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Serotonin and its metabolites reduce oxidative stress in murine RAW264.7 macrophages and prevent inflammation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F20%3A00524249" target="_blank" >RIV/68081707:_____/20:00524249 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/20:00117037

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s13105-019-00714-3" target="_blank" >https://link.springer.com/article/10.1007/s13105-019-00714-3</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s13105-019-00714-3" target="_blank" >10.1007/s13105-019-00714-3</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Serotonin and its metabolites reduce oxidative stress in murine RAW264.7 macrophages and prevent inflammation

  • Original language description

    In this study, we focused on comparing the effects of serotonin and its metabolites on the functions of RAW264.7 cells (emphasis on oxidative burst and production of nitric oxide and cytokines), thereby expanding the scope of existing knowledge with advent of novel findings in this field. Changes in production of reactive oxygen species (ROS) by RAW264.7 cells after treatment with serotonin, N-acetylserotonin and melatonin were determined using the chemiluminescence (CL) assay. To exclude the direct scavenging effects of the studied compounds on the CL response, the antioxidant properties of all respective compounds were measured using TRAP and amperometrical method. Nitric oxide (NO) production was measured by Griess reagent and inducible NO synthase (iNOS) expression by Western blot. Cytokine production was assessed using the Mouse Cytokine Panel A Array kit and ELISA. We showed that all tested compounds were able to reduce oxidative stress, as well as inhibit production of inflammatory cytokines by macrophages. Of the tested compounds, serotonin and N-acetylserotonin were markedly better antioxidants than melatonin. In comparison, other effects of tested compounds were very similar. It can be concluded that antioxidant capacity of tested compounds is a major advantage in the early stages of inflammation. Since plasma concentrations of N-acetylserotonin and melatonin are lower than serotonin, it can be deduced that serotonin plays a key role in modulation of inflammation and the regulatory functions of immune cells, while also protecting cells against oxidative stress.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/LD14030" target="_blank" >LD14030: Molecular mechanisms of serotoninergic system interactions with cells of immune system</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Physiology and Biochemistry

  • ISSN

    1138-7548

  • e-ISSN

  • Volume of the periodical

    76

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    ES - SPAIN

  • Number of pages

    12

  • Pages from-to

    49-60

  • UT code for WoS article

    000520009600004

  • EID of the result in the Scopus database

    2-s2.0-85077282839