Protective effect of carvacrol on ketamine induced testicular damage in mouse model of schizophrenia

Introduction: Ketamine is applied to induce symptoms of schizophrenia in animal models. Besides the nervous system, ketamine also affects male lower genitourinary tracts. The present study evaluated the effects of carvacrol on antioxidant enzymes and examined the histopathologic changes in the testes of ketamine induced schizophrenic mice.Methods: A total of 48 male mice were treated with 25 mg/kg ketamine or saline for a period of 14 days. Between the 8th and 14th days, the animals received carvacrol (25 and 50 mg/kg) or saline. At the end of the experiment, blood samples were taken to measure luteinizing hormone (LH), follicle-stimulating hormone (FSH) and testosterone; the testes were also collected for biochemical and histopathological evaluations. Results: The results indicated that induction of schizophrenia by ketamine led to an oxidative stress by increasing malondialdehyde (MDA) level (P < 0.05). Treatment with 50 mg/kg carvacrol resulted in significant decrease in oxidative injury by decreasing MDA level and increasing antioxidant enzymes (P < 0.05). Testosterone, FSH and LH levels showed no significant difference between treatment groups and control groups except for testosterone which increased in mice treated with 50 mg/kg carvacrol (P < 0.05). Administration of carvacrol reduced the deleterious histopathologic changes caused by ketamine.Conclusion: The present study showed that ketamine causes oxidative stress and damage in testicular tissues and co-administration with carvacrol prevents the harmful effects of ketamine

Ameliorative action of farnesol on cyclophosphamide induced toxicity in mice

Introduction: Cyclophosphamide is an alkylating agent with antineoplastic and immunosuppressive effects. Acrolein, one of its metabolites, is responsible for different toxic side effects such as oxidative stress, and cell death. The present study aimed to evaluate protective effects of farnesol, a natural terpenoid with antioxidant effects, on cyclophosphamide induced side effects. Methods: For this purpose, mice received 200 mg/kg of cyclophosphamide plus 5 or 10 mg/kg of farnesol as pretreatment for 7 days. At the end of the study, samples from blood and different organs were collected. Histopathological and biochemical analyses including malondialdehyde (MDA), catalase (CAT) and glutathione (GSH) content as well as alanine transaminase (ALT) and aspartate aminotransferase (AST) were done to determine the toxic effects of cyclophosphamide and probable protective effect of farnesol. Results: Application of farnesol as a pretreatment could reduce tissue damages induced by cyclophosphamide particularly in testis, liver and spleen. The kidney did not show any relapse in tissue damages induced by cyclophosphamide. The testis demonstrated the most improvement by administration of farnesol, and the anti-oxidant enzymes increased in testicular tissues. Conclusion: This study indicated the protective effect of farnesol against oxidative stress induced by cyclophosphamide in the tissues, especially at the dose of 10 mg/kg on the testicular tissue. Hence, it might be beneficial in patients who are using cyclophosphamide

Systemic delivery of menstrual blood stem cells is more effective in preventing remote organ injuries following myocardial infarction in comparison with bone marrow stem cells in rat

Objective(s): Remote organ injury is a phenomenon that could happen following myocardial infarction (MI). We evaluated the potency of menstrual blood stromal (stem) cells (MenSCs) and bone marrow stem cells (BMSCs) to alleviate remote organ injuries following MI in rats.Materials and Methods: 2 × 106 MenSCs or BMSCs were administrated seven days after MI induction via the tail vein. Four weeks after cell therapy, activities of aspartate aminotransferase (AST), urea, creatinine, and Blood Urea Nitrogen (BUN) were evaluated. The level of tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6 were determined by ELISA assay. The expression of Nuclear Factor-κB (NF-κB) was evaluated by immunohistochemical staining. Apoptosis activity and tissue damage were also determined by TUNEL and H&E staining, respectively.Results: MenSCs and BMSCs administration caused a significant reduction in AST, urea, and BUN levels compared with the MI group. In addition, systemic injection of MenSCs significantly decreased the IL-1β level compared with BMSCs and MI groups (P0.05).Conclusion: MenSCs are probably more protective than BMSCs on remote organ injuries following MI via decreasing cell death and immunoregulatory properties

Effect of Quaternary Ammonium Salt on Shear Bond Strength of Orthodontic Brackets to Enamel

Objectives: This study sought to assess the effect of quaternary ammonium salt (QAS) on shear bond strength of orthodontic brackets to enamel. Materials and Methods: In this in vitro experimental study, 0, 10, 20 and 30% concentrations of QAS were added to Transbond XT primer. Brackets were bonded to 60 premolar teeth using the afore-mentioned adhesive mixtures, and the shear bond strength of the four groups (n=15) was measured using a universal testing machine. After debonding, the adhesive remnant index (ARI) score was determined under a stereomicroscope. Data were analyzed using one-way ANOVA. Results: The mean and standard deviation of shear bond strength of the control and 10%, 20% and 30% groups were 23.54±6.31, 21.81±2.82, 20.83±8.35 and 22.91±5.66 MPa, respectively. No significant difference was noted in shear bond strength of the groups (P=0.83). Study groups were not different in terms of ARI scores (P=0.80). Conclusions: The results showed that addition of QAS to Transbond XT primer had no adverse effect on shear bond strength of orthodontic brackets