Page 22 - A. Aging
P. 22

[A. Aging-12]



                  Long-term administration of red ginseng non-saponin


                   fraction rescues the loss of skeletal muscle mass and


                              function associated with aging in mice



             Da Eun Cho¹, Gwang Muk Choi¹, Hyein Song², Mijung Yeom³, Bombi Lee³, Dae Hyun Hahm¹˙³˙⁴


           ¹Department of Biomedical Sciences, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea,

          ²Department of Medicinal Bioscience, Nonsan Interdisciplinary & Creative Studies Campus, Konyang University,
         Nonsan-si 32992, Republic of Korea, ³Acupuncture and Meridian Science Research Center, Kyung Hee University,

           Seoul 02447, Republic of Korea, ⁴Department of Physiology, College of Medicine, Kyung Hee University, Seoul
                                                 02447, Republic of Korea




        Korean red ginseng has been known to relieve fatigue and enhance the physical performance especially in the

        elderly.  Anti-sarcopenic  effect  of  its  non-saponin  fraction  (RGNS)  was  investigated  in  22-month-old  mice,
        administered with 0.08% RGNS chow diet for another 4 months. Aging-associated weight loss of hindlimb skeletal

        muscles  such  as  tibials  anterior,  extensor  digitorum  longus  (EDL),  gastrocnemius  and  soleus  was  significantly
        alleviated by RGNS treatment. The cross-sectional areas of soleus, decreased by 40 % in aged mice raised from 22

        to 26 months, were mitigated to 12.5%, and a shift of fast- to slow-twitch muscle type, observed in soleus and EDL
        was also retarded. In order to elicit a senescence in C2C12 myoblasts, the cells were treated with C2-ceramide, and

        RGNS  1h  earlier.  RGNS  significantly  alleviated  C2-ceramide-induced  senescence  indicated  by  intracellular  lipid
        accumulation, increased amount of lysosomal β-galactosidase, cell cycle retardation, and reduced cell proliferative

        capacity.  RGNS  restored  C2-ceramide-stimulated  expression  of  p21, p57,  p16, MuRF1 and  atrogen-1,  and  the
        suppression  of  Pax-7  in  a  dose  dependent  manner.  RGNS  thus  might  be  invaluable  for  the  development  of

        therapeutic medicines to rescue sarcopenia and its accompanying muscle dysfunction.
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