IPSIndian Journal of Pharmacology
Home  IPS  Feedback Subscribe Top cited articles Login 
Users Online : 5786 
Small font sizeDefault font sizeIncrease font size
Navigate Here
 » Next article
 » Previous article 
 » Table of Contents
Resource Links
 »  Similar in PUBMED
 »  Search Pubmed for
 »  Search in Google Scholar for
 »Related articles
 »  Article in PDF (136 KB)
 »  Citation Manager
 »  Access Statistics
 »  Reader Comments
 »  Email Alert *
 »  Add to My List *
* Registration required (free)

In This Article
 »  Abstract
 »  Introduction
 »  Material and Methods
 »  Results
 »  Discussion
 »  Acknowledgement
 »  References

 Article Access Statistics
    PDF Downloaded596    
    Comments [Add]    
    Cited by others 11    

Recommend this journal

Year : 2004  |  Volume : 36  |  Issue : 5  |  Page : 296-302

Effects of Pterocarpus marsupium on NIDDM-induced rat gastric ulceration and mucosal offensive and defensive factors

Department of Pharmacology, Institute of Medical Sciences, Banaras Hindu University, Varanasi - 221 005, India

Date of Submission12-Sep-2003
Date of Decision23-Feb-2004
Date of Acceptance29-Feb-2004

Correspondence Address:
Department of Pharmacology, Institute of Medical Sciences, Banaras Hindu University, Varanasi - 221 005, India
[email protected]

 » Abstract 

OBJECTIVE: To evaluate the vulnerability of gastric mucosa to ulceration in non-insulin-dependent diabetes mellitus (NIDDM) rats vis-ŕ-vis the protective effects of the methanolic extract of Pterocarpus marsupium heartwood (PMS, an antidiabetic herbal plant). MATERIAL AND METHODS: NIDDM was produced in 5-day-old rat pups by administering streptozotocin (70 mg/kg, i.p). The animals showing blood glucose level > 140 mg/dl after 12 weeks of STZ administration were considered as NIDDM positive rats. The effective hypoglycemic dose of PMS (750 mg/kg/day, p.o.) for 6 days was studied for its gastric ulcer (GU) protective effects against cold restraint stress (CRS), aspirin (ASP), ethanol (EtOH) and pylorus ligation (PL)-induced GU both in normal (NR) and NIDDM rats. To ascertain the mechanism of action, the effects of NIDDM and that of PMS treatment in NIDDM rats on mucosal offensive acid-pepsin, free-radicals (LPO,NO) and defensive mucin secretion, cell shedding, cell proliferation, glycoproteins and antioxidant enzymes (SOD and CAT) were studied. RESULTS: PMS (750 mg/kg) decreased the blood sugar level both in NR and NIDDM rats. NIDDM rats exhibited an increased propensity to GU, induced by CRS, ASP, EtOH and PL. Though, PMS did not protect the NR rats against GU induced by the above methods it reversed their increased propensity in NIDDM rats. NIDDM PL-rats showed an increase in acid-pepsin secretion, cell shedding and decrease in mucin secretion and mucosal glycoproteins with little effect on cell proliferation. PMS treatment in NIDDM rats reversed the acid-pepsin secretion, enhanced mucin and mucosal glycoproteins and decreased cell shedding without any effect on cell proliferation. NIDDM-CRS rats showed a significant increase in LPO and NO and a decrease in SOD and CAT levels, which were, reversed by PMS treatment. CONCLUSION: NIDDM increased the propensity to GU by affecting both offensive (increased) and defensive (decreased) mucosal factors. Though PMS, a hypoglycemic agent, did not show any protection against ulceration induced by CRS, ASP, EtOH and PL in normal rats, it protected the mucosa against the same in NIDDM rats by affecting the above mucosal offensive and defensive factors.

