skip to main content
Guest
e-Shelf
My Account
Sign out
Sign in
This feature requires javascript
Tags
e-Journals
e-Books
Databases
USP Libraries
Help
Help
Language:
English
Spanish
Portuguese (Brazil)
This feature required javascript
This feature requires javascript
Primo Advanced Search
General Search
General Search
Physical Collection
Physical Collections
USP Intelectual Production
USP Production
Primo Advanced Search Query Term
Input search text:
Show Results with:
criteria input
Any
Show Results with:
Any
Primo Advanced Search prefilters
Material Type:
criteria input
All items
General Search
Simple Search
This feature requires javascript
Amelioration of cyclophosphamide-induced hepatotoxicity by the root extract of Decalepis hamiltonii in mice
Zarei, Mahsa ; Shivanandappa, T.
Food and chemical toxicology, 2013-07, Vol.57, p.179-184
[Peer Reviewed Journal]
Oxford: Elsevier Ltd
Full text available
Citations
Cited by
View Online
Details
Reviews & Tags
More
Times Cited
This feature requires javascript
Actions
Add to e-Shelf
Remove from e-Shelf
E-mail
Print
Permalink
Citation
EasyBib
EndNote
RefWorks
Delicious
Export RIS
Export BibTeX
This feature requires javascript
Title:
Amelioration of cyclophosphamide-induced hepatotoxicity by the root extract of Decalepis hamiltonii in mice
Author:
Zarei, Mahsa
;
Shivanandappa, T.
Subjects:
alanine
;
alanine transaminase
;
Alanine Transaminase - blood
;
Alanine Transaminase - genetics
;
Alanine Transaminase - metabolism
;
alkaline phosphatase
;
Alkaline Phosphatase - blood
;
Alkaline Phosphatase - genetics
;
Alkaline Phosphatase - metabolism
;
Animals
;
antioxidant activity
;
Antioxidant enzymes
;
antioxidants
;
Antioxidants - metabolism
;
Apocynaceae - chemistry
;
Aspartate
Aminotransferases
- blood
;
Aspartate
Aminotransferases
- genetics
;
Aspartate
Aminotransferases
- metabolism
;
aspartate
transaminase
;
Biological and medical sciences
;
blood serum
;
Carcinogenesis, carcinogens and anticarcinogens
;
catalase
;
Catalase - metabolism
;
Chemical agents
;
Cyclophosphamide
;
Cyclophosphamide - toxicity
;
Decalepis hamiltonii
;
drug
therapy
;
Enzymes - blood
;
Enzymes - genetics
;
Enzymes - metabolism
;
gene expression regulation
;
Gene Expression Regulation, Enzymologic -
drug
effects
;
genes
;
glutathione
;
glutathione peroxidase
;
Glutathione Peroxidase - metabolism
;
Glutathione Reductase - metabolism
;
glutathione transferase
;
Glutathione Transferase - metabolism
;
glutathione-disulfide reductase
;
Hepatotoxicity
;
lactate dehydrogenase
;
lipid peroxidation
;
Lipid Peroxidation - drug effects
;
liver
;
Liver - drug effects
;
Liver - pathology
;
Medical sciences
;
Mice
;
oxidative stress
;
Oxidative Stress - drug effects
;
Plant Extracts - pharmacology
;
Plant Roots - chemistry
;
Protective Agents - pharmacology
;
reactive oxygen species
;
roots
;
superoxide dismutase
;
Superoxide Dismutase - metabolism
;
Toxicology
;
Tumors
Is Part Of:
Food and chemical toxicology, 2013-07, Vol.57, p.179-184
Notes:
http://dx.doi.org/10.1016/j.fct.2013.03.028
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Description:
•The hepatoprotective potential of DHA against CP-induced liver damage.•DHA prevented the elevation of serum marker enzymes in CP-treated mice.•DHA enhanced the antioxidant defenses in the liver in vivo.•DHA inhibited down-regulation of antioxidant enzymes gene expressions. Hepatoprotective potential of the aqueous extract of the roots of Decalepis hamiltonii (DHA) against cyclophosphamide (CP)-induced oxidative stress has been investigated in mice. Administration of CP (25mg/kg b.w., i.p) for 10days induced hepatic damage as indicated by the serum marker enzymes aspartate and alanine transaminases (AST, ALT), alkaline phosphatase (ALP) and lactate dehydrogenase (LDH). Parallel to these changes CP induced oxidative stress in the liver as evident from the increased lipid peroxidation (LPO), reactive oxygen species (ROS), depletion of glutathione (GSH), and reduced activities of the antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), and glutathione-S-transferase (GST). Treatment with DHA (50 and 100mg/kg b.w., po) mitigated the CP-induced oxidative stress. Moreover, expression of genes for the antioxidant enzymes, were down-regulated by CP treatment which was reversed by DHA. Our study shows the DHA protected the liver from toxicity induced by CP and therefore, it could be serve as a safe medicinal supplement during cyclophosphamide chemotherapy.
Publisher:
Oxford: Elsevier Ltd
Language:
English
Links
View record in Pascal Francis
View this record in MEDLINE/PubMed
This feature requires javascript
This feature requires javascript
Back to results list
Result
1
Next
This feature requires javascript
This feature requires javascript
Searching Remote Databases, Please Wait
Searching for
in
scope:(USP_VIDEOS),scope:("PRIMO"),scope:(USP_FISICO),scope:(USP_EREVISTAS),scope:(USP),scope:(USP_EBOOKS),scope:(USP_PRODUCAO),primo_central_multiple_fe
Show me what you have so far
This feature requires javascript
This feature requires javascript