Bai Fengju, Yin Tinggui, Johnstone Edward M, Su Chen, Varga Gabor, Little Sheila P, Nelson David L
Lilly Research Laboratories, Eli Lilly and Co., Indianapolis, IN 46285, USA.
Eur J Pharmacol. 2004 Jan 26;484(2-3):127-39. doi: 10.1016/j.ejphar.2003.11.019.
The human 5-HT(1E) receptor gene was cloned more than a decade ago. Little is known about its function, and there have been no reports of its existence in the genome of small laboratory animals. In this study, attempts to clone the 5-HT(1E) gene from the rat and mouse were unsuccessful. In fact, a search of the mouse genome database revealed that the 5-HT(1E) receptor gene is missing from the mouse genome. However, the 5-HT(1E) gene was cloned from guinea pig genomic DNA and was characterized. The guinea pig 5-HT(1E) receptor gene encodes a protein of 365 amino acids. It shares 88% (nucleic acid) and 95% (amino acid) homology with the human receptor. The guinea pig 5-HT(1E) receptor showed similar pharmacology to the human 5-HT(1E) receptor in radioligand binding assays. Serotonin (5-hydroxytryptamine, 5-HT) dose-dependently stimulated [35S]GTPgammaS binding to the guinea pig 5-HT(1E) receptor with an EC(50) of 13.6+/-1.92 nM, similar to that of the human 5-HT(1E) receptor (13.7+/-1.78 nM). Activation of the guinea pig 5-HT(1E) receptor was also achieved by ergonovine, alpha-methyl-5-HT, 1-naphthylpiperazine, methysergide, tryptamine, and 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI). Methiothepin exhibited antagonist activity. Quantitative real-time polymerase chain reaction (qRT-PCR) analysis showed that 5-HT(1E) mRNA was present in the guinea pig brain with the greatest abundance in the hippocampus, followed by the olfactory bulb. Lower levels were detected in the cortex, thalamus, pons, hypothalamus, midbrain, striatum, and cerebellum. Our current study marks the first identification of the 5-HT(1E) receptor gene in a commonly used laboratory animal species. This finding should allow the elucidation of the receptor's role(s) in the complex coordination of central serotonergic effects.
人类5-HT(1E)受体基因在十多年前就已被克隆出来。关于其功能人们知之甚少,而且在小型实验动物的基因组中也没有其存在的相关报道。在本研究中,从大鼠和小鼠中克隆5-HT(1E)基因的尝试均未成功。事实上,对小鼠基因组数据库的搜索显示,小鼠基因组中缺少5-HT(1E)受体基因。然而,从豚鼠基因组DNA中克隆出了5-HT(1E)基因并对其进行了表征。豚鼠5-HT(1E)受体基因编码一种由365个氨基酸组成的蛋白质。它与人类受体的核酸同源性为88%,氨基酸同源性为95%。在放射性配体结合试验中,豚鼠5-HT(1E)受体表现出与人类5-HT(1E)受体相似的药理学特性。血清素(5-羟色胺,5-HT)以剂量依赖性方式刺激[35S]GTPγS与豚鼠5-HT(1E)受体结合,其半数有效浓度(EC(50))为13.6±1.92 nM,与人类5-HT(1E)受体(13.7±1.78 nM)相似。麦角新碱、α-甲基-5-HT、1-萘基哌嗪、美西麦角、色胺和1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(DOI)也能激活豚鼠5-HT(1E)受体。甲硫哒嗪表现出拮抗活性。实时定量聚合酶链反应(qRT-PCR)分析表明,5-HT(1E) mRNA存在于豚鼠脑中,在海马体中丰度最高,其次是嗅球。在皮质、丘脑、脑桥、下丘脑、中脑、纹状体和小脑中检测到的水平较低。我们目前的研究首次在一种常用的实验动物物种中鉴定出5-HT(1E)受体基因。这一发现应有助于阐明该受体在中枢5-羟色胺能效应复杂协调中的作用。