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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">AJMB</journal-id>
			<journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
			<issn pub-type="ppub">2008-2835</issn>
			<issn pub-type="epub">2008-4625</issn>
			<publisher>
				<publisher-name>Avicenna Research Institute</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="publisher-id">AJMB-3-31</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Original Article</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Protective Effects of <italic>Capparis zeylanica</italic> Linn. Leaf Extract on Gastric Lesions in Experimental Animals</article-title>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author" corresp="yes">
					<name>
						<surname>Sini</surname>
						<given-names>Karanayil R.</given-names>
					</name>
					<xref ref-type="aff" rid="AF0001">1</xref>
					<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Sinha</surname>
						<given-names>Barij N.</given-names>
					</name>
					<xref ref-type="aff" rid="AF0002">2</xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Rajasekaran</surname>
						<given-names>Aiyolu</given-names>
					</name>
					<xref ref-type="aff" rid="AF0003">3</xref>
				</contrib>
			</contrib-group>
			<aff id="AF0001">
				<label>1</label>Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Palakkad, India</aff>
			<aff id="AF0002">
				<label>2</label>Department of Pharmaceutical Sciences, Jharkhand, India</aff>
			<aff id="AF0003">
				<label>3</label>KMCH College of Pharmacy, Coimbatore, India</aff>
			<author-notes>
				<corresp id="cor1">
				<label>&#x002A;</label>
				<bold>Corresponding author:</bold> Karanayil R Sini, M.Pharm., Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Palakkad, India. <bold>E-mail:</bold> <email xlink:href="sinikaranayil@gmail.com">sinikaranayil@gmail.com</email>
				</corresp>
			</author-notes>
			<pub-date pub-type="ppub">
				<season>January-March</season>
				<year>2011</year>
			</pub-date>
			<volume>3</volume>
			<issue>1</issue>
			<fpage>31</fpage>
			<lpage>35</lpage>
			<history>
				<date date-type="received">
					<day>11</day>
					<month>10</month>
					<year>2010</year>
				</date>
				<date date-type="accepted">
					<day>12</day>
					<month>01</month>
					<year>2011</year>
				</date>
			</history>
			<permissions>
			<copyright-statement>Copyright &#x00A9; 2011 Avicenna Research Institute</copyright-statement>
				<copyright-year>2011</copyright-year>
				<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">
					<p>This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.</p>
				</license>
			</permissions>
			<abstract>
				<p>The aim of the study was to study the anti-ulcer activity of the methanolic extract of the leaves of <italic>Capparis zeylanica</italic> Linn on experimental animal models. The methanol extract of <italic>Capparis zeylanica</italic> Linn. leaves was investigated for anti-ulcer activity against aspirin plus pylorus ligation induced gastric ulcer in rats. HCl-Ethanol induced ulcer in mice and indomethacin induced ulcer in rats at 200 <italic>mg/kg</italic> body weight <italic>p.o</italic>. A significant (p&#x003C;0.01, p&#x003C;0.001) anti-ulcer activity was observed in all the models. Pylorus ligation showed significant (p&#x003C;0.01) reduction in gastric volume, free acidity and ulcer index as compared to control. It also showed 88.5% ulcer inhibition in HCl-ethanol induced ulcer and 83.78% inhibition in indomethacin induced ulcer.</p>
			</abstract>
			<kwd-group>
				<kwd>Aspirin</kwd>
				<kwd>Indomethacin</kwd>
				<kwd>Rats</kwd>
				<kwd>Plant extract</kwd>
				<kwd>Mice</kwd>
				<kwd>Gastric ulcer</kwd>
			</kwd-group>
		</article-meta>
	</front>
	<body>
		<sec id="S0001" sec-type="intro">
			<title>Introduction</title>
