Study on the interaction of taurine and hepatic protein in rats with cirrhotic portal hypertension by spectrometry

  • YU Ye ,
  • LIAO Juan ,
  • WEN Bin ,
  • DENG Xin
Expand
  • 1. Traditional Chinese Medicine Hospital of Guilin, Guilin 541000, China;
    2. Ruikang Hospital affiliated to Guangxi University of Traditional Chinese Medicine;
    3. Guangxi University of traditional Chinese Medicine, Guilin 541000, China

Received date: 2023-11-30

  Online published: 2024-03-22

Abstract

Objective: To study the interaction of taurine with hepatic proteins in rats with cirrhotic portal hypertension and its underlying mechanism using spectroscopy. Methods: A total of 120 rats were randomly divided into the normal group, model group, propranolol group and taurine group, with 30 rats in each group. Except for the normal group, the other three groups were treated with carbon tetrachloride (CCL4) to prepare a cirrhotic portal hypertension rat model. When modeling, the propranolol group was given propranolol, the taurine group was treated with taurine, and rats in the model group were fed with the same amount of normal saline. All rats were treated for a course of 10 weeks. After treatment, values of portal hypertension in each group were compared. The fluorescence spectra of hepatic protein and the ultraviolet absorption spectrum of taurine of rats in each group at different temperatures were measured and analyzed. Results: Compared to the propranolol group and model group, portal venous flow (PVF), portal venous pressure (PVP), portal vascular resistance (PVR) and heart rate were lower and mean arterial pressure (MAP) was higher in the taurine group. Kq values of hepatic protein for each rats were greater than the maximum dynamic quenching rate of 2.0×1010L/(mol·s), with the enthalpy change(△H)of -8707.6336 and entropy change(△S)of 33.41395. △G and △H of Gibbs free energy change in the normal group were both negative, and △S was positive. △G and △H in the taurine group were positive, with negative △S, while the model group had no obvious regularity. The R values were 1.77, 2.35, and 2.28 nm in the normal, model and taurine group respectively, with the r values of 1.24, 1.31 and 6.56 respectively. Conclusion: Taurine can inhibit fibrosis and attenuate portal hypertension, and this mechanism may alter the protein structure of liver tissue in cirrhotic portal hypertension rats to alleviate liver damage.

Cite this article

YU Ye , LIAO Juan , WEN Bin , DENG Xin . Study on the interaction of taurine and hepatic protein in rats with cirrhotic portal hypertension by spectrometry[J]. Journal of Baotou Medical College, 2024 , 40(3) : 42 -49 . DOI: 10.16833/j.cnki.jbmc.2024.03.008

References

[1] Simonetto DA, Liu MF, Kamath PS. Portal hypertension and related complications: diagnosis and management[J]. Mayo Clin Proc, 2019, 94(4): 714-726.
[2] 梁健, 邓鑫, 王勤, 等. 应用基因芯片分析牛磺酸对肝星状细胞基因表达的调控[J]. 第二军医大学学报, 2010, 31(2): 226-227.
[3] 邓鑫, 梁健, 李益忠, 等. 天然牛磺酸对肝纤维化大鼠肝线粒体的保护作用[J]. 西安交通大学学报(医学版), 2007, 28(6): 648-650, 703.
[4] Wen B, Liang J, Deng X, et al. Effect of fluid shear stress on portal vein remodeling in a rat model of portal hypertension[J]. Gastroenterol Res Pract, 2015, 2015: 545018.
[5] Liang J, Deng X, Lin ZX, et al. Attenuation of portal hypertension by natural taurine in rats with liver cirrhosis[J]. World J Gastroenterol, 2009, 15(36): 4529-4537.
[6] Wang C, Wu QH, Li CR, et al. Interaction of tetrandrine with human serum albumin: a fluorescence quenching study[J]. Anal Sci, 2007, 23(4): 429-433.
[7] Xie MX, Xu XY, Wang YD. Interaction between hesperetin and human serum albumin revealed by spectroscopic methods[J]. Biochim Biophys Acta, 2005, 1724(1/2): 215-224.
[8] 赵静. 药物小分子与生物大分子相互作用机理的研究[D]. 大连: 辽宁师范大学, 2011.
[9] Hu YJ, Li W, Liu Y, et al. Fluorometric investigation of the interaction between methylene blue and human serum albumin[J]. J Pharm Biomed Anal, 2005, 39(3/4): 740-745.
[10] Hu YJ, Liu Y, Zhao RM, et al. Interaction of colchicine with human serum albumin investigated by spectroscopic methods[J]. Int J Biol Macromol, 2005, 37(3): 122-126.
[11] Hu YJ, Yue HL, Li XL, et al. Molecular spectroscopic studies on the interaction of morin with bovine serum albumin[J]. J Photochem Photobiol B, 2012, 112: 16-22.
[12] Bogdan M, Pirnau A, Floare C, et al. Binding interaction of indomethacin with human serum albumin[J]. J Pharm Biomed Anal, 2008, 47(4/5): 981-984.
[13] Shahabadi N, Maghsudi M, Rouhani S. Study on the interaction of food colourant quinoline yellow with bovine serum albumin by spectroscopic techniques[J]. Food Chem, 2012, 135(3): 1836-1841.
[14] Li GX, Liu BS, Zhang QJ, et al. Investigation on the effect of fluorescence quenching of bovine serum albumin by cefoxitin sodium using fluorescence spectroscopy and synchronous fluorescence spectroscopy[J]. Luminescence, 2016, 31(5): 1054-1062.
[15] Chaudhry S, Tandon B, Gupta A, et al. Taurine: a potential mediator for periodontal therapy[J]. Indian J Dent Res, 2018, 29(6): 808-811.
[16] Wen CY, Li FN, Zhang LY, et al. Taurine is involved in energy metabolism in muscles, adipose tissue, and the liver[J]. Mol Nutr Food Res, 2019, 63(2): e1800536.
[17] Eftink MR. Fluorescence quenching: theory and applications[M]//Topics in Fluorescence Spectroscopy. Boston: Kluwer Academic Publishers, 2006: 53-126.
[18] Toprak M. Fluorescence study on the interaction of human serum albumin with butein in liposomes[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2016, 154: 108-113.
Outlines

/