نتایج جستجو برای: paraoxonase 55genotype

تعداد نتایج: 2123  

Journal: :iranian journal of allergy, asthma and immunology 0
fariborz bahrehmand molecular diagnostic research center, kermanshah university of medical sciences, kermanshah, iran. asad vaisi-raygani molecular diagnostic research center, kermanshah university of medical sciences, kermanshah, iran and  fertility and infertility research center, kermanshah university of medical sciences, kermanshah, iran. reza ahmadi molecular diagnostic research center, kermanshah university of medical sciences, kermanshah, iran. amir kiani department of pharmacology  and toxicology, shahid beheshti university of medical sciences, tehran, iran. zohreh rahimi department of clinical biochemistry, kermanshah university of medical sciences, kermanshah, iran and medical biology research center, kermanshah university of medical sciences, kermanshah, iran. heidar tavilani department of clinical biochemistry, hamadan university of medical sciences, hamadan, iran.

paraoxonase-1 (pon1) is a serum hdl-bound enzyme that hydrolyzes a number of aromatic carboxylic acid esters including lipid peroxides, preventing ldl oxidation. systemic lupus erythematosus (sle) patients are at greater risk of oxidative stress, which is associated with abnormal plasma lipid metabolism. in this study, association of pon-55 polymorphism with serum arylesterase (are) activities,...

زواره‌ای, عباس, فیروزرای, محسن, نفیسی, نرگس, حسینی گوهری, لادن ,

    Paraoxonase can hydrolyse organophosphate esters and paraxon is its most important substrate in laboratory studies. This enzyme circulates in blood with HDL. It seems that reduced paraoxonase activity in human may increase risk of coronary artery disease. Genetic variations in two autosomal genes may reduce its activity. These variations produce three phenotypes: A, AB and B. B phenotype ac...

Journal: :applied biotechnology reports 0
kobra chehari department of biology, faculty of science, razi university, kermanshah, iran farideh sepahvand department of biology, faculty of science, lorestan university, khorrtamabad, iran sirous ghobadi department of biology, faculty of science, razi university, kermanshah, iran ahmad ismaili department of agronomy and plant breeding, faculty of agriculture, lorestan university, khorramabad, iran ezat rafiei alavy department of pathology, school of medicine, lorestanuniversity of medical sciences, khorramabad, iran

human serum paraoxonase (hupon1:   ec 3.1.8.1), a calcium-dependent esterase, is synthesized in the liver and   widely distributed in tissues including liver, kidney, intestine, and serum,   where it is associated exclusively with high-density lipoprotein.  human paraoxonase-1 plays an important role   in prevention of atherosclerosis and also protection against organophosphate-induced   neurot...

Journal: :Archives of Iranian medicine 2008
Ali Jalilian Ebrahim Javadi Mohamad Akrami Hossin Fakhrzadeh Ramin Heshmat Mazaher Rahmani Fatemeh Bandarian

BACKGROUND Recently another member of the paraoxonase gene family designated paraoxonase-2 has been identified. Paraoxonase-2 has antioxidant properties similar to paraoxonase-1 and paraoxonase-3. However, in contrast to paraoxonase-1 and paraoxonase-3, paraoxonase-2 is not associated with high-density lipoprotein and may only exert its antioxidant function at the cellular level. METHODS We a...

2017
Gülben Sayılan Özgün Eray Özgün Kıymet Tabakçıoğlu Selma Süer Gökmen Sevgi Eskiocak Erol Çakır

BACKGROUND Apolipoprotein A-1, paraoxonase-1 and paraoxonase-3 are antioxidant and anti-atherosclerotic structural high-density lipoprotein proteins that are mainly synthesized by the liver. No study has ever been performed to specifically examine the effects of caffeine on paraoxonase enzymes and on liver apolipoprotein A-1 protein levels. AIMS To investigate the dose-dependent effects of ca...

Journal: :medical journal of islamic republic of iran 0
a a. samadi from the dept of biochemistry, pasteur institute of iran, tehran s alvani the dept. of biochemistry, kashan medical university, kashan, iran m ghazi-khonsari the dept. of toxicology, tehran university of medical sciences, tehran, iran.

human serum paraoxonase (pon) associated with high density lipoprotein (hdl) , has been postulated to have a role in protecting low-density lipoprotein (ldl) against oxidative damage, which has led to the proposal that pon is an anti-atherogenic and anti-inflammatory enzyme. it has genetic polymorphism at the 191 (r ->q) and two alloenzymes a and b and three phenotypes a, b, and ab. we examined...

Nabatchian, Fariba, Zarei, Nazanin,

The paraoxonase family in humans includes the PON1, PON2, and PON3 genes. These genes are located on the long arm of chromosome 7 and are structurally similar .Between the nucleotide sequences of these three genes is about 70% and between their amino acid    sequences is about 60% compatibility. The three have 9 exons, which in the case of PON1 exists an addition code in position 106 (lysine) i...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2007
Sara Deakin Xenia Moren Richard W James

OBJECTIVE The purpose of this study was to analyze the consequences of HDL oxidation for paraoxonase-1 metabolism and function. METHODS AND RESULTS HDL was oxidized with AAPH, copper ions, and hypochlorite. Secretion studies were performed using human paraoxonase-1-transfected cells lines and primary rat hepatocytes. Stability studies were performed with recombinant paraoxonase. Conditioned m...

Journal: :Journal of lipid research 2004
Su Duy Nguyen Dai-Eun Sok

To determine the causes responsible for a preferential decrease of paraoxonase activity, which has been observed in the serum of patients with cardiovascular diseases, the inactivation or inhibition of paraoxonase 1 (PON1) by various endogenous factors was examined using paraoxon or phenyl acetate as a substrate. When purified PON1 was incubated with various endogenous oxidants or aldehydes, th...

A Jahangiri A Shafiee H Jalalizadeh M Mahmoudian

There are many evidences that human serum paraoxonase activity modifies plasma lipid profile and paraoxonase has an antiatherogenic property. Non-selective beta-blockers affect plasma lipid profile too, but they have atherogenic property when patients take these drugs in long term. In this study the effect of propranolol, a non-selective beta-blocker, on paraoxonase activity was investigated. L...

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