			<p>The exact pathogenesis of ulcer continues to elude scientists and medical researchers, but a common ground has been proposed. Ulcers are produced when any factor causes an imbalance between the protective factors (mucus and bicarbonate) and aggressive factors (acid and pepsin) in the stomach. The disease has been reported to have high recurrence and mortality rates especially in complicated cases (<xref ref-type="bibr" rid="CIT0001">1</xref>, <xref ref-type="bibr" rid="CIT0002">2</xref>). Such factors could range from natural causes (gastric cancer), infections (<italic>Helicobacter pylori-H.pylori</italic>) and lifestyle (drugs, non steroidal anti-inflammatory agents, alcohol, stress and cigarette smoking) (<xref ref-type="bibr" rid="CIT0003">3</xref>, <xref ref-type="bibr" rid="CIT0004">4</xref>).</p>
			<p>Current treatment of ulcers in developing countries has been largely suppression of pain, with little or no strategy aimed at a cure. Herbal medicine is fast emerging as an alternative treatment to available synthetic drugs for treatment of ulcer possibly due to lower costs, availability, fewer adverse effects and perceived effectiveness.</p>
			<p>Gastric ulcer, one of the most widespread, is believed to be due to an imbalance between aggressive and protective factors (<xref ref-type="bibr" rid="CIT0005">5</xref>). The gastric mucosa is continuously exposed to potentially injurious agents such as acid, pepsin, bile acids, food ingredients, bacterial products (<italic>H. pylori</italic>) and drugs (<xref ref-type="bibr" rid="CIT0006">6</xref>). These agents have been implicated in the pathogenesis of gastric ulcer including enhanced gastric acid and pepsin secretion, inhibition of prostaglandin synthesis and cell proliferation growth, diminished gastric blood flow and gastric motility (<xref ref-type="bibr" rid="CIT0007">7</xref>).</p>
			<p>The goals of treating peptic ulcer disease are to relieve pain, heal the ulcer and prevent ulcer recurrence. Currently there is no cost-effective treatment that meets all these goals. Hence, efforts are on to find a suitable treatment from natural product sources.</p>
			<p>Many tropical herbs have been scientifically reported to possess potent anti-ulcer activity (<xref ref-type="bibr" rid="CIT0008">8</xref>&#x2013;<xref ref-type="bibr" rid="CIT0010">10</xref>). <italic>Capparis zeylanica</italic> Linn. (<italic>C.zeylanica</italic>) commonly known as &#x2018;<italic>Asadhua</italic>&#x2019; in Oriya and &#x2018;<italic>Ardanda</italic>&#x2019; in Hindi is a branched thorny, sub-scandent climbing shrub found throughout India (<xref ref-type="bibr" rid="CIT0011">11</xref>). It has been used as a &#x2018;Rasayana&#x2019; drug in the traditional Ayurvedic system of medicine. In Northern India, the leaves are widely used as counter-irritant, febrifuge and as a cataplasm in swellings (<xref ref-type="bibr" rid="CIT0012">12</xref>), boils and piles (<xref ref-type="bibr" rid="CIT0013">13</xref>). Traditionally it is also used as antidote to snake bite, to cure swelling of testicle, small pox, boils, cholera, colic, hemiplegia, neuralgia, sores, pneumonic and pleurisy (<xref ref-type="bibr" rid="CIT0014">14</xref>).</p>
			<p>Whole plant showed the presence of saponin, p-hydroxybenzoic, syringic, vanillic, ferrulic and p-coumanic acid. Leaves and seeds showed presence of &#x03B2;-carotene, thioglycoside, glycocapparin, n-tricortane, &#x03B1;-amyrin and fixed oil where as root bark showed presence of an alkaloid, a phytosterol, a water soluble acid and a mucilaginous substance (<xref ref-type="bibr" rid="CIT0015">15</xref>, <xref ref-type="bibr" rid="CIT0016">16</xref>)
 <italic>. Capparis</italic> species has been reported to have antihelmintic, anti microbial and anti inflammatory activities (<xref ref-type="bibr" rid="CIT0017">17</xref>, <xref ref-type="bibr" rid="CIT0018">18</xref>). The dried leaves of few species from the genus <italic>Capparis</italic>, steeped in vinegar were reported to be used for treatment of ulcers (<xref ref-type="bibr" rid="CIT0019">19</xref>).</p>