How to cite this article:
Joshi M C, Dorababu M, Prabha T, Kumar M M, Goel R K. Effects of Pterocarpus marsupium on NIDDM-induced rat gastric ulceration and mucosal offensive and defensive factors. Indian J Pharmacol 2004;36:296-302

How to cite this URL:
Joshi M C, Dorababu M, Prabha T, Kumar M M, Goel R K. Effects of Pterocarpus marsupium on NIDDM-induced rat gastric ulceration and mucosal offensive and defensive factors. Indian J Pharmacol [serial online] 2004 [cited 2023 Sep 21];36:296-302. Available from: https://www.ijp-online.com/text.asp?2004/36/5/296/12649

 » Introduction Top

Recent experimental studies indicate that a prolonged diabetic state produces deleterious influences on various functions of the gastrointestinal tract with reports of an aggravation of gastric mucosal ulcerogenic responses to starvation or stress in diabetic rats.[1],[2] Peptic ulcer occurs due to an imbalance between offensive acid-pepsin secretion and free radical generation and defensive mucosal factors which include mucin-bicarbonate secretions, lifespan of mucosal cells, cell proliferation, glycoproteins, and antioxidant enzymes status.[3],[4]
Diabetes being a chronic disease may lead to a decrease in the mucosal defensive factors with a concomitant increase in propensity to ulceration in response to various physical (cold restraint stress and pylorus ligation) and chemical (aspirin, ethanol) agents. The changes induced by diabetes (DM) could be reversed by using drugs which can either promote mucosal defensive factors or correct the blood glucose levels or both.[5] Hence, we selected Pterocarpus marsupium (PMS, Leguminnaceae family), commonly known as vijaysar that has been recommended as early as 1000 BC by Sushruta for the treatment of diabetes. Various reports indicate the hypoglycemic activity of PMS both in experimental and clinical studies.[6]-[8] The objectives of the present study were to evaluate the effects of PMS on the susceptibility of the gastric mucosa of NIDDM rats to various ulcerogenic stimuli. The results were also compared with the standard oral hypoglycemic drug, glibenclamide and ulcer protective drug, sucralfate, on the ulcer models in NR/NIDDM rats.

