saber zahri

In the article published in Cell J, Vol 15, No 4, 2015, pages 364-371, the reference for Table 1 and Figures 1B-D, 2,and 5A, B was inadvertently omitted. The missing reference (24), originally written in Persian by the authors, has nowbeen added to the relevant Table and Figures' legends with the permission of the original publisher, Journal of ArdabilUniversity of Medical Sciences.The authors would like to apologies for any inconvenience caused.

Tissue engineering, by designing biological scaffolds and imitating the extracellular environment, helps the growth and proliferation of cells and plays a key role in replacing and repairing damaged tissues. In recent years, the addition of nanoparticles, such as carbon quantum dots, to biological scaffolds has received attention. In this research, the synthesis of polycaprolactone scaffolds containing carbon quantum dots and the investigation of biocompatibility effects and their protection have been discussed.

Carbon quantum dots were synthesized using the pyrolysis method, and polymer scaffolds containing carbon quantum dots were prepared by the electrospinning method. The physical and chemical properties of the scaffold were evaluated by scanning electron microscopy and FTIR spectroscopy. The scaffolds' biocompatibility and antioxidant properties were measured by the MTT method.

Examination of the morphology and chemical showed the appropriate porosity of the scaffold containing carbon quantum dots. The MTT assay significantly enhanced stem cell viability on scaffolds incorporating carbon quantum dots. Furthermore, these scaffolds exhibited a significant protective effect against oxidative stress.

This study showed that the polycaprolactone scaffold containing carbon quantum dots, with high biocompatibility and suitable antioxidant properties, provides an effective substrate for tissue engineering and cell protection under oxidative stress conditions.

Tissue engineering is a multidisciplinary and interdisciplinary topic that involves the development of biological implants for tissue regeneration intending to improve or enhance tissue or organ function.

This study aimed to evaluate the mechanical and histological properties of decellularized rat pancreas scaffolds, as well as to investigate the viability of adipose mesenchymal stem cells (MSCs) on the said scaffold for use in regenerative medicine and tissue engineering.

This is an experimental study that was performed in the research laboratory of Mohaghegh Ardabili University. To prepare the scaffold, male Wistar rats were anesthetized with carbon dioxide. After dissecting the mice, their pancreases were isolated and immediately transferred to a phosphate-buffered saline (PBS) solution to prepare them for decellularization. The decellularized scaffolds were evaluated histologically and mechanically. After decellularization, lipid MSCs were injected into de-cell scaffolds in the third passage.

Examination of the results of histological evaluations showed that scaffolding was completely decellularized. These results were confirmed by Mason trichrome and Dapi staining (coloring). Specialized tissue assessments by electron microscopy showed that the collagen and elastin strands were relatively conserved in the extracellular matrix (ECM).

In general, the result of this research demonstrates the successful decellularization of pancreatic tissue, effective preservation of the ECM of the desired tissue, and the viability of the MSCs on the scaffold resulting from the decellularization of the tissue.

Family history of gastric cancer (GC) in first-degree relatives may increase the risk of GC. This study aimed to assess how family history of GC in first-degree relatives really affects the risk of GC in an extremely high-risk population.

A large population-based case-control study was carried out on 1222 incident GC cases and 1235 controls in Ardabil Province-a high-risk area in North-West Iran-to assess the associations of GC family history in first-degree relatives with the risk of GC (2003-2017).

GC family history did not significantly associate with the risk of GC overall (ORadj=1.09, 95% CI: 0.80–1.47, P=0.589). It found no significant association of GC family history in a parent, and in a fa-ther, mother, and sister separately, with the risk of GC. However, GC risk was significantly associated with a history of GC in a sibling (ORadj=1.61, 95% CI: 1.11–2.35, P=0.013), especially brother (ORadj=2.24, 95% CI: 1.41–3.64, P=0.0008). The risk was greatly increased in subjects with two or more affected brothers (ORadj =5.56, 95% CI: 2.33–14.20, P=0.0002).

We did not find a familial tendency to cardia GC and non-cardia GC as well as histopatho-logic features. Determining the type of first-degree relationships with GC may, therefore, be more im-portant than assessing family history alone for predicting the risk of GC in this high-risk area.

 The goal of tissue engineering is to create biological solutions that restore, maintain, and improve the function of damaged tissue. Scaffolds are structures based on extracellular matrix materials that have undergone various treatments.

