Wistar Rats

Strawberry (Fragaria ananassa) is an herbaceous plant from the Fragaria genus. It is a well-known plant with a widely enjoyed fruit. Strawberry, like other common fruits, contains antioxidants such as ascorbic acid (vitamin C), folic acid, and essential oils It is also high in minerals like iodine, magnesium, copper, iron, and phosphorus, as well as vitamins like thiamine, riboflavin, niacin, vitamin B6, vitamin K, vitamin A, and vitamin E. Hormones have critical role in fertility management and regulation. Endocrine glands produce hormones and release them to target organs in response to stimulation via negative or positive feedback mechanisms. This study was aimed at evaluating the effect of Fragaria ananassa (strawberry fruit) extract on male reproductive function by analyzing the male hormones in adult male wistar rat. A total of twenty (20) adult male wistar rats were used for this study. The rats were divided into four (4) experimental groups (A-D) with five (n=5) rats in each group. The rats were acclimatized for two weeks before commencement of administration. Group A was the control group. Group B, C and D were administered 50mg/kg, 100mg/kg and 200mg/kg body weight of fragaria ananassa extract orally via gavage respectively. The rats were anesthetized using chloroform vapor and were terminally bled by cardiac puncture. The blood samples were collected using a heparinized tube for hormonal assay. Testosterone was determined by competitive enzyme immunoassay (TYPE 7) and Luteinizing hormone was determined by Immunoenzymometric assay (TYPE 3). The result were statistically analyzed using Graph-Pad prism version 8.0. Comparison within groups were done using one-way ANOVA. The result were presented as mean ±SEM and p-value less than 0.05(P < 0.05) was considered statistically significant. The result showed non-significant difference in the hormones (Testosterone and Luteinizing hormone) in group B, C and D when compared to the control group (Group A). In conclusion aqueous extract of Fragaria ananassa (strawberry fruit) does not have significant effect on the reproductive hormones (Testosterone and Luteinizing hormone) in adult male wistar rats.

This study investigated the effects of 28-day oral administration of the aqueous leaf extract of Sphenocentrum jollyanum on haematological parameters in wistar rats. The plant which is widely used in West African traditional medicine, is known for its therapeutic benefits, yet its prolonged safety on blood indices remains scarcely explored. Twenty-four male wistar rats were randomly distributed into four groups: a control group and three treatment groups receiving 250 mg/kg, 500 mg/kg, and 1000 mg/kg of the extract, respectively. At the end of the experimental period, blood samples were analyzed for red and white blood cell indices, as well as platelet parameters, using standard hematological techniques. The results revealed a significant reduction (p < 0.05) in total white blood cell, monocyte, and granulocyte counts at the lowest dose (250 mg/kg), while higher doses maintained values comparable to the control. Red blood cell indices—including haemoglobin, packed cell volume, and mean corpuscular volume—remained within normal physiological limits, suggesting no adverse effect on erythropoiesis. Platelet counts were greatly unaffected, though a temporary decrease in plateletcrit and platelet distribution width was observed at low dose. Overall, the extract did not produce any clinically significant haematotoxic effect but demonstrated mild dose-dependent immunomodulatory influence. These findings suggest that aqueous extract of Sphenocentrum jollyanum is relatively
safe on haematological profiles within the tested range, supporting its traditional use while emphasizing the need for dose regulation in prolonged administration.

