{"id":687,"date":"2021-03-22T22:01:40","date_gmt":"2021-03-22T22:01:40","guid":{"rendered":"https:\/\/veterinarska-stanica-journal.hr\/?post_type=article&#038;p=687"},"modified":"2021-06-16T15:01:11","modified_gmt":"2021-06-16T13:01:11","slug":"hypolipidemic-and-cardioprotective-effects-of-taraxacum-officinal-aqueous-extract-in-obese-rats","status":"publish","type":"article","link":"https:\/\/journal.h3s.org\/?article=hypolipidemic-and-cardioprotective-effects-of-taraxacum-officinal-aqueous-extract-in-obese-rats","title":{"rendered":"Hypolipidemic and cardioprotective effects of <em>Taraxacum officinal<\/em> aqueous extract in obese rats"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/04\/ToumiIKRAM.jpg\" alt=\"\" width=\"200\" height=\"250\" class=\"alignright size-full wp-image-1672\" \/><\/p>\n<p style=\"text-align: center;\">Toumi <strong>Ikram<\/strong>*, Medila <strong>Ifriqya<\/strong> and Lifa <strong>Saoussane<\/strong><\/p>\n<hr \/>\n<div class=\"info\"><strong>Toumi IKRAM<\/strong>*, DVM, Senior Professor, (Corresponding author, e-mail: toumi-ikram@univ-eloued.dz), <strong>Medila IFRIQYA<\/strong>, DVM, Senior Professor, Department of Cellular and Molecular Biology, Life and Natural Sciences Faculty, University of Hamma Lakhdar El Oued, 39000, Algeria, Biology, Environment and Health Laboratory, University of Hamma Lakhdar El Oued, 39000, Algeria; <strong>Lifa SAOUSSANE<\/strong>, Assistant Master, Biology, Environment and Health Laboratory, University of Hamma Lakhdar El Oued, 39000, Algeria<\/div>\n<div class=\"doi\"><a href=\"https:\/\/veterinarska-stanica-journal.hr\/pdf\/52\/52-4\/06-hypolipidemic-and-cardioprotective-effects-of-taraxacum-officinal-aqueous-extract-in-obese-rats.pdf\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/03\/pdf.png\" alt=\"\" width=\"32\" height=\"18\" class=\"alignleft size-full wp-image-1504\" \/><\/a><a href=\"https:\/\/doi.org\/10.46419\/vs.52.4.6\" rel=\"noopener\" target=\"_blank\">https:\/\/doi.org\/10.46419\/vs.52.4.6<\/a><\/div>\n<\/p>\n<p><a name=\"menu\"><\/a><\/p>\n<div class=\"block grey mid\"><span class=\"small\"><a class=\"btn\" href=\"#Abstract\">Abstract<\/a><a class=\"btn\" href=\"#Introduction\">Introduction<\/a><a class=\"btn\" href=\"#Materials\">Materials and methods<\/a><a class=\"btn\" href=\"#Dosage\">Dosage of serum and tissue lipid parameters<\/a><a class=\"btn\" href=\"#Results\">Results<\/a><a class=\"btn\" href=\"#Conclusions\">Conclusions<\/a><a class=\"btn\" href=\"#Literatura1\" onclick=\"toggle_visibility('Literatura');\">References<\/a><a class=\"btn\" href=\"#Sazetak\">Sa\u017eetak<\/a><\/span><\/div>\n<p><a name=\"Abstract\"><\/a><a class=\"alignright\" href=\"#\" onclick=\"scrollToTop();return false\"> &#9650;<\/a><\/p>\n<blockquote>\n<h2>Abstract<\/h2>\n<hr \/>\n<p>Obesity is a chronic disease responsible for comorbidity and excess mortality, and is considered an independent risk factor for cardiovascular pathology development. Most cardiovascular disease can be prevented by tackling behavioural risk factors, such as a sedentary lifestyle, unhealthy diet, and obesity. <em>Taraxacum officinal<\/em> is a perennial plant belonging to the <em>Asteraceae<\/em> family, commonly used for these medicinal characteristics.<br \/>\nIt has diuretic, anti-tumour, antioxidant, anti-inflammatory, hepatoprotective and immunostimulant properties. The aim of this study was to evaluate the lipid-lowering and cardioprotective effect of <em>Taraxacum officinal<\/em> aqueous extract in Wistar rats on hyper-fatty diets. A total of 24 rats weighing 200 \u00b1 6.8 g were divided into three lots: healthy control (HC) receiving a standard diet, obese control (OC) receiving a cafeteria diet without treatment and the third load (TL) receiving a cafeteria diet and treated for 20 days with 200 mg\/kg <em>Taraxacum officinal<\/em> aqueous extract. The results showed that the cafeteria diet induced obesity in rats compared to the control group, characterized by hyperglycaemia (148.75 mg\/dL), hypertriglyceridemia (59 mg\/dL) and hypercholesterolemia (160.67 mg\/dL) with an increase in total lipids (0.39 g\/g of