Determining NOEL/NOAEL in Repeated-dose Toxicity Studies, When the Low Dose Group Shows Significant Difference in Quantitative Data.
10.5625/lar.2010.26.2.133
- Author:
Katsumi KOBAYASHI
1
;
K Sadasivan PILLAI
;
Mathews MICHAEL
;
K M CHERIAN
;
Mariko OHNISHI
Author Information
1. National Institute of Technology and Evaluation (NITE), Tokyo, Japan. kobayashi-katsumi@nite.go.jp
- Publication Type:Original Article
- Keywords:
Repeated-dose toxicity study;
statistical significant difference;
rats;
low dose;
NOEL/NOAEL
- MeSH:
Animals;
Chemistry, Clinical;
Hematology;
Japan;
Jurisprudence;
No-Observed-Adverse-Effect Level;
Organ Size;
Rats;
Urinalysis
- From:Laboratory Animal Research
2010;26(2):133-137
- CountryRepublic of Korea
- Language:English
-
Abstract:
In repeated-dose 28-day oral toxicity study design, the low dose is fixed as the no observed effect level (NOEL). But, in practice the low dose usually shows significant difference in few measurable items in most of the studies. We investigated 109 of repeated-dose 28-day oral toxicity studies in rats conducted according to the Chemical Substance Control Law, Japan and examined the measurable items (functional observational battery, urinalysis, hematology, blood chemistry and absolute and relative organ weights) of the low dose group which showed a statistical significant difference (P<0.05) compared to the respective control groups. The investigation revealed that, 205/12,167 (1.6%) measurable items showed a significant difference in the low dose groups. The significant difference shown by urinalysis was high (3.3%), followed by clinical chemistry parameters, hematology, relative organ weights and absolute organ weights (1.8-1.1%). We conclude from the investigation that the low dose may be considered as NOEL, if the significant difference of measurable items of it is about 2% (maximum <5%), compared to the control. However, due consideration may be given to the clinical relevance of the items that showed a significant difference.
