CLC number: Q66; R318.01; R333.4
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2014-03-13
Cited: 4
Clicked: 10107
Ying Zhu, Yi Zheng, Yuan-yuan Shen, Xin Chen, Xin-yu Zhang, Hao-ming Lin, Yan-rong Guo, Tian-fu Wang, Si-ping Chen. Analyzing and modeling rheological behavior of liver fibrosis in rats using shear viscoelastic moduli[J]. Journal of Zhejiang University Science B,in press.Frontiers of Information Technology & Electronic Engineering,in press.https://doi.org/10.1631/jzus.B1300121 @article{title="Analyzing and modeling rheological behavior of liver fibrosis in rats using shear viscoelastic moduli", %0 Journal Article TY - JOUR
利用剪切黏弹性模量对大鼠肝纤维化流变特性进行分析和建模创新要点:本文利用剪切黏弹性模量描绘并比较了大鼠肝脏F0期到F4期的纤维化过程。 研究方法:两个黏弹性模型,即Zener模型和Voigt模型用于解释流变力学测试得到的实验数据,由此得到每个纤维化分期的肝脏弹性和黏性值。 重要结论:肝脏中度纤维化(≤F2期)与黏弹性值密切相关。Zener模型的弹性均值E1从F0期的(0.452±0.094) kPa增加到F2期的(1.311±0.717) kPa,而Voigt模型的弹性均值E从F0期的(0.618±0.089) kPa增加到 F2期的(1.701±0.844) kPa。Zener模型的黏性均值从F0期的(3.499±0.186) Pa•s 增加到F2期的(4.947±1.811) Pa•s,而Voigt模型的黏性均值从F0期的(3.379±0.316) Pa•s 增加到F2期的(4.625±1.296) Pa•s。无论选用哪个黏弹性模型,在F1期和F2期,肝脏弹性值的标准差比黏性值的标准差变化要小。因此,测得的弹性比黏性更有效地区分肝纤维化F0期到F2期。 关键词组: Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article
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