		</sec>
		<sec id="S0002" sec-type="materials|methods">
			<title>Materials and Methods</title>
			<sec id="S20003">
				<title>Plant collection</title>
				<p>The fresh leaves of <italic>C.zeylanica</italic> Linn (Capparidaceae), collected at the flowering stage in the month of March 2010 from the tribal areas of Palakkad district, Kerala state, South India were authenticated by the Botanical survey of India, Combatore, Tamilnadu (BSI). A voucher specimen (no.BSI/SRC/5/ 23/10-11/Tech-565) is deposited in the departmental herbarium.</p>
			</sec>
			<sec id="S20004">
				<title>Preparation of extract</title>
				<p>The leaves of <italic>C.zeylanica</italic> were shade dried and reduced to coarse powder in a mechanical grinder. The powdered material obtained was soxhlet extracted using methanol and the extract obtained was evaporated at 45<italic>&#x00B0;C</italic> to get a semisolid mass. The extract thus obtained was subjected to phytochemical analysis. The percentage yield of methanolic extract was found to be 36.50% <italic>w/w</italic> and was used for further studies (<xref ref-type="bibr" rid="CIT0020">20</xref>).</p>
			</sec>
			<sec id="S20005">
				<title>Animals</title>
				<p>Healthy adult albino rats of male sex weighing between 100-180 <italic>g</italic> obtained from Kerala Veterinary College, Mannuthy, Kerala. The animals were housed under standard conditions of light/dark at 12/12 <italic>hr</italic> cycle. They were fed with commercial pellet diet and water <italic>ad libitum</italic>. All animal experiments were carried out in accordance with guidelines of CPCSEA and the study was approved by the Institutional Animal Ethics Committee (NCP/IAEC/CLEAR/05/03/2007-08).</p>
			</sec>
			<sec id="S20006">
				<title>Acute oral toxicity studies</title>
				<p>A safe oral dose of the extract was determined by acute oral toxic class method of Organization of Economic Co-operation and Development (OECD) as per 423 guidelines (<xref ref-type="bibr" rid="CIT0021">21</xref>).</p>
			</sec>
			<sec id="S20007">
				<title>Anti-ulcer activity</title>
				<p>Three models (ethanol, aspirin, and indo-methacin) with effective induction of ulcer experimentally in rats were employed to evaluate the anti-ulcer activity of the methanolic extract of <italic>C.zeylanica</italic>. All the rats used were fasted for 18 <italic>hr</italic> hours but were given water <italic>ad libitum</italic> till the start of the experiment.</p>
			</sec>
			<sec id="S20008">
				<title>Ethanol-induced ulcer</title>
				<p>Thirty fasted animals were used in three groups of six animals each. Groups A and B received 5 <italic>ml/kg</italic> (<italic>p.o</italic>) of 3% Tween 80 (negative control) and 100 <italic>mg/kg p.o</italic>. sucralfate (Antepsin<sup>&#x00AE;</sup>) while rats in group C were given 200 <italic>mg/kg</italic> of MECZ orally (<italic>p.o</italic>), respectively. After 1 <italic>hr</italic> all animals received 1 <italic>ml/kg</italic> of 80% ethanol (Sigma-Aldrich, Germany) orally. The rats were sacrificed with chloroform (Sigma-Aldrich, Germany) anaesthesia after 1 <italic>hr</italic>. The stomachs were isolated, washed gently under clean flowing water and cut open along the greater curvature. The stomachs were then fixed in 10% formalin and craters observed and ulcer scores were recorded (<xref ref-type="bibr" rid="CIT0010">10</xref>).</p>
			</sec>
			<sec id="S20009">
				<title>Aspirin-induced ulcer</title>
