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Dr Richard Gordon
Dr

Richard Gordon

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Overview

Background

Dr. Richard Gordon leads a multi-disciplinary, industry-partnered research program in Translational Neuroscience which integrates immunology, drug development, pharmacology, metabolomics and microbial metagenomics. His group aims to understand and therapeutically target key pathological mechanisms which drive the onset and progression of neurodegenerative disorders such as Parkinson’s disease (PD) and Amyotrophic Lateral Sclerosis (ALS). Their work combines target validation studies in human patients with mechanistic insights from disease models to develop and test novel therapeutic strategies that can be translated towards clinical trials.

Key research themes within this program include:

  • Understanding how chronic immune and inflammasome activation contribute to neurodegeneration in the CNS
  • The role of gut dysbiosis and gastrointestinal dysfunction in Parkinson’s disease pathophysiology
  • Therapeutic targeting of the gut-brain axis for neuroprotection
  • Drug discovery, development and repositioning for novel therapeutic targets
  • Discovery and validation of clinical biomarkers for PD and ALS
  • Clinical trials for disease-modifying therapeutic strategies

Availability

Dr Richard Gordon is:
Available for supervision
Media expert

Qualifications

  • Doctor of Philosophy, University of Iowa
  • Australasian Society of Clinical & Experimental Pharmacologists & Toxicologists, Australasian Society of Clinical & Experimental Pharmacologists & Toxicologists

Research interests

  • Understanding and targeting the gut-brain axis in neurodegeneration

  • Targeting immune and inflammatory mechanisms for neuroprotection

  • Novel therapeutic approaches for regeneration of the central nervous system

  • Clinical bio-markers for early detection of Parkinson's disease

  • In silico approaches for therapeutic development

  • Drug repositioning to accelerate new treatments for progressive neurodegenerative disorders

Research impacts

Dr. Gordon’s research has contributed to ground-breaking advances in the field of neuroinflammation and Parkinson’s disease, including discovery of a novel signalling paradigm for prokineticin signalling during neurodegeneration, and inflammasome activation as a driver of synuclein pathology and disease progression in PD. He established the Queensland Drug Repurposing Initiative (QDRI) which aims to accelerate new treatments for neurological diseases through drug repositioning. He is the Research Lead for the COMBO-PD clinical trial at UQ which is evaluating the therapeutic potential of restoring beneficial gut microbiota which are depleted in people with PD.

Dr. Gordon is a Board-certified toxicologist with the American Board of Toxicology (DABT) and has served as a member of the Gene Technology Technical Advisory Committee for the Australian Federal Government. He is also a Science Ambassador for the World Parkinson Coalition (WPC) for Australia and the Asia Pacific Region.

Works

Search Professor Richard Gordon’s works on UQ eSpace

42 works between 2011 and 2023

21 - 40 of 42 works

2018

Journal Article

An overview of sleep and circadian dysfunction in Parkinson's disease

Mantovani, Susanna, Smith, Simon S., Gordon, Richard and O'Sullivan, John D. (2018). An overview of sleep and circadian dysfunction in Parkinson's disease. Journal of Sleep Research, 27 (3) e12673, e12673. doi: 10.1111/jsr.12673

An overview of sleep and circadian dysfunction in Parkinson's disease

2018

Journal Article

Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour

Giacomin, Paul R., Kraeuter, Ann Katrin, Albornoz, Eduardo A., Jin, Shuting, Bengtsson, Mia, Gordon, Richard, Woodruff, Trent M., Urich, Tim, Sarnyai, Zoltán and Soares Magalhães, Ricardo J. (2018). Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour. The Journal of Infectious Diseases, 218 (9), 1511-1516. doi: 10.1093/infdis/jiy092

Chronic helminth infection perturbs the gut-brain axis, promotes neuropathology and alters behaviour

2018

Conference Publication

C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation

Gordon, Richard, Albornoz, Eduardo, Kanthasamy, Anumantha and Woodruff, Trent (2018). C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation. 27th International Complement Workshop (ICW), Santa Fe, NM, United States, Sep 16-20, 2018. Kidlington, Oxford, United Kingdom: Pergamon Press. doi: 10.1016/j.molimm.2018.06.247

