1,2,3,4,6-Penta-O-galloyl-β-D-glucose Protects Splenocytes against Radiation-Induced Apoptosis in Murine Splenocytes

被引:10
作者
Bing, So Jin [1 ,2 ]
Kim, Min Ju [1 ,2 ]
Park, Eunjin [1 ,2 ]
Ahn, Ginnae [3 ]
Kim, Dae Seung [1 ,2 ]
Ko, Ryeo Kyeong [4 ]
Lee, Nam Ho [4 ]
Shin, Taekyun [1 ,2 ]
Park, Jae Woo [5 ]
Jee, Youngheun [1 ,2 ]
机构
[1] Jeju Natl Univ, Dept Vet Med, Cheju 690756, South Korea
[2] Jeju Natl Univ, Appl Radiol Sci Res Inst, Cheju 690756, South Korea
[3] Jeju Natl Univ, Fac Marine Life Sci, Cheju 690756, South Korea
[4] Jeju Natl Univ, Dept Chem, Coll Nat Sci, Cheju 690756, South Korea
[5] Jeju Natl Univ, Dept Nucl & Energy Engn, Cheju 690756, South Korea
关键词
1,2,3,4,6-penta-O-galloyl-beta-D-glucose; Nymphaea; radioprotection; IN-VITRO; CELLS; RADIOPROTECTION; AMIFOSTINE; INDUCTION; GROWTH; PGG;
D O I
10.1248/bpb.33.1122
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antioxidant property and hematopoietic repair capacity are important characteristics of radioprotective agents. Some studies have demonstrated that 1,2,3,4,6-penta-O-galloyl-beta-D-glucose (PGG), a molecule isolated from the waterlily, has antioxidant, hematopoietic repair, and anti-inflammatory activities. In this study, we try to determine whether PGG extracted from a lily, Nymphaea tetragona var. angusta, has radioprotective effects on splenocytes in vitro against Co-60 gamma-ray irradiation with absorption doses of 2 Gy and 4 Gy. Results show that PGG treatment dramatically enhances the proliferation of splenocytes compared with irradiated but untreated controls. In addition, PGG treatment before irradiation protects the splenocytes from lethal effects of irradiation and decreases DNA damages as identified by the alkaline comet assay. PGG-treated cells also show less radiation-induced apoptosis. These cells have lower concentrations of the pro-apoptotic protein p53 and more of the antiapoptotic protein Bcl-2. The results presented in this study suggest that PGG has a cytoprotective effect on immune cells exposed to normally damaging amount of radiation. Thus, PGG could be an effective, non-toxic radioprotective agent.
引用
收藏
页码:1122 / 1127
页数:6
相关论文
共 31 条
[1]   RADIATION-INDUCED SALIVARY GLAND DYSFUNCTION RESULTS FROM p53-DEPENDENT APOPTOSIS [J].
Avila, Jennifer L. ;
Grundmann, Oliver ;
Burd, Randy ;
Limesand, Kirsten H. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2009, 73 (02) :523-529
[2]   1,2,3,4,6-Penta-O-galloyl-beta-D-glucose protects rat neuronal cells (Neuro 2A) from hydrogen peroxide-mediated cell death via the induction of heme oxygenase-1 [J].
Choi, BM ;
Kim, HJ ;
Oh, GS ;
Pae, HO ;
Oh, H ;
Jeong, S ;
Kwon, TO ;
Kim, YM ;
Chung, HT .
NEUROSCIENCE LETTERS, 2002, 328 (02) :185-189
[3]   Curcumin induces apoptosis in human breast cancer cells through p53-dependent Bax induction [J].
Choudhuri, T ;
Pal, S ;
Agwarwal, ML ;
Das, T ;
Sa, G .
FEBS LETTERS, 2002, 512 (1-3) :334-340
[4]  
Crouzet J, 1999, NATURALLY OCCURRING GLYCOSIDES, P225
[5]   Mathematical model of a network of interaction between p53 and Bcl-2 during genotoxic-induced apoptosis [J].
Dogu, Yasam ;
Diaz, Jose .
BIOPHYSICAL CHEMISTRY, 2009, 143 (1-2) :44-54
[6]   The screening and isolation of an effective anti-endotoxin monomer from Radix Paeoniae Rubra using affinity biosensor technology [J].
Genfa, L ;
Jiang, Z ;
Hong, Z ;
Zheng, YM ;
Wang, LX ;
Guo, W ;
Ming, H ;
Jiang, DL ;
Wei, LZ .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2005, 5 (06) :1007-1017
[7]   Foundation review: Trends in the development of radioprotective agents [J].
Hosseinimehr, Seyed Jalal .
DRUG DISCOVERY TODAY, 2007, 12 (19-20) :794-805
[8]   Vasodilatory and anti-inflammatory effects of the 1,2,3,4,6-penta-O-galloyl-β-D-glucose (PGG) via a nitric oxide-cGMP pathway [J].
Kang, DG ;
Moon, MK ;
Choi, DH ;
Lee, JK ;
Kwon, TO ;
Lee, HS .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 524 (1-3) :111-119
[9]  
Kim Y.H., 2007, INT J COSMETIC SCI, V29, P487, DOI DOI 10.1111/J.1468-2494.2007.00391_3.X
[10]   Subcutaneous administration of amifostine during fractionated radiotherapy: A randomized phase II study [J].
Koukourakis, MI ;
Kyrias, G ;
Kakolyris, S ;
Kouroussis, C ;
Frangiadaki, C ;
Giatromanolaki, A ;
Retalis, G ;
Georgoulias, V .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (11) :2226-2233