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作 者:季淑梅[1] 薛建梅[2] 王川[2] 苏素文[2] 何瑞荣[3]
机构地区:[1]燕山大学生物医学工程系,秦皇岛066004 [2]河北医科大学药理室,石家庄050017 [3]河北医科大学生理室,石家庄050017
出 处:《生理学报》2005年第3期340-345,共6页Acta Physiologica Sinica
摘 要:经荧光探针Fluo 3-AM标记细胞内游离钙后,用激光共聚焦显微镜检测肾上腺髓质素(adrenomedullin,ADM)对原代培养大鼠海马神经元内游离钙浓度([Ca2+]i)的影响.实验结果如下:(1)ADM(0.01~1.0μmol/L)浓度依赖性地降低细胞内钙浓度.(2)降钙素基因相关肽受体阻断剂(calcitonin gene-related peptide,CGRP8-37)预处理可部分抑制ADM的效应.(3)ADM可显著抑制高钾引起的[Ca2+]i增加.(4)ADM可显著抑制三磷酸肌醇(inositol 1,4,5-trisphosphate,IP3)引起的内钙释放,而对兰尼定(ryanodine)引起的内钙释放无显著影响.以上结果提示,ADM降低培养海马神经元内游离钙浓度,此作用与其抑制IP3引起的内钙释放有关,ADM对静息状态下的Ca2+内流无影响,但可显著抑制高钾引起的Ca2+内流,CGRP受体介导了ADM的上述效应.The effects of adrenomedullin (ADM) on intracellular calcium concentration ([Ca2+]i) were investigated in cultured hippoc-ampal neurons. Changes in [Ca2+]i were detected by laser scanning confocal microscopy using Fluo 3-AM as the calcium fluorescentprobe. [Ca2+]i was represented by relative fluorescent intensity. The results showed that: (1) ADM (0.01~1.0 μmol/L) decreased theresting [Ca2+]i in a concentration-dependent manner. (2) Calcitonin gene-related peptide receptor antagonist CGRP8-37 significantlyinhibited the effects of ADM. (3) ADM significantly reduced the increase in [Ca2+]i induced by high K+. (4) ADM markedly inhibitedthe inositol 1,4,5-trisphosphate (IP3)-induced increase in [Ca2+]i, while did not influence ryanodine-evoked increase in [Ca2+]i. Theseresults suggest that ADM reduces [Ca2+]i in cultured hippocampal neurons through suppressing Ca2+ release from IP3-sensitive stores.Although ADM does not alter resting Ca2+ influx, it significantly suppresses Ca2+ influx activated by high K+. These effects may bepartly mediated by CGRP receptors. ADM in the CNS may act as a cytoprotective factor in ischemic/hypoxic conditions.
关 键 词:肾上腺髓质素 海马神经元 细胞内钙 降钙素基因相关肽受体阻断剂CGRP哪 三磷酸肌醇 兰尼定 激光共聚焦显微镜
分 类 号:R33[医药卫生—人体生理学]
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