Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2004-12-8
pubmed:abstractText
Acute increases of the key counterregulatory hormone epinephrine can be modified by a number of physiological and pathological conditions in type 1 diabetic patients (T1DM). However, it is undecided whether the physiological effects of epinephrine are also reduced in T1DM. Therefore, the aim of this study was to determine whether target organ (liver, muscle, adipose tissue, pancreas, cardiovascular) responses to epinephrine differ between healthy subjects and T1DM patients. Thirty-four age- and weight-matched T1DM (n = 17) and healthy subjects (n = 17) underwent two randomized, single-blind, 2-h hyperinsulinemic euglycemic clamp studies with (Epi) and without epinephrine infusion. Muscle biopsy was performed at the end of each study. Epinephrine levels during Epi were similar in all groups (4,039 +/- 384 pmol/l). Glucose (5.3 +/- 0.06 mmol/l) and insulin levels (462 +/- 18 pmol/l) were also similar in all groups during the glucose clamps. Glucagon responses to Epi were absent in T1DM and significantly reduced compared with healthy subjects. Endogenous glucose production during the final 30 min was significantly greater during Epi in healthy subjects compared with T1DM (8.4 +/- 1.3 vs. 4.4 +/- 0.6 micromol.kg(-1).min(-1), P = 0.041). Glucose uptake showed almost a twofold greater decrease with Epi in healthy subjects vs. T1DM (Delta31 +/- 2 vs. Delta17 +/- 2 nmol.kg(-1).min(-1), respectively, P = 0.026). Glycerol, beta-hydroxybutyrate, and nonesterified fatty acid (NEFA) all increased significantly more in T1DM compared with healthy subjects. Increases in systolic blood pressure were greater in healthy subjects, but reductions of diastolic blood pressure were greater in T1DM patients with Epi. Reduction of glycogen synthase was significantly greater during epinephrine infusion in T1DM vs. healthy subjects. In summary, despite equivalent epinephrine, insulin, and glucose levels, changes in glucose flux, glucagon, and cardiovascular responses were greater in healthy subjects compared with T1DM. However, T1DM patients had greater lipolytic responses (glycerol and NEFA) during Epi. Thus we conclude that there is a spectrum of significant in vivo physiological differences of epinephrine action at the liver, muscle, adipose tissue, pancreas, and cardiovascular system between T1DM and healthy subjects.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0193-1849
pubmed:author
pubmed:issnType
Print
pubmed:volume
288
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E178-86
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:15585598-Adult, pubmed-meshheading:15585598-Autonomic Nervous System, pubmed-meshheading:15585598-Biopsy, pubmed-meshheading:15585598-Blood Glucose, pubmed-meshheading:15585598-Blood Pressure, pubmed-meshheading:15585598-Calorimetry, Indirect, pubmed-meshheading:15585598-Diabetes Mellitus, Type 1, pubmed-meshheading:15585598-Epinephrine, pubmed-meshheading:15585598-Female, pubmed-meshheading:15585598-Glucagon, pubmed-meshheading:15585598-Glucose Clamp Technique, pubmed-meshheading:15585598-Heart Rate, pubmed-meshheading:15585598-Human Growth Hormone, pubmed-meshheading:15585598-Humans, pubmed-meshheading:15585598-Hydrocortisone, pubmed-meshheading:15585598-Insulin, pubmed-meshheading:15585598-Male, pubmed-meshheading:15585598-Muscle, Skeletal, pubmed-meshheading:15585598-Norepinephrine, pubmed-meshheading:15585598-Pancreatic Polypeptide, pubmed-meshheading:15585598-Sympathomimetics
pubmed:year
2005
pubmed:articleTitle
Differing physiological effects of epinephrine in type 1 diabetes and nondiabetic humans.
pubmed:affiliation
Division of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232-6303, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, U.S. Gov't, P.H.S., Randomized Controlled Trial, Research Support, Non-U.S. Gov't