Flavonoid is a secondary metabolite produced by plants. In plants, flavonoid
can be found as aglycone from glycoside. For example, flavonoid quercetin is an
aglycone from glycoside rutin. Quercetin has free hydroxyl groups which have
been proven can inhibit cytochrome P450. Rutin, as a glycoside of quercetin is
assumed having similiar activity. One of many drugs which metabolism is
catalyzed by P450 is paracetamol. This research aimed to obtain the relation
between rutin towards analgesic activity and hepatotoxicity of paracetamol.
This study used male mice from Balb/C strain (Mus musculus). They were
divided randomly into groups of two kinds of treatment, with and without rutin.
Both groups were observed upon analgesic and hepatotoxicity test. As for
treatment with rutin, mice were given rutin suspension in CMC 0,5% orally once
per day for seven days and followed by paracetamol. Dosage of rutin used in this
study was 10 mg/kgBW and 40 mg/kgBW. Analgesic activity was measured with
its percentage, while hepatotoxicity was observed through liver organ
histopathology based on abnormality of tissue structure. The result was analyzed
by Kolmogorov Smirnov, ANOVA, and LSD tests with confidence level of 95%.
This study showed that treatment of 10 mg/kgBW and 40 mg/kgBW rutin
increased analgesic activity of paracetamol. However only at 40 mg/kgBW
treatment gave significant result compared to control. The significant effect could
be obtained at 91 mg/kgBW therapeutic dose and also at 300 mg/kgBW toxic
dose. Analgesic activity of paracetamol is proportional to the increase in rutin
dosage given . Furthermore the hepatotoxicity test showed 10 mg/kgBW or 40
mg/kgBW rutin could not decrease hepatotoxicity that caused by paracetamol at
toxic dose.