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尼古丁对大鼠主动脉平滑肌细胞舒缩功能的影响 被引量:2

Effect of nicotine on systolic and diastolic function of rat aortic smooth muscle cells
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摘要 目的:观察尼古丁对大鼠主动脉血管平滑肌细胞(vascular smooth muscle cells,VSMCs)舒缩功能的影响。方法:体外培养大鼠原代主动脉VSMCs。用不同浓度尼古丁对大鼠主动脉VSMCs干预24 h后,用罗丹明-鬼笔环肽染细胞骨架,拍摄不同实验组的照片,通过测量不同细胞表面积的大小来反映细胞收缩水平;用胶原收缩法观察不同浓度的尼古丁对大鼠VSMCs收缩功能影响。结果:原代大鼠主动脉VSMCs被成功培养。用不同浓度(0.1μmol/L、1μmol/L、10μmol/L和100μmol/L)尼古丁处理VSMCs 24 h后,其骨架呈现显著收缩,细胞板状化明显增强,且呈浓度依赖性关系;10μmol/L为尼古丁对VSMCs的最适刺激浓度(P<0.01)。胶原收缩法也显示,10μmol/L尼古丁对大鼠主动脉VSMCs有收缩作用,随着作用时间的增加,其收缩效应逐渐增强,作用60 min收缩作用最显著(P<0.01)。结论:尼古丁对大鼠主动脉VSMCs具有较强收缩作用,其收缩作用具有浓度依赖性和时间依赖性。 AIM: To observe the effects of nicotine on systolic and diastolic function of rat aortic vascular smooth muscle cells(VSMCs). METHODS: The primary rat aortic VSMCs were cultured in vitro. After exposed to nicotine at different concentrations for 24 h, the cytoskeleton of the VSMCs was stained with rhodamine-phalloidin,the photographs of the VSMCs in different experimental groups were taken and the surface area was measured to reflect the cell contractility. Collagen contraction method was also used to determine the effect of nicotine on the contractility of rat aortic VSMCs. RESULTS: The primary rat aortic VSMCs were successfully cultured. After the VSMCs were treated with nicotine(0.1 μmol/L, 1 μmol/L, 10 μmol/L and 100 μmol/L) for 24 h, the skeleton showed a significant contraction, and the cell plate shape was obviously enhanced in a concentration-dependent manner. The results showed that 10 μmol/L was the optimal concentration of nicotine for VSMCs(P<0.01). The collagen contraction method also showed that 10 μmol/L nicotine contracted the rat aortic VSMCs. With the increase in the nicotine action time, the maximum contraction effect was observed at 60 min(P<0.01). CONCLUSION: Nicotine has a strong contractile effect on VSMCs of rat aorta, and its contractile effect is dependent on concentration and time.
作者 刘继斌 秦小江 岳晗 伊淑贤 侯晓敏 LIU Ji-bin;QIN Xiao-jiang;YUE Han;YI Shu-xian;HOU Xiao-min(Office of Educational Administration, Shanxi Medical University, Taiyuan 030001 , China;School of Public Health, Shanxi Medical University, Taiyuan 030001 , China;School of Basic Medicine, Shanxi Medical University, Taiyuan 030001 , China)
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2019年第6期1142-1145,1152,共5页 Chinese Journal of Pathophysiology
基金 山西省高等学校科技创新项目(No.2017146 No.2017147) 山西省青年科技研究基金资助项目(No.201701D221247
关键词 尼古丁 主动脉 血管平滑肌细胞 收缩功能 Nicotine Aorta Vascular smooth muscle cells Systolic function
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  • 1高彦彬,赵慧玲,关崧,周晖,庚及娣,谢培风,赵翠芳,商学征,郝青春.糖肾宁治疗气阴两虚、络脉瘀滞型早期糖尿病肾病临床研究[J].中华中医药杂志,2006,21(7):409-411. 被引量:42
  • 2Chen HF, Xie LD, Xu CS. The signal transduetion pathways of heat shock protein 27 phosphorylation in vascular smooth muscle cells[J]. Mol Cell Biochem,2010,333(1/2):49-56.
  • 3Somara S, Bitar KN. Tropomyosin interacts with phosphorylated HSP27 in agonist-induced contraction of smooth muscle[J]. Am J Physiol Cell Physiol, 2004,286 (6) : C1290-C1301.
  • 4Bitar KN. HSP27 phosphorylation and interaction with actin-myosin in smooth muscle contraction[J]. Am J Physiol Gastrointest Liver Physiol,2002,282(6):G894-G903.
  • 5Hirano S, Shelden EA, Gilmont RR. HSP27 regulates fibroblast adhesion, motility, and matrix contraction[J]. Cell Stress Chaperones,2004,9(l) :29-37.
  • 6Keezer SM, Ivie SE, Krutzseh HC, etal. Angiogenesis inhibitors target the endothelial cell eytoskeleton through altered regulation of heat shock protein 27 and cofilin[J]. Cancer Res, 2003,63 (19) : 6405-6412.
  • 7Voeqeli TS, Currie RW. siRNA knocks down Hsp27 and increases angiotensin Ⅱ-induced phosphorylated NF-kappaB p65 levels in aortic smooth muscle cells[J]. Inflamm Res, 2009,58 (6) :336- 343.
  • 8Meloche S, Landry J, Huot J, et al. P38 MAP kinase pathway regulates angiotensin Ⅱ-indueed contraetion of rat vascular smooth muscle[J]. Am J Physiol Heart Circ Physiol, 2000, 279 (2) : H741-H751.
  • 9谢良地,陈海峰,许昌声.阿魏酸钠对血管平滑肌细胞热休克蛋白27磷酸化的影响[J].中国病理生理杂志,2008,24(12):2352-2355. 被引量:7
  • 10黄捷,谢良地,许昌声,王华军.大鼠HSP27基因RNA干扰慢病毒载体的构建与鉴定[J].中国药理学通报,2009,25(4):488-492. 被引量:4

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