نتایج جستجو برای: prostacyclin

تعداد نتایج: 3701  

Journal: :Journal of cardiovascular pharmacology 2014
Laith Alkukhun Nancy D Bair Raed A Dweik Adriano R Tonelli

INTRODUCTION Prostacyclin analogs are Food and Drug Administration-approved therapies for the treatment of pulmonary arterial hypertension and can be administered by inhalational, intravenous (IV), or subcutaneous (SQ) routes. Because there are limited data to guide the transition between SQ to IV prostacyclin analogs, we describe our experience. METHODS We performed a retrospective review of...

Journal: :Blood 2015
Evi X Stavrou Chao Fang Alona Merkulova Omar Alhalabi Nadja Grobe Silvio Antoniak Nigel Mackman Alvin H Schmaier

The precise mechanism for reduced thrombosis in prekallikrein null mice (Klkb1(-/-)) is unknown. Klkb1(-/-) mice have delayed carotid artery occlusion times on the rose bengal and ferric chloride thrombosis models. Klkb1(-/-) plasmas have long-activated partial thromboplastin times and defective contact activation-induced thrombin generation that partially corrects upon prolonged incubation. Ho...

2014
Nicholas S. Kirkby Martina H. Lundberg William R. Wright Timothy D. Warner Mark J. Paul-Clark Jane A. Mitchell

Cyxlo-oxygenase (COX)-2 inhibitors, including traditional nonsteroidal anti-inflammatory drugs (NSAIDs) are associated with increased cardiovascular side effects, including myocardial infarction. We and others have shown that COX-1 and not COX-2 drives vascular prostacyclin in the healthy cardiovascular system, re-opening the question of how COX-2 might regulate cardiovascular health. In diseas...

Journal: :Hypertension 1987
I Antonipillai J L Nadler E C Robin R Horton

Release of arachidonic acid from membrane phospholipids is a limiting step in the synthesis of both cyclooxygenase products and lipoxygenase products. The direct effects of prostacyclin and some lipoxygenase products on renin release were studied using rat renal cortical slices. Prostacyclin, at concentrations of 10(-5) M, stimulated renin secretion, but this effect was short-lived. Leukotriene...

Journal: :Experimental eye research 1990
P L Robertson D Ar G W Goldstein

Phosphoinositide lipid metabolism and prostacyclin production are implicated in endothelium dependent vascular relaxation in large blood vessels. To determine if these biochemical pathways might be involved in the regulation of microvascular tone in the retina, we measured the formation of 6-keto-prostaglandin-F1 alpha, the stable end product of prostacyclin, and inositol phosphates from 3H-lab...

Journal: :Hypertension 1988
R J Gryglewski R M Botting J R Vane

This review discusses the role of three mediators, synthesized by vascular endothelial cells, that help to keep the surface of the normal endothelium nonthrombogenic. The first is prostacyclin, a product of arachidonic acid metabolism discovered in 1976. This labile prostanoid, with a half-life of approximately 3 minutes, relaxes vascular smooth muscle and inhibits the aggregation of blood plat...

2015
Thomas Klein Günther Klaus Martin Kömhoff

Prostacyclin (PGI2) plays a critical role in nephrogenesis and renal physiology. However, our understanding of how prostacyclin release in the kidney is regulated remains poorly defined. We studied expression of prostacyclin synthase (PGIS) in developing and adult human kidneys, and also in selected pediatric renal diseases. We also examined PGI2 formation in human mesangial cells in vitro. We ...

Journal: :Circulation 2001
J K Hennan J Huang T D Barrett E M Driscoll D E Willens A M Park L J Crofford B R Lucchesi

BACKGROUND Prostanoid synthesis via the action of cyclooxygenase-2 (COX-2) is a component of the inflammatory response. Prostacyclin, a product of COX-2 in vascular endothelium, has important physiological roles, such as increasing blood flow to injured tissues, reducing leukocyte adherence, and inhibiting platelet aggregation. We examined the possibility that selective COX-2 inhibition could s...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2003
Candice D Fike Mark R Kaplowitz Sandra L Pfister

Our purpose was to determine whether production of arachidonic acid metabolites, particularly cyclooxygenase (COX) metabolites, is altered in 100-400-microm-diameter pulmonary arteries of piglets at an early stage of pulmonary hypertension. Piglets were raised in either room air (control) or hypoxia for 3 days. A cannulated artery technique was used to measure responses of 100-400-microm-diamet...

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