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L-精氨酸、L-硝基精氨酸对红藻氨酸诱导大鼠癫痫及其海马结构中iNOS mRNA表达的影响
引用本文:孙艺平,孙长凯,范明,赵杰,韩大跃,王吉庆,王冬梅,彭岩,宫德正,傅雷,戴淑芳,徐红. L-精氨酸、L-硝基精氨酸对红藻氨酸诱导大鼠癫痫及其海马结构中iNOS mRNA表达的影响[J]. 中国药理学通报, 2003, 19(8): 889-891
作者姓名:孙艺平  孙长凯  范明  赵杰  韩大跃  王吉庆  王冬梅  彭岩  宫德正  傅雷  戴淑芳  徐红
作者单位:1. 大连医科大学脑疾病研究所,大连,116027
2. 大连医科大学脑疾病研究所,大连,116027;解放军210医院神经科,大连,116021
3. 军事医学科学院基础医学研究所神经生物研究室,北京,100850
4. 解放军210医院神经科,大连,116021
5. 大连医科大学机能实验室,大连,116027
基金项目:国家自然科学基金资助 (No 3954 0 0 0 2 30 0 70 2 6 7),辽宁省教育厅高校科研项目基金资助 (No 2 0 2 2 0 32 4 6 )
摘    要:目的 观察诱导型一氧化氮合酶 (iNOS)在红藻氨酸(KA)癫痫大鼠海马内的表达及L 精氨酸 (L Arg)和L 硝基精氨酸 (L NNA)慢性干预的影响。方法 采用惊厥剂量的KA(1 0mg·kg- 1 )诱导大鼠癫痫发作 ,以NOS抑制剂L NNA(50mg·kg- 1 )和NO前体L Arg(40mg·kg- 1 )进行干预 ,对大鼠的癫痫发作行为及KA后不同时间点的海马内i NOSmRNA ,通过RT PCR观察其表达。结果 KA可使动物发生时间相关性癫痫发作 ,L NNA预处理后使KA诱导的癫痫发作明显加重 ,而L Arg预处理后使KA诱导的癫痫发作减弱。iNOSmRNA在KA处理后 3h开始有微弱的表达 ,且随着时间的延长逐渐增加 ,2 4h达到最高水平 ,2d及3d时未见表达 ,但 7d时又出现高表达 ;经L NNA预处理的动物 ,KA后 1h其海马结构中未出现iNOSmRNA ,但L Arg预处理后再给予KA后 1h ,可见微弱的iNOSmRNA表达。结论 红藻氨酸给药后一定时间 ,癫痫大鼠海马结构中可出现iNOSmRNA表达 ,L Arg慢性干预也有一定影响

关 键 词:诱导型一氧化氮合酶  组成型一氧化氮合酶  L-硝基精氨酸  L-精氨酸  红藻氨酸  癫痫
文章编号:1001-1978(2003)08-0889-03
修稿时间:2003-03-12

Effect of L-arginine or L-nitroarginine on kainic acid induced seizure and expression of iNOS mRNA in the rats'' hippocampus
SUN Yi-Ping ,SUN Chang-Kai ,,FAN Ming ,ZHAO Jie ,HAN Da-Yue ,WANG Ji-Qing ,WANG Dong-Mei ,PENG Yan ,GONG De-Zheng ,FU Lei ,DAI Shu-Fang ,XU Hong. Effect of L-arginine or L-nitroarginine on kainic acid induced seizure and expression of iNOS mRNA in the rats'' hippocampus[J]. Chinese Pharmacological Bulletin, 2003, 19(8): 889-891
Authors:SUN Yi-Ping   SUN Chang-Kai     FAN Ming   ZHAO Jie   HAN Da-Yue   WANG Ji-Qing   WANG Dong-Mei   PENG Yan   GONG De-Zheng   FU Lei   DAI Shu-Fang   XU Hong
Affiliation:SUN Yi-Ping 1,SUN Chang-Kai 1,2,FAN Ming 3,ZHAO Jie 1,HAN Da-Yue 2,WANG Ji-Qing 2,WANG Dong-Mei 4,PENG Yan 4,GONG De-Zheng 4,FU Lei 4,DAI Shu-Fang 4,XU Hong 4
Abstract:AIM To observe the expression of inducible nitric ox ide synthase (iNOS) in the rats' hippocampus of kainic acid (KA) induced-seizur es and the effect of L-arginine(L-Arg) or L-nitroarginine(L- NNA) chronic intervention before KA. METHODS The expression of iN OS mRNA by RT-PCR and behaviour were observed after administration of convulsan t dose of KA (10 mg·kg -1 ) and pretreatment with NO predecessor (L-Ar g, 40 mg·kg -1 ) or a inhibitor of NOS(L-NNA, 50 mg·kg -1 ) befo re KA. RESULTS The time-dependent seizures were induced on rats after giving KA, and were improved and serious in the animals with L-NNA pr etreatment, but they were alleviated by L-Arg pretreatment before KA. Compa red with control, iNOS mRNA expression was feebly at KA 3 h, continuative improv ement accompanying KA time prolonged, and it was markedly enhanced at KA 24 h. I t couldn't be examined at KA 2 d or 3 d, and was obviously improved at KA 7 d a gain. iNOS mRNA appeared weak in the rats hippocampus with L-Arg pretreatme nt after KA 1 h, whereas it wasn't found in L-NNA pretreatment animals. CONCLUSION iNOS mRNA expression appeared in the hippocampus of seizu re rats at a few time after KA, and L-Arg chronic intervention before KA ha s a little effect on it.
Keywords:inducible nitric oxide synthase  component nitric oxide synthase  L-nitroarginine  L-arginine  kainic acid  seizure
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