mahani
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BackgroundChronic usage of morphine elicits the production of inflammatory factors by glial cells andinduces neuroinflammation. Ginger (Zingiber Officinale Roscoe) is a medicinal herb that has antiinflammatory properties. It has been reported that ginger shows anti-addictive effects against chronic usageof morphine; however, its influence on morphine-induced neuroinflammation has not yet been clarified.MethodsMorphine (12 mg/kg) was administrated intraperitoneally for 6 consecutive days. To evaluate theeffect of ginger on morphine-induced neuroinflammation, ginger extract (100 mg/kg) was given orally 30minutes before morphine. Glial fibrillary acidic protein (GFAP) and P38 mitogen-activated protein kinase(p38 MAPK) levels were assayed by immunoblotting in the rat nucleus accumbens (NAcc).FindingsThe injection of chronic morphine increased the levels of proteins involved in neuroinflammation(p38 MAPK and GFAP) in NAcc. Furthermore, the levels of p38 MAPK and GFAP significantly returned tothe control levels by ginger extract.ConclusionThe results suggest that the ginger extract can reduce morphine-induced neuroinflammation in NAcc.Keywords: Morphine, ginger, p38 Mitogen-Activated Protein Kinases, Glial fibrillary acidic protein, Nucleus Accumbens, Rats
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Objective(s)The protective effect of regular running on sleep deprivation (SD)-induced cognitive impairment has been revealed. In this study, we focused on the effects of regular exercise, sleep deprivation and both of them together on the microRNA-1b (miR-1b) expression and their relation to the behavioral parameters and brain-derived neurotrophic factor (BDNF) expression.Materials and MethodsWe used ovariectomized (OVX) female rats. The exercise program was mild-moderate treadmill training for 4 weeks. 72 hr SD was achieved using the multiple platform method and the spatial learning and memory parameters have been evaluated by the Morris water maze (MWM) test. The levels of studied genes were quantified by real-time PCR.ResultsSD down-regulated pri-miR-1b, miR-1b (P˂0.05), and BDNF mRNA (P˂0.01) in the hippocampus. Furthermore, female rats under exercise conditions showed significant up-regulation of the miR-1b and BDNF mRNA (P˂0.001). In addition, miR-1b positively correlated with cognitive function (P˂0.05) and BDNF mRNA (P˂0.01).ConclusionOur data demonstrated that regular treadmill exercise could reverse the down-regulation of hippocampal miR-1b, which has a probable role in the SD-induced cognitive impairment.Keywords: Female rats, Hippocampus, Mir-1b, Sleep deprivation, Treadmill training
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PurposeTo investigate the protective effect of preconditioning with non-toxic dose of hydrogen peroxide (H2O2) as a possible cell signaling molecule, against cell death induced by toxic concentration of H2O2 or by serum deprivation in human Wharton’s jelly-derived mesenchymal stem cells (HWJ-MSCs) and underlying mechanisms.MethodsHWJ-MSCs were isolated and identified using flow cytometry. After finding non-toxic concentration of H2O2, cells preconditioning was performed by H2O2 (20 μM) for 12 h and cell tolerance against serum deprivation or toxic levels of H2O2 was assayed by MTT test. Effect of preconditioning on mRNA and protein expression of Akt-1, Bcl-2 and Bax were examined using reverse transcription polymerase chain reaction (RT-PCR) and western blotting respectively. Role of hypoxia-inducible factor (HIF)-1α was explored in presence HIF-1α inhibitor.ResultsPreconditioning with 20 μM H2O2 for 12 h was non-toxic and decreased cell death induced by oxidative stress and serum deprivation in MSC cultures. However, the increased tolerance reversed in the presence of inhibitor of HIF-1α. By regards to RT-PCR and western blotting data, although expression of Akt-1, Bcl-2 and Bax was not change considerably but phosphorylated Akt-1 (pAkt-1) was up regulated after treatment with 20 μM H2O2 compared to control group. Moreover after exposure to 100 μM H2O2, western blotting analysis showed that cell pretreatment with 20 μM H2O2, decremented Bax/Bcl2 ratio and up-regulated HIF-1α and pAkt-1 compared to the control group.ConclusionIncreased tolerance of H2O2-pretreated cells led to the suggestion that transplantation of H2O2 preconditioned MSCs may improve therapeutic potential of stem cells in cell therapy procedures.Keywords: Wharton’s jelly derived mesenchymal stem cells, Preconditioning, Hydrogen peroxide, Serum deprivation, HIF-1α, Oxidative stress
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زمینه و هدفتاثیرات مثبت ورزش بر عملکرد مغز و همچنین افزایش بیان برخی از عوامل رشد نورونی از جمله فاکتور نوروترفیک مشتق شده از مغز یا BDNF (Brain-derived neurotrophic factor) ، اثبات شده است. برای بررسی بیشتر مکانیزم های مولکولی این تغییرات و همچنین با اطلاع از این موضوع که miR-10b یکی از تنظیم کننده های بیان BDNFاست، تاثیر ورزش بر بیان نسبی miR-10b (microRNA-10) در موش های صحرایی ماده ارزیابی گردید. از آنجا که مطالعات قبلی نشان داده اند، ورزش از طریق برهمکنش با هورمون استروژن باعث افزایش بیان BDNF می شود، اثر ورزش بر بیان miR-10b در موش های فاقد تخمدان نیز سنجیده شد. روش تحقیق: در این مطالعه، تعداد 42سر موش صحرایی ماده از نژاد ویستار، انتخاب و در قالب دو گروه دست نخورده و فاقد تخمدان بررسی شدند. موش های فاقد تخمدان، جراحی تخمدان برداری را سپری کرده و بعد از گذشت یک ماه برای انجام آزمایش استفاده شدند. پروتکل ورزش، چهار هفته دویدن بر روی تردمیل بود. برای تعیین بیان نسبی miR-10b در هیپوکامپ موش ها از روش Real time PCR استفاده شد.