Nickel chloride (NiCl2) is a widespread environmental contaminant that causes neurotoxicity, with the cerebellum showing particular vulnerability due to its central role in motor coordination and high metabolic demands. Memantine, a non-competitive
N-methyl-D-aspartate (NMDA) receptor antagonist. It is hypothesized that its neuroprotective properties could be beneficial in the mitigation of cerebellar damage caused by nickel chloride. This study was aimed at investigating the effects of memantine on the nickel chloride induced cerebellar toxicity in wistar rats. Forty-eight rats were divided into eight groups: Control, nickel chloride only, high dose of memantine + nickel chloride, low dose of memantine + nickel chloride, high dose of memantine, low dose of memantine. The treatment protocol ran for 28 days. A served as control and received 1ml of distilled water daily to compensate for stress of administration, whereas, rats in group B received 2.5mg/kg of NiCl₂, rats in group C received 10mg/kg Og memantine(low dose) and 2.5mg/kg of NiCl₂, rats in group D received 20mg/kg of memantine (high dose) and 2.5mg/kg of NiCl₂, rats in group E received 10mg/kg of memantine (low dose) and rats in group F received 20mg/kg of memantine (high dose). Administration of memantine was done orally using an orogastric tube while the administration of nickel chloride was done via intraperitoneal injection. It lasted for 28days. The body weight of the rats were recorded daily. At the end of the experimental period, the rats were sacrificed by cervical dislocation and the organ( cerebrum) weight was recorded. The parameters accessed include cerebral antioxidant enzymes (SOD, CAT, GPx and GSH), MDA concentration and the histology of the cerebrum using
Hematoxylin and Eosin staining technique. Results obtained showed no significant change (p>0.05) in the initial body weight and final body weight. A significant decrease (p<0.05) was observed in the weight change of rats in group B when compared to control, however, a significant increase (p<0.05) was observed in the weight of groups C and D when compared to group B. No significant change (p>0.05) was observed in the cerebellar and relative cerebellar weight of rats across experimental groups. A significant decrease (p<0.05) was observed in cerebellar SOD, CAT, GPx and GSH activity of rats in group B (2.5 mg/kg bw. NiCl2) when compared to the control. A significant increase (p>0.05) in cerebellar MDA concentrations was observed in the weights of rates in group B (2.5 mg/kg bw. NiCl2 ) when compared with group A. Severe histological alterations in the cerebellum of nickel-chloride exposed rats were observed. However, pre-treatment with memantine mitigated the adverse effects induced by NiCl2. In conclusion, findings from this study shows that memantine exerted antioxidant properties as well as mitigating the histological alterations in the cerebellum.

Acute toxicity studies is essential for determining the immediate safety of substances following a single high-dose exposure, providing early indicators of potential adverse effects or lethality. CellifeIQ, a multi-component nutraceutical formulated with antioxidant-rich herbal extracts, vitamins, and minerals, is widely promoted for supporting cellular health, yet its toxicological safety has not been scientifically evaluated.This study evaluated the acute oral toxicity of CellifeIQ in male Wistar rats. Using Lorke’s method,male wistar rats received single oral doses of 10, 100, 1000, 1600, 2900, and 5000 mg/kg and were observed for 14 days for mortality, behavioural changes, body-weight trends, feed and water intake, and gross pathological alterations in major organs. No mortality occurred at any tested dose, indicating an LD₅₀ greater than 5000mg/kg. Mild and transient effects, such as slight restlessness or sedation, were observed at higher doses but resolved within hours, while delayed mild itching was noted only at doses ≥1000 mg/kg. Body-weight progression, feed consumption, water intake, and feed efficiency showed no significant differences compared to controls (p>0.05). Gross necropsy revealed no visible abnormalities in the liver, kidneys, heart, lungs, or spleen. CellifeIQ demonstrated very low acute oral toxicity and may be considered practically non-toxic under single-dose exposure conditions in male Wistar rats. However,further studies including sub acute and chronic toxicity,biochemical assays,histopathology, and genotoxicity evaluations are recommended to fully characterize its long-term safety profile.

Bisphenol-A (BPA) is an industrial chemical primarily used in the production of polycarbonate plastics and epoxy resins. Selenium (Se) is an essential trace element, vital for the health of humans and other living organisms. The aim of this study was to investigate the effects of Bisphenol-A (BPA) on some oxidative stress markers in adult male rats and evaluate the potential effect of Selenium (Se) in BPA-induced oxidative damage. A total of twenty (20) male Wistar rats weighing between 180g and 200g were purchased and kept in standard cages for two weeks to enable them acclimatize to their new environment. After acclimatization period, the twenty-adult male Wistar rats were divided into four (4) different groups A, B, C, D: control, BPA-only, Se-only, and BPA+Se. Group A served as control, Groups B D received 20mg/kg BPA, 2mg/kg Se, and both, respectively, for 54 days. Blood was collected and analyzed for oxidative stress parameters such as malondialdehyde (MDA), superoxide Distumates (SOD) and catalase (CAT). All statistical analyses were carried out using Graph Pad prism statistical software version 10.0. The data from all the groups were presented as Mean ± S.E.M (Standard Error of Mean), (n=5) in each group and analyze for statistical significance using one-way Analysis of Variance (ANOVA). Values were considered significant at P<0.05. The result shows that exposure to BPA resulted in significant (p<0.05) reduction in body weight. There was significant (p<0.05) increase in MDA levels in all groups compared with the control. On the other hand, SOD and CAT activities were significantly (p<0.05) reduced in all groups compared with the control, thereby indicating decreased antioxidant enzyme activities. In conclusion, these finding shows that Selenium (Se) supplementation did not mitigate the adverse effects of BPA and instead worsened oxidative stress, implying that Selenium (Se) may not provide protection against the harmful effect of Bisphenol-A (BPA) even at this dose but rather potentiated the effect of Bisphenol-A (BPA).

