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1.
Toxicol Mech Methods ; 34(5): 495-506, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38166540

ABSTRACT

The current study aimed to assess the antioxidant and antiproliferative effects of teucrium polium extract: computational and in vivo study in rats. Three groups of animals: Group (i) constitute the control group; Group (ii) HeLa group received an intrafemoral inoculation of HeLa cells and Group (iii) constitue the combination between HeLa + T. polium. The plant was administered by gavage. Our results revealed that HeLa cell injection showed an elevation in aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), total bilirubin (TB), creatinine, urea, calcium and phosphorus. The pretreatment with the plant extract reduced the level of these parameters. Injection of HeLa cells showed a significant decrease in phosphorus and calcium respectively. However, the pretreatment by T. polium modulated the level of these two minerals. Rats treated with HeLa cells line showed an increase in the level of lipid peroxidation as evaluated by the TBARS substances, at the same time, a significant decreases in SOD, CAT and GPx activities were noted in the HeLa group compared to the control. On the other hand, pretreatment with the plant improved the level of these enzymes. Our results revealed that T.polium has a therapeutic effect on some health problems. HeLa cell line induced a small infiltration in liver and kidney. T. polium reduced the damage in both liver and kidney, but did not reveal any proliferation of tumor cells from trabecular bone tissue. The computational study revealed that T. polium compound bound with high free binding energies and established promising network of molecular interactions with COX-2 and TNF-α macromolecules.


Subject(s)
Antioxidants , Cell Proliferation , Plant Extracts , Teucrium , Animals , Teucrium/chemistry , Plant Extracts/pharmacology , Plant Extracts/chemistry , Humans , HeLa Cells , Antioxidants/pharmacology , Cell Proliferation/drug effects , Male , Rats, Wistar , Rats , Liver/drug effects , Liver/metabolism , Liver/pathology , Kidney/drug effects , Kidney/metabolism , Kidney/pathology , Lipid Peroxidation/drug effects , Antineoplastic Agents, Phytogenic/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Oxidative Stress/drug effects , Molecular Docking Simulation
2.
Toxicol Mech Methods ; 26(9): 685-691, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27580939

ABSTRACT

Kalach 360 SL (KL) is a commercial herbicide which contains 360 g/l of glyphosate used in both agricultural and urban areas throughout the world including Tunisia. We aimed to evaluate the effects of KL on rats' renal system. Female Wistar rats were divided into three groups: group 1 (n = 6) received a standard diet and served as control, groups 2 and 3 (n = 12 each) received 0.07 ml (D1: 126 mg/kg), and 0.175 ml (D2: 315 mg/kg) of KL, respectively, for 60 d. The chronic exposure to KL induced a significant increase in plasma creatinine, urea, and uric acid levels. Creatinine clearance decreased in KL-treated groups, compared with controls. Several urine parameters, such as urine-specific gravity and urine osmolality, significantly decreased, while dieresis and urinary Na/K + ratio increased in KL-treated groups. These findings suggested a distal tubular damage caused by tubular necrosis. Moreover, the chronic exposure to KL induced an increase in lipid peroxidation (LPO) and a decrease in antioxidant status, enzymatic activities (superoxide dismutase and catalase) and non-enzymatic levels (vitamin C), which led to an oxidative stress. Histopathological studies showed a peritubular inflammatory reaction, nephrose, fragmented glomeruli, necrotic epithelial cells, and tubular dilatation. These results could have significant health implications for animal and human populations. Further data are necessary to investigate the potential consequences of chronic dose exposure during life.