یافته هابیان miR-10b در گروه شم- ورزش نسبت به گروه کنترل در هر دو نوع موش های دست نخورده و فاقد تخمدان، تفاوت معنی داری نشان نداد. ورزش اجباری با تردمیل، تغییرات معنی دار در بیان این ژن در هر دو نوع موش دست نخورده و فاقد تخمدان ایجاد نکرد (0/05˃P) ؛ اما بیان BDNF در موش های دست نخورده به طور معنی دار افزایش یافت (0/05˂P). در واقع بیان miR-10b با تغییرات بیان BDNF در اثر ورزش، هیچ گونه همبستگی نداشت.نتیجه گیریدر واقع این مطالعه نتوانست ارتباط بیان miR-10b با افزایش بیان BDNF که حاصل برهمکنش ورزش و هورمون استروژن است را اثبات نماید؛ بنابراینmiRNA نمی تواند جز عوامل تنظیم کننده بیان BDNF محسوب گردد.کلید واژگان: ورزش منظم با تردمیل, موش صحرایی ماده, هیپوکامپ, MiR-10bBackground and AimThe positive effects of exercise on brain function and increased expression of neuronal growth factors, including brain-derived neurotrophic factor or (BDNF), have been proven. To the further investigate the molecular mechanisms of these changes, As well as knowing that miR-10b is one of the BDNF expression regulators, the effect of exercise on the relative expression of miR-10b (microRNA-10) in female rats was evaluated. Since they have shown in previous studies, Exercise through the interaction with estrogen hormone increases the expression of BDNF, The effect of exercise on the expression of miR-10b in rats without ovarian was also measured.Materials and MethodsIn this study, 42 female Wistar rats were selected and divided into two groups: intact and without ovarian. The rats without ovarian have spent ovariectomy surgery and were used in the experiments after a month. The exercise protocol was four weeks running on the treadmill. Real time PCR was used to determine the relative expression of miR-10b in the hippocampus of rats.ResultsThe expression of miR-10b in the Sham-exercise group didn’t show any significant difference as compared to the control group in both intact and OVX rats. Compulsive exercise with treadmill did not make any significant changes in the expression of this gene in both types intact and OVX rats (P ˃0.05). But the BDNF expression of OVX rats was significantly increased (P ˂0.05). In fact, there was no correlation between miR-10b expression and exercise-induced BDNF expression changes. Conclusion: In fact, this study failed to prove the association of expression of miR-10b with the increase of BDNF expression which is the result of the interaction of exercise and estrogen hormone and this miRNA can’t be as a regulator of BDNF expression.Keywords: Regular Treadmill Exercise, Female Rats, Hippocampus, MiR-10b
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BackgroundBDNF is a critical regulator of the cognitive functions of the brain. According to the modulatory role of BDNF in the chronic pain state, this study focused on changes in BDNF expression in the hippocampus and anxiety-like behavior, following an injury to the sciatic nerve.Methods30 adult male Wistar rats were randomly divided into three subsets as neuropathic, sham, and control. The neuropathic pain was induced due to chronic constriction injury of the sciatic nerve. Anxiety-like behavior was observed using the open field and elevated plus-maze tests. The level of BDNF was determined by real-time polymerase chain reaction analysis.ResultsThe results showed that the pain threshold decreased two weeks after CCI. Simultaneously, there was a decrease in the BDNF levels (P < 0.001, F = 15. 03). In addition, the anxiety-like behaviors increased in the open field (P < 0.01, F = 25.67; P < 0.05, F = 23.02) and elevated plus-maze (P < 0.05, F = 6.01; P < 0.001, F = 5.95) tests. In the third week after CCI, the increased pain threshold was accompanied by an increase in the level of BDNF, latency to leave the first quadrant, number of rearing behaviors (P < 0.05, F = 26.07, F = 24.04), and time spent in open arms (P < 0.05, F = 5.30) while time spent in closed arms decreased (P < 0.05, F = 4.70).ConclusionsAlteration in BDNF expression is involved in CCI-induced anxiety-like behavior.Keywords: Brain-Derived Neurotrophic Factor (BDNF), Anxiety-Like Behavior, Chronic Constriction Injury of the Sciatic Nerve (CCI)
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In this report, a rare case of pregnancy in a mouse without mating and during breastfeeding is presented. Out-bred NMRI mice were prepared for mating. Two female mice without superovulation were caged with one male. The next morning, vaginal plaque was not detected; therefore, females were kept in the cage with the same male for 4 more days. One of the females delivered 4 offspring: one female and three males. This female conceived again without mating, 21 days after the first delivery and during the breastfeeding period and this time delivered 16 offspring: 13 males and 3 females. The more likely explanation for this rare, second parturition is embryonic diapause.Keywords: Pregnancy, Breastfeeding, Embryonic diapause, Parthenogenesis, Mouse
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IntroductionLearning and memory requires a brain-derived neurotrophic factor (BDNF)-dependent phase in the hippocampus. It has been reported that chronic pain decreases hippocampal BDNF levels. We have also previously reported that noxious stimulation of the rat tooth pulp impairs learning and memory. Therefore, we decided to find the changes in the hippocampal BDNF expression which are associated with tooth pain and learning and memory impairment.MethodsDental pulp nociception was induced by intradental injection of capsaicin (100μg) in male Wistar rats. BDNF expression levels were determined by semi-quantitative RT-PCR and western blotting.ResultsThe data indicated that capsaicin elicited pain behaviors and impaired learning and memory in Morris water maze test. The protein and mRNA levels of BDNF were significantly (P<0.05) decreased in capsaicin-treated rats as compared with control animals. Furthermore, iboprofen (120mg/kg, ip) treatment caused a significant (P<0.05) up-regulation of the BDNF protein and mRNA in the hippocampus of capsaicin-injected animals.ConclusionThese findings suggest that inflammatory dental pain induces hippocampal function impairments by decreasing in BDNF expression.Keywords: Dental pain, Learning, memory, Hippocampus, BDNF expression
