نتایج جستجو برای: antagonists

تعداد نتایج: 51229  

Journal: :iranian chemical communication 2016
alireza banaei eslam pourbasheer fatemeh haggi

quantitative structure-activity relationship (qsar) models were employed for prediction the activity of p2x7 receptor antagonists. a data set consisted of 50 purine derivatives was utilized in the model construction where 40 and 10 of these compounds were in the training and test sets respectively. a suitable group of calculated molecular descriptors was selected by employing stepwise multiple ...

Journal: :emergency journal 0
bita dadpour addiction research centre, imam reza hospital, mashhad university of medical sciences, mashhad, iran. arash gholoobi atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. shahrad tajoddini medical toxicology research centre, imam reza hospital, mashhad university of medical sciences, mashhad, iran. amir habibi addiction research centre, imam reza hospital, mashhad university of medical sciences, mashhad, iran.

cardiovascular effects of opioid withdrawal have long been studied. it was reported that patients with underlying ischemic heart disease and atherosclerotic vessels may be complicated by a sudden physical and emotional stress due to withdrawal syndrome. but some other believes sudden increase in catecholamine level as a sympathetic overflow might effect on heart with and without underlying isch...

Journal: :iranian journal of medical sciences 0
aditi maitra department of clinical and experimental pharmacology, calcutta school of tropical medicine, kolkata, india; shashwat bhattacharyya department of ophthalmology, calcutta national medical college, kolkata, india sabyasachi paik department of clinical and experimental pharmacology, calcutta school of tropical medicine, kolkata, india; prerna pathak department of dermatology and venereology, calcutta school of tropical medicine, kolkata, india santanu kumar tripathi department of clinical and experimental pharmacology, calcutta school of tropical medicine, kolkata, india;

abstract fixed drug eruption (fde) is a unique type of cutaneous drug reaction that typically recurs in the identical locations on re-exposure to the attributed drug. fde is characterized by the appearance of a single or multiple sharply demarcated violaceous erythematous plaques which heal with residual hyperpigmentation. a 27-year-old woman presented with multiple dark patches over her eyelid...

Journal: :physiology and pharmacology 0
mitra mahmoudi dept. pharmacology, school of medicine, tehran univ. med. sci., tehran, iran mohammad reza zarrindast

in the present study, the effect of gaba (γ-aminobutyric acid) receptor agonists and antagonists on morphine-induced antinociception was investigated in formalin test in rats. intraperitoneal (i.p.) injection of different doses of morphine (1, 3, 6 and 9 mg/kg) and intracerebroventricular (i.c.v.) injection of different doses of muscimol (0.5, 1 and 2 g/rat) or baclofen (0.25, 0.5 and 1 g/rat) ...

2016
Adrian John Clark Rachel Forfar Mashal Hussain Jeff Jerman Ed McIver Debra Taylor Li Chan

Adrenocorticotropin (ACTH) acts via a highly selective receptor that is a member of the melanocortin receptor subfamily of type 1 G protein-coupled receptors. The ACTH receptor, also known as the melanocortin 2 receptor (MC2R), is unusual in that it is absolutely dependent on a small accessory protein, melanocortin receptor accessory protein (MRAP) for cell surface expression and function. ACTH...

Losartan potassium, Valsartan , Telmisartan and Irbesartan are angiotensin-II-receptor antagonists (ARA II) group which used in treatment of hypertension alone or in combination with other drugs mainly Hydrochlorothiazide. RP- HPLC method was developed for the assay of three angiotensin-II-receptor antagonists (ARA-IIs) in presence of Hydrochlorothiazide. The method was performed by reversed ph...

GR TAGHIZADEH-JAHROMI, M REZAYAT, MR ZARRINDAST,

The effect of NMDA (N-methyl-D-aspartate) receptor antagonists on tolerance to morphine antinociception was investigated in mice. Daily subcutaneous administration of 50 mg/kg of morphine hydrochloride for three days induced tolerance to different (3,6 and 9 mg/kg) test doses of morphine. The tolerance obtained was decreased by pretreatment of animals with single or repeated doses of compe...

2017
Ayman Samman Tahhan Pratik B. Sandesara Arshed A. Quyyumi

There is strong experimental and clinical support for a causal role of immune dysregulation and inflammation in atherosclerosis and heart failure. Atherosclerotic lesions are infiltrated by monocytes, macrophages, and T lymphocytes (predominantly Th1). Cytokines, including interleukin-6 (IL6) and tumor necrosis factor-α (TNF-α), are released by the infiltrating inflammatory cells and stimulate ...

2003
David P. Westfall

Drugs that produce responses by interacting with adrenoceptors are referred to as adrenoceptor agonists or adrenergic agonists. Norepinephrine and isoproterenol are examples of such compounds. Agents that inhibit responses mediated by adrenoceptor activation are known as adrenoceptor antagonists, adrenergic antagonists, or adrenergic blocking agents. Prazosin and propranolol are examples of rec...

Journal: :Frontiers in computer science 2021

The visual design of antagonists—typically thought as “bad guys”—is crucial for game design. Antagonists are key to providing the backdrop a game's setting and motivating player's actions. representation antagonists is important because it affects player expectations about character's personality potential Particularly how players perceive an antagonist's morality. For example, antagonist appea...

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