Michael Ritchie Moore

B.Sc., Ph.D., D.Sc., FACTRA
Australian College of Toxicology and Risk Assessment · Vice-President

Topics (31) View all

Skills (4)

Research experience

  • Teaching: Toxicology and Risk Assessment
  • Apr 2012–
    present
    Research: Strategic Pesticides Advisory Working Group (SPAWG)
    GRDC
    Australia · Canberra
  • May 2010–
    Jun 2013
    Research: JFES
    Mater Hospital · Mater Research
    Defence
  • Mar 2009–
    present
    Research: Emeritus Professor
    University of Queensland 
    Australia · Brisbane
  • Jul 2008–
    present
    Research: Water Quality Research
    WQRA · Corporate
    Water
  • Jul 2008–
    present
    Research: UPTECH Adjunct Professor
    Queensland University of Technology · Queensland University of Technology
    BNE
    ultrafine particulates and Health
  • Jan 2006–
    present
    Research: Vitamin D and sun exposure Adjunct Professor
    Queensland University of Technology · IHBI, NHMRC Centre for Research Excellence in Sunlight & Health · Queensland University of Technology
    Australia · BNE
    Sun, Cancer, Osteomalacia, Vitamin D
  • Jan 2006–
    present
    Research: Queensland University of Technology Adjunct Professor
    Queensland University of Technology · Faculty of Health
    Australia · Brisbane
  • Jul 2002–
    present
    Research: Adjunct Professor
    University of the Sunshine Coast
    Australia
  • Jan 2002
    Research: Queensland Government
    Queensland Government
    Australia · Brisbane
  • Jun 2001–
    present
    Research: SmartWater Honorary Professor
    Griffith University · SmartWater · Griffith University
    Gold Coast
    Water quality, DBPs, Risk assessment
  • Jan 1998
    Research: Director
    Queensland Health · Queensland Health Scientific Services
    Australia · Brisbane
  • Jul 1997–
    Jul 2007
    Research: Water Quality
    CRC · n/a · CRC
    CRC WQT · BNE
    Water, Cyanobacteria, Risk assessment
  • Jul 1995–
    present
    Research: Honorary Professor
    Griffith University
    Australia · Brisbane
  • Jul 1994–
    Dec 2009
    Research: University of Queensland  Director and Professor
    University of Queensland  · National Research Centre for Environmental Toxicology
    Australia · Brisbane
  • Jul 1994–
    Feb 2009
    Research: Drugs and Porphyria
    University of Queensland  · EnTox · University of Queensland 
    Porphyrias group · BNE
    Porphyria, Drugs, Drug lists
  • Jan 1994
    Research: The University of Edinburgh
    The University of Edinburgh · Division of Psychiatry
    United Kingdom · Edinburgh
  • Jan 1993
    Research: Universidad de Oviedo
    Universidad de Oviedo · Department of Cell Biology and Morphology
    Spain · Oviedo
  • Jan 1993
    Research: Glasgow Royal Infirmary
    Glasgow Royal Infirmary
    United Kingdom · Glasgow
  • Jan 1990–
    Dec 1991
    Research: City of Glasgow College
    City of Glasgow College
    United Kingdom · Glasgow
  • Jun 1982–
    Jul 1983
    Research: University of Cape Town
    University of Cape Town · Department of Medicine · Porphyrias
    South Africa · Cape Town
  • Nov 1979–
    Jul 1994
    Research: Porphyrinogenicity of Drugs
    University of Glasgow · Medicine · University of Glasgow
    Porphyrias Group · Glasgow
    Porphyrins, Porphyria, Drugs
  • Jan 1975–
    Jul 1994
    Research: University of Strathclyde
    University of Strathclyde
    United Kingdom · Glasgow
  • Sep 1967–
    Jun 1994
    Research: Lead toxicology
    University of Glasgow · Medicine, Materia Medica, Medicine & Therapeutics · University of Glasgow
    MRC Group in Iron & Porphyrin Metabolism · Glasgow
    Lead
  • Jan 1967–
    Jun 1994
    Research: University of Glasgow
    University of Glasgow · School of Medicine
    United Kingdom · Glasgow

Education

  • Apr 1992–
    May 1992
    National Health Service
    Management
    United Kingdom · Glasgow
  • Mar 1983
    Royal postgraduate Medical School
    United Kingdom · London
  • Sep 1962–
    Nov 1989
    University of Glasgow
    B.Sc., Ph.D., D.Sc.
    United Kingdom · Glasgow