 This study aimed to prepare polycaprolactone/silymarin and polycaprolactane/tragacanth scaffolds and compare the morphology and viability of PC12 cell lines.

 A 7% polycaprolactane solution (dissolved in acetic acid) was mixed with a 0.9% silymarin solution to prepare the polycaprolactane scaffold and silymarin loading, and a 7% polycaprolactane solution was mixed to prepare the polycaprolactane and tragacanth scaffold. Tragacanth solution was mixed at a concentration of 0.7% by weight, and then two scaffolds were prepared by electrospinning. The morphology of the scaffolds was studied by scanning electron microscopy (SEM), and the chemical structure of the scaffolds was studied by ATR-FTIR spectroscopy. The biocompatibility of the scaffolds and cell survival of PC12 cells was investigated by MTT assay.

 The morphology of the scaffolds and their chemical structure showed good porosity and successful loading of silymarin onto PCL and a suitable combination of tragacanth with PCL. The biocompatibility of the scaffolds was evaluated at 24, 48, and 72 hours after PC12 cell culture. Cell survival was found to increase on polycaprolactane/silymarin scaffolds compared to polycaprolactane/tragacanth.

 From the results of this study, loading polycaprolactane scaffold with silymarin increases the proliferation and survivability of PC12 cells compared to polycaprolactane/supporting scaffold, which may be a good candidate for neural tissue engineering.

Tissue engineering is a set of methods that can replace or repair damaged tissues with natural or artificial tissue. Tragacanth is a natural polymer that has excellent biological properties such as biodegradability and biocompatibility. Silymarin biochemically has cleansing and antioxidant properties and also has anti-inflammatory effects. The aim of this study is the production of polycaprolactone (PCL) / tragacanth / silymarin nanoscaffold and to investigate the biocompatibility of dental cells on it.

To create a polycaprolactone /tragacanth nanoscaffold and add silymarin to it, acetic acid was used to dissolve 7 percent of the polycaprolactone, 0.7 weight percent of the tragacanth solution, and 0.9 percent of the silymarin solution. The scaffold was then created using an electrospinning machine. Scanning electron microscope (SEM) analysis and FTIR analysis were used to analyze the scaffold's chemical structure and shape, respectively.

The scaffold's correct porosity and the successful loading of silymarin on it were revealed by analyzing the scaffold's morphology and chemical composition. The biocompatibility of the scaffold was investigated 24, 48 and 72 hours after the cultivation of dental cells, and the results showed an increase in cell viability and proper attachment of cells on the scaffold.

The findings of this study demonstrated that silymarin loading on the polycaprolactone/catira scaffold improves dental cell proliferation and survival. This scaffold may therefore be a good choice for tissue engineering.

Vanadium is an essential dietary microelement that plays a key role in the metabolic pathways and has anti-neoplastic effects. In this regard, vanadium oxide 3-methoxy salen complex was produced and its anticancer effects were evaluated.

Schiff bases produced from equivamounts of Vanadyl acetylacetonate [VO(acac)2] in methanol were used to make a vanadium oxide 3-methoxy salen complex. Then, antioxidant property of compound, cell viability and cytotoxicity assay, DNA fragmentation analysis and determination of the apoptosis pathway genes were evaluated.

Result showed that compound with an RC50 value of 126.3 µM, the compound demonstrated considerable free radical scavenging activity. The combination strongly suppressed the viability and proliferation of HeLa and McCoy cell lines in a dose-dependent manner, with IC50 values of 213 µM and 175 µM, respectively. When the viability and cytotoxicity values of the treated cells were compared, it was discovered that the cells had died of apoptosis, which was validated by DNA fragmentation analysis. Capspase 3, Bcl2 antagonist/killer, and Bcl2 associated X protein (Bax) gene expression levels all increased significantly in a quantitative investigation of apoptotic pathway genes, with 2-CT values of 2.36, 2.63, and 3.18, respectively.

In malignant cell lines, lower quantities of the complex caused programmed cell death. This potential of complex can be used in cancer chemoprevention and cancer therapy.

