scholarly journals Evaluation of the Neuroprotective Effects of Eugenol on Formaldehyde Induced Neurotoxicity in Wistar Rats

2020 ◽  
Vol 11 (2) ◽  
pp. 62-70
Author(s):  
Samuel Mesole ◽  
◽  
Omachonu Okpanachi ◽  
Sunday Adebisi ◽  
Uthman Yusuf ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Wistar Rats ◽  
Activity Level ◽  
Object Recognition Test ◽  
Neuroprotective Effects ◽  
Group Iii ◽  
Group I ◽  
Therapeutic Value ◽  
Cornu Ammonis ◽  
Male Wistar Rats

Over the years, Formaldehyde (FA) has been linked to increased generation of reactive oxygen species (ROS), leading to oxidative stress and cognitive decline. However limited numbers of studies have shown the effect of eugenol on FA induced toxicity in Wistar rats. Therefore this study aimed at investigating the effects of eugenol on the FA induced toxicity in Wistar rats. A total of twenty male Wistar rats where divided into four groups: (Group I. 150 mg/kg eugenol; Group II, 5 mg/kg FA; Group III, 150 mg/kg eugenol + 5 mg/kg FA; Group IV/control, 2ml/kg distilled water) for thirty days. FA and eugenol were administered orally. Rats were humanely sacrificed under 0.8 mg/kg ketamine anaesthesia administered intraperitoneally. Cognitive tests using Morris water maze and Novel object recognition test were carried out, Oxidative stress parameters, acetylcholine activity and histometric analysis of hippocampal Cornu Ammonis (CA 1 and 3) pyramidal neuronal cells. Administration of FA resulted in significant (p<0.05) increased activity of malondialdehyde (MDA), intra-mitochondrial accumulation of 8-hydroxydeoxyguanosine (8-OHdG), reduced activity level of superoxide dismutase (SOD) and acetylcholine levels. However co-administration of eugenol and FA resulted in significant (p<0.05) enhancement of cognitive ability and also significantly (p<0.05) reduced MDA and 8-OHdG levels, and increased SOD and acetylcholine levels. Our results indicate that eugenol would provide therapeutic value against FA induced oxidative stress and cognitive impairments.

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 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.

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 OXYCAROTENOID LUTEIN REVERSES THE TOXICITY INDUCED BY CARBOFURAN IN WISTAR RATS

2018 ◽  
Vol 10 (7) ◽  
pp. 10
Author(s):  
Binitha P Purushothaman ◽  
Gayathri Valsan ◽  
Ramadasan Kuttan
Keyword(s):  
Oxidative Stress ◽  
Grip Strength ◽  
Wistar Rats ◽  
Pain Threshold ◽  
Strength Test ◽  
Endurance Capacity ◽  
Marker Enzymes ◽  
Threshold Test ◽  
Group I ◽  
Male Wistar Rats

Objective: Elucidation of the protective effect of lutein against carbofuran induced toxicity in Wistar rats.Methods: Male Wistar rats were assigned into 5 groups of five animals. Group I normal received sunflower oil, Group 2 received carbofuran (5 mg/kg b. w.) alone. Group 3-5 received carbofuran plus lutein (50, 100 and 200 mg/kg body weight) respectively. Carbofuran and lutein administration were continued for 14 d. Neurobehavioural markers such as rotarod, grip strength test and pain threshold tests were carried out. After sacrifice, tissues were analysed for marker enzymes, antioxidant enzymes as well as oxidative stress markers.Results: Low dose of carbofuran was found to produce neurobehavioral problems as seen from the decreased retention time during rotarod test, endurance capacity in grip strength test and increased endurance capacity in pain threshold test. They were found to be significantly reversed by oral lutein administration. Administration of lutein restored the decreased acetylcholinesterase produced by carbofuran. Serum and tissue marker enzymes such as lactate dehydrogenase, creatine kinase and gamma-glutamyltransferase, which were increased by carbofuran were decreased by lutein administration. Lutein administration also reduced oxidative stress parameters which were increased by carbofuran.Conclusion: The results showed that carbofuran induced toxicity in male Wistar rats was reversed by carotenoid lutein.