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The aim of this study was to evaluate anti bacterial and antibiofilm activity of PCL/gelatin nanofibers containing Lawsone against four pathogenic bacteria. Different concentrations of Lawsone (2-hydroxy-1, 4- naphthoquinone) (1, 3, 5 and 10%) were incorporated into polycaprolactone (PCL), gelatin (GEL) nanofibers via electrospinning technique. Presence of Lawsone in the scaffold confirmed by scanning electron microscopy (SEM) and Fourier-transform infrared spectroscopy (FTIR). Antibacterial and antibiofilm activity of Lawsone loaded scaffolds against clinically isolated Staphylococcus aureus, Methicillin-resistant Staphylococcus aureus (MRSA), Pseudomonas aeruginosa and Proteus mirabilis were investigated by disc diffusion method. All scaffolds were able to inhibit the growth of S. aureus and MRSA. Additionally, PCL/GEL/Lawsone 10% had bactericidal efficacy against P. mirabilis. Obtained results of the biofilm formation assay revealed that PCL/GEL/Lawsone 10% inhibited the biofilm of S. aureus, MRSA and P. mirabilis by 56%, 32%, and 15%, respectively. Due to good antibacterial and antibiofilm activity of Lawsone containing scaffolds, PCL/GEL 10% can be a good candidate for application in wound dressing patches.Keywords: Antibacterial, Anti-biofilm activity, Lawsone, Polycaprolactone, Gelatin, Electrospinning
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ارکسین A و ارکسین B ، نوروپپتیدهای هیپوتالاموسی می باشند که نقش مهمی در تنظیم پاسخ های فیزیولوژیک از جمله درد دارند. c-fos یکی از شاخص های فعالیت نورونی در شرایط بروز درد می باشد. پژوهش حاضر به منظور بررسی نقش گیرنده ارکسین 1 هسته دمی عصب سه قلو در بروز درد دهانی صورتی ناشی از کپسایسین و بیان c-fos در این ناحیه طراحی شد. در این مطالعه تجربی از 70 سر موش صحرایی نر نژاد ویستار، در محدوده وزنی 250 – 200 گرم استفاده شد، که به طور تصادفی در 10 گروه 7 تایی شامل: کنترل ، درد، شم جراحی، شم کاپسایسین، جراحی و درد، شم ارکسین A و درد ، ارکسین A (pM/rat 50) و درد ، شم SB-334867 و درد، SB-334867 (nM/rat 40) به عنوان آنتاگونیست و درد و گروه دریافت کننده ارکسین A و SB-334867 به صورت توام و درد، قرار گرفتند. پس از کانول گذاری و دوره بهبودی، تزریق داروها و 20 دقیقه بعد تزریق کاپسایسین صورت پذیرفت. میزان بیان c-fos با روش ایمونوهیستوشیمی در هسته دمی عصب سه قلو ارزیابی شد. نتایج حاصل نشان داد که تزریق کاپسایسین به صورت معنی داری موجب افزایش پاسخهای درد و افزایش بیان c-fos می گردد (001/0p<). ارکسین A منجر به مهار درد القا شده توسط کاپسایسین و بیان c-fos گردید (001/0p<). پیش درمانی با SB-334867 این اثر را حذف نمود (001/0p<). تزریق SB-334867 به تنهایی سبب تشدید پاسخ های درد ناشی از کپسایسین گردید (001/0p<). بیان c-fos در گروه دریافت کننده SB-334867 همانند گروه درد بالا بود (001/0p<). SB-334867 باعث مهار نسبی اثر کاهشی ارکسین A بر c-fos گردید.کلید واژگان: درد دهانی- صورتی, هسته دمی عصب سه قلو, ارکسین A, SB-334867Orexin A and orexin B are hypothalamic neuropeptides that have critical roles in the regulation of physiological responses such as pain. C-fos is neural activity markers in painful situations. This study was designed to evaluate the role of trigeminal nucleus caudalis (TNC) orexin 1 receptor on capsaicin-induced orofacial pain and c-fos expression in TNC. In this experimental study, 70 male Wistar rats (200-250 g) were randomly allocated into 10 groups: control, pain, sham surgery, sham capsaicin, surgery and pain, sham orexin A and pain, orexin A (50 pM/rat) and pain, sham SB-334867 and pain, SB-334867 (40 nM/rat) as antagonist and pain, orexin A plus SB-334867 and pain. Following cannula implantation and recovery period, the drugs were administration 20 min before capsaicin injection. C-fos expression in TNC was evaluated using immunohistochemistry. The capsaicin-injected rats showed a significant pain behavior and expression c-fos (p<0.001). Orexin A significantly inhibited capsaicin-induced pain and decreased c-fos expression (p<0.001). Pretreatment with SB-334867 could prevent the effects of orexin A. SB-334867 alone exaggerated capsaicin-induced pain responses. The level of c-fos was high in SB-334867–treated rats some as capsaicin group. SB-334867 could partially inhibit the effect of orexin A on c-fos orexin A expression.Keywords: C-FOS, Orexin A, orofacial pain, SB-334867, trigeminal nucleus caudalis