Various factors may result in peripheral nerve injury leading to permanent functional loss. Here, we review the role of calcium and potassium ions in peripheral nerve regeneration and repair. This narrative review of the literature collected its data by searching Google Scholar, PubMed, Elsevier, Springer, Wiley, EBSCO, Scopus, and Science Direct. Publications were searched with no particular time restriction from 1997 to 2021, including all types of study. About 100 relevant papers were found from 1997, 77 of which were selected for this study. Both beta subunits of sodium channels are expressed in peripheral neurons, and drugs that affect those channels may facilitate nerve repair. Riluzole is a sodium/glutamate antagonist which has recently entered clinical trials for spinal cord injury. Riluzole's neuroprotective effects are due to sodium channel blockade and, subsequently, the prevention of Ca2+ overflow. Besides, 4-aminopyridine (4-AP) is a neurotransmitter of potassium channel blockers that increases the rate of functional improvement following peripheral nerve damage by promoting remyelination. Verapamil is a calcium channel blocker that stimulates an endogenous anti-inflammatory response and reduces pro-inflammatory processes, thus causing pain modulation. Inhibition of ROCKs accelerate the regeneration and functional restoration after spinal-cord damage in mammals, and inhibition of the Rho/ROCK pathway has been additionally proven efficacious in animal models of stroke, inflammatory and demyelinating diseases, Alzheimer’s disease, and neuropathic ache. Therefore, the neurite outgrowth of surviving neurons is necessary for nerve regeneration to reinnervate target tissue after nerve damage. One of the critical components of the damage response process is a local translation in axons, and it is critical for the regenerative outcome. On the other hand, it provides new axonal regrowth molecules and induces signals returning to the cell's soma to partake in regenerative pathways and survival.

Tissue engineering is a growing field to repair and replace the defective function of damaged tissue or organ, and today it is proposed as a new treatment to replace conventional transplant methods. For this purpose, polymeric biomaterials (scaffolds) and living cells are used. The purpose of this study is to fabricate polycaprolactan (PCL) nanoscaffold and load silymarin on the nanoscaffold to check the biocompatibility and proliferation ability of pc12 cells on it.

In order to prepare polycaprolactan nanoscaffold and load silymarin on it, 7% polycaprolactan solution (dissolved in acetic acid) was mixed with silymarin solution with a concentration of 0.9% (weight percent), and then the scaffold was prepared using electrospinning device. The morphology of the scaffold was evaluated by scanning electron microscope (SEM) and the chemical structure of the scaffold was evaluated by ATR-FTIR spectroscopy. Toxicity of the scaffold and cell survival of PC12 cells were investigated by MTT test and SEM microscope respectively.

Examining the morphology of the scaffold and its chemical structure showed the appropriate porosity of the scaffold and the successful loading of silymarin on the PCL scaffold. The toxicity of the scaffold was investigated 24, 48 and 72 hours after the cultivation of PC12 cells, and the results showed an increase in cell viability and proper attachment of cells on the scaffold.

The results of this research showed that the loading of silymarin on polycaprolactan scaffold increases the proliferation and survival of PC12 cells. Therefore, this scaffold can be a suitable candidate for nerve tissue engineering.

Tissue engineering is a part of biotechnology that includes the development of biological implants for tissue regeneration to improve tissue or organ function. This study aimed to investigate the effect of cerium oxide nanoparticles on the interactions between adipose tissue stem cells and decellularized sciatic nerve scaffolds in rats.

Rats were anesthetized by injecting a mixture of ketamine (80 mg/kg) and xylazine (10 mg/kg). Sciatic nerve fragments (15 mm) were removed above the three-pronged site in the thigh muscle and decellularized after cleaning the surrounding tissues using the Sandal method. Then, adipose tissue mesenchymal cells were implanted on the scaffold, and the growth and viability of the cells implanted on the scaffold in the presence of cerium oxide nanoparticles were measured by MTT assay.

The results of histological evaluations showed that the scaffolds were completely decellularized and hematoxylin/eosin and Dapi staining confirmed these results. Specialized tissue evaluation by Masson trichrome staining as well as biomechanical analysis showed that collagen and elastin fibers were relatively preserved in the extracellular matrix. Cell viability on the scaffold increased in the presence of nanoparticles.

Cerium oxide nanoparticles increase cell stability, proliferation, and maintenance of adipose tissue mesenchymal cells and may be beneficial in the treatment of peripheral nerve lesions.

Bone tissue engineering aims to heal bone defects that do not repair on their own. To construct an implantable osteogenic implant in tissue engineering, cells and bioactive molecules are seeded onto three-dimensional (3D) biomaterial scaffolds.

The aim of this study was to provide an appropriate micro-environment for hUC-MSCs attachment and proliferation over a biocompatible and non-toxic nanofibrous scaffold in order to differentiate into osteoblast cells.