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.

scholarly journals Methyl Gallate Attenuates Doxorubicin-Induced Cardiotoxicity in Rats by Suppressing Oxidative Stress

Scientifica ◽  
2021 ◽  
Vol 2021 ◽  
pp. 1-12
Author(s):  
Akheruz Zaman Ahmed ◽  
Shakta Mani Satyam ◽  
Prakashchandra Shetty ◽  
Melanie Rose D’Souza
Keyword(s):  
Oxidative Stress ◽  
Normal Control ◽  
Wistar Rats ◽  
Group Iv ◽  
Control Group ◽  
Methyl Gallate ◽  
Group Iii ◽  
Group I ◽  
Female Wistar Rats ◽  
Group Ii

Doxorubicin-induced cardiotoxicity is the leading cause of morbidity and mortality among cancer survivors. The present study was aimed to investigate the cardioprotective potential of methyl gallate; an active polyphenolic nutraceutical, against doxorubicin-induced cardiotoxicity in Wistar rats. Twenty-four female Wistar rats (150–200 g) were divided into four groups (n = 6) which consist of normal control (group I), doxorubicin control (group II), test-A (group III), and test-B (group IV). Group III and group IV animals were prophylactically treated with methyl gallate 150 mg/kg/day and 300 mg/kg/day orally, respectively, for seven days. Doxorubicin (25 mg/kg; single dose) was administered through an intraperitoneal route to group II, III, and IV animals on the seventh day to induce acute cardiotoxicity. On the 8th day, besides ECG analysis, serum CK, CK-MB, LDH, AST, MDA, and GSH were assayed. Following gross examination of isolated hearts, histopathological evaluation was performed by light microscopy. A significant ( p  < 0.05) cardiac injury, as well as oxidative stress, was observed in doxorubicin control rats in comparison to normal control rats. Methyl gallate at both the doses significantly ( p  < 0.05) reduced doxorubicin-induced ECG changes, dyslipidaemia, and elevation of CK, CK-MB, LDH, AST, MDA and increased GSH level. Methyl gallate reversed the doxorubicin-induced histopathological changes in the heart. The present study revealed that methyl gallate exerts cardioprotection against doxorubicin-induced cardiotoxicity in female Wistar rats by suppressing oxidative stress. Our study opens the perspective to clinical studies for consideration of methyl gallate as a potential chemoprotectant nutraceutical in the combination chemotherapy with doxorubicin to limit its cardiotoxicity.

scholarly journals Study of Humoral Factors Regulating the Production of Leukocytes. I. Demonstration of a "Neutropoietin" in the Plasma after Administration of Triamcinolone to Rats

Blood ◽  
1961 ◽  
Vol 17 (4) ◽  
pp. 434-443 ◽  
Author(s):  
SHU CHU SHEN ◽  
TAKASHI HOSHINO
Keyword(s):  
Bone Marrow ◽  
Peripheral Blood ◽  
Wistar Rats ◽  
Significant Alteration ◽  
Humoral Factors ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Group Ii ◽  
Blood Elements

Abstract Male Wistar rats were divided into 3 groups: Group I. Rats given the triamcinolone daily by gastric catheter all developed neutrophilia accompanied by lymphopenia. Group II. Rats given daily intraperitoneal injections of plasma from normal rats manifested no significant alteration in the peripheral blood elements. Group III. Rats given daily intraperitoneal injections of plasma from rats given triamcinolone invariably developed neutrophilia without lymphopenia. Studies of the bone marrow of these groups at the end of the experiments revealed increased myeloid:erythroid ratios in Groups I and III but not II. It is therefore believed that this experiment suggests the existence of a neutrophilia-promoting factor in the plasma following the administration of triamcinolone.

scholarly journals Evaluation of Memory Impairment Following Prenatal Exposure to Mosquito Coil Smoke

2021 ◽  
Vol 1 (1) ◽  
Author(s):  
Shehu K ◽  
Badamosi Im ◽  
Saleh MS
Keyword(s):  
Oxidative Stress ◽  
Entorhinal Cortex ◽  
Prenatal Exposure ◽  
Wistar Rats ◽  
Neurofibrillary Tangle ◽  
Mosquito Coil ◽  
Object Recognition Test ◽  
Animal Group ◽  
Group I ◽  
Significant Impairment

Background: Developmental Neurotoxicity can lead to the buildup of reactive oxygen species which is an indicator to oxidative stress in the prenatally exposed offspring. Neuronal oxidative stress induces neuroinflammation, precedes tangle formation, and disrupts synaptic plasticity. The result of such changes may be expressed into adulthood as behavioral deficits. All together, these mechanisms are implicated in memory disorders. Objectives: To investigate the histochemical changes in the hippocampus and entorhinal cortex of Wistar rats' offspring after prenatal exposure to mosquito coil smoke and its effect on memory. . Methods: 12 pregnant Wistar rats were grouped into four, 3 animals per group. Group I was exposed to fresh air. Groups II, III, and IV were exposed to mosquito coil smoke for 4, 6 and 8 hours daily respectively throughout gestation period. On Post-natal day (PND) 28 and 29, shortterm spatial and recognition memory of adolescent wistar rats were assessed using water licking task and novel object recognition test respectively. For each animal group (I-IV), a total of 8 animals were randomly selected from the litters for neurobehavioral studies. Experimental animals were humanely sacrificed and sections from the hippocampus and entorhinal cortex were processed for histochemical studies using Bielschowsky stain. Data were presented as mean ± SEM; analysed using One-way analysis of variance and Tukey's Multiple Comparison Test (p<0.05). Results and Conclusion: Our results showed significant impairment in short-term recognition and spatial memory of group III and IV adolescent wistar rats when compared with the control (p<0.05) and the formation of neurofibrillary tangle-like structures in neurons of the studied regions. .