Subject(s)
Environmental Pollutants/toxicity , Glycine/analogs & derivatives , Kidney/drug effects , Oxidative Stress/drug effects , Animals , Antioxidants/metabolism , Biomarkers/blood , Biomarkers/urine , Body Weight/drug effects , Dose-Response Relationship, Drug , Environmental Pollutants/chemistry , Female , Glycine/chemistry , Glycine/toxicity , Kidney/metabolism , Kidney/pathology , Kidney Function Tests , Lipid Peroxidation/drug effects , Organ Size/drug effects , Rats, Wistar , Glyphosate
3.
Toxicology ; 436: 152412, 2020 04 30.
Article in English | MEDLINE | ID: mdl-32145347

ABSTRACT

We investigated the effects of Kalach 360 SL (KL), Glyphosate (G)-based herbicide, on bone tissue in different groups of female Wistar rats. Group 1 (n = 6) received a standard diet and served as a control, groups 2 and 3 (n = 6 each) received 0.07 ml (D1: 126 mg/Kg) and 0.175 ml (D2: 315 mg/Kg) of KL dissolved in the water for 60 days. The plasma was used to examine the metabolic balance markers (calcium, phosphorus, phosphatase alkaline (PAL), and vitamin D (vit D) and hormonal status (oestrogen and thyroid hormones). As a result, sub-chronic exposure to KL induced a perturbation of bone metabolism (calcium and phosphorus) and hormonal status disturbance. The histological and immunohistochemical study of the thyroid gland revealed a disturbance in morphological structure and thyroid cells function. Moreover, the KL disrupting eff ;ect on thyroid function was investigated by measuring changes in plasma levels of thyroid hormones. Free triiodothyronine (FT3) and thyroxine (FT4) were decreased in female rats breast-fed from rats treated with D and D2 of KL. This eff ;ect was associated with an increase in the plasma level of thyroid-stimulating hormone (TSH). Thus, that KL leads to hypothyroidism. Decrease in levels of oestrogen and thyroid dysfunction led to a disruption in the skeletal bone. The histological study and SEM in bone results allowed us to observe, in rats exposed to KL, the thinning and discontinuity of bone trabecular with a significant decrease in the number of nodes (intertrabecular links).In conclusion, KL sub-chronic exposure caused an aspect of osteoporosis.


Subject(s)
Bone Density/drug effects , Bone Remodeling/drug effects , Femur/drug effects , Glycine/analogs & derivatives , Herbicides/toxicity , Animals , Biomarkers/blood , Estrogens/blood , Female , Femur/metabolism , Femur/ultrastructure , Glycine/toxicity , Hypothyroidism/blood , Hypothyroidism/chemically induced , Hypothyroidism/pathology , Osteoporosis/blood , Osteoporosis/chemically induced , Osteoporosis/pathology , Rats, Wistar , Thyroid Gland/drug effects , Thyroid Gland/metabolism , Thyroid Gland/pathology , Thyroid Hormones/blood , Glyphosate
4.
Environ Sci Pollut Res Int ; 26(36): 36634-36646, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31732955

ABSTRACT

We investigated the effects of sub-chronic exposure to Kalach 360 SL (KL), glyphosate-based herbicide used in Tunisia, on liver and hematological system in different groups of female rats. Group 1 was used as a control, while animals of groups 2 and 3 received orally 0.07 mL and 0.175 mL of KL, respectively (126 and 315 mg of glyphosate/kg), for 60 days. As a result, the KL-exposed groups exhibited hypochromic microcytic anemia, systemic inflammation, cytolysis, decrease in hepatic enzyme activity, and cholestasis. Exposure to different doses of KL could induce erythrocyte destruction (hemolysis) in hematopoietic organs (bones). Moreover, lipid peroxidation contents and protein oxidation markers significantly increased in exposed groups, while enzymatic and non-enzymatic antioxidant activities decreased considerably, in both erythrocytes and liver tissues, compared with those in controls. Liver histological studies confirmed the presence of inflammatory reaction with pathology involving the damage or necrosis of hepatocytes, however, without fibrosis remodulation. Thus, KL sub-chronic exposure caused hepatonecrosis, systemic inflammation, and hemolysis.


