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  1. Article ; Online: The impact of oleuropein on miRNAs regulating cell death signaling pathway in human cervical cancer cells.

    Amini-Farsani, Zeinab / Hashemi Sheikhshabani, Somayeh / Shaygan, Nasibeh / Asgharzade, Samira

    Biotechnology and applied biochemistry

    2023  Volume 71, Issue 1, Page(s) 61–71

    Abstract: Cervical cancer is known as the second most pervasive malignancy in women across the globe. The role played by microRNAs (miRNAs) in the initiation, progression, and metastasis of this cancer has received specific attention. The use of natural compounds ... ...

    Abstract Cervical cancer is known as the second most pervasive malignancy in women across the globe. The role played by microRNAs (miRNAs) in the initiation, progression, and metastasis of this cancer has received specific attention. The use of natural compounds leading cancer cells toward apoptosis is a feasible strategy for cancer therapy. Oleuropein, an olive-extracted phenolic substance, displays anticancer properties. Here, it was attempted to assess the role played by oleuropein in cell viability in cervical cancer and changes in the expression of some miRNAs associated with cervical cancer as well as some of their possible target genes selected using bioinformatics analysis. For this purpose, HeLa cell line was exposed to several oleuropein concentrations for 48 and 72 h. After that, 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide assay and flow cytometry were employed to assess cell viability and apoptosis, respectively. In addition, to conduct bioinformatics analysis, Cytoscape computer program was used based on STRING database. Furthermore, to examine the role played by oleuropein in the expression of miRNAs of interest as well as their potential target genes, real-time PCR was employed. The findings indicated that oleuropein reduced cell viability through inducing apoptosis. As a result of treatment with oleuropein, miR-34a, miR-125b, and miR-29a showed increased expression levels, whereas miR-181b, miR-221, and miR-16 showed decreased expression levels. Furthermore, oleuropein reduced the expression of the anti-apoptotic genes Bcl-2 and Mcl1, whereas it elevated the expression of the pro-apoptotic Bid, Fas, and TNFRSF10B genes and the p53 tumor suppressor. Our results indicate that the apoptosis induction is a mechanism of action of oleuropein in HeLa cells. Because of its effect on the reflation of the expression of genes and miRNAs effective in the pathogenesis of cervical cancer, oleuropein shows potential as an effective research tool for developing new natural drugs for treating cervical cancer.
    MeSH term(s) Humans ; Female ; MicroRNAs/metabolism ; HeLa Cells ; Uterine Cervical Neoplasms/drug therapy ; Uterine Cervical Neoplasms/genetics ; Uterine Cervical Neoplasms/pathology ; Apoptosis ; Cell Death ; Signal Transduction ; Cell Proliferation/genetics ; Gene Expression Regulation, Neoplastic ; Cell Line, Tumor ; Iridoid Glucosides
    Chemical Substances MicroRNAs ; oleuropein (2O4553545L) ; Iridoid Glucosides
    Language English
    Publishing date 2023-10-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 883433-7
    ISSN 1470-8744 ; 0885-4513
    ISSN (online) 1470-8744
    ISSN 0885-4513
    DOI 10.1002/bab.2521
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: MicroRNAs in Noise-Induced Hearing Loss and their Regulation by Oxidative Stress and Inflammation.

    Forouzanfar, Fatemeh / Asgharzade, Samira

    Current drug targets

    2020  Volume 21, Issue 12, Page(s) 1216–1224

    Abstract: Noise exposure (NE) has been recognized as one of the causes of sensorineural hearing loss (SNHL), which can bring about irreversible damage to sensory hair cells in the cochlea, through the launch of oxidative stress pathways and inflammation. ... ...

