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Insulin receptor number and binding affinity in newborn dogs
V Johnston1, V Frazzini, S Davidheiser
1Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Pediatric Research
|June 1, 1991
Summary
Neonatal insulin resistance may stem from receptor defects. Newborn canine skeletal muscle and heart show increased insulin receptors, suggesting a potential role in neonatal insulin resistance.
Area of Science:
- Endocrinology
- Metabolic Research
- Mammalian Physiology
Background:
- Neonatal insulin resistance is a clinical concern.
- Insulin resistance may involve receptor or postreceptor defects.
- Limited data exists on insulin receptors in neonatal non-hepatic tissues.
Purpose of the Study:
- To investigate insulin receptor characteristics in neonatal canine skeletal muscle, heart, and liver.
- To compare insulin receptor number and affinity between neonatal and adult canines.
- To elucidate the role of insulin receptors in neonatal insulin resistance.
Main Methods:
- Wheat germ lectin affinity chromatography for receptor purification.
- Competition binding studies to assess insulin receptor binding.
- Scatchard plot analysis to estimate receptor number and affinity.
Main Results:
- Increased specific insulin binding in newborn skeletal muscle and heart compared to adults.
- Higher high-affinity insulin receptor numbers in newborn skeletal muscle and heart.
- No significant differences in insulin receptor affinity or liver tissue characteristics between newborns and adults.
Conclusions:
- Neonatal skeletal muscle and heart exhibit altered insulin receptor numbers.
- These alterations may contribute to neonatal insulin resistance.
- Liver insulin receptor characteristics remain similar between neonatal and adult canines.