safety assessment of osthole isolated from prangos ferulacea: acute and subchronic toxicities and modulation of cytochrome p450

background: osthole (7-methoxy-8-(3-methyl-2-butenyl)-2h-1-benzopyran-2-one), a natural coumarin derivative, has exhibited var- ious pharmacological properties. in addition, the possibility of its development as a promising lead compound for drug discovery has been proposed. however, there is little toxicological information regarding safety of repeated exposure to this coumarin. objective: the present study evaluated the potential toxicity of osthole after acute and subchronic administration in rodents. in addition, we investigated the effect of osthole on different hepatic cyp gene expressions in male rats receiving the highest dose of osthole. methods: in the acute toxicity study, single doses of osthole (100, 500, and 1000 mg/kg) were administered intraperitoneally to mice and the mice were then monitored for 14 days. in the subchronic toxicity study, osthole was administered orally to rats at doses of 5, 25, and 50 mg/kg/day for 45 days. results: the results of acute study indicated that ld50 of osthole is about 710 mg/kg. there was no significant difference in body weight, relative organ weight, and hematological parameters in the subchronic toxicity study. biochemical analysis showed some significant changes including in creatinine, potassium, glucose, albumin, and urea levels. the results of histopathological studies showed that all the removed organs, specially kidney, were affected by subchronic exposure to osthole. the change in the kidney included peritubular capillary congestion, hemorrhage in renal parenchyma, mild tubular dilatation, and mild interstitial infiltra- tion of inflammatory cells. furthermore, osthole treatment caused an induction in cyp1a2, cyp2e1, and cyp2c11. conclusions: finally, concerning the common classification of relative toxicity of chemicals, acute toxicity results suggested that osthole is a moderately toxic substance when administered i.p. the obtained data from subchronic study supported the evidence of renal function impairment by osthole. the no-observed adverse-effect level (noael) of the extract for both male and female rats is considered less than 5 mg/kg.