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A novel purine analogue bearing nitrate ester prevents platelet activation by ROCK activity inhibition

Kardeby, Caroline, 1989- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,Cardiovascular Research Centre
Paramel Varghese, Geena, 1985- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,Cardiovascular Research Centre
Pournara, Dimitra (author)
National Hellenic Research Foundation, Institute of Biology, Medicinal Chemistry and Biotechnology, Athens, Greece
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Fotopoulou, Theano (author)
National Hellenic Research Foundation, Institute of Biology, Medicinal Chemistry and Biotechnology, Athens, Greece
Sirsjö, Allan, 1959- (author)
Örebro universitet,Institutionen för medicinska vetenskaper
Koufaki, Maria (author)
National Hellenic Research Foundation, Institute of Biology, Medicinal Chemistry and Biotechnology, Athens, Greece
Fransén, Karin, 1973- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,Cardiovascular Research Centre
Grenegård, Magnus, 1963- (author)
Örebro universitet,Institutionen för medicinska vetenskaper
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 (creator_code:org_t)
Elsevier, 2019
2019
English.
In: European Journal of Pharmacology. - : Elsevier. - 0014-2999 .- 1879-0712. ; 857
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Natural purines like ATP, ADP and adenosine have crucial roles in platelet physiology. This knowledge has been significant in drug development and today ADP receptor antagonists are widely used for prevention of thrombotic events following myocardial infarction and ischaemic stroke.Recent studies have shown that a purine analogue bearing nitrate ester group (denoted MK128) has anti-inflammatory effects probably due to its ability to donate nitric oxide (NO). However, other pharmacological mechanisms may contribute to the observed effect. The aim of the present study was to establish the anti-platelet activity and elucidate the underlying molecular mechanism(s) of the purine analogue MK128.We found that MK128 reduced aggregation and secretion induced by the thrombin receptor agonist SFLLRN and nearly abolished aggregation and secretion induced by thromboxane A2 (TxA2) and collagen receptor agonists. The inhibition took place despite blockage of the NO/cGMP signalling system. Furthermore, interaction between MK128 and platelet purinergic receptors did not explain the observed inhibition. Instead, we found that MK128 concentration-dependently inhibited Rho-associated kinase (ROCK), which led to decreased ROCK-dependent myosin phosphatase target subunit (MYPT)-1 phosphorylation and suppression of platelet functional responses.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

Nitric oxide
Platelet inhibitor
Purinergic receptors
Rho associated protein kinase
Thromboxane A2

Publication and Content Type

ref (subject category)
art (subject category)

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