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作 者:张淑坤[1] 杨荣慧[2] 张翠欣[3] 姜玲玲[1] 侯艳宁[2]
机构地区:[1]河北医科大学生物化学与分子生物学教研室 [2]白求恩国际和平医院,河北石家庄050082 [3]河北医科大学第三医院,河北石家庄050051
出 处:《第四军医大学学报》2008年第10期869-871,共3页Journal of the Fourth Military Medical University
基 金:国家自然科学基金(30371566);河北省自然科学基金(303472)
摘 要:目的:研究肝X受体(LXR)激活对海马神经元神经甾体合成的影响.方法:将大鼠海马神经元体外培养至第7日,在培养液中加入2.0μmol/L TO901317,继续培养48 h.应用高效液相-质谱联用(HPLC-MS)分离测定培养液中游离型神经甾体孕烯醇酮(PREG)、脱氢表雄酮(DHEA)和结合型神经甾体孕烯醇酮硫酸酯(PREGS)、脱氢表雄酮硫酸酯(DHEAS)的含量;RT-PCR方法观察海马神经元P450侧链裂解酶(P450scc)、甾体合成快速调节蛋白(StAR)和3β-羟基甾醇脱氢酶(3β-HSD)等神经甾体合成关键酶基因的mRNA的表达.结果:TO901317激活LXR,促进P450scc,StAR和3β-HSD的mRNA表达,增加海马神经元培养液中神经甾体PREG,DHEA,PREGS和DHEAS含量.结论:LXR激活时,可通过上调海马神经元P450scc,StAR和3β-HSD的mRNA表达,促进神经甾体的合成.AIM: To investigate the effect of liver X receptor (LXR) activation on the synthesis of neurosteriod in hippocampal neurons. METHODS : On day 7 of culture, hippocampal neurons were treated with 2.0 μmoL/L TO901317 dissolved in dimethylsulfoxide for 48 h. The mRNA expressions of P450 side chain cleavage (P450scc), steroidogenic acute regulatory protein (STAR) and 3β-hydroxysteroid dehydrogenase ( 3β-HSD ) were measured by RT-PCR and the contents of unconjugated neurosteriods pregnenolone (PREG) , dehydroepiandrosterone ( DHEA ) and conjugated neurosteroids pregnenolone sulfate(PREGS) , dehydroepiandrosterone sulfate (DHEAS) in medium were analyzed and determined using high-performance liquid chromatography-mass spectrometry (HPLC-MS). RESULTS: Incubation of hippocampal neurons with TO901317 significantly increased the expressions of P450scc, STAR and 3β-HSD mRNA and the levels of PREG, DHEA, PREGS and DHEAS. CONCLUSION: Activation of LXR contributes to the synthesis of neurosteriod by up-regulating the expressions of P450scc, StAR and 3β-HSD in hippocampal neurons.
关 键 词:肝X受体 P450侧链裂解酶 神经甾体 海马 神经元
分 类 号:R917[医药卫生—药物分析学] Q189[医药卫生—药学]
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