نتایج جستجو برای: nω hydroxy nor l arginine

تعداد نتایج: 764458  

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Gökce Topal Annie Brunet Laurence Walch J-L Boucher Monique David-Dufilho

Reduced synthesis of nitric oxide (NO) contributes to the endothelial dysfunction and may be related to limited availability of L-arginine, the common substrate of constitutive nitric-oxide synthase (NOS) and cytosolic arginase I and mitochondrial arginase II. To determine whether arginases modulate the endothelial NO synthesis, we investigated the effects of the competitive arginase inhibitor ...

2017
Patricia U Simioni Luis GR Fernandes Wirla MSC Tamashiro

Dendritic cells (DC) are potential tools for therapeutic applications and several strategies to generate tolerogenic DCs are under investigation. When activated by cytokines and microbial products, DCs express mediators that modulate immune responses. In this regard, the metabolites generated by the activities of inducible nitric oxide synthase (iNOS) and arginase in DCs seem to play important ...

Journal: :The European respiratory journal 2001
R B Muijsers N H ten Hacken I Van Ark G Folkerts F P Nijkamp D S Postma

Unlike murine mononuclear phagocytes, human macrophages do not release high amounts of nitric oxide (NO) in vitro despite the presence of nitric oxide synthase (NOS). To determine whether this limited NO synthesis in vitro is due to limited availability of the NOS substrate L-arginine, and putative NOS inhibiting factors present in foetal serum preparations, both alveolar macrophages (AM) and m...

Journal: :Journal of applied physiology 2014
Paul-André Risse Anouk Lavoie-Lamoureux Taisuke Jo Kimitake Tsuchiya Sana Siddiqui James G Martin

Innate airway hyperresponsiveness (AHR) is well modeled by two strains of rat, the hyperresponsive Fischer 344 rat and the normoresponsive Lewis rat. Arginase has been implicated in AHR associated with allergic asthma models. We addressed the role of arginase in innate AHR using the Fischer-Lewis model. In vivo arginase inhibition with N(ω)-hydroxy-nor-arginine (nor-NOHA) was evaluated on metha...

Journal: :The Biochemical journal 2012
Davide Papale Chiara Bruckmann Ben Gazur Caroline S Miles Christopher G Mowat Simon Daff

The vital signalling molecule NO is produced by mammalian NOS (nitric oxide synthase) enzymes in two steps. L-arginine is converted into NOHA (Nω-hydroxy-L-arginine), which is converted into NO and citrulline. Both steps are thought to proceed via similar mechanisms in which the cofactor BH4 (tetrahydrobiopterin) activates dioxygen at the haem site by electron transfer. The subsequent events ar...

Journal: :The Journal of biological chemistry 1993
P Klatt K Schmidt G Uray B Mayer

Brain NO (nitric oxide) synthase contains FAD, FMN, heme, and tetrahydrobiopterin as prosthetic groups and represents a multi-functional oxidoreductase catalyzing oxidation of L-arginine to NO and L-citrulline, formation of H2O2, and reduction of cytochrome c. We show that substrate analogues and inhibitors interacting with the heme block both the reductive activation of oxygen and the oxidatio...

Journal: :The European respiratory journal 2009
H Maarsingh B E Bossenga I S T Bos H H Volders J Zaagsma H Meurs

Peroxynitrite has been shown to be crucially involved in airway hyperresponsiveness (AHR) after the late asthmatic reaction (LAR). Peroxynitrite production may result from simultaneous synthesis of nitric oxide (NO) and superoxide by inducible NO-synthase (iNOS) at low L-arginine concentrations. L-arginine availability to iNOS is regulated by its cellular uptake, which can be inhibited by eosin...

Journal: :American journal of physiology. Heart and circulatory physiology 2011
Julia Grönros Christian Jung Jon O Lundberg Ruha Cerrato Claes-Göran Ostenson John Pernow

Nitric oxide (NO) is crucial for maintaining normal endothelial function and vascular integrity. Increased arginase activity in diabetes might compete with NO synthase (NOS) for their common substrate arginine, resulting in diminished production of NO. The aim of this study was to evaluate coronary microvascular function in type 2 diabetic Goto-Kakizaki (GK) rats using in vivo coronary flow vel...

Journal: :Circulation 2003
Dan E Berkowitz Ron White Dechun Li Khalid M Minhas Amy Cernetich Soonyul Kim Sean Burke Artin A Shoukas Daniel Nyhan Hunter C Champion Joshua M Hare

BACKGROUND Although abnormal L-arginine NO signaling contributes to endothelial dysfunction in the aging cardiovascular system, the biochemical mechanisms remain controversial. L-arginine, the NO synthase (NOS) precursor, is also a substrate for arginase. We tested the hypotheses that arginase reciprocally regulates NOS by modulating L-arginine bioavailability and that arginase is upregulated i...

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