 » Material and Methods Top

Animals: Adult Inbred Charles-Foster (CF) albino mice (20-22 g) and rats (130-180 g), of either sex, obtained from the central animal house of the Institute of Medical Sciences, Banaras Hindu University, Varanasi, were kept in the departmental animal house at 26±2o C and relative humidity 44-56%, light and dark cycles of 10 and 14 h respectively. The mice were used for acute toxicity study to find the LD50 dose of the test drug, PMS, while the rats were kept for breeding to obtain pups. The 5-day-old pups were divided into two groups, one group received streptozotocin to induce non-insulin dependent diabetes mellitus (NIDDM), while the other group served as normal (NR) control. Animals were provided with standard rodent pellet diet (Hind liver) and the food was withdrawn 18 h before the experiment though water was allowed ad libitum. 'Principles of laboratory animal care' guidelines were followed and prior permission was sought from the Institute Animal Ethics Committee for conducting the study.
Drug collection and extraction: The heartwood of PMS (Ayurvedic Gardens, Banaras Hindu University) was collected and identified with the standard sample preserved in the department of Dravyaguna, Institute of Medical Sciences, Varanasi. The heartwood was cut into very small pieces and macerated with methanol for 7 days. The extract (PMS) was vacuum dried and stored in a refrigerator until further use. The yield was 9.2 %.
Drug treatment
Acute toxicity study (Mice): To find the LD50 of PMS, six groups of mice, containing six in each group, were given PMS in the doses of 500, 1000, 2000, 4000 and 8000 mg/kg orally, while the control group received 1% carboxymethyl cellulose (CMC) in distilled water. The concentration of test drug/vehicle was so prepared that each animal received 1 ml/100 g body weight of the test solution/suspension. The animals were observed for 5 min every 30 min till 2 h and then at 4, 8 and 24 h after treatment for any behavioral changes/mortality. They were further observed daily for 7 days for mortality.
Rat study: PMS, glibenclamide (GLC, 0.6 mg/kg)[9] and sucralfate (SFT, 500 mg/kg)[4] were suspended in 1% CMC in distilled water (1 ml/100 g, bw). The test drugs were administered orally, once daily for five days and a last dose on Day 6 in 18 hr-fasted rats, one hour before the experiments on NR or NIDDM rats. The control group of animals received suspension of 1% CMC in distilled water. A dose-dependent hypoglycemic effect of PMS (500, 750 and 1000 mg/kg) was seen on the blood glucose level, both in NR and NIDDM rats and an optimal dose of 750 mg/kg was selected for antiulcer studies.
Experimental methods
Induction of Type II Diabetes mellitus (NIDDM) in rats: NIDDM was induced by injecting streptozotocin (STZ, 70 mg/kg, i.p.) to 5-day-old rat pups.[10] The control pups received saline alone. The pups were weaned after one month. Twelve weeks after injection of STZ, the rats were checked for fasting glucose level and those with glucose level greater than 140 mg/dl were considered as NIDDM rats and used for further studies.
Estimation of blood glucose: Blood samples were collected from the retro-orbital plexus of the rat and the blood glucose level was estimated by the GOD-POD method (Ranbaxy diagnostic kits, New Delhi).
Antiulcer study
The following experimental rat gastric ulcer models were used.[4]
Cold restraint stress (CRS)-induced ulcers: On Day 6, 18 h-fasted normal (NR) and NIDDM rats were subjected to cold restraint stress by strapping on a wooden plank and keeping them for 2 h at 4-6oC. The animals were then sacrificed by cervical dislocation and ulcers were scored on the dissected stomachs. The ulcer index was calculated by adding the total number of ulcers per stomach and the total severity of ulcers per stomach.[11]
Pylorus-ligation (PL)-induced ulcers: Drugs were administered for a period of 5 days as described above. On Day 6, 1 h after administration of the test drugs, the animals (fasted for 18 h) were anaesthetized using pentobarbitone (35 mg/kg, i.p.), the abdomen was opened and pylorus ligation was done without causing any damage to its blood supply. The stomach was replaced carefully and the abdomen closed in layers. The animals were deprived of water during the postoperative period and were sacrificed with an overdose of ether after 4 h. Stomachs were dissected out and the contents collected for estimation of biochemical parameters. Ulcer index was calculated as described in the CRS group.
