In a human vascular smooth muscle cell line, oxytocin competed for [3H]-AVP binding with the highest potency of the compounds tested.
In plain wordsIn cells, oxytocin competed for vasopressin binding sites more strongly than the other compounds tested.
- Peptide
- Oxytocin
- Outcome
- Not applicableCompetition for [3H]-AVP binding
- Study
humann: not reported in source
human vascular smooth muscle cell line (HVSMC)- Outcome group
- Receptor activity and mechanism · Pharmacology
- Studied dose
- Dose not stated
Source sentences
Nonlabelled compounds compete for [3H]-AVP binding in the HVSMC membrane with an order of potency of oxytocin > lyspressin > or = AVP > Thr4, Gly7-oxytocin > (beta-mercapto-beta-beta-cyclopentamethylenepropionyl-O-Me Tyr2, Arg8) vasopressin > desmopressin > OPC21268 > OPC31260.
1 context sentence(design, population, supporting numbers)
In a human vascular smooth muscle cell line (HVSMC), binding experiments with [3H]-arginine8-vasopressin (AVP) have shown the existence of a homogeneous population of binding sites with affinity (Kd value) of 0.65 nM and a maximum number of binding sites (Bmax) of 122 fmol mg-1 protein.