2012
DOI: 10.1507/endocrj.ej12-0192
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Prompt increases in retinol-binding protein 4 and endothelial progenitor cells during acute exercise load in diabetic subjects

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Cited by 6 publications
(3 citation statements)
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“…There are several trials dealing with the effect of exercise on EPC biology in diabetic patients. Acute exercise loads promptly increased the EPC (CD34+/CD133+) count in patients with type 2 diabetes with and without nephropathy [102]. In patients with type 2 diabetes and diagnosed coronary artery disease, an elevated level of microparticles and EPC could be detected.…”
Section: Lifestyle Modificationmentioning
confidence: 92%
“…There are several trials dealing with the effect of exercise on EPC biology in diabetic patients. Acute exercise loads promptly increased the EPC (CD34+/CD133+) count in patients with type 2 diabetes with and without nephropathy [102]. In patients with type 2 diabetes and diagnosed coronary artery disease, an elevated level of microparticles and EPC could be detected.…”
Section: Lifestyle Modificationmentioning
confidence: 92%
“…An interesting approach for evaluation of vascular function might be the determination of the EPCs level. Although the potential of acute (sub-maximal) exercise to stimulate and mobilize the EPCs has been shown to be blunted in T2DM patients as compared to healthy controls [65], Aoki et al [86] have proven an increment of EPCs during acute exercise load in diabetic patients, which seems an additional promising beneficial effect of exercise [65]. A recent study, however, by Waclawovsky et al failed to show an increase of EPCs after an acute combined, aerobic and resistance training (ART) session in young T1DM patients in spite of increased response to postocclusive reactive hyperaemia (PORH), assessed by venous occlusion plethysmography [87].…”
Section: Impact Of Acute Exercise In Diabetic Microcirculationmentioning
confidence: 99%
“…52 Augmenting Mobilization and Migration: Role of Stromal Derived Factor-1 (SDF-1) SDF-1 is a chemokine for EPCs that, while constitutively expressed in the bone marrow, is also induced in peripheral tissues in the setting of ischemia by HIF-1 dependent mechanisms. 53 EPCs express the cell surface receptor for SDF-1, CXCR4, allowing these cells to egress from the bone marrow and migrate along an SDF-1 gradient to initiate and support angiogenesis in areas of ischemia.…”
Section: Indirect Strategies To Augment Epc Numbermentioning
confidence: 99%