				<p>The wistar albino rats weighing 100-200 <italic>g</italic> of either sex were divided into three groups, each group consists of 6 animals. All the animals received 200 <italic>mg/kg</italic> of aspirin once daily for three days. Group1 served as control received 5 <italic>ml/kg</italic> (<italic>p.o</italic>) of 3% Tween 80, group 2 treated with 50 <italic>mg/kg</italic> (<italic>p.o</italic>) ranitidine as standard and group 3 treated with 200 <italic>mg/kg</italic> (<italic>p.o</italic>) methanol extract of <italic>C. zeylanica</italic>. On the fourth day pylorus part was ligated following 36 <italic>hr</italic> fasting (<xref ref-type="bibr" rid="CIT0022">22</xref>). Four <italic>hrs</italic> after the pylorus ligation the animals were sacrificed by decapitation. The stomach was opened and the ulcer index was determined (<xref ref-type="bibr" rid="CIT0023">23</xref>). The gastric contents were titrated against 0.01 <italic>N</italic> NaOH to determine the free acidity and total acidity (<xref ref-type="bibr" rid="CIT0024">24</xref>).</p>
			</sec>
			<sec id="S20010">
				<title>Indomethacin-induced ulcer</title>
				<p>Animals (three groups of six rats each) in groups received 5 <italic>ml/kg</italic> (<italic>p.o</italic>) of 3% Tween 80, Omeprazole 20 <italic>mg/kg</italic> (<italic>p.o</italic>) and 200<italic>mg/kg</italic> (<italic>p.o</italic>) of extract, respectively. After 30 <italic>min</italic>, indomethacin 40 <italic>mg/kg</italic> (<italic>p.o</italic>) was administered to each rat. After 8 <italic>hr</italic> of drug treatment, stomachs were isolated, cut and ulcers counted as before (<xref ref-type="bibr" rid="CIT0025">25</xref>).</p>
			</sec>
			<sec id="S20011">
				<title>Statistical analysis</title>
				<p>Ulcer indices were shown as the mean standard error of mean and level of ulcer protection presented as percentage inhibition. The statistical analysis was carried out using one-way ANOVA followed by Dunnetts multiple comparisons using graph pad in stat3.</p>
			</sec>
		</sec>
		<sec id="S0012" sec-type="results">
			<title>Results</title>
			<p>Preliminary phytochemical screening of the Methanolic Extract of <italic>C.zeylanica</italic> (MECZ) revealed that presence of alkaloids, flavonoids, carbohydrates, glycosides, tannins, terpenoids, phenols and absence of fixed oils and steroids. No visible change was observed in any animal and all survived till 24 <italic>hr</italic>; thus based on preliminary study, different extracts of <italic>C.zeylanica</italic> were found to be safe for further biological studies, as no lethality was observed at 1000 <italic>mg/kg</italic> (<italic>p.o</italic>) in mice. Acute toxicity results showed that the LD50 was greater than 5000 <italic>mg/kg</italic>.</p>
			<p>In aspirin plus pylorus ligation induced gastric ulcer, the methanol extract of <italic>C.zeylanica</italic> showed significant reduction in gastric volume, free acidity and ulcer score (% ulcer inhibition 57.83% as compared to control (<xref ref-type="table" rid="T0001">Table 1</xref>). From <xref ref-type="table" rid="T0002">Table 2</xref> it can be observed that the number of lesions in HCl-ethanol induced peptic ulcer group was significantly high and the methanol extract of <italic>C.zeylanica</italic> pre-treated group depicted marked reduction (p&#x003C;0.01) in gastric lesion (% ulcer inhibition 88.5%) as compared to control (<xref ref-type="table" rid="T0002">Table 2</xref>).
</p>
			<table-wrap id="T0001">
			<label>Table 1</label>
				<caption>
					<p>Effect of methanol extract of <italic>C. zeylanica</italic> (MECZ) on gastric secretion, acidity, pH and ulcer score in aspirin plus pylorus ligated rats</p>
				</caption>
				<table frame="hsides" rules="groups">
					<thead>
						<tr>
							<th align="left">Treatment</th>
							<th align="center">Volume of gastric secretion (100 <italic>ml/g</italic>)</th>
							<th align="center">Free acidity (eq/100<italic>mg</italic>)</th>
							<th align="center">Total acidity (eq/100<italic>mg</italic>)</th>
							<th align="center">pH</th>
							<th align="center">Ulcer score</th>
							<th align="center">Ulcer inhibition (%)</th>
						</tr>
					</thead>
					<tbody>
						<tr>
							<td align="left">
								<bold>3%Tween 80</bold>
							</td>
							<td align="center">2.669&#x00B1;0.022</td>
							<td align="center">227.00&#x00B1;4.124</td>
							<td align="center">592.00&#x00B1;6.500</td>
