The possible neuroprotective effects of GLP-1 agonists on experimentally induced alzheimer’s disease in mice / (Record no. 176093)

MARC details
000 -LEADER
fixed length control field 05134namaa22004331i 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GICUC
005 - أخر تعامل مع التسجيلة
control field 20251225115313.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 251122s2025 ua a|||frm||| 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloguing agency EG-GICUC
Language of cataloging eng
Transcribing agency EG-GICUC
Modifying agency EG-GICUC
Description conventions rda
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract eng
-- ara
049 ## - Acquisition Source
Acquisition Source Deposit
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 615.78
092 ## - LOCALLY ASSIGNED DEWEY CALL NUMBER (OCLC)
Classification number 615.78
Edition number 21
097 ## - Degree
Degree Ph.D
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Local Call Number Cai01.08.09.Ph.D.2025.No.P
100 0# - MAIN ENTRY--PERSONAL NAME
Authority record control number or standard number Norhan Nabil Mohammed El-Badawy,
Preparation preparation.
245 14 - TITLE STATEMENT
Title The possible neuroprotective effects of GLP-1 agonists on experimentally induced alzheimer’s disease in mice /
Statement of responsibility, etc. by Norhan Nabil Mohammed El-Badawy ; Supervision of Prof. Dr. Noha Fawzy Abdelkader, Prof. Dr. Maha Ali Eissa Ahmed.
246 ## - VARYING FORM OF TITLE
Title proper/short title التأثيرات المحتملة الواقية للأعصاب لمستضادات جي إل بي-1 فى مرض الزهايمر المحدث تجريبياً فى الفئران
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 2025.
300 ## - PHYSICAL DESCRIPTION
Extent 121 pages :
Other physical details illustrations ;
Dimensions 25 cm. +
Accompanying material CD.
336 ## - CONTENT TYPE
Content type term text
Source rda content
337 ## - MEDIA TYPE
Media type term Unmediated
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term volume
Source rdacarrier
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Ph.D)-Cairo University, 2025.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Bibliography: pages 94-121.
520 #3 - SUMMARY, ETC.
Summary, etc. Tau hyper-phosphorylation has been recognized as an essential contributor to neurodegeneration in Alzheimer’s disease (AD) and related tauopathies. In the last decade, tau hyper-phosphorylation has gained considerable concern in AD therapeutic development. Tauopathies are manifested with a broad spectrum of symptoms, from dementia to cognitive decline and motor impairments. Tau undergoes conformational changes and abnormal phosphorylation that mediate its detaching from microtubules, forming neurofibrillary tangles (NFTs). In the current study, a widely used P301S transgenic mice model of tauopathy was employed to evaluate the possible neuroprotective effects of semaglutide as an autophagy regulator through modifications of the brain renin-angiotensin system (RAS). Mice were divided into two groups according to their genotypes (wild type (Wt) and P301S), which were further subdivided to receive either vehicle (saline) or semaglutide (25 nmol/kg, i.p.), once every 2 days for 28 days. Current data suggest that semaglutide ameliorated the hyperactive pattern and alleviated the cognitive decline of P301S mice. It also hastened the autophagic flux through augmenting angiotensin-converting enzyme 2/sirtuin 1/forkhead box protein O1 signaling. Semaglutide also hindered the expression of phosphorylated adenosine monophosphate-activated protein kinase and phosphorylated glycogen synthase kinase-3 beta at serine 9, reducing the propagation of neuroinflammatory cytokines and oxidative reactions. Finally, semaglutide protected against hippocampal degeneration and reduced the immunoreactivity for total tau and ionized calcium-binding adapter molecule. Semaglutide showed promising neuroprotective implications in alleviating tauopathy-related AD’s molecular and behavioral deficits through controlling autophagy and brain RAS.
520 #3 - SUMMARY, ETC.
Summary, etc. إن مرض الزهايمر هو أكثر أنواع التاوبيات انتشارا حيث يتميز بفقدان الخلايا العصبية وضمور الدماغ الشديد مما يؤدي إلى ظهور الخرف والعيوب الإدراكية. إن تراكم رواسب البروتين (أميلويد-بيتا و التاو) هو السمة المرضية المميزة لمرض الزهايمر. وتكمن عيوب الأدوية التقليدية المعتمدة لعلاج مرض الزهايمر في تخفيف الأعراض بشكل محدود وعدم قدرتها على معالجة السبب الفعلي أو تثبيط تقدم المرض. كما أن فشل الأدوية المضادة للأميلويد قد أبرز الحاجة إلى تطوير تدخلات علاجية جديدة تركز على علم الأمراض الناتج عن بروتين التاو لإعاقة أو تأجيل ظهور الخرف. إن نموذج الفئران بى 301 اس (P301S) يُستخدم على نطاق واسع لإعادة تجسيد أمراض التاو المرتبطة بمرض الزهايمر، وبالتالي تيسير إمكانية فهم ودمج خطوط علاجية جديدة تستهدف بشكل خاص تجمعات التاو وتشابكات التاو بروتين العصبية.
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Issues CD Issues also as CD.
546 ## - LANGUAGE NOTE
Text Language Text in English and abstract in Arabic & English.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Drugs that affect the nervous system
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element الأدوية المؤثرة على الجهاز العصبى
653 #1 - INDEX TERM--UNCONTROLLED
Uncontrolled term Tauopathy
-- Alzheimer's disease
-- Semaglutide
-- Autophagy
-- ACE2/SIRT1/FOXO1
-- Microglia Polarization
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Noha Fawzy Abdelkader
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Maha Ali Eissa Ahmed
Relator term thesis advisor.
900 ## - Thesis Information
Grant date 01-01-2025
Supervisory body Noha Fawzy Abdelkader
-- Maha Ali Eissa Ahmed
Universities Cairo University
Faculties Faculty of Pharmacy
Department Department of Pharmacology & Toxicology
905 ## - Cataloger and Reviser Names
Cataloger Name Shimaa
Reviser Names Eman Ghareb
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Edition 21
Suppress in OPAC No
Holdings
Source of classification or shelving scheme Home library Current library Date acquired Inventory number Full call number Barcode Date last seen Effective from Koha item type
Dewey Decimal Classification المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 22.11.2025 92657 Cai01.08.09.Ph.D.2025.No.P 01010110092657000 22.11.2025 22.11.2025 Thesis
Cairo University Libraries Portal Implemented & Customized by: Eng. M. Mohamady Contacts: new-lib@cl.cu.edu.eg | cnul@cl.cu.edu.eg
CUCL logo CNUL logo
© All rights reserved — Cairo University Libraries
CUCL logo
Implemented & Customized by: Eng. M. Mohamady Contact: new-lib@cl.cu.edu.eg © All rights reserved — New Central Library
CNUL logo
Implemented & Customized by: Eng. M. Mohamady Contact: cnul@cl.cu.edu.eg © All rights reserved — Cairo National University Library