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هدفمطالعه حاضر جهت بررسی اثرات مخرب مانکوزب بر سد خونی- بیضوی در مدل برون تنی طراحی شده است.مواد و روش هاموشهای نر با غلظتهای 250 و500 میلیگرم/ کیلوگرم (وزنی/وزنی) مانکوزب برای 40 روز متوالی بهصورت خوراکی تیمار شدند. نفوذپذیری سد خونی- بیضوی با استفاده از رنگ ایوانس بلو ارزیابی شد. بیان نسبی mRNA برخی از ژنهای سد خونی- بیضوی از جمله N- کادهرین، کلائودین- 11 و زونولا آکلودنس با روش Real time-PCRدر گروه های مختلف تعیین شد.نتایجغلظت رنگ ایوانس بلو در لومن لوله های منیساز حیواناتی که مانکوزب دریافت کرده بودند افزایش یافته بود. همچنین میزان بیانmRNA ژنهای N- کادهرین، کلائودین- 11 و زونولا آکلودنس بویژه در گروه با غلظت 500 میلیگرم/ کیلوگرم مانکوزب در مقایسه با گروه شاهد بهطور معنیداری کاهش یافت. نتیجه گیری: بر اساس نتایج حاصل از مطالعه حاضر میتوان نتیجه گرفت که مانکوزب با تغییر در بیان ژنهای درگیر در تمامیت سد خونی- بیضوی، نفوذ پذیری آن را افزایش داده و باعث اختلال در عملکرد بیضه میشود.کلید واژگان: سد خونی- بیضوی, مانکوزب, اختلالات تولید مثلی, بیضهThe effects of mancozeb on the integrity of blood- testis barrier and expression of associated genesAimThe current study was designed to understand the destructive effects of mancozeb on BTB in an in vitro model. Material and Methods: Male mice were gavage- administered MZB (250, 500 mg/kg w. w) for 40 consecutive days. Integrity of BTB was evaluated using Evans blue dye. The relative mRNA expression of BTB- associated genes; including N- cadherin, claudin-11 and zonula occludens-1 was investigated by quantitative real-time reverse transcription–polymerase chain reaction in different groups (qRT-PCR).ResultsConcentration of Evans Blue dye in the lumen of seminiferous tubules was increased in mancozeb-treated animals. The mRNA expression levels of N-cadherin, claudin-11 and zonula occludens-1 genes were decreased significantly in the MZB 500 mg/kg group compared with the control group.ConclusionAccording to the obtained data, it could be concluded that mancozeb increase BTB permeability leading to testicular dysfunction by the alteration of BTB-associated genes.Keywords: Blood- testis barrier, Mancozeb, Reproductive dysfunctions, Testis
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IntroductionG-proteins have an important role in the cell signaling of numerous receptors. The situation of G-proteins in health and disease and their critical role in the development of diabetic side effects is an interested scientific field. Here, the changes in the expression of G-protein subunits (Gαi, Gαs and Gβ) were evaluated in hyperglycemic situation of PC12 cells as a cellular model for the induction of diabetic side effect.MethodsRat pheochromocytoma PC12 cells were grown in normal or high-glucose (4X normal glucose) medium. Cell viability was determined by MTT assay and the generation of intracellular reactive oxygen species (ROS) studied using fluorescence spectrophotometry. RT-PCR and immunobloting were performed to evaluate the expression of specific G-protein subunits in the levels of mRNA and protein, respectively.ResultsIn high glucose condition (100 mM glucose for 48h), the cell viability was significantly decreased and intracellular ROS increased. In addition, Gαi expression level was significantly decreased in hyperglycemic PC12 cells. However, the levels of Gαs and Gβ mRNAs and their proteins were not altered in high glucose-treated cells.ConclusionThe results demonstrate that deregulation or disruption in the signaling of Gai coupled receptors can be occurred in hyperglycemic condition.Keywords: G, proteins, Gene expression, Hyperglycemia, PC12 cells
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زمینه و هدفگیاه مشگک از گیاهان دارویی معطر و مورد استفاده در طب سنتی ایران است که در اسانس آن ترکیبات موثر بر سیستم عصبی وجود دارد. این مطالعه به منظور تعیین اثر اسانس گیاه مشگک بر یادگیری و حافظه فضایی موش های صحرایی انجام شد.روش بررسیاین مطالعه تجربی روی 35 سر موش صحرایی نر بالغ نژاد ویستار در 5 گروه 7 تایی انجام شد. گروه ها شامل کنترل، شم (دریافت کننده نرمال سالین) و گروه های دریافت کننده اسانس گیاه مشگک به صورت روزانه با دوزهای 0.5 و 0.25 و 0.125 میلی لیتر بر کیلوگرم وزن بدن بود. اسانس گیاه طی چهار روز 20 دقیقه قبل از آزمون یادگیری به صورت درون صفاقی تزریق گردید. حافظه و یادگیری فضایی با استفاده از ماز آبی موریس اندازه گیری شد.یافته هادر روزهای دوم ، سوم و چهارم یادگیری، تاخیر رسیدن به سکو پنهان با دوز 0.5 ml/kg/bw اسانس گیاه مشگک در مقایسه با کنترل کاهش یافت (P<0.05). همچنین زمان رسیدن به سکو با دوز 0.25 ml/kg/bw در تمام روزها به جز روز اول و با دوز 0.125 ml/kg/bw در روزهای دوم و سوم یادگیری، نسبت به کنترل کاهش آماری معنی دار نشان داد (P<0.05). بررسی حافظه فضایی با آزمون پروب نشان دهنده افزایش درصد زمان و مسافت طی شده در ربع هدف در گروه دریافت کننده دوز 0.5 ml/kg/bw اسانس در مقایسه با گروه کنترل بود (P<0.05).نتیجه گیریاسانس گیاه مشگک با دوزهای 0.5 ml/kg/bw و 0.25 ml/kg/bw طی چهار روز سبب بهبود یادگیری و حافظه فضایی موش های صحرایی گردید.کلید واژگان: گیاه مشگک, یادگیری, حافظه فضایی, ماز آبی موریس, موش صحراییBackground And ObjectiveDucrosia anethifolia (Dc.) is a medicinal odor plant contains CNS effective compounds which has been used in Iranian traditional medicine. This study was done to determine the effect of Ducrosia anethifolia (Dc.) Boiss essential oil on spatial learning and memory in adult male rats.MethodsIn this experimental study, 35 wistar adult male rats were randomly allocated into the five groups (n=7) including: control, sham (injected vehicle) and Ducrosia anethifolia (Dc.) Boiss essential oil groups 0.125, 0.25 and 0.5ml/kg/bw, intraperitonally during four days. Morris water maze test was used to assess learning and memory.ResultsDucrosia anethifolia (Dc.) Boiss essential oil (0.5 ml/kg/bw) was significantly increased escape latency in the second and third (PConclusionIntraperental administration of the Ducrosia anethifolia (Dc.) Boiss essential oil at doses of 0.5 and 0.25 ml/kg/bw during four days can improves spatial learning and memory in adult male rats.Keywords: Ducrosia anethifolia (Dc.) Boiss, Learning, Memory, Morris water maze, Rat
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International Journal of Reproductive BioMedicine، سال چهاردهم شماره 9 (پیاپی 80، Sep 2016)، صص 567 -576مقدمه
اگرچه سرم خون جنین گاو (FBS) به طور گسترده ای در آزمایشگاه های کشت سلول استفاده می شود، اما خصوصیاتی از جمله خطر انتقال عفونت و اثرات جانبی حساسیت زا استفاده آن را جهت کشت سلول ها برای مصارف بالینی محدود کرده است. بنابراین تقاضا برای یک مکمل جایگزین با قابلیت کمک به رشد و تکثیر سلول ها وجود دارد.