tissue) associated with a state of oxidative stress in the cardiac tissue. Oral administration of the aqueous extract of <em>Taraxacum officinal<\/em> improved the lipid profile in serum and tissue. The findings showed a drop in blood sugar (1.02 mg\/dL), total cholesterol (135 mg\/dL), LDL cholesterol, (67 mg\/dL), triglycerides (36 mg\/dL), total lipids (1.37g\/g of tissue), and lipid peroxidation MDA (0.25 \u00b1 0.02 \u03bcmoL\/g protein), and an increase in the level of GSH (0.51 nM \/mg protein) in treated rats compared to the controls. In conclusion, the results obtained showed the effectiveness of the aqueous extract of <em>Taraxacum officinal<\/em> against dyslipidemia, obesity, and hyperglycaemia. The plant was shown to have both cardioprotective and antioxidant effect.<\/p>\n<p><strong>Key words:<\/strong> <em>Cardiac disease; Dyslipidemia; Obesity; Oxidative stress; Risk factor; Taraxacum officinal<\/em><\/p><\/blockquote>\n<p><a name=\"Introduction\"><\/a><a class=\"alignright\" href=\"#menu\"> &#9650;<\/a><\/p>\n<h2>Introduction<\/h2>\n<hr \/>\n<p>The key risk factors for cardiac disease and stroke are unhealthy diet, lack of physical activity, smoking and excessive alcohol intake. The consequences of lifestyle risk factors can affect people with hypertension, hyperglycaemia, hyperlipidaemia, excessive body weight and obesity. Obesity is the state of an organism with excess adiposities or excess fat mass resulting from a positive energy balance, in proportions that may have negative health effects. Visceral and massive obesity is a well-established risk factor for high blood pressure (hypertension), coronary heart disease and excess cardiovascular mortality (Corcos, 2012). The risk of coronary artery disease in obese and overweight people is partially explained by the frequent coexistence of other cardiovascular risk factors. Studies have also shown that there is a longitudinal linear relationship between obesity and coronary artery disease (Jousilahti <em>et al<\/em>., 1996).<\/p>\n<p>Obese subjects are often distinguished by a dyslipidemic state in which plasma triglycerides are increased, HDL-C concentrations are lowered, and LDL apolipoprotein (Apo B-100) concentrations are increased. Hence central fat distribution plays a significant role in lipid abnormalities (Despres and Lemieux, 2006). The main risk of these pathologies is the appearance of cardiovascular disease through the formation of atheroma plaques that gradually block the arteries, causing atherosclerosis. Hypertension, coronary insufficiency, stroke, venous thrombosis and pulmonary embolism are major cardiovascular diseases associated with obesity. Another disorder is heart failure, which results from fatigue of the heart caused by excess body weight and the associated complications (Must <em>et al<\/em>., 1999; Hensrud and Klein, 2006). Given the side effects of surgery and the harmful effects of synthetic drugs on weight loss, natural products are a better option in the treatment of excessive body weight, obesity and other medical disorders due to their efficacy (James, 2017).<\/p>\n<p><em>Taraxacum officinal<\/em> is a perennial plant belonging to the <em>Asteraceae<\/em> family, commonly used for its medicinal characteristics. It has diuretic, anti- tumour, antioxidant, anti-inflammatory, and hepatoprotective activity (Baba <em>et al<\/em>., 1981; Kisiel and Barszcz, 2000; Hu and Kitts, 2003; Jeon <em>et al<\/em>., 2008). The aim of this study was to evaluate the lipid-lowering and cardioprotective effect of <em>Taraxacum officinal<\/em> aqueous extract in obese Wistar rats.<\/p>\n<p><a name=\"Materials\"><\/a><a class=\"alignright\" href=\"#menu\"> &#9650;<\/a><\/p>\n<h2>Materials and methods<\/h2>\n<hr \/>\n<h3>Aqueous extract preparation<\/h3>\n<p>A total of 10 g powdered leaves dissolved in 150 ml distilled water was heated to reflux for 2 hours. After cold filtration; this filtrate was then evaporated to dryness reduced to 65\u00b0C using a rotating evaporator.