Title of article
Safety evaluation of α-lipoic acid (ALA)
Author/Authors
Cremer، نويسنده , , D.R. and Rabeler، نويسنده , , R. and Roberts، نويسنده , , A. and Lynch، نويسنده , , B.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
13
From page
29
To page
41
Abstract
The safety of the antioxidant α-lipoic acid (racemic form) (ALA), also called thioctic acid (CAS RN 1077-28-7) was assessed in acute and subchronic toxicity studies as well as in in vitro and in vivo mutagenicity/genotoxicity studies. ALA was not acutely toxic to rats (LD50 > 2000 mg/kg bw, OECD method 425). Administration of 31.6 or 61.9 mg ALA/kg bw/day for 4 weeks to male/female Wistar rats did not show any adverse effects. Specifically, there was no significant difference between control and treated animals at 31.6 or 61.9 mg ALA/kg bw with regard to body weight gain, feed consumption, animal behaviour, or haematological and clinical chemistry parameters. Only the high-dose of 121 mg ALA/kg bw was associated with slight alterations in liver enzymes as well as histopathological effects on the liver and mammary gland. ALA did not possess any mutagenic activity in the Ames assays conducted with various bacterial strains of Salmonella typhimurium. Moreover, there was no evidence of genotoxic activity in a mouse micronucleus assay. The results of these studies support the safety of ALA. The no-observed-adverse-effect level (NOAEL) is considered to be 61.9 mg/kg bw/day.
Keywords
TOXICITY , Clastinogenicity , Mutagenicity , Subchronic , ?-Lipoic acid , Adverse , Thioctic acid , Ames , Micronucleus , 4-Week study , Safety , Acute
Journal title
Regulatory Toxicology and Pharmacology
Serial Year
2006
Journal title
Regulatory Toxicology and Pharmacology
Record number
1487878
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