Subject(s)
Environmental Exposure/adverse effects , Glycine/analogs & derivatives , Hemolysis/drug effects , Herbicides/toxicity , Liver/drug effects , Animals , Antioxidants/metabolism , Biomarkers/metabolism , Female , Glycine/administration & dosage , Glycine/toxicity , Herbicides/administration & dosage , Lipid Peroxidation/drug effects , Liver/metabolism , Liver/pathology , Necrosis , Rats , Glyphosate
5.
Arch Physiol Biochem ; 124(1): 27-34, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28708416

ABSTRACT

Kalach 360 SL (KL), glyphosate (G) surfactant-based herbicides, is a systemic herbicide effective against weeds. It was applied in agriculture in Tunisia and throughout the world, which can represent a risk to non-target organisms. The aim of this study was to investigate the morphological and biochemical aspects of ovary injury after exposure to KL. Female Wistar rats were divided into three groups: group 1 was used as a control; group 2 orally received 0.07 ml of KL, (126 mg of G/kg) and group 3 orally received 0.175 ml of KL (315 mg of G/kg) each day for 60 days. The subchronic exposure of KL induces impaired folliculogenesis, ovary development, decreased oestrogen secretion, promoted oxidative stress and impairments of ovary histological aspects. Histological finding shows necrosis cell, vacuolisation of follicles, dissociated oocytes and granulosa cell, associated with several atretic follicles. We conclude that KL induces endocrine disruption and ovary damage in female rats.


Subject(s)
Endocrine Disruptors/toxicity , Herbicides/toxicity , Oogenesis/drug effects , Organophosphate Poisoning/physiopathology , Organophosphorus Compounds/toxicity , Ovarian Diseases/etiology , Ovary/drug effects , Surface-Active Agents/toxicity , Animals , Dose-Response Relationship, Drug , Endocrine Disruptors/administration & dosage , Estradiol/blood , Estradiol/metabolism , Estrogens/metabolism , Female , Granulosa Cells/drug effects , Granulosa Cells/metabolism , Granulosa Cells/pathology , Herbicides/administration & dosage , Lethal Dose 50 , Lipid Peroxidation/drug effects , Necrosis , Oocytes/drug effects , Oocytes/metabolism , Oocytes/pathology , Organophosphate Poisoning/etiology , Organophosphate Poisoning/metabolism , Organophosphate Poisoning/pathology , Organophosphorus Compounds/administration & dosage , Ovarian Follicle/drug effects , Ovarian Follicle/metabolism , Ovarian Follicle/pathology , Ovary/metabolism , Ovary/pathology , Oxidative Stress/drug effects , Rats, Wistar , Surface-Active Agents/administration & dosage , Toxicity Tests, Subchronic , Vacuoles/drug effects , Vacuoles/pathology
6.
Arch Physiol Biochem ; 123(5): 313-321, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28557561

ABSTRACT

The aim of this study was to evaluate the anti-inflammatory activity of Teucrium polium (TP). Rats were divided into four groups: group 1 controls received standard diet; group 2 inflamed by carrageenan (Carr) (1% Carr); group 3 as reference inflamed with Carr and treated with Indometacine (Ind) (150 mg/kg bw) and group 4 inflamed with Carr and pre0treated with TP (5 g/L). Oedema volume was measured 1 h to 5 h after injection. Administration of TP or Ind decreased the levels of hematology parameters relative to Carr and reduced the volume of rats induced by Carr. TP reduced levels of CRP, fibrinogen compared to treated, a decrease in oxidative stress (LP) and AOPP with an increase in the levels of SOD, CAT, GPx and Vit C in skin and erythrocytes. Carr increased the levels of lipid peroxidation and decreased levels of antioxidant enzymatic and Vit C. Our results were confirmed by histological sections of skin.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Carrageenan/pharmacology , Edema/chemically induced , Edema/drug therapy , Teucrium/chemistry , Water/chemistry , Animals , Anti-Inflammatory Agents/therapeutic use , Antioxidants/metabolism , C-Reactive Protein/metabolism , Edema/metabolism , Edema/pathology , Fibrinogen/metabolism , Male , Oxidative Stress/drug effects , Rats , Rats, Wistar
7.
Biomed Pharmacother ; 91: 43-48, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28448868

