Modulation of liver p‑glycoprotien expression may contribute to gossypin protection against methotrexate‑induced hepatotoxicity (Record no. 16879)

MARC details
000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220624101657.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220624b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 16776
Author Mohamed, Mervat
245 ## - TITLE STATEMENT
Title Modulation of liver p‑glycoprotien expression may contribute to gossypin protection against methotrexate‑induced hepatotoxicity
250 ## - EDITION STATEMENT
Volume, Issue number Vol.53(1), Jan-Feb
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Wolter Kluwer
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 25-30p.
520 ## - SUMMARY, ETC.
Summary, etc. OBJECTIVES: Methotrexate (MTX) is a broadly used anticancer. Its major side effect is hepatotoxicity.<br/>Gossypin is a flavonoid has a hepatoprotective effect as well as antitumor property. The study aimed<br/>at inspecting the protective effect of gossypin against MTX hepatotoxicity.<br/>MATERIALS AND METHODS: Twenty‑four adult male rats arranged into four groups (six rats each):<br/>control, gossypin control, MTX, and MTX+ gossypin. Animals were orally administered gossypin<br/>at 10 mg kg‑1 day‑1 for 7 days. MTX was injected i.p. (20 mg/kg‑1 once) on 5th day. Liver enzyme<br/>and oxidative stress markers were assessed. BAX, transforming growth factor‑beta (TGF‑β) gene<br/>expressions, and P‑glycoprotein (P‑gp) were assessed. The histopathological study as well as the<br/>immunohistochemical study for hepatic caspase 3 and nuclear factor kappa‑B (NFκ‑B) was done.<br/>RESULTS: MTX produced a significant increase of liver enzymes and distortion of hepatic architecture<br/>alongside with increased the hepatic collagen content. MTX administration significantly increased<br/>the oxidative stress markers and upregulated the pro‑apoptotic BAX and the pro‑fibrogenic TGF‑β.<br/>MTX increased caspase 3 and NFκ‑B expression, while diminished the expression of P‑gp. Gossypin<br/>pretreatment improved the previous parameters, restored the normal hepatic architecture, reduced<br/>the hepatic fibrosis, and regained nearly normal expressions for BAX, TGF‑β, caspase 3, and NFκ‑B.<br/>Gossypin caused more reduction in P‑gp hepatic expression.<br/>CONCLUSIONS: Gossypin may be a valuable adjuvant therapy that protects the liver against<br/>MTX toxicity through antioxidant, anti‑inflammatory, antiapoptotic mechanisms, and mediated P‑gp<br/>expression reduction.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4774
Topical term or geographic name entry element PHARMACOLOGY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 16777
Co-Author El Sheikh, Azza Kamal
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Andheri - Mumbai Wolters Kluwer India Private Limited
Title Indian Journal of Pharmacology
International Standard Serial Number 0253-7613
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijp-online.com/temp/IndianJPharmacol53125-1694899_044228.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 24/06/2022   2022-0856 24/06/2022 24/06/2022 Articles Abstract Database
Unique Visitors hit counter Total Page Views free counter
Implemented and Maintained by AIKTC-KRRC (Central Library).
For any Suggestions/Query Contact to library or Email: librarian@aiktc.ac.in | Ph:+91 22 27481247
Website/OPAC best viewed in Mozilla Browser in 1366X768 Resolution.