scholarly journals Effect of sitagliptin on depression in male wistar rats

2019 ◽  
Vol 9 (1) ◽  
pp. 200
Author(s):  
Vidya M. Mahalmani ◽  
Anil P. Hogade ◽  
Sanjay K. Mishra
Keyword(s):  
Oxidative Stress ◽  
Gene Expression ◽  
Wistar Rats ◽  
Cytokine Gene Expression ◽  
Antidepressant Effect ◽  
Oxidative Stress Markers ◽  
Cytokine Gene ◽  
Stress Markers ◽  
Group I ◽  
Male Wistar Rats

Background: Growing evidence supports relationship between depression and inflammation. The hypothesis of involvement of inflammatory pathways in depression is supported by the findings of increased levels of proinflammatory cytokines. So, we decided to evaluate the effect of sitagliptin on depression using forced swim test (FST) and possible effects of sitagliptin on serum oxidative stress markers and cytokine gene expression in rat hippocampus.Methods: FST model was used to evaluate antidepressant effect in male wistar rats. Rats in group I (control group) were given normal saline, group II (standard group) were given fluoxetine, group III and IV (test groups) were given sitagliptin 5 mg/kg and sitagliptin 9 mg/kg respectively. All the drugs in all groups were given per orally. At the end, animals were sacrificed and blood was collected. Hippocampus of rat brain was dissected out. Serum oxidative stress markers and hippocampal pro inflammatory cytokine gene expression analysis was carried out.Results: Sitagliptin 5 mg/kg and 9 mg/kg showed reduction in depressive symptoms and hippocampal cytokine gene expression in comparison to control. In case of serum oxidative stress markers, there was statistically significant reduction in nitric oxide levels with stagliptin 9 mg/kg. Although there was a decrease in the levels of catalase and increase in the levels of glutathione with standard and test groups, the results were not statistically significant.Conclusions: The present study showed significant antidepressant effect activity of standard and test groups. Hence, further research should be carried out to substantiate above results.

scholarly journals Diosmin Alleviates Doxorubicin-Induced Liver Injury via Modulation of Oxidative Stress-Mediated Hepatic Inflammation and Apoptosis via NfkB and MAPK Pathway: A Preclinical Study

Antioxidants ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 1998
Author(s):  
Abdullah F. AlAsmari ◽  
Metab Alharbi ◽  
Faleh Alqahtani ◽  
Fawaz Alasmari ◽  
Mohammed AlSwayyed ◽  
...  
Keyword(s):  
Wistar Rats ◽  
Mapk Pathway ◽  
Preclinical Study ◽  
Group Iv ◽  
Control Group ◽  
High Dose ◽  
Group Iii ◽  
Group I ◽  
Male Wistar Rats ◽  
Pre Treatment

Hepatotoxicity caused by chemotherapeutic drugs (e.g., doxorubicin) is of critical concern in cancer therapy. This study focused on investigating the modulatory effects of diosmin against doxorubicin-induced hepatotoxicity in Male Wistar rats. Male Wistar rats were randomly divided into four groups: Group I was served as control, Group II was treated with doxorubicin (20 mg/kg, intraperitoneal, i.p.), Group III was treated with a combination of doxorubicin and low-dose diosmin (100 mg/kg orally), and Group IV was treated with a combination of doxorubicin and high-dose diosmin (200 mg/kg orally) supplementation. A single dose of doxorubicin (i.p.) caused hepatic impairment, as shown by increases in the concentrations of serum alanine aminotransferase, aspartate aminotransferase, and alkaline phosphatase. Doxorubicin produced histological abnormalities in the liver. In addition, a single injection of doxorubicin increased lipid peroxidation and reduced glutathione, catalase, and superoxide dismutase (SOD) levels. Importantly, pre-treatment with diosmin restored hepatic antioxidant factors and serum enzymatic activities and reduced the inflammatory and apoptotic-mediated proteins and genes. These findings demonstrate that diosmin has a protective effect against doxorubicin-induced hepatotoxicity.

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