							<td align="center">2.200&#x00B1;0.143</td>
							<td align="center">3.7&#x00B1;0.100</td>
							<td align="center">---</td>
						</tr>
						<tr>
							<td align="left">
								<bold>Ranitidine 50</bold>
							</td>
							<td align="center">1.336&#x00B1;0.142</td>
							<td align="center">147.55&#x00B1;11.475<xref ref-type="table-fn" rid="TF0002">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">489.22&#x00B1;19.936<xref ref-type="table-fn" rid="TF0001">&#x002A;</xref>
							</td>
							<td align="center">3.165&#x00B1;0.112<xref ref-type="table-fn" rid="TF0001">&#x002A;</xref>
							</td>
							<td align="center">0.166&#x00B1;0.155<xref ref-type="table-fn" rid="TF0002">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">95.51</td>
						</tr>
						<tr>
							<td align="left">
								<bold>MECZ 200</bold>
							</td>
							<td align="center">0.987&#x00B1;0.079<xref ref-type="table-fn" rid="TF0002">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">141.00&#x00B1;9.582<xref ref-type="table-fn" rid="TF0002">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">532.27&#x00B1;9.741</td>
							<td align="center">2.223&#x00B1;0.110</td>
							<td align="center">1.567&#x00B1;0.200<xref ref-type="table-fn" rid="TF0002">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">57.83</td>
						</tr>
					</tbody>
				</table>
				<table-wrap-foot>
					<fn>
						<p>n= 6, Values are expressed as mean &#x00B1; SEM, p&#x003C;0.05 when compared with control</p>
					</fn>
					<fn id="TF0001">
					<label>&#x002A;</label>
						<p>p&#x003C;0.05, Significant as compared with control group</p>
					</fn>
					<fn id="TF0002">
					<label>&#x002A;&#x002A;</label>
						<p>p&#x003C;0.01 when compared with control</p>
					</fn>
				</table-wrap-foot>
			</table-wrap>
			<table-wrap id="T0002">
			<label>Table 2</label>
				<caption>
					<p>Effect of methanolic leaf extract of <italic>C. zeylanica</italic> (MECZ) on ethanol induced ulcer in rats</p>
				</caption>
				<table frame="hsides" rules="groups">
					<thead>
						<tr>
							<th align="left">Treatment</th>
							<th align="center">Dose (<italic>mg/kg</italic>)</th>
							<th align="center">Gastric lesion (Mean &#x00B1; SEM)</th>
							<th align="center">Percentage ulcer inhibition (%)</th>
						</tr>
					</thead>
					<tbody>
						<tr>
							<td align="left">
								<bold>Tween 80</bold>
							</td>
							<td align="center">5<italic>ml</italic>
							</td>
							<td align="center">21.367&#x00B1;2.407</td>
							<td align="center">----</td>
						</tr>
						<tr>
							<td align="left">
								<bold>Sucralfate</bold>
							</td>
							<td align="center">100</td>
							<td align="center">1.097&#x00B1;0.4627<xref ref-type="table-fn" rid="TF0004">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">94.86</td>
						</tr>
						<tr>
							<td align="left">
								<bold>MECZ</bold>
							</td>
							<td align="center">200</td>
							<td align="center">2.457&#x00B1;0.5333<xref ref-type="table-fn" rid="TF0004">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">88.50</td>
						</tr>
					</tbody>
				</table>
				<table-wrap-foot>
					<fn>
						<p>n= 6, Values are expressed as mean &#x00B1; SEM, p&#x003C;0.01 when compared with control</p>
					</fn>
					<fn id="TF0003">
					<label>&#x002A;</label>
						<p>p&#x003C;0.05, Significant as compared with control group</p>
					</fn>
					<fn id="TF0004">
					<label>&#x002A;&#x002A;</label>
						<p>p&#x003C;0.001 when compared with control</p>
					</fn>
				</table-wrap-foot>
			</table-wrap>
			<p>Results for indomethacin model can be viewed in <xref ref-type="table" rid="T0003">Table 3</xref>. There was an absolute production of severe ulcers in all the rats using this model and ulcer inhibition was seen in all the treatment groups. Ulcer inhibition was highest with 200 <italic>mg/kg</italic> MECZ (83.78%, p&#x003E;0.01) and lowest with Sucralfate (48.74%).
