2016
DOI: 10.1016/j.mce.2015.12.010
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PEDF attenuates insulin-dependent molecular pathways of glucose homeostasis in skeletal myocytes

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Cited by 17 publications
(15 citation statements)
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“…The insulin-dependent signaling pathways in skeletal muscle are upregulated via phosphotidylinositol-3-kinase which phosphorylates Akt at threonine 308, but only partially activates Akt and at serine 473 which fully activates Akt, thereby initiating events important for glucose uptake and metabolism [49, 50]. The results of the current study show that following glucose challenge (increased insulin), the ratio of the levels of skeletal muscle pAKT ser to total AKT was significantly increased in 12–14 year-old offspring untreated or treated with letrozole, indicating that this key component of insulin signaling in skeletal muscle was responsive to insulin in both groups of baboons.…”
Section: Discussionmentioning
confidence: 99%
“…The insulin-dependent signaling pathways in skeletal muscle are upregulated via phosphotidylinositol-3-kinase which phosphorylates Akt at threonine 308, but only partially activates Akt and at serine 473 which fully activates Akt, thereby initiating events important for glucose uptake and metabolism [49, 50]. The results of the current study show that following glucose challenge (increased insulin), the ratio of the levels of skeletal muscle pAKT ser to total AKT was significantly increased in 12–14 year-old offspring untreated or treated with letrozole, indicating that this key component of insulin signaling in skeletal muscle was responsive to insulin in both groups of baboons.…”
Section: Discussionmentioning
confidence: 99%
“…As a member of the serine protease inhibitor family, PEDF has a high a nity to type I collagen in bone tissue. The high expression of PEDF in osteoblasts and active areas of bone formation suggested that it played an important role in the process of bone angiogenesis and matrix reconstruction [24] . For SERPINF1 (serpin peptidase inhibitor, clade F, member 1), located on chromosome 17p13.3, it encodes pigment-epithelium-derived factor (PEDF) [25] .…”
Section: Discussionmentioning
confidence: 99%
“…Effects of the insulin that was released from the tablets on C2C12 myoblast cells were examined by Glut‐4 translocation. An immunofluorescence experiment was performed using an in‐house protocol on cells seeded in 96‐well plates . Before fixation with 4% paraformaldehyde and fluorescence immunocytochemistry with Glut‐4 antibody (Sigma‐Aldrich), C2C12 cells were treated with placebo tablet, insulin native powder, coated tablets and uncoated tablets for 15 min at room temperature.…”
Section: Methodsmentioning
confidence: 99%