Abstract
Ethanol-induced oxidative damage is commonly associated with the generation of reactive
oxygen molecules, leading to oxidative stress. Considering that antioxidant activity
is an important mechanism of action involved in cytoprotection, the aim of this work
was to evaluate the antioxidant properties of the alkaloid indigo (1 ) (2 mg/kg, p. o. ), obtained from the leaves of Indigofera truxillensis Kunth (Fabaceae), on rat gastric mucosa submitted to ethanol-induced (100 %, 1 mL,
p. o. ) gastric ulcer. Enzymatic assays and DNA fragmentation analysis were performed. When
ethanol was administered to the control group, the sulfhydryl content (SH) and the
glutathione peroxidase (GPx) activity decreased by 41 % and 50 %, respectively; in
contrast, superoxide dismutase (SOD) and glutathione reductase (GR) activities increased
by 56 % and 67 %, respectively. Additionally, myeloperoxidase (MPO) activity, a marker
for free radical generation caused by polymorphonuclear neutrophil (PMN) tissue infiltration,
also increased 4.5-fold after ethanol treatment. Rat gastric mucosa exposed to ethanol
showed DNA fragmentation. Indigo alkaloid pretreatment protected rats from ethanol-induced
gastric lesions. This effect was determined by the ulcerative lesion area (ULA), indicating
an inhibition of around 80 % at 2 mg/kg. This alkaloid also diminished GPx activity,
which was higher than that observed with ethanol alone. However, this effect was counterbalanced
by increased GR activity. Indigo was unable to restore alterations in SOD activity
promoted by ethanol. After indigo pretreatment, SH levels and MPO activity remained
normal and gastric mucosa DNA damage caused by ethanol was also partially prevented
by indigo. These results suggest that the gastroprotective mechanisms of indigo include
non-enzymatic antioxidant effects and the inhibition of PMN infiltration which, in
combination, partially protect the gastric mucosa against ethanol-induced DNA damage.
Key words
Alkaloids -
Indigofera truxillensis
- indigo - Fabaceae - free radicals - antioxidant enzymes - gastric ulcer - MPO activity
- DNA damage
References
1
Kwiecien S, Brzozowski T, Konuturek S J.
Effects of reactive oxygen species action on gastric mucosal in various models of
mucosal injury.
J Physiol Pharmacol.
2002;
53
39-50.
2
La Casa C, Villegas I, Alarcón de la Lastra C, Motilva V, Martín Calero M J.
Evidence for protective and antioxidant properties of rutin, a antural flavone, against
ethanol induced gastric lesions.
J Ethnopharmacol.
2000;
71
45-53.
3
Yoshinaga M, Ohtani A, Harada N, Fukuda Y, Nawata H.
Vitamin C inhibits corpus gastritis in Helicobacter pylori -infected patients during acid-suppressive therapy.
J Gastroenterol Hepatol.
2001;
16
1206-10.
4
Borrelli F, Izzo A A.
The plant kingdom as a source of anti-ulcer remedies.
Phytother Res.
2000;
14
581-91.
5 Bentham G M. Leguminosae I. In: von Martius KFP, Endlicher SFL, Urban I, Eichle
AWR, Fenzl E, editors
Flora Brasiliensis . Monachii; Friid Fleischer 1859: 15.
6
Leite S P, De Medeiros P L, Da Silva E C, De Souza Maia M B, De Menezes Lima V L,
Saul D E.
Embryotoxicity in vitro with extract of Indigofera suffruticosa leaves.
Reprod Toxicol.
2004;
18
701-5.
7 Roig J T. Plantas medicinales, aromaticas o venenosas de Cuba. La Havana; Editorial
Cientifica-Tecnica 1988: 164.
8 Cola-Miranda M, Barbastefano V, Hiruma-Lima C A, Calvo T R, Vilegas W, Brito A RMS.
Atividade altiulcerogênica de Indigofera truxillensis Kunth. Biota Neotrop advance online publication June 2006: doi: ISSN 1676 - 0603.
9
Lewis D A, Hanson P J.
Anti-ulcer drugs of plant origin.
Prog Med Chem..
1991;
28
201-31.
10
Chanayath N, Lhieochaiphant S, Phutrakul S.
Pigment extraction techiques from the leaves of Indigofera tinctoria Linn. and Baphicacanthus cusia Brem. and chemical structure analysis of their major compounds.
Chiang Mai Univ J.
2002;
1
149-60.
11
Robert A, Nezamis J, Lancaster C, Hanchar A.
Cytoprotection by prostaglandins in rats. Prevention of gastric necrosis produced
by alcohol, HCl, NaOH, hyprtonic NaCl and thermal injury.
Gastroenterology.
1979;
71
433-43.
12
Garg C P, Cho C H, Ogle C W.
The role of gastric mucosal sulfhydryl in the ulcer-protecting effects of sulphasalazine.
