Pseudoginsenoside F11 Enhances the Viability of Random-Pattern Skin Flaps by Promoting TFEB Nuclear Translocation Through AMPK-mTOR Signal Pathway

Random-pattern skin FLAP is widely used in tissue reconstruction. However, necrosis occurring in the distal part of the FLAP limits its clinical application to some extent. Activation of Autophagy has been considered as an effective approach to enhance the survival of skin flaps. Pseudoginsenoside F11 (PF11), an ocotillol-type saponin, is an important component of Panax quinquefolium which has been shown to confer protection against cerebral ischemia and alleviate oxidative stress. However, it is currently unknown whether PF11 induces Autophagy to improve the survival of skin flaps. In this study, we investigated the effects of PF11 on blood flow and tissue edema. The results of histological examination and western blotting showed that PF11 enhanced angiogenesis, alleviated Apoptosis and oxidative stress, thereby improving the survival of the FLAP. Further experiments showed that PF11 promoted nuclear translocation of TFEB and by regulating the phosphorylation of AMPK. In summary, this study demonstrates that PF11 activates Autophagy through the AMPK-TFEB signal pathway in skin flaps and it could be a promising strategy for enhancing FLAP viability.

AMPK-mTOR signaling pathway; TFEB; angiogenesis; apoptosis; autophagy; oxidative stress; pseudoginsenoside F11; random-pattern skin flaps.