نتایج جستجو برای: نیفیدیپین nifedipine

تعداد نتایج: 4448  

Journal: :Acta obstetricia et gynecologica Scandinavica 2010
Judit Hajagos-Tóth Zsolt Kormányos George Falkay Attila Pál Róbert Gáspár

OBJECTIVE We investigated how progesterone and salmeterol modify the effect of nifedipine in an in vivo preterm birth model in rats, and how terbutaline and nifedipine modify the contractions of the isolated human myometrium. DESIGN Experimental animal and human myometrial studies. SAMPLE Twenty-four female Sprague-Dawley rats and 13 human uterine tissues sampled from cesarean section. ME...

Journal: :Circulation 1983
R A McLeay T J Stallard R D Watson W A Littler

Nine patients with untreated essential hypertension (mean casual blood pressure 173/109 +/- 14/7 mm Hg) (+/- SD) were studied in the control state and after 16 weeks of treatment with nifedipine, 10 mg orally every 8 hours. Direct arterial blood pressure monitored continuously over 24 hours showed that nifedipine significantly reduced systolic and diastolic blood pressure throughout the day and...

Journal: :The Journal of infectious diseases 2011
Sabine M Mair Manfred Nairz Rosa Bellmann-Weiler Thomas Muehlbacher Andrea Schroll Igor Theurl Patrizia L Moser Heribert Talasz Ferric C Fang Guenter Weiss

BACKGROUND Iron overload can adversely influence the course of infection by increasing microbial replication and suppressing antimicrobial immune effector pathways. Recently, we have shown that the calcium channel blocker nifedipine can mobilize tissue iron in mouse models of iron overload. We therefore investigated whether nifedipine treatment affects the course of infection with intracellular...

2017
Shuang-Shuang Yu Li-Rong Jiang Yan Ling Zhong-Ming Qian Yu-Fu Zhou Juan Li Ya Ke

Nifedipine was reported to enhance urinary iron excretion in iron overloaded mice. However, it remains unknown how nifedipine stimulates urinary iron excretion in the kidney. We speculated that nifedipine might inhibit the TfR1/ DMT1 (transferrin receptor 1/divalent metal transporter1)-mediated iron uptake by proximal tubule cells in addition to blocking L-type Ca2+ channels, leading to an incr...

Journal: :Japanese heart journal 1989
R Ajisaka T Masuoka T Fujita R Matsumoto K Iida Y Sugishita I Ito T Takeda H Toyama N Ishikawa

To evaluate whether the effect of nifedipine on left ventricular function relates to the severity of coronary artery disease (CAD) or not, supine graded ergometer exercise testing was performed before and after sublingual administration of 10 mg nifedipine in 24 patients with stable effort angina. To minimize the effect of nifedipine on myocardial oxygen consumption, exercise before and after n...

Journal: :Japanese journal of pharmacology 1990
B Ceyhan Y Karaaslan O Caymaz A Oto E Oram A Oram S Ugurlu

Hypertensive crises require immediate therapy, usually by parenteral drug administration. Sublingual nifedipine has been shown to be highly effective. However, the blood pressure fall following nifedipine is frequently associated with side-effects. The use of sublingual captopril has recently been indicated in hypertensive crisis, assuming that by this route, there would be a faster absorption ...

2015
Tso-Hsiao Chen Ching-Yu Shih Wen-Lin Hsu Tz-Chong Chou

The platelet-derived soluble CD40L (sCD40L) release plays a critical role in the development of atherosclerosis. Nifedipine, a dihydropyridine-based L-type calcium channel blocker (CCB), has been reported to have an anti-atherosclerotic effect beyond its blood pressure-lowering effect, but the molecular mechanisms remain unclear. The present study was designed to investigate whether nifedipine ...

2015
Xian-Tao Li Xiao-Qing Li Xi-Mu Hu Xiao-Yue Qiu

It is well documented that nifedipine, a commonly used dihydropyridine Ca2+ channel blocker, has also significant interactions with voltage-gated K+ (Kv) channels. But to date, little is known whether nifedipine exerted an action on Kv2.1 channels, a member of the Shab subfamily with slow inactivation. In the present study, we explored the effects of nifedipine on rat Kv2.1 channels expressed i...

Journal: :Hypertension 2010
Taeko Kaimoto Osamu Yasuda Mitsuru Ohishi Masaki Mogi Yukihiro Takemura Toshimitsu Suhara Toshio Ogihara Keisuke Fukuo Hiromi Rakugi

Calcium is an essential signaling molecule that controls vascular smooth muscle cell (VSMC) contraction, proliferation, and differentiation. Here, we show that the calcium antagonist nifedipine inhibits VSMC dedifferentiation in vitro and in vivo. Differentiated VSMCs cultured on laminin-coated dishes were transferred to laminin-free dishes to induce dedifferentiation. Induction of dedifferenti...

Journal: :Chest 1999
M J Ricciardi E Bossone D S Bach W F Armstrong M Rubenfire

BACKGROUND The clinical course in primary pulmonary hypertension (PPH) is improved by calcium channel blocker therapy in those with a favorable hemodynamic response during a trial of high-dose oral nifedipine. Although trials of nifedipine are performed only in patients who demonstrate pulmonary vasodilator reserve to short-acting agents, this response does not predict the safety of nifedipine ...

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