نتایج جستجو برای: relaxant effect

تعداد نتایج: 1642918  

Journal: :Acta pharmaceutica 2017
Miyase Gözde Gündüz Gaetano Ragno Rahime Şimşek Michele De Luca Cihat Şafak Fedora Grande Ahmed El-Khouly Fatma İşli Şeniz Yildirim Gökçe Sevim Öztürk Fincan Giuseppina Ioele

This paper describes the synthesis of 1,4-dihydropyridine compounds (DHPs) endowed with good muscle relaxant activity and stability to light. Six new condensed DHPs were synthesized by the microwave irradiation method. A long-chain ester moiety [2-(methacryloyloxy)ethyl] and various substituents on the phenyl ring were demonstrated to affect the muscle relaxant activity occurring in isolated ra...

Journal: :Japanese journal of pharmacology 1966
J N Sinha B P Jaju R C Srimal

* Present address : Pharmacology Division , Central Drug Research Institute, Chatter Manzil Palace, Lucknow, India. Hafliger (1) synthesized a series of iminodibenzyl compounds which were found to possess antihistaminic, anticholinergic, sedative and analgesic properties. It was only after a clinical trial by Kuhn (2) that G 22355 (imipramine) "emerged as an antidepres sant". The exact mechanis...

1995
Chittaranjan Andrade

A case is reported of diazepam - induced amelioration of prominent auditory hallucinations experienced by a female paranoid schizophrenic. With the assumption that subvocal speech may be primary to such hallucinations, it is proposed that diazepam may have acted by exerting a relaxant effect on speech musculature. This is a hypothesis testable in future research.

Journal: :General pharmacology 1999
J Duarte C Lugnier A I Torres F Pérez-Vizcaino A Zarzuelo J Tamargo

1. Visnagin relaxed aortae previously contracted by noradrenaline. This effect was unalterated by endothelium removal and potentiated, at high concentrations, by the previous incubation with sodium nitroprusside. 2. Visnagin weakly inhibited the hydrolytic activity of the cyclic nucleotide phosphodiesterase (PDE) isozymes (PDE5, PDE4, PDE3, cyclic GMP activated PDE2 and PDE1). 3. The present re...

Journal: :Molecular human reproduction 2003
Attila Mihályi Eszter Ducza Robert Gáspár George Falkay

Results from recent studies have shown that alpha(1A)-adrenergic receptor (alpha(1A)-AR) antagonists could offer a new alternative in the treatment of preterm delivery. However, members of this group [2-(2,6-dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane hydrochloride (WB4101), 5-methylurapidil (5-MU)] are known to influence serotonin (5-hydroxy-tryptamine) (5-HT(1A)) receptors, too. Our ob...

Journal: :Biological & pharmaceutical bulletin 2014
Kyosuke Sato Daisuke Chino Nanako Nishioka Keisuke Kanai Mika Aoki Keisuke Obara Seiji Miyauchi Yoshio Tanaka

Docosahexaenoic acid (DHA) shows more pronounced relaxation when blood vessel is contracted with prostanoid receptor agonists than other stimulants. The present study was carried out to obtain information on the mechanisms underlying prostanoid receptor-selective relaxant action of DHA, particularly focusing on the possible roles for K(+) channels and its CYP epoxygenase (EOX) metabolites. In e...

2016
Hassan-Ali Soltani Seyed Jalal Hashemi Kamran Montazeri Alireza Dehghani Mehdi Nematbakhsh

BACKGROUND Muscle relaxant agents usually use to facilitate tracheal intubation; however, sometimes limitations exist. Magnesium (Mg) sulfate is a candidate for muscle relaxant substitute. This study was designed to determine the effect of Mg sulfate accompanied with propofol and fentanyl in patients undergoing ophthalmic surgery. MATERIALS AND METHODS In a double-blind randomized protocol an...

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