Lycopene modulates cholinergic dysfunction, Bcl-2/Bax balance, and antioxidant enzymes gene transcripts in monosodium glutamate (E621) induced neurotoxicity in a rat model

2016 ◽  
Vol 94 (4) ◽  
pp. 394-401 ◽  
Author(s):  
Kadry Sadek ◽  
Tarek Abouzed ◽  
Sherif Nasr
Keyword(s):  
Lipid Peroxidation ◽  
Brain Tissue ◽  
Creatine Phosphokinase ◽  
Monosodium Glutamate ◽  
Serum Cholinesterase ◽  
Glutathione S Transferase ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Induced Apoptosis

The effect of monosodium glutamate (MSG) on brain tissue and the relative ability of lycopene to avert these neurotoxic effects were investigated. Thirty-two male Wistar rats were distributed into 4 groups: group I, untreated (placebo); group II, injected with MSG (5 mg·kg−1) s.c.; group III, gastrogavaged with lycopene (10 mg·kg−1) p.o.; and group IV received MSG with lycopene with the same mentioned doses for 30 days. The results showed that MSG induced elevation in lipid peroxidation marker and perturbation in the antioxidant homeostasis and increased the levels of brain and serum cholinesterase (ChE), total creatine phosphokinase (CPK), creatine phosphokinase isoenzymes BB (CPK-BB), and lactate dehydrogenase (LDH). Glutathione S-transferase (GST), superoxide dismutase (SOD), and catalase (CAT) activities and gene expression were increased and glutathione content was reduced in the MSG-challenged rats, and these effects were ameliorated by lycopene. Furthermore, MSG induced apoptosis in brain tissues reflected in upregulation of pro-apoptotic Bax while lycopene upregulated the anti-apoptotic Bcl-2. Our results indicate that lycopene appears to be highly effective in relieving the toxic effects of MSG by inhibiting lipid peroxidation and inducing modifications in the activity of cholinesterase and antioxidant pathways. Interestingly, lycopene protects brain tissue by inhibiting apoptosis signaling induced by MSG.

scholarly journals Quality of Live Improvement Antituberculosis Consumer

2019 ◽  
Vol 2 (1) ◽  
pp. 22-25
Author(s):  
Jumasni Adnan
Keyword(s):  
Lipid Peroxidation ◽  
Liver Damage ◽  
Water Extract ◽  
Group Iv ◽  
Group V ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Group Ii

Antituberculosis is the most liver damage causes. Rifampicin and Isoniazide, in combination, are toxic compounds. Isoniazide and rifampicin metabolits causes lipid peroxidation. The hepatoprotective effect of rosella calyx water extract on liver damage induced with Isoniazide-rifampicin evaluated by examination of malondialdehid levels in the liver organ. 25 male wistar rats divided into 5 groups, ie group I (INH-rifampicin + rosella water extract 250 mg/kgBW), group II (INH-rifampicin + rosella water extract 125 mg/kgBW), group III (INH-rifampicin + rosella water extract 62.5 mg/kgBW),  group IV (healthy control) and group V (Isoniazide-rifampicin). MDA liver levels were analyzed after 35 days of treatments. The test results of each group are, group I has mean MDA levels 0.023912 + 0.011 mg/ml, group II 0.023526 + 0.009 mg/ml, group III 0.027168 + 0.007 mg/ml group IV 0.03437 + 0.009 mg/ml and group V 0.236846 + 0.118 mg/ml. The kruskal-wallis test showed significantly value 0.008 (p 0.05) and Post hoc Mann U whitney test showed that group V was significantly different to group I, II, III, and IV (p = 0.008) respectively, roselle extract can be used as a hepatoprotector antioxidant to improve the tuberculosis drug consumer quality of life through improved health by lowering lipid peroxidation that causes liver damage.

