Harpagophytum procumbens Prevents Oxidative Stress and Loss of Cell Viability In Vitro

被引:21
作者
Schaffer, Larissa Finger [1 ]
Peroza, Luis Ricardo [2 ]
Boligon, Aline Augusti [3 ]
Athayde, Margareth Linde [3 ]
Alves, Sydney Hartz [3 ]
Fachinetto, Roselei [1 ,2 ]
Wagner, Caroline [1 ,4 ]
机构
[1] Univ Fed Santa Maria, Programa Posgrad Farmacol, BR-97105900 Santa Maria, RS, Brazil
[2] Univ Fed Santa Maria, Programa Posgrad Ciencias Biol Bioquim Toxicol, BR-97105900 Santa Maria, RS, Brazil
[3] Univ Fed Santa Maria, Programa Posgrad Ciencias Farmaceut, BR-97105900 Santa Maria, RS, Brazil
[4] Univ Fed Pampa, BR-96570000 Cacapava Do Sul, RS, Brazil
关键词
Antioxidant; Devil's claw; Cerebral cortex; Catalase; Thiol levels; Lipid peroxidation; ANTIOXIDANT ACTIVITIES; NITRIC-OXIDE; DEVILS CLAW; LIPID PEROXIDES; FREE-RADICALS; IRON; INFLAMMATION; QUERCETIN; HYDROXYL; EXTRACTS;
D O I
10.1007/s11064-013-1133-x
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
Harpagophytum procumbens, popularly known as devil's claw, is a plant commonly used in the treatment of diseases of inflammatory origin. The anti-inflammatory effects of H. procumbens have been studied; however, the mechanism of action is not elucidated. It is known that excess of reactive oxygen and nitrogen species may contribute to increasing tissue damage due to inflammation. In the present study, we examined the effects of H. procumbens infusion, crude extract and fractions on lipid peroxidation (brain homogenates) induced by different pro-oxidants (Fe2+ or sodium nitroprusside) and the effects of ethyl acetate fraction (rich in phenolic compounds) on antioxidant defenses (catalase activity and thiol levels) and cell damage (brain cortical slices) induced by different pro-oxidants. All tested extracts of H. procumbens inhibited lipid peroxidation in a concentration-dependent manner. Furthermore, the ethyl acetate fraction had the highest antioxidant effects either by decreasing lipid peroxidation and cellular damage or restoring thiols levels and catalase activity. Taken together, our results showed that H. procumbens acts either by preventing oxidative stress or loss of cell viability. Thus, the previously reported anti-inflammatory effect of H. procumbens could also be attributed to its antioxidant activity.
引用
收藏
页码:2256 / 2267
页数:12
相关论文
共 70 条
[1]   Effect of the major glycosides of Harpagophytum procumbens (Devil's Claw) on epidermal cyclooxygenase-2 (COX-2) in vitro [J].
Abdelouahab, Nassima ;
Heard, Charles .
JOURNAL OF NATURAL PRODUCTS, 2008, 71 (05) :746-749
[2]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[3]   Iron metabolism [J].
Aisen, P ;
Wessling-Resnick, M ;
Leibold, EA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (02) :200-206
[4]   Effect of Isolated Fractions of Harpagophytum procumbens DC (Devil's Claw) on COX-1, COX-2 Activity and Nitric Oxide Production on Whole-Blood Assay [J].
Anauate, Maria Cecilia ;
Torres, Luce Maria ;
Verissimo de Mello, Suzana Beatriz .
PHYTOTHERAPY RESEARCH, 2010, 24 (09) :1365-1369
[5]   Evaluation of acute and chronic treatments with Harpagophytum procumbens on Freund's adjuvant-induced arthritis in rats [J].
Andersen, ML ;
Santos, EHR ;
Seabra, MD ;
da Silva, AAB ;
Tufik, S .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 91 (2-3) :325-330
[6]   Phagocytes and oxidative stress [J].
Babior, BM .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (01) :33-44
[7]   NITRIC-OXIDE GENERATION FROM NITROPRUSSIDE BY VASCULAR TISSUE - EVIDENCE THAT REDUCTION OF THE NITROPRUSSIDE ANION AND CYANIDE LOSS ARE REQUIRED [J].
BATES, JN ;
BAKER, MT ;
GUERRA, R ;
HARRISON, DG .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 :S157-S165
[8]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[9]  
Bhattacharya A, 1998, BRIT J PHYTOTHERAPY, V5, P2
[10]   In vitro exposure to quercetin and genistein alters lipid peroxides and prevents the loss of glutathione in human progenitor mononuclear (U937) cells [J].
Boadi, WY ;
Iyere, PA ;
Adunyah, SE .
JOURNAL OF APPLIED TOXICOLOGY, 2005, 25 (01) :82-88