Inverse agonist and neutral antagonist actions of synthetic compounds at an insect 5‐HT1 receptor

• Published in: British journal of pharmacology 2010-04, Vol.159 (7), p.1450-1462
• Main Authors: Troppmann, B, Balfanz, S, Baumann, A, Blenau, W
• Format: Article
• Language: English
• Subjects: 5‐HT; Amino Acid Sequence; Animals; Base Sequence; biogenic amine; Biological and medical sciences; Cell Line; cellular signalling; Cloning, Molecular; constitutive activity; DNA Primers; DNA, Complementary; G‐protein‐coupled receptor; Humans; Immunohistochemistry; insect; Medical sciences; methiothepin; Molecular Sequence Data; Neurosciences; Periplaneta - genetics; Periplaneta - metabolism; Periplaneta americana; Pharmacology. Drug treatments; Phylogeny; Receptors, Serotonin, 5-HT1 - chemistry; Receptors, Serotonin, 5-HT1 - drug effects; Receptors, Serotonin, 5-HT1 - genetics; Research Papers; Reverse Transcriptase Polymerase Chain Reaction; salivary gland; Sequence Homology, Amino Acid; serotonin; Serotonin Antagonists - pharmacology; WAY 100635
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1111/j.1476-5381.2010.00638.x

Background and purpose:  5‐Hydroxytryptamine (5‐HT) has been shown to control and modulate many physiological and behavioural functions in insects. In this study, we report the cloning and pharmacological properties of a 5‐HT1 receptor of an insect model for neurobiology, physiology and pharmacology. Experimental approach:  A cDNA encoding for the Periplaneta americana 5‐HT1 receptor was amplified from brain cDNA. The receptor was stably expressed in HEK 293 cells, and the functional and pharmacological properties were determined in cAMP assays. Receptor distribution was investigated by RT‐PCR and by immunocytochemistry using an affinity‐purified polyclonal antiserum. Key results:  The P. americana 5‐HT1 receptor (Pea5‐HT1) shares pronounced sequence and functional similarity with mammalian 5‐HT1 receptors. Activation with 5‐HT reduced adenylyl cyclase activity in a dose‐dependent manner. Pea5‐HT1 was expressed as a constitutively active receptor with methiothepin acting as a neutral antagonist, and WAY 100635 as an inverse agonist. Receptor mRNA was present in various tissues including brain, salivary glands and midgut. Receptor‐specific antibodies showed that the native protein was expressed in a glycosylated form in membrane samples of brain and salivary glands. Conclusions and implications:  This study marks the first pharmacological identification of an inverse agonist and a neutral antagonist at an insect 5‐HT1 receptor. The results presented here should facilitate further analyses of 5‐HT1 receptors in mediating central and peripheral effects of 5‐HT in insects.