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1.
Arch Dermatol Res ; 315(7): 1945-1952, 2023 Sep.
Article in English | MEDLINE | ID: mdl-36859573

ABSTRACT

Heliotropium europaeum has been traditionally used to stop bleeding and accelerate scarring. This study provides a scientific evaluation of H. europaeum haemostatic and healing potential. To evaluate the haemostatic effect of H. europaeum, the time of bleeding of fresh wounds induced experimentally in rats was studied. Excision wounds were induced upon four groups; each one contains six rats to estimate the healing properties of wounds. Group 1 was assigned as control (not treated), group 2 was daily treated with H. europaeum leaf powder, group 3 was treated with H. europaeum every 6 days and group 4 was treated with a reference drug, an emulsion containing 10% of Mimosa tenuiflora extract. All the parameters were significantly tested (p < 0.05) with comparison to a group control. The use of H. europaeum significantly shortened the bleeding time. The rats which were daily treated with H. europaeum healed in 12 days. This time period was significantly shorter than the control groups. Wound excision was uniformly induced randomly on the dorsum of rats in 4 groups (tested support and control). The post-healing biopsies were histologically assessed, revealed a better healing quality, and continued complete tissue regeneration, abundant and well-organized network of collagen fibres, and low numbers of inflammatory cells. The experimental data revealed that H. europaeum displayed remarkable haemostatic and wound healing activities.


Subject(s)
Heliotropium , Hemostatics , Rats , Animals , Hemostatics/pharmacology , Hemostatics/therapeutic use , Wound Healing , Cicatrix
2.
Environ Sci Pollut Res Int ; 25(16): 15404-15410, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29564705

ABSTRACT

Our study was designed to evaluate impacts of exposure to pollutants, released by the Gabès-Ghannouche factory complex of phosphate treatment, on biochemical biomarkers and histopathological indices in kidney tissues of Hybrid sparrow (Passer domesticus × Passer hispaniolensis) in Gabès city. Our results show evidence of a pronounced impairment in kidney function which is confirmed by remarkable blood chemical alterations in sparrows living in Ghannouche, the most polluted site. Moreover, superoxide dismutase and catalase activities were found to be decreased in birds sampled from the contaminated site when compared to less polluted areas. The population of sparrows feeding in Ghannouche had enhanced renal thiobarbituric acid reactive substance levels, indicating oxidative damage to membrane lipids. Some histopathological alterations were also observed including kidney interstitial dilatations. Overall, our findings demonstrated that the exposure to pollutants released by the factory complex possessed nephrotoxic by depleting renal antioxidant defense system and promoting kidney morphometric damage in sparrows. These results constitute an early warning of an ecological change in relation to human health.


Subject(s)
Environmental Exposure/analysis , Environmental Pollutants/toxicity , Kidney/drug effects , Sparrows , Animals , Biomarkers , Hybridization, Genetic , Kidney/pathology , Kidney Function Tests/veterinary , Male , Phosphates
3.
Carbohydr Polym ; 170: 148-159, 2017 Aug 15.
Article in English | MEDLINE | ID: mdl-28521980

ABSTRACT

A sulphated polysaccharide from brown algae Sargassum vulgare (SVSP) was extracted and examined with respect to chemical, structural characterization and hypolipidemic effects. SVSP consisted mainly of sulphate and total sugars with low levels of lipids and proteins. Its structure was studied by nuclear magnetic resonance (RMN), gas chromatography-mass spectrometry (GC-MS), infra-red spectroscopic, differential scanning calorimetry and X-ray diffraction analysis. Allowing us therefore to revealed that SVSP was composed of glucose, rhamnose, xylose, galactose, mannose and arabinose with XRD pattern that was typical for a semi-crystalline polymer and complexities of the spectra reflected its homogeneous structure. The administration of SVSP to obese rats is effective in lowering the body weight and inhibiting the lipase activity leading to notable regulation of lipid profile, increasing the activities of antioxidant enzymes, limiting lipid peroxidation; and protects liver-kidney functions proved by a decrease in the levels of toxicity parameters in blood, confirmed by histological study.


