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      • Open Access Article

        1 - The evaluation of sodium molybdate effect on liver fibrosis in a rat model of bile duct ligation
        مهسا Ale Ebrahim, اکرم Eidi, . P. Mortazavi, S.M Tavangar, داریوش Minai Tehrani,
        The accumulation of hydrophobic bile acids in bile duct ligation (BDL) animal model, plays apivotal role in the induction of hepatic fibrosis. Cholestatic liver fibrosis, characterized byexcessive accumulation of extracellular matrix (ECM) proteins, is associated with b More
        The accumulation of hydrophobic bile acids in bile duct ligation (BDL) animal model, plays apivotal role in the induction of hepatic fibrosis. Cholestatic liver fibrosis, characterized byexcessive accumulation of extracellular matrix (ECM) proteins, is associated with bile acidinducedoxidative stress and lipid peroxidation. Molybdenum is an essential trace element whichacts as a cofactor in many detoxification system enzymes. The results of our previous studysuggested that sodium molybdate could be used as a hepatoprotective agent against toxicitycaused by carbon tetrachloride in rats .The aim of the present study was to evaluate thetherapeutic or the anti-hepatofibrotic effects of sodium molybdate in a bile duct ligation (BDL)-induced cholestatic fibrosis model in rats .After BDL, rats were given sodium molybdate (0.05or 0.1 or 0.2 g/kg) or urosodeoxycholic acid (UDCA, 25 mg/kg) orally for 45 consecutive days(once per day). BDL markedly induced the accumulation of collagen, as well as infiltration ofinflammatory cells, hepatocyte necrosis and bile duct hyperplasia, as determined by Masson’strichrome staining. These alterations were significantly attenuated by sodium molybsdateadministration (0.1 and 0.2 g/kg). Simultaneously treatment of sodium molybdate may inhibitthe liver fibrosis in a BDL model of cholestatic rats. Our data suggest that sodium molybdatemay exert its antifibrotic effects via inhibition of ECM proteins. Manuscript profile
      • Open Access Article

        2 - Effect of folic acid in cholestatic hepatic fibrosis induced by bile duct ligation Model in rat
        Z. Mohammadian, A. Eidi, P. Mortazavid, SM. Tavangar, A. Asghari,
        Cholestasis is a liver disease that, if untreated and not prevented, will cause hepatic fibrosis andcirrhosis, and eventually death. As a result of bile duct ligation (BDL), toxic bile acidsaccumulate in liver. Accumulation of these toxins and subsequent events, such as More
        Cholestasis is a liver disease that, if untreated and not prevented, will cause hepatic fibrosis andcirrhosis, and eventually death. As a result of bile duct ligation (BDL), toxic bile acidsaccumulate in liver. Accumulation of these toxins and subsequent events, such as oxidativestress and inflammatory response leads to cell death and hepatic fibrosis. The liver is the mainorgan for folate storage and metabolism and folate deficiency is a common occurrence in manyliver diseases. The present study investigated the protective effect of folic acid in experimentalhepatic fibrosis. 81 male Wistar rats were classified into the nine groups؛ Control, Shamoperatedcontrol, Folic acid, Bile duct-ligated (BDL) control, and BDL+ folic acid groups. Folicacid treated groups were given oral folic acid (1, 5 and 10 mg/kg b.w) for 28 days. The severityof hepatic injury was determined by measures biochemical indicators like’s activities of AST,ALT, ALP, concentrations of bilirubin and albumin in the serum and activities of superoxidedismutase in the hepatic samples. To assess histopathological features of cholestasis (bile ducthyperplasia, fibrosis, necrosis and inflammatory cell infiltration), Masson’s trichrome stainingwas performed. In BDL rats treated with folic acid, hepatic fibrosis was significantlyameliorated and the serum and hepatic biochemical variation induced by BDL were moderated.This study suggests that folic acid has a protective effect in liver. Folic acid reduced oxidativestress and inflammatory response and thus prevented liver fibrotic changes. Manuscript profile
      • Open Access Article