Awards & achievements

  • May 2013
    Award: Fellow of the Australasian College of Toxicology & Risk Assessment
  • Jul 1997
    Award: Registered Toxicologist, Institute of Biology/BTS
  • Nov 1989
    Award: Miembro de l'Academia Ciencas Medicas
  • May 1987
    Award: Albert Szent-Gyorgi Medal University of Szeged

Other

  • Languages
    English (Scottish & Australian)
    French
  • Scientific Memberships
    ACTRA
    Biochemical Society
    British Toxicological Society
    Eurotox
    AWA
    IWA
  • Journal Referees
    Vital and health statistics. Series 21, Data on natality, marriage, and divorce
  • Other Interests
    Photography Walking, Nature, Biochem J, Science, Disorders of Porphyrin Metabolism,
    Australasian College of Toxicology and Risk Assessment (ACTRA)
    APVMA
    ACPM
    Toxikos
    ADEC
    NDPSC
    GRDC
    Monklands and Bellshill NHS Trust
    Lanarkshire Health Council
    The Clock Theatre Kilsyth

Questions and Answers (2) View all

  • Answer added in Marine Ecology
    13 Is Ciguatera Fish Poisoning a Neglected Tropical Disease?
    By Steven Kibler · National Oceanic and Atmospheric Administration
    Michael Moore · Australian College of Toxicology and Risk Assessment
    Not a disease - a poisoning. Many species of fish in the Pacific, Carribean and Indian oceans (in the peri-equatorial regions) can carry this toxin. ... [more]

