2011
DOI: 10.1615/intjmedmushr.v13.i6.20
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Developmental Toxicity Assessment of Medicinal Mushroom Antrodia cinnamomea T.T. Chang et W.N. Chou (Higher Basidiomycetes) Submerged Culture Mycelium in Rats

Abstract: Antrodia cinnamomea is a Taiwanese medicinal mushroom with high antioxidant and polysaccharide content. The objective of this study is to investigate developmental toxicity of A. cinnamomea in pregnant Sprague-Dawley rats. Animals were daily gavaged with A. cinnamomea mycelium at dosage levels of 0 (reverse osmosis water), 50, 150, and 500 mg/kg from gestation day (GD) 6 to 15. All dams were sacrificed on GD 20 and were subjected to cesarean section. Fetuses were examined for external, visceral, and skeletal a… Show more

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Cited by 12 publications
(7 citation statements)
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“…The lack of toxicity reported in previous studies might indicate that is safe for use as a functional food ingredient [33, 34]. However, the adverse events observed in patients treated with AC in our study were generally consistent with its known adverse event profile.…”
Section: Discussionsupporting
confidence: 86%
“…The lack of toxicity reported in previous studies might indicate that is safe for use as a functional food ingredient [33, 34]. However, the adverse events observed in patients treated with AC in our study were generally consistent with its known adverse event profile.…”
Section: Discussionsupporting
confidence: 86%
“…The fetal skeletal examination suggest that there was no LDAC (700⿿2800 mg/kg) treatment related abnormalities and LDAC related teratogenic toxicity. These data are well correlated with a previous study which reports that the mycelial extract of A. cinnamomea (50⿿500 mg/kg b.w) does not showed any teratogenic effects in female SD rats [4] . However, the highest oral dose of the present study was 5-fold higher than the previous report.…”
Section: Resultssupporting
confidence: 92%
“…These data are well correlated with a previous study which reports that the mycelial extract of A. cinnamomea (50-500 mg/kg b.w) does not showed any teratogenic effects in female SD rats. (Chen et al, 2011) However, the highest oral dose of the present study was 5-fold higher than the previous report.…”
Section: Reproductive and Developmental Toxicity Assessmentcontrasting
confidence: 76%