هدفجهت یافتن یک جایگزین مناسب برای FBS، این تحقیق به مقایسه قابلیت سرم خون بندناف با FBS در تکثیر سلول های بنیادی مزانشیمی مغز استخوان (BMMCs) و سلول های بنیادی مزانشیمی ماتریکس بند ناف (hUCMCs) پرداخته است.
مواد و روش هاخون بند ناف نوزادان سالم متولد شده به روش سزارین جمع آوری و سرم خون بند ناف جدا شد. سلول های بنیادی مزانشیمی مغز استخوان و سلول های بنیادی مزانشیمی ماتریکس بند ناف با بررسی مارکرهای سطحی توسط فلوسایتومتری، بررسی آلکالین فسفاتاز درون سلولی و تمایز به سلول های استخوانی و چربی شناسایی شدند. هر کدام از سلول های جدا شده در سه گروه جداگانه در محیط Iscove's Modified Dulbecco's Media (IMDM) کشت داده شدند. گروه ها عبارت بودند از: 1) کشت سلول ها با سرم خون بند ناف. 2) کشت سلول ها با FBS. 3) کشت سلول ها بدون افزودن سرم. تکثیر سلول ها به کمک معرف WST-1 و رنگ آمیزی تریپان بلو بررسی شد..
نتایجسلول های گروه اول و دوم از نظر مرفولوژی و بروز خصوصیات سلول های بنیادی مزانشیمی شبیه به هم بودند و نتایج حاصل از ارزیابی WST-1 و رنگ آمیزی تریپان بلو تفاوت معنی داری بین تکثیر سلول های کشت داده شده در حضور سرم خون بند ناف و FBS نشان نداد اما تفاوت معنی داری بین تکثیر سلول ها در گروه های دارای سرم و گروه بدون سرم مشاهده شد.
نتیجه گیرینتایج این تحقیق نشان داد که سرم خون بند ناف انسان می تواند به طرز موثری تکثیر سلول های بنیادی مزانشیمی مغز استخوان و سلول های بنیادی مزانشیمی ماتریکس بند ناف را در محیط آزمایشگاه پشتیبانی کند و به عنوان یک جایگزین مناسب در مطالعات بالینی به کار رود.
کلید واژگان: مغز استخوان, تکثیر سلول, خون بند ناف, سلول های بنیادی مزانشیمی, استرومال, بندناف, ژله وارتونBackgroundFetal bovine serum (FBS) is widely used in cell culture laboratories, risk of zoonotic infections and allergic side effects create obstacles for its use in clinical trials. Therefore, an alternative supplement with proper inherent growth-promoting activities is demanded.
ObjectiveTo find FBS substitute, we tested human umbilical cord blood serum (hUCS) for proliferation of human umbilical cord matrix derived mesenchymal stem cells (hUC-MSCs) and human bone marrow-derived mesenchymal cells (hBM-MSCs).
Materials And MethodsUmbilical cord blood of healthy neonates, delivered by Caesarian section, was collected and the serum was separated. hUC-MSCs and hBM-MSCs were isolated and characterized by assessment of cell surface antigens by flow cytometry, alkaline phosphatase activity and osteogenic/adipogenic differentiation potential. The cells were then cultured in Iscove's Modified Dulbecco's Medium (IMDM) by conventional methods in three preparations: 1- with hUCS, 2- with FBS, and 3- without serum supplements. Cell proliferation was measured using WST-1 assay, and cell viability was assessed by trypan blue staining.
ResultsThe cells cultured in hUCS and FBS exhibited similar morphology and mesenchymal stem cells properties. WST-1 proliferation assay data showed no significant difference between the proliferation rate of either cells following hUCS and FBS supplementation. Trypan blue exclusion dye test also revealed no significant difference for viability between hUCS and FBS groups. A significant difference was detected between the proliferation rate of stem cells cultured in serum-supplemented medium compared with serum-free medium.
ConclusionOur results indicate that human umbilical cord serum can effectively support proliferation of hBM-MSCS and hUC-MSCs in vitro and can be used as an appropriate substitute for FBS, especially in clinical studies.
