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  <Header>
    <ArticleTitle>L-SERINE DECREASES BASAL CA2+ IN RAT AORTIC VASCULAR SMOOTH MUSCLE CELLS</ArticleTitle>
  </Header>
  <ArticleParameters>
    <ArticleReceivingDate>2012-01-10</ArticleReceivingDate>
    <ArticleRevisedDate>2012-01-13</ArticleRevisedDate>
    <ArticleAcceptanceDate>2012-01-15</ArticleAcceptanceDate>
    <ArticlePublishedOn>2/24/2025 7:49:18 PM</ArticlePublishedOn>
    <Journal>Journal of Applied Pharmacy</Journal>
    <Volume>4</Volume>
    <Year>2012</Year>
    <ArticleType>Original research article</ArticleType>
    <FirstPage>92</FirstPage>
    <LastPage>102</LastPage>
    <CollectionYear>2012</CollectionYear>
    <PublisherId>JAppPharm (2012 ). 4. 92-102</PublisherId>
    <ArticleDoi>https://doi.org/10.21065/19204159.4.92</ArticleDoi>
    <Language>English</Language>
  </ArticleParameters>
  <Authors>
    <ArticleAuthors>Saswati Tripathy and Ramesh C Mishra</ArticleAuthors>
  </Authors>
  <keywords>
    <Articlekeywords>L-serine; Basal Ca2+; VSMC; Cytoplasm; Nucleus; Fluo 3-AM</Articlekeywords>
  </keywords>
  <Abstract>
    <ArticleAbstract>L-serine decreases mean arterial pressure (MAP) in both normotensive and hypertensive rats. However, the molecular mechanism is not clear. Therefore, we examined the effect of L-serine on intracellular calcium (Ca2+) in cultured aortic vascular smooth muscle cells (VSMC) isolated from normotensive and hypertensive rat models. Ca2+ fluorescence intensity was studied by using confocal imaging. L-serine evoked a concentration dependent (5-30 µM) decrease in basal Ca2+ fluorescence intensity in normotensive rat models. This decrease in basal Ca2+ fluorescence intensity level was also profound in hypertensive rat models despite the fact that basal Ca2+ fluorescence intensity was higher in these models compared to the normotensive rats. We also observed L-serine (20-30 µM) decreases nuclear Ca2+ fluorescence intensity in both the rat models. In presence of a neutral amino acid transporter inhibitor, 2-amino-2-norbornane-carboxylic acid (BCH), L-serine did not have any effect on basal Ca2+ fluorescence intensity in VSMC of either rat models, suggesting the inhibition of amino acid transporter blocked the entry of L-serine in to the cell to have an effect. Hence this data indicates the possible role of L-serine in regulation of intracellular Ca2+ in these rat models.</ArticleAbstract>
  </Abstract>
</ArticalData>