7 results on '"Davarpanah E"'
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2. Simulation of Gas Pipelines Leakage Using Modified Characteristics Method
- Author
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Nourollahi, E., primary, Rahimi, A. B., additional, and Davarpanah, E., additional
- Published
- 2012
- Full Text
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3. PUF Proteins as Critical RNA-Binding Proteins in TriTryp Parasites: A Review Article.
- Author
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Taheri T, Davarpanah E, Samimi-Rad K, and Seyed N
- Abstract
In eukaryotes, translation is a fundamental step in the long pathway of protein synthesis within the cell. In this process, several proteins and factors have involved directly or indirectly, individually or in association with other elements to contact mRNA. For perfect translation, many essential modifications should be done, such as cis-splicing to remove introns and two main events for capping and poly A polymerization in 5' and 3' end of mRNA, respectively. Gene expression is then regulated at both translation and stability of the target mRNA molecule levels. Pumilio/FBFs (PUFs) are the main group of RNA-binding proteins which bind to the 3'-UTR of target RNA and thereby regulate the fate, stability and subcellular localization of mRNAs and adjust the translated protein level. PUF proteins have been found both in nucleus where that bind to precursor mRNA, for processing and maturation of rRNA, and in cytoplasm where that bind to mRNA, stall the ribosomes, suppress the translation and localization of the mRNA. They can regulate the expression of mRNAs through activation or suppression of translation. Therefore, these proteins have recently garnered much attention as new generation of therapeutic targets against diseases such as cancer and neurological disorders. In comparison to other eukaryotes, trypanosomatids have a high number of PUF proteins, which function not only as gene expression regulatory factors but also in several biological processes such as differentiation and life-cycle progression of the cells. Here, we review the molecular and biological roles of known PUF proteins in TriTryp parasites ( Trypanosome brucei , T. cruzi and Leishmania ) beside some other parasites., Competing Interests: Conflict of Interest The authors declare that there is no conflict of interests., (Copyright © 2024 Taheri et al. Published by Tehran University of Medical Sciences.)
- Published
- 2024
- Full Text
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4. The outcome of arginase activity inhibition in BALB/c mice hosting Leishmania tropica.
- Author
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Nahidi S, Gholami E, Taslimi Y, Habibzadeh S, Seyed N, Davarpanah E, Ghanadan A, Rafati S, and Taheri T
- Subjects
- Animals, Antigens, Protozoan immunology, Arginine administration & dosage, Arginine analogs & derivatives, Female, Leishmania tropica drug effects, Leishmaniasis, Cutaneous parasitology, Leishmaniasis, Cutaneous pathology, Mice, Mice, Inbred BALB C, Nitric Oxide metabolism, Parasite Load, Real-Time Polymerase Chain Reaction, Arginase antagonists & inhibitors, Leishmania tropica physiology
- Abstract
Two species of Leishmania (L), L. tropica and L. major, are among the main causative agents of cutaneous leishmaniasis. Arginase (ARG) is an essential enzyme for cell growth, thus an attractive drug target. In this study, we tried to survey the inhibitory impact of ARG by nor-NOHA (N-ω-hydroxy-L-nor-arginine) on in vivo infection caused by L. tropica. BALB/c mice were inoculated with L. tropica
EGFP-LUC (Ltrop) or L. majorEGFP-LUC (Lmj) and then were treated by nor-NOHA. ARG inhibitor only indicated a delay in generation of a cutaneous lesion in inoculated footpad with nor-NOHA-Ltrop and nor-NOHA-Lmj. ARG activity has been significantly reduced in nor-NOHA-Ltrop group. In this group, ARG activity inhibition correlated with increased levels of nitric oxide (NO). In both inoculated mice with Ltrop or Lmj, parasite load showed a significant decrease at later steps during the CL course post-treatment. In vivo bioluminescence intensity did not show any ARG's inhibitory effect on treated-Ltrop. The findings verified that the ARG activity may partially control the L. tropica infection in BALB/c mice through reduction of parasite proliferation and parasite killing through NO generation. This effect is dose-dependent., (© 2019 John Wiley & Sons Ltd.)- Published
- 2020
- Full Text
- View/download PDF
5. Circulating concentration of interleukin-37 in Helicobacter pylori-infected patients with peptic ulcer: Its association with IL-37 related gene polymorphisms and bacterial virulence factor CagA.
