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  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2018-03-25</publicationDate>
    
        <volume>15</volume>
        <issue>1</issue>

 
    <startPage>01</startPage>
    <endPage>04</endPage>

	 
      <doi>10.13005/bbra/2602</doi>
        <publisherRecordId>29516</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">DPP-IV Inhibitory Potential of Methanolic Extract of Pueraria Tuberosa in Liver of Alloxan Induced Diabetic Model</title>

    <authors>
	 


      <author>
       <name>Shivani Srivastava</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Durgavati Yadav</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Yamini Bhusan Tripathi</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Medicinal Chemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, U.P, India.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">DPP-IV is usually found to be over expressed in many pathological conditions of Liver via disturbing immune system, lipid accumulation, ECM degradation etc.<b> </b>The main objective of this work was to explore the effect of methanolic extract of <em>Pueraria tuberosa </em>(PTME) against Alloxan induced liver damage with respect to its potential of inhibiting DPP-IV activity. PTME was prepared through continuous soxhlet extractor. Alloxan injections were given to the same age group with weight range of 80-100 g <em>Charles foster albino </em>male rats at the dosage of 120mg/kg bw.  Rats were divided into five groups. Group 1 was given with PTME dose of  20mg/100 g bw for 7 days, Group 2 for 14 days, Group 3 for 30 days, Group 4 for 40 days and Group 5 taken as an Alloxan control.  Animals were sacrificed at their respective time along with the normal rats. DPP-IV activity in liver homogenates were done through the kit based on fluorescence ELISA. After treatment with PTME (20 mg/100 g bw) at different time intervals, the alloxan induced stress enhanced DPP-IV activity in liver significantly decreased in a time dependent mannerin. This short study provides an idea, how PTME protects liver via its potential role as DPP-IV inhibitor. But it needs further deep study to reveal the overall mechanism at pathological, clinical and molecular basis in different models of liver diseases.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol15no1/dpp-iv-inhibitory-potential-of-methanolic-extract-of-pueraria-tuberosa-dc-in-liver-of-alloxan-induced-diabetic-model/</fullTextUrl>



      <keywords language="eng">
        <keyword>Alloxan; DPP-IV; Liver; PTME</keyword>
      </keywords>

  </record>
</records>