Digital Library
Close Browse articles from a journal
 
<< previous    next >>
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
           All articles of the corresponding issues
                                       Details for article 6 of 145 found articles
 
 
  An Evaluation of Toxicity and Mutagenicity of Sphenocentrum jollyanum
 
 
Title: An Evaluation of Toxicity and Mutagenicity of Sphenocentrum jollyanum
Author: Amidu Nafiu
Woode Eric
Owiredu K.B.A. William
Asare A. George
Boateng A. Kofi
Opoku-Okrah Clement
Appeared in: International journal of pharmacology
Paging: Volume 4 (2008) nr. 2 pages 67-77
Year: 2008
Contents: This study was designed to evaluate the toxicity of S. jollyanum using Fischer 344 male rats and the genotoxic effect of the alcoholic extract of the roots. In experiment 1, haematological, serum biochemical and histopathological parameters were determined after 30, 60 and 90 days of oral administration. Experiment 2 involved determinations of total hepatic cytochrome P-450 content. Pentobarbitone induced sleeping times was measured in experiment 3. These are indices of organ specific toxicity or potential for drug interactions. The mutagenic potential was assessed by reverse mutation test using Salmonella typhimurium TA97, TA98, TA100 and TA102 tester strains in experiment 4. There were no significant differences found in most of the hematological, serum biochemical parameters and organ/body weight ratio. No abnormality of any organ was found during histopathological examination and no mutagenicity evidence was detected in any of the mutagenic tests. It, however, caused a significant increase in cytochrome P-450 which correlates well with the decreased pentobarbitone induced sleeping times. The results showed that the no-observed adverse- effect level (NOAEL) of S. jollyanum extract (SJE) was >1000 mg kg-1 body weight per day in rats, which can be regarded as virtually non-toxic. In conclusion, SJE had no overt organ specific toxicity but demonstrates a potential for drug interactions via cytochrome P-450-mediated metabolism in the rat.
Publisher: Asian Network for Scientific Information (provided by DOAJ)
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 6 of 145 found articles
 
<< previous    next >>
 
 Koninklijke Bibliotheek - National Library of the Netherlands