Keywords: Bone marrow, Cell proliferation, Cord blood, Mesenchymal stem, stromal cells, Umbilical cord, Wharton jelly -
IntroductionFor thousands of years, plants have been used as the main source of drug worldwide. Recently, it has been found out that the plant Artemisia annua and especially its derivatives such as artemether have anticancer properties.MethodsIn this study, the anticancer effect of artemether on MCF-7 breast cancer cell line was examined. MTT assay was used to assess the viability of cancer cells.ResultsThe data showed that artemether (100-300 nM) resulted in MCF-7 growth inhibition. Artemether plus vincristine or doxorubicin compared to each drug alone showed significant cytotoxic effects. Over 50 percent of cells were killed in combination of non-effective doses of artemether and doxorubicin (50 and 160 nM, respectively).ConclusionTaken together, the combined therapy of artemether and anticancer drugs would be a promising strategy for breast cancer but the effectiveness of such combination therapy needs to be verified by experimental and clinical investigations.Keywords: Breast cancer cell line, MCF, 7, Artemether, Cell viability, Chemotherapy
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مقدمهکاهش آزمایش های غیرضروری یک مساله اساسی در بخش مراقبت های ویژه می باشد. یکی از راه های کاهش آزمایش ها، پیش بینی مقدار آزمایش و استفاده از آن جهت تشخیص بهتر ضرورت انجام یک آزمایش است. هدف این مقاله، ارائه یک سیستم تصمیم یار برای پیش بینی مقادیر آزمایش ها می باشد. داده های مورد بررسی، مربوط به آزمایش کلسیم برای سه دسته بیماران خون ریزی گوارشی فوقانی، تحتانی و خون ریزی نامشخص گوارشی می باشد.روش بررسیداده های مورد استفاده در این مطالعه از پایگاه داده MIMIC-II استخراج شده است. برای پیش بینی مقادیر آزمایش کلسیم از مدل فازی تاکاگی-سوگنو مرتبه صفر و متغیرهای ورودی ضربان قلب و مقدار قبلی آزمایش کلسیم استفاده شد.نتایجنتایج نشان می دهد که مقدار آزمایش کلسیم برای بیماران مورد بررسی با دقت مطلوبی قابل پیش بینی است. میانگین قدر مطلق خطا برای سه دسته بیماران به ترتیب برابر 27/0، 29/0 و 28/0 است.نتیجه گیریدر این مطالعه با استفاده از مدل سازی فازی و دو متغیر ضربان قلب و مقدار قبلی کلسیم، سیستم تصمیم یاری برای پیش بینی مقدار آزمایش کلسیم مربوط به سه دسته از بیماران با خون ریزی گوارشی، طراحی شد. سیستم طراحی شده با استفاده از این دو متغیر بالینی دقت مطلوبی دارد و نتایج نشان دهنده قابلیت سیستم در پیش بینی مقدار آزمایش کلسیم است. جهت بهبود نتایج، می توان اثر متغیرهای بیشتری بر سیستم را بررسی کرد. همچنین از این جهت که سیستم ارائه شده به جای تشخیص ضرورت/عدم ضرورت آزمایش، به طور مستقیم مقدار آزمایش را پیش بینی می کند؛ نسبت به سایر روش ها عمومیت بیشتری دارد و به پزشک این امکان را می دهد تا برای هر بیمار با توجه به شرایط آن بیمار تصمیم گیری کند.کلید واژگان: آزمایش های غیرضروری, بخش مراقبت های ویژه, پیش بینی مقدار آزمایش کلسیم, بیماران با خون ریزی گوارشی, مدل سازی فازیJournal of Shaeed Sdoughi University of Medical Sciences Yazd, Volume:24 Issue: 4, 2016, PP 286 -295IntroductionReducing unnecessary laboratory tests is an essential issue in the Intensive Care Unit. One solution for this issue is to predict the value of a laboratory test to specify the necessity of ordering the tests. The aim of this paper was to propose a clinical decision support system for predicting laboratory tests values. Calcium laboratory tests of three categories of patients, including upper and lower gastrointestinal bleeding, and unspecified hemorrhage of gastrointestinal tract, have been selected as the case studies for this research.MethodIn this research, the data have been collected from MIMIC-II database. For predicting calcium laboratory values, a Fuzzy Takagi-Sugeno model is used and the input variables of the model are heart rate and previous value of calcium laboratory test.ResultsThe results showed that the values of calcium laboratory test for the understudy patients were predictable with an acceptable accuracy. In average, the mean absolute errors of the system for the three categories of the patients are 0.27, 0.29, and 0.28, respectively.ConclusionIn this research, using fuzzy modeling and two variables of heart rate and previous calcium laboratory values, a clinical decision support system was proposed for predicting laboratory values of three categories of patients with gastrointestinal bleeding. Using these two clinical values as input variables, the obtained results were acceptable and showed the capability of the proposed system in predicting calcium laboratory values. For achieving better results, the impact of more input variables should be studied. Since, the proposed system predicts the laboratory values instead of just predicting the necessity of the laboratory tests; it was more generalized than previous studies. So, the proposed method let the specialists make the decision depending on the condition of each patient.Keywords: Unnecessary Laboratory Tests, Intensive Care Unit, Calcium Laboratory Value Prediction, Gastrointestinal Bleeding Patients, Fuzzy Modeling
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BackgroundDucrosia anethifolia (DA) is a medicinal plant traditionally used to treat a wide spectrum of illnesses. DA contains a series of antioxidant compounds, including alpha-pinene, which give it a sedative and relaxing effect. In spite of these effects of DA, the effects of DA essential oil on anxiety and locomotor activity in open field tests have not yet been studied. In the present study, the effects of DA essential oil and its main component of alpha-pinene on locomotor activity and anxiety were studied using open field tests..ObjectivesThe purpose of this study was to investigate the effects of DA essential oil and its main component, alpha-pinene, on locomotor activity and anxiety behaviors using open field and antioxidant capacity tests in Wistar rats..MethodsSixty-three adult male Wistar rats (weighing 200 - 250 g) were divided into 9 groups: control, positive control (diazepam), essential oil treated groups (25, 50, 100, 200, and 500 mg/kg administered intraperitoneally, (i.p.)) and alpha-pinene groups (0.2 and 0.4 mg/kg, i.p.). For precisely 30 minutes after each injection in all groups, open field tests were used to assess behaviors such as rearing, line crossing, walling, grooming, and stretched attend posturing. In addition, oxidant and antioxidant parameters (malondialdehyde [MDA] and catalase [CAT]) were assessed in the rats temporal lobes..ResultsDA (200 and 500 mg/kg doses) and alpha-pinene (0.2 and 0.4 mg/kg doses) significantly reduced locomotor activity, whereas doses of 25, 50, and 100 mg/kg of DA failed to show such an effect. Treatment with DA and alpha-pinene resulted in a significant decrease in MDA levels and a significant increase in CAT activity in comparison to controls..ConclusionsThe results of this study suggest that the main component of DA (alpha-pinene) is responsible for DAs ability to reduce locomotor activity and anxiety, which is indicative of CNS depressant activity. Moreover, it is possible that some of the motor suppression and sedation effects of the alpha-pinene in DA are due to the antioxidant capacity of this substance. However, further research and clinical evaluations are necessary to isolate and identify the other substances responsible for these activities in DA..Keywords: Ducrosia anethifolia (Boiss), Alpha, Pinen, Locomotor Activity, Anxiety, Oxidative Stress, Rats
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سابقه و هدفبا توجه به توانایی سلول های گلیا در آزادسازی فاکتورهای تغذیه ای و گلیوترانسمیتر و نیز پاسخ دهی به میانجی های عصبی آزاد شده توسط نورون ها و نقش آن ها در هومئوستاز فضای سیناپسی، به نظر می رسد این سلول ها در شکل پذیری سیناپسی نقش دارند. در این مطالعه به بررسی نقش سلول های گلیای هیپوکمپ در پاسخ سیناپسی پایه و شکل پذیری سیناپسی کوتاه مدت این ناحیه پرداختیم.مواد و روش هااین مطالعه از نوع تجربی می باشد. جهت مهار سلول های گلیای هیپوکمپ، فلوئوروسیترات، مهارکننده این سلول ها، (μl5/0nmol/1) به صورت دو طرفه در داخل هیپوکمپ پشتی تزریق شد. پاسخ سیناپسی پایه و شکل پذیری سیناپسی کوتاه مدت با تکنیک ثبت پتانسیل میدانی بررسی گردید. مسیر Schaffer Collateral تحریک و fEPSP از CA1 ثبت شد. پس از تهیه نمودار Input/output، از تحریکات زوج پالس (Paired pulse) برای القای شکل پذیری سیناپسی کوتاه مدت استفاده شد.یافته هامهار سلول های گلیای توسط ریز تزریق فلوئوروسیترات در ناحیه CA1، پاسخ سیناپسی پایه را متاثر نکرد (05/0> p). مهار این سلول ها سبب افزایش معنی دار شاخص زوج پالس (کنترل: 48/5±80/62 درصد، دریافت کننده فلوئوروسیترات: 11/12±19/87 درصد) در فاصله بین پالسی 20 میلی ثانیه گردید (05/0< p). اما بر این شاخص در فواصل بین پالسی 80 و 200 میلی ثانیه تاثیری نداشت (05/0> p).
