5,750,121 selected K± → π±π0 decays as normalization channel, a model independent differential branching ratio of K± → π±γγ has been measured to be:BR(K± → π±γγ, z ≥ 0.2) = (1.018 ± 0.038stat ± 0.039syst ± 0.004ext) ∙10-6. From the fit to the O(p6) ChPT prediction of the measured branching ratio and the shape of the z-spectrum, a value of ĉ = 1.54 ± 0.15stat ± 0.18syst has been extracted. Using the measured ĉ value and the O(p6) ChPT prediction, the branching ratio for z =mγγ2/mK2 <0.2 was computed and added to the measured result. The value obtained for the total branching ratio is:BR(K± → π±γγ) = (1.055 ± 0.038stat ± 0.039syst ± 0.004ext + 0.003ĉ -0.002ĉ) ∙10-6, where the last error reflects the uncertainty on ĉ.The branching ratio result presented here agrees with previous experimental results, improving the precision of the measurement by at least a factor of five. The precision on the ĉ measurement has been improved by approximately a factor of three. A slight disagreement with the O(p6) ChPT branching ratio prediction as a function of ĉ has been observed. This mightrnbe due to the possible existence of non-negligible terms not yet included in the theory. Within the scope of this thesis, η-η' mixing effects in O(p4) ChPT have also been measured.

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Subthreshold resonance is a characteristic membrane property of different neuronal classes, is critically involved in the generation of network oscillations, and tunes the integration of synaptic inputs to particular frequency ranges. In order to investigate whether resonance properties of distinct neuronal populations in the immature neocortex contribute to these network oscillations, I performed whole-cell patch-clamp recordings from visually identified neurons in tangential and coronal neocortical slices from postnatal day (P) P0-P7 C57Bl/6 and P6-P13 GAD67-GFP knock-in mice. Subthreshold resonance was analyzed by sinusoidal current injection of varying frequency. All Cajal-Retzius cells showed subthreshold resonance with an average frequency of 2.6 ± 0.1 Hz (n=60), which was massively reduced by ZD7288, a blocker of hyperpolarization-activated cation currents. About 65.6% (n=61) of the supragranular pyramidal neurons showed subthreshold resonance with an average frequency of 1.4 ± 0.1 Hz (n=40). Application of 1 mM Ni2+ suppressed subthreshold resonance, suggesting that low-threshold Ca2+ currents contribute to resonance in these neurons. About 63.6% (n=77) of the layer V pyramidal neurons showed subthreshold resonance with an average frequency of 1.4 ± 0.2 Hz (n=49), which was abolished by ZD7288. Only 44.1% (n=59) of the subplate neurons showed subthreshold resonance with an average frequency of 1.3 ± 0.2 Hz (n=26) and a small resonance strength. Finally, 50% of the investigated GABAergic interneurons showed subthreshold resonance with an average frequency of 2.0 ± 0.2 Hz (n=42). Membrane hyperpolarization to –86 mV attenuated the frequency and strength of subthreshold resonance. Subthreshold resonance was virtually abolished in the presence of 1 mM Ni2+, suggesting that t-type Ca2+ currents are critically involved in the generation of resonance, while ZD7288 had no effect. Application of 0.4 µM TTX suppressed subthreshold resonance at depolarized, but not hyperpolarized membrane potential, suggesting that persistent Na+ current contribute to the amplification of membrane resonance. rnIn summary, these results demonstrate that all investigated neuronal subpopulations reveal resonance behavior, with either hyperpolarization-activated cation or low-threshold Ca2+ currents contributing to the subthreshold resonance. GABAergic interneurons also express subthreshold resonance at low frequencies, with t-type Ca2+ and persistent Na+ currents underlying the generation of membrane resonance. The membrane resonance of immature neurons may contribute to the generation of slow oscillatory activity pattern in the immature neocortex and enhance the temporal precision of synaptic integration in developing cortical neurons.rn

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Rodents are most useful models to study physiological and pathophysiological processes in early development, because they are born in a relatively immature state. However, only few techniques are available to monitor non-invasively heart frequency and respiratory rate in neonatal rodents without restraining or hindering access to the animal. Here we describe experimental procedures that allow monitoring of heart frequency by electrocardiography (ECG) and breathing rate with a piezoelectric transducer (PZT) element without hindering access to the animal. These techniques can be easily installed and are used in the present study in unrestrained awake and anesthetized neonatal C57/Bl6 mice and Wistar rats between postnatal day 0 and 7. In line with previous reports from awake rodents we demonstrate that heart rate in rats and mice increases during the first postnatal week. Respiratory frequency did not differ between both species, but heart rate was significantly higher in mice than in rats. Further our data indicate that urethane, an agent that is widely used for anesthesia, induces a hypoventilation in neonates whilst heart rate remains unaffected at a dose of 1 g per kg body weight. Of note, hypoventilation induced by urethane was not detected in rats at postnatal 0/1. To verify the detected hypoventilation we performed blood gas analyses. We detected a respiratory acidosis reflected by a lower pH and elevated level in CO2 tension (pCO2) in both species upon urethane treatment. Furthermore we found that metabolism of urethane is different in P0/1 mice and rats and between P0/1 and P6/7 in both species. Our findings underline the usefulness of monitoring basic cardio-respiratory parameters in neonates during anesthesia. In addition our study gives information on developmental changes in heart and breathing frequency in newborn mice and rats and the effects of urethane in both species during the first postnatal week.