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Oxytocin receptors in rat kidney during development
A Schmidt1, S Jard, J J Dreifuss
1Centre National de la Recherche Scientifique, Institut National de la Santé et de la Recherche Médicale, Montpellier, France.
The American Journal of Physiology
|December 1, 1990
Summary
Oxytocin receptors are present in rat kidneys from embryonic development through adulthood, primarily in the cortex. Transient binding in the medulla suggests roles in both kidney development and function.
Area of Science:
- Nephrology
- Endocrinology
- Developmental Biology
Background:
- Oxytocin (OT) is a hormone primarily known for its roles in reproduction and social behavior.
- The presence and function of oxytocin receptors in the kidney, particularly during development, remain incompletely understood.
Purpose of the Study:
- To investigate the developmental expression and characteristics of oxytocin receptors in the rat kidney.
- To determine the localization and binding properties of renal oxytocin receptors.
Main Methods:
- Light-microscopic autoradiography was used to visualize oxytocin receptor distribution in rat kidneys at various developmental stages.
- Membrane preparations were utilized with an iodinated oxytocin antagonist (125I-d(CH2)5[Tyr(Me)2,Thr4,Orn8,Tyr(NH2)9]OT) to quantify binding characteristics.
Main Results:
- Specific oxytocin binding was detected in the renal cortex and medulla by embryonic day 17.
- Cortical binding persisted into adulthood, localized to the distal tubule near the juxtaglomerular apparatus.
- Medullary binding was transient, observed during early postnatal development (before postnatal day 6) and around weaning (postnatal days 20-30).
- Binding studies revealed a single class of high-affinity oxytocin binding sites in the developing kidney.
Conclusions:
- Oxytocin receptors are expressed in the rat kidney throughout development, with distinct temporal and spatial patterns.
- The findings suggest oxytocin plays a role in both renal development and mature renal function.
- Renal oxytocin receptors exhibit ligand selectivity similar to those found in other tissues.