Icacina trichantha, known for their medicinal use possessing bioactive compounds with anti inflammatory and hematopoietic properties, offer promises for novel treatments. This study explores the effect of the aqueous leave extract on Cyclooxygenase-1 (COX-1) expression to elucidate the molecular mechanisms driving its therapeutic action. Therefore, the aim of this study is to determine the effect of Icacina trichantha aqueous leaves extract on Cyclooxygenase 1 expression in Aluminum Chloride-Induced Anaemia in Albino Wistar Rats. A total of sixty (60) adult male albino Wistar rats were divided into six (6) groups; A, B, C, D, E and F representing control, aluminum chloride group, ferrous sulphate group, aluminum chloride + 100mg/kg leaf extract of Icacina trichantha, aluminum chloride + 200mg/kg leaf extract of Icacina trichantha and aluminum chloride + 400mg/kg leaf extract of Icacina trichantha groups respectively. 5 milliliters (ml) of blood sample was drawn from each rat, and haematological parameters and mRNA of COX-1 were determined using a SRFI Haematology autoanalyzer and polymerase chain reaction respectively. Data obtained was analyzed using the GraphPad prism 8.02 software.The comparison of Haematological parameters amongst the study groups showed that there was no significant difference in Total white blood cell count (TWBC μL) across the groups. Platelet Distribution Width (PDW) was significantly lower in group E (8.96±0.27) when compared to group D (10.6±0.31) (p<0.05). There was no significant difference in other platelet parameters across the groups. Group C and D showed significantly lower expressions of COX-1 when compared to group B (p<0.05).Group C, D and E had significantly lower expression of COX-1 when compared to group F (p < 0.05). Groups E had significantly higher expressions of COX-1 when compared to group A, and significantly lower expression when compared to group B (p<0.05). Groups F had significantly higher expressions of COX-1 when compared to group A (p<0.05). In conclusion, administration of aluminum chloride resulted in no significant difference in white blood cell counts. There was also no alteration in platelet parameters, except PDWwhich showed slight difference. Administration of leaf extract of Icacina trichantha led to
alteration in the gene expression of COX-1.

Palm oil is widely consumed worldwide, particularly in Africa and Asia, where improper storage often leads to increased levels of free fatty acids (FFA). Elevated FFA levels can induce oxidative stress and impair organ function, including the heart. The study aimed to determine the influence of varying FFA levels in palm oil on body weight, total ATPase activity and the histopathological integrity of cardiac tissue in rats. Palm oil samples with FFA levels ranging from 0.4% to 42.7% were fed to six groups of Wistar rats for four weeks. The study observed significant differences in weight gain across groups consuming palm oil
with different FFA levels, the control group show moderate weight gain as baseline for
comparison, the low level FFA group (0.4% FFA) show a significant weight gain suggesting optimal intake of nutrient while the higher level FFA group (28.4% FFA) showed reduce weight gain particular in the 8.4% FFA group. Total ATPase activity was assessed using standard spectrophotometric methods, while histopathological analysis of cardiac tissue was conducted to evaluate structural changes. The study revealed an initial increase in ATPase activity in groups fed moderate FFA levels (4.8%), reflecting potential adaptive metabolic responses. However, higher FFA levels (≥8.4%) led to suppressed ATPase activity, likely due
to oxidative damage. Despite the increase observed in ATPase activity and tissue structure ,no evidence of acute myocardial damage was found in the control and experimental groups. Histopathological analysis showed normal cardiac architecture in the control and palm oil fed groups. The finding underscore the importance of proper palm oil storage to limit FFA accumulation and prevent potential adverse effects on cardiac health.

