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牛磺酸对维生素D_3和尼古丁诱导的大鼠钙化血管精氨酸/NO途径的影响
引用本文:李夏,李菊香,姜志胜,张宝红,唐朝枢,杜军保. 牛磺酸对维生素D_3和尼古丁诱导的大鼠钙化血管精氨酸/NO途径的影响[J]. 中国药理学通报, 2002, 18(2): 222-225
作者姓名:李夏  李菊香  姜志胜  张宝红  唐朝枢  杜军保
作者单位:1. 现在山西职工医学院病理生理学教研室,太原,030012
2. 北京大学生理学和病理生理学系,北京,100083
3. 北京大学第一附属医院临床医学研究所,北京,100034
4. 北京大学第一附属医院儿科研究室,北京,100034
基金项目:国家重大基础研究发展项目资助 NoG2 0 0 0 5 690 5
摘    要:
目的 观察钙化血管精氨酸 /NO途径的改变和外源性牛磺酸 (taurine,Tau)对血管钙化及精氨酸 /NO途径的影响。方法 维生素D3 (vitaminD3 ,VitD3 )肌注和尼古丁(nicotine ,Nic)灌胃制备大鼠血管钙化模型 ,检测血管钙含量和血管碱性磷酸酶 (ALP)活性、血浆精氨酸和亚硝酸盐(NO-2 )含量、血管环磷酸鸟苷 (cGMP)含量、血管一氧化氮合酶 (NOS)活性及血管精氨酸 (arginine ,Arg)转运。结果 钙化组 (VDN)大鼠血管钙含量较对照组升高 6 6倍 (P <0 0 1) ,血管ALP活性高 12 6倍 (P <0 0 1) ;血浆NO生成减少 ,血管cGMP水平降低 ,血管NOS活性增高 ,其中cNOS活性高 18 9% (P <0 0 1) ,但精氨酸转运在血管平滑肌和内皮明显减少 (- 6 3 8% ,- 5 5 2 % ,P <0 0 1)。口服牛磺酸治疗的大鼠较单纯VDN组 ,血管钙含量降低 4 9 5 % (P <0 0 1) ,血管ALP活性明显降低 ,血浆NO生成增加 ,血管cGMP含量增加 2 9 1% (P均 <0 0 1) ,血管精氨酸转运在血管平滑肌和内皮分别增加 79 4 %和 5 5 1% (P <0 0 1)。结论 给予外源性牛磺酸可以减轻VitD3 加Nic大鼠的血管钙化程度 ,改善钙化血管L Arg/NOS/NO/cGMP途径紊乱 ;提示牛磺酸对防治动脉粥样硬化等疾病的血管钙化可能具有潜在临床意义

关 键 词:牛磺酸  血管钙化  L-精氨酸/一氧化氮途径
文章编号:1001-1978(2002)02-0222-04
修稿时间:2001-08-16

Taurine attenuates the vascular calcification and L-arginine/NO pathway impairement induced by vitamin D3 and nicotine in rat
LI Xia,LI Ju Xiang,JIANG Zhi Sheng,ZHANG Bao Hong,TANG Chao Shu,DU Jun Bao. Taurine attenuates the vascular calcification and L-arginine/NO pathway impairement induced by vitamin D3 and nicotine in rat[J]. Chinese Pharmacological Bulletin, 2002, 18(2): 222-225
Authors:LI Xia  LI Ju Xiang  JIANG Zhi Sheng  ZHANG Bao Hong  TANG Chao Shu  DU Jun Bao
Abstract:
AIM To investigate the characteristics of L arginine/NO pathway in vascular calcification and the effect of administration of extraneous taurine on the metablism of arginine/NO pathway in vascular calcification. METHODS The vascular calcification model was produced by vitamin D 3 plus nicotine. Vascular calcium content, activity of alkaline phosphatase(ALP), plasma arginine and nitrite content, vascular cGMP, vascular NOS activity and arginine transport were measured. RESULTS The vascular calcium content and the ALP activity increased 6 6 times and 12 6 times in VDN rats( P <0 01), respectively compared with control group, and plasma NO production, vascular cGMP content were obviously decreased ( P <0 01), the activity of total NOS was increased, mainly increased constitutive NOS( P <0 01). However, the L arginine transport of vascular was obviously decreased ( P <0 01). After administrating taurine in VDN rats, the vascular calcium content and ALP activity were decreased ( P <0 01), the production of plasma NO and vascular cGMP content were increased ( P <0 01), and the L arginine transport of vascular smooth muscle and endothelia obviously enhanced (+79 4% and 55 1%, all P values <0 01), compared with VDN group. CONCLUSION Taurine may attenuate the vascular calcification and improve the disturbance of L arginine/NOS/NO/cGMP pathway in rats induced by Vit D 3 plus nicotine. Thus, it appears that there is a potential clinical value of protection and treatment in taurine to the vascular calcification of atherosclerosis and other cardiovascular diseases.
Keywords:taurine  vascular calcification  L arginine/NO pathway
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