In this work, a poly(vinylalcohol)/gelatin (PVA/GE) nanocomposite scaffold was prepared using the electrospinning method. Glutaraldehyde/methanol was used as the treating medium to prevent the rapid dissolution of the PVA/GE scaffold in a physiological fluid. The chemical, physical, and morphological characterizations of the prepared scaffold were evaluated by Fourier transform infrared (FT-IR) spectroscopy, thermo-gravimetric analysis (TGA), and scanning electron microscopy (SEM), respectively. In addition, the porosity, swelling ratio, pH changes, degradation profiles, and hydrophobic-hydrophilic nature of the scaffold were investigated. Biocompatibility of the scaffold was evaluated by using MTT assay. Finally, under osteogenic conditions, the differentiation potential of the human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) cultured on the crosslinked scaffold was assessed for 21 days.

The obtained results demonstrated that crosslinking treatment changed water solubility of the PVA/GE scaffold. Also, additional investigations showed good biocompatibility, non-toxic nature, and appropriate degradation rate of the crosslinked scaffold in comparison with the control group.

The results indicated that the PVA/GE crosslinked scaffold with good biocompatibility, non-toxic nature, and appropriate degradation rate can be used for bone tissue engineering aims.

 Tissue engineering may be used to repair, preserve, or improve tissues and organs. In this regard, acellular biological scaffolds are mainly used to reconstruct damaged tissues in regenerative medicine.

 The present study examined the in vitro process of myocytes differentiated from bone marrow mesenchymal stem cells (BM‐MSCs) on the sheep bladder scaffold induced by 5-azacytidine.

 Decellularization was performed using a mixed method (physical and chemical) to prepare scaffolds kept at -20°C. The 5-azacytidine was used to induce BM‐MSCs to myocytes. Moreover, the muscle-specific gene expression (Desmin, α-Actinin, Myo D) was evaluated using the RT-PCR method.

 It was revealed that BM‐MSCs on the scaffold had high proliferation and differentiation potentials. Desmin and α-Actinin gene expression marked the differentiation at the end of the fourth week. Moreover, the results of Masson’s trichrome staining at the end of the second, third and, fourth weeks also indicated that the first differentiation signs emerged at the end of the second week. Furthermore, differentiation reached its maximum level during the fourth week.

 According to the findings, combining physical and chemical methods was the best technique to prepare the bladder scaffold so that the bone marrow mesenchymal stem cells can be differentiated into myocytes on the bladder scaffold affected by 5-azacytidine (5 µmol), and As the induction time increases to day 28, myocyte cells become more developed.

Since bone defects can result in different disabilities, many efforts have been made to bone tissue engineering. In this case, scaffolds play an important role as a key element of tissue engineering in providing three-dimensional structure for cell growth in vitro The aim of the present study was to provide the three-dimensional biological bioscaffold from the bovine femur dense bone and investigate the possibility of its potential for application in tissue engineering as biological 3D ECM bioscaffold via mesenchymal stem cells seeding and differentiation toward bone tissue. For the preparation of bioscaffolds, after cutting bovine femur bone into small pieces, demineralization and decellularization were done. Bioscaffolds biocompatibility was evaluated using an MTT assay. The morphological and cell adhesion characteristics of Bone marrow mesenchymal stem cells (BMSCs) on the bioscaffolds were evaluated using Scanning Electron Microscopy (SEM) technique. Finally, the cells were treated with an osteogenic differentiation medium and then evaluated for differentiation. Histological studies showed that the use of sodium dodecyl sulfate (2.5%) for 8 h eliminated the cells. Radiography and calcium oxalate test confirmed demineralization. MTT assay and SEM studies showed that the obtained bioscaffolds are biocompatible and could provide an optimum three-dimensional environment for cell adhesion and movement. Moreover, the Alizarin red staining showed a higher differentiation rate for BMSCs. In the present study, bone-derived 3D bioscaffold showed an important role in the growth and differentiation of BMSCs, due to the natural characteristics, cell adhesion properties, and potential to enhance differentiation toward bone tissue. It may have the potential for use as bioscaffold as supporting metrics for maintenance, growth in bone tissue engineering.

 Peripheral nervous system injuries are common and currently have no definitive treatment method. Phenytoin is one of the main antiepileptic drugs. Some studies have described a cerebroprotective effect of phenytoin in an established model of global cerebral ischemia.