C5aR1 is required for a-synuclein mediated NLRP3 inflammasome activation

2018

Book Chapter

Inflammasomes in CNS diseases

Albornoz, Eduardo A., Woodruff, Trent M. and Gordon, Richard (2018). Inflammasomes in CNS diseases. Inflammasomes: clinical and therapeutic implications. (pp. 41-60) edited by Mario D. Cordero and Elisabet Alcocer-Gómez. Cham, Switzerland: Springer International. doi: 10.1007/978-3-319-89390-7_3

Inflammasomes in CNS diseases

2017

Journal Article

The ketone body β-hydroxybutyrate does not inhibit synuclein mediated inflammasome activation in microglia

Deora, Vandana, Albornoz, Eduardo A., Zhu, Kevin, Woodruff, Trent M. and Gordon, Richard (2017). The ketone body β-hydroxybutyrate does not inhibit synuclein mediated inflammasome activation in microglia. Journal of Neuroimmune Pharmacology, 12 (4), 1-7. doi: 10.1007/s11481-017-9754-5

The ketone body β-hydroxybutyrate does not inhibit synuclein mediated inflammasome activation in microglia

2017

Book Chapter

Neuroinflammation as a therapeutic target in neurodegenerative diseases

Gordon, Richard and Woodruff, Trent M. (2017). Neuroinflammation as a therapeutic target in neurodegenerative diseases. Disease-modifying targets in neurodegenerative disorders: paving the way for disease-modifying therapies. (pp. 49-80) edited by Veerle Baekelandt and Evy Lobbestael. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-805120-7.00003-8

Neuroinflammation as a therapeutic target in neurodegenerative diseases

2017

Conference Publication

Motor neuron disease proteins activate complement and generate C5a

Deora, Vandana, Mantovani, Susanna, Yerbury, Justin, Clark, Richard, Atkin, Julie, Lee, John, Gordon, Richard and Woodruff, Trent M. (2017). Motor neuron disease proteins activate complement and generate C5a. 16th European Meeting on Complement in Human Disease (EMCHD), Copenhagen, Denmark, 8-12 September 2017. Kidlington, Oxford, United Kingdom: Pergamon Press. doi: 10.1016/j.molimm.2017.06.144

Motor neuron disease proteins activate complement and generate C5a

2017

Book Chapter

Neuroinflammation as a therapeutic target in neurodegenerative diseases

Gordon, Richard and Woodruff, Trent M. (2017). Neuroinflammation as a therapeutic target in neurodegenerative diseases. Disease-modifying targets in neurodegenerative disorders. (pp. 43-64) edited by Veerle Baekelandt and Evy Lobbestael. Boston, MA, United States: Academic Press (Elsevier Press).

Neuroinflammation as a therapeutic target in neurodegenerative diseases

2017

Conference Publication

Gut microbiome changes induced by experimental trichuris muris infection are associated with decreased cognitive function in mice

Magalhaes, Ricardo J. Soares, Giacomin, Paul, Sarnyay, Zoltan, Kraeuter, Ann, Urich, Tim, Bengtsson, Mia, Jin, Shuting, Albornoz, Eduardo A., Gordon, Richard and Woodruff, Trent (2017). Gut microbiome changes induced by experimental trichuris muris infection are associated with decreased cognitive function in mice. 65th Annual Meeting of the American-Society-of-Tropical-Medicine-and-Hygiene (ASTMH), Atlanta, GA, United States, 13-16 November 2016. Deerfield, United States: American Society of Tropical Medicine and Hygiene.

Gut microbiome changes induced by experimental trichuris muris infection are associated with decreased cognitive function in mice

2016

Journal Article

p73 gene in dopaminergic neurons is highly susceptible to manganese neurotoxicity

Kim, Dong-Suk, Jin, Huajun, Anantharam, Vellareddy, Gordon, Richard, Kanthasamy, Arthi and Kanthasamy, Anumantha G. (2016). p73 gene in dopaminergic neurons is highly susceptible to manganese neurotoxicity. NeuroToxicology, 59, 231-239. doi: 10.1016/j.neuro.2016.04.012

p73 gene in dopaminergic neurons is highly susceptible to manganese neurotoxicity

2016

Conference Publication

Complement C5a activates microglial NLRP3 inflammasomes and drives neurodegeneration in Parkinson's disease through C5aR1

