Author:
Bauknecht Th.,Krahe B.,Rechenbach U.,Zahradnik H. P.,Breckwoldt M.
Abstract
Abstract.
Human myometrium was studied for specific binding of PGE2 and PGF2α. PGF2α-binding was almost undetectable, but specific binding sites for PGE2 with high affinity (KD = 2.7 ± 0.4 × 10−9 m were demonstrated. The binding capacity for PGE2 exhibited a topically different distribution pattern with the highest values in the central parts and low to undetectable levels in the cervical region. Binding characteristics were analyzed by receptor kinetics, revealing a homogenous receptor population. Binding capacity in uteri obtained from post-menopausal women was of the order of 900–940 fmol/mg protein. Oestrogen pre-treatment and pregnancy were associated with a 3-fold reduction of the PGE2-binding capacity.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
41 articles.
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