 In this study, the neuroprotective effects of phenytoin were evaluated on the cultivation and maintenance of Wharton’s jelly stem cells (WJSCs) on acellularized sciatic nerve scaffolds.

 In this study, acellular scaffolds from the rat sciatic nerve were prepared by the sondell method. After extraction of cells of MSCs, flow cytometry analysis was executed. Also, cell differentiation potential was evaluated by placement in osteogenic and adipogenic differentiation media for 21 days. Biocompatibility of the scaffold and cell viability were investigated using the MTT assay. The morphological and cell adhesion characteristics of MSCs on acellular scaffolds were compared using SEM micrographs images. Data were analyzed using the one-way analysis of variance (ANOVA) and Tukey post hoc test by SPSS (version 19.0) software.

 The removal of cells from the scaffold was confirmed by stanning with hematoxylin-eosin, van Gieson's picro-fuchsin, and DAPI. With the aid of flow cytometry analysis and differentiation into bone and fat cells, it was confirmed that extracted cells were mesenchymal stem cells. The results of the MTT assay showed that phenytoin increased cell viability and retention on the scaffold.

 The study indicated that phenytoin improves the viability of cells and provided a good condition for the growth, survival, and attachment of cells to the scaffold when compared to the control group. These results suggest that phenytoin can be considered a new treatment for nerve regeneration and tissue engineering applications.

Polycystic ovary syndrome (PCOS) is associated with higher plasma levels of androgens, LH/FSH ratio and lower activity of aromatase and dopaminergic signaling pathways. In the present study, the effects of L-DOPA and dopamine receptor antagonists were investigated on aromatase (Cyp19) gene expression and LH concentration in PCOS rat model.

Following PCOS induction by estradiol valerate, The PCOS rats received saline, L-DOPA(100mg/kg) or simultaneous injections of sulpride (10mg/kg)/ SCH23390 (1mg/kg)/ L-DOPA (100mg/kg). Five intact estrous rats were used as a control group. Mean serum LH concentration and aromatase relative gene expression was evaluated by radioimmonoassay and real- time-PCR method respectively.

Mean aromatase mRNA levels significantly decreased in the hypothalamus and ovary of PCOS model rats compared to intact ones. Mean serum LH concentration significantly increased in PCOS group in comparison with intact rats. The L-DOPA significantly increased mean hypothalamic and ovarian aromatase gene expression compared to PCOS rats while it significantly declined serum LH concentration compared to PCOS rats. Dopamine receptor antagonists including sulpiride and SCH23390 blocks the stimulatory or inhibitory effects of L-DOPA on hypothalamic aromatase or serum LH levels respectively. But the sulpride and SCH23390 did not inhibit the stimulatory influences of L-DOPA on ovarian aromatase gene expression.

L-DOPA may be involved in the controling of PCOS condition via decreasing LH secretion and increasing the aromatase gene expresion.

Overexpression of EGFR is associated with carcinogenesis in more than 70% of head and neck cancers. Anti-EGFR monoclonal antibodies bind to the extracellular domain of EGFR and block the EGFR downstream signaling pathway, which results in the suppression of the growth of the tumor cells. Escherichia coli is the preferred system for expressing various recombinant proteins, including single chain antibodies, but the formation of inclusion bodies negatively affects the efficacy of this system. Several strategies have been suggested to solve this problem, notably the utilization of molecular chaperones. In this study, we attempted to increase the soluble expression of huscfv antibody via co-expression with the cytoplasmic chaperones. To achieve this purpose, chaperones plasmids pG-KJE8, pGro7, pKjE7, pTf16 and pG-Tf2 encoding cytoplasmic chaperones were co-expressed with the humanized anti-EGFR scFv construct in E. coli. Different temperatures, incubations times, and concentrations of IPTG were used to produce an active antibody with the highest solubility. Results were analyzed by SDS-PAGE. Soluble huscFv was purified by Ni-NTA column and the biologic activity of the recombinant protein was determined by ELISA. The results indicated that the highest concentrations of humanized anti-EGFR scFv were obtained by co-expression of huscFv via chaperone plasmid pG-KJE8 with 0.2 mM concentration of inducer (IPTG), culture temperature of 25 °C, and 4 h incubation time after induction. In conclusion, co-expression with chaperones could be used as an efficient strategy to produce soluble active ScFvs in E. coli.