Gordon, Richard, Albornoz, Eduardo A., Kumar, Vinod, Zhou, Kiane, Garin-Michaud, Ashoka, Mantavani, Susanna, Kanthasamy, Anumantha G. and Woodruff, Trent M. (2016). Complement C5a activates microglial NLRP3 inflammasomes and drives neurodegeneration in Parkinson's disease through C5aR1. The XXVI International Complement Workshop (ICW), Kanazawa, Japan, 4-8 September 2016. Muenchen, Germany: Elsevier. doi: 10.1016/j.imbio.2016.06.146

Complement C5a activates microglial NLRP3 inflammasomes and drives neurodegeneration in Parkinson's disease through C5aR1

2016

Conference Publication

The complement C5a receptor, C5aR2 contributes to motor deficits in mouse models of Huntington's and Parkinson's disease

Li, R., Levin, S., Lee, J., Gordon, R. and Woodruff, T. (2016). The complement C5a receptor, C5aR2 contributes to motor deficits in mouse models of Huntington's and Parkinson's disease. International Congress of Immunology (ICI), Melbourne, Australia, 21-26 August 2016. Weinheim, Germany: Wiley - VCH. doi: 10.1002/eji.201670200

The complement C5a receptor, C5aR2 contributes to motor deficits in mouse models of Huntington's and Parkinson's disease

2016

Conference Publication

A pathogenic role for the C5a receptor, C5aR2, in mouse models of Huntington's and Parkinson's disease

Li, Rui, Lee, John D., Levin, Samantha, Gordon, Richard and Woodruff, Trent M. (2016). A pathogenic role for the C5a receptor, C5aR2, in mouse models of Huntington's and Parkinson's disease. The XXVI International Complement Workshop (ICW), Kanazawa, Japan, 4-8 September 2016. Muenchen, Germany: Elsevier. doi: 10.1016/j.imbio.2016.06.186

A pathogenic role for the C5a receptor, C5aR2, in mouse models of Huntington's and Parkinson's disease

2015

Journal Article

Fyn kinase regulates microglial neuroinflammatory responses in cell culture and animal models of parkinson’s disease

Panicker, Nikhil, Saminathan, Hariharan, Jin, Huajun, Neal, Matthew, Harischandra, Dilshan S., Gordon, Richard, Kanthasamy, Kavin, Lawana, Vivek, Sarkar, Souvarish, Luo, Jie, Anantharam, Vellareddy, Kanthasamy, Anumantha G. and Kanthasamy, Arthi (2015). Fyn kinase regulates microglial neuroinflammatory responses in cell culture and animal models of parkinson’s disease. Journal of Neuroscience, 35 (27), 10058-10077. doi: 10.1523/JNEUROSCI.0302-15.2015

Fyn kinase regulates microglial neuroinflammatory responses in cell culture and animal models of parkinson’s disease

2015

Journal Article

Antiallodynic effects of alpha lipoic acid in an optimized RR-EAE mouse model of MS-neuropathic pain are accompanied by attenuation of upregulated BDNF-TrkB-ERK signalling in the dorsal horn of the spinal cord

Khan, Nemat, Gordon, Richard, Woodruff, Trent M. and Smith, Maree T. (2015). Antiallodynic effects of alpha lipoic acid in an optimized RR-EAE mouse model of MS-neuropathic pain are accompanied by attenuation of upregulated BDNF-TrkB-ERK signalling in the dorsal horn of the spinal cord. Pharmacology Research and Perspectives, 3 (3) e00137, 1-16. doi: 10.1002/prp2.137

Antiallodynic effects of alpha lipoic acid in an optimized RR-EAE mouse model of MS-neuropathic pain are accompanied by attenuation of upregulated BDNF-TrkB-ERK signalling in the dorsal horn of the spinal cord

2015

Conference Publication

Peripheral immune complement activation in neurodegenerative disease

Mantovani, S., Gordon, R., Ngo, S., Pfluger, C., O'Sullivan, J., Noakes, P., Henderson, R., McCombe, P. and Woodruff, T. (2015). Peripheral immune complement activation in neurodegenerative disease. 25th Biennial Meeting of the International-Society-for-Neurochemistry Jointly with the 13th Meeting of the Asian-Pacific-Society-for-Neurochemistry in Conjunction with the 35th Meeting of the Australasian-Neuroscience-Society, Cairns Australia, 23-27 August 2015. Chichester, West Sussex, United Kingdom: Wiley-Blackwell. doi: 10.1111/jnc.13188

