» Articles » PMID: 3059816

Rates and Tissue Sites of Non-insulin- and Insulin-mediated Glucose Uptake in Humans

Overview
Journal Am J Physiol
Specialty Physiology
Date 1988 Dec 1
PMID 3059816
Citations 225
Authors
Affiliations
Soon will be listed here.
Abstract

In vivo glucose uptake can occur via two mechanisms, namely, insulin-mediated glucose uptake (IMGU) and non-insulin-mediated glucose uptake (NIMGU). Although the principal tissue sites for IMGU are skeletal muscle, the tissue sites for NIMGU at a given serum glucose concentration are not known. To examine this issue, rates of whole body glucose uptake (Rd) were measured at basal and during glucose clamp studies performed at euglycemia (approximately 90 mg/dl) and hyperglycemia (approximately 220 mg/dl) in six lean healthy men. Studies were performed during hyperinsulinemia (approximately 70 microU/ml) and during somatostatin-induced insulinopenia to measure IMGU and NIMGU, respectively. During each study, leg glucose balance (arteriovenous catheter technique) was also measured. With this approach, rates of whole body skeletal muscle IMGU and NIMGU can be estimated, and the difference between overall Rd and skeletal muscle glucose uptake represents non-skeletal muscle Rd. The results indicate that approximately 20% of basal Rd is into skeletal muscle. During insulinopenia approximately 86% of body NIMGU occurs in non-skeletal muscle tissues at euglycemia. When hyperglycemia was created, whole body NIMGU increased from 128 +/- 6 to 213 +/- 18 mg/min (P less than 0.01); NIMGU into non-skeletal muscle tissues was 134 +/- 11 and 111 +/- 6 mg/min at hyperglycemia and euglycemia, respectively, P = NS. Therefore, virtually all the hyperglycemia induced increment in NIMGU occurred in skeletal muscle. During hyperinsulinemia, IMGU in skeletal muscle represented 75 and 95% of body Rd, at euglycemia and hyperglycemia, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

Insulin-Sensitizing Properties of Decoctions from Leaves, Stems, and Roots of L.

Mekonnen Z, Petito G, Shitaye G, DAbrosca G, Legesse B, Addisu S Molecules. 2025; 30(1.

PMID: 39795155 PMC: 11722063. DOI: 10.3390/molecules30010098.


Regulation of injury-induced skeletal myofiber regeneration by glucose transporter 4 (GLUT4).

Sermersheim T, Phillips L, Evans P, Kahn B, Welc S, Witczak C Skelet Muscle. 2024; 14(1):33.

PMID: 39695900 PMC: 11656879. DOI: 10.1186/s13395-024-00366-y.


Metabolic Syndrome Nonalcoholic Steatohepatitis Male Mouse With Adeno-Associated Viral Renin as a Novel Model for Heart Failure With Preserved Ejection Fraction.

Shi Y, Perez-Bonilla P, Chen X, Tam K, Marshall M, Morin J J Am Heart Assoc. 2024; 13(23):e035894.

PMID: 39575718 PMC: 11681587. DOI: 10.1161/JAHA.124.035894.


Effects of Obesity and Hyperglycemia on Postprandial Insulin-Mediated and Non-Insulin-Mediated Glucose Disposal.

Mittendorfer B, Patterson B, Smith G, Yoshino M, Klein S Diabetes Care. 2024; 48(1):84-92.

PMID: 39499792 PMC: 11664199. DOI: 10.2337/dc24-1280.


Artificial intelligence approaches to the volumetric quantification of glycogen granules in EM images of human tissue.

Rios E, Samso M, Figueroa L, Manno C, Tammineni E, Rios Giordano L J Gen Physiol. 2024; 156(9.

PMID: 38980209 PMC: 11233403. DOI: 10.1085/jgp.202413595.