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Background and Aim: Oral infections are common among people of any age and can trigger systemic inflammation. The microbiota is a diverse group of microorganisms that play important roles in metabolism, immune function, and homeostasis. Oral microbiota in human atherosclerotic plaques has been identified using various techniques. Therefore, the focus of this study was to determine the correlation between metabolic parameters and oral microbiota composition in patients with atherosclerosis using Denaturing Gradient Gel Electrophoresis (DGGE) assays. Materials and Methods: In this case-control study, saliva samples were collected from 139 patients with atherosclerosis and healthy individuals from Imam Ali Cardiovascular Hospital, Kermanshah, Iran. After DNA extraction, PCR products were examined and evaluated using DGGE assays. Results: The study included 89 (36%) patients with a history of atherosclerosis and 50 (36%) healthy individuals. There was a significant relationship between the mean total cholesterol, Low-Density Lipoprotein (LDL), Fasting Blood Sugar (FBS), and Blood Urea Nitrogen (BUN) in the two groups. However, there was no significant difference in the mean high-density lipoprotein (HDL) and Triglyceride levels between the study groups. Conclusion: Our results showed a relationship between metabolic parameters and oral microbiota composition in patients with atherosclerosis. Additionally, our results indicated that the DGGE assay is a useful method for diagnosing and comparing the oral microbiota of people with atherosclerosis and healthy individuals. Therefore, further examination of the oral microbiota is necessary to determine its potential as a biomarker for atherosclerosis. [ABSTRACT FROM AUTHOR]

Aim: Effects of maternal probiotics administered during pregnancy as well as consumption by offspring in the post-weaning period on anxiety behavior were examined. Methods: In addition to anxiety levels measured by EPM and OFT, the expression level of the hippocampal genes, and serum sex hormones in male and female mice that received foot shock stress were assayed in the pubertal period. Results: The results of this study showed that consumption of probiotics in the foot shock-stressed offspring in both sexes could significantly increase the length of stay in the EPM open arm compared to the control group, however, the offspring of the probiotic-treated dam did not. Consumption of probiotics by the pro-off group caused remarkable high expression of the 5HT2AC receptor gene. In the pro-off group, consumption of probiotics led to a significant decrease in 5HT1 receptor expression. Expression of GABRA2 was increased in probiotics-treated groups, thus the pro-off and the pro-dam group had a significant difference from the control group. Feeding offspring with probiotics by significantly increased progesterone concentrations compared to the control group, and maternal consumption of probiotics during pregnancy and lactation had no reducing effect on progesterone concentrations. This is due to electric shock stress. The consumption of probiotics by mice during infancy was shown to compensate for the decrease in progesterone concentration in them. Maternal use of probiotics during pregnancy and lactation did not affect this concentration. Conclusions: It is concluded that probiotics can protect against foot shock stress-induced anxiety, progesterone disturbance, and dysregulation of expression of some anxiety-related genes. [ABSTRACT FROM AUTHOR]

The current investigation was aimed to evaluate the oxidative stress (OS), blood factors, and neurocognitive state among cement factory workers who are exposed to dust during their work. Totally 41 cement exposed workers and 41 subjects as a control group were selected, and their OS, biochemical parameters, and a neurocognitive questionnaire were assessed. The results indicated that the levels of triglyceride, alanine aminotransferase, and alkaline phosphatase were higher among the exposed workers. The rate of lipid peroxidation and total antioxidant capacity were not significantly differenced among the workers while compared to the control group. Cement industry may lead to several health impairments among cement workers. A significant association between past dust exposure in the workplace and neurocognitive impairment. Occupational exposures to these dusts may result later in life in adverse mental health outcomes. [ABSTRACT FROM AUTHOR]