        3 - بررسی اثر MTBE (متیل ترشیاری بوتیل اتر) روی ساختار هموگلوبین خون موش نر نژاد ویستار
        , M Tashakori , A Eidi
        مطالعه تأثیر آلاینده­های زیستی با مولکول­های پروتئینی از سال­های گذشته مورد توجه بوده است. از جمله آلاینده‌هایی که اخیراً مورد توجه محققان علوم زیستی قرار گرفته استMTBE (متیل ترشیاری بوتیل اتر) می­باشد. این ماده سبب افزایش کارایی بنزین می‌گردد. MTBE می‌ت More
        مطالعه تأثیر آلاینده­های زیستی با مولکول­های پروتئینی از سال­های گذشته مورد توجه بوده است. از جمله آلاینده‌هایی که اخیراً مورد توجه محققان علوم زیستی قرار گرفته استMTBE (متیل ترشیاری بوتیل اتر) می­باشد. این ماده سبب افزایش کارایی بنزین می‌گردد. MTBE می‌تواند در طبیعت حضور داشته و به جریان خون وارد شود.با توجه به شباهت ساختاری هموگلوبین انسان و موش در این مطالعه تاثیر MTBE بر روی هموگلوبین موش به شکل invivo مورد بررسی قرار گرفته است. 3 غلظت از MTBE (200، 400 و 800 میلی‌گرم بر کیلوگرم وزن بدن) به موش­های تحت تیمار به صورت خوراکی منتقل شد. مطالعات اسپکتروسکوپی UV در منطقه 280 نانومتر حاکی از فشردگی و پیچیده‌تر شدن بیشتر هموگلوبین­های موش­های تحت تیمار با MTBE نسبت به نمونه نرمال است. مطالعات اسپکتروسکوپی CD جهت بررسی ساختار دوم هموگلوبین تحت تاثیر MTBE انجام گردید. مطالعه حاضر تغییرات قابل ملاحظه ای در ساختار دوم را اثبات نمی کند. با توجه به بررسی‌های انجام شده میتوان فشردگی بیشتر ساختار هموگلوبین در حضور غلظت‌های مختلف MTBE را عنوان کرد. Manuscript profile
      • Open Access Article

        4 - بررسی اثر محافظتی عصاره دانه خرفه(Portulaca oleraceae) بر آسیب بافت بیضه القا شده توسط کلرید کادمیوم در موش‌های صحرایی نر بالغ نژاد ویستار
        Ghahreman, E قهرمان , A Eidi , P Mortazavi , S. Oryan
        خرفه یک علف هرز با گستره پراکنده­ای است و در طب سنتی در بسیاری از کشورها به عنوان داروی مدر، ضد سرطان، ضد عفونی کننده و ضد اسپاسم استفاده می­شود. مطالعه حاضر با هدف بررسی نقش محافظتی عصاره اتانولی خرفه بر آسیب بافت بیضه­ای ناشی از تیمار کلرید کادمیوم با اندا More
        خرفه یک علف هرز با گستره پراکنده­ای است و در طب سنتی در بسیاری از کشورها به عنوان داروی مدر، ضد سرطان، ضد عفونی کننده و ضد اسپاسم استفاده می­شود. مطالعه حاضر با هدف بررسی نقش محافظتی عصاره اتانولی خرفه بر آسیب بافت بیضه­ای ناشی از تیمار کلرید کادمیوم با اندازه­گیری آنزیم­های آنتی­اکسیدانی در موش های صحرایی نر بالغ نژاد ویستار انجام شد.تعداد 60 سر موش­های صحرایی نر به طور تصادفی به 10 گروه تقسیم شدند: گروه کنترل سالم، گروه­های دریافت کننده عصاره خرفه (50، 100، 200 و 400 میلی­گرم بر کیلوگرم وزن بدن، روزانه به طور خوراکی)، گروه کنترل آسیب بیضه­ای (دریافت کلرید کادمیوم به میزان 3 میلی­گرم بر کیلوگرم وزن بدن، روزانه به طور خوراکی)، گروه­های دریافت کننده عصاره خرفه (50، 100، 200 و 400 میلی­گرم بر کیلوگرم وزن بدن، روزانه به طور خوراکی) همراه با کلرید کادمیوم. بعد از 28 روز تیمار، موش­ها به آسانی کشته شدند و بیضه­های آن­ها خارج گردید و فعالیت آنزیم­های آنتی­اکسیدانی و میزان پراکسیداسیون لیپیدی بافت بیضه موش­ها اندازه­گیری شد. کلرید کادمیوم باعث کاهش معنی­داری در میزان فعالیت آنزیم­های گلوتاتیون پراکسیداز، سوپراکسید دیسموتاز، کاتالاز و افزایش سطح مالون دی آلدئید بیضه شد (001/0 p<). تیمار عصاره خرفه در دوزهای 200 و 400 میلی­گرم بر کیلوگرم وزن بدن باعث افزایش معنی­داری در میزان فعالیت آنزیم­های گلوتاتیون پراکسیداز، سوپراکسید دیسموتاز، کاتالاز و افزایش سطح مالون دی آلدئید گردید (001/0 p<). مطالعه حاضر نشان داد عصاره خرفه احتمالا از طریق افزایش فعالیت آنتی­اکسیدانی، بیضه موش­های صحرایی را از آسیب ناشی از کلرید کادمیوم محافظت می­کند. Manuscript profile
      • Open Access Article

