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A thirteen week dietary toxicity study with 7-hydroxymatairesinol potassium acetate (HMRlignan) in rats

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Author: Lina, B. · Korte, H. · Nyman, L. · Unkila, M.
Institution: TNO Kwaliteit van Leven
Source:Regulatory Toxicology and Pharmacology, 1, 41, 28-38
Identifier: 238314
doi: doi:10.1016/j.yrtph.2004.09.001
Keywords: Toxicology Biology · Toxicology and Applied Pharmacology · 7-Hydroxymatairesinol · Enterolactone · Lignan · Safety · Sub-chronic · Toxicity · 7 hydroxyenterolactone · 7 hydroxymatairesinol potassium acetate · drug metabolite · enterolactone · lignan · matairesinol · phospholipid · triacylglycerol · unclassified drug · animal experiment · animal tissue · article · body weight · cholesterol blood level · chronic toxicity · cognition · controlled study · diet · dose response · drug blood level · estrus cycle · female · food intake · histopathology · kidney disease · leukocyte count · male · motor activity · nonhuman · ophthalmoscopy · organ weight · ovary · palatability · priority journal · rat · sex difference · thrombocyte count · toxicity testing · triacylglycerol blood level · weight reduction · 4-Butyrolactone · Animals · Body Weight · Diet · Female · Lignans · Male · Motor Activity · No-Observed-Adverse-Effect Level · Organ Size · Potassium Acetate · Rats · Rats, Wistar · Mammalia · Rattus norvegicus


Plant lignan 7-hydroxymatairesinol (7-HMR) is a novel precursor of the mammalian lignan enterolactone. A 13 week toxicity study at dietary levels of 0, 0.25, 1, and 4% (w/w) of potassium acetate complex of 7-HMR (HMRlignan) was conducted in the Wistar rat. These dietary levels resulted in an average daily intake of 160, 640, and 2600 mg HMRlignan/kg body weight/day, respectively. A considerable systemic exposure of HMRlignan was verified by dose-related increases in plasma total (conjugated and unconjugated) concentration of 7-HMR and metabolites enterolactone, 7-hydroxyenterolactone, and matairesinol. Enterolactone appeared to be the major metabolite. Most (>96%) of the circulating 7-HMR and enterolactone was in conjugated form as measured from the low-dose rat plasma samples. HMRlignan exposure did not significantly affect clinical signs, ophthalmoscopy or neurobehavioural observations, and motor activity. Transient reductions in food intake and body weight gain in the mid-and high-dose group were ascribed to decreased palatability of the test feed. Only in males of the high-dose group the body weights remained slightly reduced throughout the study. In the high-dose group the number of thrombocytes (females), and total white blood cell count (males) were increased. Plasma triglycerides were dose-dependently depressed in males of all test groups and in females of the mid- and high-dose group, while plasma total cholesterol, and phospholipids were decreased in high-dose males. These changes, which have also been reported for other (flaxseed) lignans, were not considered to represent adverse effects. The relative weight of the kidneys was increased in males of the high-dose group. The weight of the full and empty caecum showed dose-related increases in males of all treatment groups and in females of the high-dose group. Absolute ovary weights were decreased in all treatment groups while decreases in relative ovary weights were confined to the mid- and high-dose group. In addition, a marginal lengthening of the estrus cycle was noted in high-dose females. Apart from prevention of hyaline droplet nephropathy in all high-dose male rats, there were no treatment-related histopathological alterations. It was concluded that HMRlignan showed weak antiestrogen-like activity which may be mediated through enterolactone metabolite. Based on declined ovary weight, the no observed adverse effect level of HMRlignan was set at 0.25% in feed corresponding to 160 mg/kg body weight/day. © 2004 Elsevier Inc. All rights reserved.