Peripheral immune complement activation in neurodegenerative disease

2015

Conference Publication

Paraquat activates the NLRP3 Inflammasome in microglia via the NADPH oxidase pathway

Albornoz, E., Deora, V., Robertson, B. A., Cooper, M. A., Schroder, K., Woodruff, T. M. and Gordon, R. (2015). Paraquat activates the NLRP3 Inflammasome in microglia via the NADPH oxidase pathway. International Congress of Immunology (ICI), Melbourne, Australia, Aug 21-26, 2016. Weinheim, Germany: Wiley-Blackwell.

Paraquat activates the NLRP3 Inflammasome in microglia via the NADPH oxidase pathway

2014

Journal Article

Elevation of the terminal complement activation products C5a and C5b-9 in ALS patient blood

Mantovani, S., Gordon, R., Macmaw, J. K., Plfluger, C. M., Henderson, R. D., Noakes, P. G., McCombe, P. A. and Woodruff, T. M. (2014). Elevation of the terminal complement activation products C5a and C5b-9 in ALS patient blood. Journal of Neuroimmunology, 276 (1-2), 213-218. doi: 10.1016/j.jneuroim.2014.09.005

Elevation of the terminal complement activation products C5a and C5b-9 in ALS patient blood

2013

Conference Publication

Behavioural and pathological phenotyping of the C57BL/6J BACHD transgenic mouse model of Huntington’s disease

Mantovani, S., Li, R., Gordon, R., Kumar, V., Taylor, S. and Woodruff, T. M. (2013). Behavioural and pathological phenotyping of the C57BL/6J BACHD transgenic mouse model of Huntington’s disease. World Congress on Huntington’s disease, Rio de Janeiro, Brazil, 15-18 September 2013. Amsterdam, Netherlands: I O S Press.

Behavioural and pathological phenotyping of the C57BL/6J BACHD transgenic mouse model of Huntington’s disease

2012

Journal Article

Proteolytic activation of proapoptotic kinase protein kinase Cδ by tumor necrosis factor α death receptor signaling in dopaminergic neurons during neuroinflammation

Gordon, Richard, Anantharam, Vellareddy, Kanthasamy, Anumantha G. and Kanthasamy, Arthi (2012). Proteolytic activation of proapoptotic kinase protein kinase Cδ by tumor necrosis factor α death receptor signaling in dopaminergic neurons during neuroinflammation. Journal of Neuroinflammation, 9 (1) 82. doi: 10.1186/1742-2094-9-82

Proteolytic activation of proapoptotic kinase protein kinase Cδ by tumor necrosis factor α death receptor signaling in dopaminergic neurons during neuroinflammation

Funding

Current funding

  • 2022 - 2025
    Mining the inflammasome-gut microbiome axis to uncover new biomarkers and therapeutic targets for Parkinson's disease
    Research Donation Generic
    Open grant