Subject(s)
Body Weight/drug effects , Polysaccharides/chemistry , Sargassum/chemistry , Sulfates/chemistry , Animals , Enzyme Activation/drug effects , Lipase/metabolism , Lipid Peroxidation/drug effects , Lipids/blood , Molecular Structure , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Rats
4.
Int J Biol Macromol ; 102: 119-129, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28392390

ABSTRACT

The present study investigates the hypolipidemic effects of sulphated polysaccharide obtained from Codium fragile (CFSP) in induced obese rats (HFD). The results showed an increase in body weight of HFD rats by 21.56% as compared to control normal rats. Moreover, serum lipase activity underwent an increase which led to an increase in the levels of total cholesterol (T-Ch), triglycerides (TG) and low density lipoprotein cholesterol (LDL-Ch) in serum associeted with a decrease in the level of high density lipoprotein cholesterol (HDL-Ch) in untreated HFD rats. This diet has disrupted the antioxidant status by decreasing the activities of antioxidant enzymes (superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX)) and subsequently an increase in thiobarbituric acid reactive substances (TBARS) level in liver and kidney of obese rats. All these disturbances are significantly corrected by CFSP administration with no fatty deposits in the liver and a protective effect against renal histological alteration. This confirms the important role of this polysaccharide in the fight against oxidative stress and the prevention of hyperlipidemia.


Subject(s)
Chlorophyta/chemistry , Diet, High-Fat/adverse effects , Kidney/drug effects , Liver/drug effects , Obesity/drug therapy , Polysaccharides/chemistry , Polysaccharides/pharmacology , Animals , Anti-Obesity Agents/chemistry , Anti-Obesity Agents/pharmacology , Anti-Obesity Agents/therapeutic use , Antioxidants/metabolism , Body Weight/drug effects , Intestinal Mucosa/metabolism , Intestines/drug effects , Kidney/physiopathology , Lipase/metabolism , Lipid Peroxidation/drug effects , Lipids/blood , Liver/physiopathology , Male , Obesity/etiology , Obesity/physiopathology , Polysaccharides/therapeutic use , Rats , Rats, Wistar , Sulfates/chemistry
5.
Biomed Pharmacother ; 89: 257-267, 2017 May.
Article in English | MEDLINE | ID: mdl-28235688

ABSTRACT

This new study aimed to evaluate for the first time the effect of Cymodocea nodosa extract (CNE) on α-amylase activity, hyperglycemia and diabetes complications in the alloxan-induced diabetic rats. The in vitro evaluation and oral administration of CNE to surviving diabetic rats inhibited key enzyme related to hyperglycemia as α-amylase, helped to protect the ß cells of the rats from death and damage confirmed by oral glucose test tolerance (OGTT), which leads to decrease in blood glucose level by 49% as compared to untreated diabetic rats. The CNE also decreased the triglyceride, low density lipoprotein (LDL) cholesterol and total cholesterol rates in the plasma of diabetic rats by 46%, 35%, and 21%, respectively, and increased the high density lipoprotein (HDL) cholesterol level by 36%, which helped maintain the homeostasis of blood lipid. When compared to those of the untreated diabetic rats, the superoxide dismutase, catalase, and glutathione peroxidase levels in the pancreas, liver and kidney of the rats treated with this supplement were also enhanced significantly. Moreover, a significant decrease was observed in the lipid peroxidation level in the tested organs of diabetic rats after CNE administration. This positive effect of CNE was confirmed by histological study. Overall, the findings presented in this study demonstrate that CNE has both a promising potential with a valuable hypoglycemic and hypolipidemic functions.


Subject(s)
Alloxan/pharmacology , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/drug therapy , Metabolic Diseases/drug therapy , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Animals , Antioxidants/metabolism , Blood Glucose/drug effects , Cholesterol/blood , Diabetes Mellitus, Experimental/metabolism , Hyperglycemia/drug therapy , Hyperglycemia/metabolism , Hypoglycemic Agents/pharmacology , Insulin/metabolism , Lipid Peroxidation/drug effects , Lipids/blood , Male , Metabolic Diseases/metabolism , Pancreas/drug effects , Pancreas/metabolism , Rats , Rats, Wistar , Triglycerides/blood , alpha-Amylases/metabolism
6.
Arch Physiol Biochem ; 123(1): 31-42, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27855503

ABSTRACT

The present study investigated the effect of the Cystoseira crinita sulfated polysaccharide (CCSP) on key enzymes activities related to diabetes in vitro and in diabetic rats. We found that CCSP inhibited pancreatic α-amylase with IC50 = 39.16 µg/ml and angiotensin I-converting enzyme (ACE) activity with IC50 = 58.35 µg/ml in vitro. In diabetic rats, the administration of CCSP reduced the activity of α-amylase in serum, pancreas, and intestine by 23%, 44.38%, and 45%, respectively as compared to untreated diabetic rats. Moreover, the administration of CCSP to surviving diabetic rats protects pancreas ß cells from death and damage, which leads to insulin levels. The decrease in α-amylase and the increase in insulin level lead to a decrease in glucose rate by 56% as compared to untreated diabetic rats. The inhibitory action of α-amylase activity and hypoglycemic effect of CCSP were confirmed by oral glucose tolerance test (OGTT). In addition, the administration of CCSP to surviving diabetic rats normalizes lipid profile, stimulates antioxidant capacity, and prevents liver-kidney toxicities, evidenced by decrease in serum indices of liver and kidney toxicity and confirmed by histological analysis. The overall findings presented in this study demonstrate that the administration of CCSP to diabetic rats can make it a potentially strong candidate for industrial application as a pharmacological agent for the treatment of hyperglycemia, hyperlipidemia, and liver-kidney dysfunctions.


