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TM/MC  TM/MC
                                          PHARMACOLOGICAL ACTIVITIES - TOXICOLOGY - DRUG INTERACTIONS





            Picrorhiza kurroa (Picrorhiza)

            Rhizoma Picrorhizae is a distinguished medicinal herb of the Ayurvedic medicinal system, used
            mainly for the treatment of a variety of liver ailments. The major biologically active constituents
            are iridoid glycosides, cucurbitacin triterpenes and simple phenols (WHO, 2009). The iridoid
            glycoside  mixture kutkin (picroside and kutkoside) isolated from Rhizoma  Picrorhizae  has
            shown significant hepato-protective efficacy in animal models of galactosamine, paracetamol,
            thioacetamide and carbon tetrachloride induced hepatic damage. It has also exhibited anti-viral
            and immune-stimulant activities (Verma et al., 2009). The mechanism of action of Rhizoma
            Picrorhizae extract in liver protection involves kutkin, which can increase the activity rates
            of nucleolar polymerase A, leading to increased protein synthesis and subsequent enhanced
            regenerative ability. Kutkins scavenge free radicals and guard hepatocytes from the damage
            caused by lipid peroxidation through antioxidant activity. Apocynin, another active constituent
            of  Rhizoma  Picrorhizae,  is  a  strong  nicotinamide  adenine  dinucleotide  phosphate-oxidase
            inhibitor and has shown anti-inflammatory properties. The mechanism of action of kutkins
            appears  to  be  the  same  as that  of silymarin,  a  hepato-protective  constituent  of  Silybum
            marianum (Vaidya et al., 1996).

                    Toxicity  for  Rhizoma  Picrorhizae  has  not  been  documented  in  dogs  and  cats  when  administered  orally  in
                    therapeutic doses. In mice, the LD  for aqueous ethanol extract of Rhizoma Picrorhizae is 1.09 g/kg of body
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                TOXICOLOGY  Rhizoma Picrorhizae in mice is >2 g/kg of body weight intragastrically (Lee, 1982). In rats, the LD  of kutkin,
                    weight  intraperitoneal,  indicating  low  toxicity  (Dhar  et  al.,  1973).  The  LD   for  70%  methanol  extract  of
                                                                                       50
                                                                                                        50
                    an active constituent of Rhizoma Picrorhizae, is >2,600 mg/kg of body weight (CSIR, 1989-1990).


                    Equivalent toxic dose in 20 kg dog:   21.8 g IP of Rhizoma Picrorhizae ethanol extract.
                    Equivalent toxic dose in 5 kg cat:    5.45 g IP of Rhizoma Picrorhizae ethanol extract.



                      DRUG     Validated interactions studies do not exist for Rhizoma Picrorhizae preparations. Clinical
              INTERACTIONS     interactions with other drugs have not been reported.




























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