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  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2018-03-25</publicationDate>
    
        <volume>11</volume>
        <issue>1</issue>

 
    <startPage>325</startPage>
    <endPage>332</endPage>

	 
      <doi>10.13005/bpj/1376</doi>
        <publisherRecordId>19590</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Comparison of Rosiglitazone and Metformin in Genetically Obese and Diabetic db/db Mice and Streptozotocin-Induced Diabetic Rat Models.</title>

    <authors>
	 


      <author>
       <name>Kishor P. Patil</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Pankaj Kothavade</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Senior Scientist, Zydus Research Center, Ahmedabad - 382210, India.</affiliationName>
    

		
		<affiliationName affiliationId="2">Pharmacology Lab 1, Department of Pharmaceutical Sciences, Institute of Chemical Technology, Matunga, Mumbai-400019, India.</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Diabetes mellitus is a group of metabolic disorder which is characterized by high plasma glucose level and near or complete deficiency of insulin. It is a complex disorder, currently affecting 422 million people worldwide. This study was designed to compare the efficacy of rosiglitazone and metformin in db/db mice and STZ-induced rat models. Diabetes was induced by streptozotocin in rats. All the STZ-induced rats were orally administered with either rosiglitazone (10 mg/kg/day) or metformin (500 mg/kg/day) for 10 days. Groups of genetically diabetic <em>db/db</em> mice were orally administered with either rosiglitazone (5 mg/kg/day) or metformin (150 mg/kg/day) for 10 days. Fasting plasma glucose, serum insulin, body weight, cholesterol, triglyceride, serum glutamic pyruvic transaminase (SGPT) and serum glutamic-oxaloacetic transaminase (SGOT) were measured at 0, 5, 7 and 10 days after treatment using a Hitachi 7350 Auto analyzer. Serum insulin was measured p by enzyme-linked immunosorbent assay (ELISA). Our results indicated that fasting blood glucose levels in all the treatment groups were decreased substantially. A substantial decline in plasma glucose level was identified in rosiglitazone group (240.75 mg/dL ± 24.27, P&lt;0.05 vs control- 541.65 mg/dL) as compared to metformin group (304.35 mg/dL ±33. 34, P&lt;0.05) in db/db mice. A significant reduction in serum insulin was observed in rosiglitazone group (15.88 ng/mL ± 2.89, p&lt;0.05 vs control- 32.65 ng/mL) and cholesterol level (52.35 ± 5. 48 mg/dL, p&lt;0.05) compared with control (32.65 ng/mL ± 4.66 and 129.48 ± 15.82 mg/dL) in <em>db/db</em> mice. Moreover, significantly (p&lt;0.05) decrease in plasma glucose (467.6 ± 56.90 mg/dL, p&lt;0.05) and serum insulin (27.05 ± 7.56 ng/mL, p&lt;0.05) level were observed in the metformin group compared with the diabetic control group (649.55 ± 80.26 mg/dL and 37.68 ± 4.66 ng/mL) into STZ-induced diabetic rats. Results suggest that, rosiglitazone is more efficacious than metformin on the lipid-lowering and plasma glucose profile in <em>db/db</em> mice. In contrast, metformin is more efficacious than rosiglitazone in STZ-induced diabetic rat model with respect to antihyperglycemic effect.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol11no1/comparison-of-rosiglitazone-and-metformin-in-genetically-obese-and-diabetic-dbdb-mice-and-streptozotocin-induced-diabetic-rat-models/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Diabetic <em>db/db Genetically Obese Mice</keyword>
      

      
        <keyword></em> Mice Insulin Resistance</keyword>
      

      
        <keyword> Metformin</keyword>
      

      
        <keyword> Rosiglitazone</keyword>
      

      
        <keyword> Streptozotocin-Induced Diabetes</keyword>
      

      
        <keyword></keyword>
      
</keywords>
  </record>
</records>