Relaxin family peptide receptor 3 (RXFP3) expressing cells in the zona incerta/lateral hypothalamus augment behavioural arousal

Author:

Richards Brandon K.123ORCID,Ch'ng Sarah S.12ORCID,Simon Ariel B.12,Pang Terence Y.124,Kim Jee Hyun125,Lawrence Andrew J.12ORCID,Perry Christina J.123

Affiliation:

1. The Florey Institute of Neuroscience and Mental Health Parkville Victoria Australia

2. Florey Department of Neuroscience and Mental Health The University of Melbourne Parkville Victoria Australia

3. School of Psychological Sciences Macquarie University North Ryde New South Wales Australia

4. Institute of Health and Sports (IHES) Victoria University Footscray Victoria Australia

5. IMPACT—The Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Deakin University Geelong Victoria Australia

Abstract

AbstractFear‐related psychopathologies, such as post‐traumatic stress disorder, are linked to dysfunction in neural circuits that govern fear memory and arousal. The lateral hypothalamus (LH) and zona incerta (ZI) regulate fear, but our understanding of the precise neural circuits and cell types involved remains limited. Here, we examined the role of relaxin family peptide receptor 3 (RXFP3) expressing cells in the LH/ZI in conditioned fear expression and general arousal in male RXFP3‐Cre mice. We found that LH/ZI RXFP3+ (LH/ZIRXFP3) cells projected strongly to fear learning, stress, and arousal centres, notably, the periaqueductal grey, lateral habenula, and nucleus reuniens. These cells do not express hypocretin/orexin or melanin‐concentrating hormone but display putative efferent connectivity with LH hypocretin/orexin+ neurons and dopaminergic A13 cells. Following Pavlovian fear conditioning, chemogenetically activating LH/ZIRXFP3 cells reduced fear expression (freezing) overall but also induced jumping behaviour and increased locomotor activity. Therefore, the decreased freezing was more likely to reflect enhanced arousal rather than reduced fear. Indeed, stimulating these cells produced distinct patterns of coactivation between several motor, stress, and arousal regions, as measured by Fos expression. These results suggest that activating LH/ZIRXFP3 cells generates brain‐wide activation patterns that augment behavioural arousal.image

Funder

National Health and Medical Research Council

Australian Research Council

International Society for Neurochemistry

Publisher

Wiley

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