<\/p>\n<h3>Animals and Obesity induction<\/h3>\n<p>The experiment included 24 Wistar rats weighing 200\u00b16.8 g from the Pasteur Institute, Algeria. Rats were acclimatized for two weeks under the conditions of the Molecular and Cell Biology Department, El Oued University, Algeria: air temperature of 22\u00b12 \u00b0C, 50% humidity and a normal photoperiod (12 h light\/12 h darkness).<\/p>\n<p>To induce obesity, rats were given either a standard diet (control) or the cafeteria diet for a period of one month.<br \/>\nThe cafeteria diet is made up of 50% standard diet and 50% sausage mixture, dry cookies, cheese, chips, peanut, and chocolate in the ratio 2:2:1:1:1 (Darimont <em>et al<\/em>., 2004). Obesity perception in rats was confirmed by monitoring body weight gain and the quantity of food consumed during one month.<\/p>\n<h3>Treatment of animals<\/h3>\n<p>After one month, non-obese rats served as the healthy control lot (HC) receiving a standard diet with tap water.<br \/>\nObese rats were divided into two groups: obese control (OC) receiving a cafeteria diet without treatment, and the third load (TL) receiving a cafeteria diet and treated for 20 days with 200 mg\/kg <em>Taraxacum officinale<\/em> aqueous extract.<\/p>\n<h3>Sacrifice, blood and organs samples<\/h3>\n<p>Rats were anesthetized with chloroform (94%) and sacrificed after 12 hours of fasting. Blood samples were collected in EDTA and dry tubes. After centrifugation at 3000 rpm for 15 minutes, serum and plasma were collected and stored for lipid parameter determination.<br \/>\nThe liver, heart, adipose tissue, and kidneys were carefully removed after dissection, rinsed with saline solution, and weighed. Organ homogenates were used to evaluate oxidative stress parameters and to measure tissue lipids.<\/p>\n<p><a name=\"Dosage\"><\/a><a class=\"alignright\" href=\"#menu\"> &#9650;<\/a><\/p>\n<h2>Dosage of serum and tissue lipid parameters<\/h2>\n<hr \/>\n<p>Triglycerides (TG), total cholesterol, HDL-cholesterol and glutamate-oxalo-ac\u00e9tate-transaminase (GOT) were determined using the colorimetric method by a type autoanalyzer (BIOLIS24j) with the appropriate reagent package for each parameter. LDL-cholesterol was determined using the direct calculation method according to the formula of Friedwald <em>et al<\/em>. (1972): LDL-C = Total cholesterol &#8211; [HDL-C + TG \/ 5].<\/p>\n<p>For the quantification of total lipids at the tissue level, we used cold extraction with a mixture of polar\/apolar solvents (chloroform\/methanol) according to the Folch <em>et al<\/em>. (1957) method.<\/p>\n<h3>Oxidative stress parameters<\/h3>\n<p>To prepare homogeneous organs, 1 gram of tissue (heart, liver, kidney and adipose tissue) from each rat was used from the various study groups. After grinding and homogenizing the tissues in TBS (Tris 50 mM, NaCl 150 m M, pH 7.4), samples were centrifuged at 3000 r\/min for 15 min. The supernatant was recuperated to perform the oxidative stress parameter assay.<\/p>\n<p>The thiobarbituric acid method (TBA; Yagi, 1976) is used to determine malondialdehyde (MDA) which reacts with TBA to give pink absorbing chromophores at 532 nm. Glutathione (GSH) was determined by a SHIMATZU type spectrophotometer using the colorimetric method (Weckbecker and Cory, 1988); the measurement of optical density was the result of the formation of 2-nitro-5 mercocapturic acid from the reduction of dithio-bis2 nitrobenzoic acid. Absorbance was set at 412 nm.<\/p>\n<h3>Statistical analysis<\/h3>\n<p>The results are presented as mean \u00b1 standard deviation. The comparison of means was carried out by the Student t-test using MINITAB and EXCEL software. Differences were considered significant at <em>P<\/em><0.05.\n\n\n\n<a name=\"Results\"><\/a><a class=\"alignright\" href=\"#menu\"> &#9650;<\/a><\/p>\n<h2>Results<\/h2>\n<hr \/>\n<h3>Food consumption, weight gain and total fat content in tissue<\/h3>\n<p>The results obtained are presented in Table 1.