Multiple sclerosis (MS) is a chronic, inflammatory demyelinating disease of central nervous system with complex etiopathogenesis that impacts young adults (Lee et al., 2015), and MS impacts younger and middle aged character and leads to a range of disabilities that can alter their daily routines (Yara et al, 2010). Although, the exact cause of MS is still undetermined, the disease is mediated by adaptive immunity through the infiltration of T cells into the central nervous system (Bjelobaba et al, 2017). MS causes the Focal neurological symptomsand biochemical changes in the molecular level and the variation of neural cells such as loss or alteration of sensation, motor function, visible signs such as blurred vision or transient blindness, disturbance of conjugate eye movements, bladder and bowel dysfunction and cognitive impairment (Induruwa et al, 2012 and Jafarzadeh et al, 2014). Autoimmune diseases (ADs) are chronic conditions initiated by way of the loss of immunological tolerance to self-antigens (TodorovicDilas et al, 2011). It is a heterogeneous group of disorders in which more than one modification in the immune system can be specific to a particular tissue or organ or might also be systemic, non-specific, involving multiple tissues or organs (Ray et al, 2012). One possible cause behind this is a lack of understanding of pathogenic mechanisms driving progressive multiple sclerosis. Due to the indolent nature of symptom progression, current disease criteria used to signify the course of disease (Lublin et al, 2014) indicate diagnosis is generally retrospective and based totally on history of gradual worsening. Clearly, diagnosis is primary based on clinical judgment, as there is no fully reliable diagnostic test (Ontaneda et al, 2015). In latest years, the elements involved in the etiology of the disease have also included oxidative stress (OS), which is described as an imbalance between the generation of reactive oxygen species (ROS) and the mechanisms that are responsible for their elimination, andthe imbalance between OS agents and antioxidants leads to OS activating the inflammatory process (Phaniendra et al, 2015). In the absence of enough antioxidant defenses, ROS can reason oxidative damage to macromolecules resulting in oxidation of lipids, proteins and deoxyribonucleic acid (DNA) (Griffiths, 2002). Some reseach report that ROS play a main role in myelin phagocytosis (Ghabaee et al, 2010 and Tasset et al, 2012). The inflammatory response gives rise to the manufacturing of both ROS and Reactive Biochem. Cell. Arch. Vol. 19, No. 1, pp. 31-35, 2019 www.connectjournals.com/bca ISSN 0972-5075 Nitrogen Species RNS through monocyte interactions with brain endothelium; ROS manufacturing induces cytoskeletal rearrangements, loss of blood-brain blood BBB integrity, tight-junction alteration and the extravasation of leukocytes into the central nervous system (Van et al, 2011; Witherick et al, 2011). Aim of study The aim of this study focuses on determination 8-H2-dG, MDA and PON1 in multiple sclerosis disease and finds the relationship between newly marker 8-H-2-dG with MDA and PON1. MATERIALS AND METHODS Subjects This study was performed on 25 female patients with age (25-35) years who diagnosed by physicians as a multiple sclerosis in Misan governorate. The patients compared with 25 apparently healthful in the identic rangel of age. In this study sample was collected five mL of venous bloods, placed in to plain tubes until coagulation was performed. Serum was separated from blood cells by centrifugation 4000 r.p.m. Assay method Determination of serum of 8-H-2-dG This assay that can be used for quantification of 8- H-2-dG in urine, cell culture, plasma and other sample matrices. The ELISA utilize an 8-H-2-dG coated plate and HRP- conjugated antibody or detection which allows for any assay range of 0.94-60 ng/mL, with sensitivity of 0.59 ng/mL. Determination of MDA The concentration of MDA,which is the consequence of lipid peroxidation and a marker of oxidative stress, was measured using thiobarbiturc acid. Determination of PON1 The quantitive sandwich enzyme immunoassay (ELISA) technique was employed for determination of PON1.