Modified Diet Supplementation With Group B Vitamins Changes Antioxidant Defense Activity Of Brain

2018 ◽  
Vol 88 (5-6) ◽  
pp. 291-299 ◽  
Author(s):  
Zuzanna Goluch-Koniuszy ◽  
Radosław Drozd
Keyword(s):  
Brain Tissue ◽  
Antioxidant Status ◽  
Antioxidant Defense ◽  
Iron Concentration ◽  
B Vitamins ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Group B ◽  
Modified Diet

Abstract. The research aimed at effect of modified diet and supplementation with synthetic B vitamins on brain antioxidant status evaluation. Forty male Wistar rats were divided into 4 groups (n = 10); group I – fed Basic Diet (BD), groups II-IV – Modified Diet (MD), where wheat flour replaced 83.5 % wheat and sucrose replaced 50 % maize. Groups I-II received only water, while group III (MD + AS) was given an aqueous vitamins solution supplementing deficiency from diet modification (MD + Adequate Supplementation: B1-0.94, B2-0.48, B6-0.5, niacin-1.9 mg); group IV (MD + ES) received a solution in order to supplement deficiency resulting from the change in diet and recommended prophylactic dose of vitamins (MD + Excessive Supplementation: B1-3.1, B2-2.3, B6-2.4, niacin-6.65 mg). The experimental phase lasted 6 weeks. Blood serum was examined, to determine glucose and iron concentration; determination of FRAP in plasma, in brain tissue the activities of GST, GPx, CAT, SOD, SH content, and FRAP. It was found that MD and MD + AS did not influence cereal antioxidant status. In brain tissue, MD + ES group exhibited an increased glycaemia (7.49 mmol×l-1 p = 0.038) and increased activity of antioxidant enzymes activity (GST 0,099 U/mg protein p = 0.005; GPx 0,039 U/mg protein p = 0.007). Brain tissue of rats also exhibited larger content of protein bond SH in comparison to BD, MD and MD + AS groups (SH 414.6 mmol/g wet weight p < 0.001; p < 0.005). These findings suggest that, an excessive supplementation with vitamins B and niacin, in sucrose rich diet, may lead to enhancing activity of cellular antioxidant defense in brain tissue of rats.

Vitamin U, a novel free radical scavenger, prevents lens injury in rats administered with valproic acid

2014 ◽  
Vol 34 (9) ◽  
pp. 904-910 ◽  
Author(s):  
S Tunali ◽  
S Kahraman ◽  
R Yanardag
Keyword(s):  
Lipid Peroxidation ◽  
Valproic Acid ◽  
Antioxidant Properties ◽  
Free Radical Scavenger ◽  
Radical Scavenger ◽  
Sprague Dawley ◽  
Glutathione S Transferase ◽  
Group Iii ◽  
Group I ◽  
Vitamin U

Valproic acid (2-propyl-pentanoic acid, VPA) is the most widely prescribed antiepileptic drug due to its ability to treat a broad spectrum of seizure types. VPA exhibits various side effects such as organ toxicity, teratogenicity, and visual disturbances. S-Methylmethioninesulfonium is a derivative of the amino acid methionine and it is widely referred to as vitamin U (Vit U). This study was aimed to investigate the effects of Vit U on lens damage parameters of rats exposed to VPA. Female Sprague Dawley rats were divided into four groups. Group I comprised control animals. Group II included control rats supplemented with Vit U (50 mg/kg/day) for 15 days. Group III was given only VPA (500 mg/kg/day) for 15 days. Group IV was given VPA + Vit U (in same dose and time). Vit U was given to rats by gavage and VPA was given intraperitoneally. On the 16th day of experiment, all the animals which were fasted overnight were killed. Lens was taken from animals, homogenized in 0.9% saline to make up to 10% (w/v) homogenate. The homogenates were used for protein, glutathione, lipid peroxidation levels, and antioxidant enzymes activities. Lens lipid peroxidation levels and aldose reductase and sorbitol dehydrogenase activities were increased in VPA group. On the other hand, glutathione levels, superoxide dismutase, glutathione peroxidase, glutathione reductase, glutathione- S-transferase, and paraoxonase activities were decreased in VPA groups. Treatment with Vit U reversed these effects. This study showed that Vit U exerted antioxidant properties and may prevent lens damage caused by VPA.

scholarly journals Pancreato-protective PANCREATOPROTECTIVE EFFECT OF SILYMARIN ON OXIDATIVE STRESS IN ALLOXAN-INDUCED HYPERGLYCEMIA IN MALE WISTAR RATS

2019 ◽  
pp. 121-125
Author(s):  
UMA NARAYANAMURTHY ◽  
SYLVIA SANTHAKUMARI A ◽  
NIRMALA P
Keyword(s):  
Lipid Peroxidation ◽  
Diabetic Complications ◽  
Wistar Rats ◽  
Serum Glucose ◽  
Pancreatic Tissue ◽  
Diabetic Rats ◽  
Group Iv ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats

Objective: The objective of the study was to study the silymarin’s pancreatoprotective effect in alloxan-induced Type I diabetes mellitus. Numerous studies have evidence to prove the fact that antioxidant defense mechanism of flavonoids has overcome the progression of chronic diabetic complications. Methods: A total of 24 male Wistar rats were divided into four groups (n=6): Group I normal control, Group II, Group III, and Group IV were induced diabetes with alloxan. Group I and Group II diabetic rats received the vehicle (PO). Group III was treated with silymarin 400 mg/kg (PO). Group IV was treated with glibenclamide 0.5 mg/kg, per orally for 21 days. Fasting blood samples were collected from all four groups of animals at the end of 21 days to evaluate serum glucose and glycosylated hemoglobin (HbA1c). Pancreatic tissue extraction, to perform lipid peroxidation and histopathological study confirms the level of oxidative damage to tissues and recovery after treatment. Results: The serum glucose and HbA1c levels significantly increased in untreated diabetic rats, also a significant rise in lipid peroxidation and necrosis of beta cells in the pancreatic tissue. The rise in serum glucose levels was ameliorated in rats treated with silymarin, pancreatic tissue showed increased antioxidant levels, decreased lipid peroxides, and minimal changes and signs of regeneration of beta cells. Conclusion: This study adds experimental evidence to the fact that silymarin is an effective nutritional supplement to treasure pancreatic beta-cell reserve and to delay diabetic complications.

scholarly journals Effect of concurrent exposure of toxic concentrations of lead and endosulfan on oxidative stress indices in rats

2021 ◽  
Vol 10 (3) ◽  
pp. 192-195
Author(s):  
Ranganathan V ◽  
◽  
Malik JK ◽  
Rao GS ◽  
◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Reduced Glutathione ◽  
Group Iv ◽  
Male Rats ◽  
Technical Grade ◽  
Stress Indices ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Toxic Concentrations

The effect of concurrent exposure of toxic concentrations of lead and endosulfan were evaluated on oxidative stress parameters in male wistar rats. Group I served as untreated control whereas Group II received drinking water containing lead as lead acetate @1000 ppm (Pb1000). Group III was exposed to feed containing technical grade endosulfan @ 100 ppm (E100). Group IV was exposed to Pb (1000) +E (100). All the treatments were given daily for 28 days. Combination of lead and endosulfan modified the indices of oxidative stress in the parameters such as lipid peroxidation, reduced glutathione, superoxide dismutase and catalase in rats as compared to their individual compounds. The results suggest that the combination of these individual compounds may have the potential to modify oxidative stress produced by single compounds in male rats

scholarly journals Concentration of hepatic vitamins A and E in rats exposed to chlorpyrifos and/or enrofloxacin

2016 ◽  
Vol 19 (2) ◽  
pp. 371-378 ◽  
Author(s):  
A. Spodniewska ◽  
D. Barski
Keyword(s):  
Lipid Peroxidation ◽  
Free Radicals ◽  
Gastric Tube ◽  
Initial Period ◽  
Hplc Method ◽  
Antioxidant Vitamin ◽  
Exposure Group ◽  
Group Iii ◽  
Group I

Abstract The aim of the study was to determine the level of antioxidant vitamins A and E in the liver of rats exposed to chlorpyrifos and/or enrofloxacin. Chlorpyrifos (Group I) was administered at a dose of 0.04 LD50 (6 mg/kg b.w.) for 28 days, and enrofloxacin (Group II) at a dose of 5 mg/kg b.w. for 5 consecutive days. The animals of group III were given both of the mentioned above compounds at the same manner as groups I and II, but enrofloxacin was applied to rats for the last 5 days of chlorpyrifos exposure (i.e. on day 24, 25, 26, 27 and 28). Chlorpyrifos and enrofloxacin were administered to rats intragastrically via a gastric tube. The quantitative determination of vitamins was made by the HPLC method. The results of this study indicated a reduction in the hepatic concentrations of vitamins A and E, compared to the control, which sustained for the entire period of the experiment. The four-week administration of chlorpyrifos to rats resulted in a significant decrease of vitamins in the initial period of the experiment, i.e. up to 24 hours after exposure. For vitamin A the maximum drop was observed after 24 hours (19.24%) and for vitamin E after 6 hours (23.19%). Enrofloxacin caused a slight (3-9%) reduction in the level of the analysed vitamins. In the chlorpyrifos-enrofloxacin co-exposure group reduced vitamins A and E levels were also noted, but changes in this group were less pronounced in comparison to the animals intoxicated with chlorpyrifos only. The decrease in the antioxidant vitamin levels, particularly noticeable in the chlorpyrifos- and the chlorpyrifos combined with enrofloxacin-treated groups, may result not only from the increase in the concentration of free radicals, but also from the intensification of the secondary stages of lipid peroxidation.