Aspirin (ASP)-induced ulcers: ASP at a dose of 200 mg/kg (20 mg/ml suspension in 1% CMC) was administered orally to 18 h-fasted animals, 1 h after administration of the test drug on Day 6. The ulcers were scored after 4 h. The stomach was taken out and cut open along the greater curvature and ulcers were scored by a person unaware of the experimental protocol in the glandular portion of the stomach. Ulcer index was calculated as described in the CRS group.
Ethanol (EtOH)-induced ulcers: The test drugs were administered in the same dose and duration as mentioned above. One hour after the administration of the last dose of test drugs to 18 h-fasted rats on Day 6, gastric ulcers were induced by administering EtOH (95%, 1 ml/200 g). The animals, 1 h after administration of EtOH, were sacrificed by cervical dislocation and the stomach was taken out and incised along the greater curvature and examined for ulcers. The ulcer index was scored based upon the product of the length and width of the ulcers present in the glandular portion of the stomach (mm2/ rat).
Statistical analysis for the above models was done by using one-way analysis of variance (ANOVA) followed by Dunnett's multiple comparisons test. The difference were considered to be significant when P<0.05.
Gastric secretion study
The gastric juice was collected 4 h after PL and centrifuged for 5 min at 2000 rpm and the volume of the supernatant was expressed as ml/100g, body weight. Total acid output was determined by titrating with 0.01 N NaOH, using phenolphthalein as indicator and was expressed as µEq/4h. Peptic activity was determined using hemoglobin as substrate and was expressed as µmol of tyrosine/4 h.[12] Dissolved mucosubstances were estimated in the 90% alcoholic precipitate of the gastric juice. The precipitate thus obtained was either dissolved in 1 ml of 0.1 N NaOH or 1 ml of 0.1 N H2SO4. The former was used for the estimation of protein,[12] total hexoses, hexosamine and fucose, while the latter was used for the estimation of sialic acid.[13] The results are expressed in µg/ml. The ratio of total carbohydrate (TC) (sum of total hexoses, hexosamine, fucose and sialic acid) to protein (P) has been taken as the index of mucin activity.[14] DNA content was estimated and expressed as mg/ml gastric juice.[15]
Estimation of mucosal glycoproteins
Samples of gastric mucosal scraping were homogenized in distilled water and treated with 90% ethanol. The carbohydrates and the proteins in the samples were estimated using the methods described above for gastric juice contents.[16]
Cell proliferation
Mucosal scraping was homogenized in 2.5 ml of ice-cold 0.6 N perchloric acid (PCA). DNA[17] and protein,[13] were then estimated. Cell proliferation was expressed as mg DNA/ mg protein.
Estimation of free radical generation
The fundus of the stomach was homogenized (5%) in ice-cold 0.9% saline with a Potter - Elvehjem glass homogeniser for 30 sec. The homogenate was used for the following estimations.
Lipid peroxidase (LPO) activity: LPO product malondial-dehyde (MDA) was estimated using 1,1,3,3-tetraethoxypropane as the standard and was expressed as nmoles/g wet tissue.[18]
Superoxide dismutase (SOD) activity: SOD was estimated by following the procedure of Kakkar and associates, 1984.[19] The inhibition of the reduction of nitro blue tetrazolium (NBT) to blue-colored formozan in the presence of phenazine metha sulphate (PMS) and NADH was measured at 560 nm using n-butanol as blank. One unit of enzyme activity was defined as the amount of enzyme that inhibits the rate of reaction by 50% in 1 min under the defined assay conditions and the result has been expressed as units (U) of SOD activity/g wet tissue.
Catalase (CAT) activity: Decomposition of H2O2 in presence of catalase was followed at 240 nm.[20] One unit (U) of CAT was defined as the amount of enzyme required to decompose 1 m mol of H2O2 per min, at 25o C and pH 7.0. Result was expressed as U of CAT activity/g wet tissue.
Estimation of nitric oxide: Nitric oxide levels were estimated by the Griess reaction method[21] spectrophotometrically. Result was expressed as µmol/g wet tissue.
Statistical analysis for the above estimations was done by unpaired 't' test when control and diabetes groups were compared. One-way analysis of variance (ANOVA) followed by Dunnett's test was used for multiple comparisons. The differences were considered to be significant when P<0.05.