ABSTRACT

Herbal drugs play a crucial function to protect organisms from the toxic effect of some compounds. The present study was designed to evaluate the protective effects of Teucrium Polium (TP) aqueous extract and vitamin C (Vit C) against carbon tetrachloride (CCl4) which induced toxicity in rats. Male albino Wistar rats were divided into six groups: group I was used as controls, group II received CCl4 in olive oil (0.5ml/kg) by gavage, and group III received CCl4 in olive oil (0.5ml/kg) by gavage after three days of receiving TP (5g/l), orally, for seven days; Group IV received TP (5g/l) alone, orally, for seven days, Group V received CCl4 in olive oil (0.5ml/kg) by gavage after three days of receiving Vit C (250mg/kg) by intramuscular injection and Group VI received Vit C (250mg/kg) alone by intramuscular injection, for day seven. Some biochemical and hematological parameters were investigated. Our results showed that the administration of CCl4 caused hepatotoxicity as monitored by the significant increase in the levels of hepatic markers enzymes (lactate dehydrogenase (LDH), Alkaline phosphatase (PAL), total bilirubin (TB) and Gamma glutamyl transferase (γGT) levels) and a decrease in hematological parameters such as white blood cell (WBC), red blood cell count (RBC), mean corpuscular hemoglobin concentration (MCHC) and blood platelet count (PLT). Treatment with TP or Vit C appeared to be effective against hematotoxic and the liver changes induced by CCl4, as evidenced by the improvement of the parameters cited above. The CCl4-treated group demonstrated a significant increase of malondialdehyde (MDA) levels in erythrocytes thus causing a reduction in antioxidant defense system. Pretreatment with TP or Vit C improved the biochemical analyses, hematological parameters, and antioxidant defense system.


Subject(s)
Ascorbic Acid/pharmacology , Carbon Tetrachloride/toxicity , Plant Extracts/pharmacology , Protective Agents/pharmacology , Teucrium/chemistry , Water/chemistry , Animals , Antioxidants/pharmacology , Biomarkers/blood , Erythrocytes/drug effects , Erythrocytes/metabolism , Lipid Peroxidation/drug effects , Male , Phytotherapy , Rats, Wistar
8.
Arch Physiol Biochem ; 123(4): 225-237, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28372462

ABSTRACT

The aim of this study was to analyse cytoprotective effect of polysaccharides compound from Opuntia stricta (O. stricta) cladode (POS) in vitro including its radical scavenging activities and protective effects against hypercholesterolaemia. Our results showed that glucose was the dominant monosaccharides (30.35%). Arabinose, pyranose, fructose, galactose, glucose, sorbitol, S-inositol, M-inositol, trehalose and saccharose found in this species. O. stricta polysaccharides did not cause any cytotoxic effect on HepG2 cells within the range of concentrations tested (0-400 µgml-1). Pre-treatment of HepG2 cells with POS (100 µgml-1) significantly (p < .05) protected against cytotoxicity induced by DPPH and ABTS radicals. The POS showed strong antioxidant potential in vitro. The results indicated also that POS significantly prevented hypercholesterolaemia-induced elevation of serum biomarkers and induced increase in serum lipid profile. Moreover, the hypercholesterolaemia characterised by elevated lipid peroxidation (MDA) and reduced antioxidant enzyme defences (SOD, CAT and GPx) was restored by POS treatment.


Subject(s)
Antioxidants/pharmacology , Diet, High-Fat/adverse effects , Hyperlipidemias/prevention & control , Lipid Peroxidation/drug effects , Opuntia/chemistry , Plant Extracts/pharmacology , Polysaccharides/pharmacology , Animals , Cell Death/drug effects , Hep G2 Cells , Humans , Hyperlipidemias/etiology , Male , Oxidative Stress/drug effects , Rats , Rats, Wistar
9.
Int J Radiat Biol ; 93(7): 697-704, 2017 07.
Article in English | MEDLINE | ID: mdl-28287017