scholarly journals Assessment of the Effects of Graded Doses of Polyphenolic-Rich Fraction of Garcinia kola Seeds on Pituitary–Testicular Axis of Male Wistar Rats

Dose-Response ◽  
2017 ◽  
Vol 15 (4) ◽  
pp. 155932581772926 ◽  
Author(s):  
Mosunmola Busayo Omotola ◽  
Isaac O. Adeosun ◽  
Efere M. Obuotor ◽  
Rufus O. Akomolafe ◽  
Olugbenga A. Ayannuga
Keyword(s):  
Pituitary Gland ◽  
Wistar Rats ◽  
Seminiferous Tubules ◽  
Sodium Arsenate ◽  
Group V ◽  
Garcinia Kola ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Cervical Dislocation

This study evaluated the ameliorative and prophylactic effects of 2 different doses of polyphenolic-rich fraction of Garcinia kola (PPRF Gk) seeds on the histology and hormones of pituitary–testicular axis of male Wistar rats. Thirty-five male Wistar rats (150-200 g) were divided into 7 groups of 5 rats each. Groups I and II were given distilled water (0.5 mL/day) for 8 days followed by propylene glycol (0.2 mL/d) and 600 mg/kg of PPRF Gk, respectively, for 21 days. Group III received sodium arsenate (8 days), left untreated for 21 days. Groups IV and V received sodium arsenate (20 mg/kg) for 8 days followed by PPRF Gk (300 and 600 mg/kg, respectively) for 21 days. Groups VI and VII received PPRF Gk (300 and 600 mg/kg, respectively) for 21 days followed by sodium arsenate (20 mg/kg) for 8 days. Rats were killed by cervical dislocation 24 hours after the last dose and their blood collected through cardiac puncture. Blood sera were assayed for the levels of follicle-stimulating hormone (FSH), luteinizing hormone (LH), and testosterone using immunoassay techniques. Histology of the pituitary gland and testes was carried out. A significant reduction was observed in the concentration of FSH in groups IV, V, VI, and VII in comparison with groups I and II. The concentrations of both LH and testosterone showed significant decreases in groups IV, V, VI, and VII in comparison with group I. Group III presented with the lowest serum hormonal concentrations. Photomicrographs of the pituitary gland revealed greatly reduced basophils in group III and mildly reduced basophils in groups IV, VI, and VII in comparison with groups I and II. Group V revealed hypercellularized and distorted basophils. Photomicrographs of the testes showed detachment of the seminiferous tubules from the basement membrane and disruption of the interstitial space which was worse in group III, moderate in groups V and VI, and mild in group VII. In conclusion, PPRF Gk effected a dose-dependent reversal and prevention of the perturbations caused by arsenate in rats.

The Effect of Parathion-methyl and Antidotes on Parotid and Pancreatic Glands: A Pilot Experimental Study

2007 ◽  
Vol 26 (5) ◽  
pp. 383-388 ◽  
Author(s):  
Betul Gulalp ◽  
Yuksel Gokel ◽  
Derya Gumurdulu ◽  
Gulsah Seydaoglu ◽  
Kenan Daglioglu ◽  
...  
Keyword(s):  
Group Iv ◽  
Control Group ◽  
Blood Levels ◽  
Parotid Glands ◽  
Group V ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Histopathologic Evaluation ◽  
Histologic Changes

