In Vitro Evaluation of Antioxidant and Anti-Inflammatory Properties of Genistein-Modified Hemodialysis Membranes

被引:32
作者
Neelakandan, Chandrasekaran [1 ]
Chang, Teng [1 ]
Alexander, Thomas [2 ]
Define, Linda [2 ]
Evancho-Chapman, Michelle [3 ]
Kyu, Thein [1 ]
机构
[1] Univ Akron, Dept Polymer Engn, Akron, OH 44325 USA
[2] Summa Hlth Syst, Dept Pathol & Lab Med, Akron, OH 44304 USA
[3] Summa Hlth Syst, Falor Div Surg Res, Akron, OH 44304 USA
关键词
PROTEIN-TYROSINE KINASE; TUMOR-NECROSIS-FACTOR; ENDOTHELIAL-CELLS; NADPH OXIDASE; TROGAMID-T; TRANSCRIPTION; COMPLEMENT; ACTIVATION; IL-1-BETA; SURVIVAL;
D O I
10.1021/bm200591q
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genistein-modified poly(amide) :poly(vinyl pyrrolidone) (PA: PVP/G) hemodialysis membranes have been fabricated by coagulation via solvent (dimethyl sulfoxide, DMSO)/nonsolvent (water) exchange. The antioxidant and anti-inflammatory properties of the unmodified PA:PVP membranes were evaluated in vitro using human blood. It was found that these unmodified PA:PVP membranes were noncytotoxic to peripheral blood mononuclear cells (PBMC) but raised intracellular reactive oxygen species (ROS) levels. Pure genistein (in DMSO solution) was not only nontoxic to PBMC, but also suppressed the ROS levels in a manner dependent on genistein dosage. A similar dose-dependent suppression of ROS was found in genistein-modified PA (i.e., PA/G) membranes. However, the PVP addition had little or no effect in the suppression of ROS levels for the ternary PA:PVP/G system; the membrane ROS suppression was largely controlled by the genistein dosage. The levels of tumor necrosis factor-alpha (TNF-alpha), interleulcin-1 beta (IL-1 beta), and interleukin (IL-6) in whole blood were measured by ex vivo stimulation with lipopolysaccharide (LPS). The unmodified PA:PVP membranes drastically increased the level of TNF-alpha; however, the concentration of IL-1 beta and IL-6 remained almost the same. The PA/G membranes reduced the concentration of IL-1 beta and TNF-alpha even at very low genistein loadings, but it required a higher genistein loading to realize a similar effect in the case of IL-6. Of particular importance is that the genistein-modified blend membranes (PA:PVP/G) showed greater suppression of the concentrations of all three cytokines (TNF-alpha, IL-1 beta, and IL-6) in comparison with those of the PA/G membranes, signifying the role of PVP in the enhanced anti-inflammatory properties of these genistein-modified membranes. Ultraviolet-visible (UV-vis) spectroscopy was employed to quantify any genistein leaching during the in vitro testing.
引用
收藏
页码:2447 / 2455
页数:9
相关论文
共 27 条
[1]  
Bao Y., 2004, Phytochemicals in health and disease, DOI DOI 10.1201/9780203021408-24
[2]  
Bolch A., 1995, J AM DIETETIC ASS, V95, P493
[3]   REDOX STATE, ANTIOXIDATIVE ACTIVITY AND LIPID-PEROXIDATION IN ERYTHROCYTES AND PLASMA OF CHRONIC AMBULATORY PERITONEAL-DIALYSIS PATIENTS [J].
CANESTRARI, F ;
BUONCRISTIANI, U ;
GALLI, F ;
GIORGINI, A ;
ALBERTINI, MC ;
CAROBI, C ;
PASCUCCI, M ;
BOSSU, M .
CLINICA CHIMICA ACTA, 1995, 234 (1-2) :127-136
[4]   Immunosuppressive effects of synthetic derivative of genistein on the survival of pancreatic islet allografts [J].
Fiedor, P ;
Kozerski, L ;
Dobrowolski, JC ;
Kawecki, R ;
Biniecki, K ;
Pachecka, J ;
Rowinski, W ;
Mazurek, AP .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (02) :537-537
[5]   Biological effects of oxidant stress in haemodialysis: The possible roles of vitamin E [J].
Galli, F ;
Canestrari, F ;
Buoncristiani, U .
BLOOD PURIFICATION, 1999, 17 (2-3) :79-94
[6]  
Gohl H, 1992, Contrib Nephrol, V96, P1
[7]  
HEROLD J, 1980, MAKROMOL CHEM, V181, P2625
[8]   SOLUTION PROPERTIES OF POLYTRIMETHYLHEXAMETHYLENTEREPHTHALAMIDE (TROGAMID T) [J].
HEROLD, J ;
MEYERHOFF, G .
EUROPEAN POLYMER JOURNAL, 1979, 15 (06) :525-532
[9]   Genistein, the dietary-derived angiogenesis inhibitor, prevents LDL oxidation and protects endothelial cells from damage by atherogenic LDL [J].
Kapiotis, S ;
Hermann, M ;
Held, I ;
Seelos, C ;
Ehringer, H ;
Gmeiner, BMK .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (11) :2868-2874
[10]   Immunologic function and survival in hemodialysis patients [J].
Kimmel, PL ;
Phillips, TM ;
Simmens, SJ ;
Peterson, RA ;
Weihs, KL ;
Alleyne, S ;
Cruz, I ;
Yanovski, JA ;
Veis, JH .
KIDNEY INTERNATIONAL, 1998, 54 (01) :236-244