Literature DB >> 15019182

Toxicological evaluation of the ethanolic extract of Artemisia dracunculus L. for use as a dietary supplement and in functional foods.

David M Ribnicky1, Alexander Poulev, Joseph O'Neal, Gary Wnorowski, Dolores E Malek, Ralf Jäger, Ilya Raskin.   

Abstract

TARRALIN is an ethanolic extract of Artemisia dracunculus (Russian tarragon), a common medicinal and culinary herb with centuries of use. Artemisia dracunculus is a close relative of the French or cooking tarragon and contains components common to many herbs that are routinely consumed without reported adverse effects. Since safety information of Artemisia dracunculus and its extract is limited to historical use, TARRALIN was examined in a series of toxicological studies. Complete Ames analysis did not reveal any mutagenic activity either with or without metabolic activation. TARRALIN was tested in an acute limit test at 5000 mg/kg with no signs of toxicity noted. In a 14 day repeated dose oral toxicity study, rats appeared to well tolerate 1000 mg/kg/day. Subsequently, TARRALIN was tested in an oral subchronic 90-day toxicity study (rat) at doses of 10, 100 and 1000 mg/kg/day. No noteworthy signs of toxicity were noted in feeding or body weight, functional observational battery or motor activity. Gross necropsy and clinical chemistry did not reveal any effects on organ mass or blood chemistry and microscopic examinations found no lesions associated with treatment. Therefore, TARRALIN appears to be safe and non-toxic in these studies and a no-observed adverse effect level in rats is established at 1000 mg/kg/day.

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Year:  2004        PMID: 15019182     DOI: 10.1016/j.fct.2003.11.002

Source DB:  PubMed          Journal:  Food Chem Toxicol        ISSN: 0278-6915            Impact factor:   6.023


  13 in total

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2.  Artemisia dracunculus L. polyphenols complexed to soy protein show enhanced bioavailability and hypoglycemic activity in C57BL/6 mice.

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3.  Bioactives from Artemisia dracunculus L. enhance insulin sensitivity via modulation of skeletal muscle protein phosphorylation.

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4.  Evaluation of PMI-5011, an ethanolic extract of Artemisia dracunculus L., on peripheral neuropathy in streptozotocin-diabetic mice.

Authors:  Pierre Watcho; Roman Stavniichuk; Pierre Tane; Hanna Shevalye; Yury Maksimchyk; Pal Pacher; Irina G Obrosova
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5.  Qualitative variation of anti-diabetic compounds in different tarragon (Artemisia dracunculus L.) cytotypes.

Authors:  Sasha W Eisenman; Alexander Poulev; Lena Struwe; Ilya Raskin; David M Ribnicky
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6.  High-fat diet-induced neuropathy of prediabetes and obesity: effect of PMI-5011, an ethanolic extract of Artemisia dracunculus L.

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7.  Improved absorption and bioactivity of active compounds from an anti-diabetic extract of Artemisia dracunculus L.

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8.  Artemisia santolinifolia enhances glutamatergic neurotransmission in the nucleus of the solitary tract.

Authors:  Katie M Vance; David M Ribnicky; Richard C Rogers; Gerlinda E Hermann
Journal:  Neurosci Lett       Date:  2014-09-09       Impact factor: 3.046

9.  Molecular mechanisms for activation of the agouti-related protein and stimulation of appetite.

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Journal:  Diabetes       Date:  2010-10-27       Impact factor: 9.461

Review 10.  Methyl eugenol: its occurrence, distribution, and role in nature, especially in relation to insect behavior and pollination.

Authors:  Keng Hong Tan; Ritsuo Nishida
Journal:  J Insect Sci       Date:  2012       Impact factor: 1.857

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