        5 - Evaluation of the effect of aflatoxin B1 on neuronal differentiation and hippocampal development in rats
        سارا Alhoei Nazari Nasim Hayati Roodbari , K Parivar , A. Eidi
        Aflatoxin B1 has harmful effects on the nervous-cerebral system. Therefore, in this study the effects of Aflatoxin B1 on the development of the hippocampus of neonatal rats were investigated. After the preparation of Aflatoxin B1, 18 pregnant female Wistar rats with an More
        Aflatoxin B1 has harmful effects on the nervous-cerebral system. Therefore, in this study the effects of Aflatoxin B1 on the development of the hippocampus of neonatal rats were investigated. After the preparation of Aflatoxin B1, 18 pregnant female Wistar rats with an average weight of 85±10 g were used. Animals were divided into three groups: sham (receiving sesame oil as a solvent of Aflatoxin B1), Aflatoxin B1 and Healthy control. According to the results of immunohistochemical studies, Aflatoxin B1 treated groups showed a statistically significant decrease in Ki-67 and NeuN expression compared to the control group (P <0.01). While the expression level of the GFAP in comparison with the control group had a statistically significant increase (P <0.01). On the other hand, a significant decrease in the expression of NeuN and Ki-67 proteins and an increase in the expression of GFAP were observed, which were confirmed by observations from fluorescent immunohistochemical imaging. Aflatoxin B1 disrupts neuronal differentiation and increases brain damage by disrupting the activity and expression of vital proteins in the hippocampus, which was demonstrated by a sharp decrease in NeuN and an increase in GFAP. Manuscript profile
      • Open Access Article

        6 - Microfluidics and improving the cell culture channel: evaluation of spermatogonial stem cells using microfluidic chips
        S. Naeemi A.M. Kajbafzadeh, A. Eidi, R. Khanbabaee, H. Sadri-Ardekani
        The main purpose of the present study was to investigate the treatment of male infertility, because infertility treatment is important in the group of cancer patients treated with gonadotoxic drugs. The main approach of the mentioned study is to compare two different gr More
        The main purpose of the present study was to investigate the treatment of male infertility, because infertility treatment is important in the group of cancer patients treated with gonadotoxic drugs. The main approach of the mentioned study is to compare two different groups of spermatogonia stem cell culture methods and to evaluate the efficiency of differentiation and proliferation of these group of cells. Successful transplantation of spermatogonia stem cells (SSCs) in laboratory studies requires a suitable microenvironment for proliferation and differentiation of these cells. The natural extracellular matrix provides a good environment for stem cell culture. In the present study, themain purpose was to evaluate the ability of spermatogonial stem cells proliferation and differentiationvia the utilizing the microfluidic device (ex vivo). On the other hand, in the present study, we compared the obtained resultswith culture conditions in conventional culture plates (in vitro) to compare the SSCs proliferation and differentiation ability. In in-vitro culture method first spermatogonia stem cells from neonatal mice were isolated, then the resulted cells were seeded in culture plates on a scaffold consisting of hyaluronic acid, chitosan and decellularized testicular tissue, furthermore, in ex-vivo study the extracted spermatogonial stem cells were cultured in the microfluidic system without a scaffold. In ex vivo study, spermatogonial stem cells were extracted from neonatal male NMRI mice. The extracted cells were transferred to a microfluidic chip that was designed without an external pump, thereafter, the culture process was evaluated by IHC evaluation after one-month culture. In examined samples, cell attachment to the seminiferous tubules, DAPI staining and immunohistochemistry were evaluated. The results of immunohistochemical studies showed a significant increase in the expression of PLZF and TEKT1 markers in ex-vivo models. Finally, the results revealed that the ability of spermatogonia stem cells to induce spermatogenesis and production of haploid cells under testicular tissue culture in the microfluidic system is much more significant than conventional culture conditions in laboratory plates for these cells. Manuscript profile
      • Open Access Article

