نتایج جستجو برای: pde inhibitor

تعداد نتایج: 218917  

Journal: :Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics 1994

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2003
Marie Georget Philippe Mateo Grégoire Vandecasteele Larissa Lipskaia Nicole Defer Jacques Hanoune Jacqueline Hoerter Claire Lugnier Rodolphe Fischmeister

Hearts from AC8TG mice develop a higher contractility (LVSP) and larger Ca2+ transients than NTG mice, with (surprisingly) no modification in L-type Ca2+ channel current (ICa,L) (1). In this study, we examined the cardiac response of AC8TG mice to beta-adrenergic and muscarinic agonists and IBMX, a cyclic nucleotide phosphodiesterase (PDE) inhibitor. Stimulation of LVSP and ICa,L by isoprenalin...

Journal: :Molecular pharmacology 2000
S B Herman D M Juilfs E B Fauman P Juneau J P Menetski

Cyclic nucleotide phosphodiesterase type 4 (PDE4) is a cAMP-specific phosphodiesterase that is found as four distinct genes in the mammalian genome (PDE4A, 4B, 4C, and 4D). Mutation analysis was done to identify the amino acids involved in activity and inhibitor selectivity. Mutations at Asp333 were made in HSPDE4D3 based on mutations that affect rolipram sensitivity in RNPDE4B1. The PDE4D3 Asp...

Journal: :Circulation 2003
Thorsten Reffelmann Robert A Kloner

Several families of phosphodiesterases (PDE), the enzymes catalyzing hydrolysis of cyclic (c) nucleoside monophosphates, namely, 3 5 -cAMP (cAMP) and 3 5 cGMP (cGMP), have been identified and characterized in recent years.1 Since selective pharmacological inhibitors of isoform 5 (a cGMP-specific PDE), such as sildenafil, tadalafil, or vardenafil, have become available, the physiological functio...

2016
Yuji Hotta Naoya Ieda Ayako Fukamoto Tomoya Kataoka Yoshihiro Kawade Yasuhiro Maeda Hidehiko Nakagawa Kazunori Kimura

PURPOSE To investigate whether relaxation of the rat penile corpus cavernosum could be controlled with NOBL-1, a novel, light-controllable nitric oxide (NO) releaser. MATERIALS AND METHODS Fifteen-week-old male Wistar-ST rats were used. The penile corpus cavernosum was prepared and used in an isometric tension study. After noradrenaline (10(-5) M) achieved precontraction, the penile corpus ca...

2015
Michael Seimetz Nirmal Parajuli Alexandra Pichl Mariola Bednorz Hossein Ardeschir Ghofrani Ralph Theo Schermuly Werner Seeger Friedrich Grimminger Norbert Weissmann Tim Lahm

RATIONALE Chronic obstructive pulmonary disease (COPD) is a widespread disease, with no curative therapies available. Recent findings suggest a key role of NO and sGC-cGMP signaling for the pathogenesis of the disease. Previous data suggest a downregulation/inactivation of the cGMP producing soluble guanylate cyclase, and sGC stimulation prevented cigarette smoke-induced emphysema and pulmonary...

Journal: :International Journal of Molecular Sciences 2021

Phosphodiesterases (PDEs) hydrolyze cyclic nucleotides to modulate multiple signaling events in cells. PDEs are recognized actively associate with nucleotide receptors (protein kinases, PKs) larger macromolecular assemblies referred as signalosomes. Complexation of PKs generates an expanded active site that enhances PDE activity. This facilitates signalosome-associated preferentially catalyze h...

Journal: :Circulation 2011
Soni Savai Pullamsetti Rajkumar Savai Martina Barbara Schaefer Jochen Wilhelm Hossein Ardeschir Ghofrani Norbert Weissmann Christian Schudt Ingrid Fleming Konstantin Mayer James Leiper Werner Seeger Friedrich Grimminger Ralph Theo Schermuly

BACKGROUND Pulmonary arterial hypertension is characterized by a progressive increase in pulmonary vascular resistance caused by endothelial dysfunction, inward vascular remodeling, and severe loss of precapillary pulmonary vessel cross-sectional area. Asymmetrical dimethylarginine (ADMA), an endogenous nitric oxide synthase inhibitor, and its metabolizing enzyme dimethylarginine dimethylaminoh...

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