 » Results Top

Acute toxicity study: The result of the acute oral administration of PMS in various doses of 500, 1000, 2000, 4000 and 8000 mg/kg indicated no mortality up to 7 days after treatment.
Effect on blood glucose: PMS (500, 750 and 1000 mg/kg) dose-dependently decreased the blood glucose levels in both NR and NIDDM rats. The effect was comparable to the oral hypoglycemic drug, glibenclamide (NR 26.6% decrease and NIDDM 42.9% decrease). However, SFT did not show any effect on blood glucose level both per se as well as in NIDDM rats [Table - 1].
Ulcer-protective effects: NIDDM rats showed increased propensity to ulceration in all models of rat gastric ulcers (156.1 to 193.4% increase, P<0.05). PMS showed more ulcer protective activity in NIDDM rats in various ulcer models (25.8 to 44.5% protection) as compared to NR rats (3.1 to 16.5%), while SFT showed significant ulcer-protective effect both in NR and NIDDM rats. Glibenclamide (GLC), like PMS, did not show any ulcer-protective activity in NR rats but it reversed the increased propensity to ulceration in NIDDM rats [Table - 2] and [Table - 3].
Effect on gastric juice and mucosal parameters: NIDDM rats showed a tendency to increase gastric mucosal offensive acid-pepsin secretion (acid output- 11.8% increase; peptic output-11.5% increase) but defensive mucin secretion was decreased significantly as indicated by decrease in TC: P ratio (35.7% decrease, P<0.05). NIDDM rats also showed an increase in gastric mucosal cell shedding (as indicated by an increase in DNA content in gastric juice, 29 % increase, P<0.05) [Table - 4], a decrease in mucosal glycoproteins (28.2% decrease, P<0.05) with little or no effect on cell proliferation [Table - 5]. PMS treatment in NIDDM rats reversed the increased output of acid (16.1% reversal) and pepsin (15% reversal), decreased cell shedding (27.5 % reversal), enhanced mucin (27.8 % reversal) and mucosal glycoproteins (28.6 % reversal) without any effect on cell proliferation. Sucralfate (SFT), an ulcer-protective drug, did not show any effect on acid output but it significantly decreased the peptic output. It also increased the mucin secretion and mucosal glycoproteins and decreased cell shedding in NIDDM rats [Table - 4] and [Table - 5]. Standard oral anti-diabetic drug, GLC did not show any effect on acid-pepsin secretion but it prevented the decrease in mucin secretion and mucosal glycoproteins and increase in DNA content in gastric juice in NIDDM rats without any effect on cell proliferation [Table - 4] and [Table - 5].
Effect on free radicals: Oxidative free radicals LPO and NO levels were increased significantly both in CRS and NIDDM rats. Both LPO and NO were further increased in NIDDM-CRS rats when compared to NIDDM rats. Both PMS and GLC tended to reverse or reversed these enhanced free radicals in NIDDM-CRS rats [Table - 6].
Effect on antioxidant enzymes: Antioxidant enzymes SOD and CAT were significantly decreased in NIDDM rats. SOD level was increased but CAT level was decreased in NR-CRS rats [Table - 4]. However, both SOD and CAT were not affected further in NIDDM-CRS rats compared to the NIDDM group. Both PMS and GLC treatments significantly reversed SOD and CAT levels in NIDDM-CRS rats [Table - 6].