    Abstract Noise exposure (NE) has been recognized as one of the causes of sensorineural hearing loss (SNHL), which can bring about irreversible damage to sensory hair cells in the cochlea, through the launch of oxidative stress pathways and inflammation. Accordingly, determining the molecular mechanism involved in regulating hair cell apoptosis via NE is essential to prevent hair cell damage. However, the role of microRNAs (miRNAs) in the degeneration of sensory cells of the cochlea during NE has not been so far uncovered. Thus, the main purpose of this study was to demonstrate the regulatory role of miRNAs in the oxidative stress pathway and inflammation induced by NE. In this respect, articles related to noise-induced hearing loss (NIHL), oxidative stress, inflammation, and miRNA from various databases of Directory of Open Access Journals (DOAJ), Google Scholar, PubMed; Library, Information Science & Technology Abstracts (LISTA), and Web of Science were searched and retrieved. The findings revealed that several studies had suggested that up-regulation of miR-1229-5p, miR-451a, 185-5p, 186 and down-regulation of miRNA-96/182/183 and miR-30b were involved in oxidative stress and inflammation which could be used as biomarkers for NIHL. There was also a close relationship between NIHL and miRNAs, but further research is required to prove a causal association between miRNA alterations and NE, and also to determine miRNAs as biomarkers indicating responses to NE.
    MeSH term(s) Animals ; Apoptosis/genetics ; Gene Expression Regulation ; Hearing Loss, Noise-Induced/genetics ; Hearing Loss, Noise-Induced/metabolism ; Humans ; Inflammation/genetics ; Inflammation/metabolism ; MicroRNAs/biosynthesis ; MicroRNAs/genetics ; Oxidative Stress/genetics
    Chemical Substances MicroRNAs
    Language English
    Publishing date 2020-06-11
    Publishing country United Arab Emirates
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2064859-5
    ISSN 1873-5592 ; 1389-4501
    ISSN (online) 1873-5592
    ISSN 1389-4501
    DOI 10.2174/1389450121666200615145552
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Regenerative Medicine Approaches in COVID-19 Pneumonia.

    Asgharzade, Samira / Alizadeh, Akram / Arab, Samaneh

    Current stem cell research & therapy

    2021  Volume 16, Issue 6, Page(s) 647–655

    Abstract: Regenerative medicine (RM) is an interdisciplinary field that uses different approaches to accelerate the repair and regeneration or replace damaged or diseased human cells or tissues to achieve normal tissue function. These approaches include the ... ...

    Abstract Regenerative medicine (RM) is an interdisciplinary field that uses different approaches to accelerate the repair and regeneration or replace damaged or diseased human cells or tissues to achieve normal tissue function. These approaches include the stimulation of the body's own repair processes, transplantation of progenitor cells, stem cells, or tissues, as well as the use of cells and exosomes as delivery-vehicles for cytokines, genes, or other therapeutic agents. COVID-19 pneumonia is a specific disease consistent with diffuse alveolar damage resulting in severe hypoxemia. Therefore, the most serious cause of death from COVID-19 is lung dysfunction. Here, we consider RM approaches to cure COVID-19 pneumonia based on what RM has so far used to treat lung diseases, injuries, or pneumonia induced by other pathogens. These approaches include stem and progenitor cell transplantation, stem cell-derived exosomes, and microRNAs therapy.
    MeSH term(s) COVID-19/therapy ; Exosomes ; Humans ; Mesenchymal Stem Cells ; MicroRNAs/therapeutic use ; Pneumonia/therapy ; Regenerative Medicine ; SARS-CoV-2 ; Stem Cell Transplantation
    Chemical Substances MicroRNAs
    Language English
    Publishing date 2021-01-12
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 2251937-3
    ISSN 2212-3946 ; 1574-888X
    ISSN (online) 2212-3946
    ISSN 1574-888X
    DOI 10.2174/1574888X16999210112205826
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: MIR96 Has Good Potential to Differentiate Human Bone Marrow-Derived Mesenchymal Stem Cells into Photoreceptor-Like Cells.

    Mahmoudian-Sani, Mohammad-Reza / Fattahi, Najmeh / Hashemzadeh Chaleshtori, Morteza / Asgharzade, Samira

    Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation

    2023  Volume 22, Issue 2, Page(s) 148–155

    Abstract: Objectives: MicroRNAs play an important role in the development and function of neuron cells. Among these, the miRNA known as MIR96 is abundantly expressed in mammalian retina and significantly affects differentiation, maturation, and survival of human ... ...