</p>
			<table-wrap id="T0003">
			<label>Table 3</label>
				<caption>
					<p>Effect of methanol extract of <italic>C. zeylanica</italic> (MECZ) on indomethacin induced ulcer in rats</p>
				</caption>
				<table frame="hsides" rules="groups">
					<thead>
						<tr>
							<th align="left">Treatment</th>
							<th align="center">Dose (<italic>mg/kg</italic>)</th>
							<th align="center">Mean ulcer index &#x00B1; SEM</th>
							<th align="center">Percentage ulcer inhibition (%)</th>
						</tr>
					</thead>
					<tbody>
						<tr>
							<td align="left">
								<bold>Tween 80</bold>
							</td>
							<td align="center">5 <italic>ml</italic>
							</td>
							<td align="center">3.7&#x00B1;0.4</td>
							<td align="center">---</td>
						</tr>
						<tr>
							<td align="left">
								<bold>Omeprazole</bold>
							</td>
							<td align="center">20</td>
							<td align="center">1.9&#x00B1;0.7<xref ref-type="table-fn" rid="TF0006">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">48.64</td>
						</tr>
						<tr>
							<td align="left">
								<bold>MECZ</bold>
							</td>
							<td align="center">200</td>
							<td align="center">0.6&#x00B1;0.2<xref ref-type="table-fn" rid="TF0006">&#x002A;&#x002A;</xref>
							</td>
							<td align="center">83.78</td>
						</tr>
					</tbody>
				</table>
				<table-wrap-foot>
					<fn>
						<p>n= 6, Values are expressed as mean &#x00B1; SEM, p&#x003C;0.01 when compared with control</p>
					</fn>
					<fn id="TF0005">
					<label>&#x002A;</label>
						<p>p&#x003C;0.05, Significant as compared with control group</p>
					</fn>
					<fn id="TF0006">
					<label>&#x002A;&#x002A;</label>
						<p>p&#x003C;0.001 when compared with control</p>
					</fn>
				</table-wrap-foot>
			</table-wrap>
		</sec>
		<sec id="S0013" sec-type="discussion">
			<title>Discussion</title>
			<p>The anti-ulcer activity of the methanol extract of <italic>C.zeylanica</italic> against ethanol, aspirin and indomethacin-induced ulcers was established in this study. Results of acute toxicity showed that the plant is safe as exemplified by its use as food in domestic and wild animals. The extract protected the stomach against ethanol&#x0027;s necrotic damage and its effect was more pronounced than sucralfate, a cytoprotective agent.</p>
			<p>Ethanol has been shown to increase the risk of ulcer in humans (<xref ref-type="bibr" rid="CIT0002">2</xref>), but produces potent ulceration in rats (<xref ref-type="bibr" rid="CIT0026">26</xref>). Ethanol challenge induces gastric injury due to production of oxygen free radicals leading to increased lipid peroxidation, which causes damage to cell and cell membrane presenting as red streaks of sores (<xref ref-type="bibr" rid="CIT0027">27</xref>). The protection by the extract of this type may suggest a possible cytoprotective mechanism of action.</p>
			<p>Indomethacin model produces its ulceration by mechanism well understood. It causes an inhibition of the production of endogenous cytoprotective prostaglandins (<xref ref-type="bibr" rid="CIT0028">28</xref>). However, with the inhibition of ulcer in this model by the extract, it is possible that the plant produces a cytoprotection similar to those of Omeprazole in the indomethacin model. The secondary metabolites identified may also have been responsible for the anti-ulcer activity of this plant as flavonoids have been reported to possess anti-ulcer activity in various experimental models of ulcers (<xref ref-type="bibr" rid="CIT0029">29</xref>).</p>
			<p>In aspirin plus pylorus ligation induced gastric ulcer model, the methanol extract of <italic>C. zeylanica</italic> reduced the gastric volume, free acidity and ulcer index thus showing the anti-secretory mechanism involved in the extracts for their anti-ulcerogenic activity. Ulcer index parameter was used for the evaluation of anti-ulcer activity since ulcer formation is directly related to factors such as gastric volume, free and total acidity. In case of vehicle control, aspirin plus pylorus ligation increased the acid secretion, which in turn caused increase in gastric volume, low pH, increased free and total acidity resulting into increase in ulcer index (<xref ref-type="bibr" rid="CIT0030">30</xref>).</p>
			<p>Ulcer protection may be attributed to any of these phytochemical constituents as flavonoids, tannins and saponins which have been shown to produce anti-ulcerogenic and anti-gastric activity (<xref ref-type="bibr" rid="CIT0031">31</xref>). However, until specific constituents are isolated and characterized, exact mechanism of action cannot be ascertained. Studies on the sub acute and chronic toxicity of the extract are however in progress.</p>
		</sec>
	</body>
	<back>
		<ack>
			<title>Acknowledgement</title>
			<p>The authors are grateful to staff of forest department, Attapady for their kind help during field visits and tribal people who shared their traditional knowledge regarding medicinal plants during our field visits.</p>
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