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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2016-02-05</publicationDate>
    
        <volume>4</volume>
        <issue>2</issue>

 
    <startPage>793</startPage>
    <endPage>796</endPage>

	    <publisherRecordId>18558</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Histopathologic study in jejunum portion of intestine by different doses of diclofenac sodium (NSAIDs) in mice models</title>

    <authors>
	 


      <author>
       <name>SARFARAZ H</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>FARAH K</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>N. GANESH</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Jawaharlal Cancer Hospital and Research Centre, Idgah Hills, Bhopal - 462 001 (India).</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Diclofenac (NSAIDs) is an inhibitor of cyclooxygnase. Receiving Diclofenac died prior of
completion of the study, exhibiting massive small intestinal ulceration and perforation. The only small
intestinal abnormality observed was diffuse hypermia. So we have put our efforts to rule out the toxic
menace of diclofenac in rodent’s (Swiss albino) by administrating different does ranging from 0.1mg/kg
body weight to 10mg/kg body weight the other doses are 0.3 mg/kg and 1mg/kg. The viable number of
crypt cells in jejunal portion of intestine also reduced with increasing doses. Villi and crypt morphology
and number were affected according to the dose concentration relatively higher doses induced higher
damage and lower doses with lower damage.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol4no2/histopathologic-study-in-jejunum-portion-of-intestine-by-different-doses-of-diclofenac-sodium-nsaids-in-mice-models/</fullTextUrl>



      <keywords language="eng">
        <keyword>Non-steroidal anti-inflammatory drug (NSAIDs); Diclofenac sodium; Swiss albino; intestinal cells; Crypt and Villi</keyword>
      </keywords>

  </record>
</records>