Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Int J Mol Sci. 2021 Jun 9;22(12):6230. doi: 10.3390/ijms22126230.
Selective antagonists of thyrotropin-releasing hormone (TRH; pGlu-His-Pro-NH), in order to enable a better understanding of this peptide's central functions, have not been identified. Using pGlu-Glu-Pro-NH ([Glu]TRH) as a lead peptide and with modification at its central residue, our studies focused on some of its analogues synthesized as potential functional antagonists of TRH in the rodent brain. Among the peptides studied, the novel isomeric analogue [β-Glu]TRH was found to suppress the analeptic and antidepressant-like pharmacological activities of TRH without eliciting intrinsic effects in these paradigms. [β-Glu]TRH also completely reversed TRH's stimulation of acetylcholine turnover in the rat hippocampus without a cholinergic activity of its own, which was demonstrated through in vivo microdialysis experiments. Altogether, [β-Glu]TRH emerged as the first selective functional antagonist of TRH's prominent cholinergic actions, by which this endogenous peptide elicits a vast array of central effects.
为了更好地理解促甲状腺激素释放激素 (TRH;pGlu-His-Pro-NH) 的中枢功能,尚未鉴定出其选择性拮抗剂。我们使用 pGlu-Glu-Pro-NH([Glu]TRH) 作为先导肽,并对其中心残基进行修饰,专注于合成一些作为潜在功能性 TRH 拮抗剂的类似物,以用于啮齿动物大脑。在所研究的肽中,新型异构类似物 [β-Glu]TRH 被发现可抑制 TRH 的觉醒和抗抑郁样药理作用,而在这些模型中不会引起内在作用。[β-Glu]TRH 还完全逆转了 TRH 对大鼠海马乙酰胆碱周转率的刺激作用,而自身没有胆碱能活性,这通过体内微透析实验得到了证明。总的来说,[β-Glu]TRH 成为 TRH 突出的胆碱能作用的第一个选择性功能拮抗剂,通过这种内源性肽引发了广泛的中枢作用。