J Pharm Pharmacol.
1991;
43
733-4.
13
Yoshikawa T, Naito Y, Kishi A, Kaneko T, Linuma S, Ichikawa H. et al .
Role of active oxygen, lipid peroxidation, and antioxidants in the pathogenesis of
gastric mucosal injury induced by indomethacin in rats.
Gut.
1993;
34
732-7.
14
Worthington D J, Rosemeyer M A.
Human glutathione reductase: purification of the crystalline enzyme from erythrocytes.
Eur J Biochem.
1974;
48
167-77.
15
Winterbourn C, Hawkins R E, Brian M, Carrell R W.
The estimation of red cell superoxide dismutase activity.
J Lab Clin Med.
1975;
85
337-41.
16
Krawisz J E, Sharon P, Stenson W F.
Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity.
Assessment of inflammation in rat and hamster models.
Gastroenterology.
1984;
87
1344-50.
17
Tilly J L, Hsueh A J.
Microscale autoradiographic method for the qualitative and quantitative analysis of
apoptotic DNA fragmentation.
J Cell Physiol.
1993;
154
519-26.
18
Bradford M M.
A rapid and sensitive method for the quantitation of microgram quantities of protein
utilizing the principle of protein-dye binding.
Anal Biochem.
1976;
172
248-54.
19
Oates P J, Hakkinen J P.
Studies on the mechanisms of ethanol-induced gastric damage in rats.
Gastroenterology.
1988;
94
20-1.
20
Cnubben N HP, Rietjens I MCM, Worterlbore H, van Zanden J, van Bladeren P J.
The interplay of glutathione related process in antioxidant defense.
Environ Toxicol Pharmacol.
2001;
10
141-52.
21
Kvietys P R, Twohing B, Danzell J, Specian R D.
Ethanol-induced injury to the rat gastric mucosal. Role of neutrophil and xantine
oxidase-derived radicals.
Gastroenterol.
1990;
98
909-20.
22
Martín M J, La Casa C, Alarcón de la Lastra C, Cabeza J, Villegas I, Motilva V.
Anti-oxidant mechanisms involved in gastroprotective effects of quercetin.
Z Naturforsch.
1998;
53
82-8.
23
Tomisato W, Tsutsumi S, Tsuchiya T, Mizushima T.
NSAIDs induce both necrosis and apoptosis in guinea pig gastric mucosal cells in primary
culture.
Am J Physiol Gastrointest Liver Physiol.
2001;
281
G1092-100.
24
Tsutsumi S, Tomisato W, Takano T, Rokutan K, Tsuchiya T, Mizushima T.
Gastric irritant-induced apoptosis in guinea pig gastric mucosal cells in primary
culture.
Biochim Biophys Acta.
2002;
1589
168-80.
25
Szabo S, Vattay P.
Experimental gastric and duodenal ulcers.
Gastroenterol Clin North Am.
1990;
19
67-85.
26
Rizvi S I, Zaid M A.
Intracellular reduced glutathione content in normal and type 2 diabetic erythrocytes:
effect of insulin and (-)epicatechin.
J Physiol Pharmacol.
2001;
52
483-8.
27
Shaw S, Herbert V, Colman N, Jayatilleke E.
Effect of ethanol-generated free radicals on gastric intrinsic factor and glutathione.
Alcohol.
1990;
7
153-7.
28
Takeuchi K, Megumu O, Hiromichi N, Okabe S.
Role of sulfhydryls in mucosal injury caused by ethanol. Reaction to microvascular
permeability, gastric motility and cytoprotection.
J Pharmacol Exp Ther.
1988;
248
836-9.
29
Repetto M G, Llesuy S F.
Antioxidant properties of natural compounds used in popular medicine for gastric ulcers.
Braz J Med Biol Res.
2002;
35
523-34.
30
Martin M C, La Casa C, Alarcon de la Lastra C, Cabeza J, Villegas I, Motilva V.
Antioxidant mechanisms involved in gastroprotective effects of quercetin.
Z Naturforsch.
1998;
53
82-8.
31
Schwartz L M, Smith S W, Jone M EE, Osbone B A.
Do all programmed cell deaths occur via apoptosis?.
Proc Natl Acad Sci USA..
1993;
90
980-4.
32
Higuchi Y.
Polyunsaturated fatty acids promote 8-hydroxy-2-deoxyguanosine formation through lipid
peroxidation under the glutamate-induced GSH depletion in nrat glioma cells.
Arch Biochem Biophys.
2001;
292
65-70.
Prof. Dr. Alba Regina Monteiro Souza Brito
Departamento de Fisiologia e Biofísica
IB - UNICAMP
Cidade Universitária ”Zeferino Vaz”
Barão Geraldo
Campinas - SP
Brasil 13083-970
Phone: +55-19-3521-6188
Fax: +55-19-3521-6284
Email: abrito@unicamp.br