S. Takeda et al., IN-VIVO ASSESSMENT OF EXTRAHEPATIC METABOLISM OF PAEONIFLORIN IN RATS- RELEVANCE TO INTESTINAL FLORAL METABOLISM, Journal of Pharmacy and Pharmacology, 49(1), 1997, pp. 35-39
The extraction ratios of paeoniflorin in gut wall (E(G)), liver (E(H))
and lung (E(L)) were assessed by comparing AUCs after various routes
of its administration to estimate the first-pass effects and the metab
olism by intestinal flora. Pulmonary extraction ratio of paeoniflorin
was assessed by comparing AUCs calculated from venous and arterial pla
sma concentrations after its intravenous administration (0.5 mg kg(-1)
). The mean pulmonary extraction ratio was estimated to be 0.06. The h
epatic extraction ratio (E(H) was assessed by comparing AUCs after int
raportal and intravenous administrations (0.5 and 5 mg kg(-1)). The pl
asma concentration profiles of paeoniflorin after intraportal administ
ration were very close to those after intravenous administration, sugg
esting a negligible hepatic extraction ratio of paeoniflorin. The AUC
value after intraperitoneal administration (0.5 mg kg(-1)) was greater
than that after intraportal or intravenous administration. This findi
ng suggests that paeoniflorin is not metabolized in the gut wall. The
transference of paeoniflorin from the serosal side to the mucosal side
was evaluated by the in-vitro everted sac method. The low intestinal
permeability (19.4% at 60 min) was demonstrated by the comparison with
phenobarbital (63.1% at 60 min). We conclude that paeoniflorin is not
metabolized by gut wall, liver and lung, its poor absorption from the
intestine results in extremely low bioavailability and the unabsorbed
fraction of paeoniflorin is degraded by the intestinal flora.