The cerebrum, vital for cognition and motor control, is highly susceptible to toxic injury. Excess manganese chloride exposure induces oxidative stress, mitochon drial dysfunction, and neuroinflammation, resulting in cerebral degeneration. Vanillin, a natural antioxidant and antiinflammatory agent, may counter these effects. Thus, this study aimed to investigate the activity of vanillin against manganese chloride–induced cerebral toxicity in adult Wistar rats. Forty-eight (48) Wistar rats were randomly assigned into six groups (A-F). Group A rats served as the control group; Group B rats were administered 10 mg/kg body weight of manganese chloride; Group C rats were administered 20 mg/kg body weight of vanillin and 10 mg/kg body weight of manganese chloride; Group D was administered 40 mg/kg body weight of manganese chloride and 40 mg/kg body weight of vanillin; Group E was administered 20 mg/kg body weight of vanillin; Group F was administered 40 mg/kg body weight of vanillin. All administrations lasted for twenty-eight (28) days. Neurobehavioural activities were evaluated using the Y-Maze Test. Results from the study showed manganese chloride-exposed rats showed significant (p<0.05) weight loss, cognitive deficits, decreased antioxidant enzymes activity, and increased lipid peroxidation with vacuolization and pyknotic nuclei observed in the cerebrum histology

Arsenic exposure remains a major global health challenge, and sodium arsenite is one of the most toxic inorganic arsenic compounds known to cause severe hematological, oxidative, and immunological disturbances. This study examined the protective effects of vitamin E against sodium arsenite–induced changes in hematological parameters in Wistar rats. Thirty-five male rats were randomly divided into five groups of seven: a control group, a vitamin E–only group (50 mg/kg), a sodium arsenite–only group (10 mg/kg), and two co-treatment groups receiving sodium arsenite with either 25 mg/kg or 50 mg/kg of vitamin E. All treatments were given orally for 14 days, after which blood samples were collected for hematological analysis. Results showed that sodium arsenite caused significant hematotoxicity, marked by reductions in red blood cell count (RBC), hemoglobin concentration (Hb), lymphocyte percentage, and monocyte levels, along with increases in white blood cell count (WBC), neutrophil levels, and the neutrophil-to-lymphocyte ratio (NLR). These changes indicate anemia, oxidative stress, inflammation, and immune suppression linked to arsenic toxicity. Co-administration of vitamin E significantly reduced these effects in a dose-dependent manner. The 50 mg/kg dose of vitamin E showed the greatest improvement across all hematological parameters, demonstrating its superior protective effects. The findings suggest that vitamin E effectively reduces sodium arsenite–induced hematological damage through its strong antioxidant, anti-inflammatory, and membrane-stabilizing properties. This study highlights the potential of vitamin E as a natural antioxidant therapy to manage hematotoxicity caused by environmental arsenic exposure

The use of traditional medical therapy is an important method in the treatment and management of diseases in the African continent and this could be as a result of social, cultural and economic lifestyles. Pharmacologically, the active ingredients found in pyrenacantha staudtii can be extracted and used to cure and prevent numerous diseases. The aim of this research was to investigate the effect of aqueous extract of pyrenacantha staudtii on the undamaged spleen of adult wistar rats. Thirty adult wistar rats weighing between 110g and 200g were used for this experiment with five rats in each group. All rats were allowed two weeks of acclimatization and they all had equal access to feed and water. Group A was the control and was not administered with any extract. Group B was administered with a low dose of the extract(100mg). Group C was administered with a medium dose of the extract(200mg). Group D was administered with 400mg of the extract. Group E was administered with 800mg of the extract. Group F was administered with 1600mg of the extract. All the rats were administered with the extract for 35 days. On the 36th day, the rats were sacrificed via chloroform anaesthesia and the spleen were harvested immediately and preserved in 10% formal saline for tissue processing using H&E for histological analysis