Diversity of Thyrotropin-Releasing Hormone Receptors in the Pituitary and Discrete Brain Regions of Rats

• Published in: Japanese Journal of Pharmacology 1999, Vol.79(3), pp.313-317
• Main Authors: Hidetoshi, Asai, Kiyoshi, Kinoshita, Michio, Yamamura, Yuzo, Matsuoka
• Format: Article
• Language: English
• Subjects: Animals; Binding, Competitive - drug effects; Brain - metabolism; Brain region; Guanosine Triphosphate - pharmacology; Male; Pituitary; Pituitary Gland - metabolism; Pyrrolidonecarboxylic Acid - analogs & derivatives; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptor binding; Receptors, Thyrotropin-Releasing Hormone - metabolism; Synaptic Membranes - drug effects; Synaptic Membranes - metabolism; Taltirelin (TA-0910, TRH analog); Thyrotropin-Releasing Hormone - analogs & derivatives; Thyrotropin-Releasing Hormone - metabolism; Tissue Distribution; TRH (thyrotropin-releasing hormone); Tritium
• ISSN: 0021-5198; 1347-3506
• DOI: 10.1254/jjp.79.313

In order to analyze the receptor properties of central nervous system (CNS)-stimulant thyrotropin-releasing hormone (L-pyroglutamyl-L-histidyl-L-prolinamide, TRH), we evaluated the binding of TRH and its analog taltirelin hydrate ((—)-N-[(S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinylcar-bonyl]-L-histidyl-L-prolinamide tetrahydrate; taltirelin, TA-0910) in rat anterior pituitary and several brain regions. There was a specific binding of [3H]methyl TRH (MeTRH) in the anterior pituitary, hypothalamus, brain stem, cerebral cortex and cerebellum with Kd values of 1.0–1.6 nM. The inhibition of [3H]MeTRH binding by TRH and taltirelin was monophasic in the anterior pituitary, hypothalamus and brain stem with Ki values of 6.3 – 8.0 nM and 145.5 – 170.4 nM for TRH and taltirelin, respectively. In contrast, the biphasic inhibition was revealed in the cerebral cortex and cerebellum. The IQ values for TRH and taltirelin were 4.1 – 4.3 nM and 67.8 – 73.4 nM for the high affinity binding site and 3.6–4.2 μM and 82.3–197.5 μM for the low affinity binding site, respectively. Addition of 100 μM GTP or its analog 5'-guanylylimidodiphos-phate (Gpp[NH]p) affected neither the biphasic inhibition by TRH nor that by taltirelin. Thus the results suggest the presence of distinct high and low affinity TRH receptors in the CNS in contrast to the pituitary.