<\/p>\n<figure id=\"attachment_1683\" aria-describedby=\"caption-attachment-1683\" style=\"width: 653px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/03\/table01-hypolipidemic-and-cardioprotective-effects.png\" alt=\"\" width=\"653\" height=\"107\" class=\"size-full wp-image-1683\" srcset=\"https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table01-hypolipidemic-and-cardioprotective-effects.png 653w, https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table01-hypolipidemic-and-cardioprotective-effects-300x49.png 300w\" sizes=\"auto, (max-width: 653px) 100vw, 653px\" \/><figcaption id=\"caption-attachment-1683\" class=\"wp-caption-text\"><strong>Table 1.<\/strong> Food consumption and weight gain in control rats, obese controls and treated rats (mean \u00b1 standard error).<br \/>Comparison with control group (C): *** <em>P<\/em> &lt; 0.001, with obese control group (OC): <sup>a<\/sup><em>P<\/em> &lt; 0.05; <sup>c<\/sup><em>P<\/em> &lt; 0.001, <em>n<\/em> = 8 rats.<\/figcaption><\/figure>\n<p>During treatment, there was no difference in the amount of food consumed by rats receiving the cafeteria diet compared to the control lot. Treatment with <em>Taraxacum officinal<\/em> aqueous extract significantly decreased food intake in obese rats compared to the control (HC).<br \/>\nThe results showed that the cafeteria diet induced an increase in weight gain and tissue lipid content in obese control rats relative to the control group. In the Wistar rat, consuming a hyperlipidic and high-calorie diet increases food intake, body weight and induces lipid accumulation in adipose tissue (Milagro <em>et al<\/em>., 2006; Bouanane <em>et al<\/em>., 2010; Benkalfat <em>et al<\/em>., 2011). The accumulation of adipose tissue and its lipid enrichment is a feature of the cafeteria diet induced by obesity (Caluwaerts <em>et al<\/em>., 2007). Lipotoxicity results from an ectopic accumulation of lipids in the liver, and the muscles and heart are involved in the insulin resistance of these different tissues (Despres and Lemieux, 2006).<\/p>\n<p>However, the administration of <em>Taraxacum officinal<\/em> aqueous extract causes a considerable reduction in weight gain and in tissue lipid content in the treated group (TL) compared to the obese control group (OC). This decrease in weight may be due to several mechanisms. According to Kajimura and Saito, (2014), most natural anti-obesity products (medicinal plants) regulate body weight through an increase in compulsory energy expenditure by transforming energy from food into heat.<\/p>\n<h3>Blood glucose and lipid content<\/h3>\n<p>The results showed a significant increase in glycaemia, triglycerides, cholesterol and LDL-C levels, and a decrease in HDL-C levels in the OC group compared to the control group C.<br \/>\nHowever, significant decreases (<em>P<\/em> &lt; 0.01) in glucose and serum lipids were observed in the treated group (TL) (Table 2).<\/p>\n<figure id=\"attachment_1684\" aria-describedby=\"caption-attachment-1684\" style=\"width: 653px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/03\/table02-hypolipidemic-and-cardioprotective-effects.png\" alt=\"\" width=\"653\" height=\"180\" class=\"size-full wp-image-1684\" srcset=\"https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table02-hypolipidemic-and-cardioprotective-effects.png 653w, https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table02-hypolipidemic-and-cardioprotective-effects-300x83.png 300w\" sizes=\"auto, (max-width: 653px) 100vw, 653px\" \/><figcaption id=\"caption-attachment-1684\" class=\"wp-caption-text\"><strong>Table 2.<\/strong> Plasma concentration of glucose, triglycerides (TG), cholesterol (CL), HDL and LDL in the control and treated groups (mean \u00b1 standard error).<br \/>Comparison with control group (C): ***<em>P<\/em> &lt; 0.001, **<em>P<\/em> &lt; 0.01, *<em>P<\/em> &lt; 0.05 with obese control group (OC): <sup>a<\/sup><em>P<\/em> &lt; 0.05; <sup>c<\/sup><em>P<\/em> &lt; 0.001, <em>n<\/em> = 8 rats.<\/figcaption><\/figure>\n<p>Obesity caused by the cafeteria diet induced an increase in blood sugar.<br \/>\nStudies have reported that rats with a diet high in fat develop insulin resistance and confirmed hyperglycaemia (Stubbs and Wickremesekera 2002; Bihan <em>et al<\/em>., 2007). The hyper lipid diet increases glucose production by reducing insulin suppression and increasing gluconeogenesis (Mart\u00ednez-Gonzalez <em>et al<\/em>., 1989), resulting in elevated plasma glucose levels. Studies of <em>Taraxacum officinal<\/em> extracts revealed that it can stimulate insulin release into the \u03b2 cells of the pancreas, thus neutralizing the effects of hyperglycaemia (Hussain <em>et al<\/em>., 2004; Sch\u00fctz <em>et al<\/em>., 2006).