    Abstract Objectives: MicroRNAs play an important role in the development and function of neuron cells. Among these, the miRNA known as MIR96 is abundantly expressed in mammalian retina and significantly affects differentiation, maturation, and survival of human photoreceptor cells. In this study, a mimic to miRNA-96 was transfected into human bone marrowderived mesenchymal stem cells to explore the biological functions of MIR96 at differentiation processing.
    Materials and methods: A mimic to miRNA-96 and a competitive control were transfected into human bone marrow-derived mesenchymal stem cells using Lipofectamine. After 24 and 48 hours, we evaluated changes in expression levels of genes associated with neural progenitor and photoreceptor differentiation (OTX2, NRL, protein kinase C, SLC1A1, and recoverin) by real-time polymerase chain reaction. In addition, we measured expression of mRNA and protein of the CRX gene (neuroretinal progenitor cell marker) and the RHO gene (terminal differentiation marker) using real-time polymerase chain reaction and immunocytochemistry, respectively.
    Results: Real-time polymerase chain reaction results showed increased levels of RHO and recoverin mRNA after 24 hours in transfected cells. In addition, mRNA levels of OTX2, CRX, NRL, RHO, recoverin, and protein kinase C increased after 48 hours in transfected cells. Immunocytochemistry results confirmed these findings by demonstrating RHO and CRX at both 24 and 48 hours in transfected cells.
    Conclusions: Control of the expression of MIR96 can be a good strategy to promote cell differentiation and can be used in cell therapy for retinal degeneration. Our results showed that human bone marrow-derived mesenchymal stem cells can differentiate into photoreceptor cells after transfection with MIR96. These results support therapeutic use of MIR96 in retinal degeneration and suggest human bone marrowderived mesenchymal stem cells as a promising tool for interventions.
    MeSH term(s) Animals ; Humans ; Retinal Degeneration/metabolism ; Recoverin/metabolism ; Bone Marrow/metabolism ; Photoreceptor Cells/metabolism ; Cell Differentiation ; Mesenchymal Stem Cells/metabolism ; MicroRNAs/genetics ; MicroRNAs/metabolism ; RNA, Messenger/genetics ; Protein Kinase C/metabolism ; Mammals/genetics ; Mammals/metabolism
    Chemical Substances Recoverin (135844-11-0) ; MicroRNAs ; RNA, Messenger ; Protein Kinase C (EC 2.7.11.13) ; MIRN96 microRNA, human
    Language English
    Publishing date 2023-10-28
    Publishing country Turkey
    Document type Journal Article
    ZDB-ID 2396778-X
    ISSN 2146-8427 ; 1304-0855
    ISSN (online) 2146-8427
    ISSN 1304-0855
    DOI 10.6002/ect.2023.0300
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Neuroprotective effect of herniarin following transient focal cerebral ischemia in rats.

    Asgharzade, Samira / Khorrami, Mohammad Bagher / Forouzanfar, Fatemeh

    Metabolic brain disease

    2021  Volume 36, Issue 8, Page(s) 2505–2510

    Abstract: Ischemic stroke is a devastating central nervous disease. Despite extensive research in to this area, few innovative neuroprotective treatments have been presented. 7-methoxycoumarin, also known as herniarin, is a common natural coumarin in several plant ...

