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Glucose Homeostasis: Regulation of Blood Glucose01:02

Glucose Homeostasis: Regulation of Blood Glucose

Carbohydrates consumed through foods are converted into glucose, a crucial energy source for the body. In the prandial state, high blood glucose levels stimulate the secretion of insulin from the pancreas. Insulin inhibits hepatic glucose production and stimulates glucose uptake and metabolism by muscle and adipose tissue. The excess glucose is converted into glycogen and stored in the liver and muscles.
During fasting, when blood glucose levels are low, the pancreas secretes glucagon. it...
Glucose Absorption Into the Small Intestine01:26

Glucose Absorption Into the Small Intestine

Complex carbohydrates consumed cannot be absorbed into the small intestine in their original form. First, they must be hydrolyzed to a monosaccharide form such as glucose or galactose. These monosaccharides are then transported across the intestinal membrane and into the blood via transcellular transport. The intestinal epithelial cells allow the movement of these monosaccharides with a defined 'entry' through membrane transporter proteins present on their apical membrane and 'exit' via the...
Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Diabetic Nephropathy01:28

Diabetic Nephropathy

Definition Diabetic nephropathy is a chronic kidney complication that results from prolonged hyperglycemia.Prevalence It is the most common cause of chronic kidney disease (CKD) and end-stage renal disease (ESRD) worldwide, affecting up to half of individuals with diabetes.Pathophysiology • Sustained hyperglycemia triggers multiple hemodynamic and metabolic changes in the kidney. • Early in the disease, increased renal blood flow and glomerular hyperfiltration occur due to afferent arteriolar...
Hormones Regulating Blood Glucose01:16

Hormones Regulating Blood Glucose

Insulin is released by beta cells of the pancreas when blood glucose levels are high. It facilitates glucose absorption and utilization in insulin-dependent cells with insulin receptors on their plasma membranes. Insulin promotes glucose uptake by increasing the number of glucose transport proteins in the cell membrane, allowing glucose to enter the cell. As a result, glucose utilization and ATP production are enhanced.
In addition to accelerating glucose uptake and utilization, insulin has...
Introduction to Urinary System01:13

Introduction to Urinary System

The urinary system consists of two kidneys, two ureters, the urinary bladder, and the urethra.
The kidneys are bean-shaped organs located in the retroperitoneal space, on either side of the vertebral column, between the T12 and L3 vertebrae. They are partially protected by the rib cage and surrounded by perirenal fat, which provides cushioning. They are responsible for urine formation and play critical roles in regulating blood pressure, electrolyte levels, and hormone production. The ureters...

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Related Experiment Video

Updated: Jun 4, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
10:31

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice

Published on: May 2, 2025

Glucose handling by the kidney.

Amanda Mather1, Carol Pollock

  • 1Department of Medicine, Kolling Institute of Medical Research, University of Sydney, Sydney, NSW, Australia. amather@med.usyd.edu.au

Kidney International. Supplement
|March 2, 2011
PubMed
Summary
This summary is machine-generated.

The kidney plays a key role in glucose regulation. In type-2 diabetes, increased kidney glucose production and reabsorption contribute to high blood sugar, offering new therapeutic targets.

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Extracellular Glucose Depletion as an Indirect Measure of Glucose Uptake in Cells and Tissues Ex Vivo
10:35

Extracellular Glucose Depletion as an Indirect Measure of Glucose Uptake in Cells and Tissues Ex Vivo

Published on: April 6, 2022

Related Experiment Videos

Last Updated: Jun 4, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
10:31

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice

Published on: May 2, 2025

Extracellular Glucose Depletion as an Indirect Measure of Glucose Uptake in Cells and Tissues Ex Vivo
10:35

Extracellular Glucose Depletion as an Indirect Measure of Glucose Uptake in Cells and Tissues Ex Vivo

Published on: April 6, 2022

Area of Science:

  • Nephrology
  • Endocrinology
  • Metabolic Diseases

Background:

  • The kidney is crucial for glucose homeostasis, involving gluconeogenesis, filtration, reabsorption, and consumption.
  • These kidney functions are altered in type-2 diabetes (T2DM), presenting therapeutic opportunities.
  • The kidney accounts for up to 20% of glucose production, with renal gluconeogenesis significantly increasing in T2DM.

Purpose of the Study:

  • To explore the kidney's role in glucose homeostasis and its dysregulation in type-2 diabetes.
  • To identify potential therapeutic targets within renal glucose metabolism for T2DM management.

Main Methods:

  • Review of recent studies on renal glucose metabolism in healthy individuals and T2DM patients.
  • Analysis of the mechanisms of renal gluconeogenesis, glucose filtration, and reabsorption.
  • Examination of the roles of sodium-dependent glucose cotransporters (SGLT1, SGLT2) and facilitative glucose transporters (GLUT1, GLUT2).

Main Results:

  • Renal gluconeogenesis increases significantly in T2DM, contributing to both fasting and postprandial hyperglycemia.
  • Renal glucose reabsorption capacity is maladaptively increased in T2DM patients.
  • SGLT2 and SGLT1 are key transporters involved in renal glucose reabsorption, with GLUT1 and GLUT2 facilitating glucose transport into the interstitium.

Conclusions:

  • The kidney's contribution to hyperglycemia in T2DM is substantial, through both increased glucose production and reabsorption.
  • Targeting renal glucose transporters, particularly SGLT2, represents a promising therapeutic strategy for T2DM.