ABSTRACT

PURPOSE: Ionizing radiation (IR) is considered as a diagnostic and therapeutic tool in medicine. However, chronic occupational exposure of medical staff to IR may affect the antioxidant status and, as a result, DNA damage and cancers as well. The objective of our study was to evaluate the oxidative stress profile caused by IR in 29 Tunisian medical staff from radiology and radiotherapy departments, and to find an association between the GSTM1 null, GSTT1 null, and GSTP1 Ile105Val polymorphisms and oxidative stress biomarkers. MATERIALS AND METHODS: The oxidant biomarkers malondialdehyde (MDA) and advanced oxidation protein product (AOPP) and the activities of the antioxidant superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT) enzymes were spectrophotometrically determined in erythrocytes hemolysates. The analysis of GSTT1 null, GSTM1 null, and GSTP1 Ile105Val polymorphisms was determined for each participant using PCR methods. RESULTS: A significant increase of white blood cell (WBC) numbers (p < .05) and a significant decrease by 11% of hemoglobin (Hb) (p < .01) were noted in the exposed subjects in our study. Moreover, we report a significant increase of MDA level and the activities of SOD and CAT enzymes of the IR-exposed group compared to controls (p < .001). Interestingly, a close association was noted between the genotypes GSTP1 low active, GSTT1 null, GSTM1 null, and both GSTT1/GSTM1 null and oxidative stress biomarkers, especially with MDA level, SOD, and CAT activities. CONCLUSIONS: Our findings indicate that the medical staff exposed to low IR levels were under risk of significant oxidative stress that was enhanced by their glutathione S-transferase (GST) polymorphisms.


Subject(s)
Glutathione Transferase/genetics , Occupational Exposure/analysis , Oxidative Stress/radiation effects , Polymorphism, Single Nucleotide/genetics , Radiation Exposure/analysis , Reactive Oxygen Species/blood , Adult , Female , Glutathione Transferase/immunology , Humans , Male , Medical Staff , Middle Aged , Oxidative Stress/immunology , Polymorphism, Single Nucleotide/radiation effects , Tunisia
10.
Environ Sci Pollut Res Int ; 22(16): 12309-22, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26210702

ABSTRACT

Maneb (MB), a fungicide largely used in agriculture throughout the world including Tunisia, protects many vegetables, fruits and field crops against a wide spectrum of fungal diseases. However there is a lack of informations regarding the risks arising from MB exposure on non target organisms, especially mammals. The aim of this study was to investigate the morphological, biochemical and molecular aspects of liver injury after exposure of mice to MB. Four doses of MB corresponding to 1/8 (group D1), 1/6 (group D2), 1/4 (group D3), and 1/2 (group D4) of lethal dose (DL50 = 1500 mg/kg body weight) were administered to adult mice. Oxidative stress parameters were also objectified by molecular and histological endpoints in the liver. Maneb caused hepatotoxicity as characterized by the significant increase in the levels of malondialdehyde and protein oxidation marker, advanced oxidation protein products (AOPP). The activities of catalase, glutathione peroxidase, superoxide dismutase and the levels of glutathione decreased significantly in all treated mice, while vitamin C levels decreased only in group D4. We also noted a significant decrease in gene expression of superoxide dismutase and glutathione peroxidase enzymes. Maneb caused nucleic acids degradation testifying its genotoxicity. Yet, biochemical markers in plasma showed a decrease in total protein and an increase in aspartate, alanine amino transferases and bilirubin levels in all treatment groups. Moreover, plasma levels of cholesterol, triglycerides and low density lipoprotein-cholesterol significantly increased, while those of high density lipoprotein-cholesterol decreased. These biochemical alterations were correlated with significantly histological changes. Our data showed, for the first time, that intraperitoneal injection of very high non environmentally relevant MB concentrations to adult mice resulted in oxidative stress leading to hepatotoxicity and the impairment of defense systems, confirming the pro-oxidant and genotoxic effects of this fungicide.


Subject(s)
Gene Expression Regulation, Enzymologic/drug effects , Glutathione Peroxidase/genetics , Liver/drug effects , Liver/metabolism , Maneb/toxicity , Reactive Oxygen Species/metabolism , Superoxide Dismutase/genetics , Animals , Catalase/metabolism , Female , Fungicides, Industrial/toxicity , Glutathione/metabolism , Male , Malondialdehyde/metabolism , Mice , Mutagens/toxicity , Oxidation-Reduction/drug effects , Oxidative Stress/drug effects , Protective Agents/pharmacology , Rats , Toxicity Tests
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