<\/p>\n<p>The results indicate an observed hyperlipidaemia in OC rats, which can be explained by the high lipid content in the diet. Obesity is also distinguished by an expansion of the adipose tissue mass and an increase in the cholesterol and triglyceride storage capacity (Benkalfat <em>et al<\/em>., 2011), which raises the risk of cardiovascular disease. Kim <em>et al<\/em>. (2000) identified that triglyceride accumulation was associated with insulin resistance as a result of insulin signalling disruption in tissues.<\/p>\n<p>The results also showed a significant increase in LDH cholesterol. The increased serum LDH activity is a precursor for necrosis of cardiac tissue (Ben Amor <em>et al<\/em>., 1999). The administration of aqueous extract of <em>Taraxacum officinale<\/em> decreased the serum level of LDH thus inducing a decrease in cardiac tissue necrosis. In rats, <em>Taraxacum officinal<\/em> leaf extract has been shown to reduce serum glucose, cholesterol and triglyceride levels, possibly due to the elevation of protein kinase activated by adenosine monophosphate (AMPK) in the liver, resulting in a significant decrease in the accumulation of lipids and an improvement in sensitivity to insulin (Davaatseren <em>et al<\/em>., 2013). Several studies have reported the presence of saponins in the <em>Taraxacum officinal<\/em> aqueous extract (Mir <em>et al<\/em>., 2013), the latter having anti-hyperlipidaemia and anti-hypercholesterolemia effect (\u00d6zlem and Giuseppe, 2007).<\/p>\n<h3>GOT levels and oxidative stress biomarkers in cardiac tissue<\/h3>\n<p>The results obtained show an increase in the serum activity of GOT in the obese control group compared to the control group (<em>P<\/em> &lt; 0.01; Figure 1).<\/p>\n<figure id=\"attachment_1685\" aria-describedby=\"caption-attachment-1685\" style=\"width: 555px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/03\/fig01-hypolipidemic-and-cardioprotective-effects.jpg\" alt=\"\" width=\"555\" height=\"341\" class=\"size-full wp-image-1685\" srcset=\"https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/fig01-hypolipidemic-and-cardioprotective-effects.jpg 555w, https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/fig01-hypolipidemic-and-cardioprotective-effects-300x184.jpg 300w\" sizes=\"auto, (max-width: 555px) 100vw, 555px\" \/><figcaption id=\"caption-attachment-1685\" class=\"wp-caption-text\"><strong>Figure 1.<\/strong> Activity of GOT transaminases in control groups and treated group.<br \/>Comparison with control group (C): ** <em>P<\/em> &lt; 0.01, with obese control group (OC): <sup>b<\/sup><em>P<\/em> &lt; 0.01, <em>n<\/em> = 8 rats.<\/figcaption><\/figure>\n<p>The increase in serum transaminase activity (GOT) in obese rats is considered to be a biomarker of hepatic dysfunction or cardiac damage (Fiacre <em>et al<\/em>., 2002; Dieusaert, 2005) caused by the hyper fat diet. However, GOT was reduced after the administration of <em>Taraxacum offilcinal<\/em> aqueous extract, and this effect could be interpreted as a protective effect of the cardiovascular system.<\/p>\n<p>The results show a significant increase in the malondialdehyde (MDA) concentration (Table 3) in cardiac tissue in obese controls compared with healthy controls, which favours apparent oxidative stress.<\/p>\n<figure id=\"attachment_1686\" aria-describedby=\"caption-attachment-1686\" style=\"width: 653px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/veterinarska-stanica-journal.hr\/wp-content\/uploads\/2021\/03\/table03-hypolipidemic-and-cardioprotective-effects.png\" alt=\"\" width=\"653\" height=\"80\" class=\"size-full wp-image-1686\" srcset=\"https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table03-hypolipidemic-and-cardioprotective-effects.png 653w, https:\/\/journal.h3s.org\/wp-content\/uploads\/2021\/03\/table03-hypolipidemic-and-cardioprotective-effects-300x37.png 300w\" sizes=\"auto, (max-width: 653px) 100vw, 653px\" \/><figcaption id=\"caption-attachment-1686\" class=\"wp-caption-text\"><strong>Table 3.