Page 39 - product-manual
P. 39

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





        Boswellia serrata (Indian Frankincense)

        Boswellic acids, the major constituent of Gummi Boswellii, are thought to contribute to most of
        the herb’s pharmacological activities. Animal studies and clinical trials support the potential of
        Gummi Boswellii for the treatment of a variety of inflammatory diseases such as inflammatory
        bowel  disease,  rheumatoid  arthritis,  osteoarthritis  and  asthma.  In  inflammatory  response,  the
        molecular  targets of Gummi Boswellii  are  inhibition  of microsomal  prostaglandin  E
        synthase-1, serine protease cathepsin G, and suppression of leukotriene formation via inhibition of
        5-lipoxygenase  which  are  attributed  to  boswellic  acids  such  as  β-boswellic  acid,  11-keto-β-
        boswellic acid and acetyl-11-keto-β-boswellic acid (Safayi et al., 1997; Siemoneit et al., 2009;
        Kunnumakkara et al., 2009; Abdel-Tawab et al., 2011). In an open multi-centre veterinary clinical
        trial  in dogs with osteoarthritis and degenerative  conditions,  dietary  support with Gummi
        Boswellii demonstrated statistically significant reduction of severity and resolution of clinical
        signs such as intermittent lameness, local pain and stiff gait (Reichling et al., 2004).

        Note:
        Boswellia serrata is also an ingredient in Articulare-VM™.  In inflammatory response, the molecular targets of Gummi Boswellii are
        inhibition of microsomal prostaglandin E synthase-1, serine protease cathepsin G, and  suppression of leukotriene formation.





                 Toxicity for Gummi Boswellii has not been documented in dogs and cats when administered orally in therapeutic
            TOXICOLOGY  established at >2 g/kg of body weight (Singh & Atal, 1986).                   50
                 doses. In toxicity studies of Gummi Boswellii extract in rats and mice, the oral and intraperitoneal LD  has been



                 Equivalent toxic dose in 20 kg dog:   >40 g PO and IP of Gummi Boswellii extract.
                                                 >10 g PO and IP of Gummi Boswellii extract.
                 Equivalent toxic dose in 5 kg cat:


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





























        4  |   Antitis-VM TM
   34   35   36   37   38   39   40   41   42   43   44