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作 者:马杰[1] 周全[1] 袁苏涛[2] 孟涛[1] 林玲[1]
机构地区:[1]福建医科大学基础医学院生物化学与分子生物学系,福州350004 [2]:福建医科大学省立临床学院福建省立医院神经外科
出 处:《中华实验外科杂志》2012年第9期1703-1705,共3页Chinese Journal of Experimental Surgery
基 金:福建省自然科学基金资助项目(2010J01175);福建省大学生创新性实验计划项目
摘 要:目的观察晚期帕金森病(PD)大鼠血中褪黑素的变化,以及硫酸镁对这种变化的影响。方法6-羟基多巴胺(6-OHDA)损毁黑质纹状体通路制备PD模型,大鼠分为PD模型组(PD/H2O)、PD加镁组(PD/Mg)、对照组(对照组/H2O)、对照加镁组(对照组/Mg)。大鼠通过饮水摄入硫酸镁(每天0.36g/kg),4周后观察其对阿扑吗啡诱发的旋转行为,并采用酶联免疫吸附试验(ELISA)检测褪黑素水平。结果PD鼠血清褪黑素水平为(153.4±29.8)pg/L,明显高于对照组(77.2±13.7)pg/L;补镁后PD组和对照组大鼠的褪黑素水平分别降至(126.8±15.9)pgCL和(53.4±18.1)pg/L。PD/Mg组大鼠的旋转行为较PD/H2O组有改善。结论硫酸镁可缓解晚期PD鼠的运动症状,对PD鼠褪黑素的代偿性升高有抑制作用。Objective To explore the relationship between magnesium (Mg) and melatonin (MLT) by observation serum MLT levels in advanced Parkinson' s disease (PD) rats, and to clarify the effect of magnesium on serum melatonin in PD model. Methods PD rat model was established by a uni- lateral injection of 6-OHDA into the right substantia nigra pars compacta (SNc) and the right medial lore- brain bundle (MFB). Rats of control group received saline injection. Twenty animals were divided into four groups. PD model (PD/H20) and control/H2 O groups were vehicle-treated rats, and received drinking wa- ter (magnesium sulphate vehicle) daily. Magnesium sulphate (MgSQ 0. 36 g/kg/day dissolved in drink- ing water) was administered in rats of PD/Mg and control/Mg groups for four weeks. Then apomorphine-in- duced rotational behaviour, serum MLT levels and histological changes were tested. Results The level of MLT in PD groups was ( 153.4 ±29. 8 ) pg/L, which distinctly higher than those in the controls (77.2 ± 13.7) pg/L, while the levels of MLT in PD model and control rats receiving Mg were decreased to ( 126. 8± 15.9) pg/L and (53.4 ± 18. 1 ) pg/L respectively, MLT levels appeared to correlate well with the frequency of apomorphine-induced rotations. The fi'equency of rotations in PD/Mg group decreased com- pared with those in PD/H20 group. Conclusion The rotational behaviour in advanced PD rat might ameliorated by magnesium, and magnesium may partly inhibit compensatory increased MLT.
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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