Role of TRH receptors as possible mediators of analeptic actions of TRH-like peptides

被引:42
作者
Hinkle, PM
Pekary, AE
Senanayaki, S
Sattin, A
机构
[1] Univ Rochester, Sch Med & Dent, Dept Physiol & Pharmacol, Rochester, NY 14642 USA
[2] VA Greater Los Angeles Healthcare Syst, Psychiat & Res Serv, Los Angeles, CA 90073 USA
[3] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
[4] Dept Psychiat & Biobehav Sci, Los Angeles, CA 90073 USA
关键词
TRH; EEP; TRH receptor; calcium signaling;
D O I
10.1016/S0006-8993(02)02454-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A large family of TRH-like peptides in the limbic region of rat brain including pGlu-Glu-Pro-NH2 (EEP), pGlu-Val-Pro-NH, (Val(2) -TRH), Leu(2) -TRH, Phe(2) -TRH and Tyr(2)-TRH has recently been discovered. TRH (pGlu-His-Pro-NH2) has antidepressant, neuroprotcetive, analeptic, anticonvulsant, antiamnesic and euphoric properties, and other TRH-like peptides such as EEP exert several of these effects. A new TRH receptor (TRHR2) has been reported which is highly expressed in regions of rat brain that regulate attention and learning, arousal, sleep and processing of sensory information. The TRHR1 predominates in limbic structures involved in regulation of mood and in pituitary. This study examined the possibility that some of the newly discovered TRH-like peptides bind with high affinity to TRHR2, and that this receptor acts as the transducer for some of the CNS effects of this new class of neuropeptides. EEP, Val(2)-TRH and Leu(2)-TRH were analeptics, like TRH, but Phe(2) -TRH and Tyr2-TRH were not. The affinity and efficacy of TRH-like peptides for TRHR1 and TRHR2 were measured in HEK293 cells stably expressing these receptors. The IC50 values of TRH-like peptides for displacement of [H-3]TRH from TRHR2 were TRH <<< (Leu(2)-, Phe(2) -TRH)<(Gln(2)-, Ser(2) -TRH) << (Val(2) -, Tyr(2)-, Arg(2)-, Thr(2)-, and Glu(2) -TRH). The IC50 for Leu(2)-TRH was about 100 times that for TRH. When tested at the calculated IC50 values, TRH-like peptides stimulated calcium responses in cells expressing TRHR1 and TRHR2, indicating that the peptides act as weak agonists at both receptors. These results indicate that TRHR1 and TRHR2 do not mediate the behavioral effects of TRH-like peptides. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 21 条
[1]  
Adeoya-Osiguwa SA, 1998, MOL REPROD DEV, V51, P468, DOI 10.1002/(SICI)1098-2795(199812)51:4&lt
[2]  
468::AID-MRD14&gt
[3]  
3.0.CO
[4]  
2-6
[5]   Cloning and characterization of a cDNA encoding a novel subtype of rat thyrotropin-releasing hormone receptor [J].
Cao, J ;
O'Donnell, D ;
Vu, H ;
Payza, K ;
Pou, C ;
Godbout, C ;
Jakob, A ;
Pelletier, M ;
Lembo, P ;
Ahmad, S ;
Walker, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :32281-32287
[6]   Molecular and cellular biology of thyrotropin-releasing hormone receptors [J].
Gershengorn, MC ;
Osman, R .
PHYSIOLOGICAL REVIEWS, 1996, 76 (01) :175-191
[7]   Minireview: Insights into G protein-coupled receptor function using molecular models [J].
Gershengorn, MC ;
Osman, R .
ENDOCRINOLOGY, 2001, 142 (01) :2-10
[8]  
Heuer H, 2000, J COMP NEUROL, V428, P319
[9]   Characterization of the calcium response to thyrotropin-releasing hormone in lactotrophs and GH cells [J].
Hinkle, PM ;
Nelson, EJ ;
Ashworth, R .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1996, 7 (10) :370-374
[10]   An update on the CNS actions of TRH and its analogs [J].
Horita, A .
LIFE SCIENCES, 1998, 62 (17-18) :1443-1448