The objective of this study is to investigate the functions of parotid and pancreatic glands in response to intoxication with parathion-methyl (PM) and the effects of treatment in rats. Seventy-five male Wistar rats were divided equally into five groups: Group I, control; group II, received atropine and pralidoxime (2-PAM) for 24 h, but no PM; group III, oral PM but no atropine and 2-PAM; group IV, PM and atropine for 24 h and 2-PAM; group V, PM and atropine for 96 h and 2-PAM. After the administration of the chemicals, blood samples were drawn to test for amylase, lipase, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE), while pancreatic and parotid glands of each rat were removed for light microscopic examination. Amylase levels were found significantly elevated in groups II, III, IV, and V, whereas lipase levels were supranormal in groups III, IV, and V. The blood levels of AChE were decreased in groups III and IV and BChE were decreased in II, III, IV, and V. No evidence of pancreatitis and parotitis was identified in the histopathologic evaluation in any group in 96 h; however, hyperchromasia, irregularity in nuclei, and binuclear cells were observed in all parotid glands in group V. Parotitis and pancreatitis were not evident; however, hyperamylasemia and hyperlipasemia were found, whereas various histologic changes in parotid glands were documented in the groups that were administered organophosphate and treatment.

scholarly journals Biochemical Effects of Matured Stem Extract of Opuntia Dillenii in Male Wistar Rats

2018 ◽  
Vol 11 (1) ◽  
pp. 49-58
Author(s):  
Uche C. Njoku ◽  
Benjamin A. Amadi ◽  
Peter U. Amadi ◽  
Onyebuchi E. Ezendiokwere ◽  
Idongesit E. Archibong
Keyword(s):  
Wistar Rats ◽  
Density Lipoprotein ◽  
Control Group ◽  
Group Iii ◽  
Therapeutic Benefits ◽  
Group I ◽  
Male Wistar Rats ◽  
Stem Extract ◽  
Group Ii ◽  
Opuntia Dillenii

Summary The effect of aqueous matured stem extract of Opuntia dillenii on selected biochemical parameters in Male Wistar rats was explored. Standard analytical methods were applied. Forty Wistar rats (80-100g) were used in the animal studies, separated into four groups. The control group was solely administered normal feed and saline, group I was administered 100mgkg−1 of the extract, group II received 300mgkg−1 of the extract and group III received 500 mg/kg−1 of the extract. A significant increase (p<0.05) in the activities of alanine aminotransferase (ALT) and alkaline phosphatase was observed in group II and III rats, as compared with the controls. A significant decrease in urea and creatinine concentrations was found only in group III rats against the controls. Also, a significant (p<0.05) decrease in triglyceride, total cholesterol, and low density lipoprotein (LDL)-cholesterol was seen in group II and group III rats when compared with the control. The hematological evaluation revealed a significant (p<0.05) decrease in red blood cell and hemoglobin levels in group III rats when compared with the control. The findings showed both beneficial and toxicological effects of the plant. Hence, for optimal therapeutic benefits, a further toxicological survey could still be carried out perhaps at higher doses.

scholarly journals Oxidized tissue proteins after intestinal reperfusion injury in rats

2005 ◽  
Vol 20 (6) ◽  
pp. 434-436 ◽  
Author(s):  
Alberto Schanaider ◽  
Vinícius José Martinho Toledo Menezes ◽  
Aline Cury Borchardt ◽  
Pedro Lagerblad de Oliveira ◽  
Kalil Madi
Keyword(s):  
Oxidative Stress ◽  
Reperfusion Injury ◽  
Intestinal Ischemia ◽  
Ischemia And Reperfusion ◽  
Ischemia And Reperfusion Injury ◽  
Group Iii ◽  
Protein Levels ◽  
Group I ◽  
Carbonyl Protein ◽  
Male Wistar Rats

PURPOSE: To analyse if the carbonyl proteins measurement could be validated as a method that allows the identification of an intestinal oxidative stress after ischemia and reperfusion injury. METHODS: Twenty-five male Wistar rats (n =21) weighting 200 to 250g were divided into three groups. Group I - control (n = 10). Group II - sham (n = 5) and Group III (n = 10) subjected to 60 minutes of intestinal ischemia and equal period of reperfusion. For this purpose it was clamped the superior mesenteric artery in its distal third. Histological changes and carbonyl protein levels were determined in the samples of all groups. In group III, samples of both normal and reperfused ileal segment were studied. RESULTS: All the reperfused segments showed mucosal and submucosal swelling and inflammatory infiltrate of the lamina propria. Levels of carbonyl protein rose in group III, including in the non-ischemic segments. The sensitivity and specificity of the carbonyl protein tissue levels were respectively 94% and 88%. CONCLUSION: The carbonyl protein method is a useful biologic marker of oxidative stress after the phenomenon of intestinal ischemia and reperfusion in rats. It was also noteworthy that the effects of oxidative stress could be seen far from the locus of the primary injury.

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