<\/strong> Cardiac tissue concentrations of malondialdehyde (MDA) and reduced glutathione (GSH) in the control, obese control and treated group (mean \u00b1 standard error).<br \/>Comparison with control group (C): **<em>P<\/em> &lt;  0.01, *<em>P<\/em> &lt; 0.05 with obese control group (OC): <sup>b<\/sup><em>P<\/em> &lt; 0.01, <em>n<\/em> = 8 rats.<\/figcaption><\/figure>\n<p>These results can be explained by lipid self-oxidation (Saka <em>et al<\/em>., 2011), likely induced by obesity. A high-fat diet also leads to mitochondrial dysfunction correlated with oxidative stress (Yuzefovych <em>et al<\/em>., 2013). Nevertheless, a significant decrease in MDA was observed in the <em>Taraxacum officinal<\/em> extract treated group, showing the antioxidant effect of the plant (Hagymasi <em>et al<\/em>., 2000; Choi <em>et al<\/em>., 2010; Gonzalez-Castejon <em>et al<\/em>., 2012).<\/p>\n<p>The results of the statistical analysis show evidence a significant reduction of GSH in the cardiac tissue in obese rats.<br \/>\nOn the one hand, this reduction can be viewed as an increase in its use by liver cells, while on the other, by a reduction in the synthesis of GSH or increase of its degradation during oxidative stress (Loven <em>et al<\/em>., 1986).<\/p>\n<p>GSH can be associated with many pathways in vascular physiology and pathology. Oxyradicals and peroxides are considered to have strong effects on platelets, endothelial cells and smooth vascular muscle cells (Hennig and Chow, 1988; Rubanyi, 1988). As a product of oxidative stress, endothelial dysfunction has been identified as a possible pathological vector in the formation of atherosclerosis, and in vascular sound alterations and permeability (Boissonneault <em>et al<\/em>., 1990).<\/p>\n<p>However, a reduction in glutathione was observed in obese rats after administration of the aqueous extract of <em>Taraxacum officinal<\/em>. Ivanov, (2014) reported that <em>Taraxacum officinal<\/em> is a good source of biologically active compounds and has desirable antioxidant properties. Raising glutathione levels fights the oxidation of fatty acids in the bloodstream, including cholesterol, thereby delaying the process of plaque formation in the arteries, which is the underlying cause of most heart problems (Stamler and Slivka, 1996).<br \/>\nAdditionally, GSH plays an important role in leukotrien and prostaglandin formation and metabolism, which have a potential role in coronary artery constriction, causing ionotropic damage to cardiac muscle. The results also showed that the <em>Taraxacum officinal<\/em> aqueous extract improved the state of oxidative stress in rats, confirming that this plant could contribute to the protection of the heart against pathologies linked to the deleterious effects of reactive oxygen species.<\/p>\n<p><a name=\"Conclusions\"><\/a><a class=\"alignright\" href=\"#menu\"> &#9650;<\/a><\/p>\n<h2>Conclusions<\/h2>\n<hr \/>\n<p><em>Taraxacum officinal<\/em> aqueous extract had a cholesterol-lowering, hypotriglyceridemic, hypoglycaemic and cardioprotective effect in Wistar rats.<\/p>\n<p><a name=\"Literatura1\"><\/a><br \/>\n<strong>References<\/strong><span style=\"color: #808080;\"><a onclick=\"toggle_visibility('Literatura');\" ><span style=\"color: #808080; cursor:pointer;\"> [&#8230; show]<\/span><\/a><\/span><\/p>\n<div id=\"Literatura\" style=\"display: none;\">&nbsp;<a class=\"alignright\" href=\"#menu\" onclick=\"toggle_visibility('Literatura');\"> &#9650;<\/a><\/p>\n<p style=\"font-size: small;\"><em>1. 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WAHEED, R. A. QURESHI, D. K. BURDI, E. J. VERSPOHL, N. KHAN and M. HASAN (2004): The effect of medicinal plants of Islamabad and Murree region of Pakistan on insulin secretion from INS\u20101 cells. Phytother. Res.: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives 18, 73-77.