Sasako Takayoshi, Ueki Kohjiro
Graduate School of Medicine, The University of Tokyo/Diabetes Research Center, National Center for Global Health and Medicine, Tokyo, Japan.
Clin Calcium. 2018;28(9):1221-1228.
Insulin and IGF-1 share many of the downstream molecules involved in the signal transduction, and cooperatively maintain volume of skeletal muscle. Along with aging, however, insulin/IGF-1 signaling is impaired, mainly due to insulin resistance and lowered IGF-1 levels, which is thought to promote the development of sarcopenia, and thus they are among the promising therapeutic targets. It is also known that sarcopenia is associated with the development of frailty, one of the phenomena of systemic aging. Actually insulin/IGF-1 signaling is known to affect longevity in lower organisms, but in humans, little is known about roles of the signaling in the development of frailty, and further investigation is needed.
胰岛素和胰岛素样生长因子-1(IGF-1)共享许多参与信号转导的下游分子,并协同维持骨骼肌的体积。然而,随着衰老,胰岛素/IGF-1信号传导受损,主要是由于胰岛素抵抗和IGF-1水平降低,这被认为会促进肌肉减少症的发展,因此它们是很有前景的治疗靶点。还已知肌肉减少症与衰弱的发展有关,衰弱是全身衰老的现象之一。实际上,已知胰岛素/IGF-1信号传导会影响低等生物的寿命,但在人类中,关于该信号传导在衰弱发展中的作用知之甚少,需要进一步研究。