        7 - The effect of PM2/5 exposure on neonatal rat cerebral tissue
        مریم Momayez sefat, سعید Motesaddi Zarandi, P. Mortazavi, اکرم Eidi
        The present study, evaluated the effect of PM2/5exposure on the cerebral tissue of neonatal rats. 24 female Wistar albino rats after mating and pregnancy, classified into three groups including "control", "Exposure1", and "Exposure2".  The Control group used air wi More
        The present study, evaluated the effect of PM2/5exposure on the cerebral tissue of neonatal rats. 24 female Wistar albino rats after mating and pregnancy, classified into three groups including "control", "Exposure1", and "Exposure2".  The Control group used air with a clean standard condition, and the other two groups were exposed to gaseous pollutants and gaseous pollutants plus PM2/5 respectively for 40 days. The cerebral tissues were removed. Gene expression analysis was conducted for S100 gene using quantitative Real-Time PCR and also methylation-sensitive high-resolution melting (MS-HRM) assay was performed for the control, Exposure1, and Exposure2 groups. The amount of malondialdehyde (MDA) involved in the oxidative stress (OS) process was assessed for all groups. The results showed the significant expression of S100 gene in Exposure1 and Exposure2 groups compared with the control group. MS-HRM assays detected only hypermethylation of Exposure 1 in comparison with control group. Based on the analysis of the involved enzymes in OS, malondialdehyde increased in the Exposure1 and Exposure2 groups. These findings may help provide insight to identifying therapeutic targets for reducing human cerebral disorders caused by exposure to PM2/5 or other air pollutants. Manuscript profile
      • Open Access Article

        8 - Investigation of the effect of Deferoxamine preconditioning on VEGF, ANGP1, and TFGβ1 gene expression in diabetic adipose derived stem cells (ADSCs)
        راضیه Tajali اکرم Eidi حسین Ahmadi Tafti عبدالرضا Pazouki A.M Sharifi
        Adipose tissue-derived stem cells (ADSCs) have been considered a promising treatment for diabetic wound repair. However, the effectiveness of autologous ADSC-derived therapy for diabetic patients needs to be improved. The aim of this study was to investigate the effect More
        Adipose tissue-derived stem cells (ADSCs) have been considered a promising treatment for diabetic wound repair. However, the effectiveness of autologous ADSC-derived therapy for diabetic patients needs to be improved. The aim of this study was to investigate the effect of pretreatment with deferoxamine on the expression of the angiogenic genes in diabetic ADSCs preconditioned with deferoxamine. In this experimental study, abdominal adipose tissue was taken from three patients with type 2 diabetes and three healthy individuals, and stem cells derived from adipose tissue were extracted by the enzymatic method. Diabetic ADSCs were treated with 75, 150, and 300 μM deferoxamine concentrations for 24 and 48 hours. Then, the cell survival rate was evaluated using the WST1 test and the expression level of VEGF, ANGP1, and TFGβ1 genes in normal, diabetic, and diabetic ADSCs treated with deferoxamine using the Real-time PCR technique. The data were analyzed using Prism statistical software. Our results showed that the expression levels of VEGF, ANGP1 and TGFβ1 genes in diabetic samples were significantly decreased compared to the normal group (P<0.05). However, the expression level of all three genes after treating the cells with concentrations of 150 and 300 μM deferoxamine for 24 hours was significantly increased compared to the untreated diabetic group (P<0.05). Our results showed that deferoxamine significantly increases the expression of VEGF, ANGP1, and TGFβ1 in diabetic ADSCs and increases their angiogenic capacity. Manuscript profile