Past funding

  • 2022 - 2024
    Evaluation of Tolebrutinib as a novel disease-modifying therapeutic for Parkinson's disease
    The Michael J Fox Foundation Therapeutic Pipeline Program
    Open grant
  • 2022
    Targeting inflammasome-driven neuropathology and motor neuron death in MND using a clinically approved cancer drug.
    Motor Neurone Disease Research Institute of Australia Inc Linda Rynalski Bridge Funding Grant
    Open grant
  • 2021 - 2023
    Comparative and Cross Validation of alpha- Synuclein Seeding Assays in Peripheral Biomatrices skin, submandibular gland, CSF, Saliva and Tear Fluids
    University of Georgia
    Open grant
  • 2021 - 2023
    Validating the functional role of the pathogenic microbiome metabolite Trimethylamine (TMA) at the gut-brain axis in Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2021 - 2023
    CNS-targeted inhibitors of neuroinflammation for disease modification in Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2021 - 2023
    Validating a novel glycolipid receptor as a disease-modifying therapeutic target for Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2020 - 2022
    Targeting inflammasome-driven neuropathology and motor neuron death in MND using a clinically approved cancer drug.
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2020 - 2021
    Tipping the Scales on MND: Preclinical testing of a compound with multiple actions to slow disease progression in MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2020 - 2021
    Investigating the immunometabolic nature of motor neurone disease (MND): a study linking metabolism, inflammation, and clinical outcomes in MND patients
    Metro North Hospital and Health Service
    Open grant
  • 2019 - 2022
    Pharmacological targeting of inflammasome activation mechanisms in synuclein models of Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2018 - 2019
    Targeting peripheral inflammatory pathology in Parkinson's disease using repurposed drugs
    Wesley Medical Research Ltd
    Open grant
  • 2018
    Repurposing of clinically validated kinase inhibitors to block chronic neuroinflammation and disease progression in Parkinson's disease
    UQ Development Fellowships
    Open grant
  • 2018 - 2022
    Validating the NLRP3 Inflammasome as a Therapeutic Target in Motor Neuron Disease
    NHMRC Project Grant
    Open grant
  • 2017 - 2019
    Therapeutic switching of a licensed oncology drug to target neuropathology in Parkinson's disease
    The Cure Parkinson's Trust
    Open grant
  • 2017 - 2021
    Drug repurposing for neurodegeneration using Artificial Intelligence and machine learning
    Advance Queensland Research Fellowships
    Open grant
  • 2017 - 2023
    The Queensland Drug Repurposing Initiative
    Queensland Government Advance Queensland Innovation Partnerships
    Open grant
  • 2017 - 2018
    Targeting chronic NLRP3 mediated neuroinflammation in Parkinson?s disease using clinically validated kinase inhibitor drugs
    UQ Early Career Researcher
    Open grant
  • 2016 - 2018
    Pharmacological Targeting of Proinflammatory Kinase Signalling in Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2016 - 2020
    Blocking inflammasome-induced neuroinflammation in PD with a potent, orally available small molecule
    The Michael J Fox Foundation Therapeutic Pipeline Program
    Open grant
  • 2015
    Ian Potter Foundation Travel Award to attend the 'Experimental Biology 2015 Annual Meeting'
    Ian Potter Foundation
    Open grant
  • 2015 - 2017
    Pharmacological targeting of the NLRP3 inflammasome in pre-clinical models of Parkinson's disease using a potent orally active inhibitor
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2015
    Therapeutic targeting of inflammation in Parkinson's disease
    RL Cooper Medical Research Foundation Limited
    Open grant
  • 2015 - 2016
    Therapeutic targeting of the NLRP3 inflammasome using a potent and orally active inhibitor in experimental MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2012 - 2013
    Characterization of the role of complement activation in Parkinson's disease
    UQ New Staff Research Start-Up Fund
    Open grant

Supervision

Availability

Dr Richard Gordon is:
Available for supervision

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Available projects

  • Novel therapeutic strategies targeting the microbiota and gut-brain axis in Parkinson's disease

    Gastrointestinal pathology and alterations in the gut microbiota are often early pathogenic changes seen in Parkinson's disease (PD) and other neurological disorders. Clinical studies suggest that gastrointestinal deficits in people with PD, can often precede cardinal motor symptoms, based on which clinical diagnosis is confirmed. Emerging evidence suggests that specific alternations in the gut microbiota and gastrointestinal deficits are associated with neuronal dysfunction, chronic immune activation and progressive neurodegeneration seen in PD. Our translational research program on the gut-brain axis combines innovative preclinical mechanistic studies in model systems, with powerful big-data analytics on our clinical cohorts to understand the role of gut dysbiosis and gastrointestinal dysfunction in PD, with a focus on therapeutically tractable mechanisms that are involved. We use these insights to develop and test novel and clinically relevant neuroprotective strategies by which to slow, stop or even reverse neurodegeneration in PD.

  • Pharmacological targeting of immune and inflammatory mechanisms for neuroprotection

  • Clinical biomarkers for Parkinson's disease

  • Novel therapeutic approaches for regeneration of the central nervous system

  • AI-based approaches for therapeutic development and drug repositioning

  • Drug discovery, development and repurposing to accelerate therapies for neurodegeneration

Media

Enquiries

Contact Dr Richard Gordon directly for media enquiries about:

  • Drug Repurposing
  • Neuroinflamamtion
  • Parkinson's disease
  • Risk Assessments
  • Toxicology

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