- Author
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Davarpanah E, Jafarzadeh A, Nemati M, Bassagh A, Abasi MH, Khosravimashizi A, Kazemipoor N, Ghazizadeh M, and Mirzaee M
- Subjects
- Adult, Antibodies, Bacterial blood, Female, Gene Frequency genetics, Helicobacter Infections pathology, Helicobacter pylori pathogenicity, Humans, Immunoglobulin A blood, Immunoglobulin G blood, Male, Peptic Ulcer microbiology, Peptic Ulcer pathology, Polymorphism, Single Nucleotide genetics, Antigens, Bacterial immunology, Bacterial Proteins immunology, Helicobacter Infections blood, Interleukin-1 blood, Interleukin-1 genetics, Peptic Ulcer blood
- Abstract
The immunopathologic responses play a major role in the development of H. pylori (HP)-related gastrointestinal diseases. IL-37 is an anti-inflammatory cytokine with potent suppressive effects on innate and adaptive immune responses. Here, we investigated the IL-37 levels and two single nucleotide polymorphisms (SNPs) including rs3811047 and rs2723176 in IL-37 gene in HP-infected peptic ulcer (PU) patients to identify any relationship. Three groups, including 100 HP-infected PU patients, 100 HP-infected asymptomatic (AS) subjects and 100 non-infected healthy control (NHC) subjects were enrolled to study. Serum IL-37 levels and the genotyping at rs3811047 and rs2723176 were determined using ELISA and SSP-PCR methods, respectively. Significantly higher IL-37 levels were observed in PU patients compared with AS and NHC groups (P < 0.0001). In both PU and AS groups, the CagA
+ HP-infected participants displayed higher IL-37 levels compared with those infected with CagA- strains (P < 0.0001). There were significant differences between PU, AS and NHC groups regarding the distribution of genotypes and alleles at rs3811047 and rs2723176 SNPs. The genotype GG and allele G at IL-37 rs3811047 SNP, and the genotype CC and allele C at IL-37 rs2723176 SNP more frequently expressed in PU patients than total healthy subjects (AS + NHC groups) and were associated with an increased risk of PU development (genotype GG: RR = 3.08, P < 0.009; allele G: RR = 2.94, P < 0.01; genotype CC: RR = 5, P < 0.01; and allele C: RR = 5.0, P < 0.02, respectively). The PU patients with allele A at IL-37 rs2723176 SNP expressed higher amounts of IL-37 compared with patients carried allele C at the same position (P < 0.05). In AS carriers and NHC individuals, the IL-37 levels in subjects carried genotype AA or allele A at IL-37 rs2723176 SNP were higher than those carried genotype CC or allele C at the same location (P < 0.01 and P < 0.02 for AS group; P < 0.0001 and P < 0.001 for NHC subjects, respectively). The increased IL-37 levels may be considered as a valuable marker of PU development in HP-infected individuals. The SNPs rs3811047 and rs2723176 were associated with PU development. The CagA status of HP and IL-37 rs2723176 SNP may affect the IL-37 levels., (Copyright © 2019 Elsevier Ltd. All rights reserved.)- Published
- 2020
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6. Lactococcus lactis expressing sand fly PpSP15 salivary protein confers long-term protection against Leishmania major in BALB/c mice.
- Author
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Davarpanah E, Seyed N, Bahrami F, Rafati S, Safaralizadeh R, and Taheri T
- Subjects
- Animals, Female, Insect Proteins immunology, Lactococcus lactis genetics, Leishmaniasis, Cutaneous transmission, Mice, Inbred BALB C, Phlebotomus genetics, Recombinant Proteins immunology, Salivary Proteins and Peptides genetics, Lactococcus lactis metabolism, Leishmania major, Salivary Proteins and Peptides metabolism
- Abstract
Cutaneous leishmaniasisis a vector-borne disease transmitted by Leishmania infected sand flies. PpSP15 is an immunogenic salivary protein from the sand fly Phlebotomus papatasi. Immunization with PpSP15 was shown to protect against Leishmania major infection. Lactococcus lactis is a safe non-pathogenic delivery system that can be used to express antigens in situ. Here, the codon-optimized Ppsp15-egfp gene was cloned in pNZ8121 vector downstream of the PrtP signal peptide that is responsible for expression and secretion of the protein on the cell wall. Expression of PpSP15-EGFP recombinant protein was monitored by immunofluorescence, flow cytometry and Western blot. Also, expression of protein in cell wall compartment was verified using whole cell ELISA, Western blot and TEM microscopy. BALB/c mice were immunized three times with recombinant L. lactis-PpSP15-EGFPcwa, and the immune responses were followed up, at short-term (ST, 2 weeks) and long-term (LT, 6 months) periods. BALB/c mice were challenged with L. major plus P. papatasi Salivary Gland Homogenate. Evaluation of footpad thickness and parasite burden showed a delay in the development of the disease and significantly decreased parasite numbers in PpSP15 vaccinated animals as compared to control group. In addition, immunized mice showed Th1 type immune responses. Importantly, immunization with L. lactis-PpSP15-EGFPcwa stimulated the long-term memory in mice which lasted for at least 6 months., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2020
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- View/download PDF
7. Are gold nanoparticles and microplastics mixtures more toxic to the marine microalgae Tetraselmis chuii than the substances individually?
- Author
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Davarpanah E and Guilhermino L
- Subjects
- Biological Assay, Models, Theoretical, Chlorophyta drug effects, Gold toxicity, Metal Nanoparticles toxicity, Microalgae drug effects, Plastics toxicity, Water Pollutants, Chemical toxicity
- Abstract
The widespread use of microplastics and nanomaterials resulting in environmental contamination is of high concern. Microplastics have been found to modulate the toxicity of other environmental contaminants. Thus, the hypothesis that microplastics increase the toxicity of gold nanoparticles to the marine microalgae Tetraselmis chuii was tested. In a laboratory bioassay, T. chuii cultures were exposed for 96 h to ∼5 nm diameter gold nanoparticles (AuNP) and to virgin 1-5 μm diameter microplastics (MP), alone and in mixture. The treatments were: control; citrate-control; AuNP alone (0.1, 0.3 and 3 mg/L); MP alone (0.3, 0.9 and 4 mg/L) and mixture of the two substances in three different concentrations (0.1 mg/L AuNP + 0.3 mg/L MP; 0.3 mg/L AuNP + 0.9 mg/L MP; 3 mg/l AuNP + 4 mg/L MP). The effect criterion was the inhibition of the average specific growth rate. AuNP alone and MP alone did not cause significant decrease of T. chui average specific growth rate up to 3 mg/L and 4 mg/L, respectively. The mixture containing 3 mg/L AuNP + 4 mg/L MP significantly reduced the average specific growth rate of the microalgae. Therefore, this mixture was more toxic to T. chuii than its components individually. Overall, the results of the present study indicated that the MP and AuNP tested have a relatively low toxicity to T. chuii, but the toxicity increases when they are in mixtures containing high concentrations of both substances. These proof-of-concept findings stress the need of more research on the toxicity of mixtures containing microplastics and nanomaterials., (Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2019
- Full Text
- View/download PDF
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