Expression of TRPM8 in the distal cerebrospinal fluid-contacting neurons in the brain mesencephalon of rats

<p>Abstract</p> <p>Background</p> <p>It has been shown that distal cerebrospinal fluid-contacting neurons (dCSF-CNs) exist near the ventral midline of the midbrain aqueduct and also in the grey matter of the inferior third ventricle and the fourth ventricle floor in the superior segment of the pons. The dCSF-CNs communicate between the cerebrospinal fluid (CSF) and the brain parenchyma and may participate in the transduction and regulation of pain signals. The cold sensation receptor channel, TRPM8 is involved in analgesia for neuropathic pain, but whether the TRPM8 receptor exists on dCSF-CNs remains unknown. However, there is preliminary evidence that TRPM8 is expressed in dCSF-CNs and may participate in the transmission and regulation of sensory information between brain parenchyma and cerebrospinal fluid (CSF) in rats.</p> <p>Methods</p> <p>Retrograde tracing of the cholera toxin subunit B labeled with horseradish peroxidase (CB-HRP) injected into the lateral ventricle was used to identify dCSF-CNs. A double-labeled immunofluorescent technique and laser scanning confocal microscopy were used to identify the expression of TRPM8 in dCSF-CNs. Software Image-Pro Plus was used to count the number of neurons in three sections where CB-HRP positive neurons were located in the mesencephalon of six rats.</p> <p>Results</p> <p>The cell bodies of CB-HRP-positive dCSF-CNs were found in the brain parenchyma near the midline of the ventral Aq, also in the grey of the 3V, and the 4V floor in the superior segment of the pons. In the mesencephalon their processes extended into the CSF. TRPM8 labeled neurons were also found in the same area as were CB-HRP/TRPM8 double-labeled neurons. CB-HRP/TRPM8 double-labeled neurons were found in 42.9 ± 2.3% of neurons labeled by TRPM8, and all CB-HRP-labeled neurons were also labeled with TPRM8.</p> <p>Conclusion</p> <p>This study has demonstrated that the cold sensation receptor channel, TRPM8, is localised within the dCSF-CNs of the mesencephalon. TRPM8 acts as receptor of dCSF-CNs for sensation transmission and pain regulation.</p

A feasibility study of multi-electrode high-purity germanium detector for Ge-76 neutrinoless double beta decay searching

Experiments to search for neutrinoless double-beta (0{\nu}\b{eta}\b{eta}) decay of 76Ge using a high-purity germanium (HPGe) detector rely heavily on background suppression technologies to enhance their sensitivities. In this work, we proposed a pulse-shape analysis method based on a neural network (NN) and a light gradient boosting machine (lightGBM; LGB) to discriminate single-electron (background) and double-electrons (0{\nu}\b{eta}\b{eta} signal) events in a multi-electrode HPGe detector. In this paper, we describe a multi-electrode HPGe detector system, a data-processing system, and pulse-shape simulation procedures. We built a fully connected (FC) neural network and an LGB model to classify the single- and double-electron events. The FC network is trained with simulated single- and double-electron-induced pulses and tested in an independent dataset generated by the pulse-shape simulation. The discrimination efficiency of the FC neural network in the test set for the 0{\nu}\b{eta}\b{eta} double-electron events signal was 77.4%, the precision was 57.7%, and the training time was 430 min. The discrimination efficiency of LGB model was 73.1%, the precision was 64.0%, and the training time was 1.5 min. This study demonstrated that it is feasible to realize single- and double-electron discrimination on multi-electrode HPGe detectors using an FC neural network and LGB model. These results can be used as a reference for future 76Ge 0{\nu}\b{eta}\b{eta} experiments.Comment: 16 pages,12 figure

Totally thoracoscopic closure of ventricular septal defect without a robotically assisted surgical system: A summary of 119 cases

ObjectivesTo summarize the clinical outcomes of totally thoracoscopic closure of a ventricular septal defect (VSD).MethodsTotally thoracoscopic VSD closure was performed in 119 patients (66 boys; mean age, 7.1 ± 3.6 years). An additional 35 patients undergoing open-chest VSD closure were selected as a control group. Using 3 port incisions in the right chest, pericardiotomy, bicaval occlusion, atriotomy, and VSD closure were performed by thoracoscopy without the aid of a robotically assisted surgical system.ResultsCardiopulmonary bypass and aortic crossclamp times were 42.2 ± 9.8 and 32.5 ± 7.3 minutes, respectively. There were no deaths but 1 patient required insertion of a permanent pacemaker as a result of postoperative atrioventricular conduction block. The length of stay in the intensive care unit (11.0 ± 2.6 vs 22.9 ± 4.9 hours, P < .01) or postoperative hospital stay (4.2 ± 1.1 vs 6.6 ± 2.1 days, P < .03) in the thoracoscopic group were shorter than in the control group. The percentage of patients who required postoperative opioid analgesics in the thoracoscopic group was lower than in the control group (31.9% vs 74.2%, P < .001). Rate of blood transfusion during the operation (17.6% vs 65.7%, P = .001) and the postoperative use of opioid analgesics (31.9% vs 74.3%, P = .003) in the thoracoscopic group was lower than in the control group. Transesophageal echocardiographic analysis 4.6 ± 2.3 months after the operation showed complete closure of the defect.ConclusionsTotally thoracoscopic closure of VSD through a 3-port entry was safe and effective