Subject(s)
Antihypertensive Agents/therapeutic use , Diabetes Mellitus, Type 2/drug therapy , Enzyme Inhibitors/therapeutic use , Hypertension/drug therapy , Hypoglycemic Agents/therapeutic use , Phaeophyceae/chemistry , Polysaccharides/therapeutic use , Angiotensin-Converting Enzyme Inhibitors/chemistry , Angiotensin-Converting Enzyme Inhibitors/isolation & purification , Angiotensin-Converting Enzyme Inhibitors/metabolism , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Animals , Antihypertensive Agents/chemistry , Antihypertensive Agents/isolation & purification , Antihypertensive Agents/metabolism , Biological Products/chemistry , Biological Products/isolation & purification , Biological Products/metabolism , Biological Products/therapeutic use , Diabetes Mellitus, Type 2/metabolism , Diabetes Mellitus, Type 2/pathology , Diabetes Mellitus, Type 2/physiopathology , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/isolation & purification , Enzyme Inhibitors/metabolism , Hypertension/metabolism , Hypertension/pathology , Hypertension/physiopathology , Hypoglycemic Agents/chemistry , Hypoglycemic Agents/isolation & purification , Hypoglycemic Agents/metabolism , Intestinal Mucosa/drug effects , Intestinal Mucosa/enzymology , Intestinal Mucosa/metabolism , Intestine, Small/drug effects , Intestine, Small/enzymology , Intestine, Small/metabolism , Kidney/drug effects , Kidney/metabolism , Kidney/pathology , Kidney/physiopathology , Liver/drug effects , Liver/metabolism , Liver/pathology , Liver/physiopathology , Male , Mediterranean Sea , Pancreas/drug effects , Pancreas/metabolism , Pancreas/pathology , Pancreatic alpha-Amylases/antagonists & inhibitors , Pancreatic alpha-Amylases/blood , Pancreatic alpha-Amylases/metabolism , Peptidyl-Dipeptidase A/chemistry , Peptidyl-Dipeptidase A/metabolism , Phaeophyceae/growth & development , Polysaccharides/chemistry
7.
Arch Physiol Biochem ; 121(5): 218-27, 2015.
Article in English | MEDLINE | ID: mdl-26599334

ABSTRACT

This study aimed to evaluate for the first time the effects of Cymodocea nodosa sulphated polysaccharide (CNSP) on the α-amylase activity, hyperglycaemia, liver-kidney functions, and pancreatic architecture of alloxan-induced diabetic rats. Animals were allocated into four groups of seven rats each, the body weight and blood glucose levels were estimated periodically for 2 months of treatment by gastric gavages route. The CNSP effect was confirmed by biochemical procedures and histological study. The inhibition of α-amylase activity and protection of pancreatic ß-cells induced a decrease in the blood glucose levels and regulated the lipid profile in the plasma of the treated diabetic rats, which helped to maintain the homeostasis of blood lipid. Moreover, CNSP administration induced a significant decrease in the levels of lipid peroxidation in the pancreas, liver and kidney of diabetic rats and protects their functions attested by a decrease in the levels of toxicity parameters in blood.


Subject(s)
Alismatales/chemistry , Diabetes Mellitus, Experimental/drug therapy , Lipid Peroxidation/drug effects , Plant Extracts/pharmacology , Polysaccharides/pharmacology , alpha-Amylases/antagonists & inhibitors , Animals , Blood Glucose/metabolism , Body Weight/drug effects , Diabetes Mellitus, Experimental/etiology , Diabetes Mellitus, Experimental/metabolism , Hypoglycemic Agents/pharmacology , Kidney/drug effects , Kidney/metabolism , Liver/drug effects , Liver/metabolism , Male , Oxidative Stress/drug effects , Pancreas/drug effects , Pancreas/metabolism , Plant Leaves/chemistry , Rats , Rats, Wistar , Sulfhydryl Reagents/chemistry , alpha-Amylases/drug effects , alpha-Amylases/metabolism
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