 » Discussion Top

Our present study showed that gastric ulcers induced by various (physical and chemical) agents were aggravated in STZ-induced NIDDM rats. This confirmed the earlier observations where increased propensity to ulceration in both experimental and clinical diabetes was reported.[2] The increased susceptibility to ulceration could be due to back diffusion of hydrogen ions in the stomach of diabetic rats, which played an important role in the formation of acute hemorrhagic ulcers.[2] Gastric ulcers have multiple etiopathogenesis. Ulcers caused by ethanol are due to superficial damage to mucosal cells[22] and damage by NSAIDs are due to a decrease in PG synthesis, and ulcers due to stress are due to both physiological and psychological factors and those by pyloric ligation are due to increased accumulation of gastric acid and pepsin leading to auto digestion of the gastric mucosa.[3]
Mucus is secreted by the mucus neck cells and coats the gastric mucosa, thereby preventing physical damage and back diffusion of hydrogen ions. Even though the causative factors of ulcerogenesis may be different, the net imbalance in offensive and defensive factors brought about by these changes, is thought to be the detrimental factor in ulcerogenesis.[3] The decreased mucin secretion in NIDDM rats indicates the decreased ability of the mucosal membrane to protect the mucosa from physical damage and back diffusion of hydrogen ions. The decrease in the glycoprotein content of the gastric mucosa[18] further proved the decreased ability of the gastric mucosa to withstand the offensive onslaught.
The decrease in the DNA content of the gastric mucosa indicates decreased cell shedding and increased lifespan of cells and increase in mucosal resistance.[15] NIDDM rats showed a tendency to increase acid-pepsin secretion and increased cell shedding (in terms of DNA content of gastric juice) and decreased mucosal defensive mucin secretion and mucosal glycoproteins (in terms of TC:P ratio, a reliable index of both mucin secretion and mucosal glycoproteins).[3] Treatment with both PMS and GLC reversed the NIDDM-induced acute adverse effect on the above parameters thus indicating the deleterious effects of diabetes and its reversal by hypoglycemic agents.
Reactive oxygen species (ROS) are generated through numerous normal metabolic processes and are needed for normal functioning of the organism. Various antioxidant enzymes like SOD, CAT and glutathione peroxidase (GPX) control their accumulation.[23] Any imbalance in the activity of these enzymes normally leads to faulty disposal of free radicals and its accumulation. These ROS are responsible for the oxidation of tissues leading to lipid peroxidation and tissue damage. Oxidative damage is considered to be an important factor in the pathogenesis of ulcers as evidenced in different experimental and clinical models. Gastric mucosal LPO has been reported to increase in CRS-induced gastric ulcers[4] and there are reports which indicated an increase in the erythrocytic LPO level in STZ-induced diabetes.[4],[24],[25] In our present work, we also observed an increase in the oxidative free radicals, lipid peroxides and nitric oxide in CRS and NIDDM rats, with a further increase when CRS was given to NIDDM rats. This could be due to an increase in the generation of ROS leading to oxidative damage. Normally, the increase in damage due to O2- is contained by dismutation with SOD.[23] SOD converts the reactive O2 to H2O2, which if not scavenged by the CAT causes lipid peroxidation by an increase in the generation of hydroxyl radicals.[26] Hence, a decrease in SOD and CAT levels in NIDDM rats may lead to an increase in the accumulation of these reactive products and LPO resulting in tissue damage. The above effect could be further aggravated by the decreased activity of CAT during stress.[27] Treatment with PMS and GLC both reversed these oxidative changes induced by NIDDM and stress. The decrease in ulcer index could be due to concomitant decrease in LPO, NO and an increase in SOD and CAT as seen in NIDDM-CRS rats.
Thus, the increased propensity to ulceration as found in NIDDM rats could be due to an increase in offensive acid-pepsin secretion and free radicals along with a decrease in defensive mucosal factors like mucin secretion, mucosal glycoproteins, lifespan of mucosal cells and antioxidant enzymes. Both PMS and GLC (a known oral hypoglycemic agent) significantly decreased the blood glucose levels in NR and NIDDM rats and showed significant ulcer-protective effect in NIDDM rats but not in NR rats. This could be due to the correction of blood glucose level by PMS and GLC, which in turn could have caused the reversal of the diabetes-associated changes on mucosal offensive and defensive factors. The standard anti-ulcer drug, SFT decreased the ulceration in all ulcers models in both NR and NIDDM rats by virtue of its various effects on mucosal offensive and defensive factors. The maintenance of blood glucose level at a nearly normal level could thus possibly protect the NIDDM patient from peptic ulceration.