<br \/>\n22. IVANOV, I. G. (2014): Polyphenols content and antioxidant activities of Taraxacum officinale FH Wigg (dandelion) leaves. Int. J. Pharmacogn. Phytochem. Res. 6, 889-893.<br \/>\n23. JAMES, A. (2017): Constructing childhood: Theory, policy and social practice. Macmillan International Higher Education.<br \/>\n24. JEON, H. J., H. J. KANG, H. J. JUNG, Y. S. KANG, C.\tJ. LIM, Y. M. KIM and E. H. ARK (2008): Anti- inflammatory activity of Taraxacum officinale. J. Ethnopharmacol. 115, 82-88.<br \/>\n25. JOUSILAHTI, P., J. TUOMILEHTO, E. VARTIAINEN, J. PEKKANEN and P. PUSKA (1996): Body weight, cardiovascular risk factors, and coronary mortality.15-year follow-up of middle-aged men and women in eastern Finland. Circulation 93, 1372-1379.<br \/>\n26. KAJIMURA, S. and M. SAITO (2014): A new era in brown adipose tissue biology: molecular control of brown fat development and energy homeostasis. Annu. Rev. Physiol. 76, 225-249.<br \/>\n27. KIM, J. Y., L. A. NOLTE, P. A. HANSEN, D. H. HAN, K. FERGUSON, P. A. THOMPSON and J. O. HOLLOSZY (2000): High-fat diet-induced muscle insulin resistance: relationship to visceral fat mass. Am. J. Physiol. Regul. Integr. Comp. Physiol. 279, R2057-R2065.<br \/>\n28. KISIEL, W. and B. BARSZCZ (2000): Further sesquiterpenoids and phenolics from Taraxacum officinale. Fitoterapia 71, 269-273.<br \/>\n29. LOVEN, D., H. SCHEDL, H. WILSON, T.T. DAABEES, L. D. STEGINK, M. DIEKUS and L. OBERLEY (1986): Effect of insulin and oral glutathione on glutathione levels and superoxide dismutase activities in organs of rats with streptozocin-induced diabetes. Diabetes 35, 503- 507.<br \/>\n30. MART\u00cdNEZ-GONZ\u00c1LEZ, M. \u00c1., J. A. MARTINEZ, F. B. HU, M. J. GIBNEY and J. KEARNEY (1999): Physical inactivity, sedentary lifestyle and obesity in the European Union. Int. J. Obes. 23, 1192-1201.<br \/>\n31. MILAGRO, F. I., J. CAMPI\u00d3N and J. A. MART\u00cdNEZ (2006): Weight gain induced by high\u2010fat feeding involves increased liver oxidative stress. Obesity 14, 1118-1123.<br \/>\n32. MIR, M. A., S. S. SAWHNEY and M. M. S. JASSAL (2013): Qualitative and quantitative analysis of phytochemicals of Taraxacum officinale. Wudpecker J. Pharm. Pharmocol. 2, 001-005.<br \/>\n33. MUST, A., J. SPADANO, E. H. COAKLEY, A. E IELD, G. COLDITZ and W. H DIETZ (1999): The disease burden associated with overweight and obesity. JAMA 282, 1523-1529.<br \/>\n34. OZLEM, G. and M. GIUSEPPE (2007): Saponins: properties, applications and processing. Crit. Rev. Food Sci. Nutr. 47, 231-258.<br \/>\n35. RUBANYI, G. M. (1988): Vascular effects of oxygen- derived free radicals. Free Radic. Biol. Med. 4, 107- 120.<br \/>\n36. SAKA, S., A. BAHI, and W. AOUACHERI (2011): The effect of oxidative stress induced by lead acetate on the glutathione enzyme system in rats. Annales de Toxicologie Analytique 23, 139-145.<br \/>\n37. SCH\u00dcTZ, K., E. MUKS, R. CARLE and A. SCHIEBER (2006): Separation and quantification of inulin in selected artichoke (Cynara scolymus L.) cultivars and dandelion (Taraxacum officinale WEB. ex WIGG.) roots by high\u2010performance anion exchange chromatography with pulsed amperometric detection. Biomed. Chromatogr. 20, 1295-1303.<br \/>\n38. STAMLER, J. S. and A. SLIVKA (1996): Biological chemistry of thiols in the vasculature and in vascular-related disease. Nutr. Rev. 54, 1-30.<br \/>\n39. STUBBS, R. S. and S. K. WICKREMESEKERA (2002): Insulin resistance in the severely obese and links with metabolic co-morbidities. Obes. Surg. 12, 343-348.<br \/>\n40. WECKBECKER, G. and J. G. CORY (1988): Ribonucleotide reductase activity and growth of glutathione-depleted mouse leukemia L1210 cells in vitro. Cancer lett 40, 257-264.<br \/>\n41. YAGI, K. (1976): A simple fluorometric assay for lipoperoxide in blood plasma. Biochem. Med. 15, 212-216.<br \/>\n42. YUZEFOVYCH, L. V., S. I. MUSIYENKO, G. L. WILSON, and L. I. RACHEK (2013): Mitochondrial DNA damage and dysfunction, and oxidative stress are associated with endoplasmic reticulum stress, protein degradation and apoptosis in high fat diet-induced insulin resistance mice. PloS One 8(1), e54059.