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تأثير تعاطي الميتفورمين على فاعلية إنزيم غلوتاتيون بيروكسيداز و إنزيم سوبر اوكسيد ديسموتاز عند المرضى السكريين نمط II و الأفراد الأسوياء

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 Publication date 2016
  fields Pharmacy
and research's language is العربية
 Created by Shamra Editor




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References used
AA,ABD.Elaneea,AA.Moustaf,AMMouhamed(2014): Modulation 0f the oxidative stress by Metformin in the cerebrum of Rats exposed to global cerebral ischemia and ischemia reperfusion . Eu,Re,Med,Pha,Sci,No(18):2387-2392
Anilak.Madraju.Derk M,Erion(2014):Metformin suppross gluconeogenesis by inhybtingMetocondrial glycerphosphate Dehydrogenase .letter.macmilan publshers limited 13270
Alise Silova (2015):changes in oxidative stress parameters and correction opporrbunites in particular pathology.doctoral thesis- Biochemistry. Riga 2015
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يستخدم الميتفورمين كخط علاجي أول لضبط داء السكري من النمط الثاني غير المضبوطين بالحميه خاصة عند المرضى زائدي الوزن
Background: Diabetes mellitus is a leading public health problem with increasing incidence and long term complications. These complications are mainly a consequence of macro-vascular and microvascular damages of the target organs. The incidence of several pulmonary abnormalities during the course of Diabetes Mellitus because the presence of an extensive microvascular circulation and abundant connective tissue in the lungs , raises the possibility that lung tissue may be a target organ in diabetic patients. Objectives: This research is designed to study the impact of DM and both the duration of the disease and the glycemic control on pulmonary function tests. Methodology: This is a cross-sectional study carried out on 75 patients with type II diabetes mellitus patients at Tishreen University Hospital in the period between October 2015 and October 2016 .We compared with a control group consisted of 75 non diabetic healthy persons . Measurement of HbA1C , fasting plasma glucose (FPG) , and spirometry were made to all subjects and the following pulmonary function parameters were recorded: Forced Expiratory Volume in the first second (FEV1), Forced Vital Capacity (FVC), and Forced Expiratory Volume percent (FEV1/ FVC%) . Results were analyzed by calculating Mean ± SD, using X2 test , Karl Pearson correlation and ANOVA test. Results: The mean FEV1, FVC, FEV1/FVC% values were low in diabetics (p value <0.05) compared to healthy non-diabetics (control group). Also, uncontrolled diabetics show a greater decrease in these values than controlled diabetics. There was a greater decrease in these values in patients with long period of disease . Conclusion: The findings of the present study suggest that, the lung is a target organ for damage in DM and diabetics show a decrease in PFTs with a restrictive pattern lesion compared with non-diabetics . And this deterioration is exaggerated in uncontrolled diabetics and with the long duration of DM .
تعرف الجمعية الأميركية السكري بأنه مجموعة من الاضطرابات الاستقلابية تتميز بفرط غلوكوز الدم نتيجة نقص في افراز الانسولين او مقاومة عمله او كليهما معا
Heart disease, particularly coronary artery disease is a major cause of morbidity and mortality among patients with diabetes mellitus . In addition to the increased clinical incidence of coronary artery disease , the extent of coronary arteries st enosed is also greater among diabetics . T his study showes that diabetics, compared to non-diabetics ,have a higher incidence of multiple vessel disease (٨٤٪ vs ٤٨٪) and lower incidence of one vessel disease . It also showes that left ventricular function and left ventricular wall movement are more impaired in diabetics .
Some characteristics of β-galactosidase enzyme that was isolated from a new born goat brain were studied. This study concluded that the enzyme is glucoenzyme in which the carbohydrate part constitutes 22.1% in accordance with phenol –sulfate acid method. The optimum pH for the enzyme activity is 5.5. The enzyme lost its activity completely at pH8.5, and showed great stability at the range of pH 4-6. The results indicated that the optimum temperature for the enzyme activity is 55Co at the optimum pH. The stability temperature for the enzyme is 35-60Co. The analytical results of 5%lactose solution hydrolyzed by the enzyme have indicated that the hydrolysis rate is between 40% after 60 minutes, to 95% after 270 minutes.
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