<i>beta Vulgaris</I> L. Var. Cicla Improves Memory Deficits in Intracerebroventricular Streptozotocin Injected Rats: Role on Neuroinflammation

dc.contributor.author Ertas, Busra
dc.contributor.author Topal, Fadime
dc.contributor.author Gulhan, Rezzan
dc.contributor.author Yanardag, Refiye
dc.contributor.author Sacan, Ozlem
dc.contributor.author Sener, Goksel
dc.contributor.other Eczacılık Meslek Bilimleri Bölümü
dc.date.accessioned 2025-01-11T13:01:30Z
dc.date.available 2025-01-11T13:01:30Z
dc.date.issued 2021
dc.description GULHAN AKER, REZZAN/0000-0002-1519-3170; Sener, Goksel/0000-0001-7444-6193; Topal, Fadime/0000-0002-0962-4106 en_US
dc.description.abstract Alzheimer's disease is a challenging disease for patients due to progressive loss of cognition and behavioral disorders. Disruption of cholinergic transmission and neuroinflammation are the most important mechanisms underlying cognitive damage. Beta vulgaris L. var. cicla (BV) has been reported to have various pharmacological effects associated with its rich antioxidant content. In addition, anti-cholinesterase and antiinflammatory activities of BV have been demonstrated in vitro. The aim of this study is to elucidate the therapeutic effect of BV against cognitive impairment, reduction in cholinergic transmission and neuroinflammation caused by intracerebroventricular (ICV) administration of streptozotocin (STZ). STZ was administered bilaterally at a dose of 3 mg/kg via ICV to rats, and BV treatment at a dose of 2 g/kg for 21 days was administered orally to STZ-induced animals. After behavioral tests, AChE activity, TNF-alpha and IL-1 beta levels were measured in hippocampus and cortex tissues excised from decapitated animals. Novel object recognition and passive avoidance test showed that the treatment of BV reverted the ICV-STZ induced memory dysfunctions in rats. Furthermore, increased AChE levels in the hippocampal and cortical tissues of STZ-induced rats were significantly reduced with 21 days of BV treatment. In conclusion, these results confirm that STZ administration caused cholinergic hypofunction, neuronal inflammation and cognitive dysfunction in rats, and BV therapy significantly inhibited these changes with its potential neuroprotective activity. en_US
dc.identifier.citation 5
dc.identifier.doi 10.29228/jrp.50
dc.identifier.issn 2630-6344
dc.identifier.scopus 2-s2.0-85115789258
dc.identifier.uri https://doi.org/10.29228/jrp.50
dc.identifier.uri https://hdl.handle.net/20.500.14627/129
dc.language.iso en en_US
dc.publisher Marmara Univ en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Alzheimer'S Disease en_US
dc.subject Beta Vulgaris L. Var. Cicla en_US
dc.subject Cholinergic Dysfunction en_US
dc.subject Neuroinflammation en_US
dc.subject Cognitive Function en_US
dc.title <i>beta Vulgaris</I> L. Var. Cicla Improves Memory Deficits in Intracerebroventricular Streptozotocin Injected Rats: Role on Neuroinflammation en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id GULHAN AKER, REZZAN/0000-0002-1519-3170
gdc.author.id Sener, Goksel/0000-0001-7444-6193
gdc.author.id Topal, Fadime/0000-0002-0962-4106
gdc.author.institutional Şener, Göksel
gdc.author.scopusid 57196052987
gdc.author.scopusid 57217165395
gdc.author.scopusid 6602704843
gdc.author.scopusid 6701546641
gdc.author.scopusid 8368813400
gdc.author.scopusid 55662834600
gdc.author.wosid Ertas, Busra/IQS-8337-2023
gdc.author.wosid GULHAN AKER, REZZAN/A-2995-2010
gdc.description.department Fenerbahçe University en_US
gdc.description.departmenttemp [Ertas, Busra; Topal, Fadime] Univ Marmara, Fac Pharm, Dept Pharmacol, Istanbul, Turkey; [Gulhan, Rezzan] Univ Marmara, Fac Med, Dept Pharmacol, Istanbul, Turkey; [Yanardag, Refiye; Sacan, Ozlem] Istanbul Univ Cerrahpasa, Fac Engn, Dept Chem, Istanbul, Turkey; [Sener, Goksel] Fenerbahce Univ, Vocat Sch Hlth Serv, Istanbul, Turkey en_US
gdc.description.endpage 599 en_US
gdc.description.issue 5 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 589 en_US
gdc.description.volume 25 en_US
gdc.description.woscitationindex Emerging Sources Citation Index
gdc.identifier.trdizinid 489625
gdc.identifier.wos WOS:000701782800007
gdc.scopus.citedcount 5
gdc.wos.citedcount 5
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