نتایج جستجو برای: ht1 receptor antagonists

تعداد نتایج: 615397  

Ali Nasimi, Masoumeh Hatam,

Introduction: We previously shown that microinjection of glutamate into the hDB of rat elicited cardiovascular depressive responses. Microinjection of AP5 (an NMDA receptor antagonist, 2.5 mM, 50 nl) and CNQX (an AMPA receptor antagonist, 1 mM, 50 nl) caused no significant changes in the blood pressure and heart rate. Microinjection of bicuculline (BMI: a GABAA receptor antagonist, 1 mM, 50...

Journal: :medical journal of islamic republic of iran 0
gr taghizadeh-jahromi m rezayat mr zarrindast from the department of pharmacology, school of medicine, tehran university of medical sciences, tehran, i.r. iran.

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 competitiv...

Background and aims: Diabetic nephropathy (DN) is the most common cause of end-stage renal failure which could increase the risk of cardiovascular disease and morbidity and mortality in patients. The aim of this study was to investigate new modalities for treatment of diabetic nephropathy. Methods:This study was a mini-review research to investigate drugs that are used for DN treatment. Resul...

2017
Willem G. van Ginkel Danique van Vliet Johannes G. M. Burgerhof Pim de Blaauw M. Estela Rubio Gozalbo M. Rebecca Heiner-Fokkema Francjan J. van Spronsen

INTRODUCTION Hereditary Tyrosinemia type 1 (HT1) is a rare metabolic disease caused by a defect in the tyrosine degradation pathway. Current treatment consists of 2-(2-nitro-4-trifluoromethylbenoyl)-1,3-cyclohexanedione (NTBC) and a tyrosine and phenylalanine restricted diet. Recently, neuropsychological deficits have been seen in HT1 patients. These deficits are possibly associated with low bl...

Journal: :Human reproduction 1998
C Karlsson G Bodelsson M Bodelsson M Stjernquist

The contribution of endothelium-linked mechanisms to the contraction induced by 5-hydroxytryptamine (5-HT) was investigated in the isolated human uterine artery. 5-HT contracted the uterine artery concentration-dependently. Removal of the endothelium or treatment with the cyclooxygenase inhibitor indomethacin potentiated the contractile response to 5-HT. The nitric oxide synthase inhibitor L-N(...

Journal: :acta medica iranica 0
abbas norouzi brain and spinal cord injury repair research center, tehran university of medical sciences, tehran, iran. gohar fakhfouri department of pharmacology, school of medicine, shahid beheshti university of medical sciences, tehran, iran. reza rahimian brain and spinal cord injury repair research center, tehran university of medical sciences, tehran, iran. and department of pharmacology, school of medicine, tehran university of medical sciences, tehran, iran.

no abstract

2016
Francesca Angileri Geneviève Morrow Jean-Yves Scoazec Nicolas Gadot Vincent Roy Suli Huang Tangchun Wu Robert M. Tanguay

Hereditary tyrosinemia type 1 (HT1) is a severe inborn error of metabolism, impacting the tyrosine catabolic pathway with a high incidence of hepatocellular carcinoma (HCC). Using a HT1 murine model, we investigated the changes in profiles of circulating and hepatic miRNAs. The aim was to determine if plasma miRNAs could be used as non-invasive markers of liver damage in HT1 progression. Plasma...

B MOUSTAFAVI-MEHR , M GHAZI-KHANSARI, M REZAYAT, MR ZARRINDAST,

The effects of cholecystokinin (CCK) receptor antagonists on hypothermia induced by cocaine or morphine have been studied in mice. In the present work, subcutaneous (SC) injection of cocaine (50-150 mg/kg) or morphine (125-500 mg/kg) induced hypothermia in mice. Administration of CCKA receptor antagonist MK-329 (0.5-1.5 mg/kg), CCKB receptor antagonist L-365, 260 (0.5-1.5 mgl kg) and CCK r...

Gholamhossein Shirvani Kameh Esmailli Mohsen Javaheri Nader Saemian, Omid Khalili Arjomandi

Four amidine NR2B-selective NMDA receptor antagonists, N-( 2-methoxy benzyl) -3-phenyl-acrylamidine, N-[diduterio(2-methoxyphenyl) methyl]-3-phenyl-acrylamidine, N-benzyl-3-phenyl-acryl amidine and N-[diduterio(phenyl)methyl]-3-phenyl-acrylamidine, all fourlabeled with carbon-14 in the 1-position, have been synthesized as part of 5-step sequence fromBa14CO3.

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