    Abstract Ischemic stroke is a devastating central nervous disease. Despite extensive research in to this area, few innovative neuroprotective treatments have been presented. 7-methoxycoumarin, also known as herniarin, is a common natural coumarin in several plant species. This project examined the effects of the herniarin in rats subjected to the middle cerebral artery occlusion (MCAO). Herniarin at doses of 10 and 20 mg/kg was administered through intraperitoneal injection for 7 days before MCAO induction. Rats were subjected to a 30 min MCAO and a subsequent 24 h' reperfusion. 24 h after the termination of MCAO, neurologic outcome, volume of brain infarction, level of interleukin-1β (IL-1β) and tumor necrosis factor alpha (TNF-α), as inflammatory markers, and oxidative stress markers including levels of total thiol, malondialdehyde (MDA), and superoxide dismutase (SOD) activity were estimated. Herniarin administration decreased the MCAO-induced infarct volume and neurological deficits. Moreover, pretreatment with herniarin significantly decreased the levels of MDA while simultaneously increasing the level of total thiol and SOD activity in the brain tissues of MCAO rats. Moreover, herniarin pretreatment decreased the levels of IL-1β and TNF-α in the brain tissues of MCAO rats. These results suggest that herniarin presents beneficial effects against ischemic stroke, partly through the inhibition of oxidative stress and inflammation.
    MeSH term(s) Animals ; Brain Ischemia/drug therapy ; Brain Ischemia/pathology ; Disease Models, Animal ; Infarction, Middle Cerebral Artery/drug therapy ; Infarction, Middle Cerebral Artery/pathology ; Ischemic Attack, Transient/drug therapy ; Neuroprotective Agents/pharmacology ; Neuroprotective Agents/therapeutic use ; Oxidative Stress ; Rats ; Reperfusion Injury/drug therapy ; Umbelliferones/pharmacology
    Chemical Substances Neuroprotective Agents ; Umbelliferones ; herniarin (531-59-9)
    Language English
    Publishing date 2021-09-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632824-6
    ISSN 1573-7365 ; 0885-7490
    ISSN (online) 1573-7365
    ISSN 0885-7490
    DOI 10.1007/s11011-021-00841-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Tumor-resident adenosine-producing mesenchymal stem cells as a potential target for cancer treatment.

    Arab, Samaneh / Alizadeh, Akram / Asgharzade, Samira

    Clinical and experimental medicine

    2021  Volume 21, Issue 2, Page(s) 205–213

    Abstract: The development of new therapies based on tumor biology is one of the main topics in cancer treatment. In this regard, investigating the microenvironment and cellular composition of the tumor is of particular interest. Mesenchymal stem cells (MSCs) are a ...

    Abstract The development of new therapies based on tumor biology is one of the main topics in cancer treatment. In this regard, investigating the microenvironment and cellular composition of the tumor is of particular interest. Mesenchymal stem cells (MSCs) are a major group of cells in the tumor tissue and play a critical role in tumor growth and development. Investigating the mechanisms by which MSCs influence tumor growth and progression is very useful in establishing new therapeutic approaches. MSCs have some immunological capacities, including anti-inflammatory, immune-regulatory, and immune-suppressive abilities, which help the tumor growth in the inflammatory condition. They can suppress the proliferation and activation of CD4 + T cells and direct them toward the regulatory phenotype through the release of some factors such as indoleamine 2,3-dioxygenase, prostaglandin E2, and HO-1, PD-1 ligands (PD-L1 and PD-L2) and promote tolerance and apoptosis. Besides, these cells are able to produce adenosine. Adenosine has a key role in controlling the immune system by signaling through receptors located on the surface of immune cells. It plays a very essential role in tumor growth and progression. In the present review, we investigate and introduce adenosine-producing mesenchymal stem cells as a potential target for cancer treatment.
    MeSH term(s) 5'-Nucleotidase/antagonists & inhibitors ; Adenosine/physiology ; Humans ; Mesenchymal Stem Cells/drug effects ; Mesenchymal Stem Cells/physiology ; Neoplasms/drug therapy ; Neoplasms/etiology ; Tumor Microenvironment
    Chemical Substances 5'-Nucleotidase (EC 3.1.3.5) ; Adenosine (K72T3FS567)
    Language English
    Publishing date 2021-01-23
    Publishing country Italy
    Document type Journal Article ; Review
    ZDB-ID 2053018-3
    ISSN 1591-9528 ; 1591-8890
    ISSN (online) 1591-9528
    ISSN 1591-8890
    DOI 10.1007/s10238-020-00674-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The impact of miR-183/182/96 gene regulation on the maturation, survival, and function of photoreceptor cells in the retina.

    Amini-Farsani, Zeinab / Asgharzade, Samira

    The Journal of comparative neurology

    2019  Volume 528, Issue 9, Page(s) 1616–1625

    Abstract: MicroRNAs (MiRNAs) play important roles in posttranscriptional processes to regulate gene expression. MiRNAs control various biological processes, such as growth, development, and differentiation. The continuous physiological function of photoreceptors ... ...

