AS160 expression, but not AS160 Serine‐588, Threonine‐642, and Serine‐704 phosphorylation, is essential for elevated insulin‐stimulated glucose uptake by skeletal muscle from female rats after acute exercise

Abstract

AbstractOne exercise session can increase subsequent insulin‐stimulated glucose uptake (ISGU) by skeletal muscle in both sexes. We recently found that muscle expression and phosphorylation of key sites of Akt substrate of 160 kDa (AS160; also called TBC1D4) are essential for the full‐exercise effect on postexercise‐ISGU (PEX‐ISGU) in male rats. In striking contrast, AS160's role in increased PEX‐ISGU has not been rigorously tested in females. Our rationale was to address this major knowledge gap. Wild‐type (WT) and AS160‐knockout (KO) rats were either sedentary or acutely exercised. Adeno‐associated virus (AAV) vectors were engineered to express either WT‐AS160 or AS160 mutated on key serine and threonine residues (Ser588, Thr642, and Ser704) to alanine to prevent their phosphorylation. AAV vectors were delivered to the muscle of AS160‐KO rats to determine if WT‐AS160 or phosphorylation‐inactivated AS160 would influence PEX‐ISGU. AS160‐KO rats have lower skeletal muscle abundance of the GLUT4 glucose transporter protein. This GLUT4 deficit was rescued using AAV delivery of GLUT4 to determine if eliminating muscle GLUT4 deficiency would normalize PEX‐ISGU. The novel results were as follows: (1) AS160 expression was required for greater PEX‐ISGU; (2) rescuing muscle AS160 expression in AS160‐KO rats restored elevated PEX‐ISGU; (3) AS160's essential role for the postexercise increase in ISGU was not attributable to reduced muscle GLUT4 content; and (4) AS160 phosphorylation on Ser588, Thr642, and Ser704 was not essential for greater PEX‐ISGU. In conclusion, these novel findings revealed that three phosphosites widely proposed to influence PEX‐ISGU are not required for this important outcome in female rats.