Objective: The study aimed to assess Leucine-rich alpha-2-glycoprotein-1 biomarker serum level in hospitalized COVID-19 patients. Methods: The case control study from multi-centers in Baghdad included 45 adult patients (19 females and 26 males) with COVID-19, diagnosed with a positive real-time reverse transcription polymerase chain reaction and excluded negative RT-PCR for COVID-19 and comorbidity conditions. Second group, was 43 control (20 females and 23 males). Results: This study found a decrease Leucine-rich alpha-2-glycoprotein-1 biomarker serum level in these patients and a significant difference in D. dimer, neutrophil count, lymphocyte count, and the neutrophil-lymphocyte ratio between the patients and controls at a P valu
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FLI1 is a member of ETS family of transcription factors that regulate a variety of normal biologic activities including cell proliferation, differentiation, and apoptosis. The expression of FLI1 and its correlation with well-known breast cancer prognostic markers (ER, PR and HER2) was determined in primary breast tumors as well as four breast cancer lines including: MCF-7, T47D, MDA-MB-231 and MDA-MB-468 using RT-qPCR with either 18S rRNA or ACTB (β-actin) for normalization of data. FLI1 mRNA level was decreased in the breast cancer cell lines under study compared to the normal breast tissue; however, Jurkat cells, which were used as a positive control, showed overexpression compared to the normal breast. Regarding primary breast carcinoma
... Show MoreAfamin, which is a human plasma glycoprotein, a putative multifunctional transporter of hydrophobic molecules and a marker for metabolic syndrome. Afamin concentration have been proposed to have a significant role as a predictor of metabolic disorders. Since NAFLD is associated with metabolic risk factors, e.g., dyslipidemia, insulin resistance and visceral obesity, it is considered as the hepatic manifestation of the metabolic syndrome. The objective of this study is to determine Afamin levels in hypothyroid patients with and without fatty liver disease and compare the results with controls. Also to study the relationship of Afamin level with the Anthropometric and Clinical Features (Age, Gender, BMI and Duration of Hypothyroidism) , Serum
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Background: Although various imaging modalities are available for evaluating suspicious breast lesions, ultrasound-based Shear-Wave Elastography (SWE) is an advanced, non-invasive technique complementary to grayscale sonography. This technique evaluates the elasticity of a specific tissue by applying sonic pressure to that tissue.
Objective: The aim is to assess the role of SWE in evaluating solid breast masses in correlation to histopathological study results.
Subjects and Methods: This prospective study was done in a tertiary care teaching hospital from September 2019 to August 2020. A study population of 50 women aged 18 years or above with an
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Aromatic Schiff-bases are known to have antibacterial activity, but most of these compounds are sparingly soluble in water. The present work describes the synthesis of new Schiff-bases derived from branched aminosugars. Treatment of 3-Amino-3-Cyano-3-Deoxy-1,2:5,6-Di-O-Isopropylene-α-D-Allofuranose (1) with the aldehydes (2) under reflux in methanol afforded the Schiff-bases (3) in good yields. The new Schiff-bases were in accord with their NMR, IR spectral data and elemental analysis.
Histone deacetylase inhibitors with zinc binding groups often exhibit drawbacks like non-selectivity or toxic effects. Thus, there are continuous efforts to modify the currently available inhibitors or to discover new derivatives to overcome these problems. One approach is to synthesize new compounds with novel zinc binding groups. The present study describes the utilization of acyl thiourea functionality, known to possess the ability to complex with metals, to be a novel zinc binding group incorporated into the designed histone deacetylase inhibitors. N-adipoyl monoanilide thiourea (4) and N-pimeloyl monoanilide thiourea (5) have been synthesized and characterized successfully. They showed inhibition of growth of human colon adenoc
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The compounds 3-[4̄-(4˭-methoxybenzoyloxy) benzylideneamino]-2-thioxo-imidazolidine-4-one(3)aand 4-(1-(5-oxo- 2-thioxoimidazolidin-1-ylimino)ethyl)phenyl acetate(3)b were prepared from the reaction of aromatic aldehyde or ketone(1)a,bwith thiosemicarbazide to give aryl thiosemicarbazones(2)a,b ,followed by cyclization with ethylchloroacetate in the presence of fused sodium acetate. Treatment the compounds(3)a,bwith 4- hydroxybenzenediazoniumchloride yielded the correspondings4-((4-((4-hydroxyphenyl)diazenyl)-5-oxo-2- thioxoimidazolidin-1-ylimino)methyl)phenyl 4-methoxybenzoate(4)aand4-(1-(4-((4-hydroxyphenyl)diazenyl)-5-oxo-2- thioxoimidazolidin-1-ylimino)ethyl)phenyl acetate(4)b.The new 2-thioxo-imidazolidin-4-one with esters (5-7)a,b sy
... Show MoreThe compounds 3-[4̄-(4˭-methoxybenzoyloxy) benzylideneamino]-2-thioxo-imidazolidine-4-one(3)aand 4-(1-(5-oxo- 2-thioxoimidazolidin-1-ylimino)ethyl)phenyl acetate(3)b were prepared from the reaction of aromatic aldehyde or ketone(1)a,bwith thiosemicarbazide to give aryl thiosemicarbazones(2)a,b ,followed by cyclization with ethylchloroacetate in the presence of fused sodium acetate. Treatment the compounds(3)a,bwith 4- hydroxybenzenediazoniumchloride yielded the correspondings4-((4-((4-hydroxyphenyl)diazenyl)-5-oxo-2- thioxoimidazolidin-1-ylimino)methyl)phenyl 4-methoxybenzoate(4)aand4-(1-(4-((4-hydroxyphenyl)diazenyl)-5-oxo-2- thioxoimidazolidin-1-ylimino)ethyl)phenyl acetate(4)b.The new 2-thioxo-imidazolidin-4-one with esters (5-7)a,b sy
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