The inhibition of gastric mucosal lesion, oxidative stress and neutrophil-infiltration in rats by the lichen constituent diffractaic acid

被引:105
作者
Bayir, Y.
OdabaSoglu, F.
Cakir, A. [1 ]
Aslan, A.
Suleyman, H.
Halici, M.
Kazaz, C.
机构
[1] Ataturk Univ, Kazim Karabekir Educ Fac, Dept Chem, TR-25240 Erzurum, Turkey
[2] Ataturk Univ, Fac Pharm, Dept Biochem, TR-25240 Erzurum, Turkey
[3] Ataturk Univ, Fac Med, Dept Pharmacol, TR-25240 Erzurum, Turkey
[4] Ataturk Univ, Kazim Karabekir Educ Fac, Dept Biol, TR-25240 Erzurum, Turkey
[5] Ataturk Univ, Fac Sci, Dept Chem, TR-25240 Erzurum, Turkey
关键词
lichen; Usnea longissima; diffractaic acid; antiulcerogenic activity; antioxidants; myeloperoxidase; nitric oxide synthase; neutrophil infiltration;
D O I
10.1016/j.phymed.2005.07.002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The antiulcerogenic effect of diffractaic acid (DA) isolated from Usnea longissima, a lichen species, on indomethacin (IND)-induced gastric lesions was investigated in rats. Administration of 25, 50, 100 and 200 mg/kg doses of DA and ranitidine (RAN) (50 mg/kg dose) reduced the gastric lesions by 43.5%, 52.9%, 91.4%, 96.7% and 72.7%, respectively. It is known that oxidative stress leads to tissue injury in organisms. Thus, in all treated groups of rats, the in vivo activities of the antioxidant enzymes, superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and the levels of reduced glutathione (GSH) and lipid peroxidation (LPO) were evaluated. IND caused oxidative stress, which resulted in LPO in tissues, by decreasing the levels of GPx, SOD and GSH as compared to healthy rats. In contrast to IND, the administration of DA and RAN showed a significant decrease in LPO level and an increase in tissue SOD, GPx and GSH levels. However, while CAT activity was significantly increased by the administration of IND, the administration of DA and RAN decreased CAT activity. The administration of IND also increased the myeloperoxidase (MPx) activity, which shows neutrophil infiltration into the gastric mucosal tissues. In contrast to IND, the administration of DA and RAN decreased Wx activity. The changes in activities of gastric mucosal nitric oxide synthases (NOS) throughout the development of gastric mucosal damage induced by IND were also studied. A decrease in constitutive NOS (cNOS) activity and an increase in inducible NOS (iNOS) activity were determined in gastric damaged tissues induced by IND. The administration of DA (100 mg/kg dose) and RAN reversed the activities of iNOS and cNOS. These results suggest that the gastroprotective effect of DA can be attributed to its enhancing effects on antioxidant defense systems as well as reducing effects of neutrophil infiltration. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:584 / 590
页数:7
相关论文
共 40 条
  • [1] AEBI H, 1984, METHOD ENZYMOL, V105, P121
  • [2] OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING
    AMES, BN
    SHIGENAGA, MK
    HAGEN, TM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) : 7915 - 7922
  • [3] NONSTEROIDAL ANTIINFLAMMATORY DRUGS INHIBIT GASTRIC PEROXIDASE-ACTIVITY
    BANERJEE, RK
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1034 (03) : 275 - 280
  • [4] MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER
    BRADLEY, PP
    PRIEBAT, DA
    CHRISTENSEN, RD
    ROTHSTEIN, G
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) : 206 - 209
  • [5] Brij L., 1995, LICHENOLOGIST, V27, P77
  • [6] NITRIC-OXIDE GENERATORS AND CGMP STIMULATE MUCUS SECRETION BY RAT GASTRIC-MUCOSAL CELLS
    BROWN, JF
    KEATES, AC
    HANSON, PJ
    WHITTLE, BJR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03): : G418 - G422
  • [7] CHOPRA RN, 1958, CHOPRAS INDIGENOUS D, P1
  • [8] Hydroxyl radical is the major causative factor in stress-induced gastric ulceration
    Das, D
    Bandyopadhyay, D
    Bhattacharjee, M
    Banerjee, RK
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (01) : 8 - 18
  • [9] Oxidative stress, antioxidant defenses, and damage removal, repair, and replacement systems
    Davies, KJA
    [J]. IUBMB LIFE, 2000, 50 (4-5) : 279 - 289
  • [10] Neutrophil-mediated gastrointestinal injury
    Elliott, SN
    Wallace, JL
    [J]. CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1998, 12 (08): : 559 - 568