Conditioned medium obtained from human amniotic mesenchymal stem cells attenuates focal cerebral ischemia/reperfusion injury in rats by targeting mTOR pathway

التفاصيل البيبلوغرافية
العنوان: Conditioned medium obtained from human amniotic mesenchymal stem cells attenuates focal cerebral ischemia/reperfusion injury in rats by targeting mTOR pathway
المؤلفون: Mahin Nikougoftar, Nahid Aboutaleb, Solmaz Nasseri Maleki, Donya Nazarinia, Behnaz Mokhtari, Raheleh Gholamzadeh
المصدر: Journal of chemical neuroanatomy. 102
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Male, Ischemia, Apoptosis, Pharmacology, Neuroprotection, Brain Ischemia, 03 medical and health sciences, Cellular and Molecular Neuroscience, symbols.namesake, chemistry.chemical_compound, 0302 clinical medicine, Medicine, Animals, Humans, cardiovascular diseases, Amnion, Rats, Wistar, PI3K/AKT/mTOR pathway, Evans Blue, TUNEL assay, business.industry, TOR Serine-Threonine Kinases, Mesenchymal stem cell, Brain, Mesenchymal Stem Cells, medicine.disease, Rats, 030104 developmental biology, chemistry, Blood-Brain Barrier, Culture Media, Conditioned, Reperfusion Injury, Nissl body, symbols, business, Reperfusion injury, 030217 neurology & neurosurgery, Signal Transduction
الوصف: Conditioned medium obtained from human amniotic mesenchymal stem cells (hAMSC-CM) was recently shown to have many antioxidant, antiapoptotic and proangiogenic growth factors. The present study was performed to investigate whether protective effects of hAMSC-CM against focal cerebral ischemia/ reperfusion (I/R) injury is associated with modulation of the mammalian target of rapamycin (mTOR) pathway. A rat model of middle cerebral artery occlusion (MCAO) was created and the animals were divided into three groups including sham, MCAO and MCAO + hAMSC-CM. Drug was administrated immediately after cerebral reperfusion (i.v). The expressions of mTOR, p-mTOR and LC3 were measured using Western blotting and real time-PCR, respectively. Apoptosis and neuronal loss were determined using TUNEL and Nissl staining, respectively. Infarct volume and the blood-brain barrier (BBB) damage were evaluated using 2,3,5-triphenyltetrazolium chloride (TTC) staining and Evans Blue (EB) uptake, respectively. Compared with sham, significant infarct volume, apoptotic cell death, and neuronal loss were found in MCAO rats that reversed by hAMSC-CM (P 0.05). Likewise, MCAO rats exhibited increased mRNA level of light-chain 3 (LC3) and the LC3II/LC3I ratio as well as decreased expression level of p-mTOR that reversed by hAMSC-CM (P 0.05). There were no significant differences in the expression of total mTOR among the experimental groups. In summary, our results demonstrate that hAMSC-CM gives rise to neuroprotection following ischemic stroke by restoring mTOR activity and inhibiting autophagy.
تدمد: 1873-6300
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d133a5df8b788f41f43fcc0e7ffda751
https://pubmed.ncbi.nlm.nih.gov/31672459
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....d133a5df8b788f41f43fcc0e7ffda751
قاعدة البيانات: OpenAIRE