استنتاج: نتایج پیشنهاد می کند عملکرد سلول های گلیا هیپوکمپ بر پاسخ سیناپسی پایه اثری ندارد، اما شکل پذیری سیناپسی کوتاه مدت در ناحیه CA1 هیپوکمپ را متاثر می کند.کلید واژگان: هیپوکمپ, سلول های گلیا, شکل پذیری سیناپسیBackground andPurposeGlial cells seem to play role in synaptic plasticity because they have the ability to release trophic factors and gliotransmitters and respond to neurotransmitters. They also play important role in synaptic space homeostasis. In this study, the role of hippocampal glial cells in baseline synaptic response and short term synaptic plasticity were investigated.Materials And MethodsIn this experimental study, flourocitrate, glia inhibitor (1nmol/0.5μl), was microinjected intrahippcampally for inhibition of hippocampal glial cells. Baseline synaptic response and short term synaptic plasticity were evaluated by field potential recording. fEPSP was recorded from CA1 following Schaffer collaterals stimulation. After Input/Output curve construction, short term synaptic plasticity was induced by paired pulse stimulations.ResultsInhibition of glial cells by flourocitrate microinjection in CA1 did not have any effect on baseline synaptic response (P>0.05). Flourocitrate increased paired pulse index (PPI, control: 62.80%±5.48; flourocitrate treated: 87.19%±12.11) at 20 ms inter pulse interval (P0.05).ConclusionThe results suggest that hippocampal glial cells functions did not influence the baseline synaptic response but affected short term synaptic plasticity in CA1 area of the hippocampus.Keywords: hippocampus, Gglial cells, synaptic plasticity -
ObjectiveWorldwide, diabetes mellitus (DM) is an ever-increasing metabolic disorder. A promising approach to the treatment of DM is the implantation of insulin producing cells (IPC) that have been derived from various stem cells. Culture conditions play a pivotal role in the quality and quantity of the differentiated cells. In this experimental study, we have applied various culture conditions to differentiate human umbilical cord matrix-derived mesenchymal cells (hUCMs) into IPCs and measured insulin production.Materials And MethodsIn this experimental study, we exposed hUCMs cells to pancreatic medium and differentiated them into IPCs in monolayer and suspension cultures. Pancreatic medium consisted of serum-free Dulbeccos modified eagles medium Nutrient mixture F12 (DMEM/F12) medium with 17.5 mM glucose supplemented by 10 mM nicotinamide, 10 nM exendin-4, 10 nM pentagastrin, 100 pM hepatocyte growth factor, and B-27 serum-free supplement. After differentiation, insulin content was analyzed by gene expression, immunocytochemistry (IHC) and the chemiluminesence immunoassay (CLIA).ResultsReverse transcription-polymerase chain reaction (RT-PCR) showed efficient expressions of NKX2.2, PDX1 and INSULIN genes in both groups. IHC analysis showed higher expression of insulin protein in the hanging drop group, and CLIA revealed a significant higher insulin production in hanging drops compared with the monolayer group following the glucose challenge test.ConclusionWe showed by this novel, simple technique that the suspension culture played an important role in differentiation of hUCMs into IPC. This culture was more efficient than the conventional culture method commonly used in IPC differentiation and cultivation.Keywords: Suspension Culture, Wharton Jelly Cells, Insulin Producing Cell
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Uranium (VI) sorption using an anionic exchanger resin in the presence of sulfate anions, namely amberlite 910, was the subject of current study. Batch sorption experiments were carried out to evaluate the influence of operational parameters such as pH, contact time, initial concentration and existence of various anions (including phosphate, sulfate, chloride, fluoride, and nitrate) in the solution on amberlite 910 sorption behavior. Kinetics study revealed that the pseudo-second-order model showed better curve-fitting regression of the experimental data than the pseudo-first-order one. Freundlich isotherm was also provided well mathematical description of sorption process than the Langmuir one. It was also revealed that the existence of various anion species in the solution could strongly affect the sorption of uranium using amberlite 910 anion exchanger resin.Keywords: Uranium, Amberlite 910, Anion exchanger resin, Adsorption, Anion effect.
