14 research outputs found

    Zygophyllum album aqueous extract reduces oxidative damage in red blood cells and attenuates pro-inflammatory plasma markers in hypercholesterolemic-diabetic rats

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    Zygophyllum album (Z. album) is used in traditional medicine for a long time for its anti-diabetic activities. This study had to assess Z. album extract supplementation effects on redox and inflammatory statuses in hypercholesterolemic-diabetic rats. Male rats Wistar (n=36), weighing 200±10 g were divided into three groups (n=12). The first group was rendered hypercholesterolemic (HC) with a high cholesterol diet (1 %). The second group was rendered diabetic (D) by intraperitoneal injection of streptozotocin (STZ) (35 mg/kg of body weight). The third group was rendered hypercholesterolemic-diabetic (HC-D); each group was divided into two groups (n=6), untreated groups (HC, D, HC-D) and treated groups with 1 % Z. album extract (HC-Za, D-Za and HC-D-Za). After 28 days, Z. album treatment lead to a decrease in RBC’s TBARS contents in HC-Za (-44 %), D-Za (-66 %) and HC-D-Za (-23 %) groups. An increase in the antioxidant enzymes activities (superoxide dismutase, glutathione peroxidase, glutathione reductase and catalase) was observed in HC-Za, D-Za and HC-D-Za (p <0.05). IL-1 β and IL-6 concentrations were reduced by -44, -50 and -33 % and -49, 38 and -41 %, respectively in treated groups. A decrease in TNF-α as well as homocysteine and CRP was observed in Z. album treated groups (p <0,05). In conclusion, Z. album reduces radical attack and improves the anti-inflammatory proprieties in hypercholesterolemic-diabetic rats

    Zygophyllum album aqueous extract reduces oxidative damage in red blood cells and attenuates pro-inflammatory plasma markers in hypercholesterolemic-diabetic rats

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    Zygophyllum album (Z. album) is used in traditional medicine for a long time for its anti-diabetic activities. This study had to assess Z. album extract supplementation effects on redox and inflammatory statuses in hypercholesterolemic-diabetic rats. Male rats Wistar (n=36), weighing 200±10 g were divided into three groups (n=12). The first group was rendered hypercholesterolemic (HC) with a high cholesterol diet (1 %). The second group was rendered diabetic (D) by intraperitoneal injection of streptozotocin (STZ) (35 mg/kg of body weight). The third group was rendered hypercholesterolemic-diabetic (HC-D); each group was divided into two groups (n=6), untreated groups (HC, D, HC-D) and treated groups with 1 % Z. album extract (HC-Za, D-Za and HC-D-Za). After 28 days, Z. album treatment lead to a decrease in RBC’s TBARS contents in HC-Za (-44 %), D-Za (-66 %) and HC-D-Za (-23 %) groups. An increase in the antioxidant enzymes activities (superoxide dismutase, glutathione peroxidase, glutathione reductase and catalase) was observed in HC-Za, D-Za and HC-D-Za (p <0.05). IL-1 β and IL-6 concentrations were reduced by -44, -50 and -33 % and -49, 38 and -41 %, respectively in treated groups. A decrease in TNF-α as well as homocysteine and CRP was observed in Z. album treated groups (p <0,05). In conclusion, Z. album reduces radical attack and improves the anti-inflammatory proprieties in hypercholesterolemic-diabetic rats

    In vivo and in vitro effects of fructose on rat brain acetylcholinesterase activity: an ontogenetic study

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    Increased fructose concentrations are the biochemical hallmark of fructosemia, a group of inherited disorders on the metabolic pathway of this sugar. The main clinical findings observed in patients affected by fructosemia include neurological abnormalities with developmental delay, whose pathophysiology is still undefined. In the present work we investigated the in vitro and in vivo effects of fructose on acetylcholinesterase (AchE) activity in brain structures of developing rats. For the in vitro experiments, fructose was added at increasing concentrations to the incubation medium. It was observed that fructose provoked an inhibition of acetylcholinesterase activity in cerebral cortex of 30-day-old-rats, even at low concentrations (0.1 mM). For the in vivo experiments, rats were killed 1 h after a single fructose administration (5 µmol/g). Control group received the same volume of saline solution. We found that AchE activity was increased in cerebral cortex of 30- and 60-day-old rats receiving fructose administration. Finally, we observed that AchE activity was unaffected by acute fructose administration in cerebral cortex, striatum or hippocampus of 15- and 90-day-old rats. The present data suggest that a disruption in cholinergic homeostasis may be involved in the pathophysiology of brain damage observed in young patients affected by fructosemia

    Sardine proteins (Sardina pilchardus) combined with green lemon zest (Citrus latifolia) improve blood pressure, lipid profile and redox status in diabetic hypertensive rats

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    Purpose This paper aims to study the effect of green lemon zest combined with sardine proteins in diabetic hypertensive rats (DHRs). Design/methodology/approach Male Wistar rats (n = 30) weighing 250 ± 10 g were divided into five groups. The first group consumed a diet containing 20 per cent casein (C). The other four groups are rendered diabetic by intraperitoneal injection of streptozotocin (40 mg/kg body weight), then hypertensive by subcutaneous implantation controlled time-release pellet containing ouabain (0.25 mg/pellet). One untreated group (DHR) consumed 20 per cent casein and the three other groups consumed the same diet supplemented with 2 per cent green lemon zest (DHR-lz), or with 20 per cent of sardine protein (group DHR-sp) or with the combination of both sardine proteins and green lemon zest (group DHR-sp + lz). Findings DHRs feeding on the combination of both sardine protein (sp) and lemon zest (lz) induced a significant decrease of diastolic blood pressure and heart rates values compared with DHR (p &lt; 0.05). The HDLC values were increased by +55 per cent in DHR-sp + lz compared with DHR group. Moreover, plasma non-HDLC concentrations were decreased significantly compared to DHR, DHR-lz, DHR-sp and C groups. In DHR-sp + lzvs DHR group, TBARS values were decreased by −25 per cent in the liver. Moreover, kidney TBARS were significantly reduced by −66, −51, −65 and −67 per cent compared with C, DHR, DHR-lz and DHR-sp, respectively. Originality/value These results suggest that consumption of green lemon zest combined with sardine proteins can reduce blood pressure and tissue oxidative damage and, therefore, help to prevent cardiovascular complications in hypertensive diabetic patients. </jats:sec

    Zygophyllum album aqueous extract reduces protein oxidation and protects endothelial function in hypercholesterolemic-diabetic rats

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    Zygophyllum album (Z. album) is an endemic plant in Algeria and is known for its medicinal properties since long times. This study assess Z. album extract supplementation effects on protein oxidation and endothelial dysfunction tissues in rats rendered hypercholesterolemic-diabetic. Male Wistar rats (n=36), weighing 200±10 g were divided into three groups (n=12). The first group was rendered hypercholesterolemic with an enriched cholesterol diet (1 %) (HC). The second group was rendered diabetic by intraperitoneal injection of streptozotocin (STZ) (35 mg/kg of body weight) (D). The third group was hypercholesterolemic and diabetic (HC-D); each group was divided into two groups (n=6), untreated groups (HC, D, HC-D) and treated groups with 1 % Z. album extract (HC-Za, D-Za and HC-D-Za). At d28 of the experiment, Z. album treatment lead to a similar weight growth in HC-Za vs HC and HC-D-Za vs HC-D, while was increased in D-Za vs D (+35 %); similarly, food intake was increased by +17 %. An increase in glutathione (GSH) levels was noted in liver, heart and adipose tissue (p &lt;0.05). Therefore,reduced carbonyls tissue concentrations after Z. album supplementation in HC-Za, D-Za and HC-D-Za was noted; there was respectively a decrease by -38, -52 and -46 % in liver; -36, -32 and -35 % in kidneys and -27, -39 and -27 %, in adipose tissue. An increase in nitric monoxide (NO) levels was observed in all treated groups (p &lt;0.05). In conclusion Z. album stimulates GSH synthesis, attenuates protein oxidation and protects endothelial function in hypercholesterolemic-diabetic rats.</jats:p

    Zygophyllum album aqueous extract reduces oxidative damage in erythrocytes and attenuates pro-inflammatory markers in hypercholesterolemic-diabetic rats

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    Introduction. Zygophyllum album (Z. album) is used in traditional medicine for a long time for its anti-diabetic activities. Objective. To investigate Z. album extract supplementation effects on redox and inflammatory status in hypercholesterolemic-diabetic rats. Material and methods. Male Wistar rats (n=36), weighing 200±10g were divided into three groups (n=12). The 1st group was hypercholesterolemic (HC) by consuming cholesterol enriched diet (1%). The 2nd group was diabetic (D) by intraperi-toneal injection of streptozotocin (STZ) (35 mg/kg body weight). The 3rd group was hypercholesterolemic-diabetic (HC-D). Each group was divided into two subgroups (n=6), untreated (HC, D, HC-D) and treated groups with 1% Z. album extract (HC-Za, D-Za and HC-D-Za). Results. At d28, Z. album treatment lead to a decrease in erythrocytes thiobarbituric reactive substances (TBARS) in HC-Za (-44%), D-Za (-66%) and HC-D-Za (-23%) groups. Increased erythrocytes antioxidant enzymes activities (superoxide dismu-tase, glutathione peroxidase, glutathione reductase and catalase) were observed in HC-Za, D-Za and HC-D-Za (p&lt;0.05). In plasma, interleukin (IL-1 β and IL-6) concentrations were reduced by -44, -50 and -33%, and -49, 38 and -41%, respectively in treated groups. In plasma, a decrease of TNF-α (Tumor Necrosis Factor-α), homocysteine and protein-C reactive (CRP) was observed in Z. album treated groups (p&lt;0.05). Conclusion. Z. album reduces radical attack and improves anti-inflammatory proprieties in hypercholesterolemic-diabetic rats.</jats:p

    Beneficial effects of<i>linum usitatissimum L.</i>on dyslipidemia, oxidative stress and inflammatory cytokines in hypercholesterolemic rats

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    PurposeThis paper aims to study the effects of a diet supplemented with flaxseeds on dyslipidemia, oxidative stress and proinflammatory cytokines, in rats consuming a high-cholesterol diet.Design/methodology/approachMale Wistar rats (n= 30) weighing (250 ± 5 g) of which 10 were control and 20 were rendered hypercholesterolemic (HC) by feeding a diet enriched with 1% of cholesterol, for 15 days. After this phase, rats were divided into two groups; hypercholesterolemic group (HC) (n= 10), fed 20% casein diet enriched with 1% cholesterol; and hypercholesterolemic rats fed the same diet (n= 10), but additionally supplemented with flaxseeds (Linum usitatissimum) (Lu) powder, i.e. HC-Lu. Animals of the control group (n= 10) were fed the casein diet. All the animals were maintained on the respective diets for four weeks.FindingsThis study showed that in HC-Lu as compared to HC group, plasma total cholesterol, triacylglycerols and non-HDL cholesterol concentrations were respectively 2.4-, 1.5- and 3-fold lower. Also, the lipid peroxidation was reduced in red blood cells, organs (liver, heart and aorta) and lipoproteins (HDL2, HDL3 and VDL-LDL). A higher superoxide dismutase activity was observed in liver (+61%), heart (+62%) and aorta (+59%), whereas plasma proinflammatory cytokine (IL-1beta and IL-6) levels were decreased.Originality/valueThese results suggest that flaxseeds help to reduce hypercholesterolemia, oxidative stress and inflammation in patients with hypercholesterolemia.</jats:sec

    Favorable effects of <i>Globularia alypum</i> on cardiometabolic markers in high fructose-fed rats

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    Purpose This study aims to examine whether Globularia alypum (Ga) lyophilized aqueous leaves extract treatment improves cardiometabolic syndromes such as hyperglycemia, lipid profiles and oxidative damage resulting from a high-fructose diet induced in hypertriglyceridemic rats. Design/methodology/approach A total of 24 male Wistar rats weighing 80 ± 5 g were first randomly divided into 2 groups. A total of 12 control rats (C) were fed a standard-diet (St-D) and 12 high fructose (HF) rats were fed a high-fructose diet (HF-D) containing St-D in which cornstarch was substituted by fructose (61.4%). After 15 weeks of feeding, body weight (BW) was about 320 ± 20 g and hypertriglyceridemia was noted in HF vs C group (2.69 ± 0.49 mmol/L) vs (1.25 ± 0.33 mmol/L). Each group of rats was then divided into two equal groups (n = 6) and fed during four weeks either a St-D or HF-D, treated or not with 1% of Ga extract (C-Ga) and (HF-Ga). After 28 days, fasting rats were anesthetized and blood and tissues were removed to measure biochemical parameters. Findings The results showed no significant differences in BW and insulinemia between all groups. Ga extract supplementation reduced glycemia (−36%), glycosylated hemoglobin (−37%), Homeostasis Model of Assessment-Insulin Resistance index (−34%) and triacylglycerol’s contents in plasma (−33%), very low density lipoproteins–low density lipoproteins (VLDL-LDL) (−48%), liver (−52%) and aorta (−39%); total cholesterol concentrations in aorta was 3.7-fold lower in HF-Ga vs HF group. Ga treatment reduced lipid peroxidation in plasma, VLDL-LDL, red blood cells (RBC), liver, muscle and kidney by improving superoxide dismutase (SOD) activity and glutathione peroxidase (GPx) in RBC and catalase (CAT) activity in kidney (p &lt; 0.05). Moreover, Ga ameliorates glutathione (GSH) production in RBC (+41%) and kidney tissues (+35%). Originality/value Ga extract ameliorated cardiometabolic syndrome by its hypotriglyceridemic effect and prevented development of insulin resistance. It reduces lipid peroxidation by enhancing non-enzymatic (GSH) and enzymatic (SOD, GPx and CAT) antioxidant defense systems in high-fructose hypertriglyceridemic rats. Therefore, supplementation of Ga leaves extract as an adjuvant could be used for the treatment of hypertriglyceridemia and the prevention and/or the management of cardio-metabolic adverse effects. </jats:sec

    Effects of citrus latifolia extract on dyslipidemia and tissues redox status in rats fed a high-cholesterol diet

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    Purpose This study aims to investigate the possible effect of Citrus latifolia (CL) extract on biomarkers of oxidative stress, including lipid peroxidation products in rats fed a high cholesterol diet Design/methodology/approach Hypercholesterolemia was induced by feeding normocholesterolemic rats 1 per cent cholesterol-enriched diet for 15 days. An experimental group (n = 20) was divided into two groups (n = 10) and fed the same diet with or without CL lyophilized aqueous extract (1 per cent) for four weeks. At day 28, ten rats from each group were killed. Findings Treatment with CL lyophilized aqueous extract compared with the untreated group had decreased plasma total cholesterol (TC) (−36 per cent), triacylglycerols (−48 per cent), isoprostanes values (−74 per cent) and reduced thiobarbituric acid reactive substances in erythrocytes (−21 per cent). However, the supplementation of CL peels in the hypercholesterolemic diet enhanced superoxide dismutase (+69 per cent), glutathione reductase (+30 per cent) and catalase activities (+34 per cent). Originality/value In hypercholesterolemic rats, administering CL extract ameliorates dyslipidemia and attenuates lipid peroxidation in tissues. These results suggest that CL could be beneficial in the primary treatment of hypercholesterolemia and oxidative damage caused by a high-cholesterol diet. </jats:sec
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