Managing sports injuries is clinically challenging. Although new techniques can delay musculoskeletal deterioration and promote tissue restoration, they are not widely used. Thus, there is a critical need to promulgate these new methods. In recent years, “tissue engineering” approaches have been developed for improving the regeneration of cartilage by transplanting cells or engineered constructs into injured tissue. The mechanical environment affects the biology of a tissue and is necessary for the development and maintenance of load-bearing tissues. Platelets can be combined with other healing factors as a new therapeutic modality. Platelet-rich plasma (PRP) can be introduced as an autologous blood product that may improve wound healing. In this regard, stem cell therapy that focuses on mesenchymal stem cells (MSCs) has been proposed as a new treatment method in sports medicine. MSCs are multipotent; they have the ability to differentiate into other cells, notably osteoblasts, chondrocytes, adipocytes, myoblasts, and fibroblasts, depending on a variety of factors. In summary, recent advances in tissue regeneration have provided new perspectives for the use of tissue engineering to enhance tissue healing after sports injuries namely the microfracture method, the mechanical stimuli method, PRP therapy, and stem cell therapy

Polycystic ovary syndrome (PCOS) is associated with decreased dopamine release and increased secretion of GnRH, kisspeptin and neuropeptide Y (NPY).  In the present study, the effects of L-dopa and dopamine receptor antagonists were investigated on the expression of KiSS1 and NPY genes in PCOS rats hypothalamus. Following the induction of PCOS by Estradiol Valerate inejction, 25 PCOS rats assigend to 5 groups received saline, L-dopa (100mg/kg), simultaneous injection of SCH23390 (1 mg/kg) and L-dopa (100 mg/kg),  simultaneous injection of sulpride (10 mg/kg) and L-dopa (100 mg/kg), and simultaneous injection of SCH23390 (1 mg/kg), sulpride(10 mg/kg) and L-dopa (100 mg/kg) respectively. Five intact rats received saline. Hypothalamus samples were isolated and frozen. The relative expressions of KiSS1 and NPY were determined by real- time-PCR. Data analysis was done by one- way ANOVA and post hoc Tukey test. The mean relative expression of KiSS1 and NPY significantly increased in PCOS group compared to the healthy rat group (p = 0.009 and p = 0.001, respectively). L-dopa injection caused a significant decrease in the mean relative expression of KiSS1 and NPY compared to the PCOS group (p = 0.001 and p = 0.001 respectively). Simultaneous injections of SCH23390 and sulpride supressed the inhibitory effects of L-dopa on KiSS1 gene expression compared to L-dopa group exerting synergistic effects (p = 0.045).  Dopaminergic signaling pathway may play a role in the decrease of GnRH/LH secretion in PCOS rats by inhibiting the kisspeptin and NPY neuronal activity.

In patients suffer from Polycystic Ovary Syndrome (PCOS), the secretion of the Luteinizing Hormone (LH) increases while adiponectin secretion and dopamine release decreases. Dopamine and adiponectin exert inhibitory effecs on LH secretion. In the present study the effects of L-dopa and dopamine receptor antagonists were investigated on LH secretion and adiponectin gene expression of in PCOS model rats to determine whether dopaminergic pathway might be involved in the decreasing LH via affecting adiponectin.

 Following estradiol valerate- induced PCOS, fifteen PCOS rats were divided into 3 groups including saline receiving group, L-dopa(100 mg/kg) or simultaneous injections of sulpride(10 mg/kg), SCH23390 hydrochloride (1 mg/kg) and L-dopa(100 mg/kg), Five intact rats received saline as negative control group. Blood samples were collected via tail vein. Ovary and hypothalamus were dissected and frozen. Serum concentration of LH and relative gene expression of adiponectin in ovary and hypothalamus were determined by radioimmunoassay and real time-PCR method. 

This study was approved by the Research Committee of University of Mohaghegh Ardabili (Code: 95.125.1). 

 Induction of PCOS caused a significant increase in mean serum concentration of LH and a significant decrease in mean relative gene expression of ovarian and hypothalamic adiponectin compared to control group. L-dopa caused a significant decrease in serum concentration of LH, a significant decrease in hypothalamic gene expression of adiponectin compared to PCOS rats. But it did not significantly increase ovarian adiponectin gene expression in comparison to PCOS rats. Dopamine receptor antagonists inhibit the effects of L-dopa on LH and hypothalamic gene expression of adiponectin.