    Abstract MicroRNAs (MiRNAs) play important roles in posttranscriptional processes to regulate gene expression. MiRNAs control various biological processes, such as growth, development, and differentiation. The continuous physiological function of photoreceptors and retinal pigment epithelium requires precise regulation to maintain their homeostasis and function; hence, these cells are highly susceptible to premature death in retinal degenerative disorders. MiRNAs are essential for the retinal cell maturation and function; the miR-183 cluster represents one of the most important regulatory factors for the photoreceptor cells. Various studies together with bioinformatics analyses have shown that many genes contributing to the differentiation pathway of photoreceptors are targets of the miR-183 cluster, and the miR-183 cluster dysregulation causes certain defects in the differentiation of the photoreceptors and other retinal neurons by influencing the expression of target genes. Misexpression of miR-183 cluster in the human retinal epithelial cells leads to the reprogramming and transformation of these cells to neuron- and photoreceptor-like cells, which are associated with the expression of neuron- and photoreceptor-specific markers in human retinal pigment epitheliums cells. The knockout of this cluster causes the destruction of the outer segment of the photoreceptors, which subsequently causes the cells to exhibit severe susceptibility to light and eventually degenerate. Hundreds of target genes in this family are likely to affect the development and maintenance of the retina. Identifying the genes that are regulated by the miRNA-183 cluster provides researchers with important insights into the complex development and regeneration mechanism of the retina and may offer a new way for maintaining and regenerating photoreceptor cells in neurodegenerative diseases.
    MeSH term(s) Animals ; Cell Differentiation/genetics ; Cell Survival/genetics ; Gene Expression Regulation ; Humans ; MicroRNAs ; Photoreceptor Cells, Vertebrate/cytology ; Photoreceptor Cells, Vertebrate/metabolism
    Chemical Substances MIRN183 microRNA, human ; MIRN96 microRNA, human ; MicroRNAs ; Mirn182 microRNA, human
    Language English
    Publishing date 2019-12-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 3086-7
    ISSN 1096-9861 ; 0021-9967 ; 0092-7317
    ISSN (online) 1096-9861
    ISSN 0021-9967 ; 0092-7317
    DOI 10.1002/cne.24833
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A Review on Stem Cell Therapy for Neuropathic Pain.

    Asgharzade, Samira / Talaei, Andisheh / Farkhondeh, Tahereh / Forouzanfar, Fatemeh

    Current stem cell research & therapy

    2020  Volume 15, Issue 4, Page(s) 349–361

    Abstract: Neuropathic pain is a complex, chronic pain state that is heterogeneous in nature and caused by the consequence of a lesion or disease affecting the somatosensory system. Current medications give a long-lasting pain relief only in a limited percentage of ...

    Abstract Neuropathic pain is a complex, chronic pain state that is heterogeneous in nature and caused by the consequence of a lesion or disease affecting the somatosensory system. Current medications give a long-lasting pain relief only in a limited percentage of patients also associated with numerous side effects. Stem cell transplantation is one of the attractive therapeutic platforms for the treatment of a variety of diseases, such as neuropathic pain. Here, the authors review the therapeutic effects of stem cell transplantation of different origin and species in different models of neuropathic pain disorders. Stem cell transplantation could alleviate the neuropathic pain; indeed, stem cells are the source of cells, which differentiate into a variety of cell types and lead trophic factors to migrate to the lesion site opposing the effects of damage. In conclusion, this review suggests that stem cell therapy can be a novel approach for the treatment of neuropathic pain.
    MeSH term(s) Animals ; Cell- and Tissue-Based Therapy/methods ; Chronic Pain/therapy ; Humans ; Neuralgia/drug therapy ; Neuralgia/pathology ; Pain Management ; Stem Cell Transplantation ; Stem Cells/cytology
    Language English
    Publishing date 2020-02-13
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 2251937-3
    ISSN 2212-3946 ; 1574-888X
    ISSN (online) 2212-3946
    ISSN 1574-888X
    DOI 10.2174/1574888X15666200214112908
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Combining Growth Factor and Stem Cell Therapy for Stroke Rehabilitation, A Review.

