Hormones and Behaviour Group

Our research aims to uncover the neurobiological mechanisms driving behaviour, including alcohol use, anxiety, and adaptive or maladaptive decision-making. A key priority is understanding sex differences that shape biology and behaviour — helping to close the gap in our knowledge of women’s neurobiology and using these insights to develop more precise, tailored treatments for women.

Research interests

  • The impact of alcohol on the brain
  • Neural circuitry of alcohol-seeking behaviours
  • Identifying novel therapeutic targets
  • Interactions between stress and
    alcohol use
  • Sex differences in binge drinking
  • Alcohol and metabolic hormones
  • Decision-making and hunger hormones
  • Gut-brain axis
Techniques

  • Behavioural models
  • Neuropsychopharmacology
  • Electrophysiology
  • Fiber photometry
  • RNAScope
  • Immunohistochemistry/microscopy
  • Chemogenetics
  • Viral tracing

About our research

Our research aims to identify and to understand neurobiology driving behaviour, including alcohol use, anxiety and adaptive/maladaptive decision-making. We have a major focus on understanding differences between the sexes that may underpin aspects of biology and behaviour – and to help build our fundamental understanding of women’s biology, and how we can use this information to make more precise and tailored treatments for women.

In recent decades, alcohol misuse has risen dramatically in women — by more than 80% compared to 35% in men. Women aged 15–39 in Australia and New Zealand now have the highest global rates of harmful alcohol use. This is particularly concerning as women experience more severe alcohol-related consequences and transition more rapidly from casual drinking to problematic use. Additionally, emerging evidence suggests that some frontline treatments for alcohol use disorder may be less effective or cause more adverse effects in women.

Our lab is dedicated to uncovering the neurobiological mechanisms driving sex differences in decision-making and the development of alcohol use disorder, including its frequent co-occurrence with anxiety, depression and PTSD. By mapping the physiological, molecular and circuit-level processes that shape behaviour, we aim to identify novel treatment targets. Given the historical gap in research on women’s biology, our work is critical for understanding how treatments may differ in effectiveness — or even cause harm — in certain populations. Through this research, we strive to contribute to a more personalised and effective approach to mental health and addiction treatment.

We combine basic physiology and pharmacology with advanced neuroscience techniques (e.g. spatial transcriptomics, chemogenetics, fiber photometry, RNAscope) in close collaboration with the Addiction Neuroscience Group to understand how stress and drugs of abuse change the brain – leveraging this information to identify potential new targets for treatment.

Research team

Research team head

Dr Leigh Walker

Group Head

Team members

Dr Xavier Maddern

Research Fellow

Amy Pearl

Research Assistant

Students

  • Lauren Ursich
  • Kade Huckstep
  • Grace Bailey
  • Jarrah Kron
  • Jaime Spencer
  • Smruti Mhalgi

 

  • Qian Tan
  • Kendall Raymond
  • Isabelle Riches
  • LihFhung Hiew
  • Aaron Perena

Selected publications

  • Pearl AJ, Maddern XJ, Pinares-Garcia P, Ursich LT, Anversa RG, Shesham A, Brown RM, Reed, FM, Giardina WJ, Lawrence AJ and Walker LC (2025), ‘Midbrain ghrelin receptor signalling regulates binge drinking in a sex specific manner’, Nature Communications, doi:10.1038/s41467-025-57880-w
  • Maddern XJ, Ursich LT, Walker LC (2025). Rapid estrogen signaling drives binge drinking. Trends in Neurosciences, doi:1016/j.tins.2025.02.001
  • Maddern XJ, Ursich LT, Bailey G, Pearl A, Anversa RG, Lawrence AJ, Walker LC (2024), ‘Sex differences in alcohol use: is it all about hormones?’, Endocrinology, Sep;165(9):bqae088
  • Maddern XJ, Letherby B, Ch’ng SS, Pearl A, Gogos A, Lawrence AJ and Walker LC (2023), ‘Cocaine and amphetamine regulated transcript (CART) mediates sex differences in binge drinking through central taste circuits’, Neuropsychopharmacology, doi:10.1038/s41386-023-01712-2
  • Walker LC, Hand LJ, Letherby B, Huckstep KL, Campbell EJ and Lawrence AJ (2020), ‘Cocaine and amphetamine regulated transcript (CART) signalling in the central nucleus of the amygdala modulates stress-induced alcohol seeking’, Neuropsychopharmacology (2020) 0:1–9, doi:10.1038/s41386-020-00807-4
  • Pomrenze MB, Walker LC and Giardino WJ (2021) ‘Gray areas: Neuropeptide circuits linking the Edinger-Westphal and Dorsal Raphe nuclei in addiction’, Neuropharmacology 198 (2021) 108769
  • Walker LC, Huckstep KL, Becker HC, Langmead CJ, Lawrence AJ (2024), ‘Targeting muscarinic receptors for the treatment of alcohol use disorders: Opportunities and hurdles for clinical development’, British Journal of Pharmacology, doi: 10.1111/bph.16081

 

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