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    Clinical Nutrition Experimental

    Clinical Nutrition Experimental

    JournalISSN 2352-9393eISSN 2352-9393

    年发文量

    研究主题

    论文(141)

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    1Practical Guidance for the Use of Indirect Calorimetry During COVID 19 Pandemic
    Pierre Singer,Claude Pichard,Elisabeth De Waele

    The daily practice requires the use of indirect calorimetry to define the energy requirements of intensive care patients. In the time of COVID-19 pandemic, this practice is challenging. The purpose of this methodology paper is to provide practical guidance to health professionals to perform this measurement safely, using various metabolic monitors.

    2020引用:25
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    2Trichosanthes Dioica Roxb. Prevents Hepatic Inflammation and Fibrosis in CCl4-induced Ovariectomized Rats
    Salma Khan,Md. Mizanur Rahman,Fariha Kabir,Kamrun Nahar,Fariha Mamun,Shoumen Lasker,Nusrat Subhan,Md. Hemayet Hossain,Lutfun Nahar,Satyajit D. Sarker,Md Ashraful Alam,Md. Areeful Haque

    Plant-derived natural products have shown beneficial effects in many diseases associated with liver. The present study aimed to appraise the effects of Trichosanthes dioica (TD) peel extract on oxidative stress, inflammation as well as fibrosis exhibited by the ovariectomized rats in which hepatic damage had been induced by the administration of carbon tetrachloride (CCl4). The CCl4 administration in the ovariectomized rats elevated the plasma ALT, AST, and ALP level in comparison with the control while TD peel extract showed significant reduction of those activities. Besides, oxidative stress and lipid peroxidation also increased in CCl4-treated rats. TD peel extract significantly reduced the oxidative stress marker's concentration and improved the catalase and SOD activities in CCl4-administered ovariectomized rats. These results suggest that TD peel extract is capable of protecting the liver from CCl4induced damage through preventing oxidative stress, lipid peroxidation, inflammation, fibrosis and boosting the diminished cellular antioxidant defense.

    2020引用:12
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    3The Effect of a Single Mega Dose Injection of Vitamin D on Serum Adiponectin Concentration at First Gestational Diabetes Mellitus: A Randomized Controlled Clinical Trial
    Mahdieh Hosseinzadeh,Elham Razmpoosh,Elham shareghfarid,Elham Hosseinzadeh,Hossein Hadinedoushan,Maryam-Alsadat Salami,Maryam Khosravi,Maryam Amini,Hassan Mozaffari-Khosravi

    Background: vitamin D is being increasingly recognized for its important non-skeletal functions including endocrine actions. This study investigated if a single, large, intramuscular post‐artum injection of vitamin D improve adiponectin levels among women with gestational diabetes mellitus (GDM). Methods: A total of 45 pregnant women with GDM participated in this randomized clinical trial. They were randomly divided into intervention and control group. The intervention group received an intramuscular injection of 300,000 IU of vitamin D during 3 to 10 days after their child delivery, but controls did not. Serum 25‐hydroxyvitamin D, fasting blood glucose, HbA1c and serum adiponectin were measured at baseline and after 3 months of intervention. Results: Serum 25 OH vitamin D increase significantly in the intervention but not in the control group from 24.25 to 62.10 (nmol/l) (p-value< 0.01). Comparison in within group showed that adiponectin level increased significantly only among intervention group after the vitamin D injection from 7.45 to 8.98 (ngr/dl) (P-value=0.01), while between group comparisons showed no significant differences in adiponectin concentration after the intervention (P-value<0.05). Between and within group comparisons reported no significant alterations in the levels of glycated hemoglobin (HbA1c) and FPG (fasting plasma glucose), as well. Conclusions: The 300,000 IU single dose of intramuscular injection of vitamin D is regarded as an effective procedure to improve vitamin D status which significantly increased the adiponectin levels among mothers with gestational diabetes after delivery. Trial registration: The trial was registered in Iranian Registry of Clinical Trials available at http://www.irct.ir. The reference number is IRCT138902113840N1.

