Passage of insulin across capillary endothelium was monitored in perfused rat parametrial adipose tissue by the effect of intra-arterially infused insulin on oxidation of [U-14C]glucose to CO2. Glucose oxidation was constant at 34 nmol C.g-1.min-1 for 90 min in tissues perfused with 0 or 50 microU/ml. The rate of oxidation was doubled in 90 min at 100 microU/ml and maximal (4 X control) in 40 min at 200 microU/ml and in 20-30 min at 500 microU/ml. The slow decline in oxidation rate when insulin infusion was stopped suggested that insulin was sequestered in the tissue. Although half-maximal response to insulin occurred in perfused tissues at 100 microU/ml, it occurred at 8 microU/ml in incubated adipocytes and at 30 microU/ml in incubated tissue. In addition, the time required for maximal response to insulin was longer in perfused adipose tissue than in incubated cells and tissues. The data indicate that transfer of insulin from blood to parenchymal cells in perfused tissue was restricted. The minimal amount of insulin needed for a response by adipocytes in perfused tissue was estimated to be less than 1% of that in blood. Our findings are consistent with the concept that insulin is transferred across capillary endothelium by a receptor-mediated process.
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http://dx.doi.org/10.1152/ajpendo.1987.253.5.E475 | DOI Listing |
Sci Adv
January 2025
Division of Regenerative Medicine, Hartman Institute for Therapeutic Organ Regeneration, Ansary Stem Cell Institute, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Tissue-specific endothelial cells (ECs) are critical for the homeostasis of pancreatic islets and most other tissues. In vitro recapitulation of islet biology and therapeutic islet transplantation both require adequate vascularization, which remains a challenge. Using human reprogrammed vascular ECs (R-VECs), human islets were functionally vascularized in vitro, demonstrating responsive, dynamic glucose-stimulated insulin secretion and Ca influx.
View Article and Find Full Text PDFClin Sci (Lond)
January 2025
Center for Interdisciplinary Research in Biology, College de France, Institut National de la Santé et de la Recherche Médicale, Paris, France.
Apelin, a (neuro) vasoactive peptide, plays a prominent role in controlling water balance and cardiovascular functions. Apelin and its receptor co-localize with vasopressin in magnocellular vasopressinergic neurons. Apelin receptors (Apelin-Rs) are also expressed in the collecting ducts of the kidney, where vasopressin type 2 receptors are also present.
View Article and Find Full Text PDFPhysiol Rep
February 2025
Department of Biomedical Engineering, Toyo University, Saitama, Japan.
The present study aims to examine the effect of 4 h of continuous sitting on cerebral endothelial function, which is a crucial component of cerebral blood flow regulation. We hypothesized that 4 h of sitting may impair cerebral endothelial function similarly to how it affects lower limb vasculature. Thirteen young, healthy participants were instructed to remain seated for 4 h without moving their lower limbs.
View Article and Find Full Text PDFInt Angiol
December 2024
Vascular Surgery Research Laboratories, Division of Vascular and Endovascular Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA -
The glycocalyx is an essential structural and functional component of endothelial cells. Extensive hemodynamic changes cause endothelial glycocalyx disruption and vascular dysfunction, leading to multiple arterial and venous disorders. Chronic venous disease (CVD) is a common disorder of the lower extremities with major health and socio-economic implications, but complex pathophysiology.
View Article and Find Full Text PDFJ Ginseng Res
January 2025
The Key Laboratory of Cardiovascular and Cerebrovascular Drug Research of Liaoning Province, Jinzhou Medical University, Jinzhou, China.
Background: Vascular endothelial dysfunction (VED) is one of the main pathogenic events in pulmonary arterial hypertension (PAH). Previous studies have demonstrated that the ginsenoside Rg1 (Rg1) can ameliorate PAH, but the mechanism by which Rg1 affects pulmonary VED in hypoxia-induced PAH remains unclear.
Methods: Network pharmacology, molecular docking and other experiments were used to explore the mechanisms by which Rg1 affects PAH.
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