In vivo Effects of Ashwagandha Withania somnifera on the Activation of Lymphocytes Jeremy Mikolai, A - PowerPoint PPT Presentation

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In vivo Effects of Ashwagandha Withania somnifera on the Activation of Lymphocytes Jeremy Mikolai, A

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Title: In vivo Effects of Ashwagandha Withania somnifera on the Activation of Lymphocytes Jeremy Mikolai, A


1
In vivo Effects of Ashwagandha (Withania
somnifera) on the Activation of Lymphocytes
Jeremy Mikolai, Andrew Erlandsen, Andrew
Murison, Kimberly Brown M.S.O.M., William L.
Gregory Ph.D., Padma Raman-Caplan N.D., Heather
Zwickey Ph.D.Helfgott Research Institute at the
National College of Natural Medicine, 049 SW
Porter St., Portland, OR. 97201
  • Background Ashwagandha (Withania somnifera) is
    an herbal supplement commonly used in Ayurveda,
    the traditional medicine of India. Purported
    health benefits include effects on several organ
    systems. Previous research has suggested immune
    consequences resulting from Ashwagandha
    supplementation, though human investigations have
    been few and mechanisms of action have not been
    described. Traditional Ayurvedic practice
    includes the co-administration of herbal
    supplements with a carrier substance, anupana.
    This step has been largely left out of previous
    research investigations.
  • Objective A quasi-experimental pilot study was
    designed to determine the immunological
    mechanisms of action of Ashwagandha when
    administered with a traditional anupana, cows
    milk. The objectives were to determine
  • The effects on the activation state of CD8
    T-cells, CD4 T-cells, CD19 B cells, and CD56
    NK lymphocytes over a 96 hour period
  • The effects on expression of the early activation
    marker CD69
  • The properties of Ashwagandha most suitable for
    further investigation.
  • Design Five participants consumed 12mL liquid
    extract of Ashwagandha root daily in divided
    doses combined with 8 fl oz. of cows milk.
    Peripheral blood samples were collected from
    participants at 0, 24 and 96 hours and compared
    for differences in lymphocyte count and
    activation state.
  • Methods Analysis of lymphocyte cell count and
    surface receptor data was conducted using FACScan
    flow cytometry to assay CD3, CD4, CD8, CD19, CD56
    and CD69 cell markers. A multivariate analysis of
    variance (MANOVA) and Paired sample T-tests were
    used to analyze data for changes in investigatory
    parameters.

Further information regarding this study may be
found in an upcoming publication of The Journal
of Alternative and Complementary Medicine (JACM).
The authors of this study have no competing
financial interests to disclose.
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