    2020引用:5
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    4Biochemical Changes Associated with Low and Very Low Calorie Diets on Lipid Metabolism, Iron Profile and Kidney Function in Obese Rats
    H.A. Abdel Maksoud,Mohamed G. Elharrif,Raafat R. Mohammed,M.A. Omnia, Nihal E. El Sayed

    Obesity is the most prevalent nutritional disorder. Healthy diets helps people maintain and improve their general health. This study aimed to assessment of low and very low calorie diets through determination of its effect on lipid metabolism, iron profile and kidney function in obese male rats. To achieve our aim forty five male albino rats were used and divided into 4 groups: control group, obese group with 75 calories diet, obese group with 60 calories diet and obese group with 45 calories diet. Our result showed significant disturbance of lipid, iron and kidney profile on supplementation of 75 calories diet to obese group of male rats and significant improvement in lipid, iron and kidney profile on supplementation of 60 calories diet or 45 calories diet to obese group of male rats. The results confirmed that, high fat diet able to produce significant disturbance in lipid metabolism, iron profile and kidney function while low calorie diets able to improving the disturbance in such parameter.

    2020
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    5Possible Ameliorative Role of Green Tea on Chronic Alcohol Mediated Renal Toxicity of STZ -Induced Diabetic Rats
    Swarnalatha Kodidela,Fareeda Begum Shaik,Venkataramaiah Chinta,Subhan Ali Mohammad,Chiranjeevi Pasala,Chandra Mohan Mittameedi,Narendra Maddu,Rajendra Wudayagiri,Varadacharyulu Nallanchakravarthula

    Summary: This research was planned to assess the protective effect of aqueous green tea extract (AGTE) in alcohol treated diabetic rats. This study was examined, whether 20% v/v of 5 g/kg.b.w alcohol intake exacerbates diabetes-induced renal damage associated with an escalated nitroxidative stress and glucose homeostasis in comparison with diabetic condition alone. The present study is primarily focused to investigate the possible toxic effects of chronic alcohol intake on kidney of streptozotocin (STZ)-induced diabetic rats. Forty albino male Wistar rats were used and randomly allocated into five groups. Diabetes was induced by a single intraperitoneal injection of STZ (50 mg/kg) in rats. Alcohol was administered through orogastric tube once daily for a period of 60 days. Impact of chronic alcohol treatment on renal function and selected metabolites of catecholamines and antioxidant metabolisms have been investigated in the kidney of STZ-induced diabetic rats. Biochemical analysis of kidneys demonstrated that chronic alcohol induced alterations in vitro gluconeogenesis, significant decrease in the body weight, and activities of antioxidant enzymes in diabetic rats. A significant increase in the levels of epinephrine and sertonine was observed between alcohol treated, diabetic control and alcohol treated diabetic rat groups. Further, excessive chronic alcohol treatment caused additive deterioration of the kidney function as evidenced by increased inducible nitric oxide synthase (iNOS) protein expression and thus nitroxidative stress and histopathological aberrations leading to aggravation of diabetic nephropathy under alcohol intoxication. Treatment with aqueous green tea extract (300 mg/kg.b.w) to diabetic rats treated with alcohol renders the protection against the decreased body weight, increased hyperglycemia, hyperlipidemia, catecholamines, nitroxidative stress and further tissue damage.

    2020引用:14
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    高被引作者

    作者引用发文
    Catherine Stanton1831
    Ruairi C Robertson1831
    Clara Seira Oriach1831
    John Cryan1831
    Timothy Dinan1831
    Dan Waitzberg1243
    Raquel Susana Torrinhas1232
    Harald Hoensch1001
    Reinhard Oertel1001
    Bagga Paramdeep Singh981

    高产作者

    作者引用发文
    Dan Waitzberg1243
    Bothe Melanie K13
    Moïse Coëffier143
    Johannes Harleman13
    Nurdiana Nurdiana233
    Pierre Singer313
    André Léké462
    Peter V Van Heerden42
    Pichard Claude412
    John F Stover02

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