Reactive oxygen species mediated membrane damage induced by fullerene derivatives and its possible biological implications

被引:199
作者
Kamat, JP
Devasagayam, TPA
Priyadarsini, KI
Mohan, H [1 ]
机构
[1] Bhabha Atom Res Ctr, Div Chem, Bombay 400085, Maharashtra, India
[2] Bhabha Atom Res Ctr, Div Cell Biol, Bombay 400085, Maharashtra, India
关键词
photosensitization; fullerenes; microsome; lipid peroxidation; antioxidants;
D O I
10.1016/S0300-483X(00)00277-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fullerenes have attracted considerable attention in recent years due to their unique chemical structure and potential applications. Hence it is of interest to study their biological effects. Using rat liver microsomes as model systems we have examined the ability of the most commonly used fullerene, C-60 and its water-soluble derivative, C-60(OH)(18) to induce membrane damage on photosensitization. For photoexcitation, UV or tungsten lamps were used. Damage was assessed as lipid peroxidation products like conjugated dienes, lipid hydroperoxides and thiobarbituric acid reactive substances (TBARS), protein oxidation in the form of protein carbonyls, besides loss of membrane bound enzymes. Both fullerene derivatives induced significant oxidative damage. The alterations induced were both time- and concentration-dependent. Role of different reactive oxygen species (ROS) in the damage induced was examined by various scavengers of ROS and by deuteration of the buffer. The changes induced by C-60 were predominantly due to O-1(2) while that by C-60(OH)(18) was mainly due to radical species. Biological antioxidants such as glutathione, ascorbic acid and a-tocopherol were capable of inhibiting membrane damage induced by both the fullerenes. However, the damage induced by C-60(OH)(18) was more for both lipids and proteins than that showed by C-60. C-60 also showed enhancement in the formation of lipid peroxidation in sarcoma 180 ascites microsomes. In conclusion, our studies indicate that fullerene/its derivative can generate ROS on photoexcitation and can induce significant lipid peroxidation/protein oxidation in membranes and these phenomena can be prevented by endogenous/natural antioxidants. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:55 / 61
页数:7
相关论文
共 24 条
[1]   Protein oxidation in aging, disease, and oxidative stress [J].
Berlett, BS ;
Stadtman, ER .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20313-20316
[2]  
CHIANG LY, 1992, J CHEM SOC CHEM COMM
[3]   PREVENTION OF SINGLET OXYGEN-INDUCED DNA DAMAGE BY LIPOATE [J].
DEVASAGAYAM, TPA ;
SUBRAMANIAN, M ;
PRADHAN, DS ;
SIES, H .
CHEMICO-BIOLOGICAL INTERACTIONS, 1993, 86 (01) :79-92
[4]   DIFFERENCES IN LIPID-PEROXIDATION OF RAT-LIVER ROUGH AND SMOOTH MICROSOMES [J].
DEVASAGAYAM, TPA ;
PUSHPENDRAN, CK ;
EAPEN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 750 (01) :91-97
[5]  
Esterbauer H, 1996, PATHOL BIOL, V44, P25
[6]   Singlet oxygen generation by photodynamic agents [J].
Fernandez, JM ;
Bilgin, MD ;
Grossweiner, LI .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1997, 37 (1-2) :131-140
[7]   CHARGE RECOMBINATION REACTIONS IN PHOTOEXCITED C-60-AMINE COMPLEXES STUDIED BY PICOSECOND PUMP-PROBE SPECTROSCOPY [J].
GHOSH, HN ;
PAL, H ;
SAPRE, AV ;
MITTAL, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (25) :11722-11727
[8]   PHOTODYNAMIC LIPID-PEROXIDATION IN BIOLOGICAL-SYSTEMS [J].
GIROTTI, AW .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1990, 51 (04) :497-509
[9]   TOCOTRIENOLS FROM PALM OIL AS POTENT INHIBITORS OF LIPID-PEROXIDATION AND PROTEIN OXIDATION IN RAT-BRAIN MITOCHONDRIA [J].
KAMAT, JP ;
DEVASAGAYAM, TPA .
NEUROSCIENCE LETTERS, 1995, 195 (03) :179-182
[10]   NICOTINAMIDE-INDUCED HEPATIC-MICROSOMAL MIXED-FUNCTION OXIDASE SYSTEM IN RATS [J].
KAMAT, JP ;
NARURKAR, LM ;
MHATRE, NA ;
NARURKAR, MV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 628 (01) :26-34