M. Hosney, Alaa Sakraan, Asaad, M., E. F., Emad Elzayat
{"title":"添加/不添加牛磺酸的脂肪源性间充质干细胞(ADMSCs)在氯化铝诱导的阿尔茨海默病大鼠模型中的治疗潜力","authors":"M. Hosney, Alaa Sakraan, Asaad, M., E. F., Emad Elzayat","doi":"10.21608/eajbsz.2022.262121","DOIUrl":null,"url":null,"abstract":"Alzheimer's (AD) of characterized by its progression, neurobehavioral and neuro-pathological characteristics. Adipose-derived mesenchymal stem cells (ADMSCs) have previously proved a potential role in preventing the pathogenesis of several neurodegenerative disorders, so it is regarded as a promising new approach for AD regenerative therapy. Taurine was found to enhance stem cell activation and propagation, yielding a higher concentration of neural progenitors and stem cells, and reducing the number of activated microglia leading to down-regulated inflammation in vitro . The present study aimed to investigate the possible therapeutic potential of ADMSCs with/without taurine in treating the AD rat model. It was planned to include three successive phases: induction, withdrawal, and therapeutic phases. Fifty male Wistar rats were divided into two main groups: control (C) and AD model. Behavioral changes, as manifested by the T-maze experiment, had been recorded. β - amyloid levels had been measured in brain homogenate and serum by ELISA. Oxidative stress marker (MDA), brain and serum antioxidant enzyme activities (SOD, GSH, and CAT) as well serum acetylcholine esterase activity were spectrophotometrically determined. Pro-apoptotic (p53 and Bax) and anti-apoptotic (Bcl2) gene expression in the brain were evaluated using RT-qPCR. The histopathological alterations in brain tissues were also observed.","PeriodicalId":34551,"journal":{"name":"Egyptian Academic Journal of Biological Sciences B Zoology","volume":"50 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Therapeutic Potential of Adipose-Derived Mesenchymal Stem Cells (ADMSCs) with/without Taurine in Aluminum Chloride-Induced Alzheimer's Disease Rat Model\",\"authors\":\"M. Hosney, Alaa Sakraan, Asaad, M., E. F., Emad Elzayat\",\"doi\":\"10.21608/eajbsz.2022.262121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Alzheimer's (AD) of characterized by its progression, neurobehavioral and neuro-pathological characteristics. Adipose-derived mesenchymal stem cells (ADMSCs) have previously proved a potential role in preventing the pathogenesis of several neurodegenerative disorders, so it is regarded as a promising new approach for AD regenerative therapy. Taurine was found to enhance stem cell activation and propagation, yielding a higher concentration of neural progenitors and stem cells, and reducing the number of activated microglia leading to down-regulated inflammation in vitro . The present study aimed to investigate the possible therapeutic potential of ADMSCs with/without taurine in treating the AD rat model. It was planned to include three successive phases: induction, withdrawal, and therapeutic phases. Fifty male Wistar rats were divided into two main groups: control (C) and AD model. Behavioral changes, as manifested by the T-maze experiment, had been recorded. β - amyloid levels had been measured in brain homogenate and serum by ELISA. Oxidative stress marker (MDA), brain and serum antioxidant enzyme activities (SOD, GSH, and CAT) as well serum acetylcholine esterase activity were spectrophotometrically determined. Pro-apoptotic (p53 and Bax) and anti-apoptotic (Bcl2) gene expression in the brain were evaluated using RT-qPCR. The histopathological alterations in brain tissues were also observed.\",\"PeriodicalId\":34551,\"journal\":{\"name\":\"Egyptian Academic Journal of Biological Sciences B Zoology\",\"volume\":\"50 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-10-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Egyptian Academic Journal of Biological Sciences B Zoology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/eajbsz.2022.262121\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Egyptian Academic Journal of Biological Sciences B Zoology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/eajbsz.2022.262121","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Therapeutic Potential of Adipose-Derived Mesenchymal Stem Cells (ADMSCs) with/without Taurine in Aluminum Chloride-Induced Alzheimer's Disease Rat Model
Alzheimer's (AD) of characterized by its progression, neurobehavioral and neuro-pathological characteristics. Adipose-derived mesenchymal stem cells (ADMSCs) have previously proved a potential role in preventing the pathogenesis of several neurodegenerative disorders, so it is regarded as a promising new approach for AD regenerative therapy. Taurine was found to enhance stem cell activation and propagation, yielding a higher concentration of neural progenitors and stem cells, and reducing the number of activated microglia leading to down-regulated inflammation in vitro . The present study aimed to investigate the possible therapeutic potential of ADMSCs with/without taurine in treating the AD rat model. It was planned to include three successive phases: induction, withdrawal, and therapeutic phases. Fifty male Wistar rats were divided into two main groups: control (C) and AD model. Behavioral changes, as manifested by the T-maze experiment, had been recorded. β - amyloid levels had been measured in brain homogenate and serum by ELISA. Oxidative stress marker (MDA), brain and serum antioxidant enzyme activities (SOD, GSH, and CAT) as well serum acetylcholine esterase activity were spectrophotometrically determined. Pro-apoptotic (p53 and Bax) and anti-apoptotic (Bcl2) gene expression in the brain were evaluated using RT-qPCR. The histopathological alterations in brain tissues were also observed.