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Mitochondrial Dysfunction in Blood Platelets of Patients with Manic Episode of Bipolar Disorder

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F19%3A10385725" target="_blank" >RIV/00064165:_____/19:10385725 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/19:10385725

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=bX~eMYrH-w" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=bX~eMYrH-w</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/1871527318666181224130011" target="_blank" >10.2174/1871527318666181224130011</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Mitochondrial Dysfunction in Blood Platelets of Patients with Manic Episode of Bipolar Disorder

  • Original language description

    We measured selected mitochondrial parameters in peripheral blood components. The analyses were performed for patients suffering from a manic episode and during remission and were compared to those performed for healthy controls. Mitochondrial respiration was examined in intact and permeabilized blood platelets using high-resolution respirometry. The citrate synthase (CS) and electron transport system (ETS) complex (complex I, II, and IV) activities were examined in platelets. The CS, complex II and complex IV activities were decreased in the BAD patients, complex I activity was increased, and the ratio of complex I to CS was significantly increased. In the intact platelets, respiration after complex I inhibition and residual oxygen consumption were decreased in the BAD patients compared to the healthy controls. In the permeabilized platelets, a decreased ETS capacity was found in the BAD patients. No significant differences were found between BAD patients in mania and remission. Increased complex I activity can be a compensatory mechanism for decreased CS and complex II and IV activities. We conclude that complex I and its abnormal activity contribute to defects in cellular energy metabolism during a manic episode and that the deficiency in the complex&apos;s functioning, but not the availability of oxidative phosphorylation substrates, seems to be responsible for the decreased ETS capacity in BAD patients. The observed parameters can be further evaluated as &apos;trait&apos; markers of BAD

  • 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

    30215 - Psychiatry

Result continuities

  • Project

    <a href="/en/project/NV15-28616A" target="_blank" >NV15-28616A: Mitochondrial dysfunctions in bipolar affective disorder</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    CNS &amp; Neurological Disorders - Drug Targets

  • ISSN

    1871-5273

  • e-ISSN

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    222-231

  • UT code for WoS article

    000466102200005

  • EID of the result in the Scopus database

    2-s2.0-85065585115