Adrenergic Agonists Activate Transcriptional Activity in Immortalized Neuronal Cells From the Mouse Suprachiasmatic Nucleus

Author:

Langiu Monica12,Dehghani Faramarz3,Hohmann Urszula3,Bechstein Philipp1,Rawashdeh Oliver14ORCID,Rami Abdelhaq1,Maronde Erik1ORCID

Affiliation:

1. Institute for Anatomy II Goethe University Frankfurt Frankfurt Germany

2. Monash Institute of Pharmaceutical Sciences Monash University Parkville Victoria Australia

3. Department of Anatomy and Cell Biology, Medical Faculty Martin Luther University Halle‐Wittenberg Halle (Saale) Germany

4. School of Biomedical Sciences, Faculty of Medicine The University of Queensland Brisbane Queensland Australia

Abstract

ABSTRACTThe suprachiasmatic nucleus of the hypothalamus (SCN) houses the central circadian oscillator of mammals. The main neurotransmitters produced in the SCN are γ‐amino‐butyric acid, arginine‐vasopressin (AVP), vasoactive intestinal peptide (VIP), pituitary‐derived adenylate cyclase‐activating peptide (PACAP), prokineticin 2, neuromedin S, and gastrin‐releasing peptide (GRP). Apart from these, catecholamines and their receptors were detected in the SCN as well. In this study, we confirmed the presence of β‐adrenergic receptors in SCN and a mouse SCN‐derived immortalized cell line by immunohistochemical, immuno‐cytochemical, and pharmacological techniques. We then characterized the effects of β‐adrenergic agonists and antagonists on cAMP‐regulated element (CRE) signaling. Moreover, we investigated the interaction of β‐adrenergic signaling with substances influencing parallel signaling pathways. Our findings have potential implications on the role of stress (elevated adrenaline) on the biological clock and may explain some of the side effects of β‐blockers applied as anti‐hypertensive drugs.

Publisher

Wiley

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