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Hydrogen sulfide inhibits cell proliferation

AUTHOR Payrhuber Georg
PUBLISHER AV Akademikerverlag (03/04/2015)
PRODUCT TYPE Paperback (Paperback)

Description
Accumulating evidence suggests a very important role for the gasotransmitter hydrogen sulfide (H2S) in a great variety of invertebrate and vertebrate species, including humans. Effects of H2S in the nervous system range from enhancing neurogenesis, modulation of cell proliferation, ion channel activity to influencing behaviour and learning. In my master thesis I investigated the effect of H2S on cell proliferation and its underlying mechanisms using cell counting assays as well as calcium imaging of C6 glioma and GH3 pituitary tumour cells. My results indicate that H2S reduces the cell proliferation rate in a concentration dependent manner. The antiproliferative effect of H2S was found to be released when cells were allowed to recover for 24 hours after a previous 24 hour incubation with H2S. In GH3 cells incubated for 48 hours with H2S cell size histograms indicate a possible apoptotic mechanism of H2S. Ca2+ imaging data suggest that H2S evokes a Ca2+ influx in GH3 cells. This effect was highly significant.
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Product Details
ISBN-13: 9783639792782
ISBN-10: 3639792785
Binding: Paperback or Softback (Trade Paperback (Us))
Content Language: English
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Page Count: 76
Carton Quantity: 92
Product Dimensions: 6.00 x 0.18 x 9.00 inches
Weight: 0.27 pound(s)
Feature Codes: Illustrated
Country of Origin: US
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BISAC Categories
Science | Life Sciences - Biology
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Accumulating evidence suggests a very important role for the gasotransmitter hydrogen sulfide (H2S) in a great variety of invertebrate and vertebrate species, including humans. Effects of H2S in the nervous system range from enhancing neurogenesis, modulation of cell proliferation, ion channel activity to influencing behaviour and learning. In my master thesis I investigated the effect of H2S on cell proliferation and its underlying mechanisms using cell counting assays as well as calcium imaging of C6 glioma and GH3 pituitary tumour cells. My results indicate that H2S reduces the cell proliferation rate in a concentration dependent manner. The antiproliferative effect of H2S was found to be released when cells were allowed to recover for 24 hours after a previous 24 hour incubation with H2S. In GH3 cells incubated for 48 hours with H2S cell size histograms indicate a possible apoptotic mechanism of H2S. Ca2+ imaging data suggest that H2S evokes a Ca2+ influx in GH3 cells. This effect was highly significant.
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