نتایج جستجو برای: cilostamide

تعداد نتایج: 89  

Journal: :American journal of physiology. Lung cellular and molecular physiology 2003
Siobhán B Tarpey Darrell R Sawmiller Claire Kelly W Joseph Thompson Mary I Townsley

We hypothesized that decreases in expression and/or activity of cAMP-specific phosphodiesterases (PDE) contribute to protective adaptations observed in lung after heart failure. In this study, we compared PDE activity in lung parenchyma isolated from control dogs and those paced to heart failure by assaying cyclic nucleotide hydrolysis in fractions of homogenate supernatant eluted from DEAE-Tri...

Journal: :The Journal of clinical investigation 1991
M A Movsesian C J Smith J Krall M R Bristow V C Manganiello

Sarcoplasmic reticulum-associated cAMP phosphodiesterase activity was examined in microsomes prepared from the left ventricular myocardium of eight heart transplant recipients with end-stage idiopathic dilated cardiomyopathy and six unmatched organ donors with normal cardiac function. At cAMP concentrations less than or equal to 1.0 microM, sarcoplasmic reticulum-associated cAMP phosphodiestera...

Journal: :Journal of lipid research 2012
Marta Fernández-Galilea Patricia Pérez-Matute Pedro L Prieto-Hontoria J Alfredo Martinez Maria J Moreno-Aliaga

Lipoic acid (LA) is a naturally occurring compound with beneficial effects on obesity. The aim of this study was to evaluate its effects on lipolysis in 3T3-L1 adipocytes and the mechanisms involved. Our results revealed that LA induced a dose- and time-dependent lipolytic action, which was reversed by pretreatment with the c-Jun N-terminal kinase inhibitor SP600125, the PKA inhibitor H89, and ...

Journal: :Molecular human reproduction 2005
Allen D Seftel

The molecular mechanisms underlying the regulation of vas deferens (VD) motility and semen emission are still poorly understood. We now report evidence on VD expression of phosphodiesterase type 5 (PDE5), which regulates nitric oxide (NO)-induced relaxation and cGMP breakdown in smooth muscle cells. In human VD, the PDE5 abundance was relatively high (>3 x 10(6) molecules/microg total RNA), alt...

Journal: :iranian journal of basic medical sciences 0
azar hosseini pharmacological research centre of medicinal plants, department of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran reza shafiee-nick pharmacological research centre of medicinal plants, department of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran nasser pour ali behzad pharmacological research centre of medicinal plants, department of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran hamid sadeghian pharmacological research centre of medicinal plants, department of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran

objective(s) pde3 has a functional role in insulin secretion and action. we investigated the metabolic effects of new synthetic pde3 inhibitors (mc1, mc2, mc5 and mc6), on mice and hyperglycemic rat. materials and methods the test compound or solvent was injected subcutaneously to mice, for 7 days. on day 8, blood and liver samples were obtained. in hyperglycemic rat, 0.5 g/kg glucose with or w...

Journal: :Circulation research 2006
Francesca Rochais Aniella Abi-Gerges Kathleen Horner Florence Lefebvre Dermot M F Cooper Marco Conti Rodolphe Fischmeister Grégoire Vandecasteele

Compartmentation of cAMP is thought to generate the specificity of Gs-coupled receptor action in cardiac myocytes, with phosphodiesterases (PDEs) playing a major role in this process by preventing cAMP diffusion. We tested this hypothesis in adult rat ventricular myocytes by characterizing PDEs involved in the regulation of cAMP signals and L-type Ca2+ current (I(Ca,L)) on stimulation with beta...

Journal: :The Journal of pharmacology and experimental therapeutics 2000
J S Bian W M Zhang J M Pei T M Wong

This study determined whether phosphodiesterase (PDE) was activated by protein kinase C (PKC) upon kappa-receptor stimulation, and if so, to identify the isozyme. We first studied the effects of trans-(+/-)-3,4-dichloro-N-methyl-N-(2-[1-pyrrolidinyl] cyclohexyl) benzeneacetamide methanesulphonate (U50,488H), a selective kappa-opioid receptor (OR) agonist, and phorbol-12-myristate-13-acetate (PM...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2010
Anne-Marie Pelletier Shriram Venkataramana Kurtis G Miller Brian M Bennett Dileep G Nair Sandra Lourenssen Michael G Blennerhassett

Hyperplasia of smooth muscle contributes to the thickening of the intestinal wall that is characteristic of inflammation, but the mechanisms of growth control are unknown. Nitric oxide (NO) from enteric neurons expressing neuronal NO synthase (nNOS) might normally inhibit intestinal smooth muscle cell (ISMC) growth, and this was tested in vitro. In ISMC from the circular smooth muscle of the ad...

Journal: :Journal of receptor and signal transduction research 2015
Klaus Stahl Maximilian Stahl Hugo R de Jonge John N Forrest

CONTEXT Acting through different receptors, natriuretic peptides (atrial natriuretic peptide [ANP], brain type natriuretic peptide [BNP] and C-type natriuretic peptide [CNP]) increase intracellular cGMP, which then stimulates different pathways that activate fluid secretion. OBJECTIVE We used two-electrode voltage clamping to define the dominant pathway that is employed when natriuretic pepti...

2015
Øivind Ørstavik Ornella Manfra Kjetil Wessel Andressen Geir Øystein Andersen Tor Skomedal Jan-Bjørn Osnes Finn Olav Levy Kurt Allen Krobert

AIMS We recently published that the positive inotropic response (PIR) to levosimendan can be fully accounted for by phosphodiesterase (PDE) inhibition in both failing human heart and normal rat heart. To determine if the PIR of the active metabolite OR-1896, an important mediator of the long-term clinical effects of levosimendan, also results from PDE3 inhibition, we compared the effects of OR-...

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