    Asgharzade, Samira / Talaei, Andisheh / Farkhondeh, Tahereh / Forouzanfar, Fatemeh

    Current drug targets

    2020  Volume 21, Issue 8, Page(s) 781–791

    Abstract: Stroke is a serious, life-threatening condition demanding vigorous search for new therapies. Recent research has focused on stem cell-based therapies as a viable choice following ischemic stroke, based on studies displaying that stem cells transplanted ... ...

    Abstract Stroke is a serious, life-threatening condition demanding vigorous search for new therapies. Recent research has focused on stem cell-based therapies as a viable choice following ischemic stroke, based on studies displaying that stem cells transplanted to the brain not only survive but also cause functional recovery. Growth factors defined as polypeptides that regulate the growth and differentiation of many cell types. Many studies have demonstrated that combined use of growth factors may increase results by the stimulation of endogenous neurogenesis, anti-inflammatory, neuroprotection properties, and enhancement of stem cell survival rates and so may be more effective than a single stem cell therapy. This paper reviews and discusses the most promising new stroke recovery research, including combination treatment.
    MeSH term(s) Animals ; Drug Therapy, Combination ; Humans ; Intercellular Signaling Peptides and Proteins/pharmacology ; Intercellular Signaling Peptides and Proteins/therapeutic use ; Stem Cell Transplantation ; Stem Cells/physiology ; Stroke/etiology ; Stroke/therapy ; Stroke Rehabilitation/methods
    Chemical Substances Intercellular Signaling Peptides and Proteins
    Language English
    Publishing date 2020-01-04
    Publishing country United Arab Emirates
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2064859-5
    ISSN 1873-5592 ; 1389-4501
    ISSN (online) 1873-5592
    ISSN 1389-4501
    DOI 10.2174/1389450121666200107100747
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Protective Effect of Capparis spinosa Extract against Focal Cerebral Ischemia-reperfusion Injury in Rats.

    Rakhshandeh, Hassan / Asgharzade, Samira / Khorrami, Mohammad Bagher / Forouzanfar, Fatemeh

    Central nervous system agents in medicinal chemistry

    2021  Volume 21, Issue 2, Page(s) 148–153

    Abstract: Background: Ischemic stroke is a serious public health problem. Despite extensive researches focusing on the area, little is known about novel treatments.: Objective: In this study, we aimed to investigate the effects of Capparis spinosa (C. spinosa) ...

    Abstract Background: Ischemic stroke is a serious public health problem. Despite extensive researches focusing on the area, little is known about novel treatments.
    Objective: In this study, we aimed to investigate the effects of Capparis spinosa (C. spinosa) extract in the middle cerebral artery occlusion (MCAO) model of ischemic stroke.
    Methods: Wistar rats underwent 30-min MCAO-induced brain ischemia followed by 24 h of reperfusion. C. spinose was administrated orally once a day for 7 days before the induction of MCAO. The neurologic outcome, infarct volume (TTC staining), histological examination, and markers of oxidative stress, including total thiol content, and malondialdehyde (MDA) levels, were measured 24hr. after the termination of MCAO.
    Results: Pretreatment with C. spinosa reduced neurological deficit score, histopathological alterations, and infarct volume in treated groups compared to the stroke group. Furthermore, pretreatment with C. spinosa extract significantly reduced the level of MDA with concomitant increases in the levels of thiol in the brain tissues compared to the stroke group.
    Conclusion: Our study demonstrates that C. spinosa extract effectively protects MCAO injury through the attenuation or the suppression of the oxidative stress.
    MeSH term(s) Animals ; Capparis ; Plant Extracts/therapeutic use ; Rats ; Rats, Wistar ; Reperfusion ; Reperfusion Injury/drug therapy
    Chemical Substances Plant Extracts
    Language English
    Publishing date 2021-06-27
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 2227560-5
    ISSN 1875-6166 ; 1871-5249
    ISSN (online) 1875-6166
    ISSN 1871-5249
    DOI 10.2174/1871524921666210625112356
    Database MEDical Literature Analysis and Retrieval System OnLINE

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