Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.
about
General aspects of muscle glucose uptakeKinin B1 receptor in adipocytes regulates glucose tolerance and predisposition to obesityEvidence and evidence gaps of medical treatment of non-tumorous diseases of the head and neckGlucose, exercise and insulin: emerging conceptsGLUT4 translocation precedes the stimulation of glucose uptake by insulin in muscle cells: potential activation of GLUT4 via p38 mitogen-activated protein kinasePreclinical characterization of recombinant human tissue kallikrein-1 as a novel treatment for type 2 diabetes mellitusAltered glucose homeostasis and hepatic function in obese mice deficient for both kinin receptor genesA dominant-negative p38 MAPK mutant and novel selective inhibitors of p38 MAPK reduce insulin-stimulated glucose uptake in 3T3-L1 adipocytes without affecting GLUT4 translocation.Use of RNA interference-mediated gene silencing and adenoviral overexpression to elucidate the roles of AKT/protein kinase B isoforms in insulin actions.Activators of AMP-activated protein kinase enhance GLUT4 translocation and its glucose transport activity in 3T3-L1 adipocytes.Lysophosphatidylcholine activates adipocyte glucose uptake and lowers blood glucose levels in murine models of diabetes.Protein kinase B/Akt participates in GLUT4 translocation by insulin in L6 myoblastsOxidative stress stimulates skeletal muscle glucose uptake through a phosphatidylinositol 3-kinase-dependent pathwayG(alpha)11 signaling through ARF6 regulates F-actin mobilization and GLUT4 glucose transporter translocation to the plasma membrane.Acute effects of physical exercise in type 2 diabetes: A review.The pleckstrin homology (PH) domain-interacting protein couples the insulin receptor substrate 1 PH domain to insulin signaling pathways leading to mitogenesis and GLUT4 translocationNonallergic angioedema: role of bradykinin.VAMP2, but not VAMP3/cellubrevin, mediates insulin-dependent incorporation of GLUT4 into the plasma membrane of L6 myoblasts.Deletion of Kinin B2 Receptor Alters Muscle Metabolism and Exercise Performance.AMPK enhances insulin-stimulated GLUT4 regulation via lowering membrane cholesterol.Postexercise skeletal muscle glucose transport is normal in kininogen-deficient rats.Mechanisms behind the immediate effects of Roux-en-Y gastric bypass surgery on type 2 diabetesThe sweeter side of ACE2: physiological evidence for a role in diabetes.Angiotensin-converting enzyme in skeletal muscle: sentinel of blood pressure control and glucose homeostasis.Ceramide 1-phosphate stimulates glucose uptake in macrophages.Insulin and hypertonicity recruit GLUT4 to the plasma membrane of muscle cells by using N-ethylmaleimide-sensitive factor-dependent SNARE mechanisms but different v-SNAREs: role of TI-VAMP.SNPs in genes encoding G proteins in pharmacogenetics.Non-canonical signalling and roles of the vasoactive peptides angiotensins and kinins.Bradykinin inhibits hepatic gluconeogenesis in obese mice.Role of AMP-Activated Protein Kinase for Regulating Post-exercise Insulin Sensitivity.G alpha-q/11 protein plays a key role in insulin-induced glucose transport in 3T3-L1 adipocytes.Contraction-related stimuli regulate GLUT4 traffic in C2C12-GLUT4myc skeletal muscle cells.Labeling and imaging of GLUT4 in live L6 cells with quantum dots.Maturation of the regulation of GLUT4 activity by p38 MAPK during L6 cell myogenesis.Differential effects of phosphatidylinositol 3-kinase inhibition on intracellular signals regulating GLUT4 translocation and glucose transport.GLUT-4myc ectopic expression in L6 myoblasts generates a GLUT-4-specific pool conferring insulin sensitivity.Gi-mediated translocation of GLUT4 is independent of p85/p110alpha and p110gamma phosphoinositide 3-kinases but might involve the activation of Akt kinase.Changes in dietary sodium consumption modulate GLUT4 gene expression and early steps of insulin signaling.The trimeric GTP-binding protein (G(q)/G(11)) alpha subunit is required for insulin-stimulated GLUT4 translocation in 3T3L1 adipocytes.Cdc42 is a Rho GTPase family member that can mediate insulin signaling to glucose transport in 3T3-L1 adipocytes.
P2860
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P2860
Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.
@en
type
label
Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.
@en
prefLabel
Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.
@en
P2093
P1433
P1476
Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway
@en
P2093
P304
P356
10.2337/DIABETES.47.4.550
P407
P50
P577
1998-04-01T00:00:00Z