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






                    Platycladus orientalis

                    Toxicity for Cacumen Platycladi has not been documented in dogs and cats when administered orally in therapeutic
               TOXICOLOGY  in ruminants including bovine, caprine and ovine (Chizzola et al., 2004). Intraperitoneal LD  for Cacumen
                    doses. Ingestion of Platycladus orientalis has been associated with clinical signs of gastroenteritis and seizures
                                                                                                     50
                    Platycladi is 15.2 g/kg of body weight in mice. No deaths were recorded among mice within 72 hours of being
                    given 60 g/kg of body weight of a decoction of Cacumen Platycladi via intragastric administration (Li, 2002).

                    Equivalent toxic dose in 20 kg dog:   304 g IP of Cacumen Platycladi decoction.
                    Equivalent toxic dose in 5 kg cat:    76 g IP of Cacumen Platycladi decoction.



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





                                   Ziziphus jujuba [Ziziphus spinosa] (Chinese Jujube)

                                   Semen Ziziphi Spinosae has been used extensively for the treatment of insomnia. In an animal study,
                                   spinosin a major constituent of Semen Ziziphi Spinosae, dose-dependently augmented pentobarbital
                                   induced sleep, reflected by increased sleep time and reduced sleep latency assessed with the loss-of-
                                   righting reflex (Wang et al., 2008). Various tests on animals including dogs and cats were carried out to
                                   assess the sedative and hypnotic effects of Semen Ziziphi Spinosae and the results showed sedative
                                   effects and synergistic effects with other sedatives and hypnotics (Chang & But, 1987). It has also been
                                   found that Semen Ziziphi Spinosae possessed anxiolytic effects at a lower dose and sedative effects
                                   at a higher dose (Wen et al., 2000). In a human study, Semen Ziziphi Spinosae showed a significant
                                   improvement in sleep quality and well-being without side effects (Bone, 2001).



                    Toxicity  for  Semen  Ziziphi  Spinosae  has  not  been  documented  in  dogs  and  cats  when  administered  orally  in
                    therapeutic doses. In laboratory animals a single oral dose of 50 g/kg of body weight of Semen Ziziphi Spinosae
                TOXICOLOGY  (Dharmananda, 2001). Intraperitoneal LD  of Semen Ziziphi Spinosae decoction is 14.3 ± 2.0 g/kg of body weight
                    did not produce any toxic symptoms, and a daily dose of 20 g/kg of body weight for 30 days had no toxic reactions
                                                       50
                    in mice (Chang & But, 1987).


                    Equivalent toxic dose in 20 kg dog:   286 g IP of Semen Ziziphi Spinosae decoction.
                    Equivalent toxic dose in 5 kg cat:    71.5 g IP of Semen Ziziphi Spinosae decoction.



                          DRUG     Validated  interactions  studies  do  not  exist  for  Semen  Ziziphi  Spinosae  preparations.  Clinical
                 INTERACTIONS      interactions  with  other  drugs  have  not  been  reported.  However,  Semen  Ziziphi  Spinosae  has
                                   sedative and hypnotic effects. It potentiates the sedative effects of barbiturates (Chen & Chen,
                                   2004).





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