Abstract

The characteristics and distribution of putative thyrotropin releasing hormone (TRH) receptors were studied in rat central nervous system using the TRH analogue 3H-(3MeHis 2)TRH as a radiolabeled ligand. The analogue had a dissociation constant of 2.3 ± 0.2 nM and a receptor density of 34 ± 2 fm/mg protein in whole brain homogenates. An association rate constant of 1.6 × 10 −3 min −1nM −1 and a biphasic dissociation with rate constants of 2.6 × 10 −3 min −1 and 1.3 × 10 −4 min −1 were observed. The brain was dissected into ten regions, and detectable levels of binding were found in all regions. The highest levels were found in the amygdala/piriform cortex area and the septal region, and the lowest levels were found in the cerebellar and cerebral cortex. Competition curves showed the methylated analogue to have approximately 7-fold higher affinity for the receptor than TRH. The higher affinity, along with lower nonspecific binding, accounts for the much improved sensitivity of the binding assay of the methylated analogue (70–80% specific binding) as compared to 3H-TRH (15–20% specific binding) and enables one to work with much lower tissue amounts. Use of the tritiated analogue will greatly aid in further studies of TRH receptors.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.