 Dopaminergic signaling pathway may be involved in decreasing LH secretion via increasing hypothalamic adiponectin gene expression level in PCOS rats.

Ovarian carcinoma is one of the leading causes of cancer-related death among females. K-ras codon 12 mutations are commonly occurring mutations in different types of cancers and leads to resistance against anti-EGFR therapeutics. Hence, determination of mutations in k-ras gene is crucial for predicting response to anti-EGFR therapies. This study aimed to evaluate the prevalence of k-ras gene mutations and CA125 tumor marker in patients with ovarian carcinoma in Tabriz city.

Genomic DNA was extracted from 67 tissues pertained to women with ovarian carcinoma. Mutations in codon 12 and 13 of k-ras gene were analyzed by Nested PCR and RFLP methods. Titer of CA125 tumor marker was determined by ELISA.

Among the 67 patients, 7 patients (10.4%) had mutation in k-ras codon 12 while none of them had mutation in k-ras codon 13. Based on the results, the frequency of various genotypes were 89.55%, 10.44%, and 0%, for GG, GA, and AA alleles, respectively. The p-value for stage I and Grade I tumors were 0.022 and 0.04, respectively, indicating a statistically significant correlation between codon 12 mutation and stage I and Grade I tumors. Furthermore, we found significant correlations among CA125 tumor marker titers and histological grade (p<0.000) and stage (p<0.000). The mean serum CA125 tumor marker levels in malignant carcinomas were 499.84 U/ml.

The results in this study indicated high prevalence of k-ras codon 12 mutations and high titer of CA125 tumor marker in patients with ovarian carcinoma in the study region.

Tissue engineering is a developing multidisciplinary and interdisciplinary field involving the use of bioartificial implants for tissue remodeling with the target for repair and enhancing tissue or organ function. Acellular nerve has been used in experimental models as a peripheral nerve substitute. The purpose of the present study was to evaluate the mechanical and histological characteristics of acellular nerve scaffolds compared to the fresh nerve for application in environmental nerve repair.
This experimental study was conducted in Ferdowsi University of Mashhad Regeneration Research Laboratory, Mashhad, Iran, from May 2017 to October 2018. In this study for preparing the scaffold. The rats were sacrificed by intraperitoneal anesthesia with 10 % Chloral Hydrate solution. Then sciatic nerve fragments of the rats were removed above the nerve branching site and after cleansing of the tissues were decellularized by Sondell method, briefly nerves were treated with a series of detergent baths consisting of distilled water for 8 h, Triton X-100 for 12 h, and sodium deoxycholate for 24 hours according to the Sondell protocol. All acellularization steps were performed at room temperature. Then decellularized scaffolds were evaluated histologically and mechanically.
The results of tissue evaluations showed that decellularization of scaffolds were done completely, this was demonstrated by hematoxylin and eosin staining and DAPI staining. Also the specialized tissue evaluations by picro-fuchsin staining and evaluation the scaffolds by scanning electron microscopy (SEM) micrographs showed that the collagen and elastin strands are relatively preserved in the extracellular matrix in comparison with control groups. As well as mechanical examination of scaffolds in tensile test showed that extracellular matrix of scaffolds was relatively preserved the main components of tissue compared to control group and scaffolds have good mechanical resistance quality for use in tissue engineering.
The results of the present study showed that decellularized scaffolds that prepared with Sondell decellularization method by preserving the main components of the tissue can be a good platform for investigating cellular behaviors.

In this study, layer-by-layer deposition method by sodium alginate polymer and carbon nanoparticles were used for modification of glassy carbon electrode surface. The modified electrode surface was studied by using scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The SEM images has been utilized to estimate the size of carbon nanoparticles on electrode surface which is approximately 47-57 nm. Gallic acid and ascorbic acid the antioxidant compounds naturally present in foods were determined with modified glassy carbon electrode using differential pulse voltammetry technique. The effect of. scan rate and pH parameters were optimized. In optimal conditions, using differential pulse voltammetry, the linear range for the concentration of gallic acid and ascorbic acid are 0.1-100.0 and 1.0-1000.0 µM and the limit of detection equal to 0.057 and 0.368 µM is estimated respectively. Finally, Gallic acid was determined in some herbs such as marjoram, thyme and mallow.