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افت تحصیلی دانشجویان در نیمسالهای اول تحصیل اغلب به دلیل تغییر شیوه زندگی و عادت نداشتن به محیط جدید بوی&zwj&zwjژه خوابگاه، جدایی از خانواده و درگیر شدن در مسائل عاطفی به دلیل حساس بودن سن ورود به دانشگاه مشاهده می شود. این گزارش به وضعیت تحصیلی محمد دانشجوی پزشکی می پردازد که با پیشینه علمی عالی و رتبه بسیار خوب در رشته پزشکی دانشگاه علوم پزشکی کرمان قبول و در همان بدو ورود دو نیمسال متوالی مشروطی و دچار افت تحصیلی شدید می شود. محمد که از پشتوانه خانوادگی و وضعیت مالی نسبتا مناسبی برخوردار است در بدو ورود درگیر مشکلات عاطفی می شود و با شکست در این مرحله دچار افسردگی و افت شدید تحصیلی میگردد، خانواده محمد با تصور کمک به فرزندشان دچار اشتباهات بزرگتر شده و دانشجوی یاد شده با دو نیمسال مشروطی متوالی بعدی در معرض خطر اخراج قرار میگیرد. با توجه به حساس بودن این مرحله از زندگی دانشجویان، علاوه بر کمک و توجه اساتید، باید مرکز مشاوره در دانشگاه بسیار فعال عمل کند و دانشجویانی را که دچارمشکلات عاطفی و افت تحصیلی می شوند را شناسایی نموده، تحت مراقبت های محسوس و نامحسوس نگه دارد و دلسوزانه با مشاوره سودمند و با همکاری خانواده به آنها کمک شود که از این مرحله بحرانی عبور و با شرایط جدید سازگار شوند.
کلید واژگان: افت تحصیلی, مشاوره دانشجویی, دانشجوی رشته پزشکیEducational decline among university students during the first university terms is generally observed as a reason of the big change in lifestyle and not being accustomed to dormitory atmosphere, or it can be as a result of being involved with emotional matters, due to the special age at which they enter university. This research concerns the situation of a medical student ((Mohammad)) who enters Kerman medical university with a perfect educational background and a top rank in entrance exam of university but he encounters a noticeable underachievement in educating as soon as he starts his courses at university. Mohammad who is from a relatively supportive family and has a suitable financial situation in his family, gets involved with an emotional case and its following problems and matters, facing a breakup at this stage, he is suffered with depression and severe educational decline. His family, in order to help him, acts mistakenly and it brings about bigger problems. Therefore, after finishing two university terms with conditional educational situation, he exposes with the warning of being dropped out of university.Noticing the importance of this stage of life among university students, more than the consideration of university teachers, needs the contribution of consulting center of university in an effective way. so that they can identify students with emotional conflicts that leads them toward educational underachievement, and then offering them suitable and helpful consultation aimed to help them pass this serious phase of life and moreover, how to adopt themselves with new situations, surely with having their family support as well.Keywords: Educational Decline, Medical Student, Consultation -
Nationwide implementation of Family Physician (FP) program started in 2005 and targeted almost 25,000,000 citizens residing in rural areas and cities with less than 20,000 populations in Iran. Despite its blatant initiation that resulted in some modest achievements, the future of FP looks unclear in Iran. Thus far, no longitudinal evaluation of the implementation and impact of FP program has been conducted. However, meager evidence highlights the facilitating role of an existing and strong Primary Health Care (PHC) network in the implementation of FP in rural areas in Iran. A longstanding challenge, however, as emphasized by most stakeholders, remains to be the expansion of FP program into urban settings, where the PHC is undeveloped and fragile as well as the powerful private sector is resistant. Using an adapted conceptual framework of institutions, ideas, and interests, this policy perspective aims to shed light on main difficulties of FP implementation in urban areas of Iran. We analyze FP policy in the context of ongoing interactions and conflicts among institutions (the structures and rules that shape policies), interests (the groups and individuals influencing policy), and ideas (discourses around policies). Our argument will, we envisage, help plan for more appropriate implementation of FP in cities in Iran, and hopefully beyond.Keywords: Family physician program, ideas, institutions, interests, Iranian health system, primary health care (PHC)
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In this study, a carbon paste electrode modified with carbon nanotubes and benzoylferrocene (BF) was used to prepare a novel electrochemical sensor. The objective of this novel electrode modification was to seek new electrochemical performances for the detection of glutathione. The response of catalytic current with glutathione concentration showed a linear relation in the range from 1.0×10−7 to 1.0×10−4 M with a detection limit of 3.0×10−8 M. Finally, this method was used for the determination of glutathione in real samples.Keywords: Glutathione, Carbon nanotubes paste electrode, Voltammetry, Electrochemical sensor
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IntroductionUncontrolled diabetes mellitus could lead to neuropathy in central and peripheral nerve tissues and one of its main signs can be hyperalgesia and motor coordination defect. Due to the blood glucose lowering effect of Thymus species and the presence of polyphenolic compounds with high antioxidant capacity, in this study the effect of Thymus caramanicus jalas extract was investigated on animal model of diabetes-induced neuropJavascript:FormatThis(''B'')athy.MethodsIn the present study development of hyperalgesia was examined by tail-flick and rota-rod tests, in streptozotocin-induced diabetic male wistar rats (subcutaneous injection). Animals were given Thymus caramanicus jalas extract (50, 100, 150 and 200 mg/kg) for 6 weeks. The levels of blood glucose were measured at the beginning and the end of the experimental period.ResultsBlood glucose levels in diabetic animals which received Thymus extract at the doses of 150 and 100 mg/kg was reduced as compared to the pretreatment levels (p<0.05 and p<0.01, respectively). Untreated diabetic rats showed lower threshold in pain sensation and motor deficit compared with the control animals. However, tail-flick latency and ability to stay on rota-rod were significantly decreased in diabetic animals that received 100 mg/kg (p<0.01) and 150 mg/kg (p<0.001) of extract.ConclusionThe data show that Thymus caramanicus jalas extract has ability to reduce serum glucose levels and attenuate hyperalgesia and motor deficit induced by diabetes in rats. The mechanisms of this effect may be related to (at least in part) the attenuation of blood glucose and prevention of neural damage.Keywords: Thymus caramanicus jalas extract, Diabetes, Hyperalgesia, Motor deficit, Rats
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