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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2020-03-28</publicationDate>
    
        <volume>13</volume>
        <issue>1</issue>

 
    <startPage>325</startPage>
    <endPage>333</endPage>

	 
      <doi>10.13005/bpj/1892</doi>
        <publisherRecordId>31106</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Comparative Inotropic Effects of the Some Isoquinoline Alkaloids</title>

    <authors>
	 


      <author>
       <name>Inoyat Jumayev</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Pulat Usmanov</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Shavkat Rustamov</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Sherzod Zhurakulov</name>

		
	<affiliationId>2</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Institute of Biophysics and Biochemistry, National University of Uzbekistan, Tashkent, Uzbekistan.</affiliationName>
    

		
		<affiliationName affiliationId="2">Institute of Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent, Uzbekistan.</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">In this study, mechanisms of inotropic action of some isoquinoline alkaloids 1-(4-dimethylaminophenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (F-24), 1-(2-chloro-4,5-methylenedioxyphenyl)-2-hydroxyethyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (N-14) and 1-(2-сhloro-4,5-methylenedioxyphenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (F-14) were studied. The F-24, F-14, and N-14 alkaloids have been shown to have a negative effect on papillary muscle contraction activity, <em>IC<sub>50</sub></em> value -16,8 µM, 14,03 µM and 12 µM. Са<sup>2+</sup><sub>L</sub>-channel blocker - nifedipine, adenylate cyclase (AС) activator–forskolin, β-adrenoreceptor (β-AR) blocker – propranolol, protein kinase С (PKС) activator – phorbol 12-myristate 13-acetate and SR RyR2 activator caffeine were used. Inotropic effects of F-24, F-14 and N-14 isoquinoline alkaloids on cardiomyocytes were suggested, based on results obtained in experiments carried in cardiomyocytes β-AR → [cAMP] → PKA → [Са<sup>2+</sup>]<sub>in</sub> ↑ cascade, PKC, RyR2 and Na<sup>+</sup>/Ca<sup>2+</sup> modulation.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol13no1/comparative-inotropic-effects-of-the-some-isoquinoline-alkaloids/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Inotropic Effect</keyword>
      

      
        <keyword> Isoquinoline Alkaloids</keyword>
      

      
        <keyword> Papillary Muscle</keyword>
      
</keywords>
  </record>
</records>