Publications (607) View all

  • Article: Striking association between urinary cadmium level and albuminuria among Torres Strait Islander people with diabetes.
    [show abstract] [hide abstract]
    ABSTRACT: Indigenous people of the Torres Strait (Australia) have greater potential for cadmium exposure and renal damage than other Australians due to high cadmium in some traditional seafood and a high prevalence of Type 2 diabetes, hypertension, smoking, and obesity. This study explored associations between albuminuria and an index of cadmium exposure (urinary cadmium excretion) in the presence and absence of Type 2 diabetes. Two population-based, cross-sectional studies were undertaken in the Torres Strait to obtain data on body mass index (BMI), blood pressure, chronic disease, smoking, urinary cadmium, and albumin creatinine ratio (ACR). Age- and BMI-adjusted urinary cadmium levels were significantly higher (p<0.01) among people with diabetes and albuminuria (n=22, geometric mean (GM) 1.91 microg Cd/g creatinine) compared to those with diabetes and normal ACR (n=21, GM 0.74 microg Cd/g creatinine). Urinary cadmium was also strongly associated (p<0.001) with ACR among people with diabetes in regression models and remained significant after controlling for age, sex, BMI, smoking status, and hypertension (or continuous systolic and diastolic measurements). While the study has methodological limitations and the nature of the association is unclear, the striking dose-dependent links between markers of cadmium exposure and of Type 2 diabetic nephropathy highlight the need for further definitive research on the health effects of cadmium in the presence of diabetes.
    Environmental Research 04/2008; 106(3):379-83. · 3.40 Impact Factor
  • Article: Does a high UV environment ensure adequate vitamin D status?
    [show abstract] [hide abstract]
    ABSTRACT: This study assesses the Vitamin D status of 126 healthy free-living adults aged 18-87 years, in southeast Queensland, Australia (27 degrees S) at the end of the 2006 winter. Participants provided blood samples for analysis of 25(OH)D (the measure of an individual's Vitamin D status), PTH, Calcium, Phosphate, and Albumin, completed a questionnaire on sun-protective/sun-exposure behaviours, and were assessed for phenotypic characteristics such as skin/hair/eye colour and BMI. We found that 10.2% of the participants had serum 25(OH)D levels below 25 nmol/l (considered deficient) and a further 32.3% had levels between 25 nmol/l and 50 nmol/l (considered insufficient). Our results show that low levels of 25(OH)D can occur in a substantial proportion of the population at the end of winter, even in a sunny climate. 25(OH)D levels were higher amongst those who spent more time in the sun and lower among obese participants (BMI>30) than those who were not obese (BMI<30). 25(OH)D levels were also lower in participants who had black hair, dark/olive skin, or brown eyes, when compared with participants who had brown or fair hair, fair skin, or blue/green eyes. No associations were found between 25(OH)D status and age, gender, smoking status, or the use of sunscreen.
    Journal of Photochemistry and Photobiology B Biology 12/2007; 89(2-3):139-47. · 2.81 Impact Factor
  • Article: Exploring potential dietary contributions including traditional seafood and other determinants of urinary cadmium levels among indigenous women of a Torres Strait Island (Australia).
    [show abstract] [hide abstract]
    ABSTRACT: Indigenous people of the Torres Strait Islands have been concerned about the safety of their traditional seafoods since the discovery of high cadmium levels in the liver and kidney of dugong and turtle in 1996. This study explored links between urinary cadmium levels and consumption frequency of these traditional foods and piloted a community-based methodology to identify potential determinants of cadmium exposure and accumulation. Consultations led to selection of one community for study from which 60 women aged 30 to 50 years participated in health and food frequency survey, urine collection and a routine health check. Urinary cadmium levels were determined by inductively coupled plasma-mass spectrometry; data were analysed using SPSS-14. The geometric mean cadmium level in this group of women was 1.17 (arithmetic mean 1.86) microg/g creatinine with one-third exceeding 2.0 microg/g creatinine. Heavy smoking (>or=300 pack years) was linked to higher cadmium in urine, as was increasing age and waist circumference. Analysis of age-adjusted residuals revealed significant associations (P<0.05) between cadmium level and higher consumption of turtle liver and kidney, locally gathered clams, peanuts, coconut, chocolate and potato chips. Dugong kidney consumption approached significance (P=0.06). Multiple regression revealed that 40% (adjusted r(2)) of variation in cadmium level was explained by the sum of these associated foods plus heavy smoking, age and waist circumference. No relationships between cadmium and pregnancy history were found. This paper presents a novel approach to explore contributions of foods and other factors to exposure to toxins at community level and the first direct evidence that frequent turtle (and possibly dugong) liver and kidney and wild clam consumption is linked to higher urinary cadmium levels among Torres Strait Islander women.
    Journal of Exposure Science and Environmental Epidemiology 06/2007; 17(3):298-306. · 2.93 Impact Factor
  • Article: Extraction and purification of the zwitterions cylindrospermopsin and deoxycylindrospermopsin from Cylindrospermopsis raciborskii
    [show abstract] [hide abstract]
    ABSTRACT: The hepatotoxin cylindrospermopsin (CYN) has been isolated from the cyanobacterium Cylindrospermopsis raciborskii (C. raci.). Efforts to study this toxin have been hampered by the time-consuming requirement to extract it from cultures of the organism. It is usually extracted from lyophilized cells collected from a laboratory culture. Our preliminary work suggested far more of the toxin is available in solution in the culture media than in the cells collected. We have therefore investigated the use of commercially available solid phase extraction sorbents to extract CYN from culture media in which C. raci. has been grown. A range of reverse phase and ion-exchange sorbents were tested across a range of pHs for their ability to retain CYN without success. Subsequently, graphitized carbon cartridges were found to retain CYN strongly. Elution with 5% formic acid in methanol allowed the CYN to be regained for final purification by HPLC. Deoxy-CYN, an analog of CYN can also be extracted using this procedure. (C) 2001 John Wiley & Sons, Inc.
  • Article: A sensitive and specific assay for glutathione with potential application to glutathione disulphide, using high-performance liquid chromatography-tandem mass spectrometry
    [show abstract] [hide abstract]
    ABSTRACT: We have utilised the combination of sensitivity and specificity afforded by coupling high-performance liquid chromatography (HPLC) to a tandem mass spectrometer (MS-MS) to produce an assay which is suitable for assaying glutathione (GSH) concentrations in liver tissue. The sensitivity suggests it may also be suitable for extrahepatic tissues, The method has been validated for GSH using mouse liver samples and also allows the assay of GSSG. The stability of GSH under conditions relevant to the assay has been determined. A 20-mul amount of a diluted methanol extract of tissue is injected with detection limits of 0.2 pmol for GSH and 2 pmol for GSSG. The HPLC uses an Altima C-18 (150X4.6 mm, 5 mum) column at 35 degreesC. Chromatography utilises a linear gradient from 0 to 10% methanol in 0.1% formic acid over 5 min, with a final isocratic stage holding at 10% methanol for 5 min. Total flow rate is 0.8 ml/min. The transition from the M+H ion (308.1 m/z for GSH, and 613.3 m/z for GSSG) to the 162.0 m/z (GSH) and 355.3 m/z (GSSG) fragments are monitored. (C) 2001 Elsevier Science B.V. All rights reserved.

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