 » Acknowledgement Top

RKG is thankful to ICMR for grant-in-aid. 

 » References Top

1.Takehara K, Tashima K, Takeuchi K. Alterations in duodenal bicarbonate secretion and mucosal susceptibility to acid in diabetic rats. Gastroenterology 1997;112:418-29.  Back to cited text no. 1    
2.Takeuchi K, Ushima K, Ohuchi T, Okabe S. Induction of gastric lesions and hypoglycemic responses by food deprivation in streptozotocin-diabetic rats. Dig Dis Sci 1994;39:626-34.  Back to cited text no. 2    
3.Goel RK, Bhattacharya SK. Gastroduodenal mucosal defense and mucosal protective agents. Indian J Exp Biol 1991;29:701-14.  Back to cited text no. 3  [PUBMED]  
4.Sairam K, Rao ChV, Babu MD, Goel RK. Prophylactic and curative effects of Bacopa monniera in gastric ulcer models. Phytomedicine 2001;86:423-30.  Back to cited text no. 4    
5.Dorababu M, Prabha T, Priyambada S, Agrawal VK, Aryya NC, Goel RK. Effect of Bacopa monniera and Aazadirachta indica on gastric ulceration and healing in experimental NIDDM rats. Indian J Exp Biol 2004;42:389-97.  Back to cited text no. 5  [PUBMED]  
6.Sapha, Bose. Clinical observation of antidiabetic properties of Pterocarpus marsupium, Eugenia jambolona. J Indian Med Assoc 1956;27:388-90.  Back to cited text no. 6    
7.Shah DS. A preliminary study of indigenous hypoglycemic action of heart wood of Pterocarpus marsupium Roxb. Indian J Med Res 1967;55:166-8.  Back to cited text no. 7  [PUBMED]  
8.Pandey MC, Sharma PV. Hypoglycemic effect of bark of Pterocarpus marsupium Roxb. (Bijak)- A clinical study. Med Surg 1975;15:86-8.  Back to cited text no. 8    
9.Stanley MP, Venugopal PM, Pari L. Hypoglycemic activity of Syzigium cumini seeds: Effects on lipid peroxidation in alloxan diabetic rats. J Ethnopharmacol 1998;61:1-7.  Back to cited text no. 9    
10.Srinivasan PS, Hakim ZS, Santani DD, Goyal RK. Effect of chronic treatment with amlodipine in streptozotocin-induced diabetic and spontaneous hypertensive rats. Pharmacol Res 1997;35:423-8.  Back to cited text no. 10    
11.Sanyal AK, Panday BL, Goel RK. The effect of a traditional preparation of Copper, Thamrabasma, on experimental ulcers and gastric secretion. J Ethnopharmacol 1982;5:79-89.  Back to cited text no. 11    
12.Debnath PK, Gode KD, Das DG, Sanyal AK. Effect of propranolol on gastric secretion in albino rats. Br J Pharmacol 1974;51:213-6.  Back to cited text no. 12  [PUBMED]  
13.Lowry OH, Roseborough NJ, Farr AL, Randall RJ. Protein measurement with folin phenol reagent. J Biol Chem 1951;193:265-75.  Back to cited text no. 13    
14.Sanyal AK, Mitra PK, Goel RK. A modified method to estimate dissolved mucosubstances in gastric juice. Indian J Exp Biol 1983;21:78-80.  Back to cited text no. 14  [PUBMED]  
15.Mukhopadhyaya K, Bhattacharya D, Chakrabarti A, Goel RK, Sanyal AK. Effect of banana powder (Musa sapientum var. paradisiaca) on gastric mucosal shedding. J Ethnopharmacol 1987;21:11-9.  Back to cited text no. 15    
16.Goel RK, Maiti RN, Mukhopadhyaya K. Effect of Tamrabhasma, an Indian indigenous preparation of copper, on rat gastric mucosal resistance. Indian J Exp Biol 1994;32:559-61.  Back to cited text no. 16  [PUBMED]  
17.Goel RK, Gupta S, Shankar R, Sanyal AK. Antiulcerogenic effect of banana powder (Musa sapientum var. paradisiaca) and its effect on mucosal resistance. J Ethnopharmacol 1986;18:33-44.  Back to cited text no. 17  [PUBMED]  
18.Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351-8.  Back to cited text no. 18  [PUBMED]  
19.Kakkar P, Das B, Viswanathan PN. A modified spectrophotometric assay of superoxide dismutase. Indian J Biochem Biophys 1984;21:130-2.  Back to cited text no. 19  [PUBMED]  
20.Hans Luck. Catalase spectrometric method. Methods in Enzymatic analysis. New York: Academic press 1963.  Back to cited text no. 20    
21.Miranda KM, Espey MG, Wink DA. A rapid, simple specreophotometric method for simultaneous detection of nitrate and nitrite. Nitric Oxide 2001;5:62-5.  Back to cited text no. 21    
22.Miller TA, Henagan JM. Indomethacin decreases resistance of gastric barrier to disruption by alcohol. Dig Dis Sci 1984;29:141-9.  Back to cited text no. 22  [PUBMED]  
23.Fridovich I. Biological effects of the superoxide radicals. Arch Biochem Biophys 1986;247:1-11.  Back to cited text no. 23  [PUBMED]  
24.Garg MC, Ojha S, Bansal DD. Antioxidant status of streptozotocin diabetic rats. Indian J Exp Biol 1996;34:264-6.  Back to cited text no. 24  [PUBMED]  
25.Memisogullari R, Taysi S, Bakan E, Capoglu I. Antioxidants status and lipid peroxidation in type II diabetes mellitus. Cell Biochem Funct 2003;21:291-6.  Back to cited text no. 25  [PUBMED]  [FULLTEXT]
26.Das D, Bandyopadhyay D, Bhattacharya M, Banarjee RK. Hydroxyl radical is the major causative factor in stress-induced gastric ulceration. Free Radic Biol Med 1997;23:8-18.  Back to cited text no. 26    
27.Boyd SC, Sasame HA, Boyd MR. Gastric glutathione depletion and acute ulcerogenesis by diethylmaleate given subcutaneously to rats. Life Sci 1981;28:2987-92.  Back to cited text no. 27  [PUBMED]  
Print this article  Email this article


Site Map | Home | Contact Us | Feedback | Copyright and Disclaimer | Privacy Notice
Online since 20th July '04
Published by Wolters Kluwer - Medknow