Objective Muncl8-1 has an important role in neurotransmitter release, and controls every step in the exocy- totic pathway in the central nervous system. In the present study, whether epileptic seizure causes a change ...
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Objective Muncl8-1 has an important role in neurotransmitter release, and controls every step in the exocy- totic pathway in the central nervous system. In the present study, whether epileptic seizure causes a change of Muncl8 localization in neuronal nuclei was analyzed. Methods Epilepsy models were established by injection of kainic acid （KA） solution into hippocampus of Sprague-Dawley （SD） rats or intraperitoneal injection of KA in Kunming mice. The hippocampal neurons were prepared from embryonic day 18 SD rats, and cultured in neurobasal medium, followed by treatment with glutamate for 3 h. Neuronal and glial nuclei of hippocampus were separated by sucrose density gradient centrifugation. The nucleus-enriched fractions were stained with 0.1% Cresyl Violet for morphological assay. Immuno- chemistry and immunoelectron microscopy with anti-Muncl 8-1 antibody were used to determine the nuclear locatization of Munc 18-1. Immunoblotting was used to detect the protein level of Munc 18-1. Results The localization of Munc 18-1 in nucleus of rat hippocampal neuron was confirmed by immunochemistry, immunoelectron microscopy, and immunob- lotting detection of neuronal nucleus fraction. In animals receiving intrahippocampal or intraperitoneal injection of KA, immunostaining revealed that the expression of Muncl 8-1 decreased in pyramidal cell layer of CA regions, as well as in hilus and granular cell layer of dentate gyrus in hippocampus. Moreover, immunoblotting analysis showed that the expres- sion level of Muncl 8-1 in nucleus fraction of hippocampus significantly decreased in KA-treated animals. The relation- ship between the change of Muncl8-1 expression in neuronal nuclei and neuronal over-activation was also tested in pri- mary cultured neurons. After treatment with 50 ~tmol/L glutamate acid for 3 h, Muncl8-1 level was decreased in nucleus fraction and increased in cytoplasmic fraction of primary cultured neurons. Conclusion These results suggest that excit- atory st
谷氨酸能和GABA能支配是心迷走节前神经元(cardiac vagal neuron,CVN)的主要兴奋性和抑制性突触传入。在CVN 的活动调节中,这两种支配是否有相互作用、以及如何相互作用目前尚不清楚。本研究用神经元逆行荧光染料标记法和电压膜片钳方法证明,谷氨酸NMDA型和非NMDA型受体拈抗剂AP5和CNQX在全脑片应用条件下,对疑核(nucleus ambiguus, NA)内CVN的GABA能突触前活动无明显影响,而对迷走神经运动背核(dorsal motor nucleus of the vagus,DMNX)内CVN的 GABA能突触前活动有显著的抑制作用。这些观察结果提示:支配迷走神经运动背核内CVN的GABA能神经元可能接受紧张性谷氨酸能支配,而支配疑核内CVN的GABA能神经元则没有这种紧张性谷氨酸能支配。疑核内和迷走神经运动背核内 CVN的这种调节差异,是两个核团的CVN在心率和心功能调节中功能分工的可能机制之一。
Objective To assess whether quick cognitive screening test （QCST） could quickly identify mild cognitive impairment （MCI）. Methods QCST and a full set of standardized neuropsychological tests, including mini-mental...
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Objective To assess whether quick cognitive screening test （QCST） could quickly identify mild cognitive impairment （MCI）. Methods QCST and a full set of standardized neuropsychological tests, including mini-mental state examination （MMSE） and montreal cognitive assessment （MoCA） were performed. A total number of 121 cases of MCI [41 cases of amnestic MCI-single domain （aMCI-s）; 44 of amnestic MCI-multiple domain （aMCI-m）; 36 of nonamnestic MCI （naMCI）], 79 cases of mild Alzheimer’s disease （AD） and 186 healthy elderly volunteers were employed in the present study. All the participants （55-85 years old） had an educational level no less than 5 years. QCST subtests included word list recall, naming test, animal fluency test, similarity test, color trail-1min, clock drawing test, finger construction test, and digit span test. The total score of QCST was 90 points, 10 points for each index of subtests. Results The total scores of QCST in MCI, AD and the control groups were （58.13±8.18）, （44.53±10.54） and （72.92±6.85） points, respectively. According to the educational level, the cut off scores of participants with an educational level of 5-8 years, 9-12 years and more than 13 years were 63, 65 and 68 points, respectively. The sensitivity and specificity of QCST in detection of MCI were 87.6% （85.7% for aMCI-s, 90.1% for aMCI-m and 89.5% for naMCI） and 84.3%, respectively. The area under the curve was 0.923 （95% CI： 0.892-0.953）. Delayed memory, color trail-1min and similarity test could help distinguish between aMCI and naMCI. Conclusion QCST may have a good sensitivity and specificity for MCI detection, which warrants its further clinical application.
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