INTERNATIONAL PROGRAMME ON CHEMICAL SAFETY WORLD HEALTH ORGANIZATION SUMMARY OF TOXICOLOGICAL DATA OF CERTAIN FOOD ADDITIVES AND CONTAMINANTS WHO FOOD ADDITIVES SERIES NO. 13 The data contained in this document were examined by the Joint FAO/WHO Expert Committee on Food Additives* Rome, 3-12 April 1978 Food and Agriculture Organization of the United Nations World Health Organization * Twenty-second Report of the Joint FAO/WHO Expert Committee on Food Additives, Geneva, 1978, WHO Technical Report Series No. 631 TURMERIC/CURCUMIN Explanation These compounds have been evaluated for acceptable daily intake by the Joint FAO/WHO Expert Committee on Food Additives in 1974. Since the previous evaluation additional data have become available and are summarized below. BIOLOGICAL DATA BIOCHEMICAL ASPECTS Curcumin at 0.1% in the diet lowered the serum and liver cholesterol levels of rats fed cholesterol at 1% in their diet for seven weeks. Faecal output of bile acids was increased in rats fed curcumin with or without added cholesterol. Cholesterol excretion was also enhanced by feeding curcumin (Rao et al., 1970). TOXICOLOGICAL STUDIES Acute toxicity No data available. Short-term studies Dog Two dogs were fed for one year on a diet containing approximately 1% commercial turmeric. No adverse effects were noted compared with two controls (Truhaut, 1958). Long-term studies Rat Groups of 20 male and 20 female rats were fed for 420 days on a diet containing 0.5% of commercial turmeric with a control group of 15 males and 15 females. The average life span of test animals was 16-1/2 months compared with 17 months of the controls. Growth, haematology or reproductive function were undisturbed as well as survival of the pups. Passive congestion of the liver was seen equally in test and control animals. No tumours were found. A follow-up of the first filial generation for their life span showed no abnormalities except for one benign tumour in a female rat (Truhaut, 1958). Special studies Pharmacology "In vitro" lipid peroxidation of rat brain preparations showed 95% inhibition in the presence of 5.15 × 10-3 M curcumin (Sharma, 1976). Mutagenicity Extracts of curcumin prepared by crushing the rhyzomes of curcumin, and diluting the extract with water caused abnormalities in the metaphase stage of division of root tip cells of Alluim cepa. The predominant type of aberration produced was chromosome breakage. In addition, other effects observed included C-mitosis, somatic segregations, binucleate cells and multipolar anophases (Abraham et al., 1976). "In vitro" cell toxicity Studies on the effect of alcoholic extracts of turmeric on mammalian cells "in vitro", using cells of the Chinese hamster (Cencetulus griseus), cell line Don of the cactus mouse (Peromyseus eremicus) and of the Indian munja (Muntiacus muntjac), and short-term human lymphocyte cultures, showed changes in chromosome morphology (chromatid separation, breakage and disintegration), as well as mitotic arrest. The incorporation of labelled nuclosides into Chinese hamster cells was greatly inhibited by concentrations of the turmeric extract that did not cause detectable changes in chromosome morphology (Goodpasture and Arrighi, 1976). REFERENCES Abraham, S., Abraham, S. K. and Radhamany, G. (1976) Mutagenic potential of the condiments, ginger and turmeric, Cytologia (Tokyo), 41, 591-595 Goodpasture, C. E. and Arrighi, F. E. (1976) Effects of food seasonings on the cell cycle and chromosome morphology of mammalian cells in vitro with special reference to turmeric, Food Cosmet. Toxicol., 14, 9-14 Rao, D. S., Sekhara, N. C., Satyanarayana, M. N. and Srinivasan, M. (1970) Effect of curcumin on serum and liver cholesterol levels in the rat, J. Nutr., 100, 1307-1315 Sharma, O. P. (1976) Antioxidant activity of curcumin and related compounds, Biochem. Pharmacol., 25, 1811-1812 Truhaut, R. (1958) Resultats des experiences de toxicité à long terme effectuées avec les colorants d'origine naturelle, le curcuma et l'orseille. C.R. on 18ème Congrès de la Federation internationale de Pharmacologie, 8-15 September, 1978
See Also: Toxicological Abbreviations