Tumor-secreted vascular endothelial growth factors binding to their receptors on endothelial cells surface play as the key roles in vascular permeability and tumor angiogenesis. In this study, VEGF antagonistic peptide was designed in order to interfere with the binding VEGF to VEGFRs and inactivates their downstream signaling pathways and hence suppresses angiogenesis with high efficiency. In this study, 4T1 tumor allograft was prepared as a murine breast cancer model in BALB/c mice. After subcutaneous transplantation of tumor fragments into the animals, daily intraperitoneal injection of VGB4 at the different doses of (0.25, 1, 2.5, 5 and 10 mg/kg) was performed for two weeks. Anti-tumor potential of different doses of VGB4 was statistically examined in compare to control. VGB4 peptide reduced tumor growth dose-dependently and that the increase in the concentration from 5 mg/kg to 10 mg/kg had no significant inhibitory effect on tumor growth. Therefore, 5 mg/kg is the best effective dose of VGB4 in the prevention of growth rate of tumors. VGB4 peptide has a significant inhibitory effect on 4T1murine mammary carcinoma tumor growth. Antitumor activity of VGB4 indicates that VGB4 could be considered as an adequate candidate for cancer therapy

CagA, a 120- to 145-kD Helicobacter pylori (H. pylori) protein, increases the risk of atrophic gastritis and gastric cancer (GC). The pathogenic CagA contains a highly polymorphic Glu-Pro-Ile-Tyr-Ala (EPIYA) repeat region in the C-terminal portion of the protein. The aim of this study was to determine the number and type of EPIYA (glutamine–proline–isoleucine–tyrosine–alanine) motifs within the cagA 3' variable region among H. pylori isolates and their association with GC. The total number of 206 individuals (170 controls and 36 patients with GC) referring to the endoscopy units of several cities in Iran (2008-2014) were recruited. The polymerase chain reaction (PCR) amplification was performed to determine the presence of H. pylori, cagA gene, and EPIYA motifs. In this study, 81 (47.6%) and 22 (61.1%) of the controls and patients with GC were carriers of cagA+ strains, respectively. The overall frequency of EPIYA-AB, EPIYA-ABC, EPIYA-ABCC, and EPIYA-ABCCC in patients with GC were 0%, 59%, 9%, and 31.8%, respectively. The results of regression analysis showed a significant association between EPIYA-ABCCC motif and the risk of GC [OR = 9.99 (95%CI: 2.17-45.88), p = 0.003]. We propose that patients infected with H. pylori strains harboring more than one CagA EPIYA C motif (EPIYA-ABCCC) have an increased risk of GC, thus, testing for this genotype may have clinical usefulness.

Gastric cancer (GC) is the second leading cause of cancer-related deaths worldwide. It has been proposed that the specific genotypes of Helicobacter pylori (H. pylori) are the causative agents in the development of gastroduodenal diseases, such as chronic atrophic gastritis, peptic ulcerations, and GC. However, disease progression to GC occurs in only a small proportion of infected patients. Recently, we identified a novel polymorphic site in the 3ʹ-end region of H. pylori vacA gene. The vacA c1 genotype increased the risk of GC. This association was independent of and larger than the associations of the m-, i-, and d-type of vacA or cagA status with GC. Therefore, treatment of H. pylori infection may be an effective way to prevent GC. Expression of cytokines and their associations with inflammatory responses has been shown. Several cytokine polymorphisms, such as IL-1B, IL-8, IL-10, and TNF-α have been considered as risk factors for GC. It has been shown that the interaction of bacterial genotypes and host factors plays an essential role in developing GC. Several altered molecular pathways are involved in the pathogenesis of GC. Micro-RNAs are small, non-coding RNAs of 18-25 nucleotides in length that regulate the expression of target mRNAs. Expression pattern of cancer cells is different compared with the normal cells. Micro-RNAs plays a critical role in apoptosis and classified in two groups: pro- and anti-apoptotic agents. Recent studies have confirmed the oncogenic or tumor suppression role of micro-RNAs in cancer cells. They play a significant role in the GC cell physiology and tumor progression, by translational suppression of target genes. These small RNAs have therefore emerged as a new type of GC biomarker with immeasurable clinical potential. Generally, a variety of micro-RNAs involved in different stages of cancer, including tumorigenesis, angiogenesis, and metastasis. Considering to this issue more than 50% of cancers can be cured, if they were diagnosed in the early stages. Hence, identifying the biomarkers of GC could play an important role in prevention, early diagnosis and rapid treatment of patients. In this review article, we have reviewed the latest findings about bacterial and tissue biomarkers of GC