Objective: The aim of the present study was to investigate antibacterial and antibiofilm activity of a few medicinal plants against oral bacteria. Materials and Methods: Salvia officinalis, Lippie citriodora, Mentha piperita, Echinacea purpurea and Matricaria chamomilla were extracted. Isolates from oral cavity were identified by microbiological and molecular methods. Minimum inhibitory concentration and minimum bactericidal concentration were determined by Broth microdilution method. The anti-biofilm activity of essential oils and extracts investigated and as a mixture by Broth dilution method. Toxicity of the herbal mixture was assayed by in Wistar rats treated with intradermal injection. Wound healing properties of the herbal mixture against infected wounds on the back of the rats were investigated. Anti-biofilm activity was investigated on tooth surfaces. Bacterial structure changes and finestructure study were performed by light microscopy and Transmission electron microscopy. Results: The lowest MIC and MBC for the plant mixtures was 0.0002 mg/ml belonged to Streptococcus pyogenes and the highest values (0.025 mg/ml) belonged to Eikenella corrodens. The essential oils of S.officinalis, L.citriodora and M.piperita, but not E.purpurea and M.chamomilla extracts, were able to remove the biofilms created by the studied bacteria. The herbal mixture was able to completely heal the wound skin of rats in 21 days (p<0.05 compared to control). The mixture was able to decompose the teeth biofilm in 45 seconds. The results of light and electron microscopy showed that the bacterial structure exposed to the herbal mixture was deformed. Conclusion: It was concluded that the essential oils of S.officinalis, L.citriodora and M.piperita had significant effects on inhibition of oral bacteria biofilm formation. [ABSTRACT FROM AUTHOR]

Background and Aim Epilepsy is a common brain disorder. Brain function can be affected by the intestinal microflora. The intestinal microflora have a major role in modulating immune responses, producing essential metabolites and mediating neurotransmitters. Antibiotics can affect and reduce these roles and functions by eliminating the intestinal microflora. The aim of this study was to investigate the effect of intestinal natural micro flora removal on seizure susceptibility and seizure behavior modification with the use of probiotics in male Wistar rats. Methods & Materials This study was performed on 32 male Wistar rats with weight range 200-250 gr. The animals were randomly divided into four groups: 1. Control group; 2. Antibiotic group; 3. Probiotic group and 4. Antibiotic + probiotic group. To remove the microflora, antibiotics (neomycin, ampicillin, and metronidazole) for three weeks and for replacement of microflora, probiotics (Lactobacilli casei, Lactobacillus acidophilus and Bifidobacterium bifidum) for four weeks were administered. Seizures were performed by intraperitoneal injection of pentylentrazole. The microflora was examined by the MRS Agar medium and the Pure Plate method. The data were statistically analyzed in Graph Pad Prism V. 8. Ethical Considerations This study was approved by the Research Ethics Committee of Arak University of Medical Sciences (Code: IR.ARAKMU.REC.1395.176). Results The use of antibiotics lead to decrease the number of intestinal bacteria (P<0.0001), increased the severity and stability of seizure stages (P<0.05) and decreased the time delay of seizure onset (P<0.05) compared to the control group. Probiotic consumption by modifying the intestinal microflora (P<0.0001) reduced the severity of seizure and increased the time delay of seizure onset (P<0.05). Conclusion Elimination of microflora has the potential to induce seizures, which can be compensated by administration of probiotics. [ABSTRACT FROM AUTHOR]

In this study, C14/SiO2–Fe3O4and AC–Fe3O4nanocomposite synthesized by co-precipitation method were used as adsorbents for the removal of U(VI) from aqueous solutions. The main compositions of AC–Fe3O4and C14/SiO2–Fe3O4were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The removal efficiency of U(VI) was studied as a function of pH, contact time, ionic strength, temperature, adsorbent dose, initial U(VI) concentration, and initial benzamide concentration. Maximum adsorption of U(VI) was obtained at pH 6. The removal of U(VI) reached an equilibrium within 30 min by C14/SiO2–Fe3O4and 90 min by AC–Fe3O4, respectively. Removal efficiency of U(VI) by both adsorbents was decreased with increasing ionic strength and initial U(VI) concentration, but was increased with increasing temperature and adsorbent dosage. Kinetic study revealed that the pseudo-second order model well described the adsorption of U(VI) onto two adsorbents. When adsorption data was analyzed by both Langmuir and Freundlich adsorption isotherms, it was better described by the Langmuir model. The maximum adsorption of U(VI) was 16.29 and 15.87 mg/g by C14/SiO2–Fe3O4and AC–Fe3O4nanocomposite, respectively. The thermodynamic parameters of the adsorption process indicated that adsorption occurred through endothermic process. Overall, this work shows that C14/SiO2–Fe3O4is a more effective adsorbent than AC–Fe3O4for the removal of low concentration of U(VI). [ABSTRACT FROM AUTHOR]

Oral infections can activate local and systemic inflammation. The inflammatory response plays a main role in atherosclerosis. several studies have reported a relation between oral pathogen infection and Atherosclerosis. Recently it was indicated that some oral microbiome has a significant role in triggering atherosclerosis. Denaturing Gradient Gel Electrophoresis (DGGE) is an acceptable assay for identification of uncultivable bacteria. Therefore, we compared the bacterial population diversity in the oral microbiota between atherosclerosis patients and healthy people. Oral microbiota profiling was performed for 139 individuals including 89 patients with CAD and 50 healthy individuals. After DNA extracted from saliva, PCR products were examined and evaluated using DGGE assay. We found that significant relationship between the increased risk of atherosclerosis and the presence of Actinomyces oris, Enterococcus faecalis, Bacterium strain sulresv, Bacterium Culaenoe, NC4, NC7, and NC5 in atherosclerosis patients and healthy individuals. There was also a significant relationship between reducing the risk of atherosclerosis in the presence of NC3 and Entreococcus munotii in atherosclerosis patients and healthy individuals.  In conclusion, presence of some oral microbiota increases the risk of atherosclerosis and the presence of some oral microbiota reduces the risk, so the oral microbiota should be further examined to determine its potential as a biomarker for atherosclerosis.

The study aimed to determine the effects of probiotic consumption during pregnancy and lactation and post-weaning on acute stress-induced anxiety and gut beneficial microbiota of the female offspring mice.The female offspring mice were divided into several groups: intact, control (only stressed), PBS/dam (dams gavaged with PBS), PRO/dam (dams gavaged with probiotics), PRO/dam+off (both dams and offspring gavaged with probiotics), and PBS/dam+off (both dams and offspring gavaged with PBS)The probiotics chosen are mainly L. rhamnosus, B.breve, and B. longum (108 CFU/ml). Foot shock stress will be applied for one hour on the 43rd day after birth. Behavioral tests were conducted using the open field and elevated plus-maze. Corticosterone was measured by ELISA kit, and intestinal microflora with qPCR.The data showed that PRO/dam+off had more entries into open arms compared to the control group and decreased move distance and time spent in closed arms compared to the control group. However, there was no significant difference between the PRO/dam group and the control group. In the open field test, the control group spent less time in the inner zone compared to the intact group and in PRO/dam+off group. Corticosterone hormone was increased in the control group and was decreased in the PRO/dam+off. Bifidobacteria and Lactobacilli decreased in the control group in comparison to the intact group, and in the PRO/dam+off group increased compared with other groups. Maternal and filial supplementation with a multi-strain probiotic mixture increased levels of beneficial bacteria and reduced stress-induced anxiety in mice.

Introduction: Vancomycin Resistant Enterococci (VRE) can be found all over the world. Thus, rapid detection of the isolates could be of high importance in the treatment or prevention of the associated disease., Aim: To measure the turanose fermentation in Enterococcus faecalis clinical isolates for rapid differentiation of VRE and Vancomycin-Susceptible E. faecalis (VSE) isolates., Materials and Methods: Forty E. faecalis samples were isolated from 200 clinical samples in Tehran Medical Center, Iran, from October 2012 to December 2012. These isolates were detected according to the standard microbial and biochemical tests. Detection of VRE isolates was originally performed by disk diffusion using 1 μg vancomycin disk, followed by Polymerase Chain Reaction (PCR) amplification of the van A gene. Finally, the turanose consumption in 1%, 0.7% and 0.5% dilutions was detected by a phenotypic method., Results: Among the 40 E. faecalis isolates, 20 vancomycin-susceptible and 20 vancomycin-resistant E. faecalis were isolated according to the disk diffusion and PCR of the van A gene. There was a considerable difference between VRE and VSE isolates in 0.7% dilution of turanose. However, there was no significant difference between VRE and VSE in 1% and 0.5% dilutions of turanose., Conclusion: Since detection of VRE isolates is of high importance, especially in nosocomial infections, phenotypic methods may be highly useful for this purpose. In conclusion, our data indicate that VRE isolated from clinical samples could be distinguished from VSE isolates by turanose fermentation at dilution 0.7%.