<br \/>\n<\/em><\/p>\n<\/div>\n<p><a name=\"Sazetak\"><\/a><a class=\"alignright\" href=\"#\" onclick=\"scrollToTop();return false\"> &#9650;<\/a><\/p>\n<blockquote>\n<h2>Hipolipidemijski i kardioprotektivni u\u010dinak vodenog ekstrakta <em>Taraxacum officinal<\/em> u pretilih \u0161takora<\/h2>\n<hr \/>\n<div class=\"info\"><strong>Toumi IKRAM<\/strong>, dr. med. vet., redovita profesorica, dr. sc. <strong>Medila IFRIQYA<\/strong>, dr. med. vet., redovita profesorica, Zavod za stani\u010dnu i molekularnu biologiju, Prirodoslovni fakultet, Univerzitet u Hamma Lakhdar El Oued, 39000, Al\u017eir, Biologija, Laboratorij za okoli\u0161 i zdravlje, Univerzitet u Hamma Lakhdar El Oued, 39000, Al\u017eir; <strong>Lifa SAOUSSANE<\/strong>, vi\u0161i asistent, Biologija, Laboratorij za okoli\u0161 i zdravlje, Univerzitet u Hamma Lakhdar El Oued, 39000, Al\u017eir<\/div>\n<hr \/>\n<p>Pretilost je kroni\u010dna bolest koja je odgovorna za komorbiditet i prekomjernu smrtnost te se smatra neovisnim \u010dimbenikom rizika za razvoj kardiovaskularne patologije.<br \/>\nVe\u0107inu kardiovaskularnih bolesti mogu\u0107e je sprije\u010diti rje\u0161avanjem faktora rizika pona\u0161anja; sjedila\u010dkog na\u010dina \u017eivota, nezdrave prehrane i pretilosti. <em>Taraxacum officinal<\/em> je vi\u0161egodi\u0161nja biljka koja pripada obitelji <em>Asteraceae<\/em>, a obi\u010dno se rabi zbog svojih medicinskih svojstava. Ima diureti\u010dko, protutumorsko, antioksidativno, protuupalno, hepatoprotektivno i imunostimulacijsko djelovanje. Cilj je ove studije bio procijeniti u\u010dinak sni\u017eavanja lipida i kardioprotektivni u\u010dinak vodenog ekstrakta <em>Taraxacum officinal<\/em> u \u0161takora soja wistar na vrlo masnoj prehrani. 24 \u0161takora te\u017eine 200 \u00b1 6,8 g podijeljeno je u 3 skupine: zdravu kontrolnu (HC) koja je primala standardnu prehranu, pretilu kontrolnu (OC) koja je primala \u201ekantinsku\u201c hranu bez terapije i tre\u0107u optere\u0107enu skupinu (TL) koja je primala \u201ekantinsku dijetu\u201c i terapiju tijekom 20 dana s 200 mg\/kg vodenog ekstrakta <em>Taraxacum officinal<\/em>. Dobiveni rezultati su pokazali da je \u201ekantinska dijeta\u201c dovela do pretilosti \u0161takora u usporedbi s kontrolnom skupinom okarakteriziranom hiperglikemijom (148,75 mg\/dL), hipertrigliceridemijom (59 mg\/dL) i hiperkolesterolemijom (160,67 mg\/dL) uz pove\u0107anje ukupnih lipida (0,39 g\/g tkiva) povezano sa stanjem oksidativnog stresa u sr\u010danom tkivu. Oralna primjena vodenog ekstrakta <em>Taraxacum officinal<\/em> pobolj\u0161ala je lipidni profil u krvi i tkivu. Nalazi su pokazali pad \u0161e\u0107era u krvi (1,02 mg\/dL), ukupnog kolesterola (135 mg\/dL), LDL kolesterola, (67 mg\/dL), triglicerida (36 mg\/dL), ukupnih lipida (1,37 g\/g tkiva) i peroksidacije lipida MDA (0,25 \u00b1 0,02 \u03bcmoL\/g proteina) te pove\u0107anje razine GSH (0,51 nM\/mg proteina) u \u0161takora koji su primali terapiju u usporedbi s kontrolnim skupinama. Zaklju\u010dno, dobiveni rezultati dokazali su u\u010dinkovitost vodenog ekstrakta <em>Taraxacum officinal<\/em> protiv dislipidemije, pretilosti i hiperglikemije. Biljka ima kardioprotektivni i antioksidativni u\u010dinak.<\/p>\n<p><strong>Klju\u010dne rije\u010di:<\/strong> <em>bolest srca, dislipidemija, pretilost, oksidativni stres, faktor rizika, Taraxacum officinal<\/em><\/p><\/blockquote>\n","protected":false},"excerpt":{"rendered":"<p>Toumi Ikram*, Medila Ifriqya and Lifa Saoussane Toumi IKRAM*, DVM, Senior Professor, (Corresponding author, e-mail: toumi-ikram@univ-eloued.dz), Medila IFRIQYA, DVM, Senior<\/p>\n","protected":false},"author":8,"featured_media":0,"menu_order":6,"comment_status":"closed","ping_status":"open","template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[428,429,432,431,430,433],"issuem_issue":[93],"ppma_author":[425,426,427],"class_list":["post-687","article","type-article","status-publish","format-standard","hentry","category-original-scientific-articles","tag-bolest-srca","tag-dislipidemija","tag-faktor-rizika","tag-oksidativni